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Items: 1 to 20 of 24

1.
Tau interactome maps synaptic and mitochondrial processes associated with neurodegeneration
Tara E. Tracy, Jesus Madero-Pérez, Danielle L. Swaney, Timothy S. Chang, Michelle Moritz, Csaba Konrad, Michael E. Ward, Erica Stevenson, Ruth Hüttenhain, Grant Kauwe, Maria Mercedes, Lauren Sweetland-Martin, Xu Chen, Sue-Ann Mok, Man Ying Wong, Maria Telpoukhovskaia, Sang-Won Min, Chao Wang, Peter Dongmin Sohn, Jordie Martin, Yungui Zhou, Wenjie Luo, John Q. Trojanowski, Virginia M.Y. Lee, Shiaoching Gong, Giovanni Manfredi, Giovanni Coppola, Nevan J. Krogan, Daniel H. Geschwind, Li Gan
Cell. Author manuscript; available in PMC 2022 Feb 19.
Published in final edited form as: Cell. 2022 Feb 17; 185(4): 712–728.e14. Published online 2022 Jan 20. doi: 10.1016/j.cell.2021.12.041
PMCID:
PMC8857049
AbstractArticlePDF–3.6M
2.
An antibody-based proximity labeling map reveals mechanisms of SARS-CoV-2 inhibition of antiviral immunity
Yuehui Zhang, Limin Shang, Jing Zhang, Yuchen Liu, Chaozhi Jin, Yanan Zhao, Xiaobo Lei, Wenjing Wang, Xia Xiao, Xiuyuan Zhang, Yujiao Liu, Linlin Liu, Meng-Wei Zhuang, Qingkun Mi, Chunyan Tian, Jianwei Wang, Fuchu He, Pei-Hui Wang, Jian Wang
Cell Chem Biol. 2022 Jan 20; 29(1): 5–18.e6. Published online 2021 Oct 20. doi: 10.1016/j.chembiol.2021.10.008
PMCID:
PMC8527578
AbstractArticlePDF–4.5M
3.
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
4.
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
5.
Genome sequencing uncovers phenocopies in primary progressive multiple sclerosis
Xiaoming Jia, Lohith Madireddy, Stacy Caillier, Adam Santaniello, Federica Esposito, Giancarlo Comi, Olaf Stuve, Yuan Zhou, Bruce Taylor, Trevor Kilpatrick, Filippo Martinelli‐Boneschi, Bruce A.C. Cree, Jorge R. Oksenberg, Stephen L. Hauser, Sergio E Baranzini
Ann Neurol. 2018 Jul; 84(1): 51–63. Published online 2018 Jul 3. doi: 10.1002/ana.25263
PMCID:
PMC6119489
AbstractArticlePDF–2.0M
6.
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
7.
Hereditary Spastic Paraplegia-Linked REEP1 Modulates ER-Mitochondria Contacts
Youngshin Lim, Il-Taeg Cho, Leah J. Schoel, Ginam Cho, Jeffrey A. Golden
Ann Neurol. Author manuscript; available in PMC 2016 Nov 1.
Published in final edited form as: Ann Neurol. 2015 Nov; 78(5): 679–696. Published online 2015 Sep 16. doi: 10.1002/ana.24488
PMCID:
PMC4681538
AbstractArticlePDF–3.4M
8.
A recurrent deletion syndrome at chromosome bands 2p11.2-2p12 flanked by segmental duplications at the breakpoints and including REEP1
Servi J C Stevens, Eveline W Blom, Ingrid T J Siegelaer, Eric E J G L Smeets
Eur J Hum Genet. 2015 Apr; 23(4): 543–546. Published online 2014 Jul 2. doi: 10.1038/ejhg.2014.124
PMCID:
PMC4666567
AbstractArticlePDF–1.0M
9.
REEP1 and REEP2 proteins are preferentially expressed in neuronal and neuronal-like exocytotic tissues
Carl M. Hurt, Susann Björk, Vincent K. Ho, Ralf Gilsbach, Lutz Hein, Timothy Angelotti
Brain Res. Author manuscript; available in PMC 2015 Jan 30.
Published in final edited form as: Brain Res. 2014 Jan 30; 1545: 12–22. Published online 2013 Dec 16. doi: 10.1016/j.brainres.2013.12.008
PMCID:
PMC3919455
AbstractArticlePDF–1009K
10.
A spastic paraplegia mouse model reveals REEP1-dependent ER shaping
Christian Beetz, Nicole Koch, Mukhran Khundadze, Geraldine Zimmer, Sandor Nietzsche, Nicole Hertel, Antje-Kathrin Huebner, Rizwan Mumtaz, Michaela Schweizer, Elisabeth Dirren, Kathrin N. Karle, Andrey Irintchev, Victoria Alvarez, Christoph Redies, Martin Westermann, Ingo Kurth, Thomas Deufel, Michael M. Kessels, Britta Qualmann, Christian A. Hübner
J Clin Invest. 2013 Oct 1; 123(10): 4273–4282. Published online 2013 Sep 24. doi: 10.1172/JCI65665
Correction in:
J Clin Invest. 2014 Jun 2; 124(6): 2809.
PMCID:
PMC3784524
AbstractArticlePDF–3.8M
11.
Protrudin binds atlastins and endoplasmic reticulum-shaping proteins and regulates network formation
Jaerak Chang, Seongju Lee, Craig Blackstone
Proc Natl Acad Sci U S A. 2013 Sep 10; 110(37): 14954–14959. Published online 2013 Aug 22. doi: 10.1073/pnas.1307391110
PMCID:
PMC3773775
AbstractArticlePDF–1.5M
12.
Exome Sequencing Identifies a REEP1 Mutation Involved in Distal Hereditary Motor Neuropathy Type V
Christian Beetz, Thomas R. Pieber, Nicole Hertel, Maria Schabhüttl, Carina Fischer, Slave Trajanoski, Elisabeth Graf, Silke Keiner, Ingo Kurth, Thomas Wieland, Rita-Eva Varga, Vincent Timmerman, Mary M. Reilly, Tim M. Strom, Michaela Auer-Grumbach
Am J Hum Genet. 2012 Jul 13; 91(1): 139–145. doi: 10.1016/j.ajhg.2012.05.007
PMCID:
PMC3397265
AbstractArticlePDF–588K
13.
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
14.
Mutation Screening of Spastin, Atlastin, and REEP1 in Hereditary Spastic Paraplegia
Donald S. McCorquodale, III, Uzoezi Ozomaro, Jia Huang, Gladys Montenegro, Arielle Kushman, Luigi Citrigno, Justin Price, Fiorella Speziani, Margaret A. Pericak-Vance, Stephan Züchner
Clin Genet. Author manuscript; available in PMC 2012 Jun 1.
Published in final edited form as: Clin Genet. 2011 Jun; 79(6): 523–530. doi: 10.1111/j.1399-0004.2010.01501.x
PMCID:
PMC2990804
AbstractArticlePDF–303K
15.
Personalized Smoking Cessation: Interactions between Nicotine Dose, Dependence and Quit-Success Genotype Score
Jed E Rose, Frédérique M Behm, Tomas Drgon, Catherine Johnson, George R Uhl
Mol Med. 2010 Jul-Aug; 16(7-8): 247–253. Published online 2010 Mar 17. doi: 10.2119/molmed.2009.00159
Correction in:
Mol Med. 2012; 18(1): 729.
PMCID:
PMC2896464
AbstractArticlePDF–2.4M
16.
Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network
Seong H. Park, Peng-Peng Zhu, Rell L. Parker, Craig Blackstone
J Clin Invest. 2010 Apr 1; 120(4): 1097–1110. Published online 2010 Mar 1. doi: 10.1172/JCI40979
PMCID:
PMC2846052
AbstractArticlePDF–5.8M
17.
REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31
Christian Beetz, Rebecca Schüle, Tine Deconinck, Khanh-Nhat Tran-Viet, Hui Zhu, Berry P. H. Kremer, Suzanna G. M. Frints, Wendy A. G. van Zelst-Stams, Paula Byrne, Susanne Otto, Anders O. H. Nygren, Jonathan Baets, Katrien Smets, Berten Ceulemans, Bernard Dan, Narasimhan Nagan, Jan Kassubek, Sven Klimpe, Thomas Klopstock, Henning Stolze, Hubert J. M. Smeets, Constance T. R. M. Schrander-Stumpel, Michael Hutchinson, Bart P. van de Warrenburg, Corey Braastad, Thomas Deufel, Margaret Pericak-Vance, Ludger Schöls, Peter de Jonghe, Stephan Züchner
Brain. Author manuscript; available in PMC 2010 Mar 19.
Published in final edited form as: Brain. 2008 Apr; 131(Pt 4): 1078–1086. Published online 2008 Mar 5. doi: 10.1093/brain/awn026
PMCID:
PMC2841798
AbstractArticlePDF–645K
18.
Ubiquitin-mediated proteolysis of HuR by heat shock
Kotb Abdelmohsen, Subramanya Srikantan, Xiaoling Yang, Ashish Lal, Hyeon Ho Kim, Yuki Kuwano, Stefanie Galban, Kevin G Becker, Davida Kamara, Rafael de Cabo, Myriam Gorospe
EMBO J. 2009 May 6; 28(9): 1271–1282. Published online 2009 Mar 26. doi: 10.1038/emboj.2009.67
PMCID:
PMC2683047
AbstractArticlePDF–1.4M
19.
Autosomal dominant hereditary spastic paraplegia: Novel mutations in the REEP1 gene (SPG31)
Katharina J Schlang, Larissa Arning, Joerg T Epplen, Susanne Stemmler
BMC Med Genet. 2008; 9: 71. Published online 2008 Jul 21. doi: 10.1186/1471-2350-9-71
PMCID:
PMC2492855
AbstractArticlePDF–206K
20.
Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31
Stephan Züchner, Gaofeng Wang, Khanh-Nhat Tran-Viet, Martha A. Nance, Perry C. Gaskell, Jeffery M. Vance, Allison E. Ashley-Koch, Margaret A. Pericak-Vance
Am J Hum Genet. 2006 Aug; 79(2): 365–369. Published online 2006 May 26. doi: 10.1086/505361
PMCID:
PMC1559498
AbstractArticlePDF–2.2M

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