169 related articles for article (PubMed ID: 20209123)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Dystonia musculorum mutation and myosin heavy chain expression in skeletal and cardiac muscles.
Hartmann N; Martrette JM; Strazielle C; Westphal A
J Cell Biochem; 1999 Jul; 74(1):90-8. PubMed ID: 10381265
[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. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. 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]
16. 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]
17. 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]
18. 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]
19. Microtubule stability, Golgi organization, and transport flux require dystonin-a2-MAP1B interaction.
Ryan SD; Bhanot K; Ferrier A; De Repentigny Y; Chu A; Blais A; Kothary R
J Cell Biol; 2012 Mar; 196(6):727-42. PubMed ID: 22412020
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]