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Gene|September 14, 1990
Isolation of cDNAs encoding subunit VIb of cytochrome c oxidase and steady-state levels of coxVIb mRNA in different tissuesJ W Taanman, C Schrage, N J Ponne, et al.Human Mutation|January 1, 1995
Déjérine-Sottas neuropathy is associated with a de novo PMP22 mutationL J Valentijn, R A Ouvrier, N H van den Bosch, et al.Journal of Inherited Metabolic Disease|January 1, 1990
Muscle cell cultures in Menkes' disease: copper accumulation in myotubesG J van den Berg, J J Kroon, F A Wijburg, et al.American Journal of Human Genetics|April 1, 1997
Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21A J van der Kooi, M van Meegen, T M Ledderhof, et al.American Journal of Human Genetics|May 9, 2003
Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathyNeil Howell, Roelof-Jan Oostra, Piet A Bolhuis, et al.Human Genetics|August 1, 1990
Distribution and characterization of a Sandhoff disease-associated 50-kb deletion in the gene encoding the human beta-hexosaminidase beta-chainH Bikker, F M van den Berg, R A Wolterman, et al.Neurology|March 1, 1996
Genetic localization of Bethlem myopathyG J Jobsis, P A Bolhuis, J M Boers, et al.Biochimica Et Biophysica Acta|February 21, 1992
Isoforms of cytochrome c oxidase in tissues and cell lines of the mouseC Van den Bogert, H L Dekker, J C Cornelissen, et al.Neurology|January 1, 1987
Ganglioside storage, hexosaminidase lability, and urinary oligosaccharides in adult Sandhoff's diseaseP A Bolhuis, J G Oonk, P E Kamp, et al.Applied and Environmental Microbiology|July 2, 1999
Evaluation of bottlenecks in the late stages of protein secretion in Bacillus subtilisA Bolhuis, H Tjalsma, H E Smith, et al.Pageof 14