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

Molecular Cloning: A Laboratory Manual

2001 • 133,517 citations

Basic local alignment search tool

1990 • 87,358 citations

Basic Local Alignment Search Tool

1990 • 12,947 citations

A Laboratory manual

1989 • 6,833 citations

Three muscular dystrophies: Loss of cytoskeleton-extracellular matrix linkage

1995 • 829 citations

Type VII collagen is a major structural component of anchoring fibrils.

1986 • 545 citations

Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa

1991 • 511 citations

Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment

1991 • 491 citations

Alpha 6 beta 4 integrin heterodimer is a component of hemidesmosomes.

1990 • 486 citations

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

1995 • 440 citations

Integrin β4 mutations associated with junctional epidermolysis bullosa with pyloric atresia

1995 • 389 citations

Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

1996 • 386 citations

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

1995 • 367 citations

Desmosomes and hemidesmosomes

1993 • 310 citations

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

1995 • 279 citations

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

1992 • 268 citations

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

1995 • 250 citations

Intermediate filaments in disease

1995 • 248 citations

Cellular origin of the dermal‐epidermal basement membrane

1993 • 244 citations

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

1992 • 231 citations

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

1996 • 227 citations

A function for the integrin alpha 6 beta 4 in the hemidesmosome.

1991 • 225 citations

Human bullous pemphigoid antigen (BPAG1). Amino acid sequences deduced from cloned cDNAs predict biologically important peptide segments and protein domains.

1991 • 222 citations

Molecular complexity of the cutaneous basement membrane zone

1996 • 199 citations

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.

1991 • 188 citations

Cloning of type XVII collagen. Complementary and genomic DNA sequences of mouse 180-kilodalton bullous pemphigoid antigen (BPAG2) predict an interrupted collagenous domain, a transmembrane segment, and unusual features in the 5‘-end of the gene and the 3‘-untranslated region of the mRNA.

1993 • 175 citations

Generalized Atrophic Benign Epidermolysis Bullosa

1982 • 174 citations

180-kD bullous pemphigoid antigen (BP180) is deficient in generalized atrophic benign epidermolysis bullosa.

1995 • 170 citations

Comparative structural analysis of desmoplakin, bullous pemphigoid antigen and plectin: members of a new gene family involved in organization of intermediate filaments

1992 • 169 citations

Expression of hemidesmosomal and extracellular matrix proteins by normal and malignant human prostate tissue.

1995 • 158 citations

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

1992 • 158 citations

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

1996 • 127 citations

Human Gene Mutations Affecting RNA Processing and Translation

1993 • 123 citations

Immunolocalization of the intermediate filament-associated protein plectin at focal contacts and actin stress fibers.

1992 • 122 citations

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

1993 • 117 citations

Isolation and characterization of hemidesmosomes from bovine corneal epithelial cells

1991 • 108 citations

IFAP 300 is common to desmosomes and hemidesmosomes and is a possible linker of intermediate filaments to these junctions.

1994 • 92 citations

Junctional Epidermolysis Bullosis: Defects in Expression of Epiligrin/Nicein/Kalinin and Integrin ß4 That Inhibit Hemidesmosome Formation

1994 • 84 citations

Distribution of plectin, an intermediate filament‐associated protein, in the adult rat central nervous system

1994 • 77 citations

Autosomal Recessive Epidermolysis Bullosa Simplex

1989 • 77 citations

Epidermolysis Bullosa Simplex Associated With Muscular Dystrophy With Recessive Inheritance

1988 • 75 citations

Characterisation of Eight Monoclonal Antibodies to Involucrin

1992 • 69 citations

Genetic Skin Disorders of Keratin

1992 • 69 citations

A Homozygous Deletion Mutation in the Gene Encoding the 180-kDa Bullous Pemphigoid Antigen (BPAG2) in a Family with Generalized Atrophic Benign Epidermolysis Bullosa

1996 • 66 citations

Intermediate filament plasma membrane interactions

1991 • 65 citations

The pyloric atresia-junctional epidermolysis bullosa syndrome. Report of a case and review of the literature

1992 • 60 citations

Molecular diagnosis of inherited skin diseases: the paradigm of dystrophic epidermolysis bullosa.

1996 • 60 citations

Epidermolysis bullosa : basic and clinical aspects

1992 • 58 citations

The Pyloric Atresia—Junctional Epidermolysis Bullosa Syndrome

1992 • 53 citations

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

1994 • 49 citations

Detection of myc translocations in lymphoma cells by fluorescence in situ hybridization with yeast artificial chromosomes

1995 • 45 citations

Congenital muscular dystrophy and epidermolysis bullosa simplex

1989 • 33 citations

The Genomic Structure of an Insertional Mutation in the Dystonia Musculorum Locus

1994 • 32 citations

Epidermolysis Bullosa

1992 • 22 citations

A Case of Subepidermal Blister Disease Associated with Autoantibody against 450 kD Protein

1992 • 22 citations

Junctional Epidermolysis Bullosis: Defects in Expression of Epiligrin/Nicein/Kalinin and Integrin beta4 That Inhibit Hemidesmosome Formation.

1994 • 19 citations

Molecular Genetics of Epidermolysis Bullosa

1992 • 11 citations

Deleted Work

1955 • 0 citations