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M Vainzof

Showing results (71-80 of 85) with videos related to

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Human Molecular Genetics|May 1, 1993
No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markersM R Passos-Bueno, C Wijmenga, R E Takata, et al.
Journal of Molecular Neuroscience : MN|October 23, 2001
Dysferlin protein analysis in limb-girdle muscular dystrophiesM Vainzof, L V Anderson, E M McNally, et al.
American Journal of Medical Genetics|April 15, 1993
Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?M R Passos-Bueno, B C Byth, S Rosenberg, et al.
Journal of Child Neurology|April 11, 2000
Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical casesU C Reed, S K Marie, M Vainzof, et al.
Nature Genetics|February 2, 2000
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethoninE S Moreira, T J Wiltshire, G Faulkner, et al.
Neuromuscular Disorders : NMD|November 26, 1998
Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridizationC Rosenberg, L Navajas, D F Vagenas, et al.
Cell Transplantation|November 22, 2012
Human adipose-derived mesenchymal stromal cells injected systemically into GRMD dogs without immunosuppression are able to reach the host muscle and express human dystrophinN M Vieira, M Valadares, E Zucconi, et al.
Stem Cell Reviews and Reports|June 20, 2014
Human adipose tissue derived pericytes increase life span in Utrn (tm1Ked) Dmd (mdx) /J miceM C Valadares, J P Gomes, G Castello, et al.
Human Molecular Genetics|December 1, 1996
Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)C G Bönnemann, M R Passos-Bueno, E M McNally, et al.
Neuromuscular Disorders : NMD|March 16, 2015
A normal life without muscle dystrophinM Zatz, N M Vieira, E Zucconi, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|May 1, 1993
No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markersM R Passos-Bueno, C Wijmenga, R E Takata, et al.
Journal of Molecular Neuroscience : MN|October 23, 2001
Dysferlin protein analysis in limb-girdle muscular dystrophiesM Vainzof, L V Anderson, E M McNally, et al.
American Journal of Medical Genetics|April 15, 1993
Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?M R Passos-Bueno, B C Byth, S Rosenberg, et al.
Journal of Child Neurology|April 11, 2000
Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical casesU C Reed, S K Marie, M Vainzof, et al.
Nature Genetics|February 2, 2000
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethoninE S Moreira, T J Wiltshire, G Faulkner, et al.
Neuromuscular Disorders : NMD|November 26, 1998
Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridizationC Rosenberg, L Navajas, D F Vagenas, et al.
Cell Transplantation|November 22, 2012
Human adipose-derived mesenchymal stromal cells injected systemically into GRMD dogs without immunosuppression are able to reach the host muscle and express human dystrophinN M Vieira, M Valadares, E Zucconi, et al.
Stem Cell Reviews and Reports|June 20, 2014
Human adipose tissue derived pericytes increase life span in Utrn (tm1Ked) Dmd (mdx) /J miceM C Valadares, J P Gomes, G Castello, et al.
Human Molecular Genetics|December 1, 1996
Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)C G Bönnemann, M R Passos-Bueno, E M McNally, et al.
Neuromuscular Disorders : NMD|March 16, 2015
A normal life without muscle dystrophinM Zatz, N M Vieira, E Zucconi, et al.
Pageof 9