(Q24310411)

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I M Leigh

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J R McMillan

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E L Rugg

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D P Kelsell

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S P Bryant

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N K Spurr

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J F Geddes

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G Kirtschig

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G Milana

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A G de Bono

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K Owaribe

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G Wiche

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L Pulkkinen

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J Uitto

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W H McLean

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E B Lane

Human plectin: organization of the gene, sequence analysis, and chromosome localization (8q24)

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language of work or name

English

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publication date

August 1996

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450-7

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG0896-450

par-1, a gene required for establishing polarity in C. elegans embryos, encodes a putative Ser/Thr kinase that is asymmetrically distributed

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0896-450

Mutations in the genes for epidermal keratins in epidermolysis bullosa and epidermolytic hyperkeratosis

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

Autosomal recessive epidermolysis bullosa simplex. Generalized phenotypic features suggestive of junctional or dystrophic epidermolysis bullosa, and association with neuromuscular diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

Occurrence and immunolocalization of plectin in tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

A panel of monoclonal antibodies to rat plectin: distinction by epitope mapping and immunoreactivity with different tissues and cell lines.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

Identification of a new hemidesmosomal protein, HD1: a major, high molecular mass component of isolated hemidesmosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

Intermediate filaments in disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

Cloning and sequencing of rat plectin indicates a 466-kD polypeptide chain with a three-domain structure based on a central alpha-helical coiled coil.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

High-Mr microtubule-associated proteins: properties and functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

Distribution and ultrastructure of plectin arrays in subclones of rat glioma C6 cells differing in intermediate filament protein (vimentin) expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

Expression of plectin mutant cDNA in cultured cells indicates a role of COOH-terminal domain in intermediate filament association

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

Hemidesmosome ontogeny in digit skin of the human fetus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

19-DEJ-1, a hemidesmosome-anchoring filament complex-associated monoclonal antibody. Definition of a new skin basement membrane antigenic defect in junctional and dystrophic epidermolysis bullosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

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/10.1038%2FNG0896-450

7 January 2021

Epidermolysis bullosa: hereditary skin fragility diseases as paradigms in cell biology

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Molecular complexity of the cutaneous basement membrane zone. Revelations from the paradigms of epidermolysis bullosa

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Epidermolysis Bullosa Simplex Associated With Muscular Dystrophy With Recessive Inheritance

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Congenital muscular dystrophy associated with familial junctional epidermolysis bullosa letalis

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Identification of plectin in different human cell types and immunolocalization at epithelial basal cell surface membranes

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

The molecular biology of desmosomes and hemidesmosomes: "what's in a name"?

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

A novel hemidesmosomal plaque component: tissue distribution and incorporation into assembling hemidesmosomes in an in vitro model

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Production of Rabbit Antibodies Against Carboxy-Terminal Epitopes Encoded by Bullous Pemphigoid cDNA

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Development of a panel of monochromosomal somatic cell hybrids for rapid gene mapping.

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Genetic analysis of the BRCA1 region in a large breast/ovarian family: refinement of the minimal region containing BRCA1

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Human gene mutations affecting RNA processing and translation

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Identification and characterization of genes that are required for the accelerated degradation of mRNAs containing a premature translational termination codon

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Plectin: general overview and appraisal of its potential role as a subunit protein of the cytomatrix

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Intermediate filament-plasma membrane interactions

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Epidermolysis Bullosa Simplex (Dowling-Meara Type) Is a Genetic Disease Characterized by an Abnormal Keratin-Filament Network Involving Keratins K5 and K14

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

A functional "knockout" of human keratin 14

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Gene targeting of BPAG1: abnormalities in mechanical strength and cell migration in stratified epithelia and neurologic degeneration

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

GPT--epidermolysis bullosa simplex (EBS Ogna) linkage in man

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

The use of Michel's transport medium for immunofluorescence and immunoelectron microscopy in autoimmune bullous diseases

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Abnormal binding of an anti-amnion antibody to epidermal basement membrane provides a novel diagnostic probe for junctional epidermolysis bullosa

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

γ2 Chain of Laminin-5 Is Recognized By Monoclonal Antibody GB3

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Second generation monoclonal antibodies to the human integrin alpha 6 beta 4

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Embedding in epoxy resins for ultrathin sectioning in electron microscopy

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Demonstration of intra- and extracellular localization of bullous pemphigoid antigen using cryofixation and freeze substitution for postembedding immunoelectron microscopy

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Improved tools for biological sequence comparison

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Alignment of physical and genetic maps of human 8q23-qter using somatic cell hybrid mapping panel

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Defective expression of plectin/HD1 in epidermolysis bullosa simplex with muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-450

7 January 2021

Identifiers

DOI

10.1038/NG0896-450

1 reference

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

1020760641

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Fatcat ID

release_syczhyb3gzalrlqbezvka3mkqq

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1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

8696340

1 reference

Consolidated OpenCitations Corpus – April 2017