BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

169 related articles for article (PubMed ID: 21272373)

  • 1. Neuronal degeneration in autonomic nervous system of Dystonia musculorum mice.
    Tseng KW; Peng ML; Wen YC; Liu KJ; Chien CL
    J Biomed Sci; 2011 Jan; 18(1):9. PubMed ID: 21272373
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. The intermediate filament protein peripherin is the specific interaction partner of mouse BPAG1-n (dystonin) in neurons.
    Leung CL; Sun D; Liem RK
    J Cell Biol; 1999 Feb; 144(3):435-46. PubMed ID: 9971739
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Molecular characterization of the genetic lesion in Dystonia musculorum (dt-Alb) mice.
    Goryunov D; Adebola A; Jefferson JJ; Leung CL; Messer A; Liem RK
    Brain Res; 2007 Apr; 1140():179-87. PubMed ID: 16725123
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Prenatal onset of axonopathy in Dystonia musculorum mice.
    Bernier G; Kothary R
    Dev Genet; 1998; 22(2):160-8. PubMed ID: 9581287
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Alterations in myelination in the central nervous system of dystonia musculorum mice.
    Saulnier R; De Repentigny Y; Yong VW; Kothary R
    J Neurosci Res; 2002 Jul; 69(2):233-42. PubMed ID: 12111805
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Differentiation potential of primary myogenic cells derived from skeletal muscle of dystonia musculorum mice.
    Boudreau-Larivière C; Kothary R
    Differentiation; 2002 Aug; 70(6):247-56. PubMed ID: 12190986
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Developmental expression of BPAG1-n: insights into the spastic ataxia and gross neurologic degeneration in dystonia musculorum mice.
    Dowling J; Yang Y; Wollmann R; Reichardt LF; Fuchs E
    Dev Biol; 1997 Jul; 187(2):131-42. PubMed ID: 9242412
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Glial cell line-derived neurotrophic factor-responsive and neurotrophin-3-responsive neurons require the cytoskeletal linker protein dystonin for postnatal survival.
    Carlsten JA; Kothary R; Wright DE
    J Comp Neurol; 2001 Apr; 432(2):155-68. PubMed ID: 11241383
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Motor unit abnormalities in Dystonia musculorum mice.
    De Repentigny Y; Ferrier A; Ryan SD; Sato T; Kothary R
    PLoS One; 2011; 6(6):e21093. PubMed ID: 21698255
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.