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Items: 1 to 20 of 58

1.
Phosphoregulatory protein 14-3-3 facilitates SAC1 transport from the endoplasmic reticulum
Kanika Bajaj Pahuja, Jinzhi Wang, Anastasia Blagoveshchenskaya, Lillian Lim, M. S. Madhusudhan, Peter Mayinger, Randy Schekman
Proc Natl Acad Sci U S A. 2015 Jun 23; 112(25): E3199–E3206. Published online 2015 Jun 8. doi: 10.1073/pnas.1509119112
PMCID:
PMC4485137
AbstractArticlePDF–1.3M
2.
SAC1 degrades its lipid substrate PtdIns4P in the endoplasmic reticulum to maintain a steep chemical gradient with donor membranes
James P Zewe, Rachel C Wills, Sahana Sangappa, Brady D Goulden, Gerald RV Hammond
eLife. 2018; 7: e35588. Published online 2018 Feb 20. doi: 10.7554/eLife.35588
PMCID:
PMC5829913
AbstractArticlePDF–8.1M
3.
The Sac1 Phosphoinositide Phosphatase Regulates Golgi Membrane Morphology and Mitotic Spindle Organization in Mammals
Yang Liu, Malika Boukhelifa, Emily Tribble, Elizabeth Morin-Kensicki, Andrea Uetrecht, James E. Bear, Vytas A. Bankaitis
Mol Biol Cell. 2008 Jul; 19(7): 3080–3096. doi: 10.1091/mbc.E07-12-1290
PMCID:
PMC2441670
AbstractArticlePDF–2.6M
4.
The activity of Sac1 across ER–TGN contact sites requires the four-phosphate-adaptor-protein-1
Rossella Venditti, Maria Chiara Masone, Laura Rita Rega, Giuseppe Di Tullio, Michele Santoro, Elena Polishchuk, Ivan Castello Serrano, Vesa M. Olkkonen, Akihiro Harada, Diego L. Medina, Raffaele La Montagna, Maria Antonietta De Matteis
J Cell Biol. 2019 Mar 4; 218(3): 783–797. doi: 10.1083/jcb.201812021
PMCID:
PMC6400556
AbstractArticlePDF–3.1M
5.
Model of OSBP-Mediated Cholesterol Supply to Aichi Virus RNA Replication Sites Involving Protein-Protein Interactions among Viral Proteins, ACBD3, OSBP, VAP-A/B, and SAC1
Kumiko Ishikawa-Sasaki, Shigeo Nagashima, Koki Taniguchi, Jun Sasaki
J Virol. 2018 Apr 15; 92(8): e01952-17. Prepublished online 2018 Jan 24. Published online 2018 Mar 28. doi: 10.1128/JVI.01952-17
PMCID:
PMC5874406
AbstractArticlePDF–6.9M
6.
Dynamic formation of ER–PM junctions presents a lipid phosphatase to regulate phosphoinositides
Eamonn J. Dickson, Jill B. Jensen, Oscar Vivas, Martin Kruse, Alexis E. Traynor-Kaplan, Bertil Hille
J Cell Biol. 2016 Apr 11; 213(1): 33–48. doi: 10.1083/jcb.201508106
PMCID:
PMC4828688
AbstractArticlePDF–3.4M
7.
The ER cholesterol sensor SCAP promotes CARTS biogenesis at ER–Golgi membrane contact sites
Yuichi Wakana, Kaito Hayashi, Takumi Nemoto, Chiaki Watanabe, Masato Taoka, Jessica Angulo-Capel, Maria F. Garcia-Parajo, Hidetoshi Kumata, Tomonari Umemura, Hiroki Inoue, Kohei Arasaki, Felix Campelo, Mitsuo Tagaya
J Cell Biol. 2021 Jan 4; 220(1): e202002150. Published online 2020 Nov 6. doi: 10.1083/jcb.202002150
PMCID:
PMC7654440
AbstractArticlePDF–9.2M
8.
Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D
S. L. Clark, D. E. Adkins, K. Aberg, J. M. Hettema, J. L. McClay, R. P. Souza, E. J. C. G. van den Oord
Psychol Med. Author manuscript; available in PMC 2013 Jun 1.
Published in final edited form as: Psychol Med. 2012 Jun; 42(6): 1151–1162. Published online 2011 Nov 1. doi: 10.1017/S003329171100239X
PMCID:
PMC3627503
AbstractArticlePDF–834K
9.
Evidence of efficient stop codon readthrough in four mammalian genes
Gary Loughran, Ming-Yuan Chou, Ivaylo P. Ivanov, Irwin Jungreis, Manolis Kellis, Anmol M. Kiran, Pavel V. Baranov, John F. Atkins
Nucleic Acids Res. 2014 Aug 18; 42(14): 8928–8938. Published online 2014 Jul 10. doi: 10.1093/nar/gku608
PMCID:
PMC4132726
AbstractArticlePDF–2.3M
10.
Phosphorylation switches protein disulfide isomerase activity to maintain proteostasis and attenuate ER stress
Jiaojiao Yu, Tao Li, Yu Liu, Xi Wang, Jianchao Zhang, Xi'e Wang, Guizhi Shi, Jizhong Lou, Likun Wang, Chih‐chen Wang, Lei Wang
EMBO J. 2020 May 18; 39(10): e103841. Published online 2020 Mar 9. doi: 10.15252/embj.2019103841
PMCID:
PMC7232009
AbstractArticlePDF–5.5M
11.
The interactome of metabolic enzyme carbonic anhydrase IX reveals novel roles in tumor cell migration and invadopodia/MMP14-mediated invasion
M Swayampakula, P C McDonald, M Vallejo, E Coyaud, S C Chafe, A Westerback, G Venkateswaran, J Shankar, G Gao, E M N Laurent, Y Lou, K L Bennewith, C T Supuran, I R Nabi, B Raught, S Dedhar
Oncogene. 2017 Nov 9; 36(45): 6244–6261. Published online 2017 Jul 10. doi: 10.1038/onc.2017.219
PMCID:
PMC5684442
AbstractArticlePDF–4.4M
12.
A proteome-scale map of the SARS-CoV-2–human contactome
Dae-Kyum Kim, Benjamin Weller, Chung-Wen Lin, Dayag Sheykhkarimli, Jennifer J. Knapp, Guillaume Dugied, Andreas Zanzoni, Carles Pons, Marie J. Tofaute, Sibusiso B. Maseko, Kerstin Spirohn, Florent Laval, Luke Lambourne, Nishka Kishore, Ashyad Rayhan, Mayra Sauer, Veronika Young, Hridi Halder, Nora Marín-de la Rosa, Oxana Pogoutse, Alexandra Strobel, Patrick Schwehn, Roujia Li, Simin T. Rothballer, Melina Altmann, Patricia Cassonnet, Atina G. Coté, Lena Elorduy Vergara, Isaiah Hazelwood, Betty B. Liu, Maria Nguyen, Ramakrishnan Pandiarajan, Bushra Dohai, Patricia A. Rodriguez Coloma, Juline Poirson, Paolo Giuliana, Luc Willems, Mikko Taipale, Yves Jacob, Tong Hao, David E. Hill, Christine Brun, Jean-Claude Twizere, Daniel Krappmann, Matthias Heinig, Claudia Falter, Patrick Aloy, Caroline Demeret, Marc Vidal, Michael A. Calderwood, Frederick P. Roth, Pascal Falter-Braun
Nat Biotechnol. 2023; 41(1): 140–149. Published online 2022 Oct 10. doi: 10.1038/s41587-022-01475-z
PMCID:
PMC9849141
AbstractArticlePDF–7.1M
13.
Agrin has a pathological role in the progression of oral cancer
César Rivera, Flávia Silva Zandonadi, Celeste Sánchez-Romero, Ciro Dantas Soares, Daniela Campos Granato, Wilfredo Alejandro González-Arriagada, Adriana Franco Paes Leme
Br J Cancer. 2018 Jun 12; 118(12): 1628–1638. Published online 2018 Jun 6. doi: 10.1038/s41416-018-0135-5
PMCID:
PMC6008410
AbstractArticlePDF–2.6M
14.
IKK-mediated Regulation of the COP9 Signalosome via Phosphorylation of CSN5
Jingzi Zhang, Ruoyu Zhao, Christine L. N. Bryant, Kenneth Wu, Zhihong Liu, Yibing Ding, Yue Zhao, Bin Xue, Zhen-Qiang Pan, Chaojun Li, Lan Huang, Lei Fang
J Proteome Res. Author manuscript; available in PMC 2020 Jun 17.
Published in final edited form as: J Proteome Res. 2020 Mar 6; 19(3): 1119–1130. Published online 2020 Feb 3. doi: 10.1021/acs.jproteome.9b00626
PMCID:
PMC7299130
AbstractArticlePDF–2.2M
15.
Interaction mapping of endoplasmic reticulum ubiquitin ligases identifies modulators of innate immune signalling
Emma J Fenech, Federica Lari, Philip D Charles, Roman Fischer, Marie Laétitia-Thézénas, Katrin Bagola, Adrienne W Paton, James C Paton, Mads Gyrd-Hansen, Benedikt M Kessler, John C Christianson
eLife. 2020; 9: e57306. Published online 2020 Jul 2. doi: 10.7554/eLife.57306
PMCID:
PMC7332293
AbstractArticlePDF–2.2M
16.
Genome-wide CRISPR screening reveals genetic modifiers of mutant EGFR dependence in human NSCLC
Hao Zeng, Johnny Castillo-Cabrera, Mika Manser, Bo Lu, Zinger Yang, Vaik Strande, Damien Begue, Raffaella Zamponi, Shumei Qiu, Frederic Sigoillot, Qiong Wang, Alicia Lindeman, John S Reece-Hoyes, Carsten Russ, Debora Bonenfant, Xiaomo Jiang, Youzhen Wang, Feng Cong
eLife. 2019; 8: e50223. Published online 2019 Nov 19. doi: 10.7554/eLife.50223
PMCID:
PMC6927754
AbstractArticlePDF–5.1M
17.
Systematic identification of pathological lamin A interactors
Travis A. Dittmer, Nidhi Sahni, Nard Kubben, David E. Hill, Marc Vidal, Rebecca C. Burgess, Vassilis Roukos, Tom Misteli
Mol Biol Cell. 2014 May 1; 25(9): 1493–1510. doi: 10.1091/mbc.E14-02-0733
PMCID:
PMC4004598
AbstractArticlePDF–3.5M
18.
The ubiquitin-dependent ATPase p97 removes cytotoxic trapped PARP1 from chromatin
Dragomir B. Krastev, Shudong Li, Yilun Sun, Andrew J. Wicks, Gwendoline Hoslett, Daniel Weekes, Luned M. Badder, Eleanor G. Knight, Rebecca Marlow, Mercedes Calvo Pardo, Lu Yu, Tanaji T. Talele, Jiri Bartek, Jyoti S. Choudhary, Yves Pommier, Stephen J. Pettitt, Andrew N. J. Tutt, Kristijan Ramadan, Christopher J. Lord
Nat Cell Biol. 2022; 24(1): 62–73. Published online 2022 Jan 10. doi: 10.1038/s41556-021-00807-6
PMCID:
PMC8760077
AbstractArticlePDF–12M
19.
FAM105A/OTULINL is a pseudodebuiquitinase of the OTU-class that localizes to the ER membrane
Derek F. Ceccarelli, Sofiia Ivantsiv, Amber Anne Mullin, Etienne Coyaud, Noah Manczyk, Pierre Maisonneuve, Igor Kurinov, Liang Zhao, Chris Go, Anne-Claude Gingras, Brian Raught, Sabine Cordes, Frank Sicheri
Structure. Author manuscript; available in PMC 2020 Jun 4.
Published in final edited form as: Structure. 2019 Jun 4; 27(6): 1000–1012.e6. Published online 2019 May 2. doi: 10.1016/j.str.2019.03.022
PMCID:
PMC6551266
AbstractArticlePDF–3.4M
20.
Interpreting cancer genomes using systematic host perturbations by tumour virus proteins
Orit Rozenblatt-Rosen, Rahul C. Deo, Megha Padi, Guillaume Adelmant, Michael A. Calderwood, Thomas Rolland, Miranda Grace, Amélie Dricot, Manor Askenazi, Maria Tavares, Sam Pevzner, Fieda Abderazzaq, Danielle Byrdsong, Anne-Ruxandra Carvunis, Alyce A. Chen, Jingwei Cheng, Mick Correll, Melissa Duarte, Changyu Fan, Mariet C. Feltkamp, Scott B. Ficarro, Rachel Franchi, Brijesh K. Garg, Natali Gulbahce, Tong Hao, Amy M. Holthaus, Robert James, Anna Korkhin, Larisa Litovchick, Jessica C. Mar, Theodore R. Pak, Sabrina Rabello, Renee Rubio, Yun Shen, Saurav Singh, Jennifer M. Spangle, Murat Tasan, Shelly Wanamaker, James T. Webber, Jennifer Roecklein-Canfield, Eric Johannsen, Albert-László Barabási, Rameen Beroukhim, Elliott Kieff, Michael E. Cusick, David E. Hill, Karl Münger, Jarrod A. Marto, John Quackenbush, Frederick P. Roth, James A. DeCaprio, Marc Vidal
Nature. Author manuscript; available in PMC 2013 Jan 26.
Published in final edited form as: Nature. 2012 Jul 26; 487(7408): 491–495. doi: 10.1038/nature11288
PMCID:
PMC3408847
AbstractArticlePDF–937K

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