BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 38332109)

  • 1. A splice acceptor variant in RGS6 associated with intellectual disability, microcephaly, and cataracts disproportionately promotes expression of a subset of RGS6 isoforms.
    Ahlers-Dannen KE; Yang J; Spicer MM; Fu D; DeVore A; Fisher RA
    J Hum Genet; 2024 Apr; 69(3-4):145-152. PubMed ID: 38332109
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Protein Profiling of RGS6, a Pleiotropic Gene Implicated in Numerous Neuropsychiatric Disorders, Reveals Multi-Isoformic Expression and a Novel Brain-Specific Isoform.
    Ahlers-Dannen KE; Yang J; Spicer MM; Maity B; Stewart A; Koland JG; Fisher RA
    eNeuro; 2022; 9(1):. PubMed ID: 34880111
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Human RGS6 gene structure, complex alternative splicing, and role of N terminus and G protein gamma-subunit-like (GGL) domain in subcellular localization of RGS6 splice variants.
    Chatterjee TK; Liu Z; Fisher RA
    J Biol Chem; 2003 Aug; 278(32):30261-71. PubMed ID: 12761221
    [TBL] [Abstract][Full Text] [Related]  

  • 4. RGS6 interacts with SCG10 and promotes neuronal differentiation. Role of the G gamma subunit-like (GGL) domain of RGS6.
    Liu Z; Chatterjee TK; Fisher RA
    J Biol Chem; 2002 Oct; 277(40):37832-9. PubMed ID: 12140291
    [TBL] [Abstract][Full Text] [Related]  

  • 5. RGS6 interacts with DMAP1 and DNMT1 and inhibits DMAP1 transcriptional repressor activity.
    Liu Z; Fisher RA
    J Biol Chem; 2004 Apr; 279(14):14120-8. PubMed ID: 14734556
    [TBL] [Abstract][Full Text] [Related]  

  • 6. RGS6: a novel gene associated with congenital cataract, mental retardation, and microcephaly in a Tunisian family.
    Chograni M; Alkuraya FS; Maazoul F; Lariani I; Chaabouni-Bouhamed H
    Invest Ophthalmol Vis Sci; 2014 Dec; 56(2):1261-6. PubMed ID: 25525169
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mild heat and proteotoxic stress promote unique subcellular trafficking and nucleolar accumulation of RGS6 and other RGS proteins. Role of the RGS domain in stress-induced trafficking of RGS proteins.
    Chatterjee TK; Fisher RA
    J Biol Chem; 2003 Aug; 278(32):30272-82. PubMed ID: 12761220
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Fidelity of G protein beta-subunit association by the G protein gamma-subunit-like domains of RGS6, RGS7, and RGS11.
    Snow BE; Betts L; Mangion J; Sondek J; Siderovski DP
    Proc Natl Acad Sci U S A; 1999 May; 96(11):6489-94. PubMed ID: 10339615
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Regulators of G protein signaling 6 and 7. Purification of complexes with gbeta5 and assessment of their effects on g protein-mediated signaling pathways.
    Posner BA; Gilman AG; Harris BA
    J Biol Chem; 1999 Oct; 274(43):31087-93. PubMed ID: 10521509
    [TBL] [Abstract][Full Text] [Related]  

  • 10. RGS6 as a Novel Therapeutic Target in CNS Diseases and Cancer.
    Ahlers KE; Chakravarti B; Fisher RA
    AAPS J; 2016 May; 18(3):560-72. PubMed ID: 27002730
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Splice variant in ARX leading to loss of C-terminal region in a boy with intellectual disability and infantile onset developmental and epileptic encephalopathy.
    Shoubridge C; Jackson M; Grinton B; Berkovic SF; Scheffer IE; Huskins S; Thomas A; Ware T
    Am J Med Genet A; 2019 Aug; 179(8):1483-1490. PubMed ID: 31145546
    [TBL] [Abstract][Full Text] [Related]  

  • 12. RGS6, but not RGS4, is the dominant regulator of G protein signaling (RGS) modulator of the parasympathetic regulation of mouse heart rate.
    Wydeven N; Posokhova E; Xia Z; Martemyanov KA; Wickman K
    J Biol Chem; 2014 Jan; 289(4):2440-9. PubMed ID: 24318880
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Christianson syndrome: A novel splicing variant of SLC9A6 causes exon skipping in a Chinese boy and a literature review.
    Zhang X; Wu X; Liu H; Song T; Jiang Y; He H; Yang S; Xie Y
    J Clin Lab Anal; 2022 Jan; 36(1):e24123. PubMed ID: 34791706
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Regulator of G protein signaling 6 (RGS6) protein ensures coordination of motor movement by modulating GABAB receptor signaling.
    Maity B; Stewart A; Yang J; Loo L; Sheff D; Shepherd AJ; Mohapatra DP; Fisher RA
    J Biol Chem; 2012 Feb; 287(7):4972-81. PubMed ID: 22179605
    [TBL] [Abstract][Full Text] [Related]  

  • 15. RGS6 and RGS7 Discriminate between the Highly Similar Gα
    Israeli R; Asli A; Avital-Shacham M; Kosloff M
    J Mol Biol; 2019 Aug; 431(17):3302-3311. PubMed ID: 31153905
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Instability of GGL domain-containing RGS proteins in mice lacking the G protein beta-subunit Gbeta5.
    Chen CK; Eversole-Cire P; Zhang H; Mancino V; Chen YJ; He W; Wensel TG; Simon MI
    Proc Natl Acad Sci U S A; 2003 May; 100(11):6604-9. PubMed ID: 12738888
    [TBL] [Abstract][Full Text] [Related]  

  • 17. HA117 endows HL60 cells with a stem-like signature by inhibiting the degradation of DNMT1 via its ability to down-regulate expression of the GGL domain of RGS6.
    Li S; Jin X; Wu H; Wang Y; Li X; Guo Y; Liang S
    PLoS One; 2017; 12(6):e0180142. PubMed ID: 28665981
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hepatic Regulator of G Protein Signaling 6 (RGS6) drives non-alcoholic fatty liver disease by promoting oxidative stress and ATM-dependent cell death.
    Mahata T; Sengar AS; Basak M; Das K; Pramanick A; Verma SK; Singh PK; Biswas S; Sarkar S; Saha S; Chatterjee S; Das M; Stewart A; Maity B
    Redox Biol; 2021 Oct; 46():102105. PubMed ID: 34534913
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Age-dependent nigral dopaminergic neurodegeneration and α-synuclein accumulation in RGS6-deficient mice.
    Luo Z; Ahlers-Dannen KE; Spicer MM; Yang J; Alberico S; Stevens HE; Narayanan NS; Fisher RA
    JCI Insight; 2019 May; 5(13):. PubMed ID: 31120439
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Revealing the functions of novel mutations in RAB3GAP1 in Martsolf and Warburg micro syndromes.
    Koparir A; Karatas OF; Yilmaz SS; Suer I; Ozer B; Yuceturk B; Ozen M
    Am J Med Genet A; 2019 Apr; 179(4):579-587. PubMed ID: 30730599
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.