Localization of the mdx mutation within the mouse dystrophin gene.
about
Short telomeres and stem cell exhaustion model Duchenne muscular dystrophy in mdx/mTR miceAssignment of human genes for phosphorylase kinase subunits alpha (PHKA) to Xq12-q13 and beta (PHKB) to 16q12-q13Granulocyte-colony stimulating factor improves MDX mouse response to peripheral nerve injuryBiochemical and Functional Comparisons of mdx and Sgcg(-/-) Muscular Dystrophy Mouse Models.Chronic hypoxia impairs muscle function in the Drosophila model of Duchenne's muscular dystrophy (DMD).Transcriptome-scale similarities between mouse and human skeletal muscles with normal and myopathic phenotypesEvaluation of skeletal and cardiac muscle function after chronic administration of thymosin beta-4 in the dystrophin deficient mouse.Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.Localization of murine X and autosomal sequences homologous to the human Y located testis-determining region.A molecular genetic linkage map of mouse chromosome 9 with regional localizations for the Gsta, T3g, Ets-1 and Ldlr loci.A genetic linkage map of mouse chromosome 10: localization of eighteen molecular markers using a single interspecific backcrossRapid depletion of muscle progenitor cells in dystrophic mdx/utrophin-/- mice.Influence of genetic background on ex vivo and in vivo cardiac function in several commonly used inbred mouse strainsCarbamylated erythropoietin does not alleviate signs of dystrophy in mdx mice.Feline muscular dystrophy with dystrophin deficiency.Pulse-field linkage of the P3, G6pd and Cf-8 genes on the mouse X chromosome: demonstration of synteny at the physical levelDystrophin deficiency reduces atherosclerotic plaque development in ApoE-null miceRNA interference inhibits DUX4-induced muscle toxicity in vivo: implications for a targeted FSHD therapy.Effect of genetic background on the dystrophic phenotype in mdx mice.Loss of cIAP1 attenuates soleus muscle pathology and improves diaphragm function in mdx mice.Dystrophin-deficient cardiomyopathy in mouse: expression of Nox4 and Lox are associated with fibrosis and altered functional parameters in the heartRecent developments in the treatment of Duchenne muscular dystrophy and spinal muscular atrophy.CRISPR/Cas9-Mediated Genome Editing Corrects Dystrophin Mutation in Skeletal Muscle Stem Cells in a Mouse Model of Muscle Dystrophy.Black bear parathyroid hormone has greater anabolic effects on trabecular bone in dystrophin-deficient mice than in wild type miceAberrant development of neuromuscular junctions in glycosylation-defective Large(myd) mice.Dystrophin-glycoprotein complex sequesters Yap to inhibit cardiomyocyte proliferation.Humanizing the mdx mouse model of DMD: the long and the short of it.
P2860
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P2860
Localization of the mdx mutation within the mouse dystrophin gene.
description
1988 nî lūn-bûn
@nan
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
1988年论文
@zh
1988年论文
@zh-cn
name
Localization of the mdx mutation within the mouse dystrophin gene.
@ast
Localization of the mdx mutation within the mouse dystrophin gene.
@en
type
label
Localization of the mdx mutation within the mouse dystrophin gene.
@ast
Localization of the mdx mutation within the mouse dystrophin gene.
@en
prefLabel
Localization of the mdx mutation within the mouse dystrophin gene.
@ast
Localization of the mdx mutation within the mouse dystrophin gene.
@en
P2093
P2860
P1433
P1476
Localization of the mdx mutation within the mouse dystrophin gene.
@en
P2093
A S Ryder-Cook
E A Barnard
K E Davies
M G Darlison
P J Barnard
P Sicinski
R G Worton
P2860
P304
P407
P577
1988-10-01T00:00:00Z