BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 30590232)

  • 1. Implication of GATA4 synonymous variants in congenital heart disease: A comprehensive in-silico approach.
    Dixit R; Kumar A; Mohapatra B
    Mutat Res; 2019 Jan; 813():31-38. PubMed ID: 30590232
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A gain-of-function mutation in CITED2 is associated with congenital heart disease.
    Yadav ML; Jain D; Neelabh ; Agrawal D; Kumar A; Mohapatra B
    Mutat Res; 2021; 822():111741. PubMed ID: 33706167
    [TBL] [Abstract][Full Text] [Related]  

  • 3. In silico investigation of the impact of synonymous variants in ABCB4 gene on mRNA stability/structure, splicing accuracy and codon usage: Potential contribution to PFIC3 disease.
    Khabou B; Siala-Sahnoun O; Gargouri L; Mkaouar-Rebai E; Keskes L; Hachicha M; Fakhfakh F
    Comput Biol Chem; 2016 Dec; 65():103-109. PubMed ID: 27788395
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification and in silico characterization of CSRP3 synonymous variants in dilated cardiomyopathy.
    Giri P; Jain D; Kumar A; Mohapatra B
    Mol Biol Rep; 2023 May; 50(5):4105-4117. PubMed ID: 36877346
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children.
    Behiry EG; Al-Azzouny MA; Sabry D; Behairy OG; Salem NE
    Mol Genet Genomic Med; 2019 May; 7(5):e612. PubMed ID: 30834692
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of intronic-splice site mutations in GATA4 gene in Indian patients with congenital heart disease.
    Bose D; D V; Shetty M; J K; Kutty AVM
    Mutat Res; 2017 Oct; 803-805():26-34. PubMed ID: 28843068
    [TBL] [Abstract][Full Text] [Related]  

  • 7. c.620C>T mutation in GATA4 is associated with congenital heart disease in South India.
    Mattapally S; Nizamuddin S; Murthy KS; Thangaraj K; Banerjee SK
    BMC Med Genet; 2015 Feb; 16():7. PubMed ID: 25928801
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel Point Mutations in 3'-Untranslated Region of GATA4 Gene Are Associated with Sporadic Non-syndromic Atrial and Ventricular Septal Defects.
    Khatami M; Ghorbani S; Adriani MR; Bahaloo S; Naeini MA; Heidari MM; Hadadzadeh M
    Curr Med Sci; 2022 Feb; 42(1):129-143. PubMed ID: 34652630
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of functional mutations in GATA4 in patients with congenital heart disease.
    Wang E; Sun S; Qiao B; Duan W; Huang G; An Y; Xu S; Zheng Y; Su Z; Gu X; Jin L; Wang H
    PLoS One; 2013; 8(4):e62138. PubMed ID: 23626780
    [TBL] [Abstract][Full Text] [Related]  

  • 10. GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co-occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous GATA4 mutation in a family with autosomal dominant congenital heart disease.
    Kalayinia S; Maleki M; Rokni-Zadeh H; Changi-Ashtiani M; Ahangar H; Biglari A; Shahani T; Mahdieh N
    J Clin Lab Anal; 2019 Sep; 33(7):e22923. PubMed ID: 31115957
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD).
    Reamon-Buettner SM; Cho SH; Borlak J
    BMC Med Genet; 2007 Jun; 8():38. PubMed ID: 17592645
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease.
    LaHaye S; Corsmeier D; Basu M; Bowman JL; Fitzgerald-Butt S; Zender G; Bosse K; McBride KL; White P; Garg V
    Circ Cardiovasc Genet; 2016 Aug; 9(4):320-9. PubMed ID: 27418595
    [TBL] [Abstract][Full Text] [Related]  

  • 13. GATA4 mutations in 357 unrelated patients with congenital heart malformation.
    Butler TL; Esposito G; Blue GM; Cole AD; Costa MW; Waddell LB; Walizada G; Sholler GF; Kirk EP; Feneley M; Harvey RP; Winlaw DS
    Genet Test Mol Biomarkers; 2010 Dec; 14(6):797-802. PubMed ID: 20874241
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Functional analysis of rare variants of GATA4 identified in Chinese patients with congenital heart defect.
    Zhao Z; Zhan Y; Chen W; Ma X; Sheng W; Huang G
    Genesis; 2019 Nov; 57(11-12):e23333. PubMed ID: 31513339
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification and functional study of GATA4 gene regulatory variants in atrial septal defects.
    Fan D; Pang S; Chen J; Shan J; Cheng Q; Yan B
    BMC Cardiovasc Disord; 2021 Jun; 21(1):321. PubMed ID: 34193080
    [TBL] [Abstract][Full Text] [Related]  

  • 16. GATA4 mutations in 486 Chinese patients with congenital heart disease.
    Zhang W; Li X; Shen A; Jiao W; Guan X; Li Z
    Eur J Med Genet; 2008; 51(6):527-35. PubMed ID: 18672102
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Mutations in the GATA4 gen in patients with non-syndromic congenital heart disease].
    Orjuela Quintero DC; Núñez F; Caicedo V; Pachón S; Salazar Salazar M
    Invest Clin; 2014 Sep; 55(3):207-16. PubMed ID: 25272520
    [TBL] [Abstract][Full Text] [Related]  

  • 18. GATA4 sequence variants in patients with congenital heart disease.
    Tomita-Mitchell A; Maslen CL; Morris CD; Garg V; Goldmuntz E
    J Med Genet; 2007 Dec; 44(12):779-83. PubMed ID: 18055909
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Intronic Polymorphisms in Gene of Second Heart Field as Risk Factors for Human Congenital Heart Disease in a Chinese Population.
    Wang E; Nie Y; Fan X; Zheng Z; Hu S
    DNA Cell Biol; 2019 Jun; 38(6):521-531. PubMed ID: 31013439
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 3'UTR SNPs and Haplotypes in the GATA4 Gene Contribute to the Genetic Risk of Congenital Heart Disease.
    Pulignani S; Vecoli C; Sabina S; Foffa I; Ait-Ali L; Andreassi MG
    Rev Esp Cardiol (Engl Ed); 2016 Aug; 69(8):760-5. PubMed ID: 27118528
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.