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Oncogene|August 8, 2012
BMK1 is involved in the regulation of p53 through disrupting the PML-MDM2 interactionQ Yang, L Liao, X Deng, et al.Analytical Chemistry|February 15, 1997
Direct analysis and identification of proteins in mixtures by LC/MS/MS and database searching at the low-femtomole levelA L McCormack, D M Schieltz, B Goode, et al.Neuropediatrics|March 6, 2004
Coats' plus: a progressive familial syndrome of bilateral Coats' disease, characteristic cerebral calcification, leukoencephalopathy, slow pre- and post-natal linear growth and defects of bone marrow and integumentY J Crow, J McMenamin, C A Haenggeli, et al.Human Molecular Genetics|December 6, 2001
Mutations in the general transcription factor TFIIH result in beta-thalassaemia in individuals with trichothiodystrophyV Viprakasit, R J Gibbons, B C Broughton, et al.Journal of Medical Genetics|November 1, 1996
Improved genetic mapping of X linked retinoschisisN D George, S J Payne, R M Bill, et al.Molecular and Cellular Biology|September 22, 1999
The ADA complex is a distinct histone acetyltransferase complex in Saccharomyces cerevisiaeA Eberharter, D E Sterner, D Schieltz, et al.The Journal of Investigative Dermatology|June 1, 1996
The gene encoding collagen alpha1(V)(COL5A1) is linked to mixed Ehlers-Danlos syndrome type I/IIN P Burrows, A C Nicholls, J R Yates, et al.Journal of Medical Genetics|August 1, 1989
Evidence for genetic heterogeneity in tuberous sclerosisJ R Sampson, J R Yates, L A Pirrit, et al.Neuromuscular Disorders : NMD|March 11, 2000
Two distal mutations in the gene encoding emerin have profoundly different effects on emerin protein expressionJ A Ellis, C A Brown, L D Tilley, et al.Electrophoresis|November 18, 2000
Proteomics of rat liver Golgi complex: minor proteins are identified through sequential fractionationR S Taylor, C C Wu, L G Hays, et al.Pageof 56