PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
29605876-0	2018	Cdc20/p55 mediates the resistance to docetaxel in castration-resistant prostate cancer in a Bim-dependent manner.	Docetaxel	37-46	H3 histone pseudogene 44	Homo sapiens	6-9
24465991-3	2014	Importantly, boosting CE-primed macaques with DNA expressing full-length p55(gag) increased both magnitude of CE responses and breadth of Gag immunity, demonstrating alteration of the hierarchy of epitope recognition in the presence of pre-existing CE-specific responses.	Glycosaminoglycans	138-141	H3 histone pseudogene 44	Homo sapiens	73-76
28715197-1	2017	The effects of electrochemical preconditioning of P-55 pitch-based carbon-fiber microelectrodes were quantitatively examined in this study.	Carbon	67-73	H3 histone pseudogene 44	Homo sapiens	50-54
26230322-9	2015	We observed that Ala mutations of Trp664, Trp668 and Trp670 in MPER moderately lowered the intracellular and intraviral contents of Env while significantly elevating the content of another viral structural protein, p55/Gag and its derivative p24/capsid.	Alanine	17-20	H3 histone pseudogene 44	Homo sapiens	215-218
25397470-14	2014	Gp120 Mn and Bal, nef and p55-gag treatment had no effect on OC differentiation.	Glycosaminoglycans	30-33	H3 histone pseudogene 44	Homo sapiens	26-29
22759308-6	2012	In addition, the 5"-UTR regulates expression in an RNA concentration-dependent manner, with a high concentration of RNA triggering specific reduction of full-length Gag p55 production.	Glycosaminoglycans	165-168	H3 histone pseudogene 44	Homo sapiens	169-172
23164996-7	2013	The MAbF12 binding site in the p55(gag), p36 and p22 proteins was found to be a linear epitope with cross-linked sulphide bonds.	Sulfides	113-121	H3 histone pseudogene 44	Homo sapiens	31-34
15246272-4	2004	We found instead that nonactivated mixed glial cells expressed almost 10-fold less Gag protein, but more importantly, analysis of the intracellular Gag products in quiescent cells showed an aberrant p55/p24 Gag processing phenotype that appeared to be due to the premature activity of the viral protease.	Glycosaminoglycans	148-151	H3 histone pseudogene 44	Homo sapiens	199-202
20661277-4	2010	In erythrocytes, p55 forms a tripartite complex with protein 4.1R and glycophorin C promoting the assembly of actin filaments and the interaction of whirlin with p55 indicates that it plays a similar role in OHC stereocilia.	tripartite	29-39	H3 histone pseudogene 44	Homo sapiens	17-20
19459409-5	2009	Peptide A was shown to inhibit Gag precursor p55 transport from the nuclei to the plasma membrane, the site of virus assembly.	Glycosaminoglycans	31-34	H3 histone pseudogene 44	Homo sapiens	45-48
18160010-6	2007	In OBs, HIV p55-gag and gp120 were seen to reduce calcium deposition, ALP activity, levels of secreted BMP-2, -7, and RANK-L, and the expression and activity of RUNX-2.	Calcium	50-57	H3 histone pseudogene 44	Homo sapiens	12-15
18160010-7	2007	The levels of osteocalcin were also significantly reduced by p55-gag treatment, while gp120 also increased PPARgamma activity.	Glycosaminoglycans	65-68	H3 histone pseudogene 44	Homo sapiens	61-64
18160010-9	2007	The ability of MSCs to develop into functioning OBs was also affected by the presence of HIV proteins, with p55-gag inducing a decrease in osteogenesis, while rev induced an increase.	Glycosaminoglycans	112-115	H3 histone pseudogene 44	Homo sapiens	108-111
22792193-10	2012	In addition, the predicted Gag peptides were found to induce broader polyfunctional CD4+ T cell responses compared to the commonly used Gag-p55 peptide pool.	Glycosaminoglycans	27-30	H3 histone pseudogene 44	Homo sapiens	140-143
22393785-1	2011	HIV-1 matrix protein (MA) is multifunctional structural protein located on N-terminus of Gag precursor p55 and responsible for its transport to plasma membrane, the site of virus assembly.	Glycosaminoglycans	89-92	H3 histone pseudogene 44	Homo sapiens	103-106
21211021-10	2011	However, antibody reactivity to gag antigens varied among the women, being 100%, 90%, 70% and 63% for p24, p17, p39 and p55, respectively.	Glycosaminoglycans	32-35	H3 histone pseudogene 44	Homo sapiens	120-123
16679673-9	2006	WB indeterminate results were largely due to non-specific reactivity to gag protein (p55).	Glycosaminoglycans	72-75	H3 histone pseudogene 44	Homo sapiens	85-88
16537608-8	2006	The presence of chromosome 2 did not have consistent effects on the amount of unspliced viral RNA, whereas the amount of cell-associated Gag p55 was increased a fewfold.	Glycosaminoglycans	137-140	H3 histone pseudogene 44	Homo sapiens	141-144
15790028-6	2005	The "early" virus phenomenon, which is deprived of any mature structure or the ability to infect and does not contain mature Gag and Env proteins, illustrates that the proteolytic pressing of the Gag p55 precursor is not enough for the maturation of the virus and additional viral or cellular factors are needed for the virus to become infectious.	Glycosaminoglycans	196-199	H3 histone pseudogene 44	Homo sapiens	200-203
15246272-4	2004	We found instead that nonactivated mixed glial cells expressed almost 10-fold less Gag protein, but more importantly, analysis of the intracellular Gag products in quiescent cells showed an aberrant p55/p24 Gag processing phenotype that appeared to be due to the premature activity of the viral protease.	Glycosaminoglycans	148-151	H3 histone pseudogene 44	Homo sapiens	199-202
1932206-6	1991	Two nuclear matrix proteins, p52 and p55, incorporated [3H] retinoic acid rapidly, were cell-cycle-related, and disappeared within 12 h of dosing.	Tritium	56-58	H3 histone pseudogene 44	Homo sapiens	37-40
14989901-6	2004	These results indicated that sodium arsenite increase p55 gene expression, and inhibited PL and HOXA10 gene expression.	sodium arsenite	29-44	H3 histone pseudogene 44	Homo sapiens	54-57
16276928-6	2003	Sequencing result indicate that amino acid sequences are p245: LeuGlnGlnLysHisLeuLeu; p40, p55: GlnLeuIleMetIleArgHis; p69, p274 IleThrProArgAsnArgSer.	leuglnglnlyshisleuleu	63-84	H3 histone pseudogene 44	Homo sapiens	91-94
12477806-6	2003	Finally, incubation of antigen-presenting cells with SIV Gag p55 immune complexes in the presence of lactacystin or of bafilomycin indicated that the mechanism of antibody-mediated enhancement of cross presentation required both the proteasomal and the endosomal pathways.	lactacystin	101-112	H3 histone pseudogene 44	Homo sapiens	61-64
12477806-6	2003	Finally, incubation of antigen-presenting cells with SIV Gag p55 immune complexes in the presence of lactacystin or of bafilomycin indicated that the mechanism of antibody-mediated enhancement of cross presentation required both the proteasomal and the endosomal pathways.	bafilomycin	119-130	H3 histone pseudogene 44	Homo sapiens	61-64
12015689-2	2002	For the assessable recipients of cefazolin-probenecid (n=59) and ceftriaxone-placebo (n=57), clinical cure occurred at the end of treatment in 86% and 96% (P=.11), respectively, and was maintained at 1 month of follow-up in 96% and 91% (P=.55), respectively.	Cefazolin	33-42	H3 histone pseudogene 44	Homo sapiens	237-242
11238669-5	2001	Among them, two proteins, p64--78 and p55--61, present in urea-DTT and guanidine extracts, were shown by immunoblotting to be specifically targeted by AFA.	Urea	58-62	H3 histone pseudogene 44	Homo sapiens	38-41
11238669-5	2001	Among them, two proteins, p64--78 and p55--61, present in urea-DTT and guanidine extracts, were shown by immunoblotting to be specifically targeted by AFA.	Dithiothreitol	63-66	H3 histone pseudogene 44	Homo sapiens	38-41
11238669-5	2001	Among them, two proteins, p64--78 and p55--61, present in urea-DTT and guanidine extracts, were shown by immunoblotting to be specifically targeted by AFA.	Guanidine	71-80	H3 histone pseudogene 44	Homo sapiens	38-41
8277293-1	1993	The p55 gag gene of simian immunodeficiency virus macaque strain (SIVmac) and the core p27 gag component linked to a synthetic AUG codon have been cloned into adenovirus type 5 vectors to generate either viable E3-replacement or defective E1-replacement viruses.	Glycosaminoglycans	8-11	H3 histone pseudogene 44	Homo sapiens	4-7
7903507-6	1993	Neo-resistant clones exhibited an integrated viral DNA, low viral mRNA expression and (as in F12 cells) the presence of uncleaved gp160, no gp41 and a small amount of p55 gag precursor.	Glycosaminoglycans	171-174	H3 histone pseudogene 44	Homo sapiens	167-170
1715604-2	1991	All monoclonal antibodies recognized HIV-1IIIB infected MOLT3 cells by fluorescence and gave positive Western blot signals with viral gag peptides (p55 and/or p24).	Glycosaminoglycans	134-137	H3 histone pseudogene 44	Homo sapiens	148-151
1529643-3	1992	The HIV-2BEN gag precursor p55, its mature cleavage products p24 and p17 as well as the pol reverse transcriptase (RT) p66 were detected in VV-infected CV-1 cells.	Glycosaminoglycans	13-16	H3 histone pseudogene 44	Homo sapiens	27-30
1652374-6	1991	We propose that the p77 is involved in cyp C native function and that the p55 is involved in signal transduction events blocked by treatment with immunosuppressive levels of CsA.	Cyclosporine	174-177	H3 histone pseudogene 44	Homo sapiens	74-77
1932206-6	1991	Two nuclear matrix proteins, p52 and p55, incorporated [3H] retinoic acid rapidly, were cell-cycle-related, and disappeared within 12 h of dosing.	Tretinoin	60-73	H3 histone pseudogene 44	Homo sapiens	37-40
2405486-3	1990	Moreover, 10 micromolar concentrations of U-81749 significantly inhibited proteolysis of the HIV-1 gag polyprotein (p55) to the mature viral structural proteins p24 and p17 in cells infected with a recombinant vaccinia virus expressing the HIV-1 gag-pol genes.	U 81749	42-49	H3 histone pseudogene 44	Homo sapiens	116-119
2105740-5	1990	This method is applied to the structure determination of an 18-residue peptide with an amino acid sequence comprising the first zinc fingerlike domain from the gag protein p55 of HIV.	Glycosaminoglycans	160-163	H3 histone pseudogene 44	Homo sapiens	172-175
2702040-2	1989	Wild-type cells contained three major nickel-binding proteins with molecular masses of 68 kDa (p68), 55 kDa (p55), and 48 kDa (p48).	Nickel	38-44	H3 histone pseudogene 44	Homo sapiens	109-112
2785991-0	1989	Identification of protein intermediates in the processing of the p55 HIV-1 gag precursor in cells infected with recombinant vaccinia virus.	Glycosaminoglycans	75-78	H3 histone pseudogene 44	Homo sapiens	65-68
2785991-3	1989	Sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis revealed that processing of the p55 precursor involves three major intermediates (p41a, p41b, and p39).	sodium dodecyl sulfate-polyacrylamide	0-37	H3 histone pseudogene 44	Homo sapiens	99-102
2785991-7	1989	We conclude that the myristylated HIV-1 gag p55 precursor is initially cleaved at random either at the p17/p24 junction or at two sites between p24 and p15 proteins, resulting in three intermediates (p41a, p41b, and p39) which are subsequently cleaved to yield mature gag proteins.	Glycosaminoglycans	40-43	H3 histone pseudogene 44	Homo sapiens	44-47
2500366-8	1989	Phosphoamino acid analysis of protein p55 from 32P-labeled S-phase and M-phase HeLa cell extracts after immunoprecipitation with anti-p55 antibodies revealed that threonine was extensively phosphorylated in p55 during G2-M but not in S phase, whereas serine was phosphorylated during both S and M phases.	Phosphoamino Acids	0-17	H3 histone pseudogene 44	Homo sapiens	38-41
2500366-8	1989	Phosphoamino acid analysis of protein p55 from 32P-labeled S-phase and M-phase HeLa cell extracts after immunoprecipitation with anti-p55 antibodies revealed that threonine was extensively phosphorylated in p55 during G2-M but not in S phase, whereas serine was phosphorylated during both S and M phases.	Phosphoamino Acids	0-17	H3 histone pseudogene 44	Homo sapiens	134-137
2500366-8	1989	Phosphoamino acid analysis of protein p55 from 32P-labeled S-phase and M-phase HeLa cell extracts after immunoprecipitation with anti-p55 antibodies revealed that threonine was extensively phosphorylated in p55 during G2-M but not in S phase, whereas serine was phosphorylated during both S and M phases.	Phosphoamino Acids	0-17	H3 histone pseudogene 44	Homo sapiens	134-137
2500366-8	1989	Phosphoamino acid analysis of protein p55 from 32P-labeled S-phase and M-phase HeLa cell extracts after immunoprecipitation with anti-p55 antibodies revealed that threonine was extensively phosphorylated in p55 during G2-M but not in S phase, whereas serine was phosphorylated during both S and M phases.	Phosphorus-32	47-50	H3 histone pseudogene 44	Homo sapiens	38-41
2500366-8	1989	Phosphoamino acid analysis of protein p55 from 32P-labeled S-phase and M-phase HeLa cell extracts after immunoprecipitation with anti-p55 antibodies revealed that threonine was extensively phosphorylated in p55 during G2-M but not in S phase, whereas serine was phosphorylated during both S and M phases.	Threonine	163-172	H3 histone pseudogene 44	Homo sapiens	38-41
2500366-8	1989	Phosphoamino acid analysis of protein p55 from 32P-labeled S-phase and M-phase HeLa cell extracts after immunoprecipitation with anti-p55 antibodies revealed that threonine was extensively phosphorylated in p55 during G2-M but not in S phase, whereas serine was phosphorylated during both S and M phases.	Threonine	163-172	H3 histone pseudogene 44	Homo sapiens	134-137
2500366-8	1989	Phosphoamino acid analysis of protein p55 from 32P-labeled S-phase and M-phase HeLa cell extracts after immunoprecipitation with anti-p55 antibodies revealed that threonine was extensively phosphorylated in p55 during G2-M but not in S phase, whereas serine was phosphorylated during both S and M phases.	Threonine	163-172	H3 histone pseudogene 44	Homo sapiens	134-137
2785991-7	1989	We conclude that the myristylated HIV-1 gag p55 precursor is initially cleaved at random either at the p17/p24 junction or at two sites between p24 and p15 proteins, resulting in three intermediates (p41a, p41b, and p39) which are subsequently cleaved to yield mature gag proteins.	Glycosaminoglycans	268-271	H3 histone pseudogene 44	Homo sapiens	44-47
2702040-5	1989	Both the p55 and p48 proteins appeared to be present in similar amounts in wild-type and nickel-resistant cell lines, based upon silver staining of two-dimensional gels, yet in the nickel-resistant B200 cells, these proteins could not be visualized by [63Ni] binding.	Nickel	89-95	H3 histone pseudogene 44	Homo sapiens	9-12
2702040-5	1989	Both the p55 and p48 proteins appeared to be present in similar amounts in wild-type and nickel-resistant cell lines, based upon silver staining of two-dimensional gels, yet in the nickel-resistant B200 cells, these proteins could not be visualized by [63Ni] binding.	Silver	129-135	H3 histone pseudogene 44	Homo sapiens	9-12
2702040-5	1989	Both the p55 and p48 proteins appeared to be present in similar amounts in wild-type and nickel-resistant cell lines, based upon silver staining of two-dimensional gels, yet in the nickel-resistant B200 cells, these proteins could not be visualized by [63Ni] binding.	Nickel	181-187	H3 histone pseudogene 44	Homo sapiens	9-12
2702040-8	1989	Among the nickel-binding proteins studied, the p55 contained nickel-binding sites that were the most resistant to exchange by excess nickel ions.	Nickel	10-16	H3 histone pseudogene 44	Homo sapiens	47-50
2702040-8	1989	Among the nickel-binding proteins studied, the p55 contained nickel-binding sites that were the most resistant to exchange by excess nickel ions.	Nickel	61-67	H3 histone pseudogene 44	Homo sapiens	47-50
2702040-8	1989	Among the nickel-binding proteins studied, the p55 contained nickel-binding sites that were the most resistant to exchange by excess nickel ions.	Nickel	61-67	H3 histone pseudogene 44	Homo sapiens	47-50
2702040-9	1989	The microsomal fraction that contained the highest concentration of p55 also had the highest nickel-binding activity when standardized for protein concentration.	Nickel	93-99	H3 histone pseudogene 44	Homo sapiens	68-71
2447023-5	1988	Putative gag proteins of p55, p24 and p17 were recognized by sera of human AIDS patients, but the corresponding env proteins of 32-40 and 120 kDa showed only weak cross-reactivity with those of HIV.	Glycosaminoglycans	9-12	H3 histone pseudogene 44	Homo sapiens	25-28
3290901-3	1988	The HIV protease gene product was expressed in Escherichia coli and observed to cleave HIV gag p55 to gag p24 and gag p17 in vitro.	Glycosaminoglycans	91-94	H3 histone pseudogene 44	Homo sapiens	95-98
3290901-3	1988	The HIV protease gene product was expressed in Escherichia coli and observed to cleave HIV gag p55 to gag p24 and gag p17 in vitro.	Glycosaminoglycans	102-105	H3 histone pseudogene 44	Homo sapiens	95-98
3290901-4	1988	Substitution of aspartic acid residue 25 (Asp-25) of this protein with an asparagine residue did not affect the expression of the protein, but it eliminated detectable in vitro proteolytic activity against HIV gag p55.	Aspartic Acid	16-29	H3 histone pseudogene 44	Homo sapiens	214-217
3290901-4	1988	Substitution of aspartic acid residue 25 (Asp-25) of this protein with an asparagine residue did not affect the expression of the protein, but it eliminated detectable in vitro proteolytic activity against HIV gag p55.	Aspartic Acid	42-45	H3 histone pseudogene 44	Homo sapiens	214-217
3290901-6	1988	SW480 human colon carcinoma cells transfected with the Asn-25 mutant proviral DNA produced virions that contained gag p55 but not gag p24, whereas virions from cells transfected with the wild-type DNA contained both gag p55 and gag p24.	Asparagine	55-58	H3 histone pseudogene 44	Homo sapiens	118-121
3290901-6	1988	SW480 human colon carcinoma cells transfected with the Asn-25 mutant proviral DNA produced virions that contained gag p55 but not gag p24, whereas virions from cells transfected with the wild-type DNA contained both gag p55 and gag p24.	Asparagine	55-58	H3 histone pseudogene 44	Homo sapiens	220-223
3165484-3	1988	This antibody response is mainly directed against the env-encoded envelope proteins gp160, gp120 and gp41, against the gag-encoded core proteins p55, p24 and p17 as well as against the pol-encoded enzymatic proteins p66, p51 and p31.	Glycosaminoglycans	119-122	H3 histone pseudogene 44	Homo sapiens	145-148
2841007-1	1988	Proteins P51 and P55 were photolabeled by [3H]flunitrazepam, [3H]clonazepam or 3H-Ro 15-4513 and then compared by peptide mapping after limited digestion with various proteases.	Flunitrazepam	42-59	H3 histone pseudogene 44	Homo sapiens	17-20
2841007-1	1988	Proteins P51 and P55 were photolabeled by [3H]flunitrazepam, [3H]clonazepam or 3H-Ro 15-4513 and then compared by peptide mapping after limited digestion with various proteases.	[3h]clonazepam	61-75	H3 histone pseudogene 44	Homo sapiens	17-20
2841007-1	1988	Proteins P51 and P55 were photolabeled by [3H]flunitrazepam, [3H]clonazepam or 3H-Ro 15-4513 and then compared by peptide mapping after limited digestion with various proteases.	3h-ro 15-4513	79-92	H3 histone pseudogene 44	Homo sapiens	17-20
688068-1	1978	Synaptic junctional complexes (SJCs), isolated by a procedure which preserves presynaptic dense projections (PDPs) contain as their major component a polypeptide (P55) which comigrates with tubulin on sodium dodecyl sulfate - polyacrylamide gels and another major polypeptide (P45) which comigrates with muscle actin.	Sodium Dodecyl Sulfate	201-223	H3 histone pseudogene 44	Homo sapiens	163-166
2893245-4	1987	The data indicate polymorphism in the apparent size of gag gene-encoded p55 and env gene-encoded p41 proteins.	Glycosaminoglycans	55-58	H3 histone pseudogene 44	Homo sapiens	72-75
3126770-5	1987	Extracted, infected glial cells revealed bands for three major gag proteins, p18, p24 and p55, in Western blotting.	Glycosaminoglycans	63-66	H3 histone pseudogene 44	Homo sapiens	90-93
6092547-2	1984	[3H]Flunitrazepam reproducibly and irreversibly labeled mainly one protein (P51) in cerebellum and at least two proteins (P51 and P55) in hippocampus at both temperatures.	Tritium	1-3	H3 histone pseudogene 44	Homo sapiens	130-133
6092547-2	1984	[3H]Flunitrazepam reproducibly and irreversibly labeled mainly one protein (P51) in cerebellum and at least two proteins (P51 and P55) in hippocampus at both temperatures.	Flunitrazepam	4-17	H3 histone pseudogene 44	Homo sapiens	130-133
6092547-3	1984	Differential inhibition at 37 degrees C of irreversible [3H]flunitrazepam binding to the individual proteins by several selective benzodiazepine receptor ligands supports the hypothesis that P51 and P55 are associated with different benzodiazepine receptors.	Flunitrazepam	56-73	H3 histone pseudogene 44	Homo sapiens	199-202
6436129-2	1984	Both TPA and teleocidin B caused a marked increase in the synthesis of two polypeptides with molecular weights of 44 kilodaltons (p44) and 55 kilodaltons (p55).	Tetradecanoylphorbol Acetate	5-8	H3 histone pseudogene 44	Homo sapiens	155-158
6436129-2	1984	Both TPA and teleocidin B caused a marked increase in the synthesis of two polypeptides with molecular weights of 44 kilodaltons (p44) and 55 kilodaltons (p55).	teleocidins	13-25	H3 histone pseudogene 44	Homo sapiens	155-158
6436129-5	1984	No such specific increase in polypeptide synthesis was observed following treatment with either EGF or 4-O-MeTPA, suggesting that the increase in synthesis of p44 and p55 is specific to TPA and teleocidin, both agents with strong promoting activities.	teleocidins	194-204	H3 histone pseudogene 44	Homo sapiens	167-170
6357785-4	1983	Analysis by sucrose gradient centrifugation of the nuclear material released in these conditions indicated that p55 co-migrated with core histones.	Sucrose	12-19	H3 histone pseudogene 44	Homo sapiens	112-115
688068-1	1978	Synaptic junctional complexes (SJCs), isolated by a procedure which preserves presynaptic dense projections (PDPs) contain as their major component a polypeptide (P55) which comigrates with tubulin on sodium dodecyl sulfate - polyacrylamide gels and another major polypeptide (P45) which comigrates with muscle actin.	polyacrylamide	226-240	H3 histone pseudogene 44	Homo sapiens	163-166
688068-2	1978	We report here the characterization of P55 and P45 by two-dimensional polyacrylamide gel electrophoresis and by peptide mapping of the radioiodinated polypeptides.	polyacrylamide	70-84	H3 histone pseudogene 44	Homo sapiens	39-42
688068-4	1978	Comparison of the sodium dodecyl sulfate - polyacrylamide gel electrophoresis patterns of SJCs and postsynaptic densities (PSDs) indicates that P55 and P45 are associated mainly with PDPs but are also found in the PSD.	Sodium Dodecyl Sulfate	18-40	H3 histone pseudogene 44	Homo sapiens	144-147
688068-4	1978	Comparison of the sodium dodecyl sulfate - polyacrylamide gel electrophoresis patterns of SJCs and postsynaptic densities (PSDs) indicates that P55 and P45 are associated mainly with PDPs but are also found in the PSD.	polyacrylamide	43-57	H3 histone pseudogene 44	Homo sapiens	144-147
13926156-0	1961	[Experience in the use of 21-hydroxypregnandione sodium succinate (P-55) in anesthesiology with special reference to its use, associated with neuroplegic premedication, in general surgery.	21-hydroxypregnandione sodium succinate	26-65	H3 histone pseudogene 44	Homo sapiens	67-71
13825771-0	1959	[Experience in anesthesia with P-55 (21-hydroxypregnano-3-20-dione sodium succinate) in thoracopulmonary surgery].	21-hydroxypregnano-3-20-dione sodium succinate	37-83	H3 histone pseudogene 44	Homo sapiens	31-35
13308901-0	1956	[An intravenous steroid with anesthetic activity: P-55 or Viadril; preliminary clinical experience].	Steroids	16-23	H3 histone pseudogene 44	Homo sapiens	50-54
32064576-6	2020	Immuno-blotting of semen samples of control and 0.031 mug/mL mercury-treated groups showed low intensity bands of p55, p70, p80, p105 and p190 kDa tyrosine phosphorylation proteins while higher concentration-treated groups showed no such bands.	Mercury	61-68	H3 histone pseudogene 44	Homo sapiens	114-117