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Expression of laminin subunits in human fetal skeletal muscle.

Data up to Jan 2025

Published1995
Citations34
References28

Total Citations Per Year

Abstract

References (28)

Contact and adhesive specificities in the associations, migrations, and targeting of cells and axons

1992 • 895 citations

A new nomenclature for the laminins

1994 • 753 citations

Molecular heterogeneity of basal laminae: isoforms of laminin and collagen IV at the neuromuscular junction and elsewhere.

1990 • 588 citations

Congenital progressive muscular dystrophy of the fukuyama type — clinical, genetic and pathological considerations —

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Congenital muscular dystrophy with merosin deficiency.

1994 • 449 citations

Merosin, a tissue-specific basement membrane protein, is a laminin-like protein.

1990 • 398 citations

Merosin, a protein specific for basement membranes of Schwann cells, striated muscle, and trophoblast, is expressed late in nerve and muscle development.

1988 • 371 citations

Basal lamina assembly

1994 • 322 citations

Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus.

1994 • 299 citations

Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues

1994 • 262 citations

THE DEVELOPMENT AND GROWTH OF THE EXTERNAL DIMENSIONS OF THE HUMAN BODY IN THE FETAL PERIOD.

1930 • 257 citations

Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse.

1994 • 254 citations

Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31–33

1993 • 248 citations

Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping

1994 • 195 citations

Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal

1995 • 180 citations

Abnormal localization of laminin subunits in muscular dystrophies

1993 • 161 citations

Dystrophin-related protein, utrophin, in normal and dystrophic human fetal skeletal muscle

1993 • 144 citations

Laminin variants: Why, where and when?

1993 • 130 citations

Expression of laminin subunits in congenital muscular dystrophy

1995 • 108 citations

The agyria-pachygyria complex: A spectrum of cortical malformations

1991 • 107 citations

Neural abnormalities in the dystrophic mouse

1975 • 92 citations

Laminin in Animal Models for Muscular Dystrophy Defect of Laminin M in Skeletal and Cardiac Muscles and Peripheral Nerve of the Homozygous Dystrophic dy/dy Mice.

1993 • 90 citations

Age of foetus determined from its measures

1947 • 68 citations

Somatosensory and Visual Evoked Potentials in Congenital Muscular Dystrophy: Correlation with MRI Changes and Muscle Merosin Status

1995 • 64 citations

Localization of the Gene (LAMA4) to Chromosome 6q21 and Isolation of a Partial cDNA Encoding a Variant Laminin A Chain

1994 • 56 citations

Characterisation of dystrophin during development of human skeletal muscle

1992 • 53 citations

Expression of dystrophin-associated glycoproteins during human fetal muscle development: A preliminary immunocytochemical study

1994 • 45 citations

Deleted Work

1955 • 0 citations

Cited By (0)

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Expression of laminin subunits in human fetal skeletal muscle. (1995) – PubMed | Metascience Observatory Explorer