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 *

116 related articles for article (PubMed ID: 10964697)

  • 1. 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]  

  • 2. 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]  

  • 3. Functional characterization of three mutations of the endothelin B receptor gene in patients with Hirschsprung's disease: evidence for selective loss of Gi coupling.
    Fuchs S; Amiel J; Claudel S; Lyonnet S; Corvol P; Pinet F
    Mol Med; 2001 Feb; 7(2):115-24. PubMed ID: 11471546
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease.
    Amiel J; Attié T; Jan D; Pelet A; Edery P; Bidaud C; Lacombe D; Tam P; Simeoni J; Flori E; Nihoul-Fékété C; Munnich A; Lyonnet S
    Hum Mol Genet; 1996 Mar; 5(3):355-7. PubMed ID: 8852660
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Reduced endothelin-3 expression in sporadic Hirschsprung disease.
    Kenny SE; Hofstra RM; Buys CH; Vaillant CR; Lloyd DA; Edgar DH
    Br J Surg; 2000 May; 87(5):580-5. PubMed ID: 10792313
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan.
    Lin YC; Lai HS; Hsu WM; Lee PI; Chen HL; Chang MH
    J Pediatr Gastroenterol Nutr; 2008 Jan; 46(1):36-40. PubMed ID: 18162831
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SOX10 mutations in chronic intestinal pseudo-obstruction suggest a complex physiopathological mechanism.
    Pingault V; Girard M; Bondurand N; Dorkins H; Van Maldergem L; Mowat D; Shimotake T; Verma I; Baumann C; Goossens M
    Hum Genet; 2002 Aug; 111(2):198-206. PubMed ID: 12189494
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations of the endothelin-B receptor and endothelin-3 genes in Hirschsprung's disease.
    Kusafuka T; Puri P
    Pediatr Surg Int; 1997; 12(1):19-23. PubMed ID: 9035203
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease.
    Puffenberger EG; Hosoda K; Washington SS; Nakao K; deWit D; Yanagisawa M; Chakravart A
    Cell; 1994 Dec; 79(7):1257-66. PubMed ID: 8001158
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Novel mutations of the endothelin B receptor gene in patients with Hirschsprung's disease and their characterization.
    Tanaka H; Moroi K; Iwai J; Takahashi H; Ohnuma N; Hori S; Takimoto M; Nishiyama M; Masaki T; Yanagisawa M; Sekiya S; Kimura S
    J Biol Chem; 1998 May; 273(18):11378-83. PubMed ID: 9556633
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Functional analysis of cell-free-produced human endothelin B receptor reveals transmembrane segment 1 as an essential area for ET-1 binding and homodimer formation.
    Klammt C; Srivastava A; Eifler N; Junge F; Beyermann M; Schwarz D; Michel H; Doetsch V; Bernhard F
    FEBS J; 2007 Jul; 274(13):3257-69. PubMed ID: 17535295
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Truncation of the receptor carboxyl terminus impairs membrane signaling but not ligand binding of human ETB endothelin receptor.
    Koshimizu T; Tsujimoto G; Ono K; Masaki T; Sakamoto A
    Biochem Biophys Res Commun; 1995 Dec; 217(1):354-62. PubMed ID: 8526934
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Endothelin-B receptor mutations in patients with isolated Hirschsprung disease from a non-inbred population.
    Auricchio A; Casari G; Staiano A; Ballabio A
    Hum Mol Genet; 1996 Mar; 5(3):351-4. PubMed ID: 8852659
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.