BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 23273860)

  • 1. Cellular and molecular biology of neuronal dystonin.
    Ferrier A; Boyer JG; Kothary R
    Int Rev Cell Mol Biol; 2013; 300():85-120. PubMed ID: 23273860
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dystonin/Bpag1--a link to what?
    Young KG; Kothary R
    Cell Motil Cytoskeleton; 2007 Dec; 64(12):897-905. PubMed ID: 17849487
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Functional and Genetic Analysis of Neuronal Isoforms of BPAG1.
    Lynch-Godrei A; Kothary R
    Methods Enzymol; 2016; 569():355-72. PubMed ID: 26778567
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Disruption of actin-binding domain-containing Dystonin protein causes dystonia musculorum in mice.
    Horie M; Watanabe K; Bepari AK; Nashimoto J; Araki K; Sano H; Chiken S; Nambu A; Ono K; Ikenaka K; Kakita A; Yamamura K; Takebayashi H
    Eur J Neurosci; 2014 Nov; 40(10):3458-71. PubMed ID: 25195653
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI.
    Ferrier A; Sato T; De Repentigny Y; Gibeault S; Bhanot K; O'Meara RW; Lynch-Godrei A; Kornfeld SF; Young KG; Kothary R
    Hum Mol Genet; 2014 May; 23(10):2694-710. PubMed ID: 24381311
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Trafficking of macromolecules and organelles in cultured Dystonia musculorum sensory neurons is normal.
    Pool M; Rippstein P; McBride H; Kothary R
    J Comp Neurol; 2006 Feb; 494(4):549-58. PubMed ID: 16374799
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dystonin is essential for maintaining neuronal cytoskeleton organization.
    Dalpé G; Leclerc N; Vallée A; Messer A; Mathieu M; De Repentigny Y; Kothary R
    Mol Cell Neurosci; 1998 Apr; 10(5-6):243-57. PubMed ID: 9604204
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Neuronal dystonin isoform 2 is a mediator of endoplasmic reticulum structure and function.
    Ryan SD; Ferrier A; Sato T; O'Meara RW; De Repentigny Y; Jiang SX; Hou ST; Kothary R
    Mol Biol Cell; 2012 Feb; 23(4):553-66. PubMed ID: 22190742
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dystonin-deficient mice exhibit an intrinsic muscle weakness and an instability of skeletal muscle cytoarchitecture.
    Dalpé G; Mathieu M; Comtois A; Zhu E; Wasiak S; De Repentigny Y; Leclerc N; Kothary R
    Dev Biol; 1999 Jun; 210(2):367-80. PubMed ID: 10357897
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Disruption in the autophagic process underlies the sensory neuropathy in dystonia musculorum mice.
    Ferrier A; De Repentigny Y; Lynch-Godrei A; Gibeault S; Eid W; Kuo D; Zha X; Kothary R
    Autophagy; 2015; 11(7):1025-36. PubMed ID: 26043942
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic alterations at the Bpag1 locus in dt mice and their impact on transcript expression.
    Pool M; Boudreau Larivière C; Bernier G; Young KG; Kothary R
    Mamm Genome; 2005 Dec; 16(12):909-17. PubMed ID: 16341670
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dystonin/Bpag1 is a necessary endoplasmic reticulum/nuclear envelope protein in sensory neurons.
    Young KG; Kothary R
    Exp Cell Res; 2008 Sep; 314(15):2750-61. PubMed ID: 18638474
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dissecting the sequence specific functions of alternative N-terminal isoforms of mouse bullous pemphigoid antigen 1.
    Jefferson JJ; Leung CL; Liem RK
    Exp Cell Res; 2006 Sep; 312(15):2712-25. PubMed ID: 16797530
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A possible cellular mechanism of neuronal loss in the dorsal root ganglia of Dystonia musculorum (dt) mice.
    Tseng KW; Lu KS; Chien CL
    J Neuropathol Exp Neurol; 2006 Apr; 65(4):336-47. PubMed ID: 16691115
    [TBL] [Abstract][Full Text] [Related]  

  • 15. MAP1B and clathrin are novel interacting partners of the giant cyto-linker dystonin.
    Bhanot K; Young KG; Kothary R
    J Proteome Res; 2011 Nov; 10(11):5118-27. PubMed ID: 21936565
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The survival of vagal and glossopharyngeal sensory neurons is dependent upon dystonin.
    Ichikawa H; De Repentigny Y; Kothary R; Sugimoto T
    Neuroscience; 2006; 137(2):531-6. PubMed ID: 16289886
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cloning and characterization of the neural isoforms of human dystonin.
    Brown A; Dalpé G; Mathieu M; Kothary R
    Genomics; 1995 Oct; 29(3):777-80. PubMed ID: 8575775
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hearts of dystonia musculorum mice display normal morphological and histological features but show signs of cardiac stress.
    Boyer JG; Bhanot K; Kothary R; Boudreau-Larivière C
    PLoS One; 2010 Mar; 5(3):e9465. PubMed ID: 20209123
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.
    Brown A; Bernier G; Mathieu M; Rossant J; Kothary R
    Nat Genet; 1995 Jul; 10(3):301-6. PubMed ID: 7670468
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The number of nociceptors in the trigeminal ganglion but not proprioceptors in the mesencephalic trigeminal tract nucleus is reduced in dystonin deficient dystonia musculorum mice.
    Ichikawa H; Terayama R; Yamaai T; De Repentigny Y; Kothary R; Sugimoto T
    Brain Res; 2008 Aug; 1226():33-8. PubMed ID: 18619576
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.