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 *

151 related articles for article (PubMed ID: 19780835)

  • 1. The tetralogy of Fallot-associated G274D mutation impairs folding of the second epidermal growth factor repeat in Jagged-1.
    Guarnaccia C; Dhir S; Pintar A; Pongor S
    FEBS J; 2009 Nov; 276(21):6247-57. PubMed ID: 19780835
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Variable expression of Alagille syndrome in a family with a new JAG1 gene mutation.
    Ziesenitz VC; Loukanov T; Gläser C; Gorenflo M
    Cardiol Young; 2016 Jan; 26(1):164-7. PubMed ID: 25613755
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Human Jagged 1 mutants cause liver defect in Alagille syndrome by overexpression of hepatocyte growth factor.
    Yuan ZR; Kobayashi N; Kohsaka T
    J Mol Biol; 2006 Feb; 356(3):559-68. PubMed ID: 16403414
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Gene symbol: JAG1. Disease: tetralogy of Fallot.
    Glaeser C; Kotzot D; Caliebe A; Kottke R; Schulz S; Schweigmann U; Hansmann I
    Hum Genet; 2006 Jul; 119(6):674. PubMed ID: 17128462
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.
    Marchetti D; Iascone MR; Pezzoli L
    Hum Genet; 2009 Aug; 126(2):345. PubMed ID: 19694043
    [No Abstract]   [Full Text] [Related]  

  • 13. Novel human pathological mutations. Gene symbol: JAG1. Disease: Allagille syndrome.
    Ellison J
    Hum Genet; 2009 Aug; 126(2):331. PubMed ID: 19693994
    [No Abstract]   [Full Text] [Related]  

  • 14. Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.
    Marchetti D; Iascone MR; Pezzoli L
    Hum Genet; 2009 Aug; 126(2):349-50. PubMed ID: 19694054
    [No Abstract]   [Full Text] [Related]  

  • 15. Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.
    Marchetti D; Iascone MR; Pezzoli L
    Hum Genet; 2009 Aug; 126(2):347-8. PubMed ID: 19694049
    [No Abstract]   [Full Text] [Related]  

  • 16. Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.
    Marchetti D; Iascone MR; Pezzoli L
    Hum Genet; 2009 Aug; 126(2):344-5. PubMed ID: 19694039
    [No Abstract]   [Full Text] [Related]  

  • 17. Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.
    Marchetti D; Iascone MR; Pezzoli L
    Hum Genet; 2009 Aug; 126(2):344. PubMed ID: 19694036
    [No Abstract]   [Full Text] [Related]  

  • 18. Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.
    Marchetti D; Iascone MR; Pezzoli L
    Hum Genet; 2009 Aug; 126(2):348. PubMed ID: 19694051
    [No Abstract]   [Full Text] [Related]  

  • 19. Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.
    Marchetti D; Iascone MR; Pezzoli L
    Hum Genet; 2009 Aug; 126(2):345-6. PubMed ID: 19694044
    [No Abstract]   [Full Text] [Related]  

  • 20. Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.
    Marchetti D; Iascone MR; Pezzoli L
    Hum Genet; 2009 Aug; 126(2):350-1. PubMed ID: 19694056
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.