165 related articles for article (PubMed ID: 24573017)
1. Associations between the CDKN2A/B, ADTRP and PDGFD polymorphisms and the development of coronary atherosclerosis in Japanese patients.
Dechamethakun S; Ikeda S; Arai T; Sato N; Sawabe M; Muramatsu M
J Atheroscler Thromb; 2014; 21(7):680-90. PubMed ID: 24573017
[TBL] [Abstract][Full Text] [Related]
2. GATA2 regulates the CAD susceptibility gene ADTRP rs6903956 through preferential interaction with the G allele.
Luo C; Tang B; Qin S; Yuan C; Du Y; Yang J
Mol Genet Genomics; 2021 Jul; 296(4):799-808. PubMed ID: 33856550
[TBL] [Abstract][Full Text] [Related]
3. Common Variants in Promoter of ADTRP Associate with Early-Onset Coronary Artery Disease in a Southern Han Chinese Population.
Huang EW; Peng LY; Zheng JX; Wang D; Xu QY; Huang L; Wu QP; Tang SB; Luo B; Liu SP; Liu XS; Li ZH; Quan L; Li Y; Shi H; Lv GL; Zhao J; Cheng JD; Liu C
PLoS One; 2015; 10(9):e0137547. PubMed ID: 26375920
[TBL] [Abstract][Full Text] [Related]
4. Functional Genetic Single-Nucleotide Polymorphisms (SNPs) in Cyclin-Dependent Kinase Inhibitor 2A/B (CDKN2A/B) Locus Are Associated with Risk and Prognosis of Osteosarcoma in Chinese Populations.
Zhang H; Mao JS; Hu WF
Med Sci Monit; 2019 Feb; 25():1307-1313. PubMed ID: 30774116
[TBL] [Abstract][Full Text] [Related]
5. Functional genomics of the CDKN2A/B locus in cardiovascular and metabolic disease: what have we learned from GWASs?
Hannou SA; Wouters K; Paumelle R; Staels B
Trends Endocrinol Metab; 2015 Apr; 26(4):176-84. PubMed ID: 25744911
[TBL] [Abstract][Full Text] [Related]
6. Association Study Between Coronary Artery Disease and rs1333049 Polymorphism at 9p21.3 Locus in Italian Population.
Pignataro P; Pezone L; Di Gioia G; Franco D; Iaccarino G; Iolascon A; Ciccarelli M; Capasso M
J Cardiovasc Transl Res; 2017 Dec; 10(5-6):455-458. PubMed ID: 28639227
[TBL] [Abstract][Full Text] [Related]
7. Association study of the miRNA-binding site polymorphisms of CDKN2A/B genes with gestational diabetes mellitus susceptibility.
Wang X; Li W; Ma L; Gao J; Liu J; Ping F; Nie M
Acta Diabetol; 2015 Oct; 52(5):951-8. PubMed ID: 25990668
[TBL] [Abstract][Full Text] [Related]
8. Genetic risk variants in the CDKN2A/B, RTEL1 and EGFR genes are associated with somatic biomarkers in glioma.
Ghasimi S; Wibom C; Dahlin AM; Brännström T; Golovleva I; Andersson U; Melin B
J Neurooncol; 2016 May; 127(3):483-92. PubMed ID: 26839018
[TBL] [Abstract][Full Text] [Related]
9. A case-control study provides evidence of association for a common SNP rs974819 in PDGFD to coronary heart disease and suggests a sex-dependent effect.
Zhou J; Huang Y; Huang RS; Wang F; Xu L; Le Y; Yang X; Xu W; Huang X; Lian J; Duan S
Thromb Res; 2012 Oct; 130(4):602-6. PubMed ID: 22704460
[TBL] [Abstract][Full Text] [Related]
10. A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease.
Coronary Artery Disease (C4D) Genetics Consortium
Nat Genet; 2011 Mar; 43(4):339-44. PubMed ID: 21378988
[TBL] [Abstract][Full Text] [Related]
11. Polymorphisms of LTA, LGALS2, and PSMA6 genes and coronary atherosclerosis: a pathological study of 1503 consecutive autopsy cases.
Ikeda S; Tanaka N; Arai T; Chida K; Muramatsu M; Sawabe M
Atherosclerosis; 2012 Apr; 221(2):458-60. PubMed ID: 22310064
[TBL] [Abstract][Full Text] [Related]
12. Interaction of type 2 diabetes mellitus with chromosome 9p21 rs10757274 polymorphism on the risk of myocardial infarction: a case-control study in Chinese population.
Zhang LW; Li JP; Duan FF; Liu ZK; Zhan SY; Hu YH; Jiang J; Zhang Y; Huo Y; Chen DF
BMC Cardiovasc Disord; 2014 Nov; 14():170. PubMed ID: 25430018
[TBL] [Abstract][Full Text] [Related]
13. Identification of a molecular signaling gene-gene regulatory network between GWAS susceptibility genes ADTRP and MIA3/TANGO1 for coronary artery disease.
Luo C; Wang F; Ren X; Ke T; Xu C; Tang B; Qin S; Yao Y; Chen Q; Wang QK
Biochim Biophys Acta Mol Basis Dis; 2017 Jun; 1863(6):1640-1653. PubMed ID: 28341552
[TBL] [Abstract][Full Text] [Related]
14. Genetic variants at the 9p21 locus contribute to atherosclerosis through modulation of ANRIL and CDKN2A/B.
Congrains A; Kamide K; Oguro R; Yasuda O; Miyata K; Yamamoto E; Kawai T; Kusunoki H; Yamamoto H; Takeya Y; Yamamoto K; Onishi M; Sugimoto K; Katsuya T; Awata N; Ikebe K; Gondo Y; Oike Y; Ohishi M; Rakugi H
Atherosclerosis; 2012 Feb; 220(2):449-55. PubMed ID: 22178423
[TBL] [Abstract][Full Text] [Related]
15. A genome-wide association study of a coronary artery disease risk variant.
Lee JY; Lee BS; Shin DJ; Woo Park K; Shin YA; Joong Kim K; Heo L; Young Lee J; Kyoung Kim Y; Jin Kim Y; Bum Hong C; Lee SH; Yoon D; Jung Ku H; Oh IY; Kim BJ; Lee J; Park SJ; Kim J; Kawk HK; Lee JE; Park HK; Lee JE; Nam HY; Park HY; Shin C; Yokota M; Asano H; Nakatochi M; Matsubara T; Kitajima H; Yamamoto K; Kim HL; Han BG; Cho MC; Jang Y; Kim HS; Euy Park J; Lee JY
J Hum Genet; 2013 Mar; 58(3):120-6. PubMed ID: 23364394
[TBL] [Abstract][Full Text] [Related]
16. Replication of GWAS identifies RTEL1, CDKN2A/B, and PHLDB1 SNPs as risk factors in Portuguese gliomas patients.
Viana-Pereira M; Moreno DA; Linhares P; Amorim J; Nabiço R; Costa S; Vaz R; Reis RM
Mol Biol Rep; 2020 Feb; 47(2):877-886. PubMed ID: 31721021
[TBL] [Abstract][Full Text] [Related]
17. Polymorphisms of TGFβ-1 and TGFBR2 in relation to coronary artery disease in a Chinese population.
Yang M; Zhu M; Tang L; Zhu H; Lu Y; Xu B; Jiang J; Chen X
Clin Biochem; 2016 Aug; 49(12):873-8. PubMed ID: 27234600
[TBL] [Abstract][Full Text] [Related]
18. Androgen inhibits key atherosclerotic processes by directly activating ADTRP transcription.
Luo C; Pook E; Tang B; Zhang W; Li S; Leineweber K; Cheung SH; Chen Q; Bechem M; Hu JS; Laux V; Wang QK
Biochim Biophys Acta Mol Basis Dis; 2017 Sep; 1863(9):2319-2332. PubMed ID: 28645652
[TBL] [Abstract][Full Text] [Related]
19. Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.
O'Donnell CJ; Kavousi M; Smith AV; Kardia SL; Feitosa MF; Hwang SJ; Sun YV; Province MA; Aspelund T; Dehghan A; Hoffmann U; Bielak LF; Zhang Q; Eiriksdottir G; van Duijn CM; Fox CS; de Andrade M; Kraja AT; Sigurdsson S; Elias-Smale SE; Murabito JM; Launer LJ; van der Lugt A; Kathiresan S; ; Krestin GP; Herrington DM; Howard TD; Liu Y; Post W; Mitchell BD; O'Connell JR; Shen H; Shuldiner AR; Altshuler D; Elosua R; Salomaa V; Schwartz SM; Siscovick DS; Voight BF; Bis JC; Glazer NL; Psaty BM; Boerwinkle E; Heiss G; Blankenberg S; Zeller T; Wild PS; Schnabel RB; Schillert A; Ziegler A; Münzel TF; White CC; Rotter JI; Nalls M; Oudkerk M; Johnson AD; Newman AB; Uitterlinden AG; Massaro JM; Cunningham J; Harris TB; Hofman A; Peyser PA; Borecki IB; Cupples LA; Gudnason V; Witteman JC
Circulation; 2011 Dec; 124(25):2855-64. PubMed ID: 22144573
[TBL] [Abstract][Full Text] [Related]
20. The association of polymorphic variants, rs2267788, rs1333049 and rs2383207 with coronary artery disease, its severity and presentation in North Indian population.
Kashyap S; Kumar S; Agarwal V; Misra DP; Rai MK; Kapoor A
Gene; 2018 Mar; 648():89-96. PubMed ID: 29309886
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
