(Q41444959)

English

The myoblast defect identified in Duchenne muscular dystrophy is not a primary expression of the DMD mutation. Clonal analysis of myoblasts from five double heterozygotes for two X-linked loci: DMD and G6PD.

scientific article published on September 1986

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scholarly article

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Europe PubMed Central

PubMed publication ID

30 September 2017

The myoblast defect identified in Duchenne muscular dystrophy is not a primary expression of the DMD mutation. Clonal analysis of myoblasts from five double heterozygotes for two X-linked loci: DMD and G6PD. (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

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Duchenne muscular dystrophy

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inferred from title

7

object named as

H M Blau

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Europe PubMed Central

PubMed publication ID

30 September 2017

author name string

C Webster

1

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Europe PubMed Central

PubMed publication ID

30 September 2017

G Filippi

2

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

A Rinaldi

3

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

C Mastropaolo

4

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

M Tondi

5

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Europe PubMed Central

PubMed publication ID

30 September 2017

M Siniscalco

6

1 reference

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30 September 2017

language of work or name

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publication date

1 September 1986

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30 September 2017

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Europe PubMed Central

PubMed publication ID

30 September 2017

74

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30 September 2017

1

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30 September 2017

74-80

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PubMed publication ID

30 September 2017

https://scigraph.springernature.com/pub.10.1007/bf00278789

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Isolation of mammalian cell mutants deficient in glucose-6-phosphate dehydrogenase activity: linkage to hypoxanthine phosphoribosyl transferase

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Surface antigen differentiation during human myogenesis in culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of glucose-6-phosphate dehydrogenase variants. I. Occurrence of a G6PD Seattle-like variant in Sardinia and its interaction with the G6PD Mediterranean variant

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differentiation properties of pure populations of human dystrophic muscle cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duchenne muscular dystrophy. Genetic aspects, carrier detection and antenatal diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective myoblasts identified in Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for defective myoblasts in Duchenne muscular dystrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

THE LIMITED IN VITRO LIFETIME OF HUMAN DIPLOID CELL STRAINS

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https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population genetics of haemoglobin variants, thalassaemia and glucose-6-phosphate dehydrogenase deficiency, with particular reference to the malaria hypothesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Developmental progression of myosin gene expression in cultured muscle cells.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replicative life-span of cultivated human cells. Effects of donor's age, tissue, and genotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Developmental appearance of myosin heavy and light chain isoforms in vivo and in vitro in chicken skeletal muscle.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

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Clinically manifesting carriers in Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three myosin heavy-chain isozymes appear sequentially in rat muscle development

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Continued expression of neonatal myosin heavy chain in adult dystrophic skeletal muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New approaches to the study of human dystrophic muscle cells in culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemizygous expression of glucose-6-phosphate dehydrogenase in erythrocytes of heterozygotes for the Lesch-Nyhan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies of Glucose-6-Phosphate Dehydrogenase Activity of Individual Erythrocytes: The Methemoglobin-Elution Test for Identification of Females Heterozygous for G6PD Deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reprogramming cell differentiation in the absence of DNA synthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Embryonic and foetal myosins in human skeletal muscle. The presence of foetal myosins in duchenne muscular dystrophy and infantile spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and characterization of human muscle cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463532

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00278789

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

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