Pietro V De Camilli

Summary

Affiliation: Yale University
Country: USA

Publications

  1. ncbi The ENTH domain
    Pietro De Camilli
    Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06510, USA
    FEBS Lett 513:11-8. 2002
  2. ncbi Phosphoinositides in cell regulation and membrane dynamics
    Gilbert Di Paolo
    Department of Pathology and Cell Biology, The Taub Institute for Research on Alzheimer s Disease and the Aging Brain, Columbia University Medical Center, New York, New York 10032, USA
    Nature 443:651-7. 2006
  3. ncbi Loss of endocytic clathrin-coated pits upon acute depletion of phosphatidylinositol 4,5-bisphosphate
    Roberto Zoncu
    Department of Cell Biology and Howard Hughes Medical Institute, Kavli Institute For Neuroscience and Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, New Haven, CT 06510, USA
    Proc Natl Acad Sci U S A 104:3793-8. 2007
  4. ncbi Rapid Ca2+-dependent decrease of protein ubiquitination at synapses
    Hong Chen
    Howard Hughes Medical Institute and Department of Cell Biology, Yale University School of Medicine, New Haven, CT 06510, USA
    Proc Natl Acad Sci U S A 100:14908-13. 2003

Research Grants

  1. OCRL and the pathogenesis of Lowe Syndrome and Dent Disease
    Pietro De Camilli; Fiscal Year: 2010
  2. MOLECULAR MECHANISMS IN SYNAPTIC VESICLE RECYCLING
    Pietro De Camilli; Fiscal Year: 2009
  3. MOLECULAR MECHANISMS IN SYNAPTIC VESICLE RECYCLING
    Pietro De Camilli; Fiscal Year: 2009
  4. MOLECULAR MECHANISMS IN SYNAPTIC VESICLE RECYCLING
    Pietro De Camilli; Fiscal Year: 2007
  5. MOLECULAR MECHANISMS IN SYNAPTIC VESICLE RECYCLING
    Pietro De Camilli; Fiscal Year: 2005
  6. MOLECULAR AND FUNCTIONAL ANALYSIS OF ICA 512
    Pietro De Camilli; Fiscal Year: 2002
  7. MOLECULAR MECHANISMS IN SYNAPTIC VESICLE RECYCLING
    Pietro De Camilli; Fiscal Year: 2000

Collaborators

Detail Information

Publications4

  1. ncbi The ENTH domain
    Pietro De Camilli
    Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06510, USA
    FEBS Lett 513:11-8. 2002
    ..The ENTH domain is structurally similar to the VHS domain. These domains define two families of adaptor proteins which function in membrane traffic and whose interaction with membranes is regulated, in part, by phosphoinositides...
  2. ncbi Phosphoinositides in cell regulation and membrane dynamics
    Gilbert Di Paolo
    Department of Pathology and Cell Biology, The Taub Institute for Research on Alzheimer s Disease and the Aging Brain, Columbia University Medical Center, New York, New York 10032, USA
    Nature 443:651-7. 2006
    ..Their functions, besides classical signal transduction at the cell surface, include regulation of membrane traffic, the cytoskeleton, nuclear events and the permeability and transport functions of membranes...
  3. ncbi Loss of endocytic clathrin-coated pits upon acute depletion of phosphatidylinositol 4,5-bisphosphate
    Roberto Zoncu
    Department of Cell Biology and Howard Hughes Medical Institute, Kavli Institute For Neuroscience and Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, New Haven, CT 06510, USA
    Proc Natl Acad Sci U S A 104:3793-8. 2007
    ..These findings demonstrate the critical importance of PI(4,5)P(2) in clathrin coat dynamics and Arp2/3-dependent actin regulation...
  4. ncbi Rapid Ca2+-dependent decrease of protein ubiquitination at synapses
    Hong Chen
    Howard Hughes Medical Institute and Department of Cell Biology, Yale University School of Medicine, New Haven, CT 06510, USA
    Proc Natl Acad Sci U S A 100:14908-13. 2003
    ..In nerve terminals, protein ubiquitination may play a role both in the regulation of synaptic function, including vesicle traffic, and in the coordination of protein turnover with synaptic use...

Research Grants18

  1. OCRL and the pathogenesis of Lowe Syndrome and Dent Disease
    Pietro De Camilli; Fiscal Year: 2010
    ..The goal of this proposal is to understand how disruption of OCRL function leads to kidney disease with the hope that this information may help to develop therapeutic strategies for these conditions. ..
  2. MOLECULAR MECHANISMS IN SYNAPTIC VESICLE RECYCLING
    Pietro De Camilli; Fiscal Year: 2009
    ..The importance of this field is underscored by several disorders of the nervous system in mice and humans that have already been shown to result from abnormal phosphoinositide metabolism. ..
  3. MOLECULAR MECHANISMS IN SYNAPTIC VESICLE RECYCLING
    Pietro De Camilli; Fiscal Year: 2009
    ..The importance of this field is underscored by several disorders of the nervous system in mice and humans that have already been shown to result from abnormal phosphoinositide metabolism. ..
  4. MOLECULAR MECHANISMS IN SYNAPTIC VESICLE RECYCLING
    Pietro De Camilli; Fiscal Year: 2007
    ..The importance of this field is underscored by several disorders of the nervous system in mice and humans that have already been shown to result from abnormal phosphoinositide metabolism. ..
  5. MOLECULAR MECHANISMS IN SYNAPTIC VESICLE RECYCLING
    Pietro De Camilli; Fiscal Year: 2005
    ....
  6. MOLECULAR AND FUNCTIONAL ANALYSIS OF ICA 512
    Pietro De Camilli; Fiscal Year: 2002
    ..In addition, since atypical PTP domains similar to that of ICA512 are present in an increasing number of orphan genes, our studies on ICA512 may provide insight into the general significance of such protein motifs. ..
  7. MOLECULAR MECHANISMS IN SYNAPTIC VESICLE RECYCLING
    Pietro De Camilli; Fiscal Year: 2000
    ....