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M Zatz

Showing results (231-240 of 252) with videos related to

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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.
Molecular Psychiatry|September 30, 2015
A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disabilityT Figueiredo, U S Melo, A L S Pessoa, et al.
Psychiatric Genetics|November 4, 1998
Linkage analysis between bipolar affective disorder and markers on chromosome XH P Vallada, L Vasques, D Curtis, et al.
Journal of Neurochemistry|December 21, 2004
Molecular cloning, localization and circadian expression of chicken melanopsin (Opn4): differential regulation of expression in pineal and retinal cell typesS S Chaurasia, M D Rollag, G Jiang, 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.
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.
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.
Genetics and Molecular Research : GMR|March 14, 2009
A novel COL1A1 gene-splicing mutation (c.1875+1G>C) in a Brazilian patient with osteogenesis imperfectaC Barbirato, M G Almeida, M Milanez, et al.
Journal of Medical Genetics|February 1, 1996
Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian familiesM R Passos-Bueno, E S Moreira, S K Marie, et al.
Pageof 26

Showing results (231-240 of 252) with videos related to

Sort By:
Pageof 26
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.
Molecular Psychiatry|September 30, 2015
A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disabilityT Figueiredo, U S Melo, A L S Pessoa, et al.
Psychiatric Genetics|November 4, 1998
Linkage analysis between bipolar affective disorder and markers on chromosome XH P Vallada, L Vasques, D Curtis, et al.
Journal of Neurochemistry|December 21, 2004
Molecular cloning, localization and circadian expression of chicken melanopsin (Opn4): differential regulation of expression in pineal and retinal cell typesS S Chaurasia, M D Rollag, G Jiang, 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.
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.
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.
Genetics and Molecular Research : GMR|March 14, 2009
A novel COL1A1 gene-splicing mutation (c.1875+1G>C) in a Brazilian patient with osteogenesis imperfectaC Barbirato, M G Almeida, M Milanez, et al.
Journal of Medical Genetics|February 1, 1996
Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian familiesM R Passos-Bueno, E S Moreira, S K Marie, et al.
Pageof 26