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Neuromuscular Disorders : NMD
|
November 26, 1998
Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization
C 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 disability
T 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 X
H 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 types
S 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 dystrophin
N 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 dystrophin
M 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 mice
M 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 imperfecta
C 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 families
M R Passos-Bueno, E S Moreira, S K Marie, et al.
Page
of 26
Search research articles
Search
Showing results (231-240 of 252) with videos related to
Sort By:
Page
of 26
Neuromuscular Disorders : NMD
|
November 26, 1998
Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization
C 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 disability
T 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 X
H 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 types
S 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 dystrophin
N 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 dystrophin
M 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 mice
M 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 imperfecta
C 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 families
M R Passos-Bueno, E S Moreira, S K Marie, et al.
Page
of 26