(Q34335333)

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The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus

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scholarly article

1 reference

Europe PubMed Central

1 August 2017

The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus (English)

1 reference

Europe PubMed Central

1 August 2017

facioscapulohumeral muscular dystrophy

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1

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Europe PubMed Central

1 August 2017

author name string

Winokur ST

2

1 reference

Europe PubMed Central

1 August 2017

Padberg GW

3

1 reference

Europe PubMed Central

1 August 2017

Skraastad MI

4

1 reference

Europe PubMed Central

1 August 2017

Altherr MR

5

1 reference

Europe PubMed Central

1 August 2017

Wasmuth JJ

6

1 reference

Europe PubMed Central

1 August 2017

Murray JC

7

1 reference

Europe PubMed Central

1 August 2017

Hofker MH

8

1 reference

Europe PubMed Central

1 August 2017

Frants RR

9

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Europe PubMed Central

1 August 2017

publication date

1 September 1993

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Europe PubMed Central

1 August 2017

1 reference

Europe PubMed Central

1 August 2017

92

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Europe PubMed Central

1 August 2017

2

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Europe PubMed Central

1 August 2017

198-203

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Europe PubMed Central

1 August 2017

https://scigraph.springernature.com/pub.10.1007/bf00219692

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Deficiency of complex III of the mitochondrial respiratory chain in a patient with facioscapulohumeral disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemistry of muscle membranes in Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic sequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Freeze fracture studies of muscle plasma membrane in human muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cell hybrid and recombinant DNA library that facilitate identification of polymorphic loci in the vicinity of the Huntington disease gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

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/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic counterselective procedure to isolate interspecific cell hybrids containing single human chromosomes: construction of cell hybrids and recombinant DNA libraries specific for human chromosomes 3 and 4.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial "mitochondrial" myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. 1. Clinical, electrophysiological and pathological findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA sequencing with chain-terminating inhibitors

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

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/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dinucleotide repeat polymorphism adjacent to the ANT1 gene on 4q35.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A human muscle adenine nucleotide translocator gene has four exons, is located on chromosome 4, and is differentially expressed

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzymatic synthesis of biotin-labeled polynucleotides: novel nucleic acid affinity probes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficient computations in multilocus linkage analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8103757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00219692

1 reference

Europe PubMed Central

1 August 2017

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

1 August 2017

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