Laminins and human disease (Q34071975)

30 July 2017

1 reference

title

Laminins and human disease (English)

1 reference

30 July 2017

McGowan KA

1

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30 July 2017

Marinkovich MP

series ordinal

2

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30 July 2017

publication date

1 November 2000

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Microscopy Research and Technique

30 July 2017

published in

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30 July 2017

volume

51

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30 July 2017

issue

3

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30 July 2017

page(s)

262-279

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Congenital muscular dystrophy: light and electron microscopic observations

30 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

The structural and functional diversity of dystrophin

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chain

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

The influence of fibronectin and laminin during Schwann cell migration and peripheral nerve regeneration through silicon chambers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

A novel homozygous nonsense mutation in the LAMC2 gene in patients with the Herlitz junctional epidermolysis bullosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Junctional epidermolysis bullosa of the larynx. Report of a case and literature review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Epidermolysis Bullosa Simplex: Evidence in Two Families for Keratin Gene Abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Native chick laminin-4 containing the beta 2 chain (s-laminin) promotes motor axon growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Laminin inhibits amyloid-beta-peptide fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Extracellular matrix regulates the amount of the beta-amyloid precursor protein and its amyloidogenic fragments

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

A new nomenclature for the laminins

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Alternatively spliced isoforms of nerve- and muscle-derived agrin: their roles at the neuromuscular junction

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Agrin is a differentiation-inducing "stop signal" for motoneurons in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Association of dystrophin and an integral membrane glycoprotein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Distinct functions for integrins alpha 3 beta 1 in focal adhesions and alpha 6 beta 4/bullous pemphigoid antigen in a new stable anchoring contact (SAC) of keratinocytes: relation to hemidesmosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

The role of integrins alpha 2 beta 1 and alpha 3 beta 1 in cell-cell and cell-substrate adhesion of human epidermal cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Human amnion contains a novel laminin variant, laminin 7, which like laminin 6, covalently associates with laminin 5 to promote stable epithelial-stromal attachment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

A homozygous nonsense mutation in the PLEC1 gene in patients with epidermolysis bullosa simplex with muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: Genetic and functional analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Sarcospan, the 25-kDa Transmembrane Component of the Dystrophin-Glycoprotein Complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Axonal Elongation into Peripheral Nervous System "Bridges" After Central Nervous System Injury in Adult Rats

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Corrective transduction of human epidermal stem cells in laminin-5-dependent junctional epidermolysis bullosa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Sustainable cutaneous gene delivery

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Epiligrin, the major human keratinocyte integrin ligand, is a target in both an acquired autoimmune and an inherited subepidermal blistering skin disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Laminin 1 attenuates beta-amyloid peptide Abeta(1-40) neurotoxicity of cultured fetal rat cortical neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Dystroglycan in development and disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Progression of disease in ocular cicatricial pemphigoid

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

The functions of laminins: lessons from in vivo studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Merosin promotes cell attachment and neurite outgrowth and is a component of the neurite-promoting factor of RN22 schwannoma cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Membrane organization of the dystrophin-glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Astrocytes and axon regeneration in the central nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa. A consensus report by the Subcommittee on Diagnosis and Classification of the National Epidermolysis Bullosa Registry

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Functional Re-expression of laminin-5 in laminin-gamma2-deficient human keratinocytes modifies cell morphology, motility, and adhesion

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Defective neuromuscular synaptogenesis in agrin-deficient mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Induction of Cell Migration by Matrix Metalloprotease-2 Cleavage of Laminin-5

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Differentiation of motor nerve terminals formed in the absence of muscle fibres

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Ultrastructure of blister formation in epidermolysis bullosa hereditaria: V. Epidermolysis bullosa simplex localisata type Weber-Cockayne

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Congenital muscular dystrophy with laminin alpha 2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Dystrophin abnormalities in Duchenne/Becker muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Detection of a specific isoform of alpha-actinin with antisera directed against dystrophin

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Monoclonal antibodies to human amnion

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Primary sequence of a motor neuron-selective adhesive site in the synaptic basal lamina protein S-laminin

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Expression of s-laminin and laminin in the developing rat central nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Anti-basement membrane autoantibodies in patients with anti-epiligrin cicatricial pemphigoid bind the alpha subunit of laminin 5.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Mutational hotspots in the LAMB3 gene in the lethal (Herlitz) type of junctional epidermolysis bullosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Amyloid beta-protein as a substrate interacts with extracellular matrix to promote neurite outgrowth

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Disruption of the lama2 gene in embryonic stem cells: laminin alpha 2 is necessary for sustenance of mature muscle cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Cellular interaction of integrin alpha3beta1 with laminin 5 promotes gap junctional communication

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Passive transfer of anti-laminin 5 antibodies induces subepidermal blisters in neonatal mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Pemphigus and pemphigoid. A review of the advances made since 1964.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

The sarcoglycan complex in limb-girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Laminin promotes neuritic regeneration from cultured peripheral and central neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Update on inherited bullous dermatoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

The dermal-epidermal junction of human skin contains a novel laminin variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

A synaptic localization domain in the synaptic cleft protein laminin beta 2 (s-laminin)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Expression and functional roles of neural cell surface molecules and extracellular matrix components during development and regeneration of peripheral nerves

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Untangling the pathophysio-chemistry of β-amyloid

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Mutations in the 180-kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Altered laminin 5 expression due to mutations in the gene encoding the beta 3 chain (LAMB3) in generalized atrophic benign epidermolysis bullosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Moderation of phenotypic severity in dystrophic and junctional forms of epidermolysis bullosa through in-frame skipping of exons containing non-sense or frameshift mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Neuritic pathology and dementia in Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin status

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Dystrophia Muscularis: A HEREDITARY PRIMARY MYOPATHY IN THE HOUSE MOUSE.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Laminin alpha2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Laminin inhibits Aβ42 fibril formation in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Extracellular matrix influences the biogenesis of amyloid precursor protein in microglial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Laminin and its neurite outgrowth-promoting domain in the brain in Alzheimer's disease and Down's syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Mutations in the laminin alpha2-chain gene in two children with early-onset muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Aberrant differentiation of neuromuscular junctions in mice lacking s-laminin/laminin beta 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

The renal glomerulus of mice lacking s-laminin/laminin beta 2: nephrosis despite molecular compensation by laminin beta 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Muscle fiber necrosis in murine dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Human type VII collagen: cDNA cloning and chromosomal mapping of the gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Synaptic laminin prevents glial entry into the synaptic cleft

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Development of presynaptic specializations induced by basic polypeptide-coated latex beads in spinal cord cultures

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

A motoneuron-selective stop signal in the synaptic protein S-laminin

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Compound heterozygosity for an out-of-frame deletion and a splice site mutation in the LAMB3 gene causes nonlethal junctional epidermolysis bullosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

A Homozygous Nonsense Mutation in the β3 Chain Gene of Laminin 5 (LAMB3) in Herlitz Junctional Epidermolysis Bullosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Mutations in the gamma 2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Cloning of the beta 3 chain gene (LAMB3) of human laminin 5, a candidate gene in junctional epidermolysis bullosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Predominance of the recurrent mutation R635X in the LAMB3 gene in European patients with Herlitz junctional epidermolysis bullosa has implications for mutation detection strategy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Neurite extension by peripheral and central nervous system neurons in response to substratum-bound fibronectin and laminin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Laminin 5 Binds the NC-1 Domain of Type VII Collagen

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

A homozygous mutation in the integrin alpha6 gene in junctional epidermolysis bullosa with pyloric atresia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Targeted disruption of the LAMA3 gene in mice reveals abnormalities in survival and late stage differentiation of epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Genetic linkage of type VII collagen (COL7A1) to dominant dystrophic epidermolysis bullosa in families with abnormal anchoring fibrils

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Type VII collagen is a major structural component of anchoring fibrils

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Development of the vertebrate neuromuscular junction

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Reinnervation of muscle fiber basal lamina after removal of myofibers. Differentiation of regenerating axons at original synaptic sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Expression of Laminin Chains in Skin in Merosin-Deficient Congenital Muscular Dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Induction of presynaptic differentiation in cultured neurons by extracellular matrix components

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Muscular dystrophies and the dystrophin-glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Identification of a novel mutant transcript of laminin α2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Novel Mutations in the LAMB3 Gene Shared by Two Japanese Unrelated Families with Herlitz Junctional Epidermolysis Bullosa, and Their Application for Prenatal Testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Evaluation of anchoring fibrils and other components of the dermal-epidermal junction in dystrophic epidermolysis bullosa by a quantitative ultrastructural technique

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

The eye in epidermolysis bullosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Molecular genetics of the cutaneous basement membrane zone. Perspectives on epidermolysis bullosa and other blistering skin diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

The genes for nicein/kalinin 125- and 100-kDa subunits, candidates for junctional epidermolysis bullosa, map to chromosomes 1q32 and 1q25-q31

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

The 100-kDa chain of nicein/kalinin is a laminin B2 chain variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Identification of a homozygous one-basepair deletion in exon 14 of the LAMB3 gene in a patient with Herlitz junctional epidermolysis bullosa and prenatal diagnosis in a family at risk for recurrence

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Corrective gene transfer of keratinocytes from patients with junctional epidermolysis bullosa restores assembly of hemidesmosomes in reconstructed epithelia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Monoclonal antibody GB3, a new probe for the study of human basement membranes and hemidesmosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Integrin beta 4 mutations associated with junctional epidermolysis bullosa with pyloric atresia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Partial laminin alpha2 chain restoration in alpha2 chain-deficient dy/dy mouse by primary muscle cell culture transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Myoblast transplantations lead to the expression of the laminin alpha 2 chain in normal and dystrophic (dy/dy) mouse muscles

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Congenital muscular dystrophies: 1997 update

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Human beta 2 chain of laminin (formerly S chain): cDNA cloning, chromosomal localization, and expression in carcinomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Muscular dystrophies: diseases of the dystrophin-glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Studies of patients with anti-epiligrin cicatricial pemphigoid

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Glycoprotein complex anchoring dystrophin to sarcolemma

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Structure of the human laminin alpha2-chain gene (LAMA2), which is affected in congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Genetic Linkage Between the Collagen VII (COL7A1) Gene and the Autosomal Dominant Form of Dystrophic Epidermolysis Bullosa in Two Dutch Kindreds

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

Immunoelectron microscopic localization of dystrophin in myofibres

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

10.1002/1097-0029(20001101)51:3<262::AID-JEMT6>3.0.CO;2-V

21 January 2018

Identifiers

DOI

1 reference

30 July 2017

1 reference