A H Beggs - JoVE Visualize

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Pediatric Neurology|November 1, 1992

Prediction of dystrophin phenotype by DNA analysis in Duchenne/Becker muscular dystrophyL A Specht, A H Beggs, B Korf, et al.

Neurology|May 11, 1992

Differential glucocorticoid effects on the fusion of Duchenne/Becker and control muscle cultures: pharmacologic detection of accelerated aging in dystrophic muscleO Hardiman, R H Brown, A H Beggs, et al.

Neurology|May 1, 1990

Enormous dystrophin in a patient with Becker muscular dystrophyC Angelini, A H Beggs, E P Hoffman, et al.

BMC Genetics|July 17, 2001

Genomic organization and single-nucleotide polymorphism map of desmuslin, a novel intermediate filament protein on chromosome 15q26.3Y Mizuno, A A Puca, K F O'Brien, et al.

Archives of Biochemistry and Biophysics|May 18, 1999

alpha-actinin-2 is a new component of the dystrophin-glycoprotein complexJ E Hance, S Y Fu, S C Watkins, et al.

Journal of Child Neurology|July 1, 1996

Congenital muscular dystrophy associated with merosin deficiencyK N North, L A Specht, R K Sethi, et al.

Circulation|January 28, 1998

Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of Long-QT syndromeP Duggal, M R Vesely, D Wattanasirichaigoon, et al.

Human Genetics|April 17, 1998

Multiple different missense mutations in the pore region of HERG in patients with long QT syndromeC A Satler, M R Vesely, P Duggal, et al.

American Journal of Human Genetics|May 1, 1997

A gene for isolated congenital ptosis maps to a 3-cM region within 1p32-p34.1E C Engle, A E Castro, M E Macy, et al.

Virology|July 1, 1994

Expression of the myelin basic protein gene in transgenic mice expressing human neurotropic virus, JCV, early proteinS Haas, N S Haque, A H Beggs, et al.

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Showing results (21-30 of 75) with videos related to

Sort By:

Pageof 8

Pediatric Neurology|November 1, 1992

Prediction of dystrophin phenotype by DNA analysis in Duchenne/Becker muscular dystrophyL A Specht, A H Beggs, B Korf, et al.

Neurology|May 11, 1992

Differential glucocorticoid effects on the fusion of Duchenne/Becker and control muscle cultures: pharmacologic detection of accelerated aging in dystrophic muscleO Hardiman, R H Brown, A H Beggs, et al.

Neurology|May 1, 1990

Enormous dystrophin in a patient with Becker muscular dystrophyC Angelini, A H Beggs, E P Hoffman, et al.

BMC Genetics|July 17, 2001

Genomic organization and single-nucleotide polymorphism map of desmuslin, a novel intermediate filament protein on chromosome 15q26.3Y Mizuno, A A Puca, K F O'Brien, et al.

Archives of Biochemistry and Biophysics|May 18, 1999

alpha-actinin-2 is a new component of the dystrophin-glycoprotein complexJ E Hance, S Y Fu, S C Watkins, et al.

Journal of Child Neurology|July 1, 1996

Congenital muscular dystrophy associated with merosin deficiencyK N North, L A Specht, R K Sethi, et al.

Circulation|January 28, 1998

Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of Long-QT syndromeP Duggal, M R Vesely, D Wattanasirichaigoon, et al.

Human Genetics|April 17, 1998

Multiple different missense mutations in the pore region of HERG in patients with long QT syndromeC A Satler, M R Vesely, P Duggal, et al.

American Journal of Human Genetics|May 1, 1997

A gene for isolated congenital ptosis maps to a 3-cM region within 1p32-p34.1E C Engle, A E Castro, M E Macy, et al.

Virology|July 1, 1994

Expression of the myelin basic protein gene in transgenic mice expressing human neurotropic virus, JCV, early proteinS Haas, N S Haque, A H Beggs, et al.

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