127 related articles for article (PubMed ID: 11186893)
1. Polymorphisms at the Werner locus: II. 1074Leu/Phe, 1367Cys/Arg, longevity, and atherosclerosis.
Castro E; Edland SD; Lee L; Ogburn CE; Deeb SS; Brown G; Panduro A; Riestra R; Tilvis R; Louhija J; Penttinen R; Erkkola R; Wang L; Martin GM; Oshima J
Am J Med Genet; 2000 Dec; 95(4):374-80. PubMed ID: 11186893
[TBL] [Abstract][Full Text] [Related]
2. Polymorphisms at the Werner locus: I. Newly identified polymorphisms, ethnic variability of 1367Cys/Arg, and its stability in a population of Finnish centenarians.
Castro E; Ogburn CE; Hunt KE; Tilvis R; Louhija J; Penttinen R; Erkkola R; Panduro A; Riestra R; Piussan C; Deeb SS; Wang L; Edland SD; Martin GM; Oshima J
Am J Med Genet; 1999 Feb; 82(5):399-403. PubMed ID: 10069711
[TBL] [Abstract][Full Text] [Related]
3. Paraoxonase polymorphisms PON1 192 and 55 and longevity in Italian centenarians and Irish nonagenarians. A pooled analysis.
Rea IM; McKeown PP; McMaster D; Young IS; Patterson C; Savage MJ; Belton C; Marchegiani F; Olivieri F; Bonafe M; Franceschi C
Exp Gerontol; 2004 Apr; 39(4):629-35. PubMed ID: 15050299
[TBL] [Abstract][Full Text] [Related]
4. Human evidence that the cystatin C gene is implicated in focal progression of coronary artery disease.
Eriksson P; Deguchi H; Samnegård A; Lundman P; Boquist S; Tornvall P; Ericsson CG; Bergstrand L; Hansson LO; Ye S; Hamsten A
Arterioscler Thromb Vasc Biol; 2004 Mar; 24(3):551-7. PubMed ID: 14726415
[TBL] [Abstract][Full Text] [Related]
5. Linkage disequilibrium between four MTTP gene polymorphisms in a Mexican population.
Luévano KE; González JR; Perea FJ; Magaña MT
Ann Hum Biol; 2009; 36(2):211-9. PubMed ID: 19255880
[TBL] [Abstract][Full Text] [Related]
6. Mitochondrial genotypes and cytochrome b variants associated with longevity or Parkinson's disease.
Tanaka M
J Neurol; 2002 Sep; 249 Suppl 2():II11-8. PubMed ID: 12375058
[TBL] [Abstract][Full Text] [Related]
7. [A related analysis for alpha, beta fibrinogen gene haplotypes and nucleotide polymorphisms associated with the ischemic stroke in Hainan Han population].
Liang L; Sun C; Liao XP; Xiao F; Chen XD; Huang SX; Tang XL; Wen GQ; Long ZG; Wang XY; Liu GX; Cheng S; Cai WW
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):316-9. PubMed ID: 16767673
[TBL] [Abstract][Full Text] [Related]
8. Carrier detection of Werner's syndrome using a microsatellite that exhibits linkage disequilibrium with the Werner's syndrome locus.
Kihara K; Nakura J; Ye L; Mitsuda N; Kamino K; Zhao Y; Fujioka Y; Miki T; Ogihara T
Jpn J Hum Genet; 1994 Dec; 39(4):403-9. PubMed ID: 7873752
[TBL] [Abstract][Full Text] [Related]
9. Mitochondrial DNA polymorphisms associated with longevity in a Finnish population.
Niemi AK; Hervonen A; Hurme M; Karhunen PJ; Jylhä M; Majamaa K
Hum Genet; 2003 Jan; 112(1):29-33. PubMed ID: 12483296
[TBL] [Abstract][Full Text] [Related]
10. The differential effects of age on the association of KLOTHO gene polymorphisms with coronary artery disease.
Rhee EJ; Oh KW; Lee WY; Kim SY; Jung CH; Kim BJ; Sung KC; Kim BS; Kang JH; Lee MH; Kim SW; Park JR
Metabolism; 2006 Oct; 55(10):1344-51. PubMed ID: 16979405
[TBL] [Abstract][Full Text] [Related]
11. Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population.
Ye L; Miki T; Nakura J; Oshima J; Kamino K; Rakugi H; Ikegami H; Higaki J; Edland SD; Martin GM; Ogihara T
Am J Med Genet; 1997 Feb; 68(4):494-8. PubMed ID: 9021029
[TBL] [Abstract][Full Text] [Related]
12. Excess of rare cancers in Werner syndrome (adult progeria).
Goto M; Miller RW; Ishikawa Y; Sugano H
Cancer Epidemiol Biomarkers Prev; 1996 Apr; 5(4):239-46. PubMed ID: 8722214
[TBL] [Abstract][Full Text] [Related]
13. LMNA mutations in progeroid syndromes.
Huang S; Kennedy BK; Oshima J
Novartis Found Symp; 2005; 264():197-202; discussion 202-7, 227-30. PubMed ID: 15773755
[TBL] [Abstract][Full Text] [Related]
14. Association between the eNOS (Glu298Asp) and the RAS genes polymorphisms and premature coronary artery disease in a Turkish population.
Berdeli A; Sekuri C; Sirri Cam F; Ercan E; Sagcan A; Tengiz I; Eser E; Akin M
Clin Chim Acta; 2005 Jan; 351(1-2):87-94. PubMed ID: 15563875
[TBL] [Abstract][Full Text] [Related]
15. Secular trends towards delayed onsets of pathologies and prolonged longevities in Japanese patients with Werner syndrome.
Goto M; Matsuura M
Biosci Trends; 2008 Apr; 2(2):81-7. PubMed ID: 20103906
[TBL] [Abstract][Full Text] [Related]
16. Polymorphism R25P in the gene encoding transforming growth factor-beta (TGF-beta1) is a newly identified risk factor for proliferative diabetic retinopathy.
Beránek M; Kanková K; Benes P; Izakovicová-Hollá L; Znojil V; Hájek D; Vlková E; Vácha J
Am J Med Genet; 2002 May; 109(4):278-83. PubMed ID: 11992481
[TBL] [Abstract][Full Text] [Related]
17. Possible association of p53 codon 72 polymorphism with susceptibility to adult and pediatric high-grade astrocytomas.
Parhar P; Ezer R; Shao Y; Allen JC; Miller DC; Newcomb EW
Brain Res Mol Brain Res; 2005 Jun; 137(1-2):98-103. PubMed ID: 15950766
[TBL] [Abstract][Full Text] [Related]
18. Polymorphisms of the TP53 codon 72 and WRN codon 1367 in individuals from Northern Brazil with gastric adenocarcinoma.
Khayat AS; Lobo Gatti L; Moura Lima E; de Assumpção PP; Nascimento Motta FJ; Harada ML; Casartelli C; Marques Payão SL; Cardoso Smith MA; Burbano RR
Clin Exp Med; 2005 Dec; 5(4):161-8. PubMed ID: 16362795
[TBL] [Abstract][Full Text] [Related]
19. Carrier-state of D allele in ACE gene insertion/deletion polymorphism is associated with coronary artery disease, in contrast to the C677-->T transition in the MTHFR gene.
Zak I; Niemiec P; Sarecka B; Balcerzyk A; Ciemniewski Z; Rudowska E; Dylag S
Acta Biochim Pol; 2003; 50(2):527-34. PubMed ID: 12833177
[TBL] [Abstract][Full Text] [Related]
20. Renin-angiotensin system and haemostasis gene polymorphisms and outcome after coronary artery bypass graft surgery.
Völzke H; Kleine V; Robinson DM; Grimm R; Hertwig S; Schwahn C; Eckel L; Rettig R
Int J Cardiol; 2005 Jan; 98(1):133-9. PubMed ID: 15676177
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]