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D J Duggan

Showing results (1-10 of 17) with videos related to

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Neuromuscular Disorders : NMD|December 1, 1996
Autosomal recessive muscular dystrophy and mutations of the sarcoglycan complexD J Duggan, E P Hoffman
Nature Genetics|January 23, 1999
Expression profiling using cDNA microarraysD J Duggan, M Bittner, Y Chen, et al.
Journal of the Neurological Sciences|September 1, 1996
alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutationsD J Duggan, M Fanin, E Pegoraro, et al.
The New England Journal of Medicine|February 27, 1997
Mutations in the sarcoglycan genes in patients with myopathyD J Duggan, J R Gorospe, M Fanin, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 1, 1994
Genetics of CYP1A1: coamplification of specific alleles by polymerase chain reaction and association with breast cancerT R Rebbeck, E A Rosvold, D J Duggan, et al.
Muscle & Nerve|May 19, 1998
Homozygous alpha-sarcoglycan mutation in two siblings: one asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patientC Angelini, M Fanin, E Menegazzo, et al.
Neurology|January 28, 1999
The clinical spectrum of sarcoglycanopathiesC Angelini, M Fanin, M P Freda, et al.
Neurogenetics|May 1, 1997
Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2)D J Duggan, D Manchester, K P Stears, et al.
Annals of Neurology|December 16, 1998
A dystrophin missense mutation showing persistence of dystrophin and dystrophin-associated proteins yet a severe phenotypeL R Goldberg, I Hausmanowa-Petrusewicz, A Fidzianska, et al.
Cancer Research|June 19, 2001
Human prostate cancer and benign prostatic hyperplasia: molecular dissection by gene expression profilingJ Luo, D J Duggan, Y Chen, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Neuromuscular Disorders : NMD|December 1, 1996
Autosomal recessive muscular dystrophy and mutations of the sarcoglycan complexD J Duggan, E P Hoffman
Nature Genetics|January 23, 1999
Expression profiling using cDNA microarraysD J Duggan, M Bittner, Y Chen, et al.
Journal of the Neurological Sciences|September 1, 1996
alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutationsD J Duggan, M Fanin, E Pegoraro, et al.
The New England Journal of Medicine|February 27, 1997
Mutations in the sarcoglycan genes in patients with myopathyD J Duggan, J R Gorospe, M Fanin, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 1, 1994
Genetics of CYP1A1: coamplification of specific alleles by polymerase chain reaction and association with breast cancerT R Rebbeck, E A Rosvold, D J Duggan, et al.
Muscle & Nerve|May 19, 1998
Homozygous alpha-sarcoglycan mutation in two siblings: one asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patientC Angelini, M Fanin, E Menegazzo, et al.
Neurology|January 28, 1999
The clinical spectrum of sarcoglycanopathiesC Angelini, M Fanin, M P Freda, et al.
Neurogenetics|May 1, 1997
Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2)D J Duggan, D Manchester, K P Stears, et al.
Annals of Neurology|December 16, 1998
A dystrophin missense mutation showing persistence of dystrophin and dystrophin-associated proteins yet a severe phenotypeL R Goldberg, I Hausmanowa-Petrusewicz, A Fidzianska, et al.
Cancer Research|June 19, 2001
Human prostate cancer and benign prostatic hyperplasia: molecular dissection by gene expression profilingJ Luo, D J Duggan, Y Chen, et al.
Pageof 2