BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 25772041)

  • 1. From Mice to Men: TRPC3 in Cerebellar Ataxia.
    Becker EBE
    Cerebellum; 2017 Dec; 16(5-6):877-879. PubMed ID: 25772041
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Candidate screening of the TRPC3 gene in cerebellar ataxia.
    Becker EB; Fogel BL; Rajakulendran S; Dulneva A; Hanna MG; Perlman SL; Geschwind DH; Davies KE
    Cerebellum; 2011 Jun; 10(2):296-9. PubMed ID: 21321808
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The Moonwalker mouse: new insights into TRPC3 function, cerebellar development, and ataxia.
    Becker EB
    Cerebellum; 2014 Oct; 13(5):628-36. PubMed ID: 24797279
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Modeling Suggests TRPC3 Hydrogen Bonding and Not Phosphorylation Contributes to the Ataxia Phenotype of the Moonwalker Mouse.
    Hanson SM; Sansom MS; Becker EB
    Biochemistry; 2015 Jul; 54(26):4033-41. PubMed ID: 26112884
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The mutant Moonwalker TRPC3 channel links calcium signaling to lipid metabolism in the developing cerebellum.
    Dulneva A; Lee S; Oliver PL; Di Gleria K; Kessler BM; Davies KE; Becker EB
    Hum Mol Genet; 2015 Jul; 24(14):4114-25. PubMed ID: 25908616
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice.
    Becker EB; Oliver PL; Glitsch MD; Banks GT; Achilli F; Hardy A; Nolan PM; Fisher EM; Davies KE
    Proc Natl Acad Sci U S A; 2009 Apr; 106(16):6706-11. PubMed ID: 19351902
    [TBL] [Abstract][Full Text] [Related]  

  • 7. TRPC3-dependent synaptic transmission in central mammalian neurons.
    Hartmann J; Konnerth A
    J Mol Med (Berl); 2015 Sep; 93(9):983-9. PubMed ID: 26041382
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Early onset of ataxia in moonwalker mice is accompanied by complete ablation of type II unipolar brush cells and Purkinje cell dysfunction.
    Sekerková G; Kim JA; Nigro MJ; Becker EB; Hartmann J; Birnbaumer L; Mugnaini E; Martina M
    J Neurosci; 2013 Dec; 33(50):19689-94. PubMed ID: 24336732
    [TBL] [Abstract][Full Text] [Related]  

  • 9. P/Q-type and T-type calcium channels, but not type 3 transient receptor potential cation channels, are involved in inhibition of dendritic growth after chronic metabotropic glutamate receptor type 1 and protein kinase C activation in cerebellar Purkinje cells.
    Gugger OS; Hartmann J; Birnbaumer L; Kapfhammer JP
    Eur J Neurosci; 2012 Jan; 35(1):20-33. PubMed ID: 22188405
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The puzzling role of TRPC3 channels in motor coordination.
    Trebak M
    Pflugers Arch; 2010 Feb; 459(3):369-75. PubMed ID: 19823866
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Recent advance in genetic study of hereditary autosomal recessive cerebellar ataxia].
    Guan WJ; Wang JL; Tang BS
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec; 29(6):673-6. PubMed ID: 23225047
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Activation of native TRPC3 cation channels by phospholipase D.
    Glitsch MD
    FASEB J; 2010 Jan; 24(1):318-25. PubMed ID: 19741172
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Increased GABA receptor binding in dominantly-inherited cerebellar ataxias.
    Kish SJ; Perry TL; Hornykiewicz O
    Brain Res; 1983 Jun; 269(2):370-3. PubMed ID: 6309324
    [TBL] [Abstract][Full Text] [Related]  

  • 14. SnapShot: Biology of Genetic Ataxias.
    Eidhof I; van de Warrenburg BP; Schenck A
    Cell; 2018 Oct; 175(3):890-890.e1. PubMed ID: 30340048
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?
    Fogel BL; Hanson SM; Becker EB
    Mov Disord; 2015 Feb; 30(2):284-6. PubMed ID: 25477146
    [No Abstract]   [Full Text] [Related]  

  • 16. Murine cardiac growth, TRPC channels, and cGMP kinase I.
    Domes K; Patrucco E; Loga F; Dietrich A; Birnbaumer L; Wegener JW; Hofmann F
    Pflugers Arch; 2015 Oct; 467(10):2229-34. PubMed ID: 25547873
    [TBL] [Abstract][Full Text] [Related]  

  • 17. TRPC3 is a major contributor to functional heterogeneity of cerebellar Purkinje cells.
    Wu B; Blot FG; Wong AB; Osório C; Adolfs Y; Pasterkamp RJ; Hartmann J; Becker EB; Boele HJ; De Zeeuw CI; Schonewille M
    Elife; 2019 Sep; 8():. PubMed ID: 31486767
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutational analysis of ITPR1 in a Taiwanese cohort with cerebellar ataxias.
    Hsiao CT; Liu YT; Liao YC; Hsu TY; Lee YC; Soong BW
    PLoS One; 2017; 12(11):e0187503. PubMed ID: 29186133
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Tottering mouse motor dysfunction is abolished on the Purkinje cell degeneration (pcd) mutant background.
    Campbell DB; North JB; Hess EJ
    Exp Neurol; 1999 Nov; 160(1):268-78. PubMed ID: 10630211
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Transient receptor potential channel 3 in human liver and gallbladder - An investigation in body donors.
    Kaul NL; Diebolt CM; Meier C; Tschernig T
    Ann Anat; 2023 Oct; 250():152150. PubMed ID: 37633502
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.