PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
32797910-3	2020	Here we report an efficient one-pot method for the immobilization of chiral MOF [Cu2((+)-Cam)2Dabco] (Cu2C2D) onto microspheric silica particles, generating a uniform core-shell microsphere with SiO2@CMOF@CMOF morphology as CSP packing material.	cu2(	81-85	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	224-227
33233251-2	2020	In this study, a novel and effective multifunctional PEG modified CeO2@SiO2 nanoparticle (CSP-NPs) system was successfully fabricated.	Polyethylene Glycols	53-56	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	90-93
33233251-2	2020	In this study, a novel and effective multifunctional PEG modified CeO2@SiO2 nanoparticle (CSP-NPs) system was successfully fabricated.	Silicon Dioxide	71-75	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	90-93
32797910-3	2020	Here we report an efficient one-pot method for the immobilization of chiral MOF [Cu2((+)-Cam)2Dabco] (Cu2C2D) onto microspheric silica particles, generating a uniform core-shell microsphere with SiO2@CMOF@CMOF morphology as CSP packing material.	Silicon Dioxide	128-134	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	224-227
33233251-3	2020	Food derived proanthocyanidin (PAC) and curcumin (Cur) were loaded onto CSP-NPs and formed as PAC-NPs and Cur-NPs.	proanthocyanidin	13-29	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	72-75
33233251-3	2020	Food derived proanthocyanidin (PAC) and curcumin (Cur) were loaded onto CSP-NPs and formed as PAC-NPs and Cur-NPs.	proanthocyanidin	31-34	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	72-75
34923255-6	2022	The homochiral Co-MOF-74-L-Tyr CSP gave superior enantioseparation performance for the eight chiral drugs and drug intermediates, such as nitrendipine, nimodipine, benzoin, 2,2"-furoin and bi-2-naphthol to the commercial columns under normal phase condition.	co-mof-74-l-tyr	15-30	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	31-34
33233251-3	2020	Food derived proanthocyanidin (PAC) and curcumin (Cur) were loaded onto CSP-NPs and formed as PAC-NPs and Cur-NPs.	Curcumin	40-48	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	72-75
33233251-8	2020	Therefore, CSP-NPs might be a promising delivery system for hydrophilic molecule proanthocyanidin and hydrophobic molecule curcumin against the oxidative damage, neurodegenerative diseases and cancer, which could facilitate the application of food derived nutrients in functional foods industry.	proanthocyanidin	81-97	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	11-14
33233251-8	2020	Therefore, CSP-NPs might be a promising delivery system for hydrophilic molecule proanthocyanidin and hydrophobic molecule curcumin against the oxidative damage, neurodegenerative diseases and cancer, which could facilitate the application of food derived nutrients in functional foods industry.	Curcumin	123-131	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	11-14
34875432-1	2022	To optimize the extraction of polysaccharides from coix seeds (CSP), an auxiliary method of ultrasound was developed by response surface methodology (RSM).	Polysaccharides	30-45	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	63-66
34875432-3	2022	Compared to hot water extraction (HE), UE-treated CSP led to a higher extraction efficiency and decreased average CSP molecular weight.	Water	16-21	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	114-117
34875432-4	2022	FT-IR indicated that CSP extracted by UE and HE were neutral polysaccharides, and linkages between sugar units were mainly in the alpha-conformation.	Polysaccharides	61-76	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	21-24
34875432-4	2022	FT-IR indicated that CSP extracted by UE and HE were neutral polysaccharides, and linkages between sugar units were mainly in the alpha-conformation.	Sugars	99-104	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	21-24
34875432-5	2022	Furthermore, NMR spectra indicated that UE-treated CSP was a neutral polysaccharide with (1   6)-linked alpha-d-glucopyranose in the main chain.	ue	40-42	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	51-54
34875432-5	2022	Furthermore, NMR spectra indicated that UE-treated CSP was a neutral polysaccharide with (1   6)-linked alpha-d-glucopyranose in the main chain.	Polysaccharides	69-83	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	51-54
34875432-5	2022	Furthermore, NMR spectra indicated that UE-treated CSP was a neutral polysaccharide with (1   6)-linked alpha-d-glucopyranose in the main chain.	)-linked alpha-d-glucopyranose	95-125	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	51-54
34923255-6	2022	The homochiral Co-MOF-74-L-Tyr CSP gave superior enantioseparation performance for the eight chiral drugs and drug intermediates, such as nitrendipine, nimodipine, benzoin, 2,2"-furoin and bi-2-naphthol to the commercial columns under normal phase condition.	Nitrendipine	138-150	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	31-34
34923255-6	2022	The homochiral Co-MOF-74-L-Tyr CSP gave superior enantioseparation performance for the eight chiral drugs and drug intermediates, such as nitrendipine, nimodipine, benzoin, 2,2"-furoin and bi-2-naphthol to the commercial columns under normal phase condition.	Nimodipine	152-162	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	31-34
34923255-6	2022	The homochiral Co-MOF-74-L-Tyr CSP gave superior enantioseparation performance for the eight chiral drugs and drug intermediates, such as nitrendipine, nimodipine, benzoin, 2,2"-furoin and bi-2-naphthol to the commercial columns under normal phase condition.	Benzoin	164-171	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	31-34
34923255-6	2022	The homochiral Co-MOF-74-L-Tyr CSP gave superior enantioseparation performance for the eight chiral drugs and drug intermediates, such as nitrendipine, nimodipine, benzoin, 2,2"-furoin and bi-2-naphthol to the commercial columns under normal phase condition.	2,2"-furoin	173-184	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	31-34
34923255-6	2022	The homochiral Co-MOF-74-L-Tyr CSP gave superior enantioseparation performance for the eight chiral drugs and drug intermediates, such as nitrendipine, nimodipine, benzoin, 2,2"-furoin and bi-2-naphthol to the commercial columns under normal phase condition.	BINOL, naphthol	189-202	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	31-34
34923255-7	2022	The good repeatability and stability of this CSP was verified by the replicate enantioseparation for nimodipine and flavanone.	Nimodipine	101-111	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	45-48
34923255-7	2022	The good repeatability and stability of this CSP was verified by the replicate enantioseparation for nimodipine and flavanone.	flavanone	116-125	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	45-48
34236859-4	2021	The process begins with regioselective trapping of a 3-trifloxybenzyne intermediate by an O-silyl phosphite in an Abramov-like reaction to bond the strained Csp carbons with phosphorus and silicon.	3-trifloxybenzyne	53-70	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	157-160
34748617-1	2021	Rare and potent monoclonal antibodies (mAbs) against the Plasmodium falciparum (Pf) circumsporozoite protein (CSP) on infective sporozoites (SPZ) preferentially bind the PfCSP junctional tetrapeptide NPDP or NVDP minor repeats while cross-reacting with NANP major repeats in vitro.	nvdp	208-212	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	110-113
34378926-3	2021	Late-stage Csp-Csp3 cross-coupling of a highly functionalized bromoalkyne featured in the pseurotin A2 side-chain assembly.	bromoalkyne	62-73	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	11-14
34378926-3	2021	Late-stage Csp-Csp3 cross-coupling of a highly functionalized bromoalkyne featured in the pseurotin A2 side-chain assembly.	pseurotin	90-99	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	11-14
34236859-4	2021	The process begins with regioselective trapping of a 3-trifloxybenzyne intermediate by an O-silyl phosphite in an Abramov-like reaction to bond the strained Csp carbons with phosphorus and silicon.	o-silyl phosphite	90-107	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	157-160
34236859-4	2021	The process begins with regioselective trapping of a 3-trifloxybenzyne intermediate by an O-silyl phosphite in an Abramov-like reaction to bond the strained Csp carbons with phosphorus and silicon.	Carbon	161-168	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	157-160
34236859-4	2021	The process begins with regioselective trapping of a 3-trifloxybenzyne intermediate by an O-silyl phosphite in an Abramov-like reaction to bond the strained Csp carbons with phosphorus and silicon.	Phosphorus	174-184	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	157-160
34236859-4	2021	The process begins with regioselective trapping of a 3-trifloxybenzyne intermediate by an O-silyl phosphite in an Abramov-like reaction to bond the strained Csp carbons with phosphorus and silicon.	Silicon	189-196	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	157-160
34236859-7	2021	Specifically, the distortion in the internal bond angles at each of the Csp atoms was strongly influenced by both the electronegativity of the phosphonate ester groups as well as the dielectric of the computational solvation model.	phosphonate ester	143-160	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	72-75
35617910-8	2022	With the preferred CSP, the enantioselectivity could be increased for a chiral probe (FMOC-Phe) and the mass transfer resistance (C-term) bisected compared to the corresponding CSP prepared from benchmark MPTMS-modified silica (2.54 vs 5.72 ms).	fmoc	86-90	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	19-22
35257708-1	2022	In this work, the effect of Co substitution in the Fe1-xS (CSP) on the activation of H2O2 to degrade tetracycline (TC) is investigated.	Hydrogen Peroxide	85-89	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	59-62
35257708-1	2022	In this work, the effect of Co substitution in the Fe1-xS (CSP) on the activation of H2O2 to degrade tetracycline (TC) is investigated.	Tetracycline	101-113	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	59-62
35257708-1	2022	In this work, the effect of Co substitution in the Fe1-xS (CSP) on the activation of H2O2 to degrade tetracycline (TC) is investigated.	Tetracycline	115-117	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	59-62
35257708-4	2022	The investigation of Behnajady-Modirshahla-Ghanbery kinetic model (BMG) showed that the maximum initial degradation rate of TC over 1.0% CSP/H2O2 was 1.6 times than that of in CSP/H2O2 system.	Tetracycline	124-126	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	137-140
35257708-4	2022	The investigation of Behnajady-Modirshahla-Ghanbery kinetic model (BMG) showed that the maximum initial degradation rate of TC over 1.0% CSP/H2O2 was 1.6 times than that of in CSP/H2O2 system.	Tetracycline	124-126	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	176-179
35257708-4	2022	The investigation of Behnajady-Modirshahla-Ghanbery kinetic model (BMG) showed that the maximum initial degradation rate of TC over 1.0% CSP/H2O2 was 1.6 times than that of in CSP/H2O2 system.	Hydrogen Peroxide	141-145	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	137-140
35257708-4	2022	The investigation of Behnajady-Modirshahla-Ghanbery kinetic model (BMG) showed that the maximum initial degradation rate of TC over 1.0% CSP/H2O2 was 1.6 times than that of in CSP/H2O2 system.	Hydrogen Peroxide	180-184	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	176-179
35257708-6	2022	The quenching experiments and ESR determined that  OH,  O2- and 1O2 were involved in TC degradation with the treatment of 1.0% CSP/H2O2 system.	Tetracycline	85-87	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	127-130
35257708-6	2022	The quenching experiments and ESR determined that  OH,  O2- and 1O2 were involved in TC degradation with the treatment of 1.0% CSP/H2O2 system.	Hydrogen Peroxide	131-135	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	127-130
34082927-0	2021	Probiotic bacteria cell surface-associated protein mineralized hydroxyapatite incorporated in porous scaffold: In vitro evaluation for bone cell growth and differentiation.	Durapatite	63-77	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	19-50
34082927-2	2021	The present study describes a facile route of HANP synthesis through mineralization of the cell surface-associated protein (CSP) from the human probiotic lactic acid bacteria (LAB) Lactobacillus rhamnosus GG.	hanp	46-50	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	91-122
34082927-2	2021	The present study describes a facile route of HANP synthesis through mineralization of the cell surface-associated protein (CSP) from the human probiotic lactic acid bacteria (LAB) Lactobacillus rhamnosus GG.	hanp	46-50	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	124-127
34082927-2	2021	The present study describes a facile route of HANP synthesis through mineralization of the cell surface-associated protein (CSP) from the human probiotic lactic acid bacteria (LAB) Lactobacillus rhamnosus GG.	Lactic Acid	154-165	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	91-122
34082927-2	2021	The present study describes a facile route of HANP synthesis through mineralization of the cell surface-associated protein (CSP) from the human probiotic lactic acid bacteria (LAB) Lactobacillus rhamnosus GG.	Lactic Acid	154-165	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	124-127
35617910-8	2022	With the preferred CSP, the enantioselectivity could be increased for a chiral probe (FMOC-Phe) and the mass transfer resistance (C-term) bisected compared to the corresponding CSP prepared from benchmark MPTMS-modified silica (2.54 vs 5.72 ms).	Phenylalanine	91-94	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	19-22
35617910-8	2022	With the preferred CSP, the enantioselectivity could be increased for a chiral probe (FMOC-Phe) and the mass transfer resistance (C-term) bisected compared to the corresponding CSP prepared from benchmark MPTMS-modified silica (2.54 vs 5.72 ms).	(3-mercaptopropyl)trimethoxysilane	205-210	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	177-180
35617910-8	2022	With the preferred CSP, the enantioselectivity could be increased for a chiral probe (FMOC-Phe) and the mass transfer resistance (C-term) bisected compared to the corresponding CSP prepared from benchmark MPTMS-modified silica (2.54 vs 5.72 ms).	Silicon Dioxide	220-226	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	177-180
35484155-0	2022	Reactant-induced photoactivation of in situ generated organogold intermediates leading to alkynylated indoles via Csp2-Csp cross-coupling.	organogold	54-64	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	119-122
35620055-4	2022	Intriguingly, recent studies on DNAJC5/CSPalpha, a membrane associated HSC70 co-chaperone, have unexpectedly linked lipofuscin accumulation to two intimately coupled protein quality control processes at endolysosomes.	Lipofuscin	116-126	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	32-47
35506243-0	2022	Abnormal triaging of misfolded proteins by adult neuronal ceroid lipofuscinosis-associated DNAJC5/CSPalpha mutants causes lipofuscin accumulation.	Lipofuscin	122-132	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	91-97
35506243-1	2022	Mutations in DNAJC5/CSPalpha are associated with adult neuronal ceroid lipofuscinosis (ANCL), a dominant-inherited neurodegenerative disease featuring lysosome-derived autofluorescent storage materials (AFSMs) termed lipofuscin.	Lipofuscin	217-227	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	13-28
35506243-5	2022	Importantly, uncoupling these two processes, as seen in cells lacking SLC3A2 or expressing ANCL-associated DNAJC5 mutants, generates DNAJC5-containing AFSMs resembling NCL patient-derived lipofuscin and induces neurodegeneration in a Drosophila ANCL model.	Lipofuscin	188-198	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	107-113
35325772-11	2022	DISCUSSION: Prenatal exposure to phthalates was associated with DNAm variation at CpGs annotated to genes associated with endocrine hormone activity (i.e., SLCO4A1, TPO), immune pathways and DNA damage (i.e., RASGEF1B, KAZN, HLA-A, MYO18A, DIP2C, C1or109), and neurodevelopment (i.e., AMPH, NOTCH3, DNAJC5).	phthalic acid	33-43	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	299-305
35484155-0	2022	Reactant-induced photoactivation of in situ generated organogold intermediates leading to alkynylated indoles via Csp2-Csp cross-coupling.	alkynylated indoles	90-109	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	119-122
35186935-11	2022	Results: OE-CSP A549 and H1975 cells were more sensitive to gefitinib, demonstrating significant amounts of apoptosis and decreased viability.	Gefitinib	60-69	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	12-15
35470299-15	2022	CONCLUSIONS: CSP can be used for resection of <=10 mm PPs.	pps	54-57	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	13-16
35184138-2	2022	Hypoxic-ischemic (HI) insults in term infants produce neonatal encephalopathy (NE), and it remains unclear whether HI-induced pathology alters baseline CSP expression in the normothermic brain.	hi	115-117	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	152-155
35186935-12	2022	In the OE-CSP group, autophagy was significantly inhibited, and there was a decrease in LC3B protein after exposure to gefitinib.	Gefitinib	119-128	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	10-13
35186935-13	2022	Cell viability and colony formed ability were recovered when OE-CSP cells were exposed to rapamycin.	Sirolimus	90-99	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	64-67
33934190-3	2021	Herein, an aggregation-induced emission (AIE) probe CSP, by introducing a pyridinium cation as the mitochondria-targeted group to an AIE active core cyanostilbene skeleton, is highly sensitive to viscosity changes due to the restriction of intramolecular motion (RIM) and inhibition of twisted intramolecular charge transfer (TICT) in high-viscosity systems.	pyridine	74-84	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	52-55
19738892-1	1987	Surface plasmons on opposite sides of a thin metal film surrounded by identical dielectrics interact to form coupled surface plasmons (CSP"s).	Metals	45-50	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	135-138
19738892-2	1987	Corrugation of the metal film permits interaction of the CSP"s with the radiation field.	Metals	19-24	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	57-60
19738892-3	1987	We report the observation of optical emission from CSP"s excited by the near-field coupling of molecules adjacent to a corrugated thin metal film embedded in photoresist.	Metals	135-140	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	51-54
35069097-7	2021	We demonstrate that the molecular chaperone, cysteine string protein (CSPalpha; DnaJC5), facilitates export of disease-causing-polyglutamine-expanded huntingtin cargo in 180-240 nm vesicles as well as larger 10-30 mum vesicles.	polyglutamine	127-140	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	80-86
2625456-1	1989	An assay for the plasma concentration of the enantiomers of verapamil and its metabolite norverapamil has been developed using the improved version of the alpha 1-acid glycoprotein chiral stationary phase (CHIRAL AGP-CSP) coupled to a shielded hydrophobic phase (Hisep) column.	Verapamil	60-69	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	217-220
2625456-3	1989	The eluents containing verapamil and norverapamil are then selectively transferred to the CHIRAL AGP-CSP where the enantiomers were stereochemically resolved and the enantiomeric composition determined.	Verapamil	23-32	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	101-104
2625456-3	1989	The eluents containing verapamil and norverapamil are then selectively transferred to the CHIRAL AGP-CSP where the enantiomers were stereochemically resolved and the enantiomeric composition determined.	norverapamil	37-49	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	101-104
33934190-3	2021	Herein, an aggregation-induced emission (AIE) probe CSP, by introducing a pyridinium cation as the mitochondria-targeted group to an AIE active core cyanostilbene skeleton, is highly sensitive to viscosity changes due to the restriction of intramolecular motion (RIM) and inhibition of twisted intramolecular charge transfer (TICT) in high-viscosity systems.	cyanostilbene	149-162	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	52-55
33934190-4	2021	As expected, with the viscosity increasing from 0.903 cP (0% glycerol) to 965 cP (99% glycerol), CSP exhibited a significant enhancement (more than 117-fold) in fluorescence intensity at 625 nm, with an excellent linear relationship between log I 625 nm and log eta (R2 = 0.9869, slope as high as 0.6727).	Glycerol	61-69	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	97-100
33934190-4	2021	As expected, with the viscosity increasing from 0.903 cP (0% glycerol) to 965 cP (99% glycerol), CSP exhibited a significant enhancement (more than 117-fold) in fluorescence intensity at 625 nm, with an excellent linear relationship between log I 625 nm and log eta (R2 = 0.9869, slope as high as 0.6727).	Glycerol	86-94	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	97-100
33253958-5	2021	Various management of CSP have been used such as systemic or local methotrexate, surgical resection and uterine artery chemoembolization.	Methotrexate	67-79	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	22-25
33729782-0	2021	Computational Insight into Cu-Catalyzed Csp-S Coupling to Form a Macrocyclic Alkynyl Sulfide.	Copper	27-29	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	40-43
33729782-0	2021	Computational Insight into Cu-Catalyzed Csp-S Coupling to Form a Macrocyclic Alkynyl Sulfide.	alkynyl sulfide	77-92	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	40-43
32871377-0	2020	HPLC enantio-separation and chiral recognition mechanism of quinolones on vancomycin CSP.	Quinolones	60-70	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	85-88
33719443-3	2021	Herein, we report the Csp3-Csp cross-coupling reaction of aryl esters with terminal alkynes using the B(C6F5)3/Mes3P FLP.	aryl esters	58-69	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	22-25
33719443-3	2021	Herein, we report the Csp3-Csp cross-coupling reaction of aryl esters with terminal alkynes using the B(C6F5)3/Mes3P FLP.	Alkynes	84-91	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	22-25
33719443-4	2021	Significantly, when the 1-ethynyl-4-vinylbenzene substrate was employed, the exclusive formation of Csp3-Csp cross-coupled products was observed.	1-Ethynyl-4-vinyl-benzene	24-48	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	100-103
33719443-5	2021	However, when 1-ethynyl-2-vinylbenzene was employed, solvent-dependent site-selective Csp3-Csp or Csp3-Csp2 cross-coupling resulted.	2-ethynylstyrene	14-38	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	86-89
33413417-3	2021	It was previously reported that exposure to SMC reduced antibody levels to AMA1, MSP-142 and CSP, but the duration of exposure to SMC up to three 3 years, had no effect on antibody levels to MSP-142 and CSP.	S-Methyl-L-cysteine	44-47	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	93-96
32873145-1	2020	In this study, we investigated the effects of menthol application on the cortical and cutaneous silent period (CSP/cutSP).	Menthol	46-53	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	111-114
32873145-7	2020	Paired t-tests showed no difference in the cutSP duration between the two conditions, whereas a significant increase in the CSP was detected with the Menthol condition.	Menthol	150-157	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	124-127
32871377-0	2020	HPLC enantio-separation and chiral recognition mechanism of quinolones on vancomycin CSP.	Vancomycin	74-84	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	85-88
32871377-1	2020	A new HPLC method was developed for the enantio-separation and chiral recognition mechanism of quinolones (lomefloxacine, ofloxacine, primaquine and quinacrine) on Vancomycin CSP.	Quinolones	95-105	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	175-178
32871377-1	2020	A new HPLC method was developed for the enantio-separation and chiral recognition mechanism of quinolones (lomefloxacine, ofloxacine, primaquine and quinacrine) on Vancomycin CSP.	lomefloxacin	107-120	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	175-178
32871377-1	2020	A new HPLC method was developed for the enantio-separation and chiral recognition mechanism of quinolones (lomefloxacine, ofloxacine, primaquine and quinacrine) on Vancomycin CSP.	Ofloxacin	122-132	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	175-178
32871377-1	2020	A new HPLC method was developed for the enantio-separation and chiral recognition mechanism of quinolones (lomefloxacine, ofloxacine, primaquine and quinacrine) on Vancomycin CSP.	Primaquine	134-144	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	175-178
32871377-1	2020	A new HPLC method was developed for the enantio-separation and chiral recognition mechanism of quinolones (lomefloxacine, ofloxacine, primaquine and quinacrine) on Vancomycin CSP.	Quinacrine	149-159	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	175-178
32871377-1	2020	A new HPLC method was developed for the enantio-separation and chiral recognition mechanism of quinolones (lomefloxacine, ofloxacine, primaquine and quinacrine) on Vancomycin CSP.	Vancomycin	164-174	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	175-178
32830238-11	2020	CONCLUSION: AMC-AP is featured by recording comparable retrograde atrial activation times at CSp, CSl, and HB with the latest recordings at the posterior CS.	amc-ap	12-18	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	93-96
32603426-0	2020	Sirolimus with CSP and MMF as GVHD prophylaxis for allogeneic transplantation with HLA antigen mismatched donors.	Sirolimus	0-9	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	15-18
32956589-7	2020	Radical capture represents the key Csp-Csp3 bond forming step in the copper catalyzed C-H functionalization of benzylic substrates R-H with alkynes H-C CR" (R" = (hetero)aryl, silyl) that provide Csp-Csp3 coupled products R-C CR via radical relay with tBuOOtBu as oxidant.	Copper	69-75	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	35-38
32956589-7	2020	Radical capture represents the key Csp-Csp3 bond forming step in the copper catalyzed C-H functionalization of benzylic substrates R-H with alkynes H-C CR" (R" = (hetero)aryl, silyl) that provide Csp-Csp3 coupled products R-C CR via radical relay with tBuOOtBu as oxidant.	Copper	69-75	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	39-42
32956589-7	2020	Radical capture represents the key Csp-Csp3 bond forming step in the copper catalyzed C-H functionalization of benzylic substrates R-H with alkynes H-C CR" (R" = (hetero)aryl, silyl) that provide Csp-Csp3 coupled products R-C CR via radical relay with tBuOOtBu as oxidant.	Arginine	0-1	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	35-38
32956589-7	2020	Radical capture represents the key Csp-Csp3 bond forming step in the copper catalyzed C-H functionalization of benzylic substrates R-H with alkynes H-C CR" (R" = (hetero)aryl, silyl) that provide Csp-Csp3 coupled products R-C CR via radical relay with tBuOOtBu as oxidant.	Arginine	0-1	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	39-42
32956589-7	2020	Radical capture represents the key Csp-Csp3 bond forming step in the copper catalyzed C-H functionalization of benzylic substrates R-H with alkynes H-C CR" (R" = (hetero)aryl, silyl) that provide Csp-Csp3 coupled products R-C CR via radical relay with tBuOOtBu as oxidant.	Alkynes	140-147	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	35-38
32956589-7	2020	Radical capture represents the key Csp-Csp3 bond forming step in the copper catalyzed C-H functionalization of benzylic substrates R-H with alkynes H-C CR" (R" = (hetero)aryl, silyl) that provide Csp-Csp3 coupled products R-C CR via radical relay with tBuOOtBu as oxidant.	Alkynes	140-147	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	39-42
32956589-7	2020	Radical capture represents the key Csp-Csp3 bond forming step in the copper catalyzed C-H functionalization of benzylic substrates R-H with alkynes H-C CR" (R" = (hetero)aryl, silyl) that provide Csp-Csp3 coupled products R-C CR via radical relay with tBuOOtBu as oxidant.	Chromium	152-154	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	35-38
32956589-7	2020	Radical capture represents the key Csp-Csp3 bond forming step in the copper catalyzed C-H functionalization of benzylic substrates R-H with alkynes H-C CR" (R" = (hetero)aryl, silyl) that provide Csp-Csp3 coupled products R-C CR via radical relay with tBuOOtBu as oxidant.	Chromium	152-154	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	39-42
32956589-7	2020	Radical capture represents the key Csp-Csp3 bond forming step in the copper catalyzed C-H functionalization of benzylic substrates R-H with alkynes H-C CR" (R" = (hetero)aryl, silyl) that provide Csp-Csp3 coupled products R-C CR via radical relay with tBuOOtBu as oxidant.	tert-butyl peroxide	252-260	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	35-38
32956589-7	2020	Radical capture represents the key Csp-Csp3 bond forming step in the copper catalyzed C-H functionalization of benzylic substrates R-H with alkynes H-C CR" (R" = (hetero)aryl, silyl) that provide Csp-Csp3 coupled products R-C CR via radical relay with tBuOOtBu as oxidant.	tert-butyl peroxide	252-260	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	39-42
32632918-10	2020	The spray prolonged CSP duration, which appears a promising tool for assessing and monitoring the analgesic effects of THC-CBD in MS.	thc-cbd	119-126	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	20-23
32211642-0	2020	Copper-catalysed Csp3-Csp cross-couplings between cyclobutanone oxime esters and terminal alkynes induced by visible light.	Copper	0-6	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	17-20
32762179-4	2020	An increase of free cortisol/free cortisone ratio in the urine (UFF/UFE) for CSP patients in comparison of CSA was obtained by HPLC method.	Hydrocortisone	20-28	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	77-80
32762179-4	2020	An increase of free cortisol/free cortisone ratio in the urine (UFF/UFE) for CSP patients in comparison of CSA was obtained by HPLC method.	Cortisone	34-43	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	77-80
32762179-5	2020	Decreased urinary excretion of UFF and UFE by more than 60% after the 8 mg dexamethasone suppression test had 100% sensitivity and specificity of more than 90% for the diagnosis of CSP.	uff	31-34	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	181-184
32762179-5	2020	Decreased urinary excretion of UFF and UFE by more than 60% after the 8 mg dexamethasone suppression test had 100% sensitivity and specificity of more than 90% for the diagnosis of CSP.	Fe(Iii) Uroporphyrin	39-42	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	181-184
32762179-5	2020	Decreased urinary excretion of UFF and UFE by more than 60% after the 8 mg dexamethasone suppression test had 100% sensitivity and specificity of more than 90% for the diagnosis of CSP.	Dexamethasone	75-88	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	181-184
32667204-0	2020	General Cu-Catalyzed Csp-S Coupling.	Copper	8-10	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	21-24
31919451-9	2020	Independently occurring variants in the genomic sequence of DNAJC5 encoding the cysteine-string domain of CSPalpha suggest that this region may be more prone to DNA replication errors and that insertions or duplications within this domain should be considered in unsolved ANCL cases.	Cysteine	80-88	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	60-66
32211642-0	2020	Copper-catalysed Csp3-Csp cross-couplings between cyclobutanone oxime esters and terminal alkynes induced by visible light.	cyclobutanone oxime esters	50-76	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	17-20
32211642-0	2020	Copper-catalysed Csp3-Csp cross-couplings between cyclobutanone oxime esters and terminal alkynes induced by visible light.	Alkynes	90-97	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	17-20
32211642-1	2020	A novel transformation for the construction of Csp3-Csp bonds was achieved via a photo-induced copper-catalysed C-C bond cleavage.	Copper	95-101	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	47-50
32040522-4	2020	METHODS: Cryopreserved PBMCs from nine HLA-typed subjects were stimulated with 23 8-10mer CSP peptides from the 3D7 parasite in IFN-gamma ELISpot assays.	Peptides	94-102	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	90-93
32040522-4	2020	METHODS: Cryopreserved PBMCs from nine HLA-typed subjects were stimulated with 23 8-10mer CSP peptides from the 3D7 parasite in IFN-gamma ELISpot assays.	ifn-gamma	128-137	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	90-93
31005344-3	2019	This study aims to assess the technical and clinical results of uterine artery embolization (UAE) combined with intra-arterial methotrexate (MTX) infusion for CSP and CP.	Methotrexate	141-144	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	159-169
31423667-6	2019	The preparations of optically pure CLD were evaluated on a semi-preparative (2 x 25 cm) column packed with 30% ADMPC-coated CSP under HPLC and SFC conditions.	Chiralpak AD	111-116	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	124-127
32042150-0	2020	Aggregation of mutant cysteine string protein-alpha via Fe-S cluster binding is mitigated by iron chelators.	Iron	56-60	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	22-51
32042150-0	2020	Aggregation of mutant cysteine string protein-alpha via Fe-S cluster binding is mitigated by iron chelators.	Iron	93-97	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	22-51
31573119-3	2019	Herein, we report a selective, practical and fast iron-based cross-coupling reaction which enables the formation of Csp-Csp3 and Csp2-Csp3 bonds.	Iron	50-54	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	116-119
31005344-3	2019	This study aims to assess the technical and clinical results of uterine artery embolization (UAE) combined with intra-arterial methotrexate (MTX) infusion for CSP and CP.	Methotrexate	127-139	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	159-169
30336057-1	2018	The first example of constructing a Csp3-Csp bond with substituted Hantzsch ester and Meyer nitrile is reported.	etidin	67-81	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	36-39
31803420-3	2019	Further, the reactivity of the in situ generated Au(iii)-acetylide complex is governed by the nature of the anionic ligands transferred by the I(iii) oxidant: while halogen ligands remain unreactive, acetato ligands are efficiently displaced by the arene to yield the observed Csp2-Csp cross-coupling products through an irreversible reductive elimination step.	Gold	49-66	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	277-280
30465838-1	2019	In this study, novel polysaccharides extracted from cuttlefish skin (CSP) and muscle (CMP), by precipitation with cetylpyridinium, were characterized and their antioxidant and antibacterial activities were investigated.	Polysaccharides	21-36	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	69-72
30465838-1	2019	In this study, novel polysaccharides extracted from cuttlefish skin (CSP) and muscle (CMP), by precipitation with cetylpyridinium, were characterized and their antioxidant and antibacterial activities were investigated.	Cetylpyridinium	114-129	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	69-72
30465838-3	2019	Infrared spectroscopic analysis indicated the presence of sulfonyl (OSO) and acetyl (CH3CO-) groups for both CSP and CMP.	oso	68-71	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	109-112
30465838-4	2019	In addition, CSP showed the presence of glucuronic acid (GlcA) and galacturonic acid (GalA) as major components, while CMP showed highest amount of GalA in its monosaccharide composition.	Glucuronic Acid	40-55	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	13-16
30465838-4	2019	In addition, CSP showed the presence of glucuronic acid (GlcA) and galacturonic acid (GalA) as major components, while CMP showed highest amount of GalA in its monosaccharide composition.	Glucuronic Acid	57-61	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	13-16
30465838-4	2019	In addition, CSP showed the presence of glucuronic acid (GlcA) and galacturonic acid (GalA) as major components, while CMP showed highest amount of GalA in its monosaccharide composition.	galacturonic acid	86-90	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	13-16
30465838-7	2019	Fractionation of cuttlefish polysaccharides, by DEAE-cellulose column showed one peak during the buffer elution phase and three major fractions for CMP and two peaks for CSP during the linear gradient of NaCl.	Polysaccharides	28-43	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	170-173
30281847-6	2019	In methanotrophs, a Csp exported from the cytosol stores CuI for the active site of the ubiquitous enzyme that catalyses the oxidation of methane.	Methane	138-145	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	20-23
30336057-1	2018	The first example of constructing a Csp3-Csp bond with substituted Hantzsch ester and Meyer nitrile is reported.	meyer nitrile	86-99	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	36-39
30336057-2	2018	When benziodoxole-activated alkyne was applied as the alkynyl donor, products containing Csp3-Csp bonds involving primary, secondary, and tertiary carbon centers were achieved in up to 97% yields.	o-iodoxybenzoic acid	5-17	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	89-92
30336057-2	2018	When benziodoxole-activated alkyne was applied as the alkynyl donor, products containing Csp3-Csp bonds involving primary, secondary, and tertiary carbon centers were achieved in up to 97% yields.	Alkynes	28-34	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	89-92
30336057-2	2018	When benziodoxole-activated alkyne was applied as the alkynyl donor, products containing Csp3-Csp bonds involving primary, secondary, and tertiary carbon centers were achieved in up to 97% yields.	Carbon	147-153	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	89-92
29465727-0	2018	Nucleophilic trifluoromethylthiolation of bromoalkynones with AgSCF3: C(sp)-SCF3 bond formation towards ynonyl trifluoromethyl sulfides.	bromoalkynones	42-56	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	70-80
29864801-6	2018	Preliminary tests were also carried on a ternary molten salt for Concentrated Solar Power (CSP) (18% in mass of NaNO3, 52% KNO3, and 30% LiNO3) at 120  C and 150  C. Obtained results are within lambda range of the Hitec  salt (53% KNO3, 7% NaNO3, 40% NaNO2).	Salts	56-60	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	65-95
29240251-13	2018	The pathological changes affect CTP-Cs in Csp and Cdp cartilage zones differently.	Cytidine Triphosphate	32-35	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	42-45
29240251-13	2018	The pathological changes affect CTP-Cs in Csp and Cdp cartilage zones differently.	Cesium	36-38	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	42-45
29240251-14	2018	The heterogeneity among the available CTP-Cs in Csp and Cdp suggests performance-based selection to optimize cell-sourcing strategies for therapy.	ctp-cs	38-44	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	48-51
29429743-3	2018	Herein, a novel homochiral zeolite-like metal-organic framework (ZMOF) JLU-Liu23 with unique DNA like double-helicity structure was firstly utilized as the CSP in open tubular capillary electrochromatography (OT-CEC) for enantioseparation of chiral monoamine neurotransmitters and analogues.	Metals	40-45	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	156-159
29429743-3	2018	Herein, a novel homochiral zeolite-like metal-organic framework (ZMOF) JLU-Liu23 with unique DNA like double-helicity structure was firstly utilized as the CSP in open tubular capillary electrochromatography (OT-CEC) for enantioseparation of chiral monoamine neurotransmitters and analogues.	monoamine	249-258	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	156-159
29465727-0	2018	Nucleophilic trifluoromethylthiolation of bromoalkynones with AgSCF3: C(sp)-SCF3 bond formation towards ynonyl trifluoromethyl sulfides.	ynonyl trifluoromethyl sulfides	104-135	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	70-80
28525832-3	2017	Therefore, the NiCo2O4/NiO electrode delivers a superior specific capacitance (Csp) (992.85Fg-1 at the current density of 1Ag-1), good rate capability (79.14% Csp retention even at 10Ag-1) and considerable cycle life (79.82% Csp retention at 10Ag-1 after 5000 times).	nico2o4	15-22	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	79-82
29506599-10	2018	CONCLUSIONS: This report describes the clinical history of autosomal dominant Kufs disease, the genetic mutation within the DNAJC5 gene, and the neuropathological findings demonstrating depletion of choline acetyltransferase in the brain.	Choline	199-206	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	124-130
28917599-7	2017	In nano-LC, the CSP was stressed under the use of strong organic solvents such as ethyl acetate, acetone and methyl t-butyl ether (MTBE).	ethyl acetate	82-95	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	16-19
28917599-7	2017	In nano-LC, the CSP was stressed under the use of strong organic solvents such as ethyl acetate, acetone and methyl t-butyl ether (MTBE).	Acetone	97-104	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	16-19
28917599-7	2017	In nano-LC, the CSP was stressed under the use of strong organic solvents such as ethyl acetate, acetone and methyl t-butyl ether (MTBE).	methyl tert-butyl ether	109-129	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	16-19
28917599-7	2017	In nano-LC, the CSP was stressed under the use of strong organic solvents such as ethyl acetate, acetone and methyl t-butyl ether (MTBE).	methyl tert-butyl ether	131-135	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	16-19
28763120-3	2017	Fourteen new terminal alkynes containing either Csp -S or Csp -Se bonds were selectively prepared through the retro-Favorskii reaction from the respective carbinol precursors.	Alkynes	22-29	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	48-51
28763120-3	2017	Fourteen new terminal alkynes containing either Csp -S or Csp -Se bonds were selectively prepared through the retro-Favorskii reaction from the respective carbinol precursors.	Alkynes	22-29	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	58-61
28525832-3	2017	Therefore, the NiCo2O4/NiO electrode delivers a superior specific capacitance (Csp) (992.85Fg-1 at the current density of 1Ag-1), good rate capability (79.14% Csp retention even at 10Ag-1) and considerable cycle life (79.82% Csp retention at 10Ag-1 after 5000 times).	nico2o4	15-22	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	159-162
28525832-3	2017	Therefore, the NiCo2O4/NiO electrode delivers a superior specific capacitance (Csp) (992.85Fg-1 at the current density of 1Ag-1), good rate capability (79.14% Csp retention even at 10Ag-1) and considerable cycle life (79.82% Csp retention at 10Ag-1 after 5000 times).	nico2o4	15-22	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	159-162
28525832-3	2017	Therefore, the NiCo2O4/NiO electrode delivers a superior specific capacitance (Csp) (992.85Fg-1 at the current density of 1Ag-1), good rate capability (79.14% Csp retention even at 10Ag-1) and considerable cycle life (79.82% Csp retention at 10Ag-1 after 5000 times).	nio	23-26	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	79-82
28525832-3	2017	Therefore, the NiCo2O4/NiO electrode delivers a superior specific capacitance (Csp) (992.85Fg-1 at the current density of 1Ag-1), good rate capability (79.14% Csp retention even at 10Ag-1) and considerable cycle life (79.82% Csp retention at 10Ag-1 after 5000 times).	nio	23-26	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	159-162
28525832-3	2017	Therefore, the NiCo2O4/NiO electrode delivers a superior specific capacitance (Csp) (992.85Fg-1 at the current density of 1Ag-1), good rate capability (79.14% Csp retention even at 10Ag-1) and considerable cycle life (79.82% Csp retention at 10Ag-1 after 5000 times).	nio	23-26	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	159-162
28457453-2	2017	Because of the H-bond formed via CH3-pi interaction, the CSP bearing methyl substituent exhibited high tolerance than the ones bearing dichloro substituents.	dichloro	135-143	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	57-60
28686014-1	2017	An engineered supercharged coiled-coil protein (CSP) and the cationic transfection reagent Lipofectamine 2000 are combined to form a lipoproteoplex for the purpose of dual delivery of siRNA and doxorubicin.	Doxorubicin	194-205	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	48-51
28686014-2	2017	CSP, bearing an external positive charge and axial hydrophobic pore, demonstrates the ability to condense siRNA and encapsulate the small-molecule chemotherapeutic, doxorubicin.	Doxorubicin	165-176	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	0-3
28686014-5	2017	When the lipoproteoplex is loaded with doxorubicin, the improved doxorubicin loading (~40 mug Dox/mg CSP) results in a substantial decrease in MCF-7 cell viability.	Doxorubicin	39-50	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	101-104
28686014-5	2017	When the lipoproteoplex is loaded with doxorubicin, the improved doxorubicin loading (~40 mug Dox/mg CSP) results in a substantial decrease in MCF-7 cell viability.	Doxorubicin	65-76	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	101-104
28686014-5	2017	When the lipoproteoplex is loaded with doxorubicin, the improved doxorubicin loading (~40 mug Dox/mg CSP) results in a substantial decrease in MCF-7 cell viability.	Doxorubicin	94-97	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	101-104
28457453-3	2017	The CSP derived from the chitosan bis(3,5-dichlorophenylcarbamate)-(n-pentyl amide) with a higher molecular weight possessed high tolerance to mobile phases, whereas the enantioseparation capability of this CSP was not as good as that of the one prepared from the chitosan derivative with a lower molecular weight.	bis(3,5-dichlorophenylcarbamate)-(n-pentyl amide	34-82	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	4-7
28457453-3	2017	The CSP derived from the chitosan bis(3,5-dichlorophenylcarbamate)-(n-pentyl amide) with a higher molecular weight possessed high tolerance to mobile phases, whereas the enantioseparation capability of this CSP was not as good as that of the one prepared from the chitosan derivative with a lower molecular weight.	Chitosan	25-33	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	4-7
28353346-0	2017	Csp-Csp3 Bond Formation via Iron(III)-Promoted Hydroalkynylation of Unactivated Alkenes.	ferric sulfate	28-37	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	0-3
28596090-12	2017	These results demonstrate that soluble CSP can induce a potent and sterile protective immune response when formulated with the QS-21 containing adjuvant ALFQ.	saponin QA-21V1	127-132	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	39-42
28596090-12	2017	These results demonstrate that soluble CSP can induce a potent and sterile protective immune response when formulated with the QS-21 containing adjuvant ALFQ.	alfq	153-157	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	39-42
28353346-0	2017	Csp-Csp3 Bond Formation via Iron(III)-Promoted Hydroalkynylation of Unactivated Alkenes.	Alkenes	80-87	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	0-3
28353346-1	2017	An iron(III)-promoted hydroalkynylation of unactivated alkenes toward Csp-Csp3 bond formation has been developed.	ferric sulfate	3-12	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	70-73
28353346-1	2017	An iron(III)-promoted hydroalkynylation of unactivated alkenes toward Csp-Csp3 bond formation has been developed.	Alkenes	55-62	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	70-73
28031457-3	2017	Here, we report the structural and mechanical properties of the CSP studied using single-molecule force spectroscopy on several constructs, one including the central region of CSP, which is rich in NANP amino acid repeats (CSPrep), and a second consisting of a near full-length sequence without the signal and anchor hydrophobic domains (CSPDeltaHP).	nanp amino acid	198-213	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	64-67
28405234-3	2017	The role of the hydroxy group in ortho position of salicylaldehyde has been explored, which presumably activates the Csp-H bond of the terminal alkyne leading to the formation of propargylamines in good to excellent yields, thus negating the function of the metal catalyst.	salicylaldehyde	51-66	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	117-120
28405234-3	2017	The role of the hydroxy group in ortho position of salicylaldehyde has been explored, which presumably activates the Csp-H bond of the terminal alkyne leading to the formation of propargylamines in good to excellent yields, thus negating the function of the metal catalyst.	Alkynes	144-150	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	117-120
28405234-3	2017	The role of the hydroxy group in ortho position of salicylaldehyde has been explored, which presumably activates the Csp-H bond of the terminal alkyne leading to the formation of propargylamines in good to excellent yields, thus negating the function of the metal catalyst.	propargylamine	179-194	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	117-120
28405234-3	2017	The role of the hydroxy group in ortho position of salicylaldehyde has been explored, which presumably activates the Csp-H bond of the terminal alkyne leading to the formation of propargylamines in good to excellent yields, thus negating the function of the metal catalyst.	Metals	258-263	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	117-120
28370343-5	2017	In particular, the poly-Ac-based CSP with a helicity memory efficiently separated racemic benzoin derivatives into enantiomers.	poly-ac	19-26	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	33-36
28370343-5	2017	In particular, the poly-Ac-based CSP with a helicity memory efficiently separated racemic benzoin derivatives into enantiomers.	Benzoin	90-97	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	33-36
26177794-1	2015	A protocol has been developed for direct Csp(3)-Csp(2) bond formation at the 4- and 6-positions of dibenzothiophenes using a gold(I) catalyst with terminal alkynes and dibenzothiophene-S-oxides.	dibenzothiophene	99-116	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	41-44
27258090-1	2016	Photoredox/nickel dual catalysis via single electron transmetalation allows coupling of Csp(3)-Csp(2) hybridized centers under mild conditions.	Nickel	11-17	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	88-91
27258090-1	2016	Photoredox/nickel dual catalysis via single electron transmetalation allows coupling of Csp(3)-Csp(2) hybridized centers under mild conditions.	Nickel	11-17	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	95-98
26828317-1	2016	Single-electron transmetalation via photoredox/nickel dual catalysis provides the opportunity for the construction of Csp(3)-Csp(2) bonds through the transfer of alkyl radicals under very mild reaction conditions.	Nickel	47-53	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	118-121
26828317-1	2016	Single-electron transmetalation via photoredox/nickel dual catalysis provides the opportunity for the construction of Csp(3)-Csp(2) bonds through the transfer of alkyl radicals under very mild reaction conditions.	Nickel	47-53	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	125-128
26828317-1	2016	Single-electron transmetalation via photoredox/nickel dual catalysis provides the opportunity for the construction of Csp(3)-Csp(2) bonds through the transfer of alkyl radicals under very mild reaction conditions.	alkyl radicals	162-176	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	118-121
26828317-1	2016	Single-electron transmetalation via photoredox/nickel dual catalysis provides the opportunity for the construction of Csp(3)-Csp(2) bonds through the transfer of alkyl radicals under very mild reaction conditions.	alkyl radicals	162-176	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	125-128
26673642-1	2015	Selective reductive elimination of ethane (Csp(3)-Csp(3) RE) was observed following bromide abstraction and subsequent thermolysis of a Pt(IV) complex bearing both Csp(3)- and Csp(2)-hybridized hydrocarbyl ligands.	Ethane	35-41	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	164-179
26571021-8	2015	When formulated with adjuvants lacking a TLR4 agonist (Alum, SE and Montanide) the Qbeta-CSP induced higher anti-NANP repeat titers, higher levels of cytophilic IgG2b/c antibodies and a trend towards higher protection against transgenic parasite challenge as compared to soluble CSP formulated in the same adjuvant.	montanide	68-77	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	89-92
26571021-8	2015	When formulated with adjuvants lacking a TLR4 agonist (Alum, SE and Montanide) the Qbeta-CSP induced higher anti-NANP repeat titers, higher levels of cytophilic IgG2b/c antibodies and a trend towards higher protection against transgenic parasite challenge as compared to soluble CSP formulated in the same adjuvant.	montanide	68-77	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	279-282
26571021-8	2015	When formulated with adjuvants lacking a TLR4 agonist (Alum, SE and Montanide) the Qbeta-CSP induced higher anti-NANP repeat titers, higher levels of cytophilic IgG2b/c antibodies and a trend towards higher protection against transgenic parasite challenge as compared to soluble CSP formulated in the same adjuvant.	N-4-Azido-2-nitrophenylpyridoxyl-5-phosphate	113-117	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	89-92
27472556-4	2016	By using this photoredox catalysis and nickel catalysis approach, a direct Csp(2)-Csp(3) reductive cross-coupling of aryl bromides with alkyl bromides is achieved under mild conditions without stoichiometric metal reductants.	Nickel	39-45	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	75-78
27472556-4	2016	By using this photoredox catalysis and nickel catalysis approach, a direct Csp(2)-Csp(3) reductive cross-coupling of aryl bromides with alkyl bromides is achieved under mild conditions without stoichiometric metal reductants.	Nickel	39-45	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	82-85
27472556-4	2016	By using this photoredox catalysis and nickel catalysis approach, a direct Csp(2)-Csp(3) reductive cross-coupling of aryl bromides with alkyl bromides is achieved under mild conditions without stoichiometric metal reductants.	aryl bromides	117-130	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	75-78
27472556-4	2016	By using this photoredox catalysis and nickel catalysis approach, a direct Csp(2)-Csp(3) reductive cross-coupling of aryl bromides with alkyl bromides is achieved under mild conditions without stoichiometric metal reductants.	aryl bromides	117-130	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	82-85
27472556-4	2016	By using this photoredox catalysis and nickel catalysis approach, a direct Csp(2)-Csp(3) reductive cross-coupling of aryl bromides with alkyl bromides is achieved under mild conditions without stoichiometric metal reductants.	alkyl bromides	136-150	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	75-78
27472556-4	2016	By using this photoredox catalysis and nickel catalysis approach, a direct Csp(2)-Csp(3) reductive cross-coupling of aryl bromides with alkyl bromides is achieved under mild conditions without stoichiometric metal reductants.	alkyl bromides	136-150	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	82-85
27472556-4	2016	By using this photoredox catalysis and nickel catalysis approach, a direct Csp(2)-Csp(3) reductive cross-coupling of aryl bromides with alkyl bromides is achieved under mild conditions without stoichiometric metal reductants.	Metals	208-213	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	75-78
27472556-4	2016	By using this photoredox catalysis and nickel catalysis approach, a direct Csp(2)-Csp(3) reductive cross-coupling of aryl bromides with alkyl bromides is achieved under mild conditions without stoichiometric metal reductants.	Metals	208-213	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	82-85
26770522-8	2015	CONCLUSION: The conservative treatments UAE-MTX and USG-MTX were similarly effective in treating CSP patients.	Methotrexate	44-47	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	97-100
26770522-8	2015	CONCLUSION: The conservative treatments UAE-MTX and USG-MTX were similarly effective in treating CSP patients.	usg-mtx	52-59	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	97-100
26333771-1	2015	In this study we demonstrate that molecular fragments, which can be readily coupled via a simple, in situ RO-C OR bond-forming reaction, can subsequently undergo metal insertion-decarboxylation-recombination to generate Csp(2)-Csp(3) bonds when subjected to metallaphotoredox catalysis.	Metals	162-167	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	220-223
26333771-1	2015	In this study we demonstrate that molecular fragments, which can be readily coupled via a simple, in situ RO-C OR bond-forming reaction, can subsequently undergo metal insertion-decarboxylation-recombination to generate Csp(2)-Csp(3) bonds when subjected to metallaphotoredox catalysis.	Metals	162-167	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	227-230
26177794-1	2015	A protocol has been developed for direct Csp(3)-Csp(2) bond formation at the 4- and 6-positions of dibenzothiophenes using a gold(I) catalyst with terminal alkynes and dibenzothiophene-S-oxides.	dibenzothiophene	99-116	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	48-51
26177794-1	2015	A protocol has been developed for direct Csp(3)-Csp(2) bond formation at the 4- and 6-positions of dibenzothiophenes using a gold(I) catalyst with terminal alkynes and dibenzothiophene-S-oxides.	Alkynes	156-163	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	41-44
26177794-1	2015	A protocol has been developed for direct Csp(3)-Csp(2) bond formation at the 4- and 6-positions of dibenzothiophenes using a gold(I) catalyst with terminal alkynes and dibenzothiophene-S-oxides.	Alkynes	156-163	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	48-51
26177794-1	2015	A protocol has been developed for direct Csp(3)-Csp(2) bond formation at the 4- and 6-positions of dibenzothiophenes using a gold(I) catalyst with terminal alkynes and dibenzothiophene-S-oxides.	dibenzothiophene 5-oxide	168-193	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	41-44
26177794-1	2015	A protocol has been developed for direct Csp(3)-Csp(2) bond formation at the 4- and 6-positions of dibenzothiophenes using a gold(I) catalyst with terminal alkynes and dibenzothiophene-S-oxides.	dibenzothiophene 5-oxide	168-193	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	48-51
25553040-3	2014	Atoms attached to the pendent Csp (3)-S bond are arranged in a staggered conformation with one of the Cl atoms anti to the C atom in the aromatic ring [C-S-C-Cl torsion angles = 178.41 (11) and -176.70 (13) ].	Sulfur	38-39	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	30-33
25555197-1	2015	An efficient method for the construction of Csp(2)-Csp(3) bond in a regio- and stereoselective fashion involving 1,3-terminal dienes, enol triflates/nonaflates, and sodium formate under Pd(0)-catalysis is described.	dienes	126-132	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	44-47
25555197-1	2015	An efficient method for the construction of Csp(2)-Csp(3) bond in a regio- and stereoselective fashion involving 1,3-terminal dienes, enol triflates/nonaflates, and sodium formate under Pd(0)-catalysis is described.	dienes	126-132	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	51-54
25555197-1	2015	An efficient method for the construction of Csp(2)-Csp(3) bond in a regio- and stereoselective fashion involving 1,3-terminal dienes, enol triflates/nonaflates, and sodium formate under Pd(0)-catalysis is described.	enol triflates	134-148	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	44-47
25555197-1	2015	An efficient method for the construction of Csp(2)-Csp(3) bond in a regio- and stereoselective fashion involving 1,3-terminal dienes, enol triflates/nonaflates, and sodium formate under Pd(0)-catalysis is described.	enol triflates	134-148	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	51-54
25555197-1	2015	An efficient method for the construction of Csp(2)-Csp(3) bond in a regio- and stereoselective fashion involving 1,3-terminal dienes, enol triflates/nonaflates, and sodium formate under Pd(0)-catalysis is described.	formic acid	165-179	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	44-47
25555197-1	2015	An efficient method for the construction of Csp(2)-Csp(3) bond in a regio- and stereoselective fashion involving 1,3-terminal dienes, enol triflates/nonaflates, and sodium formate under Pd(0)-catalysis is described.	formic acid	165-179	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	51-54
25555197-1	2015	An efficient method for the construction of Csp(2)-Csp(3) bond in a regio- and stereoselective fashion involving 1,3-terminal dienes, enol triflates/nonaflates, and sodium formate under Pd(0)-catalysis is described.	pd(0)	186-191	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	44-47
25555197-1	2015	An efficient method for the construction of Csp(2)-Csp(3) bond in a regio- and stereoselective fashion involving 1,3-terminal dienes, enol triflates/nonaflates, and sodium formate under Pd(0)-catalysis is described.	pd(0)	186-191	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	51-54
25878891-4	2015	These chains are connected by Csp (2)-H piac (piac is the acetyl-inic C-C triple bond) close contacts [2.794 (1) A], resulting in a rolling sheet structure parallel to the ac plane and aromatic pi-pi stacking inter-actions between the sheets [centroid-centroid distance = 3.593 (2) A] generate a three-dimensional network.	acetyl-inic c	58-71	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	30-33
25553040-3	2014	Atoms attached to the pendent Csp (3)-S bond are arranged in a staggered conformation with one of the Cl atoms anti to the C atom in the aromatic ring [C-S-C-Cl torsion angles = 178.41 (11) and -176.70 (13) ].	Carbon	102-103	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	30-33
25553040-3	2014	Atoms attached to the pendent Csp (3)-S bond are arranged in a staggered conformation with one of the Cl atoms anti to the C atom in the aromatic ring [C-S-C-Cl torsion angles = 178.41 (11) and -176.70 (13) ].	Sulfur	154-155	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	30-33
25553040-3	2014	Atoms attached to the pendent Csp (3)-S bond are arranged in a staggered conformation with one of the Cl atoms anti to the C atom in the aromatic ring [C-S-C-Cl torsion angles = 178.41 (11) and -176.70 (13) ].	Carbon	102-103	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	30-33
24910297-7	2014	The PCA biplot analysis showed that retention is governed by the size of the R1 substituent in the case of derivatized cyclofructan and cyclodextrin CSPs, and enantiomeric resolution closely correlated with the size of the R2 group in the case of non-derivatized gamma-cyclodextrin CSP.	Cyclodextrins	136-148	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	149-152
25315319-1	2014	In this study, for distal-selective beta-hydride elimination to produce exomethylene compounds with a newly formed Csp(3)-Csp(3) bond between tertiary alkyl halides and alpha-alkylated styrenes, a combination of a Cu(I) salt and a pyridine-based amine ligand (TPMA) is found to be a very efficient catalyst system.	exomethylene	72-84	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	115-118
25315319-1	2014	In this study, for distal-selective beta-hydride elimination to produce exomethylene compounds with a newly formed Csp(3)-Csp(3) bond between tertiary alkyl halides and alpha-alkylated styrenes, a combination of a Cu(I) salt and a pyridine-based amine ligand (TPMA) is found to be a very efficient catalyst system.	exomethylene	72-84	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	122-125
25315319-1	2014	In this study, for distal-selective beta-hydride elimination to produce exomethylene compounds with a newly formed Csp(3)-Csp(3) bond between tertiary alkyl halides and alpha-alkylated styrenes, a combination of a Cu(I) salt and a pyridine-based amine ligand (TPMA) is found to be a very efficient catalyst system.	alkyl halides	151-164	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	115-118
25315319-1	2014	In this study, for distal-selective beta-hydride elimination to produce exomethylene compounds with a newly formed Csp(3)-Csp(3) bond between tertiary alkyl halides and alpha-alkylated styrenes, a combination of a Cu(I) salt and a pyridine-based amine ligand (TPMA) is found to be a very efficient catalyst system.	alkyl halides	151-164	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	122-125
25315319-1	2014	In this study, for distal-selective beta-hydride elimination to produce exomethylene compounds with a newly formed Csp(3)-Csp(3) bond between tertiary alkyl halides and alpha-alkylated styrenes, a combination of a Cu(I) salt and a pyridine-based amine ligand (TPMA) is found to be a very efficient catalyst system.	alpha-alkylated styrenes	169-193	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	115-118
25315319-1	2014	In this study, for distal-selective beta-hydride elimination to produce exomethylene compounds with a newly formed Csp(3)-Csp(3) bond between tertiary alkyl halides and alpha-alkylated styrenes, a combination of a Cu(I) salt and a pyridine-based amine ligand (TPMA) is found to be a very efficient catalyst system.	alpha-alkylated styrenes	169-193	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	122-125
25315319-1	2014	In this study, for distal-selective beta-hydride elimination to produce exomethylene compounds with a newly formed Csp(3)-Csp(3) bond between tertiary alkyl halides and alpha-alkylated styrenes, a combination of a Cu(I) salt and a pyridine-based amine ligand (TPMA) is found to be a very efficient catalyst system.	cu(i) salt	214-224	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	115-118
25315319-1	2014	In this study, for distal-selective beta-hydride elimination to produce exomethylene compounds with a newly formed Csp(3)-Csp(3) bond between tertiary alkyl halides and alpha-alkylated styrenes, a combination of a Cu(I) salt and a pyridine-based amine ligand (TPMA) is found to be a very efficient catalyst system.	cu(i) salt	214-224	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	122-125
25315319-1	2014	In this study, for distal-selective beta-hydride elimination to produce exomethylene compounds with a newly formed Csp(3)-Csp(3) bond between tertiary alkyl halides and alpha-alkylated styrenes, a combination of a Cu(I) salt and a pyridine-based amine ligand (TPMA) is found to be a very efficient catalyst system.	pyridine	231-239	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	115-118
25315319-1	2014	In this study, for distal-selective beta-hydride elimination to produce exomethylene compounds with a newly formed Csp(3)-Csp(3) bond between tertiary alkyl halides and alpha-alkylated styrenes, a combination of a Cu(I) salt and a pyridine-based amine ligand (TPMA) is found to be a very efficient catalyst system.	pyridine	231-239	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	122-125
25315319-1	2014	In this study, for distal-selective beta-hydride elimination to produce exomethylene compounds with a newly formed Csp(3)-Csp(3) bond between tertiary alkyl halides and alpha-alkylated styrenes, a combination of a Cu(I) salt and a pyridine-based amine ligand (TPMA) is found to be a very efficient catalyst system.	Amines	246-251	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	115-118
25315319-1	2014	In this study, for distal-selective beta-hydride elimination to produce exomethylene compounds with a newly formed Csp(3)-Csp(3) bond between tertiary alkyl halides and alpha-alkylated styrenes, a combination of a Cu(I) salt and a pyridine-based amine ligand (TPMA) is found to be a very efficient catalyst system.	Amines	246-251	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	122-125
25315319-1	2014	In this study, for distal-selective beta-hydride elimination to produce exomethylene compounds with a newly formed Csp(3)-Csp(3) bond between tertiary alkyl halides and alpha-alkylated styrenes, a combination of a Cu(I) salt and a pyridine-based amine ligand (TPMA) is found to be a very efficient catalyst system.	NSC625031	260-264	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	115-118
25315319-1	2014	In this study, for distal-selective beta-hydride elimination to produce exomethylene compounds with a newly formed Csp(3)-Csp(3) bond between tertiary alkyl halides and alpha-alkylated styrenes, a combination of a Cu(I) salt and a pyridine-based amine ligand (TPMA) is found to be a very efficient catalyst system.	NSC625031	260-264	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	122-125
24947438-0	2014	Caenorhabditis elegans dnj-14, the orthologue of the DNAJC5 gene mutated in adult onset neuronal ceroid lipofuscinosis, provides a new platform for neuroprotective drug screening and identifies a SIR-2.1-independent action of resveratrol.	Resveratrol	226-237	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	53-59
24947438-2	2014	Recently, the mutations that cause ANCL were mapped to the DNAJC5 gene, which encodes cysteine string protein alpha.	Cysteine	86-94	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	59-65
25137653-1	2014	As an effort to develop improved ligand exchange chiral stationary phases (CSPs) for the resolution of chiral drugs, the residual silanol groups on the silica surface of a CSP based on sodium N-[(S)-1-hydroxymethyl-3-methylbutyl]-N-undecylaminoacetate, a (S)-leucinol derivative, were protected with n-octyl groups.	silanol	130-137	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	75-78
25137653-1	2014	As an effort to develop improved ligand exchange chiral stationary phases (CSPs) for the resolution of chiral drugs, the residual silanol groups on the silica surface of a CSP based on sodium N-[(S)-1-hydroxymethyl-3-methylbutyl]-N-undecylaminoacetate, a (S)-leucinol derivative, were protected with n-octyl groups.	Silicon Dioxide	152-158	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	75-78
25137653-2	2014	The residual silanol group-protected CSP was applied to the resolution of proton pump inhibitors (PPIs) such as omeprazole, pantoprazole, lansoprazole and rabeprazole.	silanol	13-20	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	37-40
25137653-2	2014	The residual silanol group-protected CSP was applied to the resolution of proton pump inhibitors (PPIs) such as omeprazole, pantoprazole, lansoprazole and rabeprazole.	Omeprazole	112-122	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	37-40
25137653-2	2014	The residual silanol group-protected CSP was applied to the resolution of proton pump inhibitors (PPIs) such as omeprazole, pantoprazole, lansoprazole and rabeprazole.	Pantoprazole	124-136	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	37-40
25137653-2	2014	The residual silanol group-protected CSP was applied to the resolution of proton pump inhibitors (PPIs) such as omeprazole, pantoprazole, lansoprazole and rabeprazole.	Lansoprazole	138-150	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	37-40
25137653-2	2014	The residual silanol group-protected CSP was applied to the resolution of proton pump inhibitors (PPIs) such as omeprazole, pantoprazole, lansoprazole and rabeprazole.	Rabeprazole	155-166	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	37-40
25137653-3	2014	The resolution of PPIs on the residual silanol group-protected CSP was excellent with the separation factors (alpha) in the range of 4.32-6.42 and the resolution factors (RS) in the range of 6.70-7.15.	silanol	39-46	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	63-66
25137653-4	2014	The improved chiral recognition ability of the residual silanol group-protected CSP was rationalized to be originated from the protection of the non-enantioselective interaction sites on the silica surface and the improved lipophilicity of the stationary phase.	silanol	56-63	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	80-83
25137653-4	2014	The improved chiral recognition ability of the residual silanol group-protected CSP was rationalized to be originated from the protection of the non-enantioselective interaction sites on the silica surface and the improved lipophilicity of the stationary phase.	Silicon Dioxide	191-197	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	80-83
24910297-7	2014	The PCA biplot analysis showed that retention is governed by the size of the R1 substituent in the case of derivatized cyclofructan and cyclodextrin CSPs, and enantiomeric resolution closely correlated with the size of the R2 group in the case of non-derivatized gamma-cyclodextrin CSP.	gamma-cyclodextrin	263-281	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	149-152
25068595-0	2014	PhI(OAc)2-mediated intramolecular oxidative aryl-aldehyde Csp(2)-Csp(2) bond formation: metal-free synthesis of acridone derivatives.	bis(acetoxy)iodobenzene	0-9	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	58-61
24908076-5	2014	Based on this, we hypothesize the fusion protein with introducing the CSP I-plus sequence into rEndostatin (rES-CSP) of which not only targets the liver, but also inhibits endothelial cells proliferation, migration, and tube formation.	rendostatin	95-106	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	70-73
24908076-5	2014	Based on this, we hypothesize the fusion protein with introducing the CSP I-plus sequence into rEndostatin (rES-CSP) of which not only targets the liver, but also inhibits endothelial cells proliferation, migration, and tube formation.	rendostatin	95-106	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	112-115
25068595-0	2014	PhI(OAc)2-mediated intramolecular oxidative aryl-aldehyde Csp(2)-Csp(2) bond formation: metal-free synthesis of acridone derivatives.	bis(acetoxy)iodobenzene	0-9	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	65-68
25068595-0	2014	PhI(OAc)2-mediated intramolecular oxidative aryl-aldehyde Csp(2)-Csp(2) bond formation: metal-free synthesis of acridone derivatives.	aryl-aldehyde	44-57	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	58-61
25068595-0	2014	PhI(OAc)2-mediated intramolecular oxidative aryl-aldehyde Csp(2)-Csp(2) bond formation: metal-free synthesis of acridone derivatives.	aryl-aldehyde	44-57	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	65-68
25068595-0	2014	PhI(OAc)2-mediated intramolecular oxidative aryl-aldehyde Csp(2)-Csp(2) bond formation: metal-free synthesis of acridone derivatives.	Metals	88-93	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	58-61
25068595-0	2014	PhI(OAc)2-mediated intramolecular oxidative aryl-aldehyde Csp(2)-Csp(2) bond formation: metal-free synthesis of acridone derivatives.	Metals	88-93	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	65-68
25068595-0	2014	PhI(OAc)2-mediated intramolecular oxidative aryl-aldehyde Csp(2)-Csp(2) bond formation: metal-free synthesis of acridone derivatives.	acridone	112-120	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	58-61
25068595-0	2014	PhI(OAc)2-mediated intramolecular oxidative aryl-aldehyde Csp(2)-Csp(2) bond formation: metal-free synthesis of acridone derivatives.	acridone	112-120	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	65-68
25068595-1	2014	A metal-free protocol for direct aryl-aldehyde Csp(2)-Csp(2) bond formation via a PhI(OAc)2-mediated intramolecular cross-dehydrogenative coupling (CDC) of various 2-(N-arylamino)aldehydes was developed.	Metals	2-7	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	47-50
25068595-1	2014	A metal-free protocol for direct aryl-aldehyde Csp(2)-Csp(2) bond formation via a PhI(OAc)2-mediated intramolecular cross-dehydrogenative coupling (CDC) of various 2-(N-arylamino)aldehydes was developed.	Metals	2-7	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	54-57
25068595-1	2014	A metal-free protocol for direct aryl-aldehyde Csp(2)-Csp(2) bond formation via a PhI(OAc)2-mediated intramolecular cross-dehydrogenative coupling (CDC) of various 2-(N-arylamino)aldehydes was developed.	aryl-aldehyde	33-46	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	47-50
25068595-1	2014	A metal-free protocol for direct aryl-aldehyde Csp(2)-Csp(2) bond formation via a PhI(OAc)2-mediated intramolecular cross-dehydrogenative coupling (CDC) of various 2-(N-arylamino)aldehydes was developed.	aryl-aldehyde	33-46	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	54-57
25068595-1	2014	A metal-free protocol for direct aryl-aldehyde Csp(2)-Csp(2) bond formation via a PhI(OAc)2-mediated intramolecular cross-dehydrogenative coupling (CDC) of various 2-(N-arylamino)aldehydes was developed.	bis(acetoxy)iodobenzene	82-91	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	47-50
25068595-1	2014	A metal-free protocol for direct aryl-aldehyde Csp(2)-Csp(2) bond formation via a PhI(OAc)2-mediated intramolecular cross-dehydrogenative coupling (CDC) of various 2-(N-arylamino)aldehydes was developed.	bis(acetoxy)iodobenzene	82-91	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	54-57
25068595-1	2014	A metal-free protocol for direct aryl-aldehyde Csp(2)-Csp(2) bond formation via a PhI(OAc)2-mediated intramolecular cross-dehydrogenative coupling (CDC) of various 2-(N-arylamino)aldehydes was developed.	2-(n-arylamino)aldehydes	164-188	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	47-50
25068595-1	2014	A metal-free protocol for direct aryl-aldehyde Csp(2)-Csp(2) bond formation via a PhI(OAc)2-mediated intramolecular cross-dehydrogenative coupling (CDC) of various 2-(N-arylamino)aldehydes was developed.	2-(n-arylamino)aldehydes	164-188	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	54-57
25042813-3	2014	Density Functional Theory (DFT) studies support the postulated reductive elimination pathway that leads to the formation of C sp2-Csp bonds and provide the clue to understand the divergent intramolecular reorganisation when p-H-phenylacetylene is used.	p-h-phenylacetylene	224-243	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	130-133
25042813-0	2014	Aryl-copper(III)-acetylides as key intermediates in Csp2-Csp model couplings under mild conditions.	aryl-copper(iii)-acetylides	0-27	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	52-55
25042813-4	2014	Mechanistic insights and the very mild experimental conditions to effect Caryl-Csp coupling in these model systems provide important insights for developing milder copper-catalysed Caryl-Csp coupling reactions with standard substrates in the future.	Copper	164-170	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	79-82
25042813-4	2014	Mechanistic insights and the very mild experimental conditions to effect Caryl-Csp coupling in these model systems provide important insights for developing milder copper-catalysed Caryl-Csp coupling reactions with standard substrates in the future.	Copper	164-170	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	187-190
24792697-8	2014	The CSP could be analyzed with a mobile phase of 100% ethanol.	Ethanol	54-61	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	4-7
24919056-0	2014	Atropisomerism about aryl-Csp(3) bonds: the electronic and steric influence of ortho-substituents on conformational exchange in cannabidiol and linderatin derivatives.	linderatin	144-154	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	26-29
24792697-9	2014	And the biselector CSP derived from CCPC and ADMPC could safely work in a normal phase containing 30% ethanol.	Ethanol	102-109	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	19-22
25419449-1	2014	We report mechanistic aspects of the trapping of thermally (HDDA) generated benzyne derivatives by pendant silyl ether groups, which results in net insertion of the pair of benzyne Csp-hydribized carbon atoms into the silicon-oxygen sigma bond.	1,6-hexanediol diacrylate	60-64	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	181-184
24631813-7	2014	The PCA biplot analysis showed that retention is governed by the size of the R1 substituent in the case of derivatized cyclofructan and cyclodextrin CSPs, and enantiomeric resolution closely correlated with the size of the R2 group in the case of non-derivatized gamma-cyclodextrin CSP.	Cyclodextrins	136-148	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	149-152
24631813-7	2014	The PCA biplot analysis showed that retention is governed by the size of the R1 substituent in the case of derivatized cyclofructan and cyclodextrin CSPs, and enantiomeric resolution closely correlated with the size of the R2 group in the case of non-derivatized gamma-cyclodextrin CSP.	gamma-cyclodextrin	263-281	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	149-152
24376089-3	2014	Among 17 analytes, baseline separations of 12 pairs of enantiomers are achieved on the immobilized cellulose CSP, which demonstrates that this new cellulose material exhibits almost the same enantioseparation performance as the coated cellulose CSP.	Cellulose	99-108	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	109-112
24376089-3	2014	Among 17 analytes, baseline separations of 12 pairs of enantiomers are achieved on the immobilized cellulose CSP, which demonstrates that this new cellulose material exhibits almost the same enantioseparation performance as the coated cellulose CSP.	Cellulose	99-108	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	245-248
24376089-3	2014	Among 17 analytes, baseline separations of 12 pairs of enantiomers are achieved on the immobilized cellulose CSP, which demonstrates that this new cellulose material exhibits almost the same enantioseparation performance as the coated cellulose CSP.	Cellulose	147-156	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	109-112
24376089-3	2014	Among 17 analytes, baseline separations of 12 pairs of enantiomers are achieved on the immobilized cellulose CSP, which demonstrates that this new cellulose material exhibits almost the same enantioseparation performance as the coated cellulose CSP.	Cellulose	147-156	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	109-112
24376089-4	2014	In addition, the amylose-derived CSP presents limited enantiorecognition ability but certain complementarity with the immobilized and coated cellulose-based materials.	Cellulose	141-150	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	33-36
25419449-1	2014	We report mechanistic aspects of the trapping of thermally (HDDA) generated benzyne derivatives by pendant silyl ether groups, which results in net insertion of the pair of benzyne Csp-hydribized carbon atoms into the silicon-oxygen sigma bond.	benzyne	76-83	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	181-184
25419449-1	2014	We report mechanistic aspects of the trapping of thermally (HDDA) generated benzyne derivatives by pendant silyl ether groups, which results in net insertion of the pair of benzyne Csp-hydribized carbon atoms into the silicon-oxygen sigma bond.	silyl ether	107-118	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	181-184
25419449-1	2014	We report mechanistic aspects of the trapping of thermally (HDDA) generated benzyne derivatives by pendant silyl ether groups, which results in net insertion of the pair of benzyne Csp-hydribized carbon atoms into the silicon-oxygen sigma bond.	benzyne	173-180	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	181-184
25419449-1	2014	We report mechanistic aspects of the trapping of thermally (HDDA) generated benzyne derivatives by pendant silyl ether groups, which results in net insertion of the pair of benzyne Csp-hydribized carbon atoms into the silicon-oxygen sigma bond.	Carbon	196-202	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	181-184
25419449-1	2014	We report mechanistic aspects of the trapping of thermally (HDDA) generated benzyne derivatives by pendant silyl ether groups, which results in net insertion of the pair of benzyne Csp-hydribized carbon atoms into the silicon-oxygen sigma bond.	Silicon	218-225	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	181-184
25419449-1	2014	We report mechanistic aspects of the trapping of thermally (HDDA) generated benzyne derivatives by pendant silyl ether groups, which results in net insertion of the pair of benzyne Csp-hydribized carbon atoms into the silicon-oxygen sigma bond.	Oxygen	226-232	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	181-184
23668246-1	2013	An efficient and diastereoselective synthesis of highly functionalized azetidin-2-imines has been achieved through a parallel catalysis strategy, including a copper-catalyzed azide-alkyne cycloaddition, a copper-catalyzed Csp-Csp(2) cross-coupling reaction, and an intermolecular [2 + 2] cycloaddition.	azetidin-2-imines	71-88	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	222-225
24160426-5	2014	For example, CSP (chemosensory protein) and takeout genes, the dopamine pathway, protein kinase A, and carnitines were found to be involved in the regulation of behavioral phase change and gram-negative bacteria-binding proteins in prophylaxical disease resistance of gregarious locusts.	Dopamine	63-71	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	13-16
24009095-0	2013	Disilicon complexes with two hexacoordinate Si atoms: paddlewheel-shaped isomers with (ClN4 )Si-Si(S4 Cl) and (ClN2 S2 )Si-Si(S2 N2 Cl) skeletons.	DISILANE	0-9	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	87-91
24009095-3	2013	Most interestingly, three isomers (i.e., with (ClN4 )Si Si(S4 Cl), (ClN3 S)Si Si(S3 NCl), and (ClN2 S2 )Si Si(S2 N2 Cl) skeletons as so-called (4,0), (3,1), and cis-(2,2) paddlewheels) were detected in solution by using (29) Si NMR spectroscopic analysis.	Silicon	53-55	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	47-51
23668246-1	2013	An efficient and diastereoselective synthesis of highly functionalized azetidin-2-imines has been achieved through a parallel catalysis strategy, including a copper-catalyzed azide-alkyne cycloaddition, a copper-catalyzed Csp-Csp(2) cross-coupling reaction, and an intermolecular [2 + 2] cycloaddition.	Copper	158-164	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	222-225
22978711-7	2013	DNAJC5, which encodes the cysteine string protein (CSPalpha), a presynaptic protein implicated in neurodegeneration, causes autosomal dominant Kufs disease.	Cysteine	26-34	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	0-6
23476386-3	2013	In the crystal, pi-pi stacking inter-actions [centroid-centroid distance = 3.5585 (15) A] connect mol-ecules into inversion dimers which are linked by Csp-H O=C hydrogen bonds, forming a ladder-like structure.	Hydrogen	161-169	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	151-154
23377348-5	2013	Pretreatment of NHBEs with MAL3-101 attenuated in a concentration-dependent manner PMA-stimulated mucin secretion and interactions among HSP70, MARCKS, and CSP.	mal3-101	27-35	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	156-159
23377348-5	2013	Pretreatment of NHBEs with MAL3-101 attenuated in a concentration-dependent manner PMA-stimulated mucin secretion and interactions among HSP70, MARCKS, and CSP.	Tetradecanoylphorbol Acetate	83-86	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	156-159
23473506-4	2013	3 cm teico-CSP resulted to be effective for the on-line pre-concentration, before the separation, of acebutolol, alprenolol, nadolol, oxprenolol and terbutaline with limit of detection at levels of few ng/mL.	Acebutolol	101-111	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	11-14
23473506-4	2013	3 cm teico-CSP resulted to be effective for the on-line pre-concentration, before the separation, of acebutolol, alprenolol, nadolol, oxprenolol and terbutaline with limit of detection at levels of few ng/mL.	Alprenolol	113-123	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	11-14
23473506-4	2013	3 cm teico-CSP resulted to be effective for the on-line pre-concentration, before the separation, of acebutolol, alprenolol, nadolol, oxprenolol and terbutaline with limit of detection at levels of few ng/mL.	Nadolol	125-132	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	11-14
23473506-4	2013	3 cm teico-CSP resulted to be effective for the on-line pre-concentration, before the separation, of acebutolol, alprenolol, nadolol, oxprenolol and terbutaline with limit of detection at levels of few ng/mL.	Oxprenolol	134-144	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	11-14
23473506-4	2013	3 cm teico-CSP resulted to be effective for the on-line pre-concentration, before the separation, of acebutolol, alprenolol, nadolol, oxprenolol and terbutaline with limit of detection at levels of few ng/mL.	Terbutaline	149-160	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	11-14
23300801-0	2012	A statistical interaction between circumsporozoite protein-specific T cell and antibody responses and risk of clinical malaria episodes following vaccination with RTS,S/AS01E.	as01e	169-174	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	34-58
22259433-1	2012	The title compound, C(9)H(12)ClN(4) (+) Cl(-), is a natural metabolic product of imidacloprid [systematic name: (E)-1-(6-chloro-3-pyridyl-meth-yl)-N-nitro-imidazolidin-2-yl-idene-amine] and was obtained by the reduction of the latter using Fe in HCl.	imidacloprid	81-93	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	29-35
22259433-1	2012	The title compound, C(9)H(12)ClN(4) (+) Cl(-), is a natural metabolic product of imidacloprid [systematic name: (E)-1-(6-chloro-3-pyridyl-meth-yl)-N-nitro-imidazolidin-2-yl-idene-amine] and was obtained by the reduction of the latter using Fe in HCl.	(e)-1-(6-chloro-3-pyridyl-meth-yl)-n-nitro-imidazolidin-2-yl-idene-amine	112-184	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	29-35
22259433-1	2012	The title compound, C(9)H(12)ClN(4) (+) Cl(-), is a natural metabolic product of imidacloprid [systematic name: (E)-1-(6-chloro-3-pyridyl-meth-yl)-N-nitro-imidazolidin-2-yl-idene-amine] and was obtained by the reduction of the latter using Fe in HCl.	Iron	240-242	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	29-35
22259433-1	2012	The title compound, C(9)H(12)ClN(4) (+) Cl(-), is a natural metabolic product of imidacloprid [systematic name: (E)-1-(6-chloro-3-pyridyl-meth-yl)-N-nitro-imidazolidin-2-yl-idene-amine] and was obtained by the reduction of the latter using Fe in HCl.	Hydrochloric Acid	246-249	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	29-35
22674492-0	2012	Expanding the scope of arylsulfonylacetylenes as alkynylating reagents and mechanistic insights in the formation of Csp2-Csp and Csp3-Csp bonds from organolithiums.	arylsulfonylacetylenes	23-45	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	116-119
22674492-0	2012	Expanding the scope of arylsulfonylacetylenes as alkynylating reagents and mechanistic insights in the formation of Csp2-Csp and Csp3-Csp bonds from organolithiums.	arylsulfonylacetylenes	23-45	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	121-124
22719648-2	2012	The mol-ecule shows a staggered conformation around the tartramide Csp(3)-Csp(3) bond with trans-oriented carboxyl and amide groups.	Tartaramide	56-66	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	67-70
22719648-2	2012	The mol-ecule shows a staggered conformation around the tartramide Csp(3)-Csp(3) bond with trans-oriented carboxyl and amide groups.	Tartaramide	56-66	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	74-77
22719648-2	2012	The mol-ecule shows a staggered conformation around the tartramide Csp(3)-Csp(3) bond with trans-oriented carboxyl and amide groups.	Amides	61-66	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	67-70
22719648-2	2012	The mol-ecule shows a staggered conformation around the tartramide Csp(3)-Csp(3) bond with trans-oriented carboxyl and amide groups.	Amides	61-66	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	74-77
22235333-7	2012	We conducted whole exome sequencing of three affected family members and identified a pLeu116del mutation in the gene DNAJC5, which segregated with the disease phenotype.	pleu116del	86-96	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	118-124
18951872-0	2008	Phosphorylation of cysteine string protein on Serine 10 triggers 14-3-3 protein binding.	Serine	46-52	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	19-42
20579654-2	2010	The perphenylcarbamated CD CSP (CCP-CSP) exhibited excellent chiral recognition of a wide range of analytes including racemic aryl alcohols, flavonoids, bendroflumethiazide, atropine and some beta-blockers.	Cadmium	24-26	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	27-30
20579654-2	2010	The perphenylcarbamated CD CSP (CCP-CSP) exhibited excellent chiral recognition of a wide range of analytes including racemic aryl alcohols, flavonoids, bendroflumethiazide, atropine and some beta-blockers.	Cadmium	24-26	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	36-39
20579654-2	2010	The perphenylcarbamated CD CSP (CCP-CSP) exhibited excellent chiral recognition of a wide range of analytes including racemic aryl alcohols, flavonoids, bendroflumethiazide, atropine and some beta-blockers.	aryl alcohols	126-139	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	27-30
20579654-2	2010	The perphenylcarbamated CD CSP (CCP-CSP) exhibited excellent chiral recognition of a wide range of analytes including racemic aryl alcohols, flavonoids, bendroflumethiazide, atropine and some beta-blockers.	aryl alcohols	126-139	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	36-39
20579654-2	2010	The perphenylcarbamated CD CSP (CCP-CSP) exhibited excellent chiral recognition of a wide range of analytes including racemic aryl alcohols, flavonoids, bendroflumethiazide, atropine and some beta-blockers.	Flavonoids	141-151	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	27-30
20579654-2	2010	The perphenylcarbamated CD CSP (CCP-CSP) exhibited excellent chiral recognition of a wide range of analytes including racemic aryl alcohols, flavonoids, bendroflumethiazide, atropine and some beta-blockers.	Flavonoids	141-151	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	36-39
20579654-2	2010	The perphenylcarbamated CD CSP (CCP-CSP) exhibited excellent chiral recognition of a wide range of analytes including racemic aryl alcohols, flavonoids, bendroflumethiazide, atropine and some beta-blockers.	Bendroflumethiazide	153-172	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	27-30
20579654-2	2010	The perphenylcarbamated CD CSP (CCP-CSP) exhibited excellent chiral recognition of a wide range of analytes including racemic aryl alcohols, flavonoids, bendroflumethiazide, atropine and some beta-blockers.	Bendroflumethiazide	153-172	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	36-39
20579654-2	2010	The perphenylcarbamated CD CSP (CCP-CSP) exhibited excellent chiral recognition of a wide range of analytes including racemic aryl alcohols, flavonoids, bendroflumethiazide, atropine and some beta-blockers.	Atropine	174-182	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	27-30
20579654-2	2010	The perphenylcarbamated CD CSP (CCP-CSP) exhibited excellent chiral recognition of a wide range of analytes including racemic aryl alcohols, flavonoids, bendroflumethiazide, atropine and some beta-blockers.	Atropine	174-182	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	36-39
20579654-4	2010	The "click" chemistry immobilized permethylated CD CSP (CCM-CSP) afforded poor chiral recognition for most analytes, but could resolve non-aromatic ionone derivatives which were not separated on CCP-CSP.	Cadmium	48-50	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	51-54
20579654-4	2010	The "click" chemistry immobilized permethylated CD CSP (CCM-CSP) afforded poor chiral recognition for most analytes, but could resolve non-aromatic ionone derivatives which were not separated on CCP-CSP.	Cadmium	48-50	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	60-63
20579654-4	2010	The "click" chemistry immobilized permethylated CD CSP (CCM-CSP) afforded poor chiral recognition for most analytes, but could resolve non-aromatic ionone derivatives which were not separated on CCP-CSP.	Cadmium	48-50	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	60-63
20579654-4	2010	The "click" chemistry immobilized permethylated CD CSP (CCM-CSP) afforded poor chiral recognition for most analytes, but could resolve non-aromatic ionone derivatives which were not separated on CCP-CSP.	Norisoprenoids	148-154	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	51-54
20579654-4	2010	The "click" chemistry immobilized permethylated CD CSP (CCM-CSP) afforded poor chiral recognition for most analytes, but could resolve non-aromatic ionone derivatives which were not separated on CCP-CSP.	Norisoprenoids	148-154	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	60-63
20579654-4	2010	The "click" chemistry immobilized permethylated CD CSP (CCM-CSP) afforded poor chiral recognition for most analytes, but could resolve non-aromatic ionone derivatives which were not separated on CCP-CSP.	Norisoprenoids	148-154	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	60-63
20334420-0	2010	Improved enantioselective synthesis of (-)-linderol A: hindered rotation about aryl-Csp(3) bond.	isoborneol	39-51	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	84-87
19319988-1	2010	In our recent work, a series of dendritic chiral stationary phases (CSPs) were synthesized, in which the chiral selector was L-2-(p-toluenesulfonamido)-3-phenylpropionyl chloride (selector I), and the CSP derived from three-generation dendrimer showed the best separation ability.	l-2-(p-toluenesulfonamido)-3-phenylpropionyl chloride	125-178	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	68-71
19319988-6	2010	Considering the enantioseparation ability of the CSP derived from aminated silica gel and selector II is much better than that of the one derived from aminated silica gel and selector I, it is believed that the dendrimer conformation essentially impacts enantioseparation.	Silica Gel	75-85	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	49-52
19633296-10	2009	Using this information, we modeled the NANP repeat and TSR domain of CSP.	N-4-Azido-2-nitrophenylpyridoxyl-5-phosphate	39-43	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	69-72
19633296-12	2009	Thus native CSP appears as a glycosylphosphatidylinositol-anchored, flexible rod-like protein on the sporozoite surface.	Glycosylphosphatidylinositols	29-57	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	12-15
19572578-0	2009	Aryl-Csp(3) bond rotation barriers of 2-aryl perhydropyrrolo[3,4-c]pyrrole-1,3-diones.	2-aryl perhydropyrrolo[3,4-c]pyrrole-1,3-diones	38-85	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	5-8
19407421-0	2009	Apparent shortening of the Csp(3)-Csp(3)bond analysed via a variable-temperature X-ray diffraction study in racemic 1,1"-binaphthalene-2,2"-diyl diethyl bis(carbonate).	1,1"-binaphthalene-2,2"-diyl diethyl bis(carbonate)	116-167	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	27-30
19407421-0	2009	Apparent shortening of the Csp(3)-Csp(3)bond analysed via a variable-temperature X-ray diffraction study in racemic 1,1"-binaphthalene-2,2"-diyl diethyl bis(carbonate).	1,1"-binaphthalene-2,2"-diyl diethyl bis(carbonate)	116-167	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	34-37
19407421-1	2009	Crystal structure determination at room temperature [292 (2) K] of racemic 1,1"-binaphthalene-2,2"-diyl diethyl bis(carbonate), C(26)H(22)O(6), showed that one of the terminal carbon-carbon bond lengths is very short [Csp(3)-Csp(3) = 1.327 (6) A].	1,1"-binaphthalene-2,2"-diyl diethyl bis(carbonate)	75-126	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	218-221
19407421-1	2009	Crystal structure determination at room temperature [292 (2) K] of racemic 1,1"-binaphthalene-2,2"-diyl diethyl bis(carbonate), C(26)H(22)O(6), showed that one of the terminal carbon-carbon bond lengths is very short [Csp(3)-Csp(3) = 1.327 (6) A].	1,1"-binaphthalene-2,2"-diyl diethyl bis(carbonate)	75-126	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	225-228
22199899-2	2011	The two Csp(2)-Nsp(2) bonds in the thio-urea unit differ significantly in length [1.327 (2) and 1.431 (2) A].	Thiourea	35-44	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	8-11
20847230-0	2011	A charged prominence in the linker domain of the cysteine-string protein Cspalpha mediates its regulated interaction with the calcium sensor synaptotagmin 9 during exocytosis.	Calcium	126-133	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	49-72
20954213-5	2010	Compared with a conventionally packed vancomycin-CSP, a reversal of the enantiomer elution order was obtained.	Vancomycin	38-48	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	49-52
19778051-2	2010	The formation process was studied in detail, and the morphology of walnut-like multihollow polystyrene particles could be controlled by the content of cross-linking agent, sulfonation time of CSP particles, and the weight ratio of monomer/CSP.	Polystyrenes	91-102	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	192-195
19778051-2	2010	The formation process was studied in detail, and the morphology of walnut-like multihollow polystyrene particles could be controlled by the content of cross-linking agent, sulfonation time of CSP particles, and the weight ratio of monomer/CSP.	Polystyrenes	91-102	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	239-242
19655330-8	2009	However, the dynamically coated CSP was found to be especially suitable for the separation of alpha-hydroxy acids.	alpha-hydroxy acids	94-113	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	32-35
18951872-3	2008	To identify novel phosphorylation-specific binding partners for CSP, we used a pull-down approach using synthetic peptides and recombinant proteins.	Peptides	114-122	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	64-67
18815076-5	2008	The results of these studies led to the first complete HPLC resolution of all five isomers of Brivanib Alaninate as carbobenzyloxy (CBZ) derivatives on a cellulose benzoate CSP (OJ-H).	brivanib	94-112	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	173-176
18815076-5	2008	The results of these studies led to the first complete HPLC resolution of all five isomers of Brivanib Alaninate as carbobenzyloxy (CBZ) derivatives on a cellulose benzoate CSP (OJ-H).	carbobenzyloxy (cbz)	116-136	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	173-176
18599981-1	2008	Molecules of the title compound, C(12)H(13)ClN(4), are linked by two independent N-H...N hydrogen bonds into a chain of edge-fused R(2)(2)(8) rings.	Carbon	33-34	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	43-48
18599981-1	2008	Molecules of the title compound, C(12)H(13)ClN(4), are linked by two independent N-H...N hydrogen bonds into a chain of edge-fused R(2)(2)(8) rings.	Hydrogen	89-97	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	43-48
21202919-2	2008	The torsion angle around the O-Csp(3) bond of the ester group is 108.52 (18) .	Esters	50-55	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	31-34
17089339-1	2007	A new doubly tethered chiral stationary phase (CSP 5) based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid was developed by attaching the second tethering group to silica gel through a carbon atom of the first tethering group of the corresponding singly tethered CSP (CSP 2) containing an N-CH3 tertiary amide linkage, which was previously developed in our laboratory, in order to enhance the CSP stability without the loss of chiral recognition efficiency.	-crown-6)-2,3,11	70-86	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	47-50
17580257-4	2007	The first cohort of 21 patients were given cyclosporine (CSP) and mycophenolate mofetil (MMF) as postgrafting immunosuppression, whereas the subsequent cohort was given additional methotrexate (MTX) and extended duration of CSP/MMF prophylaxis in an attempt to reduce graft-versus-host disease (GVHD).	Cyclosporine	43-55	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	57-60
17089339-2	2007	The new CSP was quite effective in the resolution of various racemic alpha-amino acids, amines, and amino alcohols, and the chiral recognition efficiency of the new CSP was even greater than that of the corresponding singly tethered CSP especially in terms of the resolution factors (RS).	Amino Acids	69-86	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	8-11
17573905-4	2007	Sporozoites and CSP increased the intracellular concentration of cyclic adenosyl mono-phosphate (cAMP) and inositol 1,4,5-triphosphate in Kupffer cells, but not in hepatocytes or liver endothelia.	cyclic adenosyl mono-phosphate	65-95	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	16-19
17573905-4	2007	Sporozoites and CSP increased the intracellular concentration of cyclic adenosyl mono-phosphate (cAMP) and inositol 1,4,5-triphosphate in Kupffer cells, but not in hepatocytes or liver endothelia.	Cyclic AMP	97-101	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	16-19
17573905-4	2007	Sporozoites and CSP increased the intracellular concentration of cyclic adenosyl mono-phosphate (cAMP) and inositol 1,4,5-triphosphate in Kupffer cells, but not in hepatocytes or liver endothelia.	Inositol 1,4,5-Trisphosphate	107-134	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	16-19
17573905-9	2007	We propose that by binding of CSP to LRP-1 and cell surface proteoglycans, malaria sporozoites induce a cAMP/EPAC-dependent, but PKA-independent signal transduction pathway that suppresses defence mechanisms in Kupffer cells.	Cyclic AMP	104-108	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	30-33
17719593-12	2007	For the five molecular enantiomeric pairs in the reversed phase mode with a teicoplanin CSP, it was found that there was an elevated contribution by the e coefficient that we interpret as a possible interaction between surface charges on the teicoplanin CSP and solute induced dipoles.	Teicoplanin	76-87	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	88-91
17719593-12	2007	For the five molecular enantiomeric pairs in the reversed phase mode with a teicoplanin CSP, it was found that there was an elevated contribution by the e coefficient that we interpret as a possible interaction between surface charges on the teicoplanin CSP and solute induced dipoles.	Teicoplanin	76-87	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	254-257
17719593-12	2007	For the five molecular enantiomeric pairs in the reversed phase mode with a teicoplanin CSP, it was found that there was an elevated contribution by the e coefficient that we interpret as a possible interaction between surface charges on the teicoplanin CSP and solute induced dipoles.	Teicoplanin	242-253	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	88-91
17719593-12	2007	For the five molecular enantiomeric pairs in the reversed phase mode with a teicoplanin CSP, it was found that there was an elevated contribution by the e coefficient that we interpret as a possible interaction between surface charges on the teicoplanin CSP and solute induced dipoles.	Teicoplanin	242-253	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	254-257
17089339-2	2007	The new CSP was quite effective in the resolution of various racemic alpha-amino acids, amines, and amino alcohols, and the chiral recognition efficiency of the new CSP was even greater than that of the corresponding singly tethered CSP especially in terms of the resolution factors (RS).	Amino Acids	69-86	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	165-168
17089339-2	2007	The new CSP was quite effective in the resolution of various racemic alpha-amino acids, amines, and amino alcohols, and the chiral recognition efficiency of the new CSP was even greater than that of the corresponding singly tethered CSP especially in terms of the resolution factors (RS).	Amino Acids	69-86	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	165-168
17089339-2	2007	The new CSP was quite effective in the resolution of various racemic alpha-amino acids, amines, and amino alcohols, and the chiral recognition efficiency of the new CSP was even greater than that of the corresponding singly tethered CSP especially in terms of the resolution factors (RS).	Amines	88-94	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	8-11
17089339-2	2007	The new CSP was quite effective in the resolution of various racemic alpha-amino acids, amines, and amino alcohols, and the chiral recognition efficiency of the new CSP was even greater than that of the corresponding singly tethered CSP especially in terms of the resolution factors (RS).	Amines	88-94	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	165-168
17089339-2	2007	The new CSP was quite effective in the resolution of various racemic alpha-amino acids, amines, and amino alcohols, and the chiral recognition efficiency of the new CSP was even greater than that of the corresponding singly tethered CSP especially in terms of the resolution factors (RS).	Amines	88-94	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	165-168
17089339-2	2007	The new CSP was quite effective in the resolution of various racemic alpha-amino acids, amines, and amino alcohols, and the chiral recognition efficiency of the new CSP was even greater than that of the corresponding singly tethered CSP especially in terms of the resolution factors (RS).	Amino Alcohols	100-114	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	8-11
17089339-2	2007	The new CSP was quite effective in the resolution of various racemic alpha-amino acids, amines, and amino alcohols, and the chiral recognition efficiency of the new CSP was even greater than that of the corresponding singly tethered CSP especially in terms of the resolution factors (RS).	Amino Alcohols	100-114	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	165-168
17089339-2	2007	The new CSP was quite effective in the resolution of various racemic alpha-amino acids, amines, and amino alcohols, and the chiral recognition efficiency of the new CSP was even greater than that of the corresponding singly tethered CSP especially in terms of the resolution factors (RS).	Amino Alcohols	100-114	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	165-168
17089339-1	2007	A new doubly tethered chiral stationary phase (CSP 5) based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid was developed by attaching the second tethering group to silica gel through a carbon atom of the first tethering group of the corresponding singly tethered CSP (CSP 2) containing an N-CH3 tertiary amide linkage, which was previously developed in our laboratory, in order to enhance the CSP stability without the loss of chiral recognition efficiency.	tetracarboxylic acid	90-110	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	47-50
17089339-1	2007	A new doubly tethered chiral stationary phase (CSP 5) based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid was developed by attaching the second tethering group to silica gel through a carbon atom of the first tethering group of the corresponding singly tethered CSP (CSP 2) containing an N-CH3 tertiary amide linkage, which was previously developed in our laboratory, in order to enhance the CSP stability without the loss of chiral recognition efficiency.	Silica Gel	168-178	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	47-50
17089339-1	2007	A new doubly tethered chiral stationary phase (CSP 5) based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid was developed by attaching the second tethering group to silica gel through a carbon atom of the first tethering group of the corresponding singly tethered CSP (CSP 2) containing an N-CH3 tertiary amide linkage, which was previously developed in our laboratory, in order to enhance the CSP stability without the loss of chiral recognition efficiency.	Carbon	189-195	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	47-50
17089339-1	2007	A new doubly tethered chiral stationary phase (CSP 5) based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid was developed by attaching the second tethering group to silica gel through a carbon atom of the first tethering group of the corresponding singly tethered CSP (CSP 2) containing an N-CH3 tertiary amide linkage, which was previously developed in our laboratory, in order to enhance the CSP stability without the loss of chiral recognition efficiency.	Nitrogen	293-294	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	47-50
17089339-1	2007	A new doubly tethered chiral stationary phase (CSP 5) based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid was developed by attaching the second tethering group to silica gel through a carbon atom of the first tethering group of the corresponding singly tethered CSP (CSP 2) containing an N-CH3 tertiary amide linkage, which was previously developed in our laboratory, in order to enhance the CSP stability without the loss of chiral recognition efficiency.	Amides	308-313	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	47-50
16715514-4	2006	Pure alcohols such ethanol or 2-propanol, with a fixed percentage of DEA added, serve as valuable alternatives to the more common n-hexane-based normal-phase eluents in resolution of Mianserin on the AD CSP.	Alcohols	5-13	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	203-206
16943324-0	2006	Dual role of the cysteine-string domain in membrane binding and palmitoylation-dependent sorting of the molecular chaperone cysteine-string protein.	Cysteine	17-25	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	124-147
16943324-3	2006	Cysteine-string protein (CSP), which is extensively palmitoylated on a "string" of 14 cysteine residues, is an example of such a protein.	Cysteine	86-94	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	0-23
16943324-3	2006	Cysteine-string protein (CSP), which is extensively palmitoylated on a "string" of 14 cysteine residues, is an example of such a protein.	Cysteine	86-94	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	25-28
16715514-4	2006	Pure alcohols such ethanol or 2-propanol, with a fixed percentage of DEA added, serve as valuable alternatives to the more common n-hexane-based normal-phase eluents in resolution of Mianserin on the AD CSP.	2-Propanol	30-40	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	203-206
16715514-4	2006	Pure alcohols such ethanol or 2-propanol, with a fixed percentage of DEA added, serve as valuable alternatives to the more common n-hexane-based normal-phase eluents in resolution of Mianserin on the AD CSP.	Mianserin	183-192	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	203-206
16715514-6	2006	Nonconventional dichloromethane-based eluents have permitted to expand the chiral resolving ability of the immobilized Chiralpak IA CSP and to perform mg-scale enantioseparations with an analytical-size column.	Methylene Chloride	16-31	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	132-135
16469739-8	2006	Csp knockdown by RNA interference produced a 5-fold increase in mature CFTR and augmented cAMP-stimulated CFTR currents.	Cyclic AMP	90-94	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	0-3
16815441-6	2006	The co-solute (NH4)2SO4 stabilizes both native Bc-Csp and the collapsed form, which suggests that the large hydrated SO4(2-) ions are excluded from the surface of the collapsed form in a similar fashion as they are excluded from folded Bc-Csp.	Ammonium Sulfate	14-23	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	50-53
16815441-6	2006	The co-solute (NH4)2SO4 stabilizes both native Bc-Csp and the collapsed form, which suggests that the large hydrated SO4(2-) ions are excluded from the surface of the collapsed form in a similar fashion as they are excluded from folded Bc-Csp.	Ammonium Sulfate	14-23	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	239-242
16815441-8	2006	The collapsed form of Bc-Csp resembles the unfolded form in its interaction with ethylene glycol, suggesting that in the collapsed form the backbone is still accessible to water and small molecules.	Ethylene Glycol	81-96	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	25-28
16815441-8	2006	The collapsed form of Bc-Csp resembles the unfolded form in its interaction with ethylene glycol, suggesting that in the collapsed form the backbone is still accessible to water and small molecules.	Water	172-177	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	25-28
16787098-0	2006	Synthesis of bicyclic p-diiodobenzenes via silver-catalyzed Csp-H iodination and ruthenium-catalyzed cycloaddition.	bicyclic p-diiodobenzenes	13-38	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	60-63
16787098-0	2006	Synthesis of bicyclic p-diiodobenzenes via silver-catalyzed Csp-H iodination and ruthenium-catalyzed cycloaddition.	Silver	43-49	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	60-63
16787098-1	2006	Highly substituted iodobenzenes were efficiently and regioselectively synthesized from readily available 1,6-diynes via two-step process consisting of silver-catalyzed Csp-H iodination and subsequent ruthenium-catalyzed [2 + 2 + 2] cycloaddition of resultant iododiynes.	Iodobenzenes	19-31	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	168-171
16787098-1	2006	Highly substituted iodobenzenes were efficiently and regioselectively synthesized from readily available 1,6-diynes via two-step process consisting of silver-catalyzed Csp-H iodination and subsequent ruthenium-catalyzed [2 + 2 + 2] cycloaddition of resultant iododiynes.	1,6-diynes	105-115	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	168-171
16830502-1	2006	The chromatographic behaviour of a poly-L-proline-derived chiral stationary phase (CSP) is compared to the corresponding single proline-derived CSP.	polyproline	35-49	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	83-86
16830502-1	2006	The chromatographic behaviour of a poly-L-proline-derived chiral stationary phase (CSP) is compared to the corresponding single proline-derived CSP.	Proline	42-49	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	83-86
16830502-3	2006	Although the application domain of the poly-L-proline-derived CSP (CSP-3) was considerably restricted, this CSP showed a higher retention and a slightly broader application domain than the monomeric analogue (CSP-1) when heptane/2-PrOH was used as mobile phase.	polyproline	39-53	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	62-65
16830502-3	2006	Although the application domain of the poly-L-proline-derived CSP (CSP-3) was considerably restricted, this CSP showed a higher retention and a slightly broader application domain than the monomeric analogue (CSP-1) when heptane/2-PrOH was used as mobile phase.	polyproline	39-53	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	67-72
16830502-3	2006	Although the application domain of the poly-L-proline-derived CSP (CSP-3) was considerably restricted, this CSP showed a higher retention and a slightly broader application domain than the monomeric analogue (CSP-1) when heptane/2-PrOH was used as mobile phase.	polyproline	39-53	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	67-70
16830502-4	2006	The presence of an alcohol in the mobile phase was essential for enantioseparation in the poly-L-proline-derived CSP when normal-phase conditions were applied.	Alcohols	19-26	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	113-116
16830502-4	2006	The presence of an alcohol in the mobile phase was essential for enantioseparation in the poly-L-proline-derived CSP when normal-phase conditions were applied.	polyproline	90-104	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	113-116
15888654-8	2005	The conditioning-dependent reduction in I(A) was blocked by preincubation of the photoreceptors with Csp antisense oligonucleotide.	Oligonucleotides	115-130	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	101-104
16243840-9	2006	In vitro 32P-phosphorylation studies revealed that Akt phosphorylates CSP on serine 10.	Phosphorus-32	9-12	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	70-73
16243840-9	2006	In vitro 32P-phosphorylation studies revealed that Akt phosphorylates CSP on serine 10.	Serine	77-83	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	70-73
16243840-11	2006	Taken together, these findings reveal a novel role for Akt phosphorylation in regulating the late stages of exocytosis and suggest that this is achieved via the phosphorylation of CSP on serine 10.	Serine	187-193	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	180-183
15972823-7	2005	Consistent with the stimulation of GTP hydrolysis, CSP(1-112) increased guanine nucleotide exchange of G alpha(s).	Guanine Nucleotides	72-90	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	51-54
15972823-9	2005	Furthermore, transient expression of CSP in HEK cells increased cellular cAMP levels in the presence of the beta2 adrenergic agonist isoproterenol.	Cyclic AMP	73-77	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	37-40
15972823-9	2005	Furthermore, transient expression of CSP in HEK cells increased cellular cAMP levels in the presence of the beta2 adrenergic agonist isoproterenol.	Isoproterenol	133-146	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	37-40
15972823-10	2005	Together, these results demonstrate that CSP modulates G protein function by preferentially targeting the inactive GDP-bound form of G alpha(s) and promoting GDP/GTP exchange.	Guanosine Diphosphate	115-118	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	41-44
15972823-10	2005	Together, these results demonstrate that CSP modulates G protein function by preferentially targeting the inactive GDP-bound form of G alpha(s) and promoting GDP/GTP exchange.	Guanosine Diphosphate	158-161	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	41-44
15972823-10	2005	Together, these results demonstrate that CSP modulates G protein function by preferentially targeting the inactive GDP-bound form of G alpha(s) and promoting GDP/GTP exchange.	Guanosine Triphosphate	162-165	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	41-44
15972823-11	2005	Our results show that the guanine nucleotide exchange activity of full-length CSP is, in turn, regulated by Hsc70-SGT.	Guanine Nucleotides	26-44	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	78-81
16755337-10	2006	In 18 of the 19 patients, the bipolar electrograms exhibited the CCW activation and a negative polarity during CSp only after complete CTI block.	titanium carbide	135-138	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	111-114
16755337-16	2006	The polarity of the bipolar electrograms recorded just lateral to the ablation line during CSp after RFCA of AFL may be used as a simple and an accurate indicator of complete CTI block.	titanium carbide	175-178	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	91-94
15972823-1	2005	Cysteine string protein (CSP) is an abundant regulated secretory vesicle protein that is composed of a string of cysteine residues, a linker domain, and an N-terminal J domain characteristic of the DnaJ/Hsp40 co-chaperone family.	Cysteine	113-121	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	0-23
15972823-1	2005	Cysteine string protein (CSP) is an abundant regulated secretory vesicle protein that is composed of a string of cysteine residues, a linker domain, and an N-terminal J domain characteristic of the DnaJ/Hsp40 co-chaperone family.	Cysteine	113-121	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	25-28
15972823-4	2005	In this report, we demonstrate that CSP selectively interacts with G alpha(s) and increases steady-state GTP hydrolysis.	Guanosine Triphosphate	105-108	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	36-39
15972823-6	2005	CSP(1-112) preferentially associated with the inactive GDP-bound conformation of G alpha(s).	Guanosine Diphosphate	55-58	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	0-3
15972823-7	2005	Consistent with the stimulation of GTP hydrolysis, CSP(1-112) increased guanine nucleotide exchange of G alpha(s).	Guanosine Triphosphate	35-38	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	51-54
15610015-5	2004	Moreover, endogenous Csp1 binds in a calcium-dependent manner to monomeric VAMP2, and this interaction requires the C-terminus of Csp.	Calcium	37-44	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	21-24
15828031-4	2005	The difference in enantioselective free energy between the aglycone CSP and the teicoplanin CSP was in the range between 0.02 and 0.97 kJ mol(-1) for these beta-lactam stereoisomer separations.	CHEBI:166892	59-67	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	68-71
15828031-4	2005	The difference in enantioselective free energy between the aglycone CSP and the teicoplanin CSP was in the range between 0.02 and 0.97 kJ mol(-1) for these beta-lactam stereoisomer separations.	Teicoplanin	80-91	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	92-95
15828031-4	2005	The difference in enantioselective free energy between the aglycone CSP and the teicoplanin CSP was in the range between 0.02 and 0.97 kJ mol(-1) for these beta-lactam stereoisomer separations.	beta-Lactams	156-167	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	68-71
15828031-4	2005	The difference in enantioselective free energy between the aglycone CSP and the teicoplanin CSP was in the range between 0.02 and 0.97 kJ mol(-1) for these beta-lactam stereoisomer separations.	beta-Lactams	156-167	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	92-95
15926915-6	2005	Strikingly, in the adult cerebellar granular layer P-CSP was highly enriched in a subset of glutamatergic synapses but undetectable in neighbouring GABA-ergic synapses.	gamma-Aminobutyric Acid	148-152	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	53-56
14570907-10	2003	These results indicate that CSP"s modulation of G protein inhibition of calcium channel activity is blocked in the presence of a huntingtin fragment with expanded polyglutamine tracts.	polyglutamine	163-176	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	28-31
15628124-1	2004	A chiral selector, mono(6A-N-allylamino-6A-deoxy)permethylated beta-cyclodextrin, was synthesized through a facile synthetic route and chemically immobilized onto porous silica gel via hydrosilylation to afford a cyclodextrin based chiral stationary phase MeCD-CSP.	mono(6a-n-allylamino-6a-deoxy)	19-49	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	261-264
15628124-1	2004	A chiral selector, mono(6A-N-allylamino-6A-deoxy)permethylated beta-cyclodextrin, was synthesized through a facile synthetic route and chemically immobilized onto porous silica gel via hydrosilylation to afford a cyclodextrin based chiral stationary phase MeCD-CSP.	betadex	63-80	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	261-264
15628124-1	2004	A chiral selector, mono(6A-N-allylamino-6A-deoxy)permethylated beta-cyclodextrin, was synthesized through a facile synthetic route and chemically immobilized onto porous silica gel via hydrosilylation to afford a cyclodextrin based chiral stationary phase MeCD-CSP.	Cyclodextrins	68-80	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	261-264
15058579-4	2004	The difference in enantioselective free energy between the aglycone CSP and the teicoplanin CSP was between 0.02 and 0.30 kcal mol(-1) for these particular amino acids.	CHEBI:166892	59-67	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	68-71
15058579-4	2004	The difference in enantioselective free energy between the aglycone CSP and the teicoplanin CSP was between 0.02 and 0.30 kcal mol(-1) for these particular amino acids.	Teicoplanin	80-91	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	92-95
12559961-2	2003	Conflicting reports support either a role for CSP: (i) in exocytosis or (ii) in the regulation of transmembrane calcium fluxes.	Calcium	112-119	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	46-49
14509341-5	2003	The former CSP could separate racemic N-(3,5-dinitrobenzoyl(DNB))amino acid isopropyl esters.	n-(3,5-dinitrobenzoyl(dnb))amino acid isopropyl esters	38-92	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	11-14
12559961-3	2003	Here we have examined the self-association of CSP to form oligomers that are stable upon SDS-PAGE.	Sodium Dodecyl Sulfate	89-92	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	46-49
12559961-7	2003	The recombinant CSP oligomers as well as the CSP monomers directly associate with Ni(2+)-NTA agarose.	nickel nitrilotriacetic acid	82-92	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	16-19
12559961-7	2003	The recombinant CSP oligomers as well as the CSP monomers directly associate with Ni(2+)-NTA agarose.	nickel nitrilotriacetic acid	82-92	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	45-48
12559961-7	2003	The recombinant CSP oligomers as well as the CSP monomers directly associate with Ni(2+)-NTA agarose.	Sepharose	93-100	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	16-19
12559961-7	2003	The recombinant CSP oligomers as well as the CSP monomers directly associate with Ni(2+)-NTA agarose.	Sepharose	93-100	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	45-48
11086994-4	2000	G. subunits interact with the J domain of CSP in an ATP-dependent manner; in contrast, Gbetagamma subunits interact with the C terminus of CSP in both the presence and absence of ATP.	Adenosine Triphosphate	52-55	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	42-45
12545465-1	2001	A chiral stationary phase(CSP) was prepared by coating cellulose-tris (3,5-dimethylphenylcarbamate) onto aminopropylated spherical silica gel.	cellulose-tris	55-69	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	26-29
12545465-1	2001	A chiral stationary phase(CSP) was prepared by coating cellulose-tris (3,5-dimethylphenylcarbamate) onto aminopropylated spherical silica gel.	3,5-dimethylphenylcarbamate	71-98	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	26-29
12545465-1	2001	A chiral stationary phase(CSP) was prepared by coating cellulose-tris (3,5-dimethylphenylcarbamate) onto aminopropylated spherical silica gel.	Silica Gel	131-141	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	26-29
12541965-2	2002	The method involved the use of an amide type chiral stationary phase(CSP) made of (R)-1-naphthylglycine and 3,5-dinitrobenzoic acid known as the Chirex 3005 column.	Amides	34-39	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	69-72
12541965-2	2002	The method involved the use of an amide type chiral stationary phase(CSP) made of (R)-1-naphthylglycine and 3,5-dinitrobenzoic acid known as the Chirex 3005 column.	(1-naphthylamino)acetic acid	82-103	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	69-72
11746798-7	2001	A benzoylated analog of the commercially available ULMO CSP is shown to be very effective in separating enantiomers of N-acyl amino acids.	n-acyl amino acids	119-137	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	56-59
10662817-0	2000	Comparison of cysteine string protein (Csp) and mutant alpha-SNAP overexpression reveals a role for csp in late steps of membrane fusion in dense-core granule exocytosis in adrenal chromaffin cells.	chromaffin	181-191	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	100-103
10575903-1	1999	BACKGROUND: We report our experience on abdominal sacral colpopexy (CSP) with a prolene mesh in women with vaginal vault prolapse.	Polypropylenes	80-87	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	68-71
11327009-1	1998	By using normal-phase HPLC with urea derivative as chiral stationary phase(CSP), the direct separation of racemic norephedrine has been investigated.	Urea	32-36	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	75-78
11327009-1	1998	By using normal-phase HPLC with urea derivative as chiral stationary phase(CSP), the direct separation of racemic norephedrine has been investigated.	Phenylpropanolamine	114-126	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	75-78
9395474-4	1997	Mutation of the histidine (H43Q) or aspartic acid (D45A) residues of this motif reduced the ability of Csp to stimulate the ATPase activity of mammalian Hsc70.	Histidine	16-25	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	103-106
9395474-4	1997	Mutation of the histidine (H43Q) or aspartic acid (D45A) residues of this motif reduced the ability of Csp to stimulate the ATPase activity of mammalian Hsc70.	h43q	27-31	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	103-106
9395474-4	1997	Mutation of the histidine (H43Q) or aspartic acid (D45A) residues of this motif reduced the ability of Csp to stimulate the ATPase activity of mammalian Hsc70.	Aspartic Acid	36-49	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	103-106
10574207-4	1999	The results were compared with data reported for chiral separations of the same substrates on similar (R)-N-(3,5-dinitrobenzoyl)-alpha-phenylglycine-derived CSP.	(r)-n-(3,5-dinitrobenzoyl)-alpha-phenylglycine	102-148	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	157-160
12552849-0	1999	[The resolution of racemic sec-phenethyl alcohol on cellulose tribenzoate-based CSP: influence of different alcohols in the mobile phase].	methylphenyl carbinol	27-48	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	80-83
12552849-0	1999	[The resolution of racemic sec-phenethyl alcohol on cellulose tribenzoate-based CSP: influence of different alcohols in the mobile phase].	cellulose tribenzoate	52-73	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	80-83
9420233-7	1998	Sedimentation analysis in sucrose density gradients showed that the CSP epitope accumulated in infected cells fused to VP0, forming 80S empty capsids which also contained native VP0.	Sucrose	26-33	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	68-71
8764987-4	1996	Exemplifying this is the fact that csp immunoreactivity is detected in Triton X-114 extracts of human blood, an observation which may facilitate blood-based diagnostic assays of csp status in man.	Nonidet P-40	71-83	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	35-38