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Genetic diseases of junctions
Joey E. Lai-Cheong
, Ken Arita
,
John A. McGrath
Department of Dermatology
Research output
:
Contribution to journal
›
Comment/debate
›
peer-review
120
Citations (Scopus)
Overview
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Medicine and Dentistry
Genetic Disorder
100%
Adherens Junction
100%
Diseases
66%
Desmosome
66%
Disease
33%
Gene Mutation
33%
In Vitro
33%
Cytotechnology
33%
Tight Junction
33%
Connexin
33%
Cell Contact
33%
Gap Junction
33%
Cell Communication
33%
Desmoglein 1
33%
Claudin 1
33%
P Cadherin
33%
Tight Junction Protein
33%
Desmoplakin
33%
Connexin 26
33%
Plakophilin
33%
Plakoglobin
33%
Keyphrases
Connexin 50
50%
Intercellular Channels
50%
Corneodesmosin
50%
Adherens Junction Proteins
50%
Connexin 30
50%
P-cadherin
50%
Human Gene mutation
50%
Unusual Phenotype
50%
Epithelial Cell Biology
50%
Pharmacology, Toxicology and Pharmaceutical Science
Desmoglein 1
50%
Plakoglobin
50%
Connexin 26
50%
Plakophilin
50%
Biochemistry, Genetics and Molecular Biology
Corneodesmosin
33%