Ret protein in the human fetal rectum

A major gene for Hirschsprung's disease (HD) recently has been mapped in chromosome 10q11.2 and identified to be the RET proto-oncogene. Mutations of the RET gene have occurred in HD patients, and abnormalities of expression and function of Ret protein (a receptor tyrosine kinase, which is the...

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Veröffentlicht in:	Journal of pediatric surgery 1996-04, Vol.31 (4), p.568-571
Hauptverfasser:	Tam, P.K.H., Gould, S.J., Martucciello, G., Biddolph, S., Takahashi, M., Jasonni, V.
Format:	Artikel
Sprache:	eng
Schlagworte:	Animals Antibodies, Monoclonal Biological and medical sciences Drosophila Proteins Enteric Nervous System - embryology Enteric Nervous System - pathology Female Gastroenterology. Liver. Pancreas. Abdomen Gene Expression - physiology Gestational Age Hirschsprung Disease - genetics Hirschsprung Disease - pathology Humans Immunoenzyme Techniques Male Malformations Medical sciences Mice Pregnancy Proto-Oncogene Proteins - genetics Proto-Oncogene Proteins c-ret Receptor Protein-Tyrosine Kinases - genetics Rectum - embryology Rectum - pathology Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
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