91 related articles for article (PubMed ID: 25956626)
1. Single-Nucleotide Polymorphisms of Tight Junction Component Claudin-1 Associated with Leukoaraiosis.
Yadav BK; Shin BS
J Stroke Cerebrovasc Dis; 2015 Jul; 24(7):1662-70. PubMed ID: 25956626
[TBL] [Abstract][Full Text] [Related]
2. Single-nucleotide polymorphisms of the adherent junction component cadherin gene are associated with leukoaraiosis.
Yadav BK; Shin BS
Gene; 2018 Nov; 676():65-72. PubMed ID: 30017735
[TBL] [Abstract][Full Text] [Related]
3. Association of Genetic Variation in a Wnt Signaling Pathway Gene (
Yadav BK; Yadav R; Kang HG; Kim KW; Lee CH; Shin BS
Genet Test Mol Biomarkers; 2020 Nov; 24(11):708-716. PubMed ID: 33026847
[No Abstract] [Full Text] [Related]
4. Association of rs2075575 and rs9951307 polymorphisms of AQP-4 gene with leukoaraiosis.
Yadav BK; Oh SY; Kim NK; Shin BS
J Stroke Cerebrovasc Dis; 2014; 23(5):1199-206. PubMed ID: 24582793
[TBL] [Abstract][Full Text] [Related]
5. Association of genetic polymorphisms of claudin-1 with small vessel vascular dementia.
Srinivasan V; Braidy N; Xu YH; Xie P; Kancherla K; Chandramohan S; Chan EKW; Chan DK
Clin Exp Pharmacol Physiol; 2017 Jun; 44(6):623-630. PubMed ID: 28273404
[TBL] [Abstract][Full Text] [Related]
6. The role of glutathione S-transferase and claudin-1 gene polymorphisms in contact sensitization: a cross-sectional study.
Ross-Hansen K; Linneberg A; Johansen JD; Hersoug LG; Brasch-Andersen C; Menné T; Thyssen JP
Br J Dermatol; 2013 Apr; 168(4):762-70. PubMed ID: 23136956
[TBL] [Abstract][Full Text] [Related]
7. Evaluation of the roles of the A185C and C406T kinesin light-chain 1 variants in the development of leukoaraiosis.
Szolnoki Z; Kondacs A; Mandi Y; Somogyvari F
Neurosci Lett; 2007 Dec; 429(2-3):101-4. PubMed ID: 17977659
[TBL] [Abstract][Full Text] [Related]
8. The tight junction gene Claudin-1 is associated with atopic dermatitis among Ethiopians.
Asad S; Winge MC; Wahlgren CF; Bilcha KD; Nordenskjöld M; Taylan F; Bradley M
J Eur Acad Dermatol Venereol; 2016 Nov; 30(11):1939-1941. PubMed ID: 27581203
[TBL] [Abstract][Full Text] [Related]
9. Leukoaraiosis is associated with genes regulating blood-brain barrier homeostasis in ischaemic stroke patients.
Fernandez-Cadenas I; Mendioroz M; Domingues-Montanari S; Del Rio-Espinola A; Delgado P; Ruiz A; Hernandez-Guillamon M; Giralt D; Chacon P; Navarro-Sobrino M; Ribo M; Molina CA; Alvarez-Sabin J; Rosell A; Montaner J
Eur J Neurol; 2011 Jun; 18(6):826-35. PubMed ID: 21122033
[TBL] [Abstract][Full Text] [Related]
10. Cyclooxygenase 2 genetic polymorphism may increase the risk of developing leukoaraiosis in Chinese.
Shan XY; Chen GZ; Cheng GP; Tao HM
J Mol Neurosci; 2013 Oct; 51(2):461-6. PubMed ID: 23852948
[TBL] [Abstract][Full Text] [Related]
11. Polymorphisms in the CLDN1 and CLDN7 genes are related to differentiation and tumor stage in colon carcinoma.
Hahn-Strömberg V; Askari S; Befekadu R; Matthiessen P; Karlsson S; Nilsson TK
APMIS; 2014 Jul; 122(7):636-42. PubMed ID: 24479816
[TBL] [Abstract][Full Text] [Related]
12. Association of rs1466535 LRP1 but not rs3019885 SLC30A8 and rs6674171 TDRD10 gene polymorphisms with abdominal aortic aneurysm in Italian patients.
Galora S; Saracini C; Pratesi G; Sticchi E; Pulli R; Pratesi C; Abbate R; Giusti B
J Vasc Surg; 2015 Mar; 61(3):787-92. PubMed ID: 24423473
[TBL] [Abstract][Full Text] [Related]
13. Association of the polymorphisms 292 C>T and 1304 G>A in the SLC38A4 gene with hyperglycaemia.
González-Renteria SM; Loera-Castañeda V; Chairez-Hernández I; Sosa-Macias M; Paniagua-Castro N; Lares-Aseff I; Rodríguez-Moran M; Guerrero-Romero F; Galaviz-Hernández C
Diabetes Metab Res Rev; 2013 Jan; 29(1):39-43. PubMed ID: 22945694
[TBL] [Abstract][Full Text] [Related]
14. Polymorphisms in genes of the endothelin system and cerebral small-vessel disease.
Gormley K; Bevan S; Hassan A; Markus HS
Stroke; 2005 Aug; 36(8):1656-60. PubMed ID: 16002759
[TBL] [Abstract][Full Text] [Related]
15. CD81 and CLDN1 polymorphisms and hepatitis C virus infection susceptibility: a case control study.
Sun S; Jin G; Kang H
Gene; 2015 Aug; 567(1):87-91. PubMed ID: 25934191
[TBL] [Abstract][Full Text] [Related]
16. Association of MMP-9 gene polymorphisms with Behçet's disease risk.
Naouali A; Kaabachi W; Tizaoui K; Amor AB; Hamzaoui A; Hamzaoui K
Immunol Lett; 2015 Mar; 164(1):18-24. PubMed ID: 25639450
[TBL] [Abstract][Full Text] [Related]
17. Family-based association study of matrix metalloproteinase-3 and -9 haplotypes with susceptibility to ischemic white matter injury.
Fornage M; Mosley TH; Jack CR; de Andrade M; Kardia SL; Boerwinkle E; Turner ST
Hum Genet; 2007 Jan; 120(5):671-80. PubMed ID: 17024375
[TBL] [Abstract][Full Text] [Related]
18. Transforming growth factor beta 1 is a novel susceptibility gene for adolescent idiopathic scoliosis.
Ryzhkov II; Borzilov EE; Churnosov MI; Ataman AV; Dedkov AA; Polonikov AV
Spine (Phila Pa 1976); 2013 May; 38(12):E699-704. PubMed ID: 23446766
[TBL] [Abstract][Full Text] [Related]
19. Association of angiotensin-converting enzyme, methylene tetrahydrofolate reductase and paraoxonase gene polymorphism and coronary artery disease in an Indian population.
Pandey U; Kumari R; Nath B; Ganesh S; Banerjee I; Hasan OM; Midha T; Pandey S
Cardiol J; 2011; 18(4):385-94. PubMed ID: 21769819
[TBL] [Abstract][Full Text] [Related]
20. NOS3 tagSNPs does not modify the chronic kidney disease progression in autosomal dominant polycystic kidney disease.
Ramanathan G; Periyasamy S; Lakkakula BV
Nephrology (Carlton); 2014 Sep; 19(9):537-41. PubMed ID: 24824375
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
