The Spir actin organizers are involved in vesicle transport processes

[1]  F. Jankovics,et al.  An interaction type of genetic screen reveals a role of the Rab11 gene in oskar mRNA localization in the developing Drosophila melanogaster oocyte. , 2001, Genetics.

[2]  Kai Simons,et al.  Multicolour imaging of post-Golgi sorting and trafficking in live cells , 2001, Nature Cell Biology.

[3]  J. Salamero,et al.  Rab11 Regulates the Compartmentalization of Early Endosomes Required for Efficient Transport from Early Endosomes to the Trans-Golgi Network , 2000, The Journal of cell biology.

[4]  Marino Zerial,et al.  Distinct Membrane Domains on Endosomes in the Recycling Pathway Visualized by Multicolor Imaging of Rab4, Rab5, and Rab11 , 2000, The Journal of cell biology.

[5]  P. Bork,et al.  The p150-Spir protein provides a link between c-Jun N-terminal kinase function and actin reorganization , 2000, Current Biology.

[6]  M. Roth,et al.  Phosphatidylinositol 4,5-bisphosphate induces actin-based movement of raft-enriched vesicles through WASP-Arp2/3 , 2000, Current Biology.

[7]  C. Larabell,et al.  Actin-Dependent Propulsion of Endosomes and Lysosomes by Recruitment of N-Wasp✪ , 2000, The Journal of cell biology.

[8]  P. Tolias,et al.  Spire contains actin binding domains and is related to ascidian posterior end mark-5. , 1999, Development.

[9]  James H. Hurley,et al.  Crystal Structure of a Phosphatidylinositol 3-Phosphate-Specific Membrane-Targeting Motif, the FYVE Domain of Vps27p , 1999, Cell.

[10]  A. Brunger,et al.  Structural Basis of Rab Effector Specificity Crystal Structure of the Small G Protein Rab3A Complexed with the Effector Domain of Rabphilin-3A , 1999, Cell.

[11]  Wei Chen,et al.  Rab11 is required for trans-golgi network-to-plasma membrane transport and a preferential target for GDP dissociation inhibitor. , 1998, Molecular biology of the cell.

[12]  Rein Aasland,et al.  FYVE fingers bind PtdIns(3)P , 1998, Nature.

[13]  C. Burd,et al.  Phosphatidylinositol(3)-phosphate signaling mediated by specific binding to RING FYVE domains. , 1998, Molecular cell.

[14]  L. Lapierre,et al.  Rab11a redistributes to apical secretory canaliculus during stimulation of gastric parietal cells. , 1998, American journal of physiology. Cell physiology.

[15]  Paul A. Janmey,et al.  Corequirement of Specific Phosphoinositides and Small GTP-binding Protein Cdc42 in Inducing Actin Assembly in Xenopus Egg Extracts , 1998, The Journal of cell biology.

[16]  M. Zerial,et al.  The diversity of Rab proteins in vesicle transport. , 1997, Current opinion in cell biology.

[17]  A. Prescott,et al.  Distinct compartmentalization of TGN46 and beta 1,4-galactosyltransferase in HeLa cells. , 1997, European journal of cell biology.

[18]  M. Zerial,et al.  Rab11 regulates recycling through the pericentriolar recycling endosome , 1996, The Journal of cell biology.

[19]  J. Calley,et al.  Profilin is required for posterior patterning of the Drosophila oocyte. , 1996, Development.

[20]  M. Robinson,et al.  Targeting signals and subunit interactions in coated vesicle adaptor complexes , 1995, The Journal of cell biology.

[21]  M. Zerial,et al.  Rab11, a small GTPase associated with both constitutive and regulated secretory pathways in PC12 cells , 1993, FEBS letters.

[22]  M. Zerial,et al.  ERGIC-53, a membrane protein of the ER-Golgi intermediate compartment, carries an ER retention motif. , 1993, European journal of cell biology.

[23]  M. Robinson,et al.  Cloning and expression of gamma-adaptin, a component of clathrin-coated vesicles associated with the Golgi apparatus , 1990, The Journal of cell biology.

[24]  J. Hurley,et al.  Signaling and subcellular targeting by membrane-binding domains. , 2000, Annual review of biophysics and biomolecular structure.