Distribution of ten laminin chains in dystrophic and regenerating muscles

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Theory and Practice of Histotechnology

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Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

1994 • 874 citations

Epiligrin, a new cell adhesion ligand for integrin α3β1 in epithelial basement membranes

1991 • 771 citations

Kalinin: an epithelium-specific basement membrane adhesion molecule that is a component of anchoring filaments.

1991 • 755 citations

A new nomenclature for the laminins

1994 • 753 citations

Utrophin-Dystrophin-Deficient Mice as a Model for Duchenne Muscular Dystrophy

1997 • 710 citations

The Laminin α Chains: Expression, Developmental Transitions, and Chromosomal Locations of α1-5, Identification of Heterotrimeric Laminins 8–11, and Cloning of a Novel α3 Isoform

1997 • 661 citations

Skeletal and Cardiac Myopathies in Mice Lacking Utrophin and Dystrophin: A Model for Duchenne Muscular Dystrophy

1997 • 625 citations

Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy

1995 • 615 citations

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

1990 • 588 citations

A laminin-like adhesive protein concentrated in the synaptic cleft of the neuromuscular junction

1989 • 566 citations

Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy

1988 • 559 citations

Animal Models for Muscular Dystrophy Show Different Patterns of Sarcolemmal Disruption

1997 • 482 citations

Congenital muscular dystrophy with merosin deficiency.

1994 • 449 citations

Absence of integrin α7 causes a novel form of muscular dystrophy

1997 • 435 citations

Distribution and Function of Laminins in the Neuromuscular System of Developing, Adult, and Mutant Mice

1997 • 433 citations

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

1990 • 398 citations

Muscular dystrophies and the dystrophin–glycoprotein complex

1997 • 379 citations

Mutations in the integrin α7 gene cause congenital myopathy

1998 • 353 citations

Murine muscular dystrophy caused by a mutation in the laminin α2 (Lama2) gene

1994 • 346 citations

Distribution and isolation of four laminin variants; tissue restricted distribution of heterotrimers assembled from five different subunits.

1990 • 346 citations

The satellite cell and muscle regeneration

1994 • 343 citations

Emerin deficiency at the nuclear membrane in patients with Emery-Dreif uss muscular dystrophy

1996 • 337 citations

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

1994 • 299 citations

Developmental Regulation of the Laminin α5 Chain Suggests a Role in Epithelial and Endothelial Cell Maturation

1997 • 261 citations

Laminin α2 chain‐null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)‐deficient congenital muscular dystrophy

1997 • 252 citations

Mutations in the Sarcoglycan Genes in Patients with Myopathy

1997 • 219 citations

Presence of Laminin α5 Chain and Lack of Laminin α1 Chain during Human Muscle Development and in Muscular Dystrophies

1997 • 210 citations

Merosin and laminin in myogenesis; specific requirement for merosin in myotube stability and survival.

1996 • 205 citations

Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models.

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Neural Targeting of Mycobacterium leprae Mediated by the G Domain of the Laminin-α2 Chain

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Fetal myosin heavy chains in regenerating muscle

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Abnormal localization of laminin subunits in muscular dystrophies

1993 • 161 citations

Domains of laminin

1996 • 158 citations

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Dystrophin in skeletal muscle II. Immunoreactivity in patients with Xp21 muscular dystrophy

1989 • 139 citations

Primary structure and expression of a novel human laminin α4 chain

1995 • 127 citations

Monoclonal antibodies against laminin A chain fragment E3 and their effects on binding to cells and proteoglycan and on kidney development

1992 • 122 citations

Mild Congenital Muscular Dystrophy in Two Patients with an Internally Deleted Laminin 2-Chain

1997 • 122 citations

Laminin α2 muscular dystrophy

1998 • 116 citations

Developmental Expression of Nicein Adhesion Protein (Laminin-5) Subunits Suggests Multiple Morphogenic Roles

1994 • 112 citations

Expression of laminin subunits in congenital muscular dystrophy

1995 • 108 citations

Primary structure of the human laminin A chain. Limited expression in human tissues

1991 • 105 citations

Selective immunoreactivities of kidney basement membranes to monoclonal antibodies against laminin: localization of the end of the long arm and the short arms to discrete microdomains.

1989 • 97 citations

Fetal myosin immunoreactivity in human dystrophic muscle

1986 • 90 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

A Synaptic Localization Domain in the Synaptic Cleft Protein Laminin β2 (s-Laminin)

1995 • 87 citations

Identification of a New Locus for a Peculiar Form of Congenital Muscular Dystrophy with Early Rigidity of the Spine, on Chromosome 1p35-36

1998 • 87 citations

Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin α2 chain

1997 • 86 citations

Laminin α2 chain-deficient congenital muscular dystrophy

1998 • 67 citations

Laminin β2 chain and adhalin deficiency in the skeletal muscle of Walker‐Warburg syndrome (cerebroocular dysplasia‐muscular dystrophy)

1995 • 66 citations

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

1994 • 56 citations

Primary ?-sarcoglycan deficiency responsive to immunosuppression over three years

1998 • 49 citations

Expression of myosin heavy chain isoforms in Duchenne muscular dystrophy patients and carriers

1991 • 46 citations

Changes of laminin β2 chain expression in congenital muscular dystrophy

1997 • 40 citations

Motor neurons and Schwann cells distinguish between synaptic and extrasynaptic isoforms of laminin.

1998 • 34 citations

Expression of laminin subunits in human fetal skeletal muscle.

1995 • 34 citations

Expression of laminin subunits in human fetal skeletal muscle

1995 • 34 citations

Early onset autosomal dominant myopathy with rigidity of the spine: a possible role for laminin β1?

1997 • 31 citations

Motor neurons and Schwann cells distinguish between synaptic and extrasynaptic isoforms of laminin

1998 • 31 citations

Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin.

1994 • 30 citations

Abnormal Expression of Laminin 1 Chain in Skeletal Muscle of Adult-Onset Limb-Girdle Muscular Dystrophy

1997 • 26 citations

Congenital muscular dystrophy syndromes distinguished by alkaline and acid phosphatase, merosin, and dystrophin staining

1996 • 26 citations

Abnormal localization of laminin subunits in muscular dystrophies

1995 • 25 citations

Congenital myasthenic syndromes in two kinships with end-plate acetylcholine receptor and utrophin deficiency

1998 • 20 citations

Laminin abnormality in severe childhood autosomal recessive muscular dystrophy.

1995 • 20 citations

Emery-Dreifuss syndrome

1997 • 19 citations

Absence of laminin ?1 chain in the skeletal muscle of dystrophic dy/dy mice

1997 • 19 citations

Increased laminin a expression in regenerating myofibers neuromuscular disorders

1995 • 17 citations

Clinical heterogeneity of adhalin deficiency

1996 • 15 citations

Muscle regeneration and aging.

1992 • 14 citations