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Items: 16

1.
Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration
Laura Lorés-Motta, Anna E. van Beek, Esther Willems, Judith Zandstra, Gerard van Mierlo, Alfred Einhaus, Jean-Luc Mary, Corinne Stucki, Bjorn Bakker, Carel B. Hoyng, Sascha Fauser, Simon J. Clark, Marien I. de Jonge, Everson Nogoceke, Elod Koertvely, Ilse Jongerius, Taco W. Kuijpers, Anneke I. den Hollander
Am J Hum Genet. 2021 Aug 5; 108(8): 1367–1384. Published online 2021 Jul 13. doi: 10.1016/j.ajhg.2021.06.002
PMCID:
PMC8387287
AbstractArticlePDF–2.4M
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.
Serum FHR1 binding to necrotic-type cells activates monocytic inflammasome and marks necrotic sites in vasculopathies
Sarah Irmscher, Silke R. Brix, Svante L. H. Zipfel, Luke D. Halder, Sibel Mutlutürk, Sonia Wulf, Evaldas Girdauskas, Hermann Reichenspurner, Rolf A. K. Stahl, Berit Jungnickel, Thorsten Wiech, Peter F. Zipfel, Christine Skerka
Nat Commun. 2019; 10: 2961. Published online 2019 Jul 4. doi: 10.1038/s41467-019-10766-0
PMCID:
PMC6609651
AbstractArticlePDF–2.4M
4.
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
5.
Sequence and Expression of Complement Factor H Gene Cluster Variants and Their Roles in Age-Related Macular Degeneration Risk
Anne E. Hughes, Stephen Bridgett, Weihua Meng, Mingyao Li, Christine A. Curcio, Dwight Stambolian, Declan T. Bradley
Invest Ophthalmol Vis Sci. 2016 May; 57(6): 2763–2769. Published online 2016 May 19. doi: 10.1167/iovs.15-18744
PMCID:
PMC4884056
AbstractArticlePDF–322K
6.
Atypical haemolytic-uraemic syndrome due to heterozygous mutations of CFH/CFHR1–3 and complement factor H 479
Preeti Chaudhary, Mehmet Hepgur, Sarmen Sarkissian, Richard J.H. Smith, Ilene C. Weitz
Blood Transfus. 2014 Jan; 12(1): 111–113. doi: 10.2450/2013.0107-13
PMCID:
PMC3926711
ArticlePDF–514K
7.
Complement factor H–related hybrid protein deregulates complement in dense deposit disease
Qian Chen, Michael Wiesener, Hannes U. Eberhardt, Andrea Hartmann, Barbara Uzonyi, Michael Kirschfink, Kerstin Amann, Maike Buettner, Tim Goodship, Christian Hugo, Christine Skerka, Peter F. Zipfel
J Clin Invest. 2014 Jan 2; 124(1): 145–155. Published online 2013 Dec 16. doi: 10.1172/JCI71866
PMCID:
PMC3871254
AbstractArticlePDF–1.7M
8.
Human Factor H-Related Protein 2 (CFHR2) Regulates Complement Activation
Hannes U. Eberhardt, Denise Buhlmann, Peter Hortschansky, Qian Chen, Sascha Böhm, Markus J. Kemper, Reinhard Wallich, Andrea Hartmann, Teresia Hallström, Peter F. Zipfel, Christine Skerka
PLoS One. 2013; 8(11): e78617. Published online 2013 Nov 18. doi: 10.1371/journal.pone.0078617
PMCID:
PMC3832495
AbstractArticlePDF–3.3M
9.
C3 glomerulopathy–associated CFHR1 mutation alters FHR oligomerization and complement regulation
Agustín Tortajada, Hugo Yébenes, Cynthia Abarrategui-Garrido, Jaouad Anter, Jesús M. García-Fernández, Rubén Martínez-Barricarte, María Alba-Domínguez, Talat H. Malik, Rafael Bedoya, Rocío Cabrera Pérez, Margarita López Trascasa, Matthew C. Pickering, Claire L. Harris, Pilar Sánchez-Corral, Oscar Llorca, Santiago Rodríguez de Córdoba
J Clin Invest. 2013 Jun 3; 123(6): 2434–2446. Published online 2013 May 24. doi: 10.1172/JCI68280
PMCID:
PMC3668852
AbstractArticlePDF–3.9M
10.
Dimerization of complement factor H-related proteins modulates complement activation in vivo
Elena Goicoechea de Jorge, Joseph J. E. Caesar, Talat H. Malik, Mitali Patel, Matthew Colledge, Steven Johnson, Svetlana Hakobyan, B. Paul Morgan, Claire L. Harris, Matthew C. Pickering, Susan M. Lea
Proc Natl Acad Sci U S A. 2013 Mar 19; 110(12): 4685–4690. Published online 2013 Mar 4. doi: 10.1073/pnas.1219260110
PMCID:
PMC3606973
AbstractArticlePDF–731K
11.
Interactions of Pathological Hallmark Proteins: TUBULIN POLYMERIZATION PROMOTING PROTEIN/p25, β-AMYLOID, AND α-SYNUCLEIN
Judit Oláh, Orsolya Vincze, Dezső Virók, Dóra Simon, Zsolt Bozsó, Natália Tőkési, István Horváth, Emma Hlavanda, János Kovács, Anna Magyar, Mária Szűcs, Ferenc Orosz, Botond Penke, Judit Ovádi
J Biol Chem. 2011 Sep 30; 286(39): 34088–34100. Published online 2011 Aug 8. doi: 10.1074/jbc.M111.243907
PMCID:
PMC3190826
AbstractArticlePDF–5.7M
12.
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
13.
The NEI/NCBI dbGAP database: Genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration
Hong Zhang, Margaux A Morrison, Andy DeWan, Scott Adams, Michael Andreoli, Nancy Huynh, Maureen Regan, Alison Brown, Joan W Miller, Ivana K Kim, Josephine Hoh, Margaret M DeAngelis
BMC Med Genet. 2008; 9: 51. Published online 2008 Jun 9. doi: 10.1186/1471-2350-9-51
PMCID:
PMC2441616
AbstractArticlePDF–1.6M
14.
Extended Haplotypes in the Complement Factor H (CFH) and CFH-related (CFHR) Family of Genes that Protect against Age-related Macular Degeneration: Identification, Ethnic Distribution and Evolutionary Implications
Gregory S. Hageman, Lisa S. Hancox, Andrew J. Taiber, Karen M. Gehrs, Don H. Anderson, Lincoln V. Johnson, Monte J. Radeke, David Kavanagh, Anna Richards, John Atkinson, Seppo Meri, Julie Bergeron, Jana Zernant, Joanna Merriam, Bert Gold, Rando Allikmets, Michael Dean, the AMD Clinical Study Group
Ann Med. Author manuscript; available in PMC 2007 Jul 2.
Published in final edited form as: Ann Med. 2006; 38(8): 592–604.
PMCID:
PMC1905836
AbstractArticlePDF–470K
15.
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
16.
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences
Mammalian Gene Collection (MGC) Program Team
Proc Natl Acad Sci U S A. 2002 Dec 24; 99(26): 16899–16903. Published online 2002 Dec 11. doi: 10.1073/pnas.242603899
PMCID:
PMC139241
AbstractArticlePDF–118K

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