Debora Rapaport
Tel Aviv University(IL)
Publications by Year
Research Areas
Muscle Physiology and Disorders, Cellular transport and secretion, Skin and Cellular Biology Research, Cardiomyopathy and Myosin Studies, Wnt/β-catenin signaling in development and cancer
Most-Cited Works
- → Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting(2013)331 cited
- → 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(2005)197 cited
- → Serum creatine-kinase (CK) and pyruvate-kinase (PK) activities in Duchenne (DMD) as compared with Becker (BMD) muscular dystrophy(1991)158 cited
- → EHD1 regulates β1 integrin endosomal transport: effects on focal adhesions, cell spreading and migration(2007)125 cited
- → RIN2 Deficiency Results in Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis: MACS Syndrome(2009)97 cited
- → The DNA Sequence of the RK Strain of Human Herpesvirus 7(1998)92 cited
- → EHD3: A Protein That Resides in Recycling Tubular and Vesicular Membrane Structures and Interacts with EHD1(2002)85 cited
- → Recycling to the Plasma Membrane is Delayed in EHD1 Knockout Mice(2005)75 cited
- → Characterization and cell type distribution of a novel, major transcript of the Duchenne Muscular Dystrophy gene(1992)72 cited
- → Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophy(1991)68 cited