132 related articles for article (PubMed ID: 12190986)
1. 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]
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. 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]
4. Cytoskeleton: missing links found?
Bousquet O; Coulombe PA
Curr Biol; 1996 Dec; 6(12):1563-6. PubMed ID: 8994813
[TBL] [Abstract][Full Text] [Related]
5. 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]
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. Novel alternative splicings of BPAG1 (bullous pemphigoid antigen 1) including the domain structure closely related to MACF (microtubule actin cross-linking factor).
Okumura M; Yamakawa H; Ohara O; Owaribe K
J Biol Chem; 2002 Feb; 277(8):6682-7. PubMed ID: 11751855
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. 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]
13. Gene targeting of BPAG1: abnormalities in mechanical strength and cell migration in stratified epithelia and neurologic degeneration.
Guo L; Degenstein L; Dowling J; Yu QC; Wollmann R; Perman B; Fuchs E
Cell; 1995 Apr; 81(2):233-43. PubMed ID: 7736575
[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. 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]
16. 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]
17. BPAG1 isoform-b: complex distribution pattern in striated and heart muscle and association with plectin and alpha-actinin.
Steiner-Champliaud MF; Schneider Y; Favre B; Paulhe F; Praetzel-Wunder S; Faulkner G; Konieczny P; Raith M; Wiche G; Adebola A; Liem RK; Langbein L; Sonnenberg A; Fontao L; Borradori L
Exp Cell Res; 2010 Feb; 316(3):297-313. PubMed ID: 19932097
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Structural analysis of the predicted coiled-coil rod domain of the cytoplasmic bullous pemphigoid antigen (BPAG1). Empirical localization of the N-terminal globular domain-rod boundary.
Tang HY; Chaffotte AF; Thacher SM
J Biol Chem; 1996 Apr; 271(16):9716-22. PubMed ID: 8621649
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
