نتایج جستجو برای: dyskeratotic acantholysis

تعداد نتایج: 294  

2010
Meryem Bektas Puneet Jolly David S. Rubenstein

Pemphigus is a group of human autoimmune blistering diseases of the skin in which autoantibodies to desmosome cadherins induce loss of cell-cell adhesion (acantholysis). In addition to steric hindrance and activation of intracellular signaling, apoptosis has been suggested to contribute to the mechanism by which pathogenic IgG induces acantholysis. We review the current literature examining the...

2009
Amirala Aghbali Firouz Pouralibaba Hossein Eslami Farzaneh Pakdel Zahra Jamali

White sponge nevus (WSN) is a rare hereditary dyskeratotic hyperplasia of mucous membranes. It is an autosomal dominant disorder with variable penetrance. We report a case of WSN in a healthy 21-year-old male with no history of familial involvement. A white smooth plaque with no erythema or other structural abnormalities was observed, which confirmed the diagnosis of WSN histopathologically.

Journal: :Archives of dermatology 2004
Vu Thuong Nguyen Juan Arredondo Alexander I Chernyavsky Mark R Pittelkow Yasuo Kitajima Sergei A Grando

BACKGROUND Pemphigus vulgaris (PV) is an autoimmune, IgG autoantibody-mediated disease of skin and mucosa leading to progressive blistering and nonhealing erosions. Patients develop autoantibodies to adhesion molecules mediating intercellular adhesion and to keratinocyte cholinergic receptors regulating cell adhesion. OBSERVATIONS To determine whether a cholinergic agonist can abolish PV IgG-...

Journal: :Experimental dermatology 2012
María P Gil Teresa Modol Agustín España María J López-Zabalza

Pemphigus vulgaris (PV) is an autoimmune blistering skin disease characterized by suprabasal acantholysis and by autoantibodies against desmoglein 3 localized on desmosomes. In addition, caspases also seem to participate in this blistering disease. Focal adhesion kinase (FAK) is a non-receptor tyrosine kinase involved in cytoskeleton remodelling and formation and disassembly of cell adhesion st...

Journal: :Journal of Investigative Dermatology 1980

Journal: :Journal of Investigative Dermatology 1964

Journal: :Military Medical and Pharmaceutical Journal of Serbia 2013

Journal: :IP Indian journal of clinical and experimental dermatology 2022

Galli- Galli disease is a rare acantholytic variant of Dowling- Degos disease, with few cases reported in the literature till date. We here, describe an interesting case prominent histopathological findings. Future studies and genotype-phenotype correlations may elucidate why acantholysis observed some patients, but not others.

Journal: :Experimental dermatology 2009
Maider Pretel Agustín España Miren Marquina Beatriz Pelacho Jose María López-Picazo Maria J López-Zabalza

Pemphigus vulgaris (PV) is an autoimmune blistering disease characterized by the presence of IgG autoantibodies against Dsg3. Our aim was to investigate the molecular events implicated in the development and localization of apoptosis and acantholysis in PV. We used a passive transfer mouse model together with immunohistochemical (IHC) techniques and the TUNEL assay, with quantification analysis...

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