Results 21 to 30 of about 12,405 (225)

Hereditary epidermolytic palmoplantar keratosis due to a novel desmoglein‐1 mutation: A case report [PDF]

open access: yesClinical Case Reports
Key Clinical Message Keratosis palmoplantaris striata type I (SPPK‐I) is a rare autosomal‐dominant type of hereditary epidermolytic palmoplantar keratoderma, which can be caused by mutations in desmoglein‐1 (DSG‐1).
Kevin Koschitzki   +8 more
doaj   +2 more sources

Staphylococcal Exfoliative Toxin B Specifically Cleaves Desmoglein 1 [PDF]

open access: bronzeJournal of Investigative Dermatology, 2002
Staphylococcal scalded skin syndrome and its localized form, bullous impetigo, show superficial epidermal blister formation caused by exfoliative toxin A or B produced by Staphylococcus aureus. Recently we have demonstrated that exfoliative toxin A specifically cleaves desmoglein 1, a desmosomal adhesion molecule, that when inactivated results in ...
Yasushi Hanakawa   +5 more
openaire   +4 more sources

Epidermal stratification requires retromer-mediated desmoglein-1 recycling. [PDF]

open access: bronzeDev Cell, 2022
Hegazy M   +10 more
europepmc   +2 more sources

Alpha-1 antitrypsin promotes re-epithelialization by regulating inflammation and migration [PDF]

open access: yesFrontiers in Immunology
PurposeRegulation of inflammation and re-epithelialization are critical for efficient wound healing. This study explores the role of human α1-antitrypsin (hAAT), an immunomodulatory protein, in modulating inflammation and promoting re-epithelialization ...
Idan Farber   +21 more
doaj   +2 more sources

Desmoglein autoantibodies and disease severity in pemphigus patients – correlations and discrepancies [PDF]

open access: yesFolia Medica, 2023
Aim: To assess the correlation between the levels of anti-desmoglein-1 and anti-desmoglein-3 autoantibodies and disease severity in pemphigus patients.
Zhaneta H. Zhelyazkova   +4 more
doaj   +3 more sources

The Role of Desmoglein 1 in Gap Junction Turnover Revealed through the Study of SAM Syndrome. [PDF]

open access: hybridJ Invest Dermatol, 2020
Cohen-Barak E   +18 more
europepmc   +2 more sources

Mutations in desmoglein-1 cause diverse inherited palmoplantar keratoderma phenotypes:implications for genetic screening [PDF]

open access: yesBr J Dermatol, 2017
Almutawa   +16 more
core   +3 more sources

The interaction between Staphylococcus aureus SdrD and desmoglein 1 is important for adhesion to host cells [PDF]

open access: yesSci Rep, 2016
Ajayi, Clement   +7 more
core   +4 more sources

Molecular Hydrogen Ameliorates Anti-Desmoglein 1 Antibody-Induced Pemphigus-Associated Interstitial Lung Disease by Inhibiting Oxidative Stress. [PDF]

open access: goldInt J Mol Sci
Tang C   +18 more
europepmc   +2 more sources

TNF receptor–related factor 3 inactivation promotes the development of intrahepatic cholangiocarcinoma through NF‐κB‐inducing kinase–mediated hepatocyte transdifferentiation

open access: yesHepatology, EarlyView., 2022
Abstract Background and Aims Intrahepatic cholangiocarcinoma (ICC) is a deadly but poorly understood disease, and its treatment options are very limited. The aim of this study was to identify the molecular drivers of ICC and search for therapeutic targets.
Yuto Shiode   +16 more
wiley   +1 more source

Home - About - Disclaimer - Privacy