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Items: 1 to 20 of 24

1.
Genome-wide screening for the G-protein-coupled receptor (GPCR) pathway-related therapeutic gene RGS19 (regulator of G protein signaling 19) in bladder cancer
Yue Liu, Weiming Lou, Guang Chen, Bing Ding, Jin Kuang, Yize Zhang, Cong Wang, Sainan Duan, Ying Deng, Xiongbing Lu
Bioengineered. 2021; 12(1): 5892–5903. Published online 2021 Sep 5. doi: 10.1080/21655979.2021.1971035
PMCID:
PMC8806424
AbstractArticlePDF–2.7M
2.
5-HT1A receptor-mediated phosphorylation of extracellular signal-regulated kinases (ERK1/2) is modulated by regulator of G protein signaling protein 19
Qin Wang, Akiko Terauchi, Christopher H. Yee, Hisashi Umemori, John R. Traynor
Cell Signal. Author manuscript; available in PMC 2021 Apr 3.
Published in final edited form as: Cell Signal. 2014 Sep; 26(9): 1846–1852. Published online 2014 May 2. doi: 10.1016/j.cellsig.2014.04.017
PMCID:
PMC8019269
AbstractArticlePDF–700K
3.
Clathrin-coated vesicles bearing GAIP possess GTPase-activating protein activity in vitro
Thierry Fischer, Eric Elenko, J. Michael McCaffery, Luc DeVries, Marilyn Gist Farquhar
Proc Natl Acad Sci U S A. 1999 Jun 8; 96(12): 6722–6727. doi: 10.1073/pnas.96.12.6722
PMCID:
PMC21982
AbstractArticlePDF–283K
4.
RGS-GAIP, a GTPase-activating Protein for Gαi Heterotrimeric G Proteins, Is Located on Clathrin-coated Vesicles
Luc De Vries, Eric Elenko, J. Michael McCaffery, Thierry Fischer, Laura Hubler, Tammie McQuistan, Nicki Watson, Marilyn G. Farquhar
Mol Biol Cell. 1998 May; 9(5): 1123–1134. doi: 10.1091/mbc.9.5.1123
PMCID:
PMC25334
AbstractArticlePDF–1.1M
5.
Pediatric Encephalopathy: Clinical, Biochemical and Cellular Insights into the Role of Gln52 of GNAO1 and GNAI1 for the Dominant Disease
Gonzalo P. Solis, Tatyana V. Kozhanova, Alexey Koval, Svetlana S. Zhilina, Tatyana I. Mescheryakova, Aleksandr A. Abramov, Evgeny V. Ishmuratov, Ekaterina S. Bolshakova, Karina V. Osipova, Sergey O. Ayvazyan, Sébastien Lebon, Ilya V. Kanivets, Denis V. Pyankov, Sabina Troccaz, Denis N. Silachev, Nikolay N. Zavadenko, Andrey G. Prityko, Vladimir L. Katanaev
Cells. 2021 Oct; 10(10): 2749. Published online 2021 Oct 14. doi: 10.3390/cells10102749
PMCID:
PMC8535069
AbstractArticlePDF–2.4M
6.
Profiling of Childhood Adversity-Associated DNA Methylation Changes in Alcoholic Patients and Healthy Controls
Huiping Zhang, Fan Wang, Henry R. Kranzler, Hongyu Zhao, Joel Gelernter
PLoS One. 2013; 8(6): e65648. Published online 2013 Jun 14. doi: 10.1371/journal.pone.0065648
PMCID:
PMC3683055
AbstractArticlePDF–758K
7.
GIPC Recruits GAIP (RGS19) To Attenuate Dopamine D2 Receptor Signaling
Freddy Jeanneteau, Olivier Guillin, Jorge Diaz, Nathalie Griffon, Pierre Sokoloff
Mol Biol Cell. 2004 Nov; 15(11): 4926–4937. doi: 10.1091/mbc.E04-04-0285
PMCID:
PMC524745
AbstractArticlePDF–1.1M
8.
GAIP, a protein that specifically interacts with the trimeric G protein G alpha i3, is a member of a protein family with a highly conserved core domain.
L De Vries, M Mousli, A Wurmser, M G Farquhar
Proc Natl Acad Sci U S A. 1995 Dec 5; 92(25): 11916–11920. doi: 10.1073/pnas.92.25.11916
PMCID:
PMC40514
SummaryPage BrowsePDF–1.2M
9.
The PDZ Protein GIPC Regulates Trafficking of the LPA1 Receptor from APPL Signaling Endosomes and Attenuates the Cell’s Response to LPA
Tal Varsano, Vanessa Taupin, Lixia Guo, Oscar Y. Baterina, Jr, Marilyn G. Farquhar
PLoS One. 2012; 7(11): e49227. Published online 2012 Nov 8. doi: 10.1371/journal.pone.0049227
PMCID:
PMC3493537
AbstractArticlePDF–3.1M
10.
Membrane-associated GAIP is a phosphoprotein and can be phosphorylated by clathrin-coated vesicles
Thierry Fischer, Eric Elenko, Lei Wan, Gary Thomas, Marilyn Gist Farquhar
Proc Natl Acad Sci U S A. 2000 Apr 11; 97(8): 4040–4045. doi: 10.1073/pnas.97.8.4040
PMCID:
PMC18141
AbstractArticlePDF–204K
11.
GIPC, a PDZ domain containing protein, interacts specifically with the C terminus of RGS-GAIP
Luc De Vries, Xiaojing Lou, Grace Zhao, Bin Zheng, Marilyn Gist Farquhar
Proc Natl Acad Sci U S A. 1998 Oct 13; 95(21): 12340–12345. doi: 10.1073/pnas.95.21.12340
PMCID:
PMC22833
AbstractArticlePDF–381K
12.
MIR16, a putative membrane glycerophosphodiester phosphodiesterase, interacts with RGS16
Bin Zheng, Dan Chen, Marilyn Gist Farquhar
Proc Natl Acad Sci U S A. 2000 Apr 11; 97(8): 3999–4004. doi: 10.1073/pnas.97.8.3999
PMCID:
PMC18131
AbstractArticlePDF–278K
13.
Interactions of GIPC with Dopamine D2, D3 but not D4 Receptors Define a Novel Mode of Regulation of G Protein-coupled Receptors
Freddy Jeanneteau, Jorge Diaz, Pierre Sokoloff, Nathalie Griffon
Mol Biol Cell. 2004 Feb; 15(2): 696–705. doi: 10.1091/mbc.E03-05-0293
PMCID:
PMC329290
AbstractArticlePDF–825K
14.
Promotion of Gαi3 subunit down-regulation by GIPN, a putative E3 ubiquitin ligase that interacts with RGS-GAIP
Thierry Fischer, Luc De Vries, Timo Meerloo, Marilyn Gist Farquhar
Proc Natl Acad Sci U S A. 2003 Jul 8; 100(14): 8270–8275. Published online 2003 Jun 25. doi: 10.1073/pnas.1432965100
PMCID:
PMC166218
AbstractArticlePDF–501K
15.
GIPC and GAIP Form a Complex with TrkA: A Putative Link between G Protein and Receptor Tyrosine Kinase Pathways
Xiaojing Lou, Hiroko Yano, Francis Lee, Moses V. Chao, Marilyn Gist Farquhar
Mol Biol Cell. 2001 Mar; 12(3): 615–627. doi: 10.1091/mbc.12.3.615
PMCID:
PMC30968
AbstractArticlePDF–1.7M
16.
GAIP is membrane-anchored by palmitoylation and interacts with the activated (GTP-bound) form of Gαi subunits
Luc De Vries, Eric Elenko, Laura Hubler, Teresa L. Z. Jones, Marilyn Gist Farquhar
Proc Natl Acad Sci U S A. 1996 Dec 24; 93(26): 15203–15208. doi: 10.1073/pnas.93.26.15203
PMCID:
PMC26381
AbstractArticlePDF–331K
17.
Association Study of 182 Candidate Genes in Anorexia Nervosa
Andrea Poyastro Pinheiro, Cynthia M. Bulik, Laura M. Thornton, Patrick F. Sullivan, Tammy L. Root, Cinnamon S. Bloss, Wade H. Berrettini, Nicholas J. Schork, Walter H. Kaye, Andrew W. Bergen, Pierre Magistretti, Harry Brandt, Steve Crawford, Scott Crow, Manfred M. Fichter, David Goldman, Katherine A. Halmi, Craig Johnson, Allan S. Kaplan, Pamela K. Keel, Kelly L. Klump, Maria La Via, James E. Mitchell, Michael Strober, Alessandro Rotondo, Janet Treasure, D. Blake Woodside
Am J Med Genet B Neuropsychiatr Genet. Author manuscript; available in PMC 2010 Oct 25.
Published in final edited form as: Am J Med Genet B Neuropsychiatr Genet. 2010 Jul; 153B(5): 1070–1080. doi: 10.1002/ajmg.b.31082
PMCID:
PMC2963154
AbstractArticlePDF–315K
18.
The RNA-mediated estrogen receptor α interactome of hormone-dependent human breast cancer cell nuclei
Giovanni Nassa, Giorgio Giurato, Annamaria Salvati, Valerio Gigantino, Giovanni Pecoraro, Jessica Lamberti, Francesca Rizzo, Tuula A. Nyman, Roberta Tarallo, Alessandro Weisz
Sci Data. 2019; 6: 173. Published online 2019 Sep 16. doi: 10.1038/s41597-019-0179-2
PMCID:
PMC6746822
AbstractArticlePDF–2.0M
19.
Quantitative mapping of RNA-mediated nuclear estrogen receptor β interactome in human breast cancer cells
Giorgio Giurato, Giovanni Nassa, Annamaria Salvati, Elena Alexandrova, Francesca Rizzo, Tuula A. Nyman, Alessandro Weisz, Roberta Tarallo
Sci Data. 2018; 5: 180031. Published online 2018 Mar 6. doi: 10.1038/sdata.2018.31
PMCID:
PMC5839158
AbstractArticlePDF–1.9M
20.
A reference map of the human binary protein interactome
Katja Luck, Dae-Kyum Kim, Luke Lambourne, Kerstin Spirohn, Bridget E. Begg, Wenting Bian, Ruth Brignall, Tiziana Cafarelli, Francisco J. Campos-Laborie, Benoit Charloteaux, Dongsic Choi, Atina G. Coté, Meaghan Daley, Steven Deimling, Alice Desbuleux, Amélie Dricot, Marinella Gebbia, Madeleine F. Hardy, Nishka Kishore, Jennifer J. Knapp, István A. Kovács, Irma Lemmens, Miles W. Mee, Joseph C. Mellor, Carl Pollis, Carles Pons, Aaron D. Richardson, Sadie Schlabach, Bridget Teeking, Anupama Yadav, Mariana Babor, Dawit Balcha, Omer Basha, Christian Bowman-Colin, Suet-Feung Chin, Soon Gang Choi, Claudia Colabella, Georges Coppin, Cassandra D’Amata, David De Ridder, Steffi De Rouck, Miquel Duran-Frigola, Hanane Ennajdaoui, Florian Goebels, Liana Goehring, Anjali Gopal, Ghazal Haddad, Elodie Hatchi, Mohamed Helmy, Yves Jacob, Yoseph Kassa, Serena Landini, Roujia Li, Natascha van Lieshout, Andrew MacWilliams, Dylan Markey, Joseph N. Paulson, Sudharshan Rangarajan, John Rasla, Ashyad Rayhan, Thomas Rolland, Adriana San-Miguel, Yun Shen, Dayag Sheykhkarimli, Gloria M. Sheynkman, Eyal Simonovsky, Murat Taşan, Alexander Tejeda, Vincent Tropepe, Jean-Claude Twizere, Yang Wang, Robert J. Weatheritt, Jochen Weile, Yu Xia, Xinping Yang, Esti Yeger-Lotem, Quan Zhong, Patrick Aloy, Gary D. Bader, Javier De Las Rivas, Suzanne Gaudet, Tong Hao, Janusz Rak, Jan Tavernier, David E. Hill, Marc Vidal, Frederick P. Roth, Michael A. Calderwood
Nature. Author manuscript; available in PMC 2020 Oct 8.
Published in final edited form as: Nature. 2020 Apr; 580(7803): 402–408. Published online 2020 Apr 8. doi: 10.1038/s41586-020-2188-x
PMCID:
PMC7169983
AbstractArticlePDF–5.4M

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