BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

360 related articles for article (PubMed ID: 12848056)

  • 1. [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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Clinical and molecular genetics of Alagille syndrome.
    Krantz ID; Piccoli DA; Spinner NB
    Curr Opin Pediatr; 1999 Dec; 11(6):558-64. PubMed ID: 10590916
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Conditional JAG1 mutation shows the developing heart is more sensitive than developing liver to JAG1 dosage.
    Lu F; Morrissette JJ; Spinner NB
    Am J Hum Genet; 2003 Apr; 72(4):1065-70. PubMed ID: 12649809
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic alterations in the JAG1 gene in Japanese patients with Alagille syndrome.
    Onouchi Y; Kurahashi H; Tajiri H; Ida S; Okada S; Nakamura Y
    J Hum Genet; 1999; 44(4):235-9. PubMed ID: 10429362
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in the human Jagged1 gene are responsible for Alagille syndrome.
    Oda T; Elkahloun AG; Pike BL; Okajima K; Krantz ID; Genin A; Piccoli DA; Meltzer PS; Spinner NB; Collins FS; Chandrasekharappa SC
    Nat Genet; 1997 Jul; 16(3):235-42. PubMed ID: 9207787
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. Twelve novel JAG1 gene mutations in Polish Alagille syndrome patients.
    Jurkiewicz D; Popowska E; Gläser C; Hansmann I; Krajewska-Walasek M
    Hum Mutat; 2005 Mar; 25(3):321. PubMed ID: 15712272
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.