77 related articles for article (PubMed ID: 24668682)
1. Is there any association between childhood cardiac septal defects and ROCK2 gene polymorphism?
Aksoy M; Uygun H; Baspinar O; Demiryurek S; Oztuzcu S; Cengiz B; Irdem A; Araz NC
Genet Mol Res; 2014 Mar; 13(1):1949-54. PubMed ID: 24668682
[TBL] [Abstract][Full Text] [Related]
2. Lack of association between the Thr431Asn and Arg83Lys polymorphisms of the ROCK2 gene and diabetic retinopathy.
Demiryurek AT; Erbagci I; Oztuzcu S; Alasehirli B; Ozkara E; Seker M; Sönmez A; Ozsan M; Camci C
Curr Eye Res; 2010 Dec; 35(12):1128-34. PubMed ID: 20961215
[TBL] [Abstract][Full Text] [Related]
3. Investigation of the Rho-kinase 2 gene Thr431Asn polymorphism in migraine.
Kuzudisli SU; Yilmaz M; Gül Z; Demiryürek S; Yigiter R; Bozkurt H; Akcali A; Neyal M; Bagci C; Cengiz B; Oztuzcu S; Demiryürek AT
Neurol India; 2014; 62(1):9-14. PubMed ID: 24608447
[TBL] [Abstract][Full Text] [Related]
4. Association between the Thr431Asn polymorphism of the ROCK2 gene and risk of developing metastases of breast cancer.
Kalender ME; Demiryürek S; Oztuzcu S; Kizilyer A; Demiryürek AT; Sevinc A; Dikilitas M; Yildiz R; Camci C
Oncol Res; 2010; 18(11-12):583-91. PubMed ID: 20939434
[TBL] [Abstract][Full Text] [Related]
5. Association between Rho-kinase (ROCK2) gene polymorphisms and Behçet's disease.
Oguz E; Alasehirli B; Pehlivan Y; Onat AM; Oztuzcu S; Ozkara E; Kisacik B; Camci C; Demiryürek AT
Transl Res; 2012 Dec; 160(6):428-34. PubMed ID: 22939913
[TBL] [Abstract][Full Text] [Related]
6. Investigation of the association between Rho/Rho-kinase gene polymorphisms and systemic sclerosis.
Pehlivan Y; Yolbas S; Cetin GY; Alibaz-Oner F; Cagatay Y; Yilmaz N; Oztuzcu S; Donmez S; Ozgen M; Koca SS; Pamuk ON; Sayarlıoglu M; Kisacik B; Direskeneli H; Demiryurek AT; Onat AM
Rheumatol Int; 2016 Mar; 36(3):421-7. PubMed ID: 26615410
[TBL] [Abstract][Full Text] [Related]
7. Investigation of the Rho-kinase Gene Polymorphism in Primary Open-angle Glaucoma.
Demiryürek S; Okumus S; Bozgeyik İ; Oztuzcu S; Coskun E; Mat E; Durucu E; Tatar MG; Erbagci İ; Gürler B; Demiryürek AT
Ophthalmic Genet; 2016; 37(1):9-13. PubMed ID: 24617500
[TBL] [Abstract][Full Text] [Related]
8. Role of rho-kinase gene polymorphisms and protein expressions in colorectal cancer development.
Sari I; Berberoglu B; Ozkara E; Oztuzcu S; Camci C; Demiryurek AT
Pathobiology; 2013; 80(3):138-45. PubMed ID: 23328676
[TBL] [Abstract][Full Text] [Related]
9. Association of Rho/Rho-kinase gene polymorphisms and expressions with obesity-related metabolic syndrome.
Tabur S; Oztuzcu S; Oguz E; Korkmaz H; Eroglu S; Ozkaya M; Demiryürek AT
Eur Rev Med Pharmacol Sci; 2015; 19(9):1680-8. PubMed ID: 26004609
[TBL] [Abstract][Full Text] [Related]
10. Association of Rho-kinase Gene Polymorphisms with Respiratory Distress Syndrome in Preterm Neonates.
Kaya G; Sivasli E; Oztuzcu S; Melekoglu NA; Ozkara E; Sarikabadayi U; Demiryürek AT
Pediatr Neonatol; 2017 Feb; 58(1):36-42. PubMed ID: 27269648
[TBL] [Abstract][Full Text] [Related]
11. A genetic variant in a homocysteine metabolic gene that increases the risk of congenital cardiac septal defects in Han Chinese populations.
Xie HH; Li J; Li PQ; Zhang AA; Li Y; Wang YZ; Xie DX; Xie XD
IUBMB Life; 2017 Sep; 69(9):700-705. PubMed ID: 28834160
[TBL] [Abstract][Full Text] [Related]
12. Two functional polymorphisms of ROCK2 enhance arterial stiffening through inhibiting its activity and expression.
Liao YC; Liu PY; Lin HF; Lin WY; Liao JK; Juo SH
J Mol Cell Cardiol; 2015 Feb; 79():180-6. PubMed ID: 25481646
[TBL] [Abstract][Full Text] [Related]
13. Genetic Variants at the rs4720169 Locus of
Hernández-Almaguer MD; Calvo-Anguiano G; Cerda-Flores RM; Salinas-Torres VM; Orozco-Galicia F; Glenn E; García-Guerra J; Sánchez-Cortés G; Lugo-Trampe J; Martínez-Garza LE
Genet Test Mol Biomarkers; 2019 Sep; 23(9):664-670. PubMed ID: 31524541
[No Abstract] [Full Text] [Related]
14. Lack of association between macrophage migration inhibitory factor gene promoter (-173 G/C) polymorphism and childhood Henoch-Schönlein purpura in Turkish patients.
Nalbantoglu S; Tabel Y; Mir S; Berdeli A
Cytokine; 2013 Apr; 62(1):160-4. PubMed ID: 23523092
[TBL] [Abstract][Full Text] [Related]
15. Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects.
Salazar M; Consoli F; Villegas V; Caicedo V; Maddaloni V; Daniele P; Caianiello G; Pachón S; Nuñez F; Limongelli G; Pacileo G; Marino B; Bernal JE; De Luca A; Dallapiccola B
Eur J Med Genet; 2011; 54(3):306-9. PubMed ID: 21276881
[TBL] [Abstract][Full Text] [Related]
16. Maternal medication use, fetal 3435 C>T polymorphism of the ABCB1 gene, and risk of isolated septal defects in a Han Chinese population.
Wang C; Zhou K; Xie L; Li Y; Zhan Y; Qiao L; Qin C; Liu R; Hua Y
Pediatr Cardiol; 2014 Oct; 35(7):1132-41. PubMed ID: 24740628
[TBL] [Abstract][Full Text] [Related]
17. Rho kinase polymorphism influences blood pressure and systemic vascular resistance in human twins: role of heredity.
Seasholtz TM; Wessel J; Rao F; Rana BK; Khandrika S; Kennedy BP; Lillie EO; Ziegler MG; Smith DW; Schork NJ; Brown JH; O'Connor DT
Hypertension; 2006 May; 47(5):937-47. PubMed ID: 16585408
[TBL] [Abstract][Full Text] [Related]
18. [Relations of methionine synthase gene variation with congenital heart disease].
Zhu W; Dao J; Cheng J; Zhao R
Wei Sheng Yan Jiu; 2004 Jan; 33(1):66-9. PubMed ID: 15098482
[TBL] [Abstract][Full Text] [Related]
19. Presenilin-1 polymorphisms are not relevant in susceptibility to ventricular septal defect: a case-control study.
Chen Y; Li H; Zhou B; Peng Y; Zheng Q; Rao L
DNA Cell Biol; 2011 Aug; 30(8):565-8. PubMed ID: 21323574
[TBL] [Abstract][Full Text] [Related]
20. Single-nucleotide polymorphisms of VEGF gene are associated with risk of congenital valvuloseptal heart defects.
Vannay A; Vásárhelyi B; Környei M; Treszl A; Kozma G; Györffy B; Tulassay T; Sulyok E
Am Heart J; 2006 Apr; 151(4):878-81. PubMed ID: 16569553
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]