Molecular insights in a multigenic malformation: Hirschsprung disease;Du monogenique au polygenique: Le modele de la maladie Hirschsprung

Pathologie Biologie

Volumn 46, Issue 9, 1998, Pages 705-707

  Salomon, R ^a   Amiel, J ^a   Attie, T ^a   Pelet, A ^a   Munnich, A ^a   Lyonnet, S ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

GDNF; Hirschsprung; Multigenism; RET proto oncogene

Indexed keywords

ENDOTHELIN RECEPTOR; LIGAND; NEUROTROPHIC FACTOR; PROTEIN TYROSINE KINASE; DROSOPHILA PROTEIN; ENDOTHELIN 3; ENDOTHELIN B RECEPTOR; GLIAL CELL LINE DERIVED NEUROTROPHIC FACTOR RECEPTOR; ONCOPROTEIN; PROTEIN RET; RET ONCOGENE PROTEIN, DROSOPHILA; RET PROTEIN, MOUSE;

CONFERENCE PAPER; GENE EXPRESSION; GENE MUTATION; HIRSCHSPRUNG DISEASE; HOMOZYGOSITY; LIGAND BINDING; MEGACOLON; MISSENSE MUTATION; MULTIGENE FAMILY; PROTO ONCOGENE; SITE DIRECTED MUTAGENESIS; WAARDENBURG SYNDROME; ANIMAL; GENETICS; HUMAN; MOUSE; MUTATION; REVIEW;

ANIMALS; DROSOPHILA PROTEINS; ENDOTHELIN-3; GLIAL CELL LINE-DERIVED NEUROTROPHIC FACTOR RECEPTORS; HIRSCHSPRUNG DISEASE; HUMANS; MICE; MULTIGENE FAMILY; MUTATION; PROTO-ONCOGENE PROTEINS; PROTO-ONCOGENE PROTEINS C-RET; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTOR, ENDOTHELIN B; RECEPTORS, ENDOTHELIN;

EID: 0032447334     PISSN: 03698114     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

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