BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 16642310)

  • 1. Inverse correlation between the formation of mitochondria-derived vacuoles and Lewy-body-like hyaline inclusions in G93A superoxide-dismutase-transgenic mice.
    Sumi H; Nagano S; Fujimura H; Kato S; Sakoda S
    Acta Neuropathol; 2006 Jul; 112(1):52-63. PubMed ID: 16642310
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Phosphorylated Smad2/3 immunoreactivity in sporadic and familial amyotrophic lateral sclerosis and its mouse model.
    Nakamura M; Ito H; Wate R; Nakano S; Hirano A; Kusaka H
    Acta Neuropathol; 2008 Mar; 115(3):327-34. PubMed ID: 18210139
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Copper chaperone for superoxide dismutase co-aggregates with superoxide dismutase 1 (SOD1) in neuronal Lewy body-like hyaline inclusions: an immunohistochemical study on familial amyotrophic lateral sclerosis with SOD1 gene mutation.
    Kato S; Sumi-Akamaru H; Fujimura H; Sakoda S; Kato M; Hirano A; Takikawa M; Ohama E
    Acta Neuropathol; 2001 Sep; 102(3):233-8. PubMed ID: 11585247
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Altered distributions of nucleocytoplasmic transport-related proteins in the spinal cord of a mouse model of amyotrophic lateral sclerosis.
    Zhang J; Ito H; Wate R; Ohnishi S; Nakano S; Kusaka H
    Acta Neuropathol; 2006 Dec; 112(6):673-80. PubMed ID: 16957927
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial amyotrophic lateral sclerosis with a two base pair deletion in superoxide dismutase 1: gene multisystem degeneration with intracytoplasmic hyaline inclusions in astrocytes.
    Kato S; Shimoda M; Watanabe Y; Nakashima K; Takahashi K; Ohama E
    J Neuropathol Exp Neurol; 1996 Oct; 55(10):1089-101. PubMed ID: 8858006
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 14-3-3 proteins in Lewy body-like hyaline inclusions in patients with sporadic amyotrophic lateral sclerosis.
    Kawamoto Y; Akiguchi I; Nakamura S; Budka H
    Acta Neuropathol; 2004 Dec; 108(6):531-7. PubMed ID: 15378322
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Colocalization of 14-3-3 proteins with SOD1 in Lewy body-like hyaline inclusions in familial amyotrophic lateral sclerosis cases and the animal model.
    Okamoto Y; Shirakashi Y; Ihara M; Urushitani M; Oono M; Kawamoto Y; Yamashita H; Shimohama S; Kato S; Hirano A; Tomimoto H; Ito H; Takahashi R
    PLoS One; 2011; 6(5):e20427. PubMed ID: 21655264
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial amyotrophic lateral sclerosis with His46Arg mutation in Cu/Zn superoxide dismutase presenting characteristic clinical features and Lewy body-like hyaline inclusions.
    Ohi T; Nabeshima K; Kato S; Yazawa S; Takechi S
    J Neurol Sci; 2004 Oct; 225(1-2):19-25. PubMed ID: 15465081
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Recent advances in research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutations: neuronal Lewy body-like hyaline inclusions and astrocytic hyaline inclusions.
    Kato S; Saito M; Hirano A; Ohama E
    Histol Histopathol; 1999 Jul; 14(3):973-89. PubMed ID: 10425565
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial amyotrophic lateral sclerosis with Cys111Tyr mutation in Cu/Zn superoxide dismutase showing widespread Lewy body-like hyaline inclusions.
    Suzuki M; Yasui K; Ishikawai H; Nomura M; Watanabe T; Mikami H; Yamano T; Ono S
    J Neurol Sci; 2011 Jan; 300(1-2):182-4. PubMed ID: 20888599
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pathological characterization of astrocytic hyaline inclusions in familial amyotrophic lateral sclerosis.
    Kato S; Hayashi H; Nakashima K; Nanba E; Kato M; Hirano A; Nakano I; Asayama K; Ohama E
    Am J Pathol; 1997 Aug; 151(2):611-20. PubMed ID: 9273821
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sporadic amyotrophic lateral sclerosis with dementia and Cu/Zn superoxide dismutase-positive Lewy body-like inclusions.
    Matsumoto S; Kusaka H; Ito H; Shibata N; Asayama T; Imai T
    Clin Neuropathol; 1996; 15(1):41-6. PubMed ID: 8998856
    [TBL] [Abstract][Full Text] [Related]  

  • 13. HtrA2/Omi-immunoreactive intraneuronal inclusions in the anterior horn of patients with sporadic and Cu/Zn superoxide dismutase (SOD1) mutant amyotrophic lateral sclerosis.
    Kawamoto Y; Ito H; Kobayashi Y; Suzuki Y; Akiguchi I; Fujimura H; Sakoda S; Kusaka H; Hirano A; Takahashi R
    Neuropathol Appl Neurobiol; 2010 Jun; 36(4):331-44. PubMed ID: 20202124
    [TBL] [Abstract][Full Text] [Related]  

  • 14. TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation.
    Tan CF; Eguchi H; Tagawa A; Onodera O; Iwasaki T; Tsujino A; Nishizawa M; Kakita A; Takahashi H
    Acta Neuropathol; 2007 May; 113(5):535-42. PubMed ID: 17333220
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Histological evidence of redox system breakdown caused by superoxide dismutase 1 (SOD1) aggregation is common to SOD1-mutated motor neurons in humans and animal models.
    Kato S; Saeki Y; Aoki M; Nagai M; Ishigaki A; Itoyama Y; Kato M; Asayama K; Awaya A; Hirano A; Ohama E
    Acta Neuropathol; 2004 Feb; 107(2):149-58. PubMed ID: 14648077
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial alterations in transgenic mice with an H46R mutant Cu/Zn superoxide dismutase gene.
    Sasaki S; Aoki M; Nagai M; Kobayashi M; Itoyama Y
    J Neuropathol Exp Neurol; 2009 Apr; 68(4):365-73. PubMed ID: 19287315
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 14-3-3 proteins in Lewy body-like hyaline inclusions in a patient with familial amyotrophic lateral sclerosis with a two-base pair deletion in the Cu/Zn superoxide dismutase (SOD1) gene.
    Kawamoto Y; Akiguchi I; Fujimura H; Shirakashi Y; Honjo Y; Sakoda S
    Acta Neuropathol; 2005 Aug; 110(2):203-4. PubMed ID: 15973542
    [No Abstract]   [Full Text] [Related]  

  • 18. Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions.
    Tu PH; Raju P; Robinson KA; Gurney ME; Trojanowski JQ; Lee VM
    Proc Natl Acad Sci U S A; 1996 Apr; 93(7):3155-60. PubMed ID: 8610185
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization and changes in neurotrophin receptor p75-Expressing motor neurons in SOD1(G93A) G1H mice [corrected].
    Smith KS; Rush RA; Rogers ML
    J Comp Neurol; 2015 Aug; 523(11):1664-82. PubMed ID: 25711805
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Colocalization of Bunina bodies and TDP-43 inclusions in a case of sporadic amyotrophic lateral sclerosis with Lewy body-like hyaline inclusions.
    Miki Y; Mori F; Seino Y; Tanji K; Yoshizawa T; Kijima H; Shoji M; Wakabayashi K
    Neuropathology; 2018 Oct; 38(5):521-528. PubMed ID: 29938835
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.