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D J Blake

Showing results (61-70 of 67) with videos related to

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Neuroscience|May 6, 2014
SGCZ mutations are unlikely to be associated with myoclonus dystoniaK J Peall, K Ritz, A J Waite, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 25, 1995
G-utrophin, the autosomal homologue of dystrophin Dp116, is expressed in sensory ganglia and brainD J Blake, J N Schofield, R A Zuellig, et al.
Nature|December 10, 1992
Primary structure of dystrophin-related proteinJ M Tinsley, D J Blake, A Roche, et al.
Genomics|December 1, 1991
Genetic and physical mapping around the properdin P geneM P Coleman, J C Murray, H F Willard, et al.
Human Molecular Genetics|May 1, 1996
A member of the MAP kinase phosphatase gene family in mouse containing a complex trinucleotide repeat in the coding regionA M Theodosiou, N R Rodrigues, M A Nesbit, et al.
American Journal of Human Genetics|October 10, 2001
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycanM Brockington, D J Blake, P Prandini, et al.
Human Molecular Genetics|December 14, 2001
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1CM Brockington, Y Yuva, P Prandini, et al.
Pageof 7

Showing results (61-70 of 67) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 67 results.
Neuroscience|May 6, 2014
SGCZ mutations are unlikely to be associated with myoclonus dystoniaK J Peall, K Ritz, A J Waite, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 25, 1995
G-utrophin, the autosomal homologue of dystrophin Dp116, is expressed in sensory ganglia and brainD J Blake, J N Schofield, R A Zuellig, et al.
Nature|December 10, 1992
Primary structure of dystrophin-related proteinJ M Tinsley, D J Blake, A Roche, et al.
Genomics|December 1, 1991
Genetic and physical mapping around the properdin P geneM P Coleman, J C Murray, H F Willard, et al.
Human Molecular Genetics|May 1, 1996
A member of the MAP kinase phosphatase gene family in mouse containing a complex trinucleotide repeat in the coding regionA M Theodosiou, N R Rodrigues, M A Nesbit, et al.
American Journal of Human Genetics|October 10, 2001
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycanM Brockington, D J Blake, P Prandini, et al.
Human Molecular Genetics|December 14, 2001
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1CM Brockington, Y Yuva, P Prandini, et al.
Pageof 7