181 related articles for article (PubMed ID: 20706826)
21. An autosomal recessive form of Alagille-like syndrome that is not linked to JAG1.
Dyack S; Cameron M; Otley A; Greer W
Genet Med; 2007 Aug; 9(8):544-50. PubMed ID: 17700393
[TBL] [Abstract][Full Text] [Related]
22. Jagged1 (JAG1) mutations in Alagille syndrome: increasing the mutation detection rate.
Warthen DM; Moore EC; Kamath BM; Morrissette JJ; Sanchez-Lara PA; Piccoli DA; Krantz ID; Spinner NB
Hum Mutat; 2006 May; 27(5):436-43. PubMed ID: 16575836
[TBL] [Abstract][Full Text] [Related]
23. Phenotypic variability in Hey2 -/- mice and absence of HEY2 mutations in patients with congenital heart defects or Alagille syndrome.
Fischer A; Klamt B; Schumacher N; Glaeser C; Hansmann I; Fenge H; Gessler M
Mamm Genome; 2004 Sep; 15(9):711-6. PubMed ID: 15389319
[TBL] [Abstract][Full Text] [Related]
24. JAGGED1 gene variations in Chinese twin sisters with Alagille syndrome.
Xie X; Lu Y; Wang X; Wu B; Yu H
Int J Clin Exp Pathol; 2015; 8(7):8506-11. PubMed ID: 26339425
[TBL] [Abstract][Full Text] [Related]
25. Jagged-1 mutation analysis in Italian Alagille syndrome patients.
Pilia G; Uda M; Macis D; Frau F; Crisponi L; Balli F; Barbera C; Colombo C; Frediani T; Gatti R; Iorio R; Marazzi MG; Marcellini M; Musumeci S; Nebbia G; Vajro P; Ruffa G; Zancan L; Cao A; DeVirgilis S
Hum Mutat; 1999; 14(5):394-400. PubMed ID: 10533065
[TBL] [Abstract][Full Text] [Related]
26. Ozzy, a Jag1 vestibular mouse mutant, displays characteristics of Alagille syndrome.
Vrijens K; Thys S; De Jeu MT; Postnov AA; Pfister M; Cox L; Zwijsen A; Van Hoof V; Mueller M; De Clerck NM; De Zeeuw CI; Van Camp G; Van Laer L
Neurobiol Dis; 2006 Oct; 24(1):28-40. PubMed ID: 16875832
[TBL] [Abstract][Full Text] [Related]
27. Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patients.
Colliton RP; Bason L; Lu FM; Piccoli DA; Krantz ID; Spinner NB
Hum Mutat; 2001 Feb; 17(2):151-2. PubMed ID: 11180599
[TBL] [Abstract][Full Text] [Related]
28. Splenic hamartomas in Alagille syndrome: case report and literature review.
James AW; Nguyen A; Said J; Genshaft S; Lassman CR; Teitell M
Fetal Pediatr Pathol; 2014 Aug; 33(4):216-25. PubMed ID: 24865822
[TBL] [Abstract][Full Text] [Related]
29. Bile duct proliferation in liver-specific Jag1 conditional knockout mice: effects of gene dosage.
Loomes KM; Russo P; Ryan M; Nelson A; Underkoffler L; Glover C; Fu H; Gridley T; Kaestner KH; Oakey RJ
Hepatology; 2007 Feb; 45(2):323-30. PubMed ID: 17366661
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. 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]
32. Alagille syndrome and the Jagged1 gene.
Piccoli DA; Spinner NB
Semin Liver Dis; 2001 Nov; 21(4):525-34. PubMed ID: 11745040
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. 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]
35. 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]
36. Alagille syndrome: an overview.
Vajro P; Ferrante L; Paolella G
Clin Res Hepatol Gastroenterol; 2012 Jun; 36(3):275-7. PubMed ID: 22521120
[TBL] [Abstract][Full Text] [Related]
37. Mutational analysis of the Jagged 1 gene in Alagille syndrome families.
Yuan ZR; Kohsaka T; Ikegaya T; Suzuki T; Okano S; Abe J; Kobayashi N; Yamada M
Hum Mol Genet; 1998 Sep; 7(9):1363-9. PubMed ID: 9700188
[TBL] [Abstract][Full Text] [Related]
38. Alagille syndrome: pathogenesis, diagnosis and management.
Turnpenny PD; Ellard S
Eur J Hum Genet; 2012 Mar; 20(3):251-7. PubMed ID: 21934706
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Identification of 36 novel Jagged1 (JAG1) mutations in patients with Alagille syndrome.
Röpke A; Kujat A; Gräber M; Giannakudis J; Hansmann I
Hum Mutat; 2003 Jan; 21(1):100. PubMed ID: 12497640
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]