225 related articles for article (PubMed ID: 12297837)
1. The significance of human jagged 1 mutations detected in severe cases of extrahepatic biliary atresia.
Kohsaka T; Yuan ZR; Guo SX; Tagawa M; Nakamura A; Nakano M; Kawasasaki H; Inomata Y; Tanaka K; Miyauchi J
Hepatology; 2002 Oct; 36(4 Pt 1):904-12. PubMed ID: 12297837
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Parental mosaicism of JAG1 mutations in families with Alagille syndrome.
Giannakudis J; Röpke A; Kujat A; Krajewska-Walasek M; Hughes H; Fryns JP; Bankier A; Amor D; Schlicker M; Hansmann I
Eur J Hum Genet; 2001 Mar; 9(3):209-16. PubMed ID: 11313761
[TBL] [Abstract][Full Text] [Related]
8. The DSL domain in mutant JAG1 ligand is essential for the severity of the liver defect in Alagille syndrome.
Yuan ZR; Okaniwa M; Nagata I; Tazawa Y; Ito M; Kawarazaki H; Inomata Y; Okano S; Yoshida T; Kobayashi N; Kohsaka T
Clin Genet; 2001 May; 59(5):330-7. PubMed ID: 11359464
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. Jagged1 (JAG1) mutation detection in an Australian Alagille syndrome population.
Heritage ML; MacMillan JC; Colliton RP; Genin A; Spinner NB; Anderson GJ
Hum Mutat; 2000 Nov; 16(5):408-16. PubMed ID: 11058898
[TBL] [Abstract][Full Text] [Related]
11. DHPLC mutation analysis of Jagged1 (JAG1) reveals six novel mutations in Australian alagille syndrome patients.
Heritage ML; MacMillan JC; Anderson GJ
Hum Mutat; 2002 Dec; 20(6):481. PubMed ID: 12442286
[TBL] [Abstract][Full Text] [Related]
12. Analysis of cardiovascular phenotype and genotype-phenotype correlation in individuals with a JAG1 mutation and/or Alagille syndrome.
McElhinney DB; Krantz ID; Bason L; Piccoli DA; Emerick KM; Spinner NB; Goldmuntz E
Circulation; 2002 Nov; 106(20):2567-74. PubMed ID: 12427653
[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):345. PubMed ID: 19694043
[No Abstract] [Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. Spectrum and frequency of jagged1 (JAG1) mutations in Alagille syndrome patients and their families.
Krantz ID; Colliton RP; Genin A; Rand EB; Li L; Piccoli DA; Spinner NB
Am J Hum Genet; 1998 Jun; 62(6):1361-9. PubMed ID: 9585603
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
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]
