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cDNA cloning, mRNA expression, and chromosomal mapping of human and mouse periplakin genes
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
9521878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9521878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
title
cDNA cloning, mRNA expression, and chromosomal mapping of human and mouse periplakin genes
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
9521878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9521878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
main subject
Periplakin
1 reference
stated in
GOA release 2020-03-11
author
Irwin McLean
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
9521878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9521878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
author name string
Aho S
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
9521878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9521878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
Li K
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
9521878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9521878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
Uitto J
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
9521878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9521878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
language of work or name
English
0 references
publication date
1 March 1998
1 reference
stated in
Europe PubMed Central
PubMed ID
9521878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9521878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
published in
Genomics
1 reference
stated in
Europe PubMed Central
PubMed ID
9521878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9521878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
volume
48
1 reference
stated in
Europe PubMed Central
PubMed ID
9521878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9521878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
9521878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9521878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
page(s)
242-247
1 reference
stated in
Europe PubMed Central
PubMed ID
9521878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9521878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
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7 January 2021
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An essential cytoskeletal linker protein connecting actin microfilaments to intermediate filaments.
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Comparative structural analysis of desmoplakin, bullous pemphigoid antigen and plectin: members of a new gene family involved in organization of intermediate filaments
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Epidermolysis bullosa: a spectrum of clinical phenotypes explained by molecular heterogeneity
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Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy
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The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.
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Plectin deficiency results in muscular dystrophy with epidermolysis bullosa
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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.
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Envoplakin, a novel precursor of the cornified envelope that has homology to desmoplakin
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7 January 2021
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Homozygous deletion mutations in the plectin gene (PLEC1) in patients with epidermolysis bullosa simplex associated with late-onset muscular dystrophy
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Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC)
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Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization
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Plectin and human genetic disorders of the skin and muscle. The paradigm of epidermolysis bullosa with muscular dystrophy
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Crossref
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7 January 2021
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Human keratin diseases: hereditary fragility of specific epithelial tissues
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Crossref
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7 January 2021
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inferred from DOI database lookup
A homozygous nonsense mutation in the PLEC1 gene in patients with epidermolysis bullosa simplex with muscular dystrophy
1 reference
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Crossref
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https://api.crossref.org/works/10.1006%2FGENO.1997.5188
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1006/GENO.1997.5188
1 reference
stated in
Europe PubMed Central
PubMed ID
9521878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9521878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
PubMed ID
9521878
1 reference
stated in
Europe PubMed Central
PubMed ID
9521878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9521878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
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