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Items: 1 to 20 of 26

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.
Systematic mapping of genetic interactions for de novo fatty acid synthesis identifies C12orf49 as a regulator of lipid metabolism
Michael Aregger, Keith A. Lawson, Maximillian Billmann, Michael Costanzo, Amy H. Y. Tong, Katherine Chan, Mahfuzur Rahman, Kevin R. Brown, Catherine Ross, Matej Usaj, Lucy Nedyalkova, Olga Sizova, Andrea Habsid, Judy Pawling, Zhen-Yuan Lin, Hala Abdouni, Cassandra J. Wong, Alexander Weiss, Patricia Mero, James W. Dennis, Anne-Claude Gingras, Chad L. Myers, Brenda J. Andrews, Charles Boone, Jason Moffat
Nat Metab. Author manuscript; available in PMC 2020 Dec 1.
Published in final edited form as: Nat Metab. 2020 Jun; 2(6): 499–513. Published online 2020 Jun 1. doi: 10.1038/s42255-020-0211-z
PMCID:
PMC7566881
AbstractArticlePDF–4.8M
3.
Three New Mutations and Mild, Asymmetrical Phenotype in the Highly Distinctive LAMM Syndrome: A Report of Eight Further Cases
Amina Al Yassin, Felice D’Arco, Matías Morín, Waheeda Pagarkar, Katherine Harrop-Griffiths, Azhar Shaida, Elena Fernández, Tom Cullup, Bianca De-Souza, Miguel Angel Moreno-Pelayo, Maria Bitner-Glindzicz
Genes (Basel) 2019 Jul; 10(7): 529. Published online 2019 Jul 12. doi: 10.3390/genes10070529
PMCID:
PMC6678228
AbstractArticlePDF–11M
4.
HER2-overexpressing breast cancers amplify FGFR signaling upon acquisition of resistance to dual therapeutic blockade of HER2
Ariella B. Hanker, Joan T. Garrett, Mónica Valeria Estrada, Preston D. Moore, Paula González Ericsson, James P. Koch, Emma Langley, Sharat Singh, Phillip S. Kim, Garrett M. Frampton, Eric Sanford, Philip Owens, Jennifer Becker, M. Reid Groseclose, Stephen Castellino, Heikki Joensuu, Jens Huober, Jan C. Brase, Samira Majjaj, Sylvain Brohée, David Venet, David Brown, José Baselga, Martine Piccart, Christos Sotiriou, Carlos L. Arteaga
Clin Cancer Res. Author manuscript; available in PMC 2018 Aug 1.
Published in final edited form as: Clin Cancer Res. 2017 Aug 1; 23(15): 4323–4334. Published online 2017 Apr 5. doi: 10.1158/1078-0432.CCR-16-2287
Correction in:
Clin Cancer Res. 2019 Feb 15; 25(4): 1434.
PMCID:
PMC5540793
AbstractArticlePDF–1.2M
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.
Mitochondrial mass, a new metabolic biomarker for stem-like cancer cells: Understanding WNT/FGF-driven anabolic signaling
Rebecca Lamb, Gloria Bonuccelli, Béla Ozsvári, Maria Peiris-Pagès, Marco Fiorillo, Duncan L. Smith, Generoso Bevilacqua, Chiara Maria Mazzanti, Liam A. McDonnell, Antonio Giuseppe Naccarato, Maybo Chiu, Luke Wynne, Ubaldo E. Martinez-Outschoorn, Federica Sotgia, Michael P. Lisanti
Oncotarget. 2015 Oct 13; 6(31): 30453–30471. Published online 2015 Sep 28. doi: 10.18632/oncotarget.5852
PMCID:
PMC4741544
AbstractArticlePDF–3.8M
7.
Fibroblast Growth Factor-23 and Incident Atrial Fibrillation: The Multi-Ethnic Study of Atherosclerosis (MESA) and the Cardiovascular Health Study (CHS)
Jehu S. Mathew, Michael C. Sachs, Ronit Katz, Kristen K. Patton, Susan R. Heckbert, Andrew N. Hoofnagle, Alvaro Alonso, Michel Chonchol, Rajat Deo, Joachim H. Ix, David S. Siscovick, Bryan Kestenbaum, Ian H. de Boer
Circulation. Author manuscript; available in PMC 2015 Jul 22.
Published in final edited form as: Circulation. 2014 Jul 22; 130(4): 298–307. Published online 2014 Jun 11. doi: 10.1161/CIRCULATIONAHA.113.005499
PMCID:
PMC4108550
AbstractArticlePDF–159K
8.
Genome-wide association study identifies five new breast cancer susceptibility loci
Clare Turnbull, Shahana Ahmed, Jonathan Morrison, David Pernet, Anthony Renwick, Mel Maranian, Sheila Seal, Maya Ghoussaini, Sarah Hines, Catherine S Healey, Deborah Hughes, Margaret Warren-Perry, William Tapper, Diana Eccles, D Gareth Evans, The Breast Cancer Susceptibility Collaboration (UK), Maartje Hooning, Mieke Schutte, Ans van den Ouweland, Richard Houlston, Gillian Ross, Cordelia Langford, Paul D P Pharoah, Michael R Stratton, Alison M Dunning, Nazneen Rahman, Douglas F Easton
Nat Genet. Author manuscript; available in PMC 2013 Apr 23.
Published in final edited form as: Nat Genet. 2010 Jun; 42(6): 504–507. Published online 2010 May 9. doi: 10.1038/ng.586
PMCID:
PMC3632836
AbstractArticlePDF–454K
9.
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
10.
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome
Saima Riazuddin, Zubair M Ahmed, Rashmi S Hegde, Shaheen N Khan, Idrees Nasir, Uzma Shaukat, Sheikh Riazuddin, John A Butman, Andrew J Griffith, Thomas B Friedman, Byung Yoon Choi
BMC Med Genet. 2011; 12: 21. Published online 2011 Feb 9. doi: 10.1186/1471-2350-12-21
PMCID:
PMC3042908
AbstractArticlePDF–1.6M
11.
Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3)
Osama Alsmadi, Brian F Meyer, Fowzan Alkuraya, Salma Wakil, Fadi Alkayal, Haya Al-Saud, Khushnooda Ramzan, MoeenAldeen Al-Sayed
Eur J Hum Genet. 2009 Jan; 17(1): 14–21. Published online 2008 Aug 13. doi: 10.1038/ejhg.2008.141
PMCID:
PMC2985964
AbstractArticlePDF–310K
12.
The Transition from Radial Glial to Intermediate Progenitor Cell Is Inhibited by FGF Signaling during Corticogenesis
Wenfei Kang, Li Chin Wong, Song-Hai Shi, Jean M. Hébert
J Neurosci. 2009 Nov 18; 29(46): 14571–14580. doi: 10.1523/JNEUROSCI.3844-09.2009
PMCID:
PMC2826126
AbstractArticlePDF–2.0M
13.
Modulation of Fgf3 dosage in mouse and men mirrors evolution of mammalian dentition
Cyril Charles, Vincent Lazzari, Paul Tafforeau, Thomas Schimmang, Mustafa Tekin, Ophir Klein, Laurent Viriot
Proc Natl Acad Sci U S A. 2009 Dec 29; 106(52): 22364–22368. Published online 2009 Dec 15. doi: 10.1073/pnas.0910086106
PMCID:
PMC2799759
AbstractArticlePDF–2.0M
14.
High-Density Association Study of 383 Candidate Genes for Volumetric BMD at the Femoral Neck and Lumbar Spine Among Older Men
Laura M. Yerges, Lambertus Klei, Jane A. Cauley, Kathryn Roeder, Candace M. Kammerer, Susan P. Moffett, Kristine E. Ensrud, Cara S. Nestlerode, Lynn M. Marshall, Andrew R. Hoffman, Cora Lewis, Thomas F. Lang, Elizabeth Barrett-Connor, Robert E. Ferrell, Eric S. Orwoll, Joseph M. Zmuda
J Bone Miner Res. 2009 Dec; 24(12): 2039–2049. Published online 2009 May 18. doi: 10.1359/JBMR.090524
PMCID:
PMC2791518
AbstractArticlePDF–759K
15.
A RECQ5–RNA polymerase II association identified by targeted proteomic analysis of human chromatin
Ozan Aygün, Jesper Svejstrup, Yilun Liu
Proc Natl Acad Sci U S A. 2008 Jun 24; 105(25): 8580–8584. Published online 2008 Jun 18. doi: 10.1073/pnas.0804424105
PMCID:
PMC2430918
AbstractArticlePDF–696K
16.
A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)
David Melzer, John R. B. Perry, Dena Hernandez, Anna-Maria Corsi, Kara Stevens, Ian Rafferty, Fulvio Lauretani, Anna Murray, J. Raphael Gibbs, Giuseppe Paolisso, Sajjad Rafiq, Javier Simon-Sanchez, Hana Lango, Sonja Scholz, Michael N. Weedon, Sampath Arepalli, Neil Rice, Nicole Washecka, Alison Hurst, Angela Britton, William Henley, Joyce van de Leemput, Rongling Li, Anne B. Newman, Greg Tranah, Tamara Harris, Vijay Panicker, Colin Dayan, Amanda Bennett, Mark I. McCarthy, Aimo Ruokonen, Marjo-Riitta Jarvelin, Jack Guralnik, Stefania Bandinelli, Timothy M. Frayling, Andrew Singleton, Luigi Ferrucci
PLoS Genet. 2008 May; 4(5): e1000072. Published online 2008 May 9. doi: 10.1371/journal.pgen.1000072
PMCID:
PMC2362067
AbstractArticlePDF–442K
17.
Receptor Specificity of the Fibroblast Growth Factor Family: THE COMPLETE MAMMALIAN FGF FAMILY
Xiuqin Zhang, Omar A. Ibrahimi, Shaun K. Olsen, Hisashi Umemori, Moosa Mohammadi, David M. Ornitz
J Biol Chem. Author manuscript; available in PMC 2007 Nov 16.
Published in final edited form as: J Biol Chem. 2006 Jun 9; 281(23): 15694–15700. Published online 2006 Apr 4. doi: 10.1074/jbc.M601252200
PMCID:
PMC2080618
AbstractArticlePDF–1.1M
18.
Impaired FGF signaling contributes to cleft lip and palate
Bridget M. Riley, M. Adela Mansilla, Jinghong Ma, Sandra Daack-Hirsch, Brion S. Maher, Lisa M. Raffensperger, Erilynn T. Russo, Alexandre R. Vieira, Catherine Dodé, Moosa Mohammadi, Mary L. Marazita, Jeffrey C. Murray
Proc Natl Acad Sci U S A. 2007 Mar 13; 104(11): 4512–4517. Published online 2007 Mar 6. doi: 10.1073/pnas.0607956104
PMCID:
PMC1810508
AbstractArticlePDF–1.7M
19.
Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia
Mustafa  Tekin, Burcu Öztürk  Hişmi, Suat  Fitoz, Hilal  Özdağ, Filiz Başak  Cengiz, Aslı  Sırmacı, İdil  Aslan, Bora  İnceoğlu, E. Berrin  Yüksel-Konuk, Seda Taşır  Yılmaz, Öztan  Yasun, Nejat  Akar
Am J Hum Genet. 2007 Feb; 80(2): 338–344. Published online 2006 Dec 27. doi: 10.1086/510920
PMCID:
PMC1785350
AbstractArticlePDF–1.3M
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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