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Items: 1 to 20 of 31

1.
AAA ATPases regulate membrane association of yeast oxysterol binding proteins and sterol metabolism
Penghua Wang, Yong Zhang, Hongzhe Li, Hai Kee Chieu, Alan L Munn, Hongyuan Yang
EMBO J. 2005 Sep 7; 24(17): 2989–2999. Published online 2005 Aug 11. doi: 10.1038/sj.emboj.7600764
PMCID:
PMC1201346
AbstractArticlePDF–364K
2.
Oxysterol-binding protein homologs mediate sterol transport from the endoplasmic reticulum to mitochondria in yeast
Siqi Tian, Akinori Ohta, Hiroyuki Horiuchi, Ryouichi Fukuda
J Biol Chem. 2018 Apr 13; 293(15): 5636–5648. Published online 2018 Feb 27. doi: 10.1074/jbc.RA117.000596
PMCID:
PMC5900766
AbstractArticlePDF–1.4M
3.
Osh proteins regulate membrane sterol organization but are not required for sterol movement between the ER and PM
Alexander Georgiev, David P. Sullivan, Michael C. Kersting, Jeremy S. Dittman, Christopher T. Beh, Anant K. Menon
Traffic. Author manuscript; available in PMC 2012 Oct 1.
Published in final edited form as: Traffic. 2011 Oct; 12(10): 1341–1355. Published online 2011 Jul 19. doi: 10.1111/j.1600-0854.2011.01234.x
PMCID:
PMC3171641
AbstractArticlePDF–2.3M
4.
Lipid-regulated sterol transfer between closely apposed membranes by oxysterol-binding protein homologues
Timothy A. Schulz, Mal-Gi Choi, Sumana Raychaudhuri, Jason A. Mears, Rodolfo Ghirlando, Jenny E. Hinshaw, William A. Prinz
J Cell Biol. 2009 Dec 14; 187(6): 889–903. doi: 10.1083/jcb.200905007
PMCID:
PMC2806323
AbstractArticlePDF–3.0M
5.
Nonvesicular sterol movement from plasma membrane to ER requires oxysterol-binding protein–related proteins and phosphoinositides
Sumana Raychaudhuri, Young Jun Im, James H. Hurley, William A. Prinz
J Cell Biol. 2006 Apr 10; 173(1): 107–119. doi: 10.1083/jcb.200510084
PMCID:
PMC2063795
AbstractArticlePDF–2.4M
6.
Co-opted Oxysterol-Binding ORP and VAP Proteins Channel Sterols to RNA Virus Replication Sites via Membrane Contact Sites
Daniel Barajas, Kai Xu, Isabel Fernández de Castro Martín, Zsuzsanna Sasvari, Federica Brandizzi, Cristina Risco, Peter D. Nagy
PLoS Pathog. 2014 Oct; 10(10): e1004388. Published online 2014 Oct 16. doi: 10.1371/journal.ppat.1004388
PMCID:
PMC4199759
AbstractArticlePDF–5.6M
7.
Overlapping functions of the yeast oxysterol-binding protein homologues.
C T Beh, L Cool, J Phillips, J Rine
Genetics. 2001 Mar; 157(3): 1117–1140. doi: 10.1093/genetics/157.3.1117
Correction in:
Genetics, volume 158 on page 1387
PMCID:
PMC1461579
SummaryPDF–865K
8.
A Lipid Transfer Protein Signaling Axis Exerts Dual Control of Cell-Cycle and Membrane Trafficking Systems
Jin Huang, Carl J. Mousley, Louis Dacquay, Nairita Maitra, Guillaume Drin, Chong He, Neale D. Ridgway, Ashutosh Tripathi, Michael Kennedy, Brian K. Kennedy, Wenshe Liu, Kristin Baetz, Michael Polymenis, Vytas A. Bankaitis
Dev Cell. Author manuscript; available in PMC 2019 Apr 2.
Published in final edited form as: Dev Cell. 2018 Feb 5; 44(3): 378–391.e5. Published online 2018 Jan 27. doi: 10.1016/j.devcel.2017.12.026
PMCID:
PMC6444186
AbstractArticlePDF–1.9M
9.
The Saccharomyces cerevisiae Hot1p regulated gene YHR087W (HGI1) has a role in translation upon high glucose concentration stress
M Gomar-Alba, E Jiménez-Martí, M del Olmo
BMC Mol Biol. 2012; 13: 19. Published online 2012 Jun 21. doi: 10.1186/1471-2199-13-19
PMCID:
PMC3441895
AbstractArticlePDF–1.5M
10.
Osh4p is needed to reduce the level of phosphatidylinositol-4-phosphate on secretory vesicles as they mature
Yading Ling, Scott Hayano, Peter Novick
Mol Biol Cell. 2014 Nov 1; 25(21): 3389–3400. doi: 10.1091/mbc.E14-06-1087
PMCID:
PMC4214785
AbstractArticlePDF–2.1M
11.
Noncanonical regulation of phosphatidylserine metabolism by a Sec14-like protein and a lipid kinase
Yaxi Wang, Peihua Yuan, Aby Grabon, Ashutosh Tripathi, Dongju Lee, Martin Rodriguez, Max Lönnfors, Michal Eisenberg-Bord, Zehua Wang, Sin Man Lam, Maya Schuldiner, Vytas A. Bankaitis
J Cell Biol. 2020 May 4; 219(5): e201907128. Published online 2020 Apr 17. doi: 10.1083/jcb.201907128
PMCID:
PMC7199851
AbstractArticlePDF–6.7M
12.
Ist2 recruits the lipid transporters Osh6/7 to ER–PM contacts to maintain phospholipid metabolism
Andrew King On Wong, Barry Paul Young, Christopher J.R. Loewen
J Cell Biol. 2021 Sep 6; 220(9): e201910161. Published online 2021 Jul 14. doi: 10.1083/jcb.201910161
PMCID:
PMC8282664
AbstractArticlePDF–7.6M
13.
Exo1 recruits Cdc5 polo kinase to MutLγ to ensure efficient meiotic crossover formation
Aurore Sanchez, Céline Adam, Felix Rauh, Yann Duroc, Lepakshi Ranjha, Bérangère Lombard, Xiaojing Mu, Mélody Wintrebert, Damarys Loew, Alba Guarné, Stefano Gnan, Chun-Long Chen, Scott Keeney, Petr Cejka, Raphaël Guérois, Franz Klein, Jean-Baptiste Charbonnier, Valérie Borde
Proc Natl Acad Sci U S A. 2020 Dec 1; 117(48): 30577–30588. Published online 2020 Nov 16. doi: 10.1073/pnas.2013012117
PMCID:
PMC7720183
AbstractArticlePDF–2.3M
14.
Recruitment of Cytosolic J-Proteins by TOM Receptors Promotes Mitochondrial Protein Biogenesis
Łukasz Opaliński, Jiyao Song, Chantal Priesnitz, Lena-Sophie Wenz, Silke Oeljeklaus, Bettina Warscheid, Nikolaus Pfanner, Thomas Becker
Cell Rep. 2018 Nov 20; 25(8): 2036–2043.e5. Published online 2018 Nov 20. doi: 10.1016/j.celrep.2018.10.083
PMCID:
PMC6280124
AbstractArticle
15.
Multiplex assay for condition-dependent changes in protein–protein interactions
Ulrich Schlecht, Molly Miranda, Sundari Suresh, Ronald W. Davis, Robert P. St.Onge
Proc Natl Acad Sci U S A. 2012 Jun 5; 109(23): 9213–9218. Published online 2012 May 21. doi: 10.1073/pnas.1204952109
PMCID:
PMC3384208
AbstractArticlePDF–2.9M
16.
Mapping the Synthetic Dosage Lethality Network of CDK1/CDC28
Christine Zimmermann, Ignacio Garcia, Manja Omerzu, Pierre Chymkowitch, Beibei Zhang, Jorrit M. Enserink
G3 (Bethesda) 2017 Jun; 7(6): 1753–1766. Published online 2017 Apr 18. doi: 10.1534/g3.117.042317
Correction in:
G3 (Bethesda). 2019 Aug; 9(8): 2787.
PMCID:
PMC5473755
AbstractArticlePDF–2.7M
17.
Nuclear pore complexes mediate subtelomeric gene silencing by regulating PCNA levels on chromatin
Sanjeev Kumar Choudhry, Maxwell L. Neal, Song Li, Arti T. Navare, Trevor Van Eeuwen, Richard W. Wozniak, Fred D. Mast, Michael P. Rout, John D. Aitchison
J Cell Biol. 2023 Sep 4; 222(9): e202207060. Published online 2023 Jun 26. doi: 10.1083/jcb.202207060
PMCID:
PMC10292210
AbstractArticlePDF–5.9M
18.
A Lipid E-MAP Identifies Ubx2 as a Critical Regulator of Lipid Saturation and Lipid Bilayer Stress
Michal A. Surma, Christian Klose, Debby Peng, Michael Shales, Caroline Mrejen, Adam Stefanko, Hannes Braberg, David E. Gordon, Daniela Vorkel, Christer S. Ejsing, Robert Farese, Jr., Kai Simons, Nevan J. Krogan, Robert Ernst
Mol Cell. Author manuscript; available in PMC 2014 Aug 22.
Published in final edited form as: Mol Cell. 2013 Aug 22; 51(4): 519–530. Published online 2013 Jul 25. doi: 10.1016/j.molcel.2013.06.014
PMCID:
PMC3791312
AbstractArticlePDF–1.9M
19.
The Hsp90 molecular chaperone governs client proteins by targeting intrinsically disordered regions
Janhavi A. Kolhe, Neethu L. Babu, Brian C. Freeman
Mol Cell. Author manuscript; available in PMC 2024 Jun 15.
Published in final edited form as: Mol Cell. 2023 Jun 15; 83(12): 2035–2044.e7. Published online 2023 Jun 8. doi: 10.1016/j.molcel.2023.05.021
PMCID:
PMC10297700
AbstractArticlePDF–2.0M
20.
A mitochondrial-focused genetic interaction map reveals a scaffold-like complex required for inner membrane organization in mitochondria
Suzanne Hoppins, Sean R. Collins, Ann Cassidy-Stone, Eric Hummel, Rachel M. DeVay, Laura L. Lackner, Benedikt Westermann, Maya Schuldiner, Jonathan S. Weissman, Jodi Nunnari
J Cell Biol. 2011 Oct 17; 195(2): 323–340. doi: 10.1083/jcb.201107053
PMCID:
PMC3198156
AbstractArticlePDF–4.1M

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