(Q40373239)

19 September 2017

1 reference

title

Dystrophin, its gene, and the dystrophinopathies (English)

1 reference

19 September 2017

Roberts RG

1

1 reference

19 September 2017

1 January 1995

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19 September 2017

1 reference

19 September 2017

33

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19 September 2017

177-231

1 reference

Analysis of quantitative PCR for the diagnosis of deletion and duplication carriers in the dystrophin gene

19 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy gene

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Two forms of mouse syntrophin, a 58 kd dystrophin-associated protein, differ in primary structure and tissue distribution.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Red cell membrane sialoglycoprotein beta in homozygous and heterozygous 4.1(-) hereditary elliptocytosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Serial position memory of boys with Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

A novel product of the Duchenne muscular dystrophy gene which greatly differs from the known isoforms in its structure and tissue distribution

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Gastric hypomotility in Duchenne's muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Beta-globin nonsense mutation: deficient accumulation of mRNA occurs despite normal cytoplasmic stability

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

[A new x-chromosomal muscular dystrophy]

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Evidence to implicate translation by ribosomes in the mechanism by which nonsense codons reduce the nuclear level of human triosephosphate isomerase mRNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Brain spectrin, a membrane-associated protein related in structure and function to erythrocyte spectrin.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Expression and localization of dystrophin in human cardiac Purkinje fibers

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Human and murine dystrophin mRNA transcripts are differentially expressed during skeletal muscle, heart, and brain development

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Cognitive functions in Duchenne muscular dystrophy: a reappraisal and comparison with spinal muscular atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cells

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Duchenne dystrophy: focal alterations in the distribution of concanavalin A binding sites at the muscle cell surface

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Identification and purification of an agrin receptor from Torpedo postsynaptic membranes: a heteromeric complex related to the dystroglycans

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Dystrophin is transcribed in brain from a distant upstream promoter.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Developmentally induced, muscle-specific trans factors control the differential splicing of alternative and constitutive troponin T exons.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

X chromosome-linked muscular dystrophy (mdx) in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Point mutation in the human dystrophin gene: identification through western blot analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

A cDNA clone from the Duchenne/Becker muscular dystrophy gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Prevalence and incidence of Becker muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Identification of a myocyte nuclear factor that binds to the muscle-specific enhancer of the mouse muscle creatine kinase gene

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

An alternative dystrophin transcript specific to peripheral nerve

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Association of dystrophin and an integral membrane glycoprotein.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Altered binding of Ricinus communis I lectin by muscle membranes in Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Duchenne muscular dystrophy: plasma membrane loss initiates muscle cell necrosis unless it is repaired

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Transcription of the dystrophin gene in human muscle and non-muscle tissue

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Dystrophin gene transcribed from different promoters in neuronal and glial cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

A genetic linkage map of five marker loci in and around the Duchenne muscular dystrophy locus

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Nonsense codons can reduce the abundance of nuclear mRNA without affecting the abundance of pre-mRNA or the half-life of cytoplasmic mRNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Construction of a 2.6-Mb contig in yeast artificial chromosomes spanning the human dystrophin gene using an STS-based approach

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

The Genetic Relationship of Progressive Muscular Dystrophy (Duchenne Type) and Mental Retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Prenatal testing for Duchenne and Becker muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Structural predictions for the central domain of dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Ultrastructural localization of dystrophin in human muscle by using gold immunolabelling

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Immunogold labelling of dystrophin in human muscle, using an antibody to the last 17 amino acids of the C-terminus

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Molecular analysis of human X-linked diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

alpha-Actinins and the DMD protein contain spectrin-like repeats

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Prevalence of left ventricular systolic dysfunction in Duchenne muscular dystrophy: an echocardiographic study

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

RNA secondary structure repression of a muscle-specific exon in HeLa cell nuclear extracts.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

The genetic linkage map of the human X chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Intellectual Impairment in Muscular Dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

The linkage relations of the loci for benign (Becker type) X-borne muscular dystrophy, colour blindness and the Xg blood groups

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Very mild muscular dystrophy associated with the deletion of 46% of dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Membrane organization of the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Recombination with pERT87 (DXS164) in families with X-linked muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Intelligence level of patients with the duchenne type of progressive muscular dystrophy (PMD-D)

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Increased activity of calcium leak channels in myotubes of Duchenne human and mdx mouse origin

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Calcium entry through stretch-inactivated ion channels in mdx myotubes

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Clinical features and classification of the muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Dystrophin deficiency causes lethal muscle hypertrophy in cats

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Haemophilia B: database of point mutations and short additions and deletions--second edition

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

1 reference

7 January 2021

Analysis of molecular deletions with cDNA probes in patients with Duchenne and Becker muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Report of the Committee on the Genetic Constitution of the X and Y Chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Expression of four alternative dystrophin transcripts in brain regions regulated by different promoters.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Protein sequence of DMD gene is related to actin-binding domain of alpha-actinin

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

DNA deletions in mild and severe Becker muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Analysis of the actin-binding domain of alpha-actinin by mutagenesis and demonstration that dystrophin contains a functionally homologous domain

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Conservation of the Duchenne muscular dystrophy gene in mice and humans

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Subcellular fractionation of dystrophin to the triads of skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Cell and fiber type distribution of dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Somatic reversion/suppression of the mouse mdx phenotype in vivo.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Binding of the Drosophila Sex-lethal gene product to the alternative splice site of transformer primary transcript

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Experimental skeletal muscle damage: the nature of the calcium-activated degenerative processes

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Diagnostic criteria for Duchenne and Becker muscular dystrophy and myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial results

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

conformation and phasing of dystrophin structural repeats.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Small-caliber skeletal muscle fibers do not suffer deleterious consequences of dystrophic gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

The subcellular distribution of chromosome 6-encoded dystrophin-related protein in the brain

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Myogenic regulation of dystrophin gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Molecular and functional analysis of the muscle-specific promoter region of the Duchenne muscular dystrophy gene

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Dystrophin-glycoprotein complex and laminin colocalize to the sarcolemma and transverse tubules of cardiac muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Orocaecal transit time in Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Muscular dystrophy in a litter of golden retriever dogs

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Mental retardation in patients with Duchenne progressive muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

The identification and characterisation of an actin-binding site in alpha-actinin by mutagenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

A housekeeping type promoter, located in the 3' region of the Duchenne muscular dystrophy gene, controls the expression of Dp71, a major product of the gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

The chicken dystrophin cDNA: striking conservation of the C-terminal coding and 3' untranslated regions between man and chicken

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

An autosomal transcript in skeletal muscle with homology to dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Characterization of deletions in the dystrophin gene giving mild phenotypes.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Tissue distribution of the dystrophin-related gene product and expression in the mdx and dy mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Brain-type and muscle-type promoters of the dystrophin gene differ greatly in structure

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Dystrophin. The gene and its product

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Detection of Duchenne muscular dystrophy carriers by dosage analysis using the DMD cDNA clone 8

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

A conserved CATTCCT motif is required for skeletal muscle-specific activity of the cardiac troponin T gene promoter

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Purification of dystrophin-related protein (utrophin) from lung and its identification in pulmonary artery endothelial cells

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Nonsense mutations and diminished mRNA levels

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Mapping of Xp21 translocation breakpoints in and around the DMD gene by pulsed field gel electrophoresis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Cardiac involvement in Becker muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Decreased osmotic stability of dystrophin-less muscle cells from the mdx mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Immunohistochemical dystrophin reaction in synaptic regions

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Duchenne dystrophy: Electron microscopic findings pointing to a basic or early abnormality in the plasma membrane of the muscle fiber

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

A yeast artificial chromosome contig containing the complete Duchenne muscular dystrophy gene

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Premature translational termination triggers mRNA decapping

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Recombination frequencies between Duchenne muscular dystrophy and intragenic markers in multigeneration families

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

The chicken fast skeletal troponin I gene: exon organization and sequence

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Becker muscular dystrophy: correlation of deletion type with clinical severity

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Expression of the putative Duchenne muscular dystrophy gene in differentiated myogenic cell cultures and in the brain

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Duchenne muscular dystrophy gene product is not identical in muscle and brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Dystrophin constitutes 5% of membrane cytoskeleton in skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Duchenne muscular dystrophy gene expression in normal and diseased human muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Two hot spots of recombination in the DMD gene correlate with the deletion prone regions

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Reproductive fitness and frequency of new mutations in Becker muscular dystrophy: implications for genetic risk estimates

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysis.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

The utrophin and dystrophin genes share similarities in genomic structure

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Cardiac rhythm and conduction in Duchenne's muscular dystrophy: a prospective study of 20 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Dystrophin protects the sarcolemma from stresses developed during muscle contraction

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Dystrophin expression in the human retina is required for normal function as defined by electroretinography

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Identification of two point mutations and a one base deletion in exon 19 of the dystrophin gene by heteroduplex formation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patient

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Intelligence and the gene for Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Posttranscriptional regulation of c-fos mRNA expression

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNA

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCR.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Point mutations in the dystrophin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Exon structure of the human dystrophin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Point mutation in a Becker muscular dystrophy patient.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Searching for the 1 in 2,400,000: a review of dystrophin gene point mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Protein truncation test (PTT) for rapid detection of translation-terminating mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Analysis of dystrophin expression after activation of myogenesis in amniocytes, chorionic-villus cells, and fibroblasts. A new method for diagnosing Duchenne's muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Molecular shape of dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Colocalization of retinal dystrophin and actin in postsynaptic dendrites of rod and cone photoreceptor synapses

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Application of the freeze fracture technique to the study of human neuromuscular disease

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Carrier detection in Duchenne muscular dystrophy. Evidence from a study of obligatory carriers and mothers of isolated cases

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

The molecular basis of muscular dystrophy in the mdx mouse: a point mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Cranin: a laminin-binding protein of cell membranes

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Erythrocyte spectrin is comprised of many homologous triple helical segments

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Identification of upstream and intragenic regulatory elements that confer cell-type-restricted and differentiation-specific expression on the muscle creatine kinase gene

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Glycoprotein-binding site of dystrophin is confined to the cysteine-rich domain and the first half of the carboxy-terminal domain

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Molecular organization at the glycoprotein-complex-binding site of dystrophin. Three dystrophin-associated proteins bind directly to the carboxy-terminal portion of dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Primary structure of dystrophin-related protein

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Increased protein degradation results from elevated free calcium levels found in muscle from mdx mice

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

The 87K postsynaptic membrane protein from Torpedo is a protein-tyrosine kinase substrate homologous to dystrophin.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Selection of Dictyostelium mutants defective in cytoskeletal proteins: use of an antibody that binds to the ends of alpha-actinin rods.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

A deletion hot spot in the Duchenne muscular dystrophy gene

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Immunoelectron microscopic localization of dystrophin in myofibres

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Expression of the N-terminal domain of dystrophin in E. coli and demonstration of binding to F-actin.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

The myoD Gene Family: Nodal Point During Specification of the Muscle Cell Lineage

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Phasing the conformational unit of spectrin

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Heterogeneity of dystrophin-associated proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Selective defect in dystrophin-associated glycoproteins 50DAG (A2) and 35DAG (A4) in the dystrophic hamster: an animal model for severe childhood autosomal recessive muscular dystrophy (SCARMD)

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Crystal structure of the repetitive segments of spectrin

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Molecular analysis of the Duchenne muscular dystrophy gene in patients with Becker muscular dystrophy presenting with dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Glycoprotein complex anchoring dystrophin to sarcolemma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

Frequency of Duchenne muscular dystrophy carriers

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2960334-X

7 January 2021

10.1016/S0065-2660(08)60334-X

Identifiers

DOI

0 references

PubMed ID

7484453

1 reference

PubMed ID

7484453