BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 26778567)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 5. Dystonin-A3 upregulation is responsible for maintenance of tubulin acetylation in a less severe dystonia musculorum mouse model for hereditary sensory and autonomic neuropathy type VI.
    Lynch-Godrei A; De Repentigny Y; Gagnon S; Trung MT; Kothary R
    Hum Mol Genet; 2018 Oct; 27(20):3598-3611. PubMed ID: 29982604
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 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. 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]  

  • 11. 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]  

  • 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. Roles of dystonin isoforms in the maintenance of neural, muscle, and cutaneous tissues.
    Yoshioka N
    Anat Sci Int; 2024 Jan; 99(1):7-16. PubMed ID: 37603210
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. HSAN-VI: A spectrum disorder based on dystonin isoform expression.
    Lynch-Godrei A; Kothary R
    Neurol Genet; 2020 Feb; 6(1):e389. PubMed ID: 32042917
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of gastrointestinal pathologies in the dystonia musculorum mouse model for hereditary sensory and autonomic neuropathy type VI.
    Lynch-Godrei A; De Repentigny Y; Yaworski RA; Gagnon S; Butcher J; Manoogian J; Stintzi A; Kothary R
    Neurogastroenterol Motil; 2020 Apr; 32(4):e13773. PubMed ID: 31814231
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.