(Q81024511)

English

Increased levels of adenine nucleotide translocator 1 protein and response to oxidative stress are early events in facioscapulohumeral muscular dystrophy muscle

scientific article published on 17 November 2004

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scholarly article

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15551024%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Increased levels of adenine nucleotide translocator 1 protein and response to oxidative stress are early events in facioscapulohumeral muscular dystrophy muscle (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15551024%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

facioscapulohumeral muscular dystrophy

1 reference

based on heuristic

inferred from title

Catherine Bisbal

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15551024%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Yegor Vassetzky

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15551024%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

author name string

Dalila Laoudj-Chenivesse

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15551024%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Gilles Carnac

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15551024%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Gerald Hugon

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15551024%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Sandrine Bouillot

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15551024%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Claude Desnuelle

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15551024%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Anne Fernandez

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15551024%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

publication date

17 November 2004

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15551024%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Journal of Molecular Medicine

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15551024%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

83

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15551024%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15551024%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

216-224

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15551024%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

https://scigraph.springernature.com/pub.10.1007/s00109-004-0583-7

0 references

Reactive oxygen species (ROS)-induced ROS release: a new phenomenon accompanying induction of the mitochondrial permeability transition in cardiac myocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Caspase 3 expression correlates with skeletal muscle apoptosis in Duchenne and facioscapulo human muscular dystrophy. A potential target for pharmacological treatment?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein oxidation in aging, disease, and oxidative stress

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD).

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscle protein analysis by two-dimensional gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human muscle proteins: analysis by two-dimensional electrophoresis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial biology, degenerative diseases and aging

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Overproduction of Cu/Zn-superoxide dismutase or Bcl-2 prevents the brain mitochondrial respiratory dysfunction induced by glutathione depletion.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial adenine nucleotide translocase is modified oxidatively during aging

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Profound misregulation of muscle-specific gene expression in facioscapulohumeral muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two different variants of the same tropomyosin polypeptide in clones from GM1386 human skin fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscle protein analysis. III. Analysis of solubilized frozen-tissue sections by two-dimensional electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD)

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adenine nucleotide translocase-1, a component of the permeability transition pore, can dominantly induce apoptosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Towards the finer mapping of facioscapulohumeral muscular dystrophy at 4q35: construction of a laser microdissection library

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment bias

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linking genome and proteome by mass spectrometry: large-scale identification of yeast proteins from two dimensional gels

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Overexpression of human copper, zinc-superoxide dismutase (SOD1) prevents postischemic injury

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inappropriate Gene Activation in FSHD

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Radicals r'aging

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High performance two-dimensional gel electrophoresis using a wetting agent Tergitol NP7

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial facioscapulohumeral muscular dystrophy: phenotypic diversity and genetic abnormality

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The expression of myosin light chains and tropomyosin in human muscle biopsies with histochemical type 1 and type 2 fiber deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Facioscapulohumeral muscular dystrophy: clinical diversity and genetic abnormalities in Japanese patients.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hydroperoxide metabolism in mammalian organs

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DECLINE IN SKELETAL MUSCLE MITOCHONDRIAL RESPIRATORY CHAIN FUNCTION: POSSIBLE FACTOR IN AGEING

1 reference

https://pubmed.ncbi.nlm.nih.gov/15551024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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