Molecular analysis of a spontaneous dystrophin 'knockout' dog.
about
Dystrophin-deficient large animal models: translational research and exon skippingGenetics of Human and Canine Dilated CardiomyopathyAnimal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapyCytoplasmic gamma-actin expression in diverse animal models of muscular dystrophyAn intronic LINE-1 element insertion in the dystrophin gene aborts dystrophin expression and results in Duchenne-like muscular dystrophy in the corgi breedA duchenne muscular dystrophy gene hot spot mutation in dystrophin-deficient cavalier king charles spaniels is amenable to exon 51 skipping.The golden retriever model of Duchenne muscular dystrophy.Pharmacologic management of Duchenne muscular dystrophy: target identification and preclinical trialsMammalian models of Duchenne Muscular Dystrophy: pathological characteristics and therapeutic applications.Gene replacement therapies for duchenne muscular dystrophy using adeno-associated viral vectors.Duchenne muscular dystrophy gene therapy: Lost in translation?Duchenne's muscular dystrophy: animal models used to investigate pathogenesis and develop therapeutic strategies.Duchenne muscular dystrophy gene therapy in the canine model.Chronic administration of a leupeptin-derived calpain inhibitor fails to ameliorate severe muscle pathology in a canine model of duchenne muscular dystrophyHistologic characterization of canine dilated cardiomyopathy.Muscle satellite cells from GRMD dystrophic dogs are not phenotypically distinguishable from wild type satellite cells in ex vivo culture.Animal models of muscular dystrophyCanine cytogenetics--from band to basepair.Comparative Genomics of X-linked Muscular Dystrophies: The Golden Retriever ModelGene therapy in large animal models of muscular dystrophy.Canine models of Duchenne muscular dystrophy and their use in therapeutic strategies.Current Translational Research and Murine Models For Duchenne Muscular Dystrophy.Mechanism of Deletion Removing All Dystrophin Exons in a Canine Model for DMD Implicates Concerted Evolution of X Chromosome PseudogenesWhole genome sequencing reveals a 7 base-pair deletion in DMD exon 42 in a dog with muscular dystrophy.Copy number variation in the domestic dog.Utrophin lacks the rod domain actin binding activity of dystrophin.Chromosome-specific single-locus FISH probes allow anchorage of an 1800-marker integrated radiation-hybrid/linkage map of the domestic dog genome to all chromosomes.Genomic Insights into Cardiomyopathies: A Comparative Cross-Species Review.Multiple Species Comparison of Cardiac Troponin T and Dystrophin: Unravelling the DNA behind Dilated Cardiomyopathy.Clinical and genetic characterisation of dystrophin-deficient muscular dystrophy in a family of Miniature Poodle dogs.Complex segregation analysis of dilated cardiomyopathy (DCM) in Irish wolfhounds.A novel canine model for Duchenne muscular dystrophy (DMD): single nucleotide deletion in DMD gene exon 20.Update on Standard Operating Procedures in Preclinical Research for DMD and SMA Report of TREAT-NMD Alliance Workshop, Schiphol Airport, 26 April 2015, The Netherlands.
P2860
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P2860
Molecular analysis of a spontaneous dystrophin 'knockout' dog.
description
1999 nî lūn-bûn
@nan
1999 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Molecular analysis of a spontaneous dystrophin 'knockout' dog.
@ast
Molecular analysis of a spontaneous dystrophin 'knockout' dog.
@en
type
label
Molecular analysis of a spontaneous dystrophin 'knockout' dog.
@ast
Molecular analysis of a spontaneous dystrophin 'knockout' dog.
@en
prefLabel
Molecular analysis of a spontaneous dystrophin 'knockout' dog.
@ast
Molecular analysis of a spontaneous dystrophin 'knockout' dog.
@en
P2093
P1476
Molecular analysis of a spontaneous dystrophin 'knockout' dog.
@en
P2093
Anderson LV
Dickens HF
Kornegay JN
Langford CF
Schatzberg SJ
P304
P356
10.1016/S0960-8966(99)00011-5
P577
1999-07-01T00:00:00Z