227 related articles for article (PubMed ID: 12111805)
1. 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]
2. 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]
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. Cytoskeletal Linker Protein Dystonin Is Not Critical to Terminal Oligodendrocyte Differentiation or CNS Myelination.
Kornfeld SF; Lynch-Godrei A; Bonin SR; Gibeault S; De Repentigny Y; Kothary R
PLoS One; 2016; 11(2):e0149201. PubMed ID: 26886550
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
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. Ultrastructural studies of an hereditary sensory neuropathy in mice (dystonia musculorum).
Janota I
Brain; 1972; 95(3):529-36. PubMed ID: 4655279
[No 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. 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]
14. 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]
15. Dystonin is an essential component of the Schwann cell cytoskeleton at the time of myelination.
Bernier G; De Repentigny Y; Mathieu M; David S; Kothary R
Development; 1998 Jun; 125(11):2135-48. PubMed ID: 9570777
[TBL] [Abstract][Full Text] [Related]
16. Abnormal cell relationships in Jimpy mice: electron microscopic and immunocytochemical findings.
Omlin FX; Anders JJ
J Neurocytol; 1983 Oct; 12(5):767-84. PubMed ID: 6644355
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Dominant-negative beta1 integrin mice have region-specific myelin defects accompanied by alterations in MAPK activity.
Lee KK; de Repentigny Y; Saulnier R; Rippstein P; Macklin WB; Kothary R
Glia; 2006 Jun; 53(8):836-44. PubMed ID: 16575886
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]