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Items: 1 to 20 of 21

1.
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
2.
A conserved acetylation switch enables pharmacological control of tubby-like protein stability
Evan M. Kerek, Kevin H. Yoon, Shu Y. Luo, Jerry Chen, Robert Valencia, Olivier Julien, Andrew J. Waskiewicz, Basil P. Hubbard
J Biol Chem. 2021 Jan-Jun; 296: 100073. Published online 2020 Nov 23. doi: 10.1074/jbc.RA120.015839
PMCID:
PMC7948452
AbstractArticlePDF–3.6M
3.
Association study of genetic variants at TTC32‐WDR35 gene cluster with coronary artery disease in Chinese Han population
Ying Xu, Yang Zhuo, Mengliang Ye, Mengmeng Li, Xiaojun Tang, Li Zhou
J Clin Lab Anal. 2021 Feb; 35(2): e23594. Published online 2020 Oct 2. doi: 10.1002/jcla.23594
PMCID:
PMC7891520
AbstractArticlePDF–504K
4.
PLEKHA4/kramer Attenuates Dishevelled Ubiquitination to Modulate Wnt and Planar Cell Polarity Signaling
Adnan Shami Shah, Alex G. Batrouni, Dongsung Kim, Amith Punyala, Wendy Cao, Chun Han, Michael L. Goldberg, Marcus B. Smolka, Jeremy M. Baskin
Cell Rep. Author manuscript; available in PMC 2019 Jun 26.
Published in final edited form as: Cell Rep. 2019 May 14; 27(7): 2157–2170.e8. doi: 10.1016/j.celrep.2019.04.060
PMCID:
PMC6594551
AbstractArticlePDF–1.4M
5.
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
6.
Intraflagellar transport-A complex mediates ciliary entry and retrograde trafficking of ciliary G protein–coupled receptors
Tomoaki Hirano, Yohei Katoh, Kazuhisa Nakayama
Mol Biol Cell. 2017 Feb 1; 28(3): 429–439. doi: 10.1091/mbc.E16-11-0813
PMCID:
PMC5341726
AbstractArticlePDF–2.7M
7.
Role for the IFT-A complex in selective transport to the primary cilium
Wenxiang Fu, Lei Wang, Sehyun Kim, Ji Li, Brian David Dynlacht
Cell Rep. Author manuscript; available in PMC 2016 Nov 25.
Published in final edited form as: Cell Rep. 2016 Nov 1; 17(6): 1505–1517. doi: 10.1016/j.celrep.2016.10.018
PMCID:
PMC5123888
AbstractArticlePDF–3.0M
8.
TNIP2 is a Hub Protein in the NF-κB Network with Both Protein and RNA Mediated Interactions
Charles A. S. Banks, Gina Boanca, Zachary T. Lee, Cassandra G. Eubanks, Gaye L. Hattem, Allison Peak, Lauren E. Weems, Juliana J. Conkright, Laurence Florens, Michael P. Washburn
Mol Cell Proteomics. 2016 Nov; 15(11): 3435–3449. Published online 2016 Sep 8. doi: 10.1074/mcp.M116.060509
PMCID:
PMC5098041
AbstractArticlePDF–2.1M
9.
An organelle-specific protein landscape identifies novel diseases and molecular mechanisms
Karsten Boldt, Jeroen van Reeuwijk, Qianhao Lu, Konstantinos Koutroumpas, Thanh-Minh T. Nguyen, Yves Texier, Sylvia E. C. van Beersum, Nicola Horn, Jason R. Willer, Dorus A. Mans, Gerard Dougherty, Ideke J. C. Lamers, Karlien L. M. Coene, Heleen H. Arts, Matthew J. Betts, Tina Beyer, Emine Bolat, Christian Johannes Gloeckner, Khatera Haidari, Lisette Hetterschijt, Daniela Iaconis, Dagan Jenkins, Franziska Klose, Barbara Knapp, Brooke Latour, Stef J. F. Letteboer, Carlo L. Marcelis, Dragana Mitic, Manuela Morleo, Machteld M. Oud, Moniek Riemersma, Susan Rix, Paulien A. Terhal, Grischa Toedt, Teunis J. P. van Dam, Erik de Vrieze, Yasmin Wissinger, Ka Man Wu, Gordana Apic, Philip L. Beales, Oliver E. Blacque, Toby J. Gibson, Martijn A. Huynen, Nicholas Katsanis, Hannie Kremer, Heymut Omran, Erwin van Wijk, Uwe Wolfrum, François Kepes, Erica E. Davis, Brunella Franco, Rachel H. Giles, Marius Ueffing, Robert B. Russell, Ronald Roepman, UK10K Rare Diseases Group
Nat Commun. 2016; 7: 11491. Published online 2016 May 13. doi: 10.1038/ncomms11491
PMCID:
PMC4869170
AbstractArticlePDF–2.0M
10.
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
11.
Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the cilium
José A. Caparrós-Martín, Alessandro De Luca, François Cartault, Mona Aglan, Samia Temtamy, Ghada A. Otaify, Mennat Mehrez, María Valencia, Laura Vázquez, Jean-Luc Alessandri, Julián Nevado, Inmaculada Rueda-Arenas, Karen E. Heath, Maria Cristina Digilio, Bruno Dallapiccola, Judith A. Goodship, Pleasantine Mill, Pablo Lapunzina, Victor L. Ruiz-Perez
Hum Mol Genet. 2015 Jul 15; 24(14): 4126–4137. Published online 2015 Apr 23. doi: 10.1093/hmg/ddv152
PMCID:
PMC4560068
AbstractArticlePDF–820K
12.
Novel Cul3 binding proteins function to remodel E3 ligase complexes
Wananit Wimuttisuk, Mark West, Brittney Davidge, Kebing Yu, Arthur Salomon, Jeffrey D Singer
BMC Cell Biol. 2014; 15: 28. Published online 2014 Jul 10. doi: 10.1186/1471-2121-15-28
PMCID:
PMC4107866
AbstractArticlePDF–2.5M
13.
WDR35 Mutation in Siblings with Sensenbrenner Syndrome: A Ciliopathy With Variable Phenotype
Carlos A. Bacino, Shweta U. Dhar, Nicola Brunetti-Pierri, Brendan Lee, Penelope E. Bonnen
Am J Med Genet A. Author manuscript; available in PMC 2014 Apr 27.
Published in final edited form as: Am J Med Genet A. 2012 Nov; 0(11): 2917–2924. Published online 2012 Sep 17. doi: 10.1002/ajmg.a.35608
PMCID:
PMC4000731
AbstractArticlePDF–1.0M
14.
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease
Xiang-feng Lu, Lai-yuan Wang, Shu-feng Chen, Lin He, Xue-li Yang, Yong-yong Shi, Jing Cheng, Liang Zhang, C. Charles Gu, Jian-feng Huang, Tang-chun Wu, Yi-tong Ma, Jian-xin Li, Jie Cao, Ji-chun Chen, Dong-liang Ge, Zhong-jie Fan, Ying Li, Lian-cheng Zhao, Hong-fan Li, Xiao-yang Zhou, Lan-ying Chen, Dong-hua Liu, Jing-ping Chen, Xiu-fang Duan, Yong-chen Hao, Li-gui Wang, Fang-hong Lu, Zhen-dong Liu, Cai-liang Yao, Chong Shen, Xiao-dong Pu, Lin Yu, Xiang-hua Fang, Li-hua Xu, Jian-jun Mu, Xian-ping Wu, Run-ping Zheng, Na-qiong Wu, Qi Zhao, Yun Li, Xiao-li Liu, Meng-qin Wang, Da-hai Yu, Dong-sheng Hu, Xu Ji, Dong-shuang Guo, Dong-ling Sun, Qian-qian Wang, Ying Yang, Fang-chao Liu, Qun-xia Mao, Xiao-hua Liang, Jing-feng Ji, Pan-pan Chen, Xing-bo Mo, Dian-jiang Li, Guo-ping Chai, Yi-da Tang, Xiang-dong Li, Zhen-han Du, Xue-hui Liu, Chen-long Dou, Zi-li Yang, Qing-jie Meng, Dong Wang, Ren-ping Wang, Jun Yang, Heribert Schunkert, Nilesh J. Samani, Sekar Kathiresan, Muredach P. Reilly, Jeanette Erdmann, the CARDIoGRAM Consortium, Xiao-zhong Peng, Xi-gui Wu, De-pei Liu, Yue-jin Yang, Run-sheng Chen, Bo-qin Qiang, Dong-feng Gu
Nat Genet. Author manuscript; available in PMC 2014 Feb 18.
Published in final edited form as: Nat Genet. 2012 Jul 1; 44(8): 890–894. Published online 2012 Jul 1. doi: 10.1038/ng.2337
PMCID:
PMC3927410
AbstractArticlePDF–526K
15.
A Census of Human Soluble Protein Complexes
Pierre C. Havugimana, G. Traver Hart, Tamás Nepusz, Haixuan Yang, Andrei L. Turinsky, Zhihua Li, Peggy I. Wang, Daniel R. Boutz, Vincent Fong, Sadhna Phanse, Mohan Babu, Stephanie A. Craig, Pingzhao Hu, Cuihong Wan, James Vlasblom, Vaqaarun-Nisa Dar, Alexander Bezginov, Gregory W. Clark, Gabriel C. Wu, Shoshana J. Wodak, Elisabeth R.M. Tillier, Alberto Paccanaro, Edward M. Marcotte, Andrew Emili
Cell. Author manuscript; available in PMC 2013 Aug 31.
Published in final edited form as: Cell. 2012 Aug 31; 150(5): 1068–1081. doi: 10.1016/j.cell.2012.08.011
PMCID:
PMC3477804
AbstractArticlePDF–7.7M
16.
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
17.
Human and Mouse Mutations in WDR35 Cause Short-Rib Polydactyly Syndromes Due to Abnormal Ciliogenesis
Pleasantine Mill, Paul J. Lockhart, Elizabeth Fitzpatrick, Hayley S. Mountford, Emma A. Hall, Martin A.M. Reijns, Margaret Keighren, Melanie Bahlo, Catherine J. Bromhead, Peter Budd, Salim Aftimos, Martin B. Delatycki, Ravi Savarirayan, Ian J. Jackson, David J. Amor
Am J Hum Genet. 2011 Apr 8; 88(4): 508–515. doi: 10.1016/j.ajhg.2011.03.015
PMCID:
PMC3071922
AbstractArticlePDF–1.4M
18.
TULP3 bridges the IFT-A complex and membrane phosphoinositides to promote trafficking of G protein-coupled receptors into primary cilia
Saikat Mukhopadhyay, Xiaohui Wen, Ben Chih, Christopher D. Nelson, William S. Lane, Suzie J. Scales, Peter K. Jackson
Genes Dev. 2010 Oct 1; 24(19): 2180–2193. doi: 10.1101/gad.1966210
PMCID:
PMC2947770
AbstractArticlePDF–1.9M
19.
Exome Sequencing Identifies WDR35 Variants Involved in Sensenbrenner Syndrome
Christian Gilissen, Heleen H. Arts, Alexander Hoischen, Liesbeth Spruijt, Dorus A. Mans, Peer Arts, Bart van Lier, Marloes Steehouwer, Jeroen van Reeuwijk, Sarina G. Kant, Ronald Roepman, Nine V.A.M. Knoers, Joris A. Veltman, Han G. Brunner
Am J Hum Genet. 2010 Sep 10; 87(3): 418–423. doi: 10.1016/j.ajhg.2010.08.004
PMCID:
PMC2933349
AbstractArticlePDF–692K
20.
The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)
Genome Res. 2004 Oct; 14(10b): 2121–2127. doi: 10.1101/gr.2596504
Correction in:
Genome Res. 2006 Jun; 16(6): 804.
PMCID:
PMC528928
AbstractArticlePDF–140K

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