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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

95 related articles for article (PubMed ID: 8852653)

  • 1. Endothelin receptor-mediated signaling in hirschsprung disease.
    Chakravarti A
    Hum Mol Genet; 1996 Mar; 5(3):303-7. PubMed ID: 8852653
    [No Abstract]   [Full Text] [Related]  

  • 2. [Endothelin B receptor system and Hirschsprung disease].
    Inoue M; Kusafuka T; Okada A
    Nihon Rinsho; 1998 Jul; 56(7):1876-80. PubMed ID: 9702069
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Functional analysis of five endothelin-B receptor mutations found in human Hirschsprung disease patients.
    Abe Y; Sakurai T; Yamada T; Nakamura T; Yanagisawa M; Goto K
    Biochem Biophys Res Commun; 2000 Aug; 275(2):524-31. PubMed ID: 10964697
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in Hirschsprung disease: when does a mutation contribute to the phenotype.
    Hofstra RM; Osinga J; Buys CH
    Eur J Hum Genet; 1997; 5(4):180-5. PubMed ID: 9359036
    [TBL] [Abstract][Full Text] [Related]  

  • 5. EDNRB/EDN3 and Hirschsprung disease type II.
    McCallion AS; Chakravarti A
    Pigment Cell Res; 2001 Jun; 14(3):161-9. PubMed ID: 11434563
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Advances in the etiology and pathogenesis of congenital megacolon].
    Xia G; Xu J; Wang G
    Zhonghua Wai Ke Za Zhi; 1997 Sep; 35(9):568-70. PubMed ID: 10678038
    [No Abstract]   [Full Text] [Related]  

  • 7. Endothelins and the color of mice: unraveling the etiopathogenesis of Hirschsprung's disease.
    Sylvester FA; Griffiths AM
    J Pediatr Gastroenterol Nutr; 1995 Nov; 21(4):478-9. PubMed ID: 8583305
    [No Abstract]   [Full Text] [Related]  

  • 8. Novel nonsense mutation of the endothelin-B receptor gene in a family with Waardenburg-Hirschsprung disease.
    Syrris P; Carter ND; Patton MA
    Am J Med Genet; 1999 Nov; 87(1):69-71. PubMed ID: 10528251
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Hirschsprung disease. A receptor defect].
    Fredholm BB
    Lakartidningen; 1995 Apr; 92(16):1662-4. PubMed ID: 7723480
    [No Abstract]   [Full Text] [Related]  

  • 10. Endothelin and neural crest development.
    Kurihara H; Kurihara Y; Nagai R; Yazaki Y
    Cell Mol Biol (Noisy-le-grand); 1999 Jul; 45(5):639-51. PubMed ID: 10512195
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Genetics of Hirschsprung disease].
    Attié T; Salomon R; Amiel J; Edery P; Pelet A; Nihoul-Fékété C; Munnich A; Lyonnet S
    C R Seances Soc Biol Fil; 1996; 190(5-6):549-56. PubMed ID: 9074720
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Endothelin receptor/physiological role].
    Abe Y; Kasuya Y
    Nihon Rinsho; 1998 Jul; 56(7):1898-905. PubMed ID: 9702073
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The RET C620S mutation causes multiple endocrine neoplasia type 2A (MEN2A) but not Hirschsprung disease (HSCR) in a family cosegregating both phenotypes.
    Fernández RM; Antiñolo G; Eng C; Borrego S
    Hum Mutat; 2003 Nov; 22(5):412-5. PubMed ID: 14517954
    [No Abstract]   [Full Text] [Related]  

  • 14. Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease.
    Attié T; Till M; Pelet A; Amiel J; Edery P; Boutrand L; Munnich A; Lyonnet S
    Hum Mol Genet; 1995 Dec; 4(12):2407-9. PubMed ID: 8634719
    [No Abstract]   [Full Text] [Related]  

  • 15. Mutations in the endothelin-receptor B gene in Hirschsprung disease in Sweden.
    Svensson PJ; Tapper-Persson M; Anvret M; Molander ML; Eng C; Nordenskjöld A
    Clin Genet; 1999 Mar; 55(3):215-7. PubMed ID: 10334478
    [No Abstract]   [Full Text] [Related]  

  • 16. A consanguineous family with Hirschsprung disease, microcephaly, and mental retardation (Goldberg-Shprintzen syndrome).
    Brooks AS; Breuning MH; Osinga J; vd Smagt JJ; Catsman CE; Buys CH; Meijers C; Hofstra RM
    J Med Genet; 1999 Jun; 36(6):485-9. PubMed ID: 10874640
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inhibitors of endothelin.
    Webb ML; Meek TD
    Med Res Rev; 1997 Jan; 17(1):17-67. PubMed ID: 8979248
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR).
    Fitze G; Appelt H; König IR; Görgens H; Stein U; Walther W; Gossen M; Schreiber M; Ziegler A; Roesner D; Schackert HK
    Hum Mol Genet; 2003 Dec; 12(24):3207-14. PubMed ID: 14600022
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Endothelin receptor-mediated Ca2+ signaling and isoform expression in bovine corneal epithelial cells.
    Tao W; Wu X; Liou GI; Abney TO; Reinach PS
    Invest Ophthalmol Vis Sci; 1997 Jan; 38(1):130-41. PubMed ID: 9008638
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Endothelin-3 frameshift mutation in congenital central hypoventilation syndrome.
    Bolk S; Angrist M; Xie J; Yanagisawa M; Silvestri JM; Weese-Mayer DE; Chakravarti A
    Nat Genet; 1996 Aug; 13(4):395-6. PubMed ID: 8696331
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.