(Q48593256)

13 February 2018

title

A splice variant of Dp71 lacking the syntrophin binding site is expressed in early stages of human neural development (English)

1 reference

13 February 2018

author name string

Ceccarini M

1

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13 February 2018

Rizzo G

2

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13 February 2018

Rosa G

3

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13 February 2018

Chelucci C

4

1 reference

13 February 2018

Macioce P

5

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13 February 2018

Petrucci TC

6

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13 February 2018

publication date

1 October 1997

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13 February 2018

number of pages

6

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Developmental Brain Research

inferred from page(s)

published in

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13 February 2018

volume

103

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13 February 2018

issue

1

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13 February 2018

page(s)

77-82

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13 February 2018

The structural and functional diversity of dystrophin

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1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

Syntrophin binds to an alternatively spliced exon of dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

Cloning and characterization of alternatively spliced isoforms of Dp71

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https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

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

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https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

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%2FS0165-3806%2897%2900122-3

7 January 2021

Dystrophin is transcribed in brain from a distant upstream promoter.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

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%2FS0165-3806%2897%2900122-3

7 January 2021

An alternative dystrophin transcript specific to peripheral nerve

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

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%2FS0165-3806%2897%2900122-3

7 January 2021

A novel dystrophin isoform is required for normal retinal electrophysiology

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

Membrane organization of the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

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%2FS0165-3806%2897%2900122-3

7 January 2021

Reduced levels of dystrophin associated proteins in the brains of mice deficient for Dp71.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental ability

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

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%2FS0165-3806%2897%2900122-3

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%2FS0165-3806%2897%2900122-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

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%2FS0165-3806%2897%2900122-3

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%2FS0165-3806%2897%2900122-3

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%2FS0165-3806%2897%2900122-3

7 January 2021

Dp140: a novel 140 kDa CNS transcript from the dystrophin locus

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoform.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

Dp71, the nonmuscle product of the Duchenne muscular dystrophy gene is associated with the cell membrane

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

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/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

Point mutations in the dystrophin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

Exon structure of the human dystrophin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

Localization of the dystrophin binding site at the carboxyl terminus of beta-dystroglycan

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

Apo-dystrophin-1 and apo-dystrophin-2, products of the Duchenne muscular dystrophy locus: expression during mouse embryogenesis and in cultured cell lines

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

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%2FS0165-3806%2897%2900122-3

7 January 2021

Mammalian alpha 1- and beta 1-syntrophin bind to the alternative splice-prone region of the dystrophin COOH terminus

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

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%2FS0165-3806%2897%2900122-3

7 January 2021

The human dystrophin gene requires 16 hours to be transcribed and is cotranscriptionally spliced

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

Apo-dystrophin-3: a 2.2kb transcript from the DMD locus encoding the dystrophin glycoprotein binding site

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

Glycoprotein complex anchoring dystrophin to sarcolemma

1 reference

https://api.crossref.org/works/10.1016%2FS0165-3806%2897%2900122-3

7 January 2021

10.1016/S0165-3806(97)00122-3

Identifiers

DOI

1 reference

13 February 2018

1 reference

13 February 2018