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Items: 1 to 20 of 24

1.
Cell fixation improves performance of in situ crosslinking mass spectrometry while preserving cellular ultrastructure
Andrew R. M. Michael, Bruno C. Amaral, Kallie L. Ball, Kristen H. Eiriksson, David C. Schriemer
Nat Commun. 2024; 15: 8537. Published online 2024 Oct 2. doi: 10.1038/s41467-024-52844-y
PMCID:
PMC11447256
AbstractArticlePDF–2.8M
2.
Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome
Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi
Cell. Author manuscript; available in PMC 2022 May 27.
Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011
PMCID:
PMC8165030
AbstractArticlePDF–2.2M
3.
Biallelic loss of function variants in SYT2 cause a treatable congenital onset presynaptic myasthenic syndrome
Sandra Donkervoort, Payam Mohassel, Lucia Laugwitz, Maha S. Zaki, Erik-Jan Kamsteeg, Reza Maroofian, Katherine R. Chao, Corien C. Verschuuren-Bemelmans, Veronka Horber, Annemarie JM. Fock, Riley M. McCarty, Minal S. Jain, Victoria Biancavilla, Grace McMacken, Matthew Nalls, Nicol C. Voermans, Hasnaa M Elbendary, Molly Snyder, Chunyu Cai, Tanya Lehky, Valentina Stanley, Susan T. Iannaccone, A. Reghan Foley, Hanns Lochmüller, Joseph Gleeson, Henry Houlden, Tobias B. Haack, Rita Horvath, Carsten G. Bönnemann
Am J Med Genet A. Author manuscript; available in PMC 2021 Mar 15.
Published in final edited form as: Am J Med Genet A. 2020 Oct; 182(10): 2272–2283. Published online 2020 Aug 10. doi: 10.1002/ajmg.a.61765
PMCID:
PMC7959540
AbstractArticlePDF–778K
4.
Identification of a Novel de Novo Variant in the SYT2 Gene Causing a Rare Type of Distal Hereditary Motor Neuropathy
Olga Mironovich, Elena Dadali, Sergey Malmberg, Tatyana Markova, Oxana Ryzhkova, Aleksander Poliakov
Genes (Basel) 2020 Nov; 11(11): 1238. Published online 2020 Oct 22. doi: 10.3390/genes11111238
PMCID:
PMC7690400
AbstractArticlePDF–2.8M
5.
A reference map of the human binary protein interactome
Katja Luck, Dae-Kyum Kim, Luke Lambourne, Kerstin Spirohn, Bridget E. Begg, Wenting Bian, Ruth Brignall, Tiziana Cafarelli, Francisco J. Campos-Laborie, Benoit Charloteaux, Dongsic Choi, Atina G. Coté, Meaghan Daley, Steven Deimling, Alice Desbuleux, Amélie Dricot, Marinella Gebbia, Madeleine F. Hardy, Nishka Kishore, Jennifer J. Knapp, István A. Kovács, Irma Lemmens, Miles W. Mee, Joseph C. Mellor, Carl Pollis, Carles Pons, Aaron D. Richardson, Sadie Schlabach, Bridget Teeking, Anupama Yadav, Mariana Babor, Dawit Balcha, Omer Basha, Christian Bowman-Colin, Suet-Feung Chin, Soon Gang Choi, Claudia Colabella, Georges Coppin, Cassandra D’Amata, David De Ridder, Steffi De Rouck, Miquel Duran-Frigola, Hanane Ennajdaoui, Florian Goebels, Liana Goehring, Anjali Gopal, Ghazal Haddad, Elodie Hatchi, Mohamed Helmy, Yves Jacob, Yoseph Kassa, Serena Landini, Roujia Li, Natascha van Lieshout, Andrew MacWilliams, Dylan Markey, Joseph N. Paulson, Sudharshan Rangarajan, John Rasla, Ashyad Rayhan, Thomas Rolland, Adriana San-Miguel, Yun Shen, Dayag Sheykhkarimli, Gloria M. Sheynkman, Eyal Simonovsky, Murat Taşan, Alexander Tejeda, Vincent Tropepe, Jean-Claude Twizere, Yang Wang, Robert J. Weatheritt, Jochen Weile, Yu Xia, Xinping Yang, Esti Yeger-Lotem, Quan Zhong, Patrick Aloy, Gary D. Bader, Javier De Las Rivas, Suzanne Gaudet, Tong Hao, Janusz Rak, Jan Tavernier, David E. Hill, Marc Vidal, Frederick P. Roth, Michael A. Calderwood
Nature. Author manuscript; available in PMC 2020 Oct 8.
Published in final edited form as: Nature. 2020 Apr; 580(7803): 402–408. Published online 2020 Apr 8. doi: 10.1038/s41586-020-2188-x
PMCID:
PMC7169983
AbstractArticlePDF–5.4M
6.
Impaired plasma membrane localization of ubiquitin ligase complex underlies 3-M syndrome development
Pu Wang, Feng Yan, Zhijun Li, Yanbao Yu, Scott E. Parnell, Yue Xiong
J Clin Invest. 2019 Oct 1; 129(10): 4393–4407. Published online 2019 Sep 9. doi: 10.1172/JCI129107
PMCID:
PMC6763242
AbstractArticlePDF–12M
7.
Architecture of the human interactome defines protein communities and disease networks
Edward L. Huttlin, Raphael J. Bruckner, Joao A. Paulo, Joe R. Cannon, Lily Ting, Kurt Baltier, Greg Colby, Fana Gebreab, Melanie P. Gygi, Hannah Parzen, John Szpyt, Stanley Tam, Gabriela Zarraga, Laura Pontano-Vaites, Sharan Swarup, Anne E. White, Devin K. Schweppe, Ramin Rad, Brian K. Erickson, Robert A. Obar, K.G. Guruharsha, Kejie Li, Spyros Artavanis-Tsakonas, Steven P. Gygi, J. Wade Harper
Nature. Author manuscript; available in PMC 2017 Nov 17.
Published in final edited form as: Nature. 2017 May 25; 545(7655): 505–509. Published online 2017 May 17. doi: 10.1038/nature22366
PMCID:
PMC5531611
AbstractArticlePDF–2.7M
8.
Genome-wide CRISPR screen identifies HNRNPL as a prostate cancer dependency regulating RNA splicing
Teng Fei, Yiwen Chen, Tengfei Xiao, Wei Li, Laura Cato, Peng Zhang, Maura B. Cotter, Michaela Bowden, Rosina T. Lis, Shuang G. Zhao, Qiu Wu, Felix Y. Feng, Massimo Loda, Housheng Hansen He, X. Shirley Liu, Myles Brown
Proc Natl Acad Sci U S A. 2017 Jun 27; 114(26): E5207–E5215. Published online 2017 Jun 13. doi: 10.1073/pnas.1617467114
PMCID:
PMC5495225
AbstractArticlePDF–1.3M
9.
Control of plasma membrane lipid homeostasis by the extended synaptotagmins
Yasunori Saheki, Xin Bian, Curtis M. Schauder, Yujin Sawaki, Michal A. Surma, Christian Klose, Frederic Pincet, Karin M. Reinisch, Pietro De Camilli
Nat Cell Biol. Author manuscript; available in PMC 2016 Oct 11.
Published in final edited form as: Nat Cell Biol. 2016 May; 18(5): 504–515. Published online 2016 Apr 11. doi: 10.1038/ncb3339
PMCID:
PMC4848133
AbstractArticlePDF–2.5M
10.
Electrophysiologic features of SYT2 mutations causing a treatable neuromuscular syndrome
Roger G. Whittaker, David N. Herrmann, Boglarka Bansagi, Bashar Awwad Shiekh Hasan, Robert Muni Lofra, Eric L. Logigian, Janet E. Sowden, Jorge L. Almodovar, J. Troy Littleton, Stephan Zuchner, Rita Horvath, Hanns Lochmüller
Neurology. 2015 Dec 1; 85(22): 1964–1971. doi: 10.1212/WNL.0000000000002185
PMCID:
PMC4664120
AbstractArticlePDF–479K
11.
The BioPlex Network: A Systematic Exploration of the Human Interactome
Edward L. Huttlin, Lily Ting, Raphael J. Bruckner, Fana Gebreab, Melanie P. Gygi, John Szpyt, Stanley Tam, Gabriela Zarraga, Greg Colby, Kurt Baltier, Rui Dong, Virginia Guarani, Laura Pontano Vaites, Alban Ordureau, Ramin Rad, Brian K. Erickson, Martin Wühr, Joel Chick, Bo Zhai, Deepak Kolippakkam, Julian Mintseris, Robert A. Obar, Tim Harris, Spyros Artavanis-Tsakonas, Mathew E. Sowa, Pietro DeCamilli, Joao A. Paulo, J. Wade Harper, Steven P. Gygi
Cell. Author manuscript; available in PMC 2016 Jul 16.
Published in final edited form as: Cell. 2015 Jul 16; 162(2): 425–440. doi: 10.1016/j.cell.2015.06.043
PMCID:
PMC4617211
AbstractArticlePDF–2.2M
12.
Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy
David N. Herrmann, Rita Horvath, Janet E. Sowden, Michael Gonzales, Avencia Sanchez-Mejias, Zhuo Guan, Roger G. Whittaker, Jorge L. Almodovar, Maria Lane, Boglarka Bansagi, Angela Pyle, Veronika Boczonadi, Hanns Lochmüller, Helen Griffin, Patrick F. Chinnery, Thomas E. Lloyd, J. Troy Littleton, Stephan Zuchner
Am J Hum Genet. 2014 Sep 4; 95(3): 332–339. doi: 10.1016/j.ajhg.2014.08.007
Correction in:
Am J Hum Genet. 2014 Oct 2; 95(4): 472.
PMCID:
PMC4157148
AbstractArticlePDF–1.3M
13.
Botulinum neurotoxin D-C uses synaptotagmin I and II as receptors, and human synaptotagmin II is not an effective receptor for type B, D-C and G toxins
Lisheng Peng, Ronnie P.-A Berntsson, William H. Tepp, Rose M. Pitkin, Eric A. Johnson, Pål Stenmark, Min Dong
J Cell Sci. 2012 Jul 1; 125(13): 3233–3242. doi: 10.1242/jcs.103564
PMCID:
PMC4067266
AbstractArticle
14.
A Possible Mechanism behind Autoimmune Disorders Discovered By Genome-Wide Linkage and Association Analysis in Celiac Disease
Malin Östensson, Caroline Montén, Jonas Bacelis, Audur H. Gudjonsdottir, Svetlana Adamovic, Johan Ek, Henry Ascher, Elisabet Pollak, Henrik Arnell, Lars Browaldh, Daniel Agardh, Jan Wahlström, Staffan Nilsson, Åsa Torinsson-Naluai
PLoS One. 2013; 8(8): e70174. Published online 2013 Aug 2. doi: 10.1371/journal.pone.0070174
PMCID:
PMC3732286
AbstractArticlePDF–1.7M
15.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas
Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042
PMCID:
PMC3178059
AbstractArticlePDF–1.0M
16.
Zea mays Annexins Modulate Cytosolic Free Ca2+ and Generate a Ca2+-Permeable Conductance
Anuphon Laohavisit, Jennifer C. Mortimer, Vadim Demidchik, Katy M. Coxon, Matthew A. Stancombe, Neil Macpherson, Colin Brownlee, Andreas Hofmann, Alex A.R. Webb, Henk Miedema, Nicholas H. Battey, Julia M. Davies
Plant Cell. 2009 Feb; 21(2): 479–493. doi: 10.1105/tpc.108.059550
PMCID:
PMC2660635
AbstractArticlePDF–939K
17.
Synaptotagmin II Negatively Regulates Ca2+-triggered Exocytosis of Lysosomes in Mast Cells
Dana Baram, Roberto Adachi, Ora Medalia, Michael Tuvim, Burton F. Dickey, Yoseph A. Mekori, Ronit Sagi-Eisenberg
J Exp Med. 1999 May 17; 189(10): 1649–1658. doi: 10.1084/jem.189.10.1649
PMCID:
PMC2193646
AbstractArticlePDF–518K
18.
Membrane Topogenesis of a Type I Signal-Anchor Protein, Mouse Synaptotagmin Ii, on the Endoplasmic Reticulum
Yuichiro Kida, Masao Sakaguchi, Mitsunori Fukuda, Katsuhiko Mikoshiba, Katsuyoshi Mihara
J Cell Biol. 2000 Aug 21; 150(4): 719–730. doi: 10.1083/jcb.150.4.719
PMCID:
PMC2175286
AbstractArticlePDF–398K
19.
Stonin 2: An Adaptor-like Protein That Interacts with Components of the Endocytic Machinery
José A. Martina, Cecilia J. Bonangelino, Rubén C. Aguilar, Juan S. Bonifacino
J Cell Biol. 2001 May 28; 153(5): 1111–1120. doi: 10.1083/jcb.153.5.1111
PMCID:
PMC2174325
AbstractArticlePDF–570K
20.
Huntingtin Interacting Proteins Are Genetic Modifiers of Neurodegeneration
Linda S Kaltenbach, Eliana Romero, Robert R Becklin, Rakesh Chettier, Russell Bell, Amit Phansalkar, Andrew Strand, Cameron Torcassi, Justin Savage, Anthony Hurlburt, Guang-Ho Cha, Lubna Ukani, Cindy Lou Chepanoske, Yuejun Zhen, Sudhir Sahasrabudhe, James Olson, Cornelia Kurschner, Lisa M Ellerby, John M Peltier, Juan Botas, Robert E Hughes
PLoS Genet. 2007 May; 3(5): e82. Published online 2007 May 11. doi: 10.1371/journal.pgen.0030082
PMCID:
PMC1866352
AbstractArticlePDF–1.2M

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