(Q40644356)

22 September 2017

1 reference

title

The structural and functional diversity of dystrophin (English)

1 reference

22 September 2017

A H Ahn

1

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22 September 2017

L M Kunkel

series ordinal

2

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22 September 2017

language of work or name

English

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publication date

1 April 1993

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22 September 2017

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22 September 2017

3

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22 September 2017

283-291

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22 September 2017

4

1 reference

https://scigraph.springernature.com/pub.10.1038/ng0493-283

22 September 2017

0 references

cites work

Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

[A new x-chromosomal muscular dystrophy]

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Structural analysis of homologous repeated domains in alpha-actinin and spectrin

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Structure and evolution of the actin crosslinking proteins

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Spectrin: a structural mediator between diverse plasma membrane proteins and the cytoplasm

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Functional diversity among spectrin isoforms

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Cell and fiber type distribution of dystrophin

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Immunohistochemical dystrophin reaction in synaptic regions

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Immunocytochemical study of dystrophin at the myotendinous junction

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

The subcellular distribution of dystrophin in mouse skeletal, cardiac, and smooth muscle

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Dystrophin colocalizes with beta-spectrin in distinct subsarcolemmal domains in mammalian skeletal muscle

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Dystrophin at the plasma membrane of human muscle fibers shows a costameric localization

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Direct visualization of the dystrophin network on skeletal muscle fiber membrane

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Confocal laser microscopy of dystrophin localization in guinea pig skeletal muscle fibers

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

7 January 2021

Characterization and cell type distribution of a novel, major transcript of the Duchenne muscular dystrophy gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

7 January 2021

An alternative dystrophin transcript specific to peripheral nerve

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Quantitative estimation of minor mRNAs by cDNA-polymerase chain reaction. Application to dystrophin mRNA in cultured myogenic and brain cells

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Proteinase-sensitive sites on isolated rabbit dystrophin

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

In vitro digestion of dystrophin by calcium-dependent proteases, calpains I and II

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

The interaction of actin with dystrophin

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

7 January 2021

Erythrocyte spectrin is comprised of many homologous triple helical segments

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Evolution of EF-hand calcium-modulated proteins. I. Relationships based on amino acid sequences

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Evolution of EF-hand calcium-modulated proteins. II. Domains of several subfamilies have diverse evolutionary histories

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Non-muscle α-actinins are calcium-sensitive actin-binding proteins

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Characterization of calcium binding to spectrins.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Isolation and characterization of different C-terminal fragments of dystrophin expressed in Escherichia coli

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

An autosomal transcript in skeletal muscle with homology to dystrophin

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Primary structure of dystrophin-related protein

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Ultrastructural localization of dystrophin in human muscle by using gold immunolabelling

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Membrane organization of the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

7 January 2021

Long-range restriction map around the Duchenne muscular dystrophy gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Long-range genomic map of the Duchenne muscular dystrophy (DMD) gene: isolation and use of J66 (DXS268), a distal intragenic marker

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

7 January 2021

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Enormous dystrophin in a patient with Becker muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

7 January 2021

Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Dystrophin abnormalities in Duchenne/Becker muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Improved diagnosis of Becker muscular dystrophy by dystrophin testing

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

The frequency of patients with dystrophin abnormalities in a limb-girdle patient population

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Familial X-linked myalgia and cramps: a nonprogressive myopathy associated with a deletion in the dystrophin gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Quadriceps myopathy: forme fruste of Becker muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Subcellular fractionation of dystrophin to the triads of skeletal muscle.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Association of dystrophin and an integral membrane glycoprotein.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Identification of dystrophin in cardiac sarcolemmal vesicles

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Dystrophin is tightly associated with the sarcolemma of mammalian skeletal muscle fibers

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Dystrophin constitutes 5% of membrane cytoskeleton in skeletal muscle

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Immunoelectron microscopic localization of dystrophin in myofibres

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Dystrophin is localized to the plasma membrane of human skeletal muscle fibers by electron-microscopic cytochemical study

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Dystrophin immunostaining and freeze-fracture studies of muscles of patients with early stage amyotrophic lateral sclerosis and Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Glycoprotein complex anchoring dystrophin to sarcolemma

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Dystrophinopathy in isolated cases of myopathy in females

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Isolated dystrophin molecules as seen by electron microscopy

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Molecular shape of dystrophin

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Spectrin-based membrane skeleton: a multipotential adaptor between plasma membrane and cytoplasm

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Spectrin-actin associations studied by electron microscopy of shadowed preparations

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Identification of functional domains of human erythrocyte spectrin

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Visualization of the protein associations in the erythrocyte membrane skeleton

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Cytoskeleton--plasma membrane interactions

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Gamma actin, spectrin, and intermediate filament proteins colocalize with vinculin at costameres, myofibril-to-sarcolemma attachment sites

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

A vinculin-containing cortical lattice in skeletal muscle: transverse lattice elements ("costameres") mark sites of attachment between myofibrils and sarcolemma

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Vinculin is a component of an extensive network of myofibril-sarcolemma attachment regions in cardiac muscle fibers

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Goblin (ankyrin) in striated muscle: identification of the potential membrane receptor for erythroid spectrin in muscle cells

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Vinculin in subsarcolemmal densities in chicken skeletal muscle: localization and relationship to intracellular and extracellular structures

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Expression of collagen adhesion proteins and their association with the cytoskeleton in cardiac myocytes.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Distribution of vinculin in the Z-disk of striated muscle: analysis by laser scanning confocal microscopy

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

7 January 2021

Segmental fibre breakdown and defects of the plasmalemma in diseased human muscles

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Mitochondrial calcium overload: A general mechanism for cell-necrosis in muscle diseases

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Intracellular calcium accumulation in Duchenne dystrophy and other myopathies: a study of 567,000 muscle fibers in 114 biopsies

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Dystrophin and the membrane hypothesis of muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

7 January 2021

Protein turnover is elevated in muscle of mdx mice in vivo

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

7 January 2021

Calcium entry through stretch-inactivated ion channels in mdx myotubes

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Calpain concentration is elevated although net calcium-dependent proteolysis is suppressed in dystrophin-deficient muscle

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

The membrane hypothesis of Duchenne muscular dystrophy: quest for functional evidence

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

7 January 2021

The α5β1 integrin associates with a dystrophin-containing lattice during muscle development

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Localization of dystrophin relative to acetylcholine receptor domains in electric tissue and adult and cultured skeletal muscle

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Asymmetric distribution of dystrophin in developing and adult Torpedo marmorata electrocyte: evidence for its association with the acetylcholine receptor-rich membrane

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Localization of dystrophin and dystrophin-related protein at the electromotor synapse and neuromuscular junction in Torpedo marmorata

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Dystrophin and a dystrophin-related protein in intrafusal muscle fibers, and neuromuscular and myotendinous junctions

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Structural domains of the muscle-tendon junction. 1. The internal lamina and the connecting domain

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Adhesive strength of single muscle cells to basement membrane at myotendinous junctions.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Dystrophin as a focal adhesion protein. Collocalization with talin and the Mr 48,000 sarcolemmal protein in cultured Xenopus muscle

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Identification of a membrane-cytoskeletal complex containing the cell adhesion molecule uvomorulin (E-cadherin), ankyrin, and fodrin in Madin-Darby canine kidney epithelial cells

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Complementary distributions of vinculin and dystrophin define two distinct sarcolemma domains in smooth muscle

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Expression and localization of dystrophin in human cardiac Purkinje fibers

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Myogenic regulation of dystrophin gene expression

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Specificity of expression of the muscle and brain dystrophin gene promoters in muscle and brain cells

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Dystrophin is transcribed in brain from a distant upstream promoter.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Nucleotide sequence of chicken dystrophin cDNA.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

7 January 2021

Dystrophin in central nervous system: a developmental, regional distribution and subcellular localization study

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

The central nervous system in Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Expression of the murine Duchenne muscular dystrophy gene in muscle and brain.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Genetic and clinical correlations of Xp21 muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Impaired non-motor learning and error detection associated with cerebellar damage. A single case study

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Dystrophin immunoreactivity in normal and Duchenne human fetal neurons in culture.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Detection of dystrophin in the postsynaptic density of rat brain and deficiency in a mouse model of Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

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/10.1038%2FNG0493-283

7 January 2021

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Antibody against the C-terminal portion of dystrophin crossreacts with the 400 kDa protein in the pia mater of dystrophin-deficient mdx mouse brain.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Immunolocalization and developmental expression of dystrophin related protein in skeletal muscle.

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Dystrophin expression and somatic reversion in prednisone-treated and untreated Duchenne dystrophy. CIDD Study Group

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Methylprednisolone increases dystrophin levels by inhibiting myotube death during myogenesis of normal human muscle in vitro

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Efficient adenovirus-mediated transfer of a human minidystrophin gene to skeletal muscle of mdx mice

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Conversion of mdx myofibres from dystrophin-negative to -positive by injection of normal myoblasts

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0493-283

7 January 2021

Identifiers

DOI

10.1038/NG0493-283

1 reference

Dimensions Publication ID

22 September 2017

0 references

1 reference