CoCites: A citation-based method for searching scientific literature

The retinal specific protein RGS-r competes with the gamma subunit of cGMP phosphodiesterase for the alpha subunit of transducin and facilitates signal termination.

T Wieland, C K Chen, M I Simon. J Biol Chem 1997
Times Cited: 50

List of co-cited articles
520 articles co-cited >1

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Times Cited

Times Co-cited

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Regulation of transducin GTPase activity by human retinal RGS.
M Natochin, A E Granovsky, N O Artemyev. J Biol Chem 1997

Structure of RGS4 bound to AlF4--activated G(i alpha1): stabilization of the transition state for GTP hydrolysis.
J J Tesmer, D M Berman, A G Gilman, S R Sprang. Cell 1997

672

Activation of transducin guanosine triphosphatase by two proteins of the RGS family.
E R Nekrasova, D M Berman, R R Rustandi, H E Hamm, A G Gilman, V Y Arshavsky. Biochemistry 1997

GAIP and RGS4 are GTPase-activating proteins for the Gi subfamily of G protein alpha subunits.
D M Berman, T M Wilkie, A G Gilman. Cell 1996

655

A GTPase-accelerating factor for transducin, distinct from its effector cGMP phosphodiesterase, in rod outer segment membranes.
J K Angleson, T G Wensel. Neuron 1993

RGS4 and GAIP are GTPase-activating proteins for Gq alpha and block activation of phospholipase C beta by gamma-thio-GTP-Gq alpha.
J R Hepler, D M Berman, A G Gilman, T Kozasa. Proc Natl Acad Sci U S A 1997

333

RGS family members: GTPase-activating proteins for heterotrimeric G-protein alpha-subunits.
N Watson, M E Linder, K M Druey, J H Kehrl, K J Blumer. Nature 1996

470

The core domain of a new retina specific RGS protein stimulates the GTPase activity of transducin in vitro.
E Faurobert, J B Hurley. Proc Natl Acad Sci U S A 1997

RGS9, a GTPase accelerator for phototransduction.
W He, C W Cowan, T G Wensel. Neuron 1998

285

RGS-r, a retinal specific RGS protein, binds an intermediate conformation of transducin and enhances recycling.
C K Chen, T Wieland, M I Simon. Proc Natl Acad Sci U S A 1996

120

Regulation of deactivation of photoreceptor G protein by its target enzyme and cGMP.
Arshavsky VYu, M D Bownds. Nature 1992

237

The GTPase-activating protein RGS4 stabilizes the transition state for nucleotide hydrolysis.
D M Berman, T Kozasa, A G Gilman. J Biol Chem 1996

292

RGS10 is a selective activator of G alpha i GTPase activity.
T W Hunt, T A Fields, P J Casey, E G Peralta. Nature 1996

309

Inhibition of G-protein-mediated MAP kinase activation by a new mammalian gene family.
K M Druey, K J Blumer, V H Kang, J H Kehrl. Nature 1996

402

EGL-10 regulates G protein signaling in the C. elegans nervous system and shares a conserved domain with many mammalian proteins.
M R Koelle, H R Horvitz. Cell 1996

484

Mammalian RGS proteins: barbarians at the gate.
D M Berman, A G Gilman. J Biol Chem 1998

422

Heterotrimeric G proteins: organizers of transmembrane signals.
E J Neer. Cell 1995

1218

The regulators of G protein signaling (RGS) domains of RGS4, RGS10, and GAIP retain GTPase activating protein activity in vitro.
S Popov, K Yu, T Kozasa, T M Wilkie. Proc Natl Acad Sci U S A 1997

153

High expression levels in cones of RGS9, the predominant GTPase accelerating protein of rods.
C W Cowan, R N Fariss, I Sokal, K Palczewski, T G Wensel. Proc Natl Acad Sci U S A 1998

139

RGS proteins and signaling by heterotrimeric G proteins.
H G Dohlman, J Thorner. J Biol Chem 1997

440

Regulation of transducin GTPase activity in bovine rod outer segments.
V Y Arshavsky, C L Dumke, Y Zhu, N O Artemyev, N P Skiba, H E Hamm, M D Bownds. J Biol Chem 1994

A G protein gamma subunit-like domain shared between RGS11 and other RGS proteins specifies binding to Gbeta5 subunits.
B E Snow, A M Krumins, G M Brothers, S F Lee, M A Wall, S Chung, J Mangion, S Arya, A G Gilman, D P Siderovski. Proc Natl Acad Sci U S A 1998

226

Cloning of a retinally abundant regulator of G-protein signaling (RGS-r/RGS16): genomic structure and chromosomal localization of the human gene.
B E Snow, L Antonio, S Suggs, D P Siderovski. Gene 1998

Structures of active conformations of Gi alpha 1 and the mechanism of GTP hydrolysis.
D E Coleman, A M Berghuis, E Lee, M E Linder, A G Gilman, S R Sprang. Science 1994

710

GTPase mechanism of Gproteins from the 1.7-A crystal structure of transducin alpha-GDP-AIF-4.
J Sondek, D G Lambright, J P Noel, H E Hamm, P B Sigler. Nature 1994

495

Inhibition of G-protein signaling by dominant gain-of-function mutations in Sst2p, a pheromone desensitization factor in Saccharomyces cerevisiae.
H G Dohlman, D Apaniesk, Y Chen, J Song, D Nusskern. Mol Cell Biol 1995

176

The GTPase activating factor for transducin in rod photoreceptors is the complex between RGS9 and type 5 G protein beta subunit.
E R Makino, J W Handy, T Li, V Y Arshavsky. Proc Natl Acad Sci U S A 1999

183

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

275

RGS4 inhibits Gq-mediated activation of mitogen-activated protein kinase and phosphoinositide synthesis.
Y Yan, P P Chi, H R Bourne. J Biol Chem 1997

132

Phospholipase C-beta 1 is a GTPase-activating protein for Gq/11, its physiologic regulator.
G Berstein, J L Blank, D Y Jhon, J H Exton, S G Rhee, E M Ross. Cell 1992

300

Wilms' tumor (WT1) gene mutations occur mainly in acute myeloid leukemia and may confer drug resistance.
L King-Underwood, K Pritchard-Jones. Blood 1998

134

Hereditary syndrome of imperforate anus with hand, foot, and ear anomalies.
P L Townes, E R Brocks. J Pediatr 1972

128

Association of the FcepsilonRIbeta gene with bronchial hyper-responsiveness in an Italian population.
E Trabetti, V Cusin, G Malerba, L C Martinati, A Casartelli, A L Boner, P F Pignatti. J Med Genet 1998

Hearing loss in Townes-Brocks syndrome.
D R Rossmiller, T R Pasic. Otolaryngol Head Neck Surg 1994

A small deletion of 16q23.1-->16q24.2 [del(16)(q23.1q24.2).ish del(16)(q23.1q24.2)(D16S395+, D16S348-, P5432+)] in a boy with iris coloboma and minor anomalies.
W Werner, S Kraft, D F Callen, O Bartsch, G K Hinkel. Am J Med Genet 1997

Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies.
E Nelis, N Haites, C Van Broeckhoven. Hum Mutat 1999

175

Variability of biochemical and clinical phenotype in X-linked liver glycogenosis with mutations in the phosphorylase kinase PHKA2 gene.
B Burwinkel, L Amat, R G Gray, N Matsuo, K Muroya, K Narisawa, R J Sokol, M A Vilaseca, M W Kilimann. Hum Genet 1998

Evidence that WT1 mutations in Denys-Drash syndrome patients may act in a dominant-negative fashion.
M H Little, K A Williamson, M Mannens, A Kelsey, C Gosden, N D Hastie, V van Heyningen. Hum Mol Genet 1993

128

Regional assignment of the human loci for uvomorulin (UVO) and chymotrypsinogen B (CTRB) with the help of two overlapping deletions on the long arm of chromosome 16.
E Natt, R E Magenis, J Zimmer, A Mansouri, G Scherer. Cytogenet Cell Genet 1989

Townes-Brocks syndrome in two mentally retarded youngsters.
T H Cameron, A M Lachiewicz, A S Aylsworth. Am J Med Genet 1991

Liver glycogenosis due to phosphorylase kinase deficiency: PHKG2 gene structure and mutations associated with cirrhosis.
B Burwinkel, S Shiomi, A Al Zaben, M W Kilimann. Hum Mol Genet 1998

p53 abnormalities in B-cell prolymphocytic leukemia.
D Lens, P J De Schouwer, R A Hamoudi, M Abdul-Rauf, N Farahat, E Matutes, T Crook, M J Dyer, D Catovsky. Blood 1997

STAT6: its role in interleukin 4-mediated biological functions.
K Takeda, T Kishimoto, S Akira. J Mol Med (Berl) 1997

Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa.
M E McLaughlin, T L Ehrhart, E L Berson, T P Dryja. Proc Natl Acad Sci U S A 1995

251

Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters.
U Suter, G J Snipes, R Schoener-Scott, A A Welcher, S Pareek, J R Lupski, R A Murphy, E M Shooter, P I Patel. J Biol Chem 1994

170

Deletion of the long arm of chromosome 16 and an unexpected Duffy blood group phenotype reveal a possible autosomal linkage.
M N Crawford, H H Punnett, G G Carpenter. Nature 1967

Charcot-Marie-Tooth disease type 1A. Association with a spontaneous point mutation in the PMP22 gene.
B B Roa, C A Garcia, U Suter, D A Kulpa, C A Wise, J Mueller, A A Welcher, G J Snipes, E M Shooter, P I Patel,[...]. N Engl J Med 1993

328

A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism.
E M Rinchik, S J Bultman, B Horsthemke, S T Lee, K M Strunk, R A Spritz, K M Avidano, M T Jong, R D Nicholls. Nature 1993

325

Phosphorylase b kinase deficiency glycogenosis with cirrhosis of the liver.
A F Kagalwalla, Y A Kagalwalla, S al Ajaji, W Gorka, M A Ali. J Pediatr 1995

Control of inflammation, cytokine expression, and germinal center formation by BCL-6.
A L Dent, A L Shaffer, X Yu, D Allman, L M Staudt. Science 1997

743

Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.

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