X-linked dilated cardiomyopathy and the dystrophin gene (Q33688402)

28 July 2017

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title

X-linked dilated cardiomyopathy and the dystrophin gene (English)

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28 July 2017

dilated cardiomyopathy

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5

Muntoni F

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28 July 2017

Ferlini A

1

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28 July 2017

Sewry C

series ordinal

2

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28 July 2017

Melis MA

series ordinal

3

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28 July 2017

Mateddu A

series ordinal

4

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28 July 2017

1 July 1999

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28 July 2017

Neuromuscular Disorders

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28 July 2017

9

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28 July 2017

339-346

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28 July 2017

5

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

28 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

Molecular genetics of dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

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%2FS0960-8966%2899%2900015-2

7 January 2021

A Point Mutation in the 5' Splice Site of the Dystrophin Gene First Intron Responsible for X-Linked Dilated Cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

A 5' dystrophin duplication mutation causes membrane deficiency of alpha-dystroglycan in a family with X-linked cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

Insertional mutation by transposable element, L1, in the DMD gene results in X-linked dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

Up-regulation of the brain and Purkinje-cell forms of dystrophin transcripts, in Becker muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

X-linked dilated cardiomyopathy. Novel mutation of the dystrophin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

Expression and regulation of the dystrophin Purkinje promoter in human skeletal muscle, heart, and brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

A muscle-specific enhancer within intron 1 of the human dystrophin gene is functionally dependent on single MEF-1/E box and MEF-2/AT-rich sequence motifs

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

Conservation of a putative AP1 binding site and complete homology to a fetal brain EST in a region upstream of the core muscle promoter in the human dystrophin gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

Signals for the selection of a splice site in pre-mRNA. Computer analysis of splice junction sequences and like sequences

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

An explanation for the constitutive exon 9 cassette splicing of the DMD gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

The divergent 5' termini of the alpha human folate receptor (hFR) mRNAs originate from two tissue-specific promoters and alternative splicing: characterization of the alpha hFR gene structure

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

Dilated cardiomyopathy associated with deficiency of the cytoskeletal protein metavinculin

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

Dystrophin and utrophin: the missing links!

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

Asymptomatic dystrophinopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

Cardiac involvement in Becker muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

Mutation of dystrophin gene and cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

A transposon-like element in the deletion-prone region of the dystrophin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

A cluster of transposon-like repetitive sequences in intron 7 of the human dystrophin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

The 5' region of intron 11 of the dystrophin gene contains target sequences for mobile elements and three overlapping ORFs.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertion

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900015-2

7 January 2021

10.1016/S0960-8966(99)00015-2

Identifiers

DOI

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28 July 2017

1 reference