These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 29631691)

  • 1. Silencing mutations in JAG1 gene may play crucial roles in the pathogenesis of Tetralogy of Fallot.
    Safari-Arababadi A; Behjati-Ardakani M; Kalantar SM; Jaafarinia M
    Cell Mol Biol (Noisy-le-grand); 2018 Mar; 64(4):103-107. PubMed ID: 29631691
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutational analysis of JAG1 gene in non-syndromic tetralogy of Fallot children.
    Kola S; Koneti NR; Golla JP; Akka J; Gundimeda SD; Mundluru HP
    Clin Chim Acta; 2011 Nov; 412(23-24):2232-6. PubMed ID: 21893051
    [TBL] [Abstract][Full Text] [Related]  

  • 3. JAG1 mutation in a patient with deletion 22q11.2 syndrome and tetralogy of Fallot.
    Digilio MC; Luca AD; Lepri F; Guida V; Ferese R; Dentici ML; Angioni A; Marino B; Dallapiccola B
    Am J Med Genet A; 2013 Dec; 161A(12):3133-6. PubMed ID: 23956173
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial Tetralogy of Fallot caused by mutation in the jagged1 gene.
    Eldadah ZA; Hamosh A; Biery NJ; Montgomery RA; Duke M; Elkins R; Dietz HC
    Hum Mol Genet; 2001 Jan; 10(2):163-9. PubMed ID: 11152664
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Jagged1 (JAG1) mutations in patients with tetralogy of Fallot or pulmonic stenosis.
    Bauer RC; Laney AO; Smith R; Gerfen J; Morrissette JJ; Woyciechowski S; Garbarini J; Loomes KM; Krantz ID; Urban Z; Gelb BD; Goldmuntz E; Spinner NB
    Hum Mutat; 2010 May; 31(5):594-601. PubMed ID: 20437614
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot.
    Rauch R; Hofbeck M; Zweier C; Koch A; Zink S; Trautmann U; Hoyer J; Kaulitz R; Singer H; Rauch A
    J Med Genet; 2010 May; 47(5):321-31. PubMed ID: 19948535
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Promoter methylation and expression of the VANGL2 gene in the myocardium of pediatric patients with tetralogy of fallot.
    Yuan Y; Gao Y; Wang H; Ma X; Ma D; Huang G
    Birth Defects Res A Clin Mol Teratol; 2014 Dec; 100(12):973-84. PubMed ID: 25200836
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel and recurrent JAG1 mutations in patients with tetralogy of Fallot.
    Guida V; Chiappe F; Ferese R; Usala G; Maestrale G; Iannascoli C; Bellacchio E; Mingarelli R; Digilio MC; Marino B; Uda M; De Luca A; Dallapiccola B
    Clin Genet; 2011 Dec; 80(6):591-4. PubMed ID: 22040217
    [No Abstract]   [Full Text] [Related]  

  • 9. Peritoneal dialysis in an adult patient with tetralogy of Fallot diagnosed with incomplete Alagille syndrome.
    Ponikowska M; Pollak A; Kotwica-Strzalek E; Brodowska-Kania D; Mosakowska M; Ploski R; Niemczyk S
    BMC Med Genet; 2020 Oct; 21(1):195. PubMed ID: 33008311
    [TBL] [Abstract][Full Text] [Related]  

  • 10. GATA4 loss-of-function mutations underlie familial tetralogy of fallot.
    Yang YQ; Gharibeh L; Li RG; Xin YF; Wang J; Liu ZM; Qiu XB; Xu YJ; Xu L; Qu XK; Liu X; Fang WY; Huang RT; Xue S; Nemer G
    Hum Mutat; 2013 Dec; 34(12):1662-71. PubMed ID: 24000169
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitogen-activated protein kinase signal pathways play an important role in right ventricular hypertrophy of tetralogy of Fallot.
    Zhang HS; Wu QY; Xu M; Zhou YX; Shui CX
    Chin Med J (Engl); 2012 Jul; 125(13):2243-9. PubMed ID: 22882842
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Tetralogy of fallot and other congenital heart defects in Hey2 mutant mice.
    Donovan J; Kordylewska A; Jan YN; Utset MF
    Curr Biol; 2002 Sep; 12(18):1605-10. PubMed ID: 12372254
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Investigation of somatic NKX2-5, GATA4 and HAND1 mutations in patients with tetralogy of Fallot.
    Wang J; Lu Y; Chen H; Yin M; Yu T; Fu Q
    Pathology; 2011 Jun; 43(4):322-6. PubMed ID: 21519287
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot.
    Pizzuti A; Sarkozy A; Newton AL; Conti E; Flex E; Digilio MC; Amati F; Gianni D; Tandoi C; Marino B; Crossley M; Dallapiccola B
    Hum Mutat; 2003 Nov; 22(5):372-7. PubMed ID: 14517948
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Jagged1 (JAG1): Structure, expression, and disease associations.
    Grochowski CM; Loomes KM; Spinner NB
    Gene; 2016 Jan; 576(1 Pt 3):381-4. PubMed ID: 26548814
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rare mutations of
    Xie Y; Ma A; Wang B; Peng R; Jing Y; Wang D; Finnell RH; Qiao B; Wang Y; Wang H; Zheng Y
    Clin Sci (Lond); 2019 Jan; 133(2):225-238. PubMed ID: 30610007
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Somatic GATA5 mutations in sporadic tetralogy of Fallot.
    Huang RT; Xue S; Xu YJ; Zhou M; Yang YQ
    Int J Mol Med; 2014 May; 33(5):1227-35. PubMed ID: 24573614
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation analysis of the Vangl2 coding region revealed no common cause for Tetralogy of Fallot.
    Erdal E; Erdal C; Bulut G; Kunter I; Kir M; Atabey N; Açikel U
    J Int Med Res; 2007; 35(6):867-72. PubMed ID: 18034999
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Methylation status of CpG sites in the NOTCH4 promoter region regulates NOTCH4 expression in patients with tetralogy of Fallot.
    Zhu Y; Ye M; Xu H; Gu R; Ma X; Chen M; Li X; Sheng W; Huang G
    Mol Med Rep; 2020 Nov; 22(5):4412-4422. PubMed ID: 33000281
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CpG site hypomethylation at ETS1‑binding region regulates DLK1 expression in Chinese patients with Tetralogy of Fallot.
    Tian G; He L; Gu R; Sun J; Chen W; Qian Y; Ma X; Yan W; Zhao Z; Xu Z; Suo M; Sheng W; Huang G
    Mol Med Rep; 2022 Mar; 25(3):. PubMed ID: 35059744
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.