PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
25739273-7	2014	Moreover, some mixtures of representative chemicals like di-substituted aromatic positional isomers, n-alkanes, alcohols, aliphatic esters and phthalates can also be separated well on CTA@ PIL-C12-NTf2.	n-alkanes	101-110	serpin family A member 2 (gene/pseudogene)	Homo sapiens	189-192
25739273-7	2014	Moreover, some mixtures of representative chemicals like di-substituted aromatic positional isomers, n-alkanes, alcohols, aliphatic esters and phthalates can also be separated well on CTA@ PIL-C12-NTf2.	n-alkanes	101-110	nuclear transport factor 2	Homo sapiens	197-201
24120453-1	2013	In the n-alkane assimilating yeast Yarrowia lipolytica, the expression of ALK1, encoding a cytochrome P450 that catalyzes terminal mono-oxygenation of n-alkanes, is induced by n-alkanes.	n-alkanes	151-160	protein kinase ALK1	Saccharomyces cerevisiae S288C	74-78
24916549-6	2014	Iterative trapping is capable of sampling and desorbing C5 through C11 n-alkanes with uniform efficiency.	n-alkanes	71-80	RNA polymerase III subunit K	Homo sapiens	67-70
24666031-3	2014	Longer n-alkanes (C13 to C14), n-alcohols, and alpha,omega-diols are taken up in folded conformations.	n-alkanes	7-16	homeobox C13	Homo sapiens	18-21
24120453-1	2013	In the n-alkane assimilating yeast Yarrowia lipolytica, the expression of ALK1, encoding a cytochrome P450 that catalyzes terminal mono-oxygenation of n-alkanes, is induced by n-alkanes.	n-alkanes	176-185	protein kinase ALK1	Saccharomyces cerevisiae S288C	74-78
23172551-2	2013	Modern ski waxes consist mainly of petroleum-derived straight-chain aliphatic hydrocarbons, perfluoro-n-alkanes or polyfluorinated n-alkanes.	n-alkanes	102-111	SKI proto-oncogene	Homo sapiens	7-10
23656617-9	2013	In terms of temperature programming, it was found that a series of n-alkanes separated on the LTCC tile provided a cumulative peak capacity of around 54 peaks when using C8 to C13 as analyte markers.	n-alkanes	67-76	homeobox C13	Homo sapiens	176-179
23397139-1	2013	Large polarizable n-alkanes (approximately C18 and larger), alcohols, and other nonpolar compounds can be detected as negative ions when sample solutions are injected directly into the sampling orifice of the atmospheric pressure interface of the time-of-flight mass spectrometer with the direct analysis in real time (DART) ion source operating in negative-ion mode.	n-alkanes	18-27	Bardet-Biedl syndrome 9	Homo sapiens	43-46
21880102-8	2011	Deuterium was completely exchanged with hydrogen at the substituted carbon atom (C-2) of the succinate adducts of n-alkanes, whereas it is retained in toluene-derived benzylsuccinate, regardless of the type of enzyme catalysing the fumarate addition reaction.	n-alkanes	114-123	complement C2	Homo sapiens	81-84
23416995-7	2013	The enzyme was found to also act as an alkane omega-hydroxylase that oxidized n-alkanes with various chain lengths (C9 to C12 and C15 to C19), as well as alkyl side chains (C3 to C9) in alkylphenols (APs).	n-alkanes	78-87	placenta associated 8	Homo sapiens	130-133
21644510-2	2011	Our previous studies revealed that certain hydrocarbons (short-chain n-alkanes [C(6)-C(10)] and monoaromatics [toluene, o-xylene, m-xylene]) in residual naphtha entrained in the tailings are biodegraded to CH(4) by a consortium of microorganisms.	n-alkanes	69-78	homeobox C10	Homo sapiens	85-90
21466181-4	2011	The triclinic ordered phase, solely formed by the single even n-alkanes (C(18) or C(20)), becomes less stable due to the weakening of the layered structure and the suppression of the terminal methyl-methyl interactions in the confined geometry, which favors the miscibility of the two components.	n-alkanes	62-71	Bardet-Biedl syndrome 9	Homo sapiens	73-78
21434671-3	2011	For the viscosity dependence of k(a) in n-alkanes, the Stokes-Einstein relation k(a) ~ eta(-1.0) does not hold.	n-alkanes	40-49	endothelin receptor type A	Homo sapiens	87-90
20303087-3	2010	The derivatization process of the pristine nanotubes was a key factor to achieve a successful separation of both the light n-alkanes (C3-C5) and the related isomers (C4-C5 branched alkanes).	n-alkanes	123-132	ADAM metallopeptidase with thrombospondin type 1 motif 1	Homo sapiens	134-139
18685198-1	2008	Disruption of an SCS2 ortholog impaired the growth of the alkane-assimilating yeast Yarrowia lipolytica on n-alkanes, particularly on n-decane, although the mRNA level of the ALK1 gene encoding a highly inducible cytochrome P450ALK was not much affected.	n-alkanes	107-116	phosphatidylinositol-binding protein SCS2	Saccharomyces cerevisiae S288C	17-21
19148778-8	2009	Intrinsic biodegradation test was carried out, yielding 85% of biodegradation of n-alkanes between C15 and C30 during 30 days of process.	n-alkanes	81-90	placenta associated 8	Homo sapiens	99-102
21174989-2	2010	The average concentration of total n-alkanes (sigma n-alkanes) from C11 to C34 was 425.72 ng/m3, ranged from 7.02 to 2893.28 ng/m3.	n-alkanes	35-44	RNA polymerase III subunit K	Homo sapiens	68-71
21174989-3	2010	The concentration distributions of n-alkanes homologues in this study exhibited peaks at C21 and C29 in heating season, and C29 in non-heating season.	n-alkanes	35-44	TBL1X/Y related 1	Homo sapiens	89-92
19421509-1	2009	The sorption in H-FAU zeolite of C4-C12 n-alkanes, and linear and branched C2-C8 alkenes has been quantified up to 800 K by combining QM-Pot(MP2//B3LYP) with statistical thermodynamics calculations.	n-alkanes	40-49	FAU ubiquitin like and ribosomal protein S30 fusion	Homo sapiens	18-21
17661223-2	2007	The aim of this study was to determine in vitro metabolic rate constants for semivolatile n-alkanes, nonane (C9), decane (C10), and tetradecane (C14), by rat liver microsomal oxidation.	n-alkanes	90-99	anti-Mullerian hormone receptor type 2	Rattus norvegicus	145-148
17029681-2	2007	The normalized distribution of n-alkanes with the peak at C22, C23, C24 or C25 suggested that fossil fuel utilization was the major source of particulate n-alkanes at both sites.	n-alkanes	31-40	nucleolin	Homo sapiens	63-66
16484076-7	2006	The degradation rate of n-alkanes with carbon numbers ranging from C10 to C15 was relatively greater than that of n-alknaes with carbon numbers ranging from C16 to C20.	n-alkanes	24-33	homeobox C10	Homo sapiens	67-70
16956242-3	2006	These results were discussed together with those in n-alkanes (C(4)-C(7)) and methylcyclohexane (MCH) that were previously reported, and it was found that DeltaV++(q) increases monotonically but DeltaV++(eta) decreases rapidly with increasing the number of carbon atoms in n-alkanes.	n-alkanes	52-61	endothelin receptor type A	Homo sapiens	204-207
16944337-5	2006	The proportion of alkB containing microorganisms was positively correlated to the concentration of n-alkanes in the soil.	n-alkanes	99-108	alkB homolog 1, histone H2A dioxygenase	Homo sapiens	18-22
16999125-3	2006	The spiked n-alkanes biodegraded in the sequence C10 > C8 > C7 > C6.	n-alkanes	11-20	homeobox C10	Homo sapiens	49-52
16999125-4	2006	Degradation of 100% C10, 97% C8, 74% C7, and 44% C6 occurred in a mixture of n-alkanes in the MFT spiked at 0.2% after 25 weeks of incubation.	n-alkanes	77-86	homeobox C10	Homo sapiens	20-23
16484076-7	2006	The degradation rate of n-alkanes with carbon numbers ranging from C10 to C15 was relatively greater than that of n-alknaes with carbon numbers ranging from C16 to C20.	n-alkanes	24-33	placenta associated 8	Homo sapiens	74-77
15727309-2	2005	According to our results, the average total concentrations of n-alkanes (n-C12 to C35) and aromatics (15 PAHs) were 4.33 microg g(-1) dry weight (ranged 0.46-22.60) and 0.59 microg g(-1) dry weight (ranged 0.09-1.75), respectively.	n-alkanes	62-71	migration and invasion enhancer 1	Homo sapiens	82-85
16245812-5	2005	In the summer, n-alkanes were heavily enhanced by vegetation emissions with a maximum carbon number (Cmax) at C29, whereas they were dominated by emissions from fossil fuels combustion with a Cmax at C22/ C23 in the winter.	n-alkanes	15-24	nucleolin	Homo sapiens	205-208
16083103-2	2005	The concentrations including n-alkanes from C13 to C36, pristane and phytane were in the range of 0.60 to 170.10 microg/g, with a median value of 4.26.	n-alkanes	29-38	homeobox C13	Homo sapiens	44-47
15355121-3	2004	The force field reproduces the sodium positions in dehydrated FAU-type zeolites known from crystallography, and it predicts how the sodium cations redistribute when n-alkanes adsorb.	n-alkanes	165-174	FAU ubiquitin like and ribosomal protein S30 fusion	Homo sapiens	62-65
14971855-6	2004	In the anaerobic microcosms, on average 44% and 15% of the initial mineral oil was removed during a 12- and 10-month anaerobic incubation, respectively, and e.g. n-alkanes from C11 to C15 were removed.	n-alkanes	162-171	aldo-keto reductase family 1 member C4	Homo sapiens	177-180
14971855-6	2004	In the anaerobic microcosms, on average 44% and 15% of the initial mineral oil was removed during a 12- and 10-month anaerobic incubation, respectively, and e.g. n-alkanes from C11 to C15 were removed.	n-alkanes	162-171	placenta associated 8	Homo sapiens	184-187
11986928-5	2002	Consortia F1AA and TD removed 100% of n-alkanes and branched alkanes, whereas with consortium AM, 91% of branched alkanes remained.	n-alkanes	38-47	fem-1 homolog B	Homo sapiens	10-14
14655710-5	2003	Alba crude oil, which is naturally depleted in n-alkanes, resulted in a relatively modest stimulation of methanogenesis and sulfate reduction.	n-alkanes	47-56	afamin	Homo sapiens	0-4
12730186-1	2003	Oxidation of n-alkanes in bacteria is normally initiated by an enzyme system formed by a membrane-bound alkane hydroxylase and two soluble proteins, rubredoxin and rubredoxin reductase.	n-alkanes	13-22	rubredoxin reductase	Pseudomonas aeruginosa PAO1	164-184
11539435-6	1994	Based on the concentration profiles and isotopic compositions, the C31 and C33 n-alkanes and n-alkenes have a similar source, and both may have a planktonic origin.	n-alkanes	79-88	CD82 molecule	Homo sapiens	75-78
11878389-7	2002	More importantly the n-alkanes that were degraded at the fastest rates (n-C15 to n-C18) also showed the largest overall isotopic fractionation (approximately 12-25 per thousand deuterium enrichment), suggesting that the lower molecular weight n-alkanes can be used to monitor in-situ bioremediation of crude oil contamination.	n-alkanes	21-30	placenta associated 8	Homo sapiens	74-77
11878389-7	2002	More importantly the n-alkanes that were degraded at the fastest rates (n-C15 to n-C18) also showed the largest overall isotopic fractionation (approximately 12-25 per thousand deuterium enrichment), suggesting that the lower molecular weight n-alkanes can be used to monitor in-situ bioremediation of crude oil contamination.	n-alkanes	21-30	Bardet-Biedl syndrome 9	Homo sapiens	83-86
11878389-7	2002	More importantly the n-alkanes that were degraded at the fastest rates (n-C15 to n-C18) also showed the largest overall isotopic fractionation (approximately 12-25 per thousand deuterium enrichment), suggesting that the lower molecular weight n-alkanes can be used to monitor in-situ bioremediation of crude oil contamination.	n-alkanes	243-252	placenta associated 8	Homo sapiens	74-77
11878389-7	2002	More importantly the n-alkanes that were degraded at the fastest rates (n-C15 to n-C18) also showed the largest overall isotopic fractionation (approximately 12-25 per thousand deuterium enrichment), suggesting that the lower molecular weight n-alkanes can be used to monitor in-situ bioremediation of crude oil contamination.	n-alkanes	243-252	Bardet-Biedl syndrome 9	Homo sapiens	83-86
7698954-8	1995	Representative strains grew on spectra of the tested n-alkanes with chain lengths between C10 and C40, as sole sources of carbon and energy.	n-alkanes	53-62	homeobox C10	Homo sapiens	90-93
7698954-8	1995	Representative strains grew on spectra of the tested n-alkanes with chain lengths between C10 and C40, as sole sources of carbon and energy.	n-alkanes	53-62	CCR4-NOT transcription complex subunit 11	Homo sapiens	98-101
9463899-5	1997	Using a non-polar trapping column enrichment factors found for n-alkanes in the range of C7 to C10 ranged from 15 to 150 and agree well with calculated values.	n-alkanes	63-72	homeobox C10	Homo sapiens	95-98
24190091-3	1993	The fact that donor and transconjugant strains simultaneously lost the capacity to utilize n-alkanes on L-broth medium suggests that the OCT plasmids are unstable.	n-alkanes	91-100	plexin A2	Homo sapiens	137-140
24234502-3	1992	GC/MS studies also identified several n-alkanes with carbon numbers from C19 to C33 in the sample.	n-alkanes	38-47	CD82 molecule	Homo sapiens	80-83
24520725-5	2013	The highest concentration of n-alkanes was observed in the mature period of fog (393.12 ng/mL) which was more than ten times that in the fog formation period (27.83 ng/mL) and the fog dissipation period (14.87 ng/mL).	n-alkanes	29-38	zinc finger protein, FOG family member 1	Homo sapiens	76-79
26019148-3	2015	The FAT1 deletion mutant exhibited decreased growth on n-alkanes of 10-18 carbons, whereas the FAA1 mutant showed growth reduction on n-alkane of 16 carbons.	n-alkanes	55-64	long-chain fatty acid transporter FAT1	Saccharomyces cerevisiae S288C	4-8
26019148-4	2015	However, FAT2-FAT4 deletion mutants did not show any growth defects, suggesting that FAT1 and FAA1 are involved in the activation of fatty acids produced during the metabolism of n-alkanes.	n-alkanes	179-188	Pcs60p	Saccharomyces cerevisiae S288C	9-13
26019148-4	2015	However, FAT2-FAT4 deletion mutants did not show any growth defects, suggesting that FAT1 and FAA1 are involved in the activation of fatty acids produced during the metabolism of n-alkanes.	n-alkanes	179-188	long-chain fatty acid transporter FAT1	Saccharomyces cerevisiae S288C	85-89
26019148-4	2015	However, FAT2-FAT4 deletion mutants did not show any growth defects, suggesting that FAT1 and FAA1 are involved in the activation of fatty acids produced during the metabolism of n-alkanes.	n-alkanes	179-188	long-chain fatty acid-CoA ligase FAA1	Saccharomyces cerevisiae S288C	94-98
25345921-7	2015	Among them, 2-ring, 3-ring, and 4-ring PAHs accounted for the majority of total PAHs, and C10-15 accounted for the majority of particulate n-alkanes.	n-alkanes	139-148	homeobox C10	Homo sapiens	90-93
24520725-5	2013	The highest concentration of n-alkanes was observed in the mature period of fog (393.12 ng/mL) which was more than ten times that in the fog formation period (27.83 ng/mL) and the fog dissipation period (14.87 ng/mL).	n-alkanes	29-38	zinc finger protein, FOG family member 1	Homo sapiens	137-140
24520725-5	2013	The highest concentration of n-alkanes was observed in the mature period of fog (393.12 ng/mL) which was more than ten times that in the fog formation period (27.83 ng/mL) and the fog dissipation period (14.87 ng/mL).	n-alkanes	29-38	zinc finger protein, FOG family member 1	Homo sapiens	137-140
35134922-0	2022	Orthologs of Saccharomyces cerevisiae SFH2, genes encoding Sec14 family proteins, implicated in utilization of n-alkanes and filamentous growth in response to n-alkanes in Yarrowia lipolytica.	n-alkanes	111-120	Csr1p	Saccharomyces cerevisiae S288C	38-42
35314750-3	2022	Fingerprint analysis on the petroleum contamination level and source was conducted by the geochemical indices of n-alkanes and PAHs, such as low to high molecular weight (LMW/HMW) hydrocarbons, n-alkanes/pristine or phytane (C17/ Pr, C18/Ph), and ratio of anthracene/ (anthracene + phenanthrene) (Ant/(Ant + Phe)).	n-alkanes	113-122	cilia and flagella associated protein 97	Homo sapiens	175-178
33232125-4	2020	An adsorption-desorption model was set up to characterize the NGD response on a large set of n-alkanes from C10 to C22 at different NGD temperatures.	n-alkanes	93-102	homeobox C10	Homo sapiens	108-111
35134922-0	2022	Orthologs of Saccharomyces cerevisiae SFH2, genes encoding Sec14 family proteins, implicated in utilization of n-alkanes and filamentous growth in response to n-alkanes in Yarrowia lipolytica.	n-alkanes	159-168	Csr1p	Saccharomyces cerevisiae S288C	38-42
35134922-6	2022	These results suggest that SFH2 orthologs are involved in the utilization of n-alkanes and filamentous growth in response to n-alkanes by Y. lipolytica.	n-alkanes	77-86	Csr1p	Saccharomyces cerevisiae S288C	27-31
35134922-6	2022	These results suggest that SFH2 orthologs are involved in the utilization of n-alkanes and filamentous growth in response to n-alkanes by Y. lipolytica.	n-alkanes	125-134	Csr1p	Saccharomyces cerevisiae S288C	27-31
33557073-4	2021	cer3-6, a known Arabidopsis wax-deficient mutant (with distinct reduction in aldehydes, n-alkanes, secondary n-alcohols, and ketones compared to wild type (WT)), was most sensitive to water loss, while dewax, a known wax overproducer (greater alkanes and ketones compared to WT), was more resistant to dehydration compared to WT.	n-alkanes	88-97	Fatty acid hydroxylase superfamily	Arabidopsis thaliana	0-6
3566799-0	1987	Stabilization of the reduced halocarbon-cytochrome P-450 complex of halothane by N-alkanes.	n-alkanes	81-90	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	40-56
2424439-0	1986	N-alkanes induce the synthesis of cytochrome P-450 mRNA in Candida maltosa.	n-alkanes	0-9	cytochrome P450 709B1	Triticum aestivum	34-50
24232516-2	1980	Exposure of the alga to paraffins for 10 days results in accumulation of n-alkanes having between C13 and C16 carbon atoms.	n-alkanes	73-82	homeobox C13	Homo sapiens	98-101
1096820-4	1975	Strains UP-2, UP-3, and UP-4 grew on RAG-1-degraded oil (specifically depleted of n-alkanes).	n-alkanes	82-91	recombination activating 1	Homo sapiens	37-42
1168904-1	1975	The so-called fungus Cladosporium resinae that often occurs in oil fuels ane increases their acidity grows well at the expense of n-alkanes from C11 to C16.	n-alkanes	130-139	RNA polymerase III subunit K	Homo sapiens	145-148
4735447-5	1973	The long chain n-alkanes (C(14) to C(18)) supported good growth of all isolates, but there was no obvious correlation between cell yields and chain lengths of these n-alkanes.	n-alkanes	15-24	Bardet-Biedl syndrome 9	Homo sapiens	35-40
33151-1	1979	When Mycobacterium convolutum R22 was grown on the n-alkanes C13 through C16, the predominant fatty acids were of the same chain length as the growth substrate.	n-alkanes	51-60	homeobox C13	Homo sapiens	61-64
33151-2	1979	Cells grown on C13 through C16 n-alkanes incorporated between 15 and 85 pmol of acetate per microgram of lipid into the fatty acids, whereas acetate- or propane-grown cells incorporated 280 and 255 pmol of acetate per microgram of lipid, respectively.	n-alkanes	31-40	homeobox C13	Homo sapiens	15-18
21171-4	1977	It was shown that n-alkanes stimulated one of three enzymic steps of lecithin biosynthesis from choline; that is, the formulation of CDP-choline catalyzed by CTP: cholinephosphate cytidyltransferase [EC 2.7.7.15], an enzyme on the microsomal membrane.	n-alkanes	18-27	cut-like homeobox 1	Rattus norvegicus	133-136
961785-2	1976	The major compounds present are a series of n-alkanes (C16 to C40), with the addition of iso and anteiso hydrocarbons.	n-alkanes	44-53	CCR4-NOT transcription complex subunit 11	Homo sapiens	62-65
31030953-6	2019	Detection over a wide volatility range from C10 to C40 n-alkanes is achieved using the dual-trap TAG.	n-alkanes	55-64	CCR4-NOT transcription complex subunit 11	Homo sapiens	51-54
33262429-8	2020	The study of RTlnVn and the specific free energy  Gsp(T) of n-alkanes and polar solvents adsorbed on the various catalysts revealed the important change in the acid properties of catalysts with both the temperature and the rhodium percentage.	n-alkanes	60-69	GSM1	Homo sapiens	50-53
31310981-2	2019	The removal kinetics of semi-volatile n-alkanes (C10, C11, C13-16) under three pulsed heating operations of soil vapor extraction (SVE) was investigated.	n-alkanes	38-47	homeobox C10	Homo sapiens	49-52
31310981-6	2019	The residual n-alkanes of C10, C11, C13 and C14 in all collected soil samples were declined to levels of lower than 10 mg/kg.	n-alkanes	13-22	homeobox C10	Homo sapiens	26-29
31310981-6	2019	The residual n-alkanes of C10, C11, C13 and C14 in all collected soil samples were declined to levels of lower than 10 mg/kg.	n-alkanes	13-22	RNA polymerase III subunit K	Homo sapiens	31-34
31310981-6	2019	The residual n-alkanes of C10, C11, C13 and C14 in all collected soil samples were declined to levels of lower than 10 mg/kg.	n-alkanes	13-22	homeobox C13	Homo sapiens	36-39
29965447-5	2018	The n-alkanes were mainly C18-C24, with C21H44 and C22H46 accounting for the greatest portion.	n-alkanes	4-13	Bardet-Biedl syndrome 9	Homo sapiens	26-29
29276955-2	2018	n-Alkanes in the range C12-C33 and C13-C34 were identified in the surface sediments and the core, respectively.	n-alkanes	0-9	CD82 molecule	Homo sapiens	27-30
31161541-3	2019	The n-alkanes extracted from the sediments contained a homologous series from C15 to C34, with a notable predominance of odd carbon compounds except for sediments from the more intensively industrialized Lake Daye, in which > C21 n-alkanes showed no odd/even predominance, and carbon preference index (CPI) approached unity.	n-alkanes	4-13	placenta associated 8	Homo sapiens	78-81
31161541-3	2019	The n-alkanes extracted from the sediments contained a homologous series from C15 to C34, with a notable predominance of odd carbon compounds except for sediments from the more intensively industrialized Lake Daye, in which > C21 n-alkanes showed no odd/even predominance, and carbon preference index (CPI) approached unity.	n-alkanes	233-242	TBL1X/Y related 1	Homo sapiens	229-232
31161541-4	2019	Abundance values of middle-chain (C21, C23, and C25) and long-chain (C27, C29, C31, and C33) n-alkanes in Lake Daye were approximately 4 to 3 times greater than the average for other lakes, reaching 272.4 and 486.3 mug/g TOC, respectively, in the study.	n-alkanes	93-102	CD82 molecule	Homo sapiens	88-91
31161541-5	2019	Short-chain n-alkanes (C15, C17, and C19) in the sediments varied in abundance from 10.0 to 76.2 mug/g TOC across the study and showed a moderate correlation with total phosphorus (TP) concentrations in the overlying water.	n-alkanes	12-21	placenta associated 8	Homo sapiens	23-26
31161541-5	2019	Short-chain n-alkanes (C15, C17, and C19) in the sediments varied in abundance from 10.0 to 76.2 mug/g TOC across the study and showed a moderate correlation with total phosphorus (TP) concentrations in the overlying water.	n-alkanes	12-21	cytokine like 1	Homo sapiens	28-31
31293354-5	2019	The diblock copolymer chosen was poly(stearyl methacrylate)-poly(2,2,2-trifluoroethyl methacrylate) (PSMA-PTFEMA), which self-assembles to form PTFEMA core spheres in n-alkanes.	n-alkanes	167-176	folate hydrolase 1	Homo sapiens	101-105
29621549-1	2018	In this study, we investigated the role of OSH6, which encodes a homolog of the oxysterol-binding protein, in the assimilation of n-alkanes in the yeast Yarrowia lipolytica.	n-alkanes	130-139	oxysterol-binding protein OSH6	Saccharomyces cerevisiae S288C	43-47
29621549-2	2018	The deletion mutant of OSH6 showed growth defects on n-alkanes of 10-16 carbons.	n-alkanes	53-62	oxysterol-binding protein OSH6	Saccharomyces cerevisiae S288C	23-27
29204943-4	2018	Total n-alkanes ranged from 3.51 mug/g to 117 mug/g and showed a strong presence of odd carbon-numbered n-alkane ratios (range of C25 to C35), suggesting source input from terrestrial biomass.	n-alkanes	6-15	migration and invasion enhancer 1	Homo sapiens	137-140
28391951-1	2017	n-Alkanes and polycyclic aromatic hydrocarbons (PAHs) bound to atmospheric particulate matter (PM1) were investigated in a traffic site located in an urban area of Venice Province (Eastern Po Valley, Italy) during the cold season.	n-alkanes	0-9	transmembrane protein 11	Homo sapiens	95-98
29964615-7	2017	Concentrations of total dissolved n-alkanes(C11-C37) were between 1.756-39.09 mug L-1 with a high carbon number predominance profile without odd-even carbon number preference.	n-alkanes	34-43	immunoglobulin kappa variable 1-16	Homo sapiens	82-85
29964615-11	2017	In the sea area with strong water exchange, concentrations of total n-alkanes were around 2.196 mug L-1, which could be considered as the environmental background level of n-alkanes in Jiaozhou Bay.	n-alkanes	68-77	immunoglobulin kappa variable 1-16	Homo sapiens	100-103
29964615-11	2017	In the sea area with strong water exchange, concentrations of total n-alkanes were around 2.196 mug L-1, which could be considered as the environmental background level of n-alkanes in Jiaozhou Bay.	n-alkanes	172-181	immunoglobulin kappa variable 1-16	Homo sapiens	100-103
28527455-2	2017	For example, we implement molecular simulation to predict the critical constants (i.e., critical temperature, critical density, critical pressure, and critical compressibility factor) for large n-alkanes that thermally decompose experimentally (as large as C48).	n-alkanes	194-203	CDK5 regulatory subunit associated protein 2	Homo sapiens	257-260
28216134-11	2017	Some sampling sites especially Kharg, Lavan, Siri and Lark indicated higher concentration of n-alkanes due to the higher maintenance of organic matter by high clay content in the sediments.	n-alkanes	93-102	RNA binding motif protein 4	Homo sapiens	54-58
27341155-0	2016	Particulate PAHs and n-alkanes in the air over Southern and Eastern Mediterranean Sea.	n-alkanes	21-30	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	82-85
28007387-2	2017	The results show that the n-alkanes in this sediment core conform to a bimodal distribution, and exhibit an odd-to-even predominance of high molecular weights compared to an even-to-odd predominance in low molecular weight n-alkanes with maxima at C16 and C18.	n-alkanes	26-35	Bardet-Biedl syndrome 9	Homo sapiens	256-259
26952993-3	2016	Through the analysis of hydrocarbon biodegradation, TCOB-4 was found to biodegrade more middle-chain n-alkanes (from C17 to C23) and long-chain n-alkanes (C31-C36).	n-alkanes	101-110	cytokine like 1	Homo sapiens	117-120
27270951-2	2016	n-Alkanes (C19-C36), fatty acids (C8-C32) and n-alcohols (C16-C32) detected in Beijing aerosols are characterized by the predominance of C23, C16 and C28, respectively.	n-alkanes	0-9	chemokine like factor	Homo sapiens	62-65
27270951-2	2016	n-Alkanes (C19-C36), fatty acids (C8-C32) and n-alcohols (C16-C32) detected in Beijing aerosols are characterized by the predominance of C23, C16 and C28, respectively.	n-alkanes	0-9	nucleolin	Homo sapiens	137-140
27270951-5	2016	delta(13)C values of n-alkanes and low molecular weight fatty acids (C16:0, C18:0) ranged from -34.1 to -24.7% and -26.9 to -24.6%, respectively, which are generally heavier on polluted days than those on clear days.	n-alkanes	21-30	Bardet-Biedl syndrome 9	Homo sapiens	76-79
27133399-3	2016	The main n-alkanes in most samples were C31 , C29 , and C33 .	n-alkanes	9-18	CD82 molecule	Homo sapiens	56-59
26632517-5	2015	In addition, CC10 also exhibits good selectivity for the separation of n-alkanes, n-alcohols, Grob mixture, and positional isomers.	n-alkanes	71-80	secretoglobin family 1A member 1	Homo sapiens	13-17