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M L Moseley

Showing results (1-10 of 9) with videos related to

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Neurology|September 12, 2000
Spinocerebellar ataxia type 8: clinical features in a large familyJ W Day, L J Schut, M L Moseley, et al.
Human Molecular Genetics|July 11, 2000
The SCA8 transcript is an antisense RNA to a brain-specific transcript encoding a novel actin-binding protein (KLHL1)J P Nemes, K A Benzow, M L Moseley, et al.
Human Molecular Genetics|August 25, 2000
SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetranceM L Moseley, L J Schut, T D Bird, et al.
Nature Genetics|January 13, 1998
Rapid cloning of expanded trinucleotide repeat sequences from genomic DNAM D Koob, K A Benzow, T D Bird, et al.
Neurology|November 24, 1999
A nonpathogenic GAAGGA repeat in the Friedreich gene: implications for pathogenesisK Ohshima, N Sakamoto, M Labuda, et al.
Nature Genetics|April 7, 1999
An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)M D Koob, M L Moseley, L J Schut, et al.
Science (New York, N.Y.)|August 4, 2001
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9C L Liquori, K Ricker, M L Moseley, et al.
American Journal of Human Genetics|April 29, 2004
Insulin receptor splicing alteration in myotonic dystrophy type 2R S Savkur, A V Philips, T A Cooper, et al.
Neurology|December 17, 1998
Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia familiesM L Moseley, K A Benzow, L J Schut, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Neurology|September 12, 2000
Spinocerebellar ataxia type 8: clinical features in a large familyJ W Day, L J Schut, M L Moseley, et al.
Human Molecular Genetics|July 11, 2000
The SCA8 transcript is an antisense RNA to a brain-specific transcript encoding a novel actin-binding protein (KLHL1)J P Nemes, K A Benzow, M L Moseley, et al.
Human Molecular Genetics|August 25, 2000
SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetranceM L Moseley, L J Schut, T D Bird, et al.
Nature Genetics|January 13, 1998
Rapid cloning of expanded trinucleotide repeat sequences from genomic DNAM D Koob, K A Benzow, T D Bird, et al.
Neurology|November 24, 1999
A nonpathogenic GAAGGA repeat in the Friedreich gene: implications for pathogenesisK Ohshima, N Sakamoto, M Labuda, et al.
Nature Genetics|April 7, 1999
An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)M D Koob, M L Moseley, L J Schut, et al.
Science (New York, N.Y.)|August 4, 2001
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9C L Liquori, K Ricker, M L Moseley, et al.
American Journal of Human Genetics|April 29, 2004
Insulin receptor splicing alteration in myotonic dystrophy type 2R S Savkur, A V Philips, T A Cooper, et al.
Neurology|December 17, 1998
Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia familiesM L Moseley, K A Benzow, L J Schut, et al.
Pageof 1