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 *

141 related articles for article (PubMed ID: 38194749)

  • 1. Jagged-mediated development and disease: Mechanistic insights and therapeutic implications for Alagille syndrome.
    Mašek J; Andersson ER
    Curr Opin Cell Biol; 2024 Feb; 86():102302. PubMed ID: 38194749
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Bile duct proliferation in Jag1/fringe heterozygous mice identifies candidate modifiers of the Alagille syndrome hepatic phenotype.
    Ryan MJ; Bales C; Nelson A; Gonzalez DM; Underkoffler L; Segalov M; Wilson-Rawls J; Cole SE; Moran JL; Russo P; Spinner NB; Kusumi K; Loomes KM
    Hepatology; 2008 Dec; 48(6):1989-97. PubMed ID: 19026002
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Alagille Syndrome Mimicking Biliary Atresia in Early Infancy.
    Dědič T; Jirsa M; Keil R; Rygl M; Šnajdauf J; Kotalová R
    PLoS One; 2015; 10(11):e0143939. PubMed ID: 26618708
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. The genetics and ocular findings of Alagille syndrome.
    Kim BJ; Fulton AB
    Semin Ophthalmol; 2007; 22(4):205-10. PubMed ID: 18097983
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A mouse model of Alagille syndrome: Notch2 as a genetic modifier of Jag1 haploinsufficiency.
    McCright B; Lozier J; Gridley T
    Development; 2002 Feb; 129(4):1075-82. PubMed ID: 11861489
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Endothelial deletion of murine Jag1 leads to valve calcification and congenital heart defects associated with Alagille syndrome.
    Hofmann JJ; Briot A; Enciso J; Zovein AC; Ren S; Zhang ZW; Radtke F; Simons M; Wang Y; Iruela-Arispe ML
    Development; 2012 Dec; 139(23):4449-60. PubMed ID: 23095891
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Gene symbol: JAG1. Disease: Alagille syndrome.
    Conidi ME; Michelucci A; Maggiore G; Simi P
    Hum Genet; 2008 Oct; 124(3):322. PubMed ID: 18846686
    [No Abstract]   [Full Text] [Related]  

  • 11. Gene symbol: JAG1. Disease: Alagille syndrome.
    Conidi ME; Michelucci A; Maggiore G; Simi P
    Hum Genet; 2008 Oct; 124(3):322. PubMed ID: 18846681
    [No Abstract]   [Full Text] [Related]  

  • 12. Renal involvement and the role of Notch signalling in Alagille syndrome.
    Kamath BM; Spinner NB; Rosenblum ND
    Nat Rev Nephrol; 2013 Jul; 9(7):409-18. PubMed ID: 23752887
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Gene symbol: JAG1. Disease: Alagille syndrome.
    Conidi ME; Michelucci A; Maggiore G; Simi P
    Hum Genet; 2008 Oct; 124(3):321-2. PubMed ID: 18846680
    [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):345. PubMed ID: 19694043
    [No Abstract]   [Full Text] [Related]  

  • 16. JAG1 Mutation Spectrum and Origin in Chinese Children with Clinical Features of Alagille Syndrome.
    Li L; Dong J; Wang X; Guo H; Wang H; Zhao J; Qiu Y; Abuduxikuer K; Wang J
    PLoS One; 2015; 10(6):e0130355. PubMed ID: 26076142
    [TBL] [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):350-1. PubMed ID: 19694056
    [No Abstract]   [Full Text] [Related]  

  • 18. Medical management of Alagille syndrome.
    Kamath BM; Loomes KM; Piccoli DA
    J Pediatr Gastroenterol Nutr; 2010 Jun; 50(6):580-6. PubMed ID: 20479679
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Spectrum of JAG1 gene mutations in Polish patients with Alagille syndrome.
    Jurkiewicz D; Gliwicz D; Ciara E; Gerfen J; Pelc M; Piekutowska-Abramczuk D; Kugaudo M; Chrzanowska K; Spinner NB; Krajewska-Walasek M
    J Appl Genet; 2014 Aug; 55(3):329-36. PubMed ID: 24748328
    [TBL] [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):344. PubMed ID: 19694036
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.