Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Dan Vodo"'
Autor:
Dan Vodo, Eli Sprecher
Publikováno v:
JEADV Clinical Practice, Vol 2, Iss 2, Pp 203-212 (2023)
Abstract The severe autoimmune blistering disease pemphigus vulgaris (PV) is most probably mainly due to autoantibodies directed against desmosomal components of the epithelium, disrupting cell‐cell adhesion. The precise mechanisms underlying the d
Externí odkaz:
https://doaj.org/article/3428e0ed239c4db3b90980f56865674d
Autor:
Sari Assaf, Dan Vodo, Kiril Malovitski, Janan Mohamad, Shir Bergson, Yarden Feller, Liron Malki, Ofer Sarig, Eli Sprecher
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract Pemphigus vulgaris (PV) is a life-threatening autoimmune mucocutaneous blistering disease which is to a large extent genetically determined, and results, at least in part, from the deleterious activity of autoantibodies directed against desm
Externí odkaz:
https://doaj.org/article/0b2e83f484d04252bfd426701c1cb9cb
Publikováno v:
Indian Journal of Dermatology, Vol 66, Iss 5, Pp 575-575 (2021)
Externí odkaz:
https://doaj.org/article/a740744abc044bdb9f18d2377107f2ce
Publikováno v:
Frontiers in Medicine, Vol 5 (2018)
Pemphigus vulgaris (PV) is a severe autoimmune blistering disease caused by auto-antibodies (auto-Abs) directed against epithelial desmosomal components and leading to disruption of cell-cell adhesion. The exact mechanisms underlying the disease path
Externí odkaz:
https://doaj.org/article/7d897d6cefa94f55963ff64a07dca14e
Autor:
Dan Vodo, Ofer Sarig, Shamir Geller, Edna Ben-Asher, Tsviya Olender, Ron Bochner, Ilan Goldberg, Judith Nosgorodsky, Anna Alkelai, Pavel Tatarskyy, Alon Peled, Sharon Baum, Aviv Barzilai, Saleh M Ibrahim, Detlef Zillikens, Doron Lancet, Eli Sprecher
Publikováno v:
PLoS Genetics, Vol 12, Iss 5, p e1006008 (2016)
Pemphigus vulgaris (PV) is a life-threatening autoimmune mucocutaneous blistering disease caused by disruption of intercellular adhesion due to auto-antibodies directed against epithelial components. Treatment is limited to immunosuppressive agents,
Externí odkaz:
https://doaj.org/article/a12a4bbe1ad744ff8c325b9792779ab8
Autor:
Sari Assaf, K. Malovitski, Alon Peled, L. Malki, Eli Sprecher, M. Pavlovsky, T. Mayer, Dan Vodo, Ofer Sarig, J. Mohamad
Publikováno v:
British Journal of Dermatology. 184:1153-1160
Background Pemphigus vulgaris (PV) is a life-threatening mucocutaneous autoimmune blistering disease. We previously showed that genetic variants within the ST18 gene promoter area confer a sixfold increase in the propensity to develop PV. ST18, a tra
Publikováno v:
Pediatric dermatologyREFERENCES. 38(2)
Superficial epidermolytic ichthyosis (formerly Ichthyosis bullosa of Siemens) is an uncommon condition caused by dominant mutations in KRT2 encoding keratin 2. Epidermolytic epidermal nevus due to somatic mutations in KRT2 is even rarer. Here, we rep
Publikováno v:
Clinical and experimental dermatologyReferences. 46(5)
Autor:
Sari Assaf, Talia Canter, Arti Nanda, Kiril Malovitski, Eli Sprecher, Nicole Cesarato, Yossi Anis, Liat Samuelov, Bethany E. Perez White, Dan Vodo, Regina C. Betz, J. Mohamad, Holger Thiele, Andrea Gat, Amy S. Paller, M. Pavlovsky, Ofer Bihari, L. Malki, Ofer Sarig
Publikováno v:
Genet Med
PURPOSE: Localized autosomal recessive hypotrichosis (LAH) has been associated with pathogenic variants in DSG4, encoding a desmosomal protein as well as in LIPH and LPAR6, encoding respectively lipase H, which catalyzes the formation of 2-acyl-lysop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9538a579fc561f5b84f567136c3adc2d
https://europepmc.org/articles/PMC7405639/
https://europepmc.org/articles/PMC7405639/
Autor:
L. Malki, Liat Samuelov, Daniel Daniely, Tom Rabinowitz, J. Mohamad, Eli Sprecher, Eden Shkury, Alon Peled, Sari Assaf, M. Pavlovsky, Talia Mayer, Noam Shomron, Dan Vodo, Ofer Sarig, Kiril Malovitski
Publikováno v:
The Journal of investigative dermatology. 140(11)
Inherited palmoplantar keratodermas refer to a large and heterogeneous group of conditions resulting from abnormal epidermal differentiation and featuring thickening of the skin of the palms and soles. Here, we aimed at delineating the genetic basis