Publications by authors named "Debora Rapaport"

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The effect of mutant GBA1 on accumulation and aggregation of α-synuclein.
Gali Maor, Debora Rapaport, Mia Horowitz

Hum Mol Genet· June 2019

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NEK3-mediated SNAP29 phosphorylation modulates its membrane association and SNARE fusion dependent processes.
Debora Rapaport, Boris Fichtman, Hilla Weidberg, Eli Sprecher, Mia Horowitz

Biochem Biophys Res Commun· March 2018

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Non-keratinocyte SNAP29 influences epidermal differentiation and hair follicle formation in mice.
Stina A Schiller, Christina Seebode, Georg L Wieser, Sandra Goebbels, Torben Ruhwedel, Debora Rapaport

Exp Dermatol· August 2016

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Parkin-mediated ubiquitination of mutant glucocerebrosidase leads to competition with its substrates PARIS and ARTS.
Inna Bendikov-Bar, Debora Rapaport, Sarit Larisch, Mia Horowitz

Orphanet J Rare Dis· June 2014

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Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting.
Liat Samuelov, Ofer Sarig, Robert M Harmon, Debora Rapaport, Akemi Ishida-Yamamoto

Nat Genet· October 2013

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Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutation.
Ofer Sarig, Sagi Nahum, Debora Rapaport, Akemi Ishida-Yamamoto, Dana Fuchs-Telem

Am J Hum Genet· August 2012

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EHD2 mediates trafficking from the plasma membrane by modulating Rac1 activity.
Sigi Benjamin, Hilla Weidberg, Debora Rapaport, Olga Pekar, Marina Nudelman

Biochem J· November 2011

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Interaction between parkin and mutant glucocerebrosidase variants: a possible link between Parkinson disease and Gaucher disease.
Idit Ron, Debora Rapaport, Mia Horowitz

Hum Mol Genet· October 2010

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Loss of SNAP29 impairs endocytic recycling and cell motility.
Debora Rapaport, Yevgenia Lugassy, Eli Sprecher, Mia Horowitz

PLoS One· March 2010

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RIN2 deficiency results in macrocephaly, alopecia, cutis laxa, and scoliosis: MACS syndrome.
Lina Basel-Vanagaite, Ofer Sarig, Dov Hershkovitz, Dana Fuchs-Telem, Debora Rapaport

Am J Hum Genet· August 2009

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EHDS are serine phosphoproteins: EHD1 phosphorylation is enhanced by serum stimulation.
Boris Fichtman, Liat Ravid, Debora Rapaport, Mia Horowitz

Cell Mol Biol Lett· December 2008

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EHD1 regulates cholesterol homeostasis and lipid droplet storage.
Naava Naslavsky, Juliati Rahajeng, Debora Rapaport, Mia Horowitz, Steve Caplan

Biochem Biophys Res Commun· June 2007

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EHD1 regulates beta1 integrin endosomal transport: effects on focal adhesions, cell spreading and migration.
Marko Jović, Naava Naslavsky, Debora Rapaport, Mia Horowitz, Steve Caplan

J Cell Sci· March 2007

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Recycling to the plasma membrane is delayed in EHD1 knockout mice.
Debora Rapaport, Wojtek Auerbach, Naava Naslavsky, Metsada Pasmanik-Chor, Emilia Galperin

Traffic· January 2006

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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

Am J Hum Genet· August 2005

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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

Traffic· August 2002

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