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Human Genetics|April 1, 1996
No evidence for 'skewed' inactivation of the X-chromosome as cause of Leber's hereditary optic neuropathy in female carriersR J Oostra, S Kemp, P A Bolhuis, et al.Muscle & Nerve|June 1, 1992
Major growth reduction and minor decrease in mitochondrial enzyme activity in cultured human muscle cells after exposure to zidovudineN H Herzberg, I Zorn, R Zwart, et al.Neuromuscular Disorders : NMD|January 1, 1994
Cultured human muscle cells and respiratory chain deficienciesN H Herzberg, P A Bolhuis, C van den Bogert, et al.International Journal of Cosmetic Science|May 22, 2009
The spectral stability of several sunscreening agents on stratum corneum sheetsA Kammeyer, W Westerhof, P A Bolhuis, et al.The Journal of Biological Chemistry|August 24, 1999
Functional analysis of paralogous thiol-disulfide oxidoreductases in Bacillus subtilisA Bolhuis, G Venema, W J Quax, et al.Nederlands Tijdschrift Voor Geneeskunde|July 1, 1995
[Leber's optic nerve atrophy; a mitochondrial hereditary disease]R J Oostra, P A Bolhuis, F A Wijburg, et al.Microbiology and Molecular Biology Reviews : MMBR|September 7, 2000
Signal peptide-dependent protein transport in Bacillus subtilis: a genome-based survey of the secretomeH Tjalsma, A Bolhuis, J D Jongbloed, et al.The Journal of Biological Chemistry|March 30, 2001
TatB and TatC form a functional and structural unit of the twin-arginine translocase from Escherichia coliA Bolhuis, J E Mathers, J D Thomas, et al.Brain Research. Molecular Brain Research|March 1, 1995
RC3/neurogranin structure and expression in the caprine brain in relation to congenital hypothyroidismP A Piosik, M van Groenigen, N J Ponne, et al.The Journal of Laboratory and Clinical Medicine|March 1, 1980
Heterogeneity of human factor VIII. III. Transitions between forms of factor VIII present in cryoprecipitate and in cryosupernatant plasmaJ Over, B N Bouma, J J Sixma, et al.Pageof 14