Facioscapulohumeral muscular dystrophy (FSHD) myoblasts demonstrate increased susceptibility to oxidative stress. (Q46776089)

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5 November 2019

title

Facioscapulohumeral muscular dystrophy (FSHD) myoblasts demonstrate increased susceptibility to oxidative stress (English)

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facioscapulohumeral muscular dystrophy

5 November 2019

main subject

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5

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5 November 2019

author name string

Sara T Winokur

1

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5 November 2019

Kathy Barrett

2

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5 November 2019

Jorge H Martin

3

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5 November 2019

James R Forrester

4

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5 November 2019

Rabi Tawil

6

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5 November 2019

Seung-Ah Chung

7

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5 November 2019

Peter S Masny

8

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5 November 2019

Denise A Figlewicz

9

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5 November 2019

publication date

1 May 2003

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5 November 2019

published in

Neuromuscular Disorders

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5 November 2019

volume

13

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5 November 2019

issue

4

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5 November 2019

page(s)

322-333

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Genetic counselling in facioscapulohumeral muscular dystrophy

5 November 2019

cites work

1 reference

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7 January 2021

FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit

1 reference

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7 January 2021

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2802%2900284-5

7 January 2021

Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)

1 reference

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7 January 2021

Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular dystrophy. The FSH-DY Group

1 reference

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7 January 2021

Two cases of chromosome 4q35-linked early onset facioscapulohumeral muscular dystrophy with mental retardation and epilepsy

1 reference

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7 January 2021

Epilepsy and mental retardation in a subset of early onset 4q35-facioscapulohumeral muscular dystrophy

1 reference

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7 January 2021

Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy

1 reference

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7 January 2021

The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease.

1 reference

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7 January 2021

The distribution of somatic H1 subtypes is non-random on active vs. inactive chromatin: distribution in human fetal fibroblasts

1 reference

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7 January 2021

Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissues

1 reference

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7 January 2021

High resolution fluorescence in situ hybridization to linearly extended DNA visually maps a tandem repeat associated with facioscapulohumeral muscular dystrophy immediately adjacent to the telomere of 4q.

1 reference

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7 January 2021

Inter- and intrachromosomal sub-telomeric rearrangements on 4q35: implications for facioscapulohumeral muscular dystrophy (FSHD) aetiology and diagnosis

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7 January 2021

Options available--from start to finish--for obtaining expression data by microarray.

1 reference

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7 January 2021

Muscle cells from mdx mice have an increased susceptibility to oxidative stress

1 reference

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7 January 2021

Expression of matrix metalloproteinases in the muscle of patients with inflammatory myopathies

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7 January 2021

Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analyses

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7 January 2021

Potential contribution of the glutathione S-transferase supergene family to resistance to oxidative stress

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7 January 2021

The glutathione S-transferase supergene family: regulation of GST and the contribution of the isoenzymes to cancer chemoprotection and drug resistance

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7 January 2021

p21 as a Common Signaling Target of Reactive Free Radicals and Cellular Redox Stress

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7 January 2021

Resistance to apoptosis conferred by Cdk inhibitors during myocyte differentiation.

1 reference

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7 January 2021

Correlation of terminal cell cycle arrest of skeletal muscle with induction of p21 by MyoD.

1 reference

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7 January 2021

p53-independent expression of p21Cip1 in muscle and other terminally differentiating cells

1 reference

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7 January 2021

MyoD-induced expression of p21 inhibits cyclin-dependent kinase activity upon myocyte terminal differentiation

1 reference

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7 January 2021

MyoD prevents cyclinA/cdk2 containing E2F complexes formation in terminally differentiated myocytes.

1 reference

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7 January 2021

Active genes in junk DNA? Characterization of DUX genes embedded within 3.3 kb repeated elements

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7 January 2021

10.1016/S0960-8966(02)00284-5

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12868502%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

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