Lam6 Regulates the Extent of Contacts between Organelles

[1]  Justin Yamada,et al.  Ltc1 is an ER-localized sterol transporter and a component of ER–mitochondria and ER–vacuole contacts , 2015, The Journal of cell biology.

[2]  A. Menon,et al.  A new family of StART domain proteins at membrane contact sites has a role in ER-PM sterol transport , 2015, eLife.

[3]  W. Prinz,et al.  Membrane contact sites, gateways for lipid homeostasis. , 2015, Current opinion in cell biology.

[4]  M. van der Laan,et al.  Cellular metabolism regulates contact sites between vacuoles and mitochondria. , 2014, Developmental cell.

[5]  M. Schuldiner,et al.  A dynamic interface between vacuoles and mitochondria in yeast. , 2014, Developmental cell.

[6]  Albert Sickmann,et al.  Composition and topology of the endoplasmic reticulum-mitochondria encounter structure. , 2011, Journal of molecular biology.

[7]  M. Schuldiner,et al.  Staying in touch: the molecular era of organelle contact sites. , 2011, Trends in biochemical sciences.

[8]  P. Walter,et al.  The conserved GTPase Gem1 regulates endoplasmic reticulum–mitochondria connections , 2011, Proceedings of the National Academy of Sciences.

[9]  Peter Walter,et al.  Supporting Online Material for An ER-Mitochondria Tethering Complex Revealed by a Synthetic Biology Screen , 2009 .

[10]  M. Mann,et al.  MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification , 2008, Nature Biotechnology.

[11]  I. Behrmann,et al.  A cost effective non-commercial ECL-solution for Western blot detections yielding strong signals and low background. , 2007, Journal of immunological methods.

[12]  R. Tibshirani,et al.  Significance analysis of microarrays applied to the ionizing radiation response , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[13]  P. Bork,et al.  GRAM, a novel domain in glucosyltransferases, myotubularins and other putative membrane-associated proteins. , 2000, Trends in biochemical sciences.

[14]  D. Goldfarb,et al.  Nucleus-vacuole junctions in Saccharomyces cerevisiae are formed through the direct interaction of Vac8p with Nvj1p. , 2000, Molecular biology of the cell.

[15]  P. Philippsen,et al.  Additional modules for versatile and economical PCR‐based gene deletion and modification in Saccharomyces cerevisiae , 1998, Yeast.

[16]  J. Boeke,et al.  Designer deletion strains derived from Saccharomyces cerevisiae S288C: A useful set of strains and plasmids for PCR‐mediated gene disruption and other applications , 1998, Yeast.

[17]  K. Tokuyasu.  Application of cryoultramicrotomy to immunocytochemistry , 1986, Journal of microscopy.

[18]  G. Daum,et al.  Import of proteins into mitochondria. Cytochrome b2 and cytochrome c peroxidase are located in the intermembrane space of yeast mitochondria. , 1982, The Journal of biological chemistry.

[19]  R. D. Gietz,et al.  Yeast transformation by the LiAc/SS carrier DNA/PEG method. , 2014, Methods in molecular biology.

[20]  M. Mann,et al.  Protocol for micro-purification, enrichment, pre-fractionation and storage of peptides for proteomics using StageTips , 2007, Nature Protocols.

[21]  N. Pfanner,et al.  Isolation of yeast mitochondria. , 2006, Methods in molecular biology.

[22]  H. Schägger.  Tricine–SDS-PAGE , 2006, Nature Protocols.

[23]  D. Goldfarb,et al.  Piecemeal microautophagy of nucleus in Saccharomyces cerevisiae. , 2003, Molecular biology of the cell.

[24]  Clifford Odets Papers.  Guide to the , 2003 .

[25]  R. Schekman,et al.  Reconstitution of transport from endoplasmic reticulum to Golgi complex using endoplasmic reticulum-enriched membrane fraction from yeast. , 1992, Methods in enzymology.