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Results: 1-7 |
Results: 7
The transcription factor GATA6 is essential for branching morphogenesis and epithelial cell differentiation during fetal pulmonary development
Authors: Keijzer, R van Tuyl, M Meijers, C Post, M Tibboel, D Grosveld, F Koutsourakis, M
Citation: R. Keijzer et al., The transcription factor GATA6 is essential for branching morphogenesis and epithelial cell differentiation during fetal pulmonary development, DEVELOPMENT, 128(4), 2001, pp. 503-511
RET and GDNF gene scanning in Hirschprung patients using two dual denaturing gel systems
Authors: Hofstra, RMW Wu, Y Stulp, RP Elfferich, P Osinga, J Maas, SM Siderius, L Brooks, AS Von der Ende, JJ Heydendael, VMR Severijnen, RSVM Bax, KMA Meijers, C Buys, CHCM
Citation: Rmw. Hofstra et al., RET and GDNF gene scanning in Hirschprung patients using two dual denaturing gel systems, HUM MUTAT, 15(5), 2000, pp. 418-429
Organization and chromosomal localization of the human ECEL1 (XCE) gene encoding a zinc metallopeptidase involved in the nervous control of respiration
Authors: Valdenaire, O Rohrbacher, E Langeveld, A Schweizer, A Meijers, C
Citation: O. Valdenaire et al., Organization and chromosomal localization of the human ECEL1 (XCE) gene encoding a zinc metallopeptidase involved in the nervous control of respiration, BIOCHEM J, 346, 2000, pp. 611-616
Cellular and molecular mechanisms involved in the development of the enteric nervous system
Authors: Meijers, C Hosgor, M Keijzer, R Lohman, FP
Citation: C. Meijers et al., Cellular and molecular mechanisms involved in the development of the enteric nervous system, EUR J MORPH, 37(4-5), 1999, pp. 227-232
A consanguineous family with Hirschsprung disease, microcephaly, and mental retardation (Goldberg-Shprintzen syndrome)
Authors: Brooks, AS Breuning, MH Osinga, J Van der Smagt, JJ Catsman, CE Buys, CHCM Meijers, C Hofstra, RMW
Citation: As. Brooks et al., A consanguineous family with Hirschsprung disease, microcephaly, and mental retardation (Goldberg-Shprintzen syndrome), J MED GENET, 36(6), 1999, pp. 485-489
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/ velocardiofacial syndrome without deletions within chromosome 22q11
Authors: Wadey, R McKie, J Papapetrou, C Sutherland, H Lohman, F Osinga, J Frohn, I Hofstra, R Meijers, C Amati, F Conti, E Pizzuti, A Dallapiccola, B Novelli, G Scambler, P
Citation: R. Wadey et al., Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/ velocardiofacial syndrome without deletions within chromosome 22q11, AM J HU GEN, 65(1), 1999, pp. 247-249
A loss-of-function mutation in the endothelin-converting enzyme 1 (ECE-1) associated with Hirschsprung disease, cardiac defects, and autonomic dysfunction
Authors: Hofstra, RMW Valdenaire, O Arch, E Osinga, J Kroes, H Loffler, BM Hamosh, A Meijers, C Buys, CHCM
Citation: Rmw. Hofstra et al., A loss-of-function mutation in the endothelin-converting enzyme 1 (ECE-1) associated with Hirschsprung disease, cardiac defects, and autonomic dysfunction, AM J HU GEN, 64(1), 1999, pp. 304-308
Risultati: 1-7 |