A mutation in Sec15l1 causes anemia in hemoglobin deficit (hbd) mice

[1]  Sunil Q. Mehta,et al.  Mutations in Drosophila sec15 Reveal a Function in Neuronal Targeting for a Subset of Exocyst Components , 2005, Neuron.

[2]  M. T. Damiani,et al.  Rab11 Promotes Docking and Fusion of Multivesicular Bodies in a Calcium‐Dependent Manner , 2005, Traffic.

[3]  D. Donoghue,et al.  Constitutively activated FGFR3 mutants signal through PLCgamma-dependent and -independent pathways for hematopoietic transformation. , 2004, Blood.

[4]  C. Mitchell,et al.  Sec15 Is an Effector for the Rab11 GTPase in Mammalian Cells* , 2004, Journal of Biological Chemistry.

[5]  H. Lodish,et al.  Constitutive activation of the MEK/ERK pathway mediates all effects of oncogenic H-ras expression in primary erythroid progenitors. , 2004, Blood.

[6]  M. Hentze,et al.  Balancing Acts Molecular Control of Mammalian Iron Metabolism , 2004, Cell.

[7]  C. Yeaman,et al.  Mechanism of recruiting Sec6/8 (exocyst) complex to the apical junctional complex during polarization of epithelial cells , 2004, Journal of Cell Science.

[8]  Mala Murthy,et al.  Mutations in the Exocyst Component Sec5 Disrupt Neuronal Membrane Traffic, but Neurotransmitter Release Persists , 2003, Neuron.

[9]  K. Broadie,et al.  Drosophila Sec10 is Required for Hormone Secretion but not General Exocytosis or Neurotransmission , 2002, Traffic.

[10]  M. Vidal,et al.  The exosome pathway in K562 cells is regulated by Rab11. , 2002, Journal of cell science.

[11]  M. Larsen,et al.  The Brain Exocyst Complex Interacts with RalA in a GTP-dependent Manner , 2001, The Journal of Biological Chemistry.

[12]  P. Novick,et al.  Exocyst is involved in cystogenesis and tubulogenesis and acts by modulating synthesis and delivery of basolateral plasma membrane and secretory proteins. , 2000, Molecular biology of the cell.

[13]  N. Andrews,et al.  Iron homeostasis: insights from genetics and animal models , 2000, Nature Reviews Genetics.

[14]  M. Loh,et al.  Stat5 is essential for the myelo- and lymphoproliferative disease induced by TEL/JAK2. , 2000, Molecular cell.

[15]  N. Andrews,et al.  The molecular defect in hypotransferrinemic mice. , 2000, Blood.

[16]  Nancy Andrews,et al.  Transferrin receptor is necessary for development of erythrocytes and the nervous system , 1999, Nature Genetics.

[17]  P. Novick,et al.  The exocyst is an effector for Sec4p, targeting secretory vesicles to sites of exocytosis , 1999, The EMBO journal.

[18]  M. Mabon,et al.  The hemoglobin-deficit mutation is located on mouse Chromosome 19 , 1998, Mammalian Genome.

[19]  R. Scheller,et al.  Sec6/8 Complex Is Recruited to Cell–Cell Contacts and Specifies Transport Vesicle Delivery to the Basal-Lateral Membrane in Epithelial Cells , 1998, Cell.

[20]  D. Sabatini,et al.  Hydrolysis of GTP on rab11 is required for the direct delivery of transferrin from the pericentriolar recycling compartment to the cell surface but not from sorting endosomes. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[21]  Philippe Soriano,et al.  The secretory protein Sec8 is required for paraxial mesoderm formation in the mouse. , 1997, Developmental biology.

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

[23]  A. Mason,et al.  Exosome formation during maturation of mammalian and avian reticulocytes: Evidence that exosome release is a major route for externalization of obsolete membrane proteins , 1991, Journal of cellular physiology.

[24]  J. Hoke,et al.  Diminished acquisition of iron by reticulocytes from mice with hemoglobin deficit. , 1987, Experimental hematology.

[25]  J. Hoke,et al.  Hemoglobin Deficit: An Inherited Hypochromic Anemia in the Mouse 1 , 1986, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[26]  C. Harding,et al.  Endocytosis and intracellular processing of transferrin and colloidal gold-transferrin in rat reticulocytes: demonstration of a pathway for receptor shedding. , 1984, European journal of cell biology.

[27]  P. Stahl,et al.  Receptor-mediated endocytosis of transferrin and recycling of the transferrin receptor in rat reticulocytes , 1983, The Journal of cell biology.

[28]  R. Eisenstein.  Iron regulatory proteins and the molecular control of mammalian iron metabolism. , 2000, Annual review of nutrition.

[29]  J. Torrance.  Tissue iron stores , 1980 .

[30]  H. Scheufler.  Eine weitere mutante der hausmaus mit anamie (hbd). (eng. Summ.) , 1969 .