164 related articles for article (PubMed ID: 19208348)
1. Ductal malformation and pancreatitis in mice caused by conditional Jag1 deletion.
Golson ML; Loomes KM; Oakey R; Kaestner KH
Gastroenterology; 2009 May; 136(5):1761-71.e1. PubMed ID: 19208348
[TBL] [Abstract][Full Text] [Related]
2. Microarray data reveal relationship between Jag1 and Ddr1 in mouse liver.
Underkoffler LA; Carr E; Nelson A; Ryan MJ; Schulz R; Loomes KM
PLoS One; 2013; 8(12):e84383. PubMed ID: 24391948
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. 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]
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. Functional analysis of the Notch ligand Jagged1 missense mutant proteins underlying Alagille syndrome.
Tada M; Itoh S; Ishii-Watabe A; Suzuki T; Kawasaki N
FEBS J; 2012 Jun; 279(12):2096-107. PubMed ID: 22487239
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Evidence of Notch pathway activation in the ectatic ducts of chronic pancreatitis.
Bhanot U; Köhntop R; Hasel C; Möller P
J Pathol; 2008 Feb; 214(3):312-9. PubMed ID: 18069660
[TBL] [Abstract][Full Text] [Related]
11. Functional role of Notch signaling in the developing and postnatal heart.
Nemir M; Pedrazzini T
J Mol Cell Cardiol; 2008 Oct; 45(4):495-504. PubMed ID: 18410944
[TBL] [Abstract][Full Text] [Related]
12. Pancreatic regeneration in chronic pancreatitis requires activation of the notch signaling pathway.
Su Y; Büchler P; Gazdhar A; Giese N; Reber HA; Hines OJ; Giese T; Büchler MW; Friess H
J Gastrointest Surg; 2006 Nov; 10(9):1230-41; discussion 1242. PubMed ID: 17114010
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
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. Jagged1 heterozygosity in mice results in a congenital cholangiopathy which is reversed by concomitant deletion of one copy of Poglut1 (Rumi).
Thakurdas SM; Lopez MF; Kakuda S; Fernandez-Valdivia R; Zarrin-Khameh N; Haltiwanger RS; Jafar-Nejad H
Hepatology; 2016 Feb; 63(2):550-65. PubMed ID: 26235536
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. A 8.26Mb deletion in 6q16 and a 4.95Mb deletion in 20p12 including JAG1 and BMP2 in a patient with Alagille syndrome and Wolff-Parkinson-White syndrome.
Le Gloan L; Pichon O; Isidor B; Boceno M; Rival JM; David A; Le Caignec C
Eur J Med Genet; 2008; 51(6):651-7. PubMed ID: 18775522
[TBL] [Abstract][Full Text] [Related]
19. [From gene to disease: arteriohepatic dysplasia or Alagille syndrome].
Brooks AS; Dooijes D
Ned Tijdschr Geneeskd; 2003 Jun; 147(25):1213-5. PubMed ID: 12848056
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]