BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 27693510)

  • 21. 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: 9618216
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. 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]  

  • 25. Isoform-specific mutation in Dystonin-b gene causes late-onset protein aggregate myopathy and cardiomyopathy.
    Yoshioka N; Kurose M; Yano M; Tran DM; Okuda S; Mori-Ochiai Y; Horie M; Nagai T; Nishino I; Shibata S; Takebayashi H
    Elife; 2022 Aug; 11():. PubMed ID: 35942699
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Central serotonin system in Dystonia musculorum mutant mice: biochemical, autoradiographic and immunocytochemical data.
    Ase AR; Strazielle C; Hébert C; Botez MI; LaLonde R; Descarries L; Reader TA
    Synapse; 2000 Sep; 37(3):179-93. PubMed ID: 10881040
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Abnormal cellular translocation of alpha-internexin in spinal motor neurons of Dystonia musculorum mice.
    Tseng KW; Chau YP; Yang MF; Lu KS; Chien CL
    J Comp Neurol; 2008 Mar; 507(1):1053-64. PubMed ID: 18092335
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Biochemical and autoradiographic studies of the central noradrenergic system in dystonia musculorum mutant mice.
    Strazielle C; Ase AR; Lalonde R; Reader TA
    J Chem Neuroanat; 2002 Feb; 23(2):143-55. PubMed ID: 11841918
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Impaired fast axonal transport in neurons of the sciatic nerves from dystonia musculorum mice.
    De Repentigny Y; Deschênes-Furry J; Jasmin BJ; Kothary R
    J Neurochem; 2003 Aug; 86(3):564-71. PubMed ID: 12859670
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Recessive mutations in the neuronal isoforms of DST, encoding dystonin, lead to abnormal actin cytoskeleton organization and HSAN type VI.
    Fortugno P; Angelucci F; Cestra G; Camerota L; Ferraro AS; Cordisco S; Uccioli L; Castiglia D; De Angelis B; Kurth I; Kornak U; Brancati F
    Hum Mutat; 2019 Jan; 40(1):106-114. PubMed ID: 30371979
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Reduced Proliferation of Oligodendrocyte Progenitor Cells in the Postnatal Brain of Dystonia Musculorum Mice.
    Hossain MI; Horie M; Takebayashi H
    Neurochem Res; 2018 Jan; 43(1):101-109. PubMed ID: 28664402
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Novel mutations in
    Manganelli F; Parisi S; Nolano M; Tao F; Paladino S; Pisciotta C; Tozza S; Nesti C; Rebelo AP; Provitera V; Santorelli FM; Shy ME; Russo T; Zuchner S; Santoro L
    Neurology; 2017 May; 88(22):2132-2140. PubMed ID: 28468842
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 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]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 9.