Testing of SHIRPA, a mouse phenotypic assessment protocol, on Dmd(mdx) and Dmd(mdx3cv) dystrophin-deficient mice.
about
Marginal level dystrophin expression improves clinical outcome in a strain of dystrophin/utrophin double knockout miceLimited Effect of Chronic Valproic Acid Treatment in a Mouse Model of Machado-Joseph DiseaseNeurotoxic autoantibodies mediate congenital cortical impairment of offspring in maternal lupus.Neuronal glucose transporter isoform 3 deficient mice demonstrate features of autism spectrum disordersENU mutagenesis reveals a novel phenotype of reduced limb strength in mice lacking fibrillin 2.Algorithms to predict cerebral malaria in murine models using the SHIRPA protocolArginylation of myosin heavy chain regulates skeletal muscle strengthMouse studies to shape clinical trials for mitochondrial diseases: high fat diet in Harlequin miceAssessing functional performance in the mdx mouse modelSynaptic Deficits at Neuromuscular Junctions in Two Mouse Models of Charcot-Marie-Tooth Type 2d.Pre- and post-exposure safety and efficacy of attenuated rabies virus vaccines are enhanced by their expression of IFNγUnderstanding the human condition: experimental strategies in mammalian genetics.Knockout of the murine cysteine dioxygenase gene results in severe impairment in ability to synthesize taurine and an increased catabolism of cysteine to hydrogen sulfide.mdx(⁵cv) mice manifest more severe muscle dysfunction and diaphragm force deficits than do mdx MiceEndpoint measures in the mdx mouse relevant for muscular dystrophy pre-clinical studies.Preservation of muscle force in Mdx3cv mice correlates with low-level expression of a near full-length dystrophin proteinRead-through compound 13 restores dystrophin expression and improves muscle function in the mdx mouse model for Duchenne muscular dystrophyAAV-based gene therapy prevents neuropathology and results in normal cognitive development in the hyperargininemic mouse.Uniform low-level dystrophin expression in the heart partially preserved cardiac function in an aged mouse model of Duchenne cardiomyopathy.A Modified Wire Hanging Apparatus for Small Animal Muscle Function TestingSimultaneous dystrophin and dysferlin deficiencies associated with high-level expression of the coxsackie and adenovirus receptor in transgenic mice.Neurobehavioral Anomalies in the Pitx3/ak Murine Model of Parkinson's Disease and MPTP.Decreased sensory responses in osteocalcin null mutant mice imply neuropeptide function.Lithium chloride therapy fails to improve motor function in a transgenic mouse model of Machado-Joseph disease.LMO7-null mice exhibit phenotypes consistent with emery-dreifuss muscular dystrophy.
P2860
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P2860
Testing of SHIRPA, a mouse phenotypic assessment protocol, on Dmd(mdx) and Dmd(mdx3cv) dystrophin-deficient mice.
description
2000 nî lūn-bûn
@nan
2000 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
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2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
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name
Testing of SHIRPA, a mouse phe ...... cv) dystrophin-deficient mice.
@ast
Testing of SHIRPA, a mouse phe ...... cv) dystrophin-deficient mice.
@en
type
label
Testing of SHIRPA, a mouse phe ...... cv) dystrophin-deficient mice.
@ast
Testing of SHIRPA, a mouse phe ...... cv) dystrophin-deficient mice.
@en
prefLabel
Testing of SHIRPA, a mouse phe ...... cv) dystrophin-deficient mice.
@ast
Testing of SHIRPA, a mouse phe ...... cv) dystrophin-deficient mice.
@en
P2093
P356
P1433
P1476
Testing of SHIRPA, a mouse phe ...... cv) dystrophin-deficient mice.
@en
P2093
P2888
P304
P356
10.1007/S003350010149
P577
2000-09-01T00:00:00Z