(Q34721268)

4 August 2017

title

The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1. (English)

1 reference

4 August 2017

1 reference

A Brown

1

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Rashmi Kothary

object named as

R Kothary

5

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author name string

G Bernier

2

1 reference

4 August 2017

M Mathieu

3

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4 August 2017

J Rossant

4

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4 August 2017

language of work or name

English

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publication date

1 July 1995

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4 August 2017

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4 August 2017

volume

10

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4 August 2017

issue

3

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4 August 2017

page(s)

301-306

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A transgene containing lacZ inserted into the dystonia locus is expressed in neural tube.

4 August 2017

cites work

1 reference

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The genomic structure of an insertional mutation in the dystonia musculorum locus.

21 January 2018

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

21 January 2018

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A beta-spectrin isoform from Drosophila (beta H) is similar in size to vertebrate dystrophin

21 January 2018

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Studies on the transcription, translation, and structure of alpha-actinin in Dictyostelium discoideum

21 January 2018

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Structural relationships of actin-binding proteins

21 January 2018

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Dystrophin-associated proteins and synapse formation: is alpha-dystroglycan the agrin receptor?

21 January 2018

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

21 January 2018

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

21 January 2018

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Dystrophin: the protein product of the Duchenne muscular dystrophy locus

21 January 2018

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Immunochemical characterization of three components of the hemidesmosome and their expression in cultured epithelial cells

21 January 2018

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par-1, a gene required for establishing polarity in C. elegans embryos, encodes a putative Ser/Thr kinase that is asymmetrically distributed

21 January 2018

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A mutant neurofilament subunit causes massive, selective motor neuron death: implications for the pathogenesis of human motor neuron disease

21 January 2018

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An electrophysiological and pathological study of peripheral nerves in Friedreich's ataxia.

21 January 2018

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Infantile onset spinocerebellar ataxia with sensory neuropathy: a new inherited disease

21 January 2018

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Molecular basis and diagnosis of neurogenetic disorders

21 January 2018

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Basic local alignment search tool

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CLINICAL AND PATHOLOGICAL STUDIES OF AN HEREDITARY NEUROPATHY IN MICE (DYSTONIA MUSCULORUM)

21 January 2018

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7 January 2021

Ultrastructural studies of an hereditary sensory neuropathy in mice (dystonia musculorum)

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7 January 2021

Pathologic changes in the CNS of dystonia musculorum mutant mouse: an animal model for human spinocerebellar ataxia

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7 January 2021

An allele of the mouse mutant dystonia musculorum exhibits lesions in red nucleus and striatum

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7 January 2021

Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer

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7 January 2021

Calcium-sensitive non-muscle alpha-actinin contains EF-hand structures and highly conserved regions

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7 January 2021

Actin and neurofilament binding domain of brain spectrin beta subunit

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7 January 2021

Chromosomal localization of mouse bullous pemphigoid antigens. BPAG1 and BPAG2: identification of a new region of homology between mouse and human chromosomes

1 reference

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7 January 2021

Human homolog of a mouse sequence from the dystonia musculorum locus is on chromosome 6p12

1 reference

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7 January 2021

Isolation of complementary DNA for bullous pemphigoid antigen by use of patients' autoantibodies

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7 January 2021

The human 230-kD bullous pemphigoid antigen gene (BPAG1). Exon-intron organization and identification of regulatory tissue specific elements in the promoter region

1 reference

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7 January 2021

Mouse 230-kDa bullous pemphigoid antigen gene: structural and functional characterization of the 5'-flanking region and interspecies conservation of the deduced amino-terminal peptide sequence of the protein

1 reference

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7 January 2021

Cytoskeleton--plasma membrane interactions

1 reference

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7 January 2021

The structural and functional diversity of dystrophin

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-301

7 January 2021

A pool of bullous pemphigoid antigen(s) is intracellular and associated with the basal cell cytoskeleton-hemidesmosome complex

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-301

7 January 2021

Gene targeting of BPAG1: abnormalities in mechanical strength and cell migration in stratified epithelia and neurologic degeneration

1 reference

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7 January 2021

Cytoskeletal protein abnormalities in neurodegenerative diseases

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7 January 2021

An intrinsic neuronal defect operates in dystonia musculorum: a study of dt/dt<==>+/+ chimeras

1 reference

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7 January 2021

Increased expression of neurofilament subunit NF-L produces morphological alterations that resemble the pathology of human motor neuron disease

1 reference

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7 January 2021

Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: a mouse model of amyotrophic lateral sclerosis

1 reference

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7 January 2021

Ultrastructural and light-microscopic studies of the developing feline spinal cord white matter. II. Cell death and myelin sheath disintegration in the early postnatal period

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-301

7 January 2021

Friedreich's ataxia. Early detection and progression of peripheral nerve abnormalities

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-301

7 January 2021

Peripheral neuropathy in spinocerebellar degenerations

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-301

7 January 2021

Sensory neuropathy in infantile onset spinocerebellar ataxia (IOSCA)

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-301

7 January 2021

Bullous pemphigoid antigen (BPAG1): cDNA cloning and mapping of the gene to the short arm of human chromosome 6

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-301

7 January 2021

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

1 reference

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7 January 2021

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1

1 reference

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7 January 2021

The gene for Machado-Joseph disease maps to human chromosome 14q

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-301

7 January 2021

Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11.

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-301

7 January 2021

https://api.crossref.org/works/10.1038%2FNG0795-301

1 reference

7 January 2021

Evidence for the existence of a fourth dominantly inherited spinocerebellar ataxia locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-301

7 January 2021

Isolation and characterization of rat and human glyceraldehyde-3-phosphate dehydrogenase cDNAs: genomic complexity and molecular evolution of the gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-301

7 January 2021

Identifiers

DOI

10.1038/NG0795-301

1 reference

Dimensions Publication ID

4 August 2017

1030951123

0 references

1 reference