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Items: 1 to 20 of 31

1.
Mutants Affecting the Structure of the Cortical Endoplasmic Reticulum in Saccharomyces cerevisiae
William A. Prinz, Lara Grzyb, Marten Veenhuis, Jason A. Kahana, Pamela A. Silver, Tom A. Rapoport
J Cell Biol. 2000 Aug 7; 150(3): 461–474. doi: 10.1083/jcb.150.3.461
PMCID:
PMC2175198
AbstractArticlePDF–897K
2.
Folding and intracellular transport of the yeast plasma-membrane H(+)-ATPase: effects of mutations in KAR2 and SEC65.
A Chang, M D Rose, C W Slayman
Proc Natl Acad Sci U S A. 1993 Jun 15; 90(12): 5808–5812. doi: 10.1073/pnas.90.12.5808
PMCID:
PMC46812
SummaryPage BrowsePDF–1.7M
3.
Sec62 Protein Mediates Membrane Insertion and Orientation of Moderately Hydrophobic Signal Anchor Proteins in the Endoplasmic Reticulum (ER)
Johannes H. Reithinger, Ji Eun Hani Kim, Hyun Kim
J Biol Chem. 2013 Jun 21; 288(25): 18058–18067. Published online 2013 Apr 30. doi: 10.1074/jbc.M113.473009
PMCID:
PMC3689950
AbstractArticlePDF–1.2M
4.
Saccharomyces SRP RNA secondary structures: A conserved S-domain and extended Alu-domain
ROB W. VAN NUES, JEREMY D. BROWN
RNA. 2004 Jan; 10(1): 75–89. doi: 10.1261/rna.5137904
PMCID:
PMC1370520
AbstractArticlePDF–1.0M
5.
Retrograde lipid traffic in yeast: identification of two distinct pathways for internalization of fluorescent-labeled phosphatidylcholine from the plasma membrane
J Cell Biol. 1993 Dec 2; 123(6): 1403–1419. doi: 10.1083/jcb.123.6.1403
PMCID:
PMC2290883
SummaryPDF–4.2M
6.
Preferential Targeting of a Signal Recognition Particle-dependent Precursor to the Ssh1p Translocon in Yeast
Michael P. Spiller, Colin J. Stirling
J Biol Chem. 2011 Jun 24; 286(25): 21953–21960. Published online 2011 Mar 28. doi: 10.1074/jbc.M111.219568
PMCID:
PMC3121340
AbstractArticlePDF–2.1M
7.
Elongation arrest is a physiologically important function of signal recognition particle
Nicola Mason, Leonora F. Ciufo, Jeremy D. Brown
EMBO J. 2000 Aug 1; 19(15): 4164–4174. doi: 10.1093/emboj/19.15.4164
PMCID:
PMC306590
AbstractArticlePDF–748K
8.
Sec63p and Kar2p are required for the translocation of SRP-dependent precursors into the yeast endoplasmic reticulum in vivo
Barry P. Young, Rachel A. Craven, Peter J. Reid, Martin Willer, Colin J. Stirling
EMBO J. 2001 Jan 15; 20(1-2): 262–271. doi: 10.1093/emboj/20.1.262
PMCID:
PMC140194
AbstractArticlePDF–262K
9.
Subunits of the Saccharomyces cerevisiae signal recognition particle required for its functional expression.
J D Brown, B C Hann, K F Medzihradszky, M Niwa, A L Burlingame, P Walter
EMBO J. 1994 Sep 15; 13(18): 4390–4400. doi: 10.1002/j.1460-2075.1994.tb06759.x
PMCID:
PMC395366
SummaryPage BrowsePDF–2.9M
10.
The RNA Helicase Ded1 from Yeast Is Associated with the Signal Recognition Particle and Is Regulated by SRP21
Hilal Yeter-Alat, Naïma Belgareh-Touzé, Agnès Le Saux, Emmeline Huvelle, Molka Mokdadi, Josette Banroques, N. Kyle Tanner
Molecules. 2024 Jun; 29(12): 2944. Published online 2024 Jun 20. doi: 10.3390/molecules29122944
PMCID:
PMC11206880
AbstractArticlePDF–5.6M
11.
The proteasome biogenesis regulator Rpn4 cooperates with the unfolded protein response to promote ER stress resistance
Rolf M Schmidt, Julia P Schessner, Georg HH Borner, Sebastian Schuck
eLife. 2019; 8: e43244. Published online 2019 Mar 13. doi: 10.7554/eLife.43244
PMCID:
PMC6415940
AbstractArticlePDF–2.7M
12.
Novel cargo-binding site in the β and δ subunits of coatomer
Kai Michelsen, Volker Schmid, Jutta Metz, Katja Heusser, Urban Liebel, Torsten Schwede, Anne Spang, Blanche Schwappach
J Cell Biol. 2007 Oct 22; 179(2): 209–217. doi: 10.1083/jcb.200704142
PMCID:
PMC2064757
AbstractArticlePDF–2.2M
13.
Analysis of the interplay of protein biogenesis factors at the ribosome exit site reveals new role for NAC
Yvonne Nyathi, Martin R. Pool
J Cell Biol. 2015 Jul 20; 210(2): 287–301. doi: 10.1083/jcb.201410086
PMCID:
PMC4508901
AbstractArticlePDF–2.3M
14.
Biogenesis of the Signal Recognition Particle (Srp) Involves Import of Srp Proteins into the Nucleolus, Assembly with the Srp-Rna, and Xpo1p-Mediated Export
Helge Grosshans, Karina Deinert, Ed Hurt, George Simos
J Cell Biol. 2001 May 14; 153(4): 745–762. doi: 10.1083/jcb.153.4.745
PMCID:
PMC2192394
AbstractArticlePDF–906K
15.
Rad5 dysregulation drives hyperactive recombination at replication forks resulting in cisplatin sensitivity and genome instability
Eric E Bryant, Ivana Šunjevarić, Luke Berchowitz, Rodney Rothstein, Robert J D Reid
Nucleic Acids Res. 2019 Sep 26; 47(17): 9144–9159. Published online 2019 Jul 27. doi: 10.1093/nar/gkz631
PMCID:
PMC6753471
AbstractArticlePDF–6.0M
16.
The SND proteins constitute an alternative targeting route to the endoplasmic reticulum
Naama Aviram, Tslil Ast, Elizabeth A. Costa, Eric C. Arakel, Silvia G. Chuartzman, Calvin H. Jan, Sarah Haßdenteufel, Johanna Dudek, Martin Jung, Stefan Schorr, Richard Zimmermann, Blanche Schwappach, Jonathan S. Weissman, Maya Schuldiner
Nature. Author manuscript; available in PMC 2017 Jul 17.
Published in final edited form as: Nature. 2016 Nov 30; 540(7631): 134–138. doi: 10.1038/nature20169
PMCID:
PMC5513701
AbstractArticlePDF–1.2M
17.
AP‐3 vesicle uncoating occurs after HOPS‐dependent vacuole tethering
Jannis Schoppe, Muriel Mari, Erdal Yavavli, Kathrin Auffarth, Margarita Cabrera, Stefan Walter, Florian Fröhlich, Christian Ungermann
EMBO J. 2020 Oct 15; 39(20): e105117. Published online 2020 Aug 25. doi: 10.15252/embj.2020105117
PMCID:
PMC7560216
AbstractArticlePDF–3.6M
18.
Global analysis of genetic circuitry and adaptive mechanisms enabling resistance to the azole antifungal drugs
Harley O’Connor Mount, Nicole M. Revie, Robert T. Todd, Kaitlin Anstett, Cathy Collins, Michael Costanzo, Charles Boone, Nicole Robbins, Anna Selmecki, Leah E. Cowen
PLoS Genet. 2018 Apr; 14(4): e1007319. Published online 2018 Apr 27. doi: 10.1371/journal.pgen.1007319
PMCID:
PMC5922528
AbstractArticlePDF–7.1M
19.
La-motif–dependent mRNA association with Slf1 promotes copper detoxification in yeast
Luca Schenk, Dominik M. Meinel, Katja Strässer, André P. Gerber
RNA. 2012 Mar; 18(3): 449–461. doi: 10.1261/rna.028506.111
PMCID:
PMC3285933
AbstractArticlePDF–812K
20.
Distinct roles for Khd1p in the localization and expression of bud-localized mRNAs in yeast
Yuko Hasegawa, Kenji Irie, André P. Gerber
RNA. 2008 Nov; 14(11): 2333–2347. doi: 10.1261/rna.1016508
PMCID:
PMC2578860
AbstractArticlePDF–1.3M

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