BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

77 related articles for article (PubMed ID: 24668682)

  • 21. Association of GDF1 rs4808863 with fetal congenital heart defects: a case-control study.
    Zhang J; Wu Q; Wang L; Li X; Ma Y; Yao L
    BMJ Open; 2015 Dec; 5(12):e009352. PubMed ID: 26656983
    [TBL] [Abstract][Full Text] [Related]  

  • 22. MTHFR C677T and A1298C gene polymorphisms and their relation to homocysteine level in Egyptian children with congenital heart diseases.
    Zidan HE; Rezk NA; Mohammed D
    Gene; 2013 Oct; 529(1):119-24. PubMed ID: 23933414
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Crucial role of ROCK2 in vascular smooth muscle cells for hypoxia-induced pulmonary hypertension in mice.
    Shimizu T; Fukumoto Y; Tanaka S; Satoh K; Ikeda S; Shimokawa H
    Arterioscler Thromb Vasc Biol; 2013 Dec; 33(12):2780-91. PubMed ID: 24135024
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Association of Cx43 rs2071166 polymorphism with an increased risk for atrial septal defect.
    Gu R; Sheng W; Ma X; Huang G
    Cardiol Young; 2018 Mar; 28(3):397-402. PubMed ID: 29198211
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic polymorphisms of the TYMS gene are not associated with congenital cardiac septal defects in a Han Chinese population.
    Zhao JY; Sun JW; Gu ZY; Wang J; Wang EL; Yang XY; Qiao B; Duan WY; Huang GY; Wang HY
    PLoS One; 2012; 7(2):e31644. PubMed ID: 22384047
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Evaluation of the rs35996865 polymorphism of the ROCK1 gene in sepsis.
    Kale A; Şener EF; Günay NE; Tahtasakal R; Demiryürek S; Günay N; Demiryürek AT
    Rev Assoc Med Bras (1992); 2022 May; 68(5):586-590. PubMed ID: 35584479
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Common 894G>T single nucleotide polymorphism in the gene coding for endothelial nitric oxide synthase (eNOS) and risk of congenital heart defects.
    van Beynum IM; Mooij C; Kapusta L; Heil S; den Heijer M; Blom HJ
    Clin Chem Lab Med; 2008; 46(10):1369-75. PubMed ID: 18844489
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Vascular endothelial growth factor gene +813CC polymorphism of foetus is associated with preterm labour but not with pre-eclampsia in Turkish pregnant women.
    Atis A; Oruc O; Aydin Y; Cetincelik U; Goker N
    Int J Immunogenet; 2012 Jun; 39(3):241-6. PubMed ID: 22257487
    [TBL] [Abstract][Full Text] [Related]  

  • 29. TNF-alpha gene 1031 T/C polymorphism in Turkish patients with Behçet's disease.
    Akman A; Sallakci N; Coskun M; Bacanli A; Yavuzer U; Alpsoy E; Yegin O
    Br J Dermatol; 2006 Aug; 155(2):350-6. PubMed ID: 16882174
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Methylenetetrahydrofolate reductase gene polymorphisms in Turkish children with attention-deficit/hyperactivity disorder.
    Ergul E; Sazci A; Kara I
    Genet Test Mol Biomarkers; 2012 Jan; 16(1):67-9. PubMed ID: 21819229
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Contribution of KCNJ10 gene polymorphisms in childhood epilepsy.
    Dai AI; Akcali A; Koska S; Oztuzcu S; Cengiz B; Demiryürek AT
    J Child Neurol; 2015 Mar; 30(3):296-300. PubMed ID: 25008907
    [TBL] [Abstract][Full Text] [Related]  

  • 32. ROCK2 allelic variants are not associated with pre-eclampsia susceptibility in the Finnish population.
    Peterson H; Laivuori H; Kerkelä E; Jiao H; Hiltunen L; Heino S; Tiala I; Knuutila S; Rasi V; Kere J; Kivinen K
    Mol Hum Reprod; 2009 Jul; 15(7):443-9. PubMed ID: 19435756
    [TBL] [Abstract][Full Text] [Related]  

  • 33. CTLA-4 gene 49A/G polymorphism in Turkish patients with Behçet's disease.
    Sallakci N; Bacanli A; Coskun M; Yavuzer U; Alpsoy E; Yegin O
    Clin Exp Dermatol; 2005 Sep; 30(5):546-50. PubMed ID: 16045690
    [TBL] [Abstract][Full Text] [Related]  

  • 34. CTLA-4 gene polymorphism of exon 1(+49 A/G) in Turkish systemic lupus erythematosus patients.
    Ulker M; Yazisiz V; Sallakci N; Avci AB; Sanlioglu S; Yegin O; Terzioglu E
    Int J Immunogenet; 2009 Aug; 36(4):245-50. PubMed ID: 19602000
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The single nucleotide polymorphisms in Smad-interacting protein 1 gene contribute to its ectopic expression and susceptibility in Hirschsprung's disease.
    Zhang S; Jiang K; Yuan Z; Wang W
    Exp Mol Pathol; 2014 Apr; 96(2):219-24. PubMed ID: 24576558
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Negative association of endothelial nitric oxide gene polymorphism with hypertension in Turkish patients: effect of ecNOS polymorphism on left ventricular hypertrophy.
    Olcay A; Ekmekci CG; Ozbek U; Sezer M; Barcin C; Arslan E; Boztosun B; Nisanci Y
    Cardiovasc Ultrasound; 2006 Aug; 4():33. PubMed ID: 16923191
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The matricellular protein CCN1 is essential for cardiac development.
    Mo FE; Lau LF
    Circ Res; 2006 Oct; 99(9):961-9. PubMed ID: 17023674
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Interleukin-10 gene promoter polymorphism in patients with schizophrenia in a region of East Turkey.
    Ozbey U; Tug E; Namli M
    World J Biol Psychiatry; 2009; 10(4 Pt 2):461-8. PubMed ID: 19153889
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Association of MTHFR A1298C polymorphism with conotruncal heart disease.
    Sayin Kocakap BD; Sanli C; Cabuk F; Koc M; Kutsal A
    Cardiol Young; 2015 Oct; 25(7):1326-31. PubMed ID: 25547204
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Plasminogen activator inhibitor-1 and angiotensin converting enzyme gene polymorphisms in Turkish asthmatic children.
    Bora E; Soylar R; Arıkan-Ayyıldız Z; Uzuner N; Giray-Bozkaya Ö; Erçal D; Karaman Ö; Ülgenalp A
    Allergol Immunopathol (Madr); 2013; 41(1):11-6. PubMed ID: 22361338
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.