PMC Links for GEO Profiles (Select 68838500) - PMC

Select item 101516151.

Cross-linking mass spectrometry discovers, evaluates, and corroborates structures and protein–protein interactions in the human cell

Tara K. Bartolec, Xabier Vázquez-Campos, Alexander Norman, Clement Luong, Marcus Johnson, Richard J. Payne, Marc R. Wilkins, Joel P. Mackay, Jason K. K. Low

Proc Natl Acad Sci U S A. 2023 Apr 25; 120(17): e2219418120. Published online 2023 Apr 18. doi: 10.1073/pnas.2219418120

PMCID:: PMC10151615

Abstract Article PDF–2.9M

Select item 81650302.

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 59921043.

Comparative Protein Interaction Network Analysis Identifies Shared and Distinct Functions for the Human ROCO Proteins

James E. Tomkins, Sybille Dihanich, Alexandra Beilina, Raffaele Ferrari, Nicolò Ilacqua, Mark R. Cookson, Patrick A. Lewis, Claudia Manzoni

Proteomics. 2018 May; 18(10): 1700444. Published online 2018 Apr 17. doi: 10.1002/pmic.201700444

PMCID:: PMC5992104

Abstract Article PDF–1.2M

Select item 52152304.

Clinical Characteristics, Mutation Spectrum, and Prevalence of Åland Eye Disease/Incomplete Congenital Stationary Night Blindness in Denmark

Marianne N. Hove, Kevser Z. Kilic-Biyik, Alana Trotter, Karen Grønskov, Birgit Sander, Michael Larsen, Joseph Carroll, Torben Bech-Hansen, Thomas Rosenberg

Invest Ophthalmol Vis Sci. 2016 Dec; 57(15): 6861–6869. doi: 10.1167/iovs.16-19445

PMCID:: PMC5215230

Abstract Article PDF–1.1M

Select item 49570505.

Characterization of C-terminal Splice Variants of Ca_v1.4 Ca²⁺ Channels in Human Retina

Françoise Haeseleer, Brittany Williams, Amy Lee

J Biol Chem. 2016 Jul 22; 291(30): 15663–15673. Published online 2016 May 17. doi: 10.1074/jbc.M116.731737

PMCID:: PMC4957050

Abstract Article PDF–741K

Select item 48487626.

Pooled‐matrix protein interaction screens using Barcode Fusion Genetics

Nozomu Yachie, Evangelia Petsalaki, Joseph C Mellor, Jochen Weile, Yves Jacob, Marta Verby, Sedide B Ozturk, Siyang Li, Atina G Cote, Roberto Mosca, Jennifer J Knapp, Minjeong Ko, Analyn Yu, Marinella Gebbia, Nidhi Sahni, Song Yi, Tanya Tyagi, Dayag Sheykhkarimli, Jonathan F Roth, Cassandra Wong, Louai Musa, Jamie Snider, Yi‐Chun Liu, Haiyuan Yu, Pascal Braun, Igor Stagljar, Tong Hao, Michael A Calderwood, Laurence Pelletier, Patrick Aloy, David E Hill, Marc Vidal, Frederick P Roth

Mol Syst Biol. 2016 Apr; 12(4): 863. Published online 2016 Apr 23. doi: 10.15252/msb.20156660

PMCID:: PMC4848762

Abstract Article PDF–2.8M

Select item 34762987.

Complex Regulation of Voltage-dependent Activation and Inactivation Properties of Retinal Voltage-gated Cav1.4 L-type Ca²⁺ Channels by Ca²⁺-binding Protein 4 (CaBP4)

Lior Shaltiel, Christos Paparizos, Stefanie Fenske, Sami Hassan, Christian Gruner, Katrin Rötzer, Martin Biel, Christian A. Wahl-Schott

J Biol Chem. 2012 Oct 19; 287(43): 36312–36321. Published online 2012 Aug 30. doi: 10.1074/jbc.M112.392811

PMCID:: PMC3476298

Abstract Article PDF–1.9M

Select item 31780598.

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 28201089.

A null mutation in CABP4 causes Leber’s congenital amaurosis-like phenotype

Mohammed A. Aldahmesh, Mohammed Al-Owain, Faisal Alqahtani, Salwa Hazzaa, Fowzan S. Alkuraya

Mol Vis. 2010; 16: 207–212. Published online 2010 Feb 10.

PMCID:: PMC2820108

Abstract Article PDF–1.3M

Select item 270631710.

Membrane targeting of the EF-hand containing calcium-sensing proteins CaBP7 and CaBP8

Hannah V. McCue, Robert D. Burgoyne, Lee P. Haynes

Biochem Biophys Res Commun. 2009 Mar 20; 380(4): 825–831. doi: 10.1016/j.bbrc.2009.01.177

PMCID:: PMC2706317

Abstract Article

Select item 159256811.

Mutations in CABP4, the Gene Encoding the Ca²⁺-Binding Protein 4, Cause Autosomal Recessive Night Blindness

Christina Zeitz, Barbara Kloeckener-Gruissem, Ursula Forster, Susanne Kohl, István Magyar, Bernd Wissinger, Gábor Mátyás, François-Xavier Borruat, Daniel F. Schorderet, Eberhart Zrenner, Francis L. Munier, Wolfgang Berger

Am J Hum Genet. 2006 Oct; 79(4): 657–667. Published online 2006 Aug 23. doi: 10.1086/508067

PMCID:: PMC1592568

Abstract Article PDF–2.1M

Select item 136446912.

Five Members of a Novel Ca²⁺-binding Protein (CABP) Subfamily with Similarity to Calmodulin

Françoise Haeseleer, Izabela Sokal, Christophe L. M. J. Verlinde, Hediye Erdjument-Bromage, Paul Tempst, Alexey N. Pronin, Jeffrey L. Benovic, Robert N. Fariss, Krzysztof Palczewski

J Biol Chem. Author manuscript; available in PMC 2006 Feb 13.

Published in final edited form as: J Biol Chem. 2000 Jan 14; 275(2): 1247–1260. doi: 10.1074/jbc.275.2.1247