BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 24608096)

  • 1. Forkhead box C2 promoter variant c.-512C>T is associated with increased susceptibility to chronic venous diseases.
    Surendran S; Girijamma A; Nair R; Ramegowda KS; Nair DH; Thulaseedharan JV; Lakkappa RB; Kamalapurkar G; Kartha CC
    PLoS One; 2014; 9(3):e90682. PubMed ID: 24608096
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Arterialization and anomalous vein wall remodeling in varicose veins is associated with upregulated FoxC2-Dll4 pathway.
    Surendran S; S Ramegowda K; Suresh A; Binil Raj SS; Lakkappa RK; Kamalapurkar G; Radhakrishnan N; C Kartha C
    Lab Invest; 2016 Apr; 96(4):399-408. PubMed ID: 26808710
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Role of the FOXC2 -512C>T polymorphism in type 2 diabetes: possible association with the dysmetabolic syndrome.
    Carlsson E; Groop L; Ridderstråle M
    Int J Obes (Lond); 2005 Mar; 29(3):268-74. PubMed ID: 15597109
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Association of polymorphisms near the FOXC2 gene with the risk of varicose veins in ethnic Russians.
    Shadrina AS; Smetanina MA; Sokolova EA; Sevost'ianova KS; Shevela AI; Demekhova MY; Shonov OA; Ilyukhin EA; Voronina EN; Zolotukhin IA; Kirienko AI; Filipenko ML
    Phlebology; 2016 Oct; 31(9):640-8. PubMed ID: 26420053
    [TBL] [Abstract][Full Text] [Related]  

  • 5. MicroRNA‑199a‑5p regulates FOXC2 to control human vascular smooth muscle cell phenotypic switch.
    Cao Y; Cao Z; Wang W; Jie X; Li L
    Mol Med Rep; 2021 Sep; 24(3):. PubMed ID: 34212977
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Association of polymorphisms in forkhead box C2 and perilipin genes with bone mineral density in community-dwelling Japanese individuals.
    Yamada Y; Ando F; Shimokata H
    Int J Mol Med; 2006 Jul; 18(1):119-27. PubMed ID: 16786163
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Functional polymorphisms in FOXC2 gene and Epithelial ovarian Cancer susceptibility in Chinese population.
    Zhou Z; Ou X; Zou Q; Chu L; Quan X; Chen Y; Liu Y
    J Ovarian Res; 2020 Mar; 13(1):34. PubMed ID: 32222147
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A variant in the transcription factor 7-like 2 (TCF7L2) gene is associated with an increased risk of gestational diabetes mellitus.
    Shaat N; Lernmark A; Karlsson E; Ivarsson S; Parikh H; Berntorp K; Groop L
    Diabetologia; 2007 May; 50(5):972-9. PubMed ID: 17342473
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limb.
    Mellor RH; Brice G; Stanton AW; French J; Smith A; Jeffery S; Levick JR; Burnand KG; Mortimer PS;
    Circulation; 2007 Apr; 115(14):1912-20. PubMed ID: 17372167
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Correlations of FOXC2 Gene Expression and Polymorphism with Type 2 Diabetes Mellitus.
    Nian X; Zhang X; Wang Y; Li H; Li J; Liu H; Qin L
    Clin Lab; 2016; 62(5):781-91. PubMed ID: 27349002
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The FOXC2 -512C>T variant is associated with hypertriglyceridaemia and increased serum C-peptide in Danish Caucasian glucose-tolerant subjects.
    Yanagisawa K; Hingstrup Larsen L; Andersen G; Drivsholm T; Cederberg A; Westergren R; Borch-Johnsen K; Pedersen O; Enerbäck S; Hansen T
    Diabetologia; 2003 Nov; 46(11):1576-80. PubMed ID: 14530861
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The forkhead transcription factors, Foxc1 and Foxc2, are required for arterial specification and lymphatic sprouting during vascular development.
    Seo S; Fujita H; Nakano A; Kang M; Duarte A; Kume T
    Dev Biol; 2006 Jun; 294(2):458-70. PubMed ID: 16678147
    [TBL] [Abstract][Full Text] [Related]  

  • 13. FOXC2-AS1 regulates phenotypic transition, proliferation and migration of human great saphenous vein smooth muscle cells.
    Zhang C; Li H; Guo X
    Biol Res; 2019 Dec; 52(1):59. PubMed ID: 31801629
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of FOXP3 and GAGE10 promoter polymorphisms and decreased FOXP3 expression in regulatory T cells with susceptibility to generalized vitiligo in Gujarat population.
    Giri PS; Patel S; Begum R; Dwivedi M
    Gene; 2021 Feb; 768():145295. PubMed ID: 33181260
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Lack of symmetry in the major lower limb veins.
    Chandrashekar A; Gasparis A; Labropoulos N
    J Vasc Surg Venous Lymphat Disord; 2017 May; 5(3):346-352. PubMed ID: 28411701
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Endothelial immune activation programmes cell-fate decisions and angiogenesis by inducing angiogenesis regulator DLL4 through TLR4-ERK-FOXC2 signalling.
    Xia S; Menden HL; Korfhagen TR; Kume T; Sampath V
    J Physiol; 2018 Apr; 596(8):1397-1417. PubMed ID: 29380370
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Impact of Hey2 and COUP-TFII on genes involved in arteriovenous differentiation in primary human arterial and venous endothelial cells.
    Korten S; Brunssen C; Poitz DM; Großklaus S; Brux M; Schnittler HJ; Strasser RH; Bornstein SR; Morawietz H; Goettsch W
    Basic Res Cardiol; 2013 Jul; 108(4):362. PubMed ID: 23744056
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Defects in vein valve PROX1/FOXC2 antithrombotic pathway in endothelial cells drive the hypercoagulable state induced by trauma and critical illness.
    Hoofnagle MH; Hess A; Nalugo M; Ghosh S; Hughes SW; Fuchs A; Welsh JD; Kahn ML; Bochicchio GV; Randolph GJ; Leonard JM; Turnbull IR
    J Trauma Acute Care Surg; 2023 Aug; 95(2):197-204. PubMed ID: 37072887
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Minor alleles of genetic variants in second heart field increase the risk of hypoplastic right heart syndrome.
    Wang E; Nie Y; Fan X; Zheng Z; Gu H; Zhang H; Hu S
    J Genet; 2019 Jun; 98(2):. PubMed ID: 31204705
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Linkage to the FOXC2 region of chromosome 16 for varicose veins in otherwise healthy, unselected sibling pairs.
    Ng MY; Andrew T; Spector TD; Jeffery S;
    J Med Genet; 2005 Mar; 42(3):235-9. PubMed ID: 15744037
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.