A cell surface abnormality in Duchenne muscular dystrophy: intercellular adhesiveness of skin fibroblasts from patients and carriers (Q41605958)

5 October 2017

A cell surface abnormality in Duchenne muscular dystrophy: intercellular adhesiveness of skin fibroblasts from patients and carriers (English)

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Duchenne muscular dystrophy

5 October 2017

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1

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2

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1 January 1983

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63

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3

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232-237

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https://scigraph.springernature.com/pub.10.1007/bf00284655

5 October 2017

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12 December 2020

Evidence for the release of enzymes from different organs in Duchenne's muscular dystrophy

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12 December 2020

Patients with myotonic dystrophy, a possible segmental progeroid syndrome, and Duchenne muscular dystrophy have fibroblasts with normal limits for in vitro lifespan and growth characteristics

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Serum Enzyme Alterations in Neuromuscular Disorders

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Reduced adhesiveness between skin fibroblasts from patients with Duchenne muscular dystrophy

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In search of non-random X inactivation: studies of fetal membranes heterozygous for glucose-6-phosphate dehydrogenase

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Glucose-6 phosphate dehydrogenase mosaicism: utilization as a tracer in the study of the development of hair root cells

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Myogenic defect in human muscular dystrophy

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Cluster formation in monolayer cultures of normal and diseased human muscle

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Mosaicism of peripheral blood lymphocyte populations in females heterozygous for the Lesch-Nyhan mutation

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Membrane abnormalities in Duchenne muscular dystrophy

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Analysis of fibroblast proteins from patients with Duchenne muscular dystrophy by two-dimensional gel electrophoresis

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Re-examination of a supposed case of specific cell adhesion

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Wiskott-Aldrich syndrome: cellular impairments and their implication for carrier detection

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Capping of lymphocytes in patients and carriers of Duchenne muscular dystrophy

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12 December 2020

Incidence of cell clusters in 318 cultured muscle biopsies from duchenne dystrophy, normal, and other neuromuscular disorders

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12 December 2020

Protein degradation in skin fibroblasts from patients with Duchenne muscular dystrophy

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12 December 2020

Analysis of skin fibroblast aggregation in Duchenne muscular dystrophy

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Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.

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Clinically manifesting carriers in Duchenne muscular dystrophy

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Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

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Cell behaviour and molecular mechanisms of cell-cell adhesion

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Non-inactivation of an X-Chromosome Locus in Man

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Evidence for selection in cultured diploid fibroblast strains

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Adenyl cyclase abnormality in Duchenne muscular dystrophy: muscle cells in culture

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The measurement of cell adhesiveness by an absolute method

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12 December 2020

Gene action in the X-chromosome of the mouse (Mus musculus L.)

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Preferential paternal X inactivation in extraembryonic tissues of early mouse embryos

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Failure of inactivation of Duchenne dystrophy X-chromosome in one of female identical twins

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Progressive muscle disease in a young woman with family history of Duchenne's muscular dystrophy

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Needle muscle biopsy for carrier detection in Duchenne muscular dystrophy. Part 1. Light microscopy--histology, histochemistry and quantitation

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Pairing of X and Y chromosomes, non-inactivation of X-linked genes, and the maleness factor

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Muscular dystrophy in young girls

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Letter to the Editor: Abnormal Growth Kinetics and 5′-Nucleotidase Activities in Cultured Skin Fibroblasts from Patients with Duchenne Muscular Dystrophy

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Cell disposition and adhesiveness in the developing chick neural retina

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Genetic heterogeneity in xeroderma pigmentosum: complementation groups and their relationship to DNA repair rates

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Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm

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Duchenne dystrophy: Electron microscopic findings pointing to a basic or early abnormality in the plasma membrane of the muscle fiber

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12 December 2020

Abnormal Growth Kinetics and 5′-Nucleotidase Activities in Cultured Skin Fibroblasts from Patients with Duchenne Muscular Dystrophy

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Premature aging of fibroblasts from patients with Duchenne muscular dystrophy

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Systemic Membrane Defect in the Proximal Muscular Dystrophies

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An (X;11) translocation in a girl with Duchenne muscular dystrophy. Repository identification No. GM1695.

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The adhesiveness of normal and SV40-transformed BALB/c 3T3 cells: Effects of culture density and shear rate

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Activity of creatine kinase in sera from healthy women, carriers of Duchenne muscular dystrophy and cord blood, determined by the “European” recommended method with NAC-EDTA activation

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12 December 2020

Lymphocyte capping in Duchenne muscular dystrophy

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12 December 2020

Human lymphocyte capping in Duchenne muscular dystrophy

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12 December 2020

Enzyme release from isolated erythrocytes and lymphocytes in Duchenne muscular dystrophy

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12 December 2020

Freeze-fracture analysis of plasma membranes in Duchenne muscular dystrophy

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12 December 2020

X-chromosome inactivation and the Xg locus

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12 December 2020

X-linked Hunter syndrome: the heterozygous phenotype in cell culture

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12 December 2020

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

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12 December 2020

Identifiers

DOI

10.1007/BF00284655

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PubMed ID

6852819

Dimensions Publication ID

5 October 2017

0 references

1 reference

PubMed ID

6852819