D
Debora Rapaport
Researcher at Tel Aviv University
Publications - 19
Citations - 1370
Debora Rapaport is an academic researcher from Tel Aviv University. The author has contributed to research in topics: Endocytic recycling & Endocytosis. The author has an hindex of 16, co-authored 19 publications receiving 1242 citations.
Papers
More filters
Journal ArticleDOI
Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting
Liat Samuelov,Ofer Sarig,Robert M. Harmon,Debora Rapaport,Akemi Ishida-Yamamoto,Ofer Isakov,Jennifer L. Koetsier,Andrea Gat,Ilan Goldberg,Reuven Bergman,Reuven Bergman,Ronen Spiegel,O. Eytan,O. Eytan,Shamir Geller,Sarit Peleg,Noam Shomron,Christabelle S M Goh,Neil J. Wilson,Frances J.D. Smith,Elizabeth Pohler,Michael A. Simpson,W.H. Irwin McLean,Alan D. Irvine,Alan D. Irvine,Mia Horowitz,John A. McGrath,Kathleen J. Green,Eli Sprecher,Eli Sprecher +29 more
TL;DR: The deciphering of the pathogenesis of SAM syndrome substantiates the notion that allergy may result from a primary structural epidermal defect and is linked to a number of genes encoding allergy-related cytokines.
Journal ArticleDOI
A Mutation in SNAP29, Coding for a SNARE Protein Involved in Intracellular Trafficking, Causes a Novel Neurocutaneous Syndrome Characterized by Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma
Eli Sprecher,Akemi Ishida-Yamamoto,Mordechai Mizrahi-Koren,Debora Rapaport,Dorit Goldsher,Margarita Indelman,Orit Topaz,Ilana Chefetz,Hanni Keren,Timothy J. O'Brien,Dani Bercovich,Stavit A. Shalev,Dan Geiger,Reuven Bergman,Mia Horowitz,Hanna Mandel +15 more
TL;DR: A novel neurocutaneous syndrome characterized by cerebral dysgenesis, neuropathy, ichthyosis, and keratoderma (CEDNIK syndrome) is described, and the importance of vesicle trafficking regulatory mechanisms for proper neuroectodermal differentiation is underscored.
Journal ArticleDOI
EHD1 regulates β1 integrin endosomal transport: effects on focal adhesions, cell spreading and migration
TL;DR: It is reported that the C-terminal Eps15-homology (EH) domain-containing protein E HD1 plays an important role in regulating β1 integrin transport, and a requirement for EHD1 in integrin-mediated downstream functions is demonstrated.
Journal ArticleDOI
Interaction between parkin and mutant glucocerebrosidase variants: a possible link between Parkinson disease and Gaucher disease
TL;DR: Testing the possibility that the association between GD and PD reflects the fact that parkin acts as an E3 ligase of mutant GCase variants showed that mutantGCase variants associate with parkin.
Journal ArticleDOI
EHD3: a protein that resides in recycling tubular and vesicular membrane structures and interacts with EHD1.
Emilia Galperin,Sigi Benjamin,Debora Rapaport,Rinat Rotem-Yehudar,Sandra Tolchinsky,Mia Horowitz +5 more
TL;DR: It is postulate that EHD3 localizes on endocytic tubular and vesicular structures and regulates their microtubule‐dependent movement, based on its specific intracellular localization and its interaction with EHD1.