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.
6. Alagille syndrome. The widening spectrum of arteriohepatic dysplasia. Crosnier C; Lykavieris P; Meunier-Rotival M; Hadchouel M Clin Liver Dis; 2000 Nov; 4(4):765-78. PubMed ID: 11232356 [TBL] [Abstract][Full Text] [Related]
7. Alagille syndrome: chipping away at the tip of the iceberg. Krantz ID Am J Med Genet; 2002 Oct; 112(2):160-2. PubMed ID: 12244549 [No Abstract] [Full Text] [Related]
8. Identification and cloning of the human homolog (JAG1) of the rat Jagged1 gene from the Alagille syndrome critical region at 20p12. Oda T; Elkahloun AG; Meltzer PS; Chandrasekharappa SC Genomics; 1997 Aug; 43(3):376-9. PubMed ID: 9268641 [TBL] [Abstract][Full Text] [Related]
9. Genetic basis of Alagille syndrome deciphered. van den Berg M; Rings E; Stokkers P J Pediatr Gastroenterol Nutr; 1998 Sep; 27(3):370-1. PubMed ID: 9740218 [No Abstract] [Full Text] [Related]
10. Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1. Li L; Krantz ID; Deng Y; Genin A; Banta AB; Collins CC; Qi M; Trask BJ; Kuo WL; Cochran J; Costa T; Pierpont ME; Rand EB; Piccoli DA; Hood L; Spinner NB Nat Genet; 1997 Jul; 16(3):243-51. PubMed ID: 9207788 [TBL] [Abstract][Full Text] [Related]
11. Identification of a larger than 3 Mb deletion including JAG1 in an Alagille syndrome patient with a translocation t(3;20)(q13.3;p12.2). Oda T; Elkahloun AG; Meltzer PS; Okajima K; Sugiyama K; Wada Y; Chandrasekharappa SC Hum Mutat; 2000 Jul; 16(1):92. PubMed ID: 10874319 [TBL] [Abstract][Full Text] [Related]
12. The cardiovascular manifestations of Alagille syndrome and JAGI mutations. Goldmuntz E; Moore E; Spinner NB Methods Mol Med; 2006; 126():217-31. PubMed ID: 16930015 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Alagille syndrome associated with a paracentric inversion 20p12.2p13 disrupting the JAG1 gene. Stankiewicz P; Rujner J; Löffler C; Krüger A; Nimmakayalu M; Piłacik B; Krajewska-Walasek M; Gutkowska A; Hansmann I; Giannakudis I Am J Med Genet; 2001 Oct; 103(2):166-71. PubMed ID: 11568926 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. The genetic basis of the Alagille syndrome. Rand EB J Pediatr Gastroenterol Nutr; 1998 Feb; 26(2):234-6. PubMed ID: 9481647 [No Abstract] [Full Text] [Related]
19. Alagille syndrome inherited from a phenotypically normal mother with a mosaic 20p microdeletion. Laufer-Cahana A; Krantz ID; Bason LD; Lu FM; Piccoli DA; Spinner NB Am J Med Genet; 2002 Oct; 112(2):190-3. PubMed ID: 12244554 [TBL] [Abstract][Full Text] [Related]
20. Alagille syndrome and the notch signaling pathway: new insights into human development. Spinner NB Gastroenterology; 1999 May; 116(5):1257-60. PubMed ID: 10220521 [No Abstract] [Full Text] [Related] [Next] [New Search]