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Items: 1 to 20 of 69

1.
Proteomic analysis of diabetes genetic risk scores identifies complement C2 and neuropilin-2 as predictors of type 2 diabetes: the Atherosclerosis Risk in Communities (ARIC) Study
Brian T. Steffen, Weihong Tang, Pamela L. Lutsey, Ryan T. Demmer, Elizabeth Selvin, Kunihiro Matsushita, Alanna C. Morrison, Weihua Guan, Mary R. Rooney, Faye L. Norby, Nathan Pankratz, David Couper, James S. Pankow
Diabetologia. Author manuscript; available in PMC 2024 Jan 1.
Published in final edited form as: Diabetologia. 2023 Jan; 66(1): 105–115. Published online 2022 Oct 4. doi: 10.1007/s00125-022-05801-7
PMCID:
PMC9742300
AbstractArticlePDF–868K
2.
Gain-of-Function Mutations R249C and S250C in Complement C2 Protein Increase C3 Deposition in the Presence of C-Reactive Protein
Aleksandra Urban, Daria Kowalska, Grzegorz Stasiłojć, Alicja Kuźniewska, Anna Skrobińska, Emilia Arjona, Eugenia Castellote Alonso, María Ángeles Fenollosa Segarra, Ilse Jongerius, Robbert Spaapen, Simon Satchell, Marcel Thiel, Stanisław Ołdziej, Santiago Rodriguez de Córdoba, Marcin Okrój
Front Immunol. 2021; 12: 724361. Published online 2021 Nov 25. doi: 10.3389/fimmu.2021.724361
PMCID:
PMC8654806
AbstractArticlePDF–15M
3.
Genetic Variations at Loci Involved in the Immune Response Are Risk Factors for Hepatocellular Carcinoma
Robert J. Clifford, Jinghui Zhang, Daoud M. Meerzaman, Myung-Soo Lyu, Ying Hu, Constance M. Cultraro, Richard P. Finney, Jenny M. Kelley, Sol Efroni, Sharon I. Greenblum, Cu V. Nguyen, William L. Rowe, Sweta Sharma, Gang Wu, Chunhua Yan, Hongen Zhang, Young-Hwa Chung, Jeong A. Kim, Neung Hwa Park, Il Han Song, Kenneth H. Buetow
Hepatology. Author manuscript; available in PMC 2021 Jul 6.
Published in final edited form as: Hepatology. 2010 Dec; 52(6): 2034–2043. doi: 10.1002/hep.23943
PMCID:
PMC8259333
AbstractArticlePDF–813K
4.
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
5.
Complement protein levels and MBL2 polymorphisms are associated with dengue and disease severity
Ngo Truong Giang, Hoang van Tong, Do Quyet, Nghiem Xuan Hoan, Trinh Huu Nghia, Nguyen Minh Nam, Hoang Vu Hung, Do Tuan Anh, Can Van Mao, Ho Anh Son, Christian G. Meyer, Thirumalaisamy P. Velavan, Nguyen Linh Toan
Sci Rep. 2020; 10: 14923. Published online 2020 Sep 10. doi: 10.1038/s41598-020-71947-2
PMCID:
PMC7484760
AbstractArticlePDF–1.3M
6.
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
7.
Hereditary Deficiency of the Second Component of Complement: Early Diagnosis and 21-Year Follow-Up of a Family
Rosa Maria Dellepiane, Lucia Augusta Baselli, Marco Cazzaniga, Vassilios Lougaris, Paolo Macor, Mara Giordano, Roberta Gualtierotti, Massimo Cugno
Medicina (Kaunas) 2020 Mar; 56(3): 120. Published online 2020 Mar 10. doi: 10.3390/medicina56030120
PMCID:
PMC7143546
AbstractArticlePDF–898K
8.
Peripheral Retinal Drusen and Reticular Pigment: Association with CFHY402H and CFHrs1410996 Genotypes in Family and Twin Studies
Johanna M. Seddon, Robyn Reynolds, Bernard Rosner
Invest Ophthalmol Vis Sci. 2009 Feb; 50(2): 586–591. doi: 10.1167/iovs.08-2514
PMCID:
PMC6498874
AbstractArticlePDF–230K
9.
The Association Between Complement Component 2/Complement Factor B Polymorphisms and Age-related Macular Degeneration: A HuGE Review and Meta-Analysis
Ammarin Thakkinstian, Mark McEvoy, Usha Chakravarthy, Subhabrata Chakrabarti, Gareth J. McKay, Euijung Ryu, Giuliana Silvestri, Inderjeet Kaur, Peter Francis, Takeshi Iwata, Masakazu Akahori, Astrid Arning, Albert O. Edwards, Johanna M. Seddon, John Attia
Am J Epidemiol. 2012 Sep 1; 176(5): 361–372. Published online 2012 Aug 5. doi: 10.1093/aje/kws031
PMCID:
PMC6483268
AbstractArticlePDF–237K
10.
Acquisition of C1 inhibitor by Bordetella pertussis virulence associated gene 8 results in C2 and C4 consumption away from the bacterial surface
Elise S. Hovingh, Bryan van den Broek, Betsy Kuipers, Elena Pinelli, Suzan H. M. Rooijakkers, Ilse Jongerius
PLoS Pathog. 2017 Jul; 13(7): e1006531. Published online 2017 Jul 24. doi: 10.1371/journal.ppat.1006531
PMCID:
PMC5542704
AbstractArticlePDF–5.2M
11.
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
12.
Solution Structures of Complement C2 and Its C4 Complexes Propose Pathway-specific Mechanisms for Control and Activation of the Complement Proconvertases
Sofia Mortensen, Jan K. Jensen, Gregers R. Andersen
J Biol Chem. 2016 Aug 5; 291(32): 16494–16507. Published online 2016 Jun 1. doi: 10.1074/jbc.M116.722017
PMCID:
PMC4974366
AbstractArticlePDF–3.1M
13.
High-throughput analyses of hnRNP H1 dissects its multi-functional aspect
Philip J. Uren, Emad Bahrami-Samani, Patricia Rosa de Araujo, Christine Vogel, Mei Qiao, Suzanne C. Burns, Andrew D. Smith, Luiz O. F. Penalva
RNA Biol. 2016 Apr; 13(4): 400–411. Published online 2016 Jan 13. doi: 10.1080/15476286.2015.1138030
PMCID:
PMC4841607
AbstractArticlePDF–1.6M
14.
Widespread Macromolecular Interaction Perturbations in Human Genetic Disorders
Nidhi Sahni, Song Yi, Mikko Taipale, Juan I. Fuxman Bass, Jasmin Coulombe-Huntington, Fan Yang, Jian Peng, Jochen Weile, Georgios I. Karras, Yang Wang, István A. Kovács, Atanas Kamburov, Irina Krykbaeva, Mandy H. Lam, George Tucker, Vikram Khurana, Amitabh Sharma, Yang-Yu Liu, Nozomu Yachie, Quan Zhong, Yun Shen, Alexandre Palagi, Adriana San-Miguel, Changyu Fan, Dawit Balcha, Amelie Dricot, Daniel M. Jordan, Jennifer M. Walsh, Akash A. Shah, Xinping Yang, Ani Stoyanova, Alex Leighton, Michael A. Calderwood, Yves Jacob, Michael E. Cusick, Kourosh Salehi-Ashtiani, Luke J. Whitesell, Shamil Sunyaev, Bonnie Berger, Albert-László Barabási, Benoit Charloteaux, David E. Hill, Tong Hao, Frederick P. Roth, Yu Xia, Albertha J.M. Walhout, Susan Lindquist, Marc Vidal
Cell. Author manuscript; available in PMC 2016 Apr 23.
Published in final edited form as: Cell. 2015 Apr 23; 161(3): 647–660. doi: 10.1016/j.cell.2015.04.013
PMCID:
PMC4441215
AbstractArticlePDF–1.2M
15.
C2 rs547154 polymorphism and polypoidal choroidal vasculopathy susceptibility: a meta-analysis
Xue Chen, Xiaoli Kang, Kanxing Zhao, Chen Zhao
Sci Rep. 2015; 5: 8709. Published online 2015 Mar 3. doi: 10.1038/srep08709
PMCID:
PMC4346790
AbstractArticlePDF–603K
16.
GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region
Don L. Armstrong, Raphael Zidovetzki, Marta E Alarcón-Riquelme, Betty P Tsao, Lindsey A Criswell, Robert P Kimberly, John B Harley, Kathy L Sivils, Timothy J Vyse, Patrick M. Gaffney, Carl D Langefeld, Chaim O. Jacob
Genes Immun. Author manuscript; available in PMC 2015 Mar 1.
Published in final edited form as: Genes Immun. 2014 Sep; 15(6): 347–354. Published online 2014 May 29. doi: 10.1038/gene.2014.23
PMCID:
PMC4156543
AbstractArticlePDF–1.5M
17.
Inhibition of C3 Convertase Activity by Hepatitis C Virus as an Additional Lesion in the Regulation of Complement Components
Hangeun Kim, Keith Meyer, Adrian M. Di Bisceglie, Ranjit Ray
PLoS One. 2014; 9(7): e101422. Published online 2014 Jul 1. doi: 10.1371/journal.pone.0101422
PMCID:
PMC4077819
AbstractArticlePDF–940K
18.
Associations of complement factor B and complement component 2 genotypes with subtypes of polypoidal choroidal vasculopathy
Koji Tanaka, Tomohiro Nakayama, Ryusaburo Mori, Naoyuki Sato, Akiyuki Kawamura, Mitsuko Yuzawa
BMC Ophthalmol. 2014; 14: 83. Published online 2014 Jun 25. doi: 10.1186/1471-2415-14-83
PMCID:
PMC4076251
AbstractArticlePDF–559K
19.
Heritability and Genome-wide Association Study To Assess Genetic Differences Between Advanced Age-Related Macular Degeneration Subtypes
Lucia Sobrin, Stephan Ripke, Yi Yu, Jesen Fagerness, Tushar R. Bhangale, Perciliz L. Tan, Eric H. Souied, Gabriëlle H.S. Buitendijk, Joanna E. Merriam, Andrea J. Richardson, Soumya Raychaudhuri, Robyn Reynolds, Kimberly A. Chin, Aaron Y. Lee, Nicolas Leveziel, Donald J. Zack, Peter Campochiaro, R. Theodore Smith, Gaetano R. Barile, Ruth E. Hogg, Usha Chakravarthy, Timothy W. Behrens, André G. Uitterlinden, Cornelia M. van Duijn, Johannes R. Vingerling, Milam A. Brantley, Jr, Paul N. Baird, Caroline C.W. Klaver, Rando Allikmets, Nicholas Katsanis, Robert R. Graham, John P.A. Ioannidis, Mark J. Daly, Johanna M. Seddon
Ophthalmology. Author manuscript; available in PMC 2014 Jan 23.
Published in final edited form as: Ophthalmology. 2012 Sep; 119(9): 1874–1885. Published online 2012 Jun 15. doi: 10.1016/j.ophtha.2012.03.014
PMCID:
PMC3899891
AbstractArticlePDF–121K
20.
CFH haplotypes and ARMS2, C2, C3, and CFB alleles show association with susceptibility to age-related macular degeneration in Mexicans
Alejandra V. Contreras, Juan Carlos Zenteno, Juan Carlos Fernández-López, Ulises Rodríguez-Corona, Ramcés Falfán-Valencia, Leticia Sebastian, Fabiola Morales, Daniel Ochoa-Contreras, Alessandra Carnevale, Irma Silva-Zolezzi
Mol Vis. 2014; 20: 105–116. Published online 2014 Jan 14.
PMCID:
PMC3891434
AbstractArticlePDF–715K

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