PMC Links for GEO Profiles (Select 96576854) - PMC

Select item 81650301.

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

Abstract Article PDF–2.2M

Select item 75668812.

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

Abstract Article PDF–4.8M

Select item 39420323.

The Imprinted NPAP1 Gene in the Prader–Willi Syndrome Region Belongs to a POM121-Related Family of Retrogenes

Lisa C. Neumann, Nathalie Feiner, Axel Meyer, Karin Buiting, Bernhard Horsthemke

Genome Biol Evol. 2014 Feb; 6(2): 344–351. Published online 2014 Jan 29. doi: 10.1093/gbe/evu019

PMCID:: PMC3942032

Abstract Article PDF–692K

Select item 31780594.

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

Abstract Article PDF–1.0M

Select item 29862735.

A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndrome

Deniz Kanber, Jacques Giltay, Dagmar Wieczorek, Corinna Zogel, Ron Hochstenbach, Almuth Caliebe, Alma Kuechler, Bernhard Horsthemke, Karin Buiting

Eur J Hum Genet. 2009 May; 17(5): 582–590. Published online 2008 Dec 10. doi: 10.1038/ejhg.2008.232

PMCID:: PMC2986273

Abstract Article PDF–274K

Select item 28013236.

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies

Carolien G. F. de Kovel, Holger Trucks, Ingo Helbig, Heather C. Mefford, Carl Baker, Costin Leu, Christian Kluck, Hiltrud Muhle, Sarah von Spiczak, Philipp Ostertag, Tanja Obermeier, Ailing A. Kleefuß-Lie, Kerstin Hallmann, Michael Steffens, Verena Gaus, Karl M. Klein, Hajo M. Hamer, Felix Rosenow, Eva H. Brilstra, Dorothée Kasteleijn-Nolst Trenité, Marielle E. M. Swinkels, Yvonne G. Weber, Iris Unterberger, Fritz Zimprich, Lydia Urak, Martha Feucht, Karoline Fuchs, Rikke S. Møller, Helle Hjalgrim, Peter De Jonghe, Arvid Suls, Ina-Maria Rückert, Heinz-Erich Wichmann, Andre Franke, Stefan Schreiber, Peter Nürnberg, Christian E. Elger, Holger Lerche, Ulrich Stephani, Bobby P. C. Koeleman, Dick Lindhout, Evan E. Eichler, Thomas Sander

Brain. 2010 Jan; 133(1): 23–32. Published online 2009 Oct 20. doi: 10.1093/brain/awp262

PMCID:: PMC2801323

Abstract Article PDF–655K

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