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The Journal of Biological Chemistry|September 17, 1998
Association of the TLX-2 homeodomain and 14-3-3eta signaling proteinsS J Tang, T C Suen, R R McInnes, et al.Nature Genetics|May 20, 1998
A mouse model for Prader-Willi syndrome imprinting-centre mutationsT Yang, T E Adamson, J L Resnick, et al.Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|October 23, 1997
Patient-based research in a tertiary pediatric centre: a pilot study of markers of scientific activity and productivityG Koren, G Barker, V Mitchell, et al.Early Human Development|September 1, 1993
Transitory neurological findings in a population of at risk infantsR Michaelis, C Asenbauer, M Buchwald-Saal, et al.American Journal of Respiratory Cell and Molecular Biology|April 1, 1994
Regional expression of CFTR in developing human respiratory tissuesE F Tizzano, H O'Brodovich, D Chitayat, et al.Mutation Research|July 1, 1991
Alteration of a nuclease in Fanconi anemiaK Sakaguchi, P V Harris, C Ryan, et al.Muscle & Nerve|May 1, 1985
The free cytoplasmic Ca2+ levels in Duchenne muscular dystrophy lymphocytesA Klip, B Elder, H P Ruiz-Funes, et al.Human Genetics|July 1, 1990
Identification of sequences of chromosome 7 that are expressed in sweat gland epithelial cellsJ Burns, G Melmer, J M Rommens, et al.Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|October 1, 1992
Expression of a mutant regulatory subunit of cAMP-dependent protein kinase in the Caco-2 human colonic carcinoma cell lineV Mihajlovic, A J Krolczyk, W Auerbach, et al.Human Molecular Genetics|June 1, 1993
A nonsense mutation and exon skipping in the Fanconi anaemia group C geneR A Gibson, A Hajianpour, M Murer-Orlando, et al.Pageof 15