PMC Links for GEO Profiles (Select 108344422) - PMC

Select item 83641811.

Protein interaction landscapes revealed by advanced in vivo cross-linking–mass spectrometry

Andrew Wheat, Clinton Yu, Xiaorong Wang, Anthony M. Burke, Ilan E. Chemmama, Robyn M. Kaake, Peter Baker, Scott D. Rychnovsky, Jing Yang, Lan Huang

Proc Natl Acad Sci U S A. 2021 Aug 10; 118(32): e2023360118. Published online 2021 Aug 4. doi: 10.1073/pnas.2023360118

PMCID:: PMC8364181

Abstract Article PDF–3.0M

Select item 64864002.

Genome-wide association study of recurrent early-onset major depressive disorder

J Shi, JB Potash, JA Knowles, MM Weissman, W Coryell, WA Scheftner, WB Lawson, JR DePaulo, Jr., PV Gejman, AR Sanders, JK Johnson, P Adams, S Chaudhury, D Jancic, O Evgrafov, A Zvinyatskovskiy, N Ertman, M Gladis, K Neimanas, M Goodell, N Hale, N Ney, R Verma, D Mirel, P Holmans, DF Levinson

Mol Psychiatry. Author manuscript; available in PMC 2019 Apr 26.

Published in final edited form as: Mol Psychiatry. 2011 Feb; 16(2): 193–201. Published online 2010 Feb 2. doi: 10.1038/mp.2009.124

PMCID:: PMC6486400

Abstract Article PDF–1.0M

Select item 59674073.

Putative Digenic Inheritance of Heterozygous RP1L1 and C2orf71 Null Mutations in Syndromic Retinal Dystrophy

Yangfan P. Liu, Daniëlle G.M. Bosch, Anna M. Siemiatkowska, Nanna Dahl Rendtorff, F. Nienke Boonstra, Claes Möller, Lisbeth Tranebjærg, Nicholas Katsanis, Frans P.M. Cremers

Ophthalmic Genet. Author manuscript; available in PMC 2018 May 24.

Published in final edited form as: Ophthalmic Genet. 2017 Mar-Apr; 38(2): 127–132. Published online 2016 Mar 30. doi: 10.3109/13816810.2016.1151898

PMCID:: PMC5967407

Abstract Article PDF–559K

Select item 48691704.

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

Abstract Article PDF–2.0M

Select item 31780595.

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 28690066.

Mutations in C2ORF71 Cause Autosomal-Recessive Retinitis Pigmentosa

Rob W.J. Collin, Christine Safieh, Karin W. Littink, Stavit A. Shalev, Hanna J. Garzozi, Leah Rizel, Anan H. Abbasi, Frans P.M. Cremers, Anneke I. den Hollander, B. Jeroen Klevering, Tamar Ben-Yosef

Am J Hum Genet. 2010 May 14; 86(5): 783–788. doi: 10.1016/j.ajhg.2010.03.016

PMCID:: PMC2869006

Abstract Article PDF–715K

Select item 28689977.

Discovery and Functional Analysis of a Retinitis Pigmentosa Gene, C2ORF71

Darryl Y. Nishimura, Lisa M. Baye, Rahat Perveen, Charles C. Searby, Almudena Avila-Fernandez, Ines Pereiro, Carmen Ayuso, Diana Valverde, Paul N. Bishop, Forbes D.C. Manson, Jill Urquhart, Edwin M. Stone, Diane C. Slusarski, Graeme C.M. Black, Val C. Sheffield

Am J Hum Genet. 2010 May 14; 86(5): 686–695. doi: 10.1016/j.ajhg.2010.03.005

PMCID:: PMC2868997

Abstract Article PDF–1.4M

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