BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

123 related articles for article (PubMed ID: 8583305)

  • 1. 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]  

  • 2. Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons.
    Baynash AG; Hosoda K; Giaid A; Richardson JA; Emoto N; Hammer RE; Yanagisawa M
    Cell; 1994 Dec; 79(7):1277-85. PubMed ID: 8001160
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice.
    Hosoda K; Hammer RE; Richardson JA; Baynash AG; Cheung JC; Giaid A; Yanagisawa M
    Cell; 1994 Dec; 79(7):1267-76. PubMed ID: 8001159
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Endothelins, pseudo-obstruction and Hirschsprung's disease.
    Milla PJ
    Gut; 1999 Feb; 44(2):148-9. PubMed ID: 9895366
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Novel mutations of the endothelin-B receptor gene in isolated patients with Hirschsprung's disease.
    Kusafuka T; Wang Y; Puri P
    Hum Mol Genet; 1996 Mar; 5(3):347-9. PubMed ID: 8852658
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Mutational analysis of the endothelin-B receptor gene in Japanese Hirschsprung's disease.
    Inoue M; Hosoda K; Imura K; Kamata S; Fukuzawa M; Nakao K; Okada A
    J Pediatr Surg; 1998 Aug; 33(8):1206-8. PubMed ID: 9721987
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A mutation in endothelin-B receptor gene causes myenteric aganglionosis and coat color spotting in rats.
    Kunieda T; Kumagai T; Tsuji T; Ozaki T; Karaki H; Ikadai H
    DNA Res; 1996 Apr; 3(2):101-5. PubMed ID: 8804863
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [From monogenic to polygenic: model of Hirschsprung disease].
    Salomon R; Amiel J; Attié T; Pelet A; Munnich A; Lyonnet S
    Pathol Biol (Paris); 1998 Nov; 46(9):705-7. PubMed ID: 9885824
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. L1cam acts as a modifier gene for members of the endothelin signalling pathway during enteric nervous system development.
    Wallace AS; Tan MX; Schachner M; Anderson RB
    Neurogastroenterol Motil; 2011 Nov; 23(11):e510-22. PubMed ID: 21395909
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome).
    Edery P; Attié T; Amiel J; Pelet A; Eng C; Hofstra RM; Martelli H; Bidaud C; Munnich A; Lyonnet S
    Nat Genet; 1996 Apr; 12(4):442-4. PubMed ID: 8630502
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Congenital central hypoventilation syndrome associated with Hirschsprung's disease: mutation analysis of the RET and endothelin-signaling pathways.
    Sakai T; Wakizaka A; Nirasawa Y
    Eur J Pediatr Surg; 2001 Oct; 11(5):335-7. PubMed ID: 11719874
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.