520 related articles for article (PubMed ID: 29506519)
1. RNAseq analysis of bronchial epithelial cells to identify COPD-associated genes and SNPs.
Yeo J; Morales DA; Chen T; Crawford EL; Zhang X; Blomquist TM; Levin AM; Massion PP; Arenberg DA; Midthun DE; Mazzone PJ; Nathan SD; Wainz RJ; Nana-Sinkam P; Willey PFS; Arend TJ; Padda K; Qiu S; Federov A; Hernandez DR; Hammersley JR; Yoon Y; Safi F; Khuder SA; Willey JC
BMC Pulm Med; 2018 Mar; 18(1):42. PubMed ID: 29506519
[TBL] [Abstract][Full Text] [Related]
2. Haplotype and diplotype analyses of variation in ERCC5 transcription cis-regulation in normal bronchial epithelial cells.
Zhang X; Crawford EL; Blomquist TM; Khuder SA; Yeo J; Levin AM; Willey JC
Physiol Genomics; 2016 Jul; 48(7):537-43. PubMed ID: 27235448
[TBL] [Abstract][Full Text] [Related]
3. Cis-acting genetic variation at an E2F1/YY1 response site and putative p53 site is associated with altered allele-specific expression of ERCC5 (XPG) transcript in normal human bronchial epithelium.
Blomquist TM; Crawford EL; Willey JC
Carcinogenesis; 2010 Jul; 31(7):1242-50. PubMed ID: 20233728
[TBL] [Abstract][Full Text] [Related]
4. Ensemble genomic analysis in human lung tissue identifies novel genes for chronic obstructive pulmonary disease.
Morrow JD; Cho MH; Platig J; Zhou X; DeMeo DL; Qiu W; Celli B; Marchetti N; Criner GJ; Bueno R; Washko GR; Glass K; Quackenbush J; Silverman EK; Hersh CP
Hum Genomics; 2018 Jan; 12(1):1. PubMed ID: 29335020
[TBL] [Abstract][Full Text] [Related]
5. CEBPG regulates ERCC5/XPG expression in human bronchial epithelial cells and this regulation is modified by E2F1/YY1 interactions.
Crawford EL; Blomquist T; Mullins DN; Yoon Y; Hernandez DR; Al-Bagdhadi M; Ruiz J; Hammersley J; Willey JC
Carcinogenesis; 2007 Dec; 28(12):2552-9. PubMed ID: 17893230
[TBL] [Abstract][Full Text] [Related]
6. Impact of SNP-SNP interactions of DNA repair gene
Sang L; Lv Z; Sun LP; Xu Q; Yuan Y
World J Gastroenterol; 2018 Feb; 24(5):602-612. PubMed ID: 29434449
[TBL] [Abstract][Full Text] [Related]
7. eQTL of bronchial epithelial cells and bronchial alveolar lavage deciphers GWAS-identified asthma genes.
Li X; Hastie AT; Hawkins GA; Moore WC; Ampleford EJ; Milosevic J; Li H; Busse WW; Erzurum SC; Kaminski N; Wenzel SE; Meyers DA; Bleecker ER
Allergy; 2015 Oct; 70(10):1309-18. PubMed ID: 26119467
[TBL] [Abstract][Full Text] [Related]
8. Genetic regulation of gene expression in the lung identifies CST3 and CD22 as potential causal genes for airflow obstruction.
Lamontagne M; Timens W; Hao K; Bossé Y; Laviolette M; Steiling K; Campbell JD; Couture C; Conti M; Sherwood K; Hogg JC; Brandsma CA; van den Berge M; Sandford A; Lam S; Lenburg ME; Spira A; Paré PD; Nickle D; Sin DD; Postma DS
Thorax; 2014 Nov; 69(11):997-1004. PubMed ID: 25182044
[TBL] [Abstract][Full Text] [Related]
9. A lung cancer risk classifier comprising genome maintenance genes measured in normal bronchial epithelial cells.
Yeo J; Crawford EL; Zhang X; Khuder S; Chen T; Levin A; Blomquist TM; Willey JC
BMC Cancer; 2017 May; 17(1):301. PubMed ID: 28464886
[TBL] [Abstract][Full Text] [Related]
10. Laryngeal cancer risk and common single nucleotide polymorphisms in nucleotide excision repair pathway genes ERCC1, ERCC2, ERCC3, ERCC4, ERCC5 and XPA.
Lu B; Li J; Gao Q; Yu W; Yang Q; Li X
Gene; 2014 May; 542(1):64-8. PubMed ID: 24582975
[TBL] [Abstract][Full Text] [Related]
11. Limited overlap in significant hits between genome-wide association studies on two airflow obstruction definitions in the same population.
van der Plaat DA; Vonk JM; Lahousse L; de Jong K; Faiz A; Nedeljkovic I; Amin N; van Diemen CC; Brusselle GG; Bossé Y; Brandsma CA; Hao K; Paré PD; van Duijn CM; Postma DS; Boezen HM
BMC Pulm Med; 2019 Mar; 19(1):58. PubMed ID: 30845926
[TBL] [Abstract][Full Text] [Related]
12. Analysis of genetically driven alternative splicing identifies FBXO38 as a novel COPD susceptibility gene.
Saferali A; Yun JH; Parker MM; Sakornsakolpat P; Chase RP; Lamb A; Hobbs BD; Boezen MH; Dai X; de Jong K; Beaty TH; Wei W; Zhou X; Silverman EK; Cho MH; Castaldi PJ; Hersh CP; ;
PLoS Genet; 2019 Jul; 15(7):e1008229. PubMed ID: 31269066
[TBL] [Abstract][Full Text] [Related]
13. Molecular mechanisms underlying variations in lung function: a systems genetics analysis.
Obeidat M; Hao K; Bossé Y; Nickle DC; Nie Y; Postma DS; Laviolette M; Sandford AJ; Daley DD; Hogg JC; Elliott WM; Fishbane N; Timens W; Hysi PG; Kaprio J; Wilson JF; Hui J; Rawal R; Schulz H; Stubbe B; Hayward C; Polasek O; Järvelin MR; Zhao JH; Jarvis D; Kähönen M; Franceschini N; North KE; Loth DW; Brusselle GG; Smith AV; Gudnason V; Bartz TM; Wilk JB; O'Connor GT; Cassano PA; Tang W; Wain LV; Soler Artigas M; Gharib SA; Strachan DP; Sin DD; Tobin MD; London SJ; Hall IP; Paré PD
Lancet Respir Med; 2015 Oct; 3(10):782-95. PubMed ID: 26404118
[TBL] [Abstract][Full Text] [Related]
14. Genetic control of gene expression at novel and established chronic obstructive pulmonary disease loci.
Castaldi PJ; Cho MH; Zhou X; Qiu W; Mcgeachie M; Celli B; Bakke P; Gulsvik A; Lomas DA; Crapo JD; Beaty TH; Rennard S; Harshfield B; Lange C; Singh D; Tal-Singer R; Riley JH; Quackenbush J; Raby BA; Carey VJ; Silverman EK; Hersh CP
Hum Mol Genet; 2015 Feb; 24(4):1200-10. PubMed ID: 25315895
[TBL] [Abstract][Full Text] [Related]
15. Genetic Association between ERCC5 rs17655 Polymorphism and Colorectal Cancer Risk: Evidence Based on a Meta-analysis.
Zeng Y; Wei L; Wang YJ; Liu C
Asian Pac J Cancer Prev; 2015; 16(13):5565-71. PubMed ID: 26225711
[TBL] [Abstract][Full Text] [Related]
16. Study on association between ERCC5 single nucleotide polymorphism and susceptibility to esophageal cancer.
Zhang C; Liao Z; Yu G; Huang W; Song X
J BUON; 2017; 22(4):979-984. PubMed ID: 28952217
[TBL] [Abstract][Full Text] [Related]
17. Human Lung DNA Methylation Quantitative Trait Loci Colocalize with Chronic Obstructive Pulmonary Disease Genome-Wide Association Loci.
Morrow JD; Glass K; Cho MH; Hersh CP; Pinto-Plata V; Celli B; Marchetti N; Criner G; Bueno R; Washko G; Choi AMK; Quackenbush J; Silverman EK; DeMeo DL
Am J Respir Crit Care Med; 2018 May; 197(10):1275-1284. PubMed ID: 29313708
[TBL] [Abstract][Full Text] [Related]
18. Identification of breast cancer associated variants that modulate transcription factor binding.
Liu Y; Walavalkar NM; Dozmorov MG; Rich SS; Civelek M; Guertin MJ
PLoS Genet; 2017 Sep; 13(9):e1006761. PubMed ID: 28957321
[TBL] [Abstract][Full Text] [Related]
19. Nucleotide Excision Repair Gene ERCC2 and ERCC5 Variants Increase Risk of Uterine Cervical Cancer.
Joo J; Yoon KA; Hayashi T; Kong SY; Shin HJ; Park B; Kim YM; Hwang SH; Kim J; Shin A; Kim JY
Cancer Res Treat; 2016 Apr; 48(2):708-14. PubMed ID: 26130668
[TBL] [Abstract][Full Text] [Related]
20. The role of WWOX polymorphisms on COPD susceptibility and pulmonary function traits in Chinese: a case-control study and family-based analysis.
Xie C; Chen X; Qiu F; Zhang L; Wu D; Chen J; Yang L; Lu J
Sci Rep; 2016 Feb; 6():21716. PubMed ID: 26902998
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]