BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

296 related articles for article (PubMed ID: 10965797)

  • 1. Nonoxidative protein glycation is implicated in familial amyotrophic lateral sclerosis with superoxide dismutase-1 mutation.
    Shibata N; Nagai R; Miyata S; Jono T; Horiuchi S; Hirano A; Kato S; Sasaki S; Asayama K; Kobayashi M
    Acta Neuropathol; 2000 Sep; 100(3):275-84. PubMed ID: 10965797
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Morphological evidence for lipid peroxidation and protein glycoxidation in spinal cords from sporadic amyotrophic lateral sclerosis patients.
    Shibata N; Nagai R; Uchida K; Horiuchi S; Yamada S; Hirano A; Kawaguchi M; Yamamoto T; Sasaki S; Kobayashi M
    Brain Res; 2001 Oct; 917(1):97-104. PubMed ID: 11602233
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Selective formation of certain advanced glycation end products in spinal cord astrocytes of humans and mice with superoxide dismutase-1 mutation.
    Shibata N; Hirano A; Hedley-Whyte ET; Dal Canto MC; Nagai R; Uchida K; Horiuchi S; Kawaguchi M; Yamamoto T; Kobayashi M
    Acta Neuropathol; 2002 Aug; 104(2):171-8. PubMed ID: 12111360
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Advanced glycation endproducts are deposited in neuronal hyaline inclusions: a study on familial amyotrophic lateral sclerosis with superoxide dismutase-1 mutation.
    Shibata N; Hirano A; Kato S; Nagai R; Horiuchi S; Komori T; Umahara T; Asayama K; Kobayashi M
    Acta Neuropathol; 1999 Mar; 97(3):240-6. PubMed ID: 10090670
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Advanced glycation endproduct-modified superoxide dismutase-1 (SOD1)-positive inclusions are common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutations and transgenic mice expressing human SOD1 with a G85R mutation.
    Kato S; Horiuchi S; Liu J; Cleveland DW; Shibata N; Nakashima K; Nagai R; Hirano A; Takikawa M; Kato M; Nakano I; Ohama E
    Acta Neuropathol; 2000 Nov; 100(5):490-505. PubMed ID: 11045671
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Protein-bound crotonaldehyde accumulates in the spinal cord of superoxide dismutase-1 mutation-associated familial amyotrophic lateral sclerosis and its transgenic mouse model.
    Shibata N; Kawaguchi M; Uchida K; Kakita A; Takahashi H; Nakano R; Fujimura H; Sakoda S; Ihara Y; Nobukuni K; Takehisa Y; Kuroda S; Kokubo Y; Kuzuhara S; Honma T; Mochizuki Y; Mizutani T; Yamada S; Toi S; Sasaki S; Iwata M; Hirano A; Yamamoto T; Kato Y; Sawada T; Kobayashi M
    Neuropathology; 2007 Feb; 27(1):49-61. PubMed ID: 17319283
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Amyotrophic lateral sclerosis associated with genetic abnormalities in the gene encoding Cu/Zn superoxide dismutase: molecular pathology of five new cases, and comparison with previous reports and 73 sporadic cases of ALS.
    Ince PG; Tomkins J; Slade JY; Thatcher NM; Shaw PJ
    J Neuropathol Exp Neurol; 1998 Oct; 57(10):895-904. PubMed ID: 9786240
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Astrocytic hyaline inclusions contain advanced glycation endproducts in familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutation: immunohistochemical and immunoelectron microscopical analyses.
    Kato S; Horiuchi S; Nakashima K; Hirano A; Shibata N; Nakano I; Saito M; Kato M; Asayama K; Ohama E
    Acta Neuropathol; 1999 Mar; 97(3):260-6. PubMed ID: 10090673
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Immunohistochemical study on superoxide dismutases in spinal cords from autopsied patients with amyotrophic lateral sclerosis.
    Shibata N; Asayama K; Hirano A; Kobayashi M
    Dev Neurosci; 1996; 18(5-6):492-8. PubMed ID: 8940623
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Proteomic analysis of 4-hydroxy-2-nonenal-modified proteins in G93A-SOD1 transgenic mice--a model of familial amyotrophic lateral sclerosis.
    Perluigi M; Fai Poon H; Hensley K; Pierce WM; Klein JB; Calabrese V; De Marco C; Butterfield DA
    Free Radic Biol Med; 2005 Apr; 38(7):960-8. PubMed ID: 15749392
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Histological evidence of protein aggregation in mutant SOD1 transgenic mice and in amyotrophic lateral sclerosis neural tissues.
    Watanabe M; Dykes-Hoberg M; Culotta VC; Price DL; Wong PC; Rothstein JD
    Neurobiol Dis; 2001 Dec; 8(6):933-41. PubMed ID: 11741389
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Accumulation of labile zinc in neurons and astrocytes in the spinal cords of G93A SOD-1 transgenic mice.
    Kim J; Kim TY; Hwang JJ; Lee JY; Shin JH; Gwag BJ; Koh JY
    Neurobiol Dis; 2009 May; 34(2):221-9. PubMed ID: 19344646
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Oxidative damage to mitochondrial DNA in spinal motoneurons of transgenic ALS mice.
    Warita H; Hayashi T; Murakami T; Manabe Y; Abe K
    Brain Res Mol Brain Res; 2001 Apr; 89(1-2):147-52. PubMed ID: 11311985
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expression of hepatocyte growth factor and c-Met in the anterior horn cells of the spinal cord in the patients with amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS and familial ALS with superoxide dismutase 1 gene mutation.
    Kato S; Funakoshi H; Nakamura T; Kato M; Nakano I; Hirano A; Ohama E
    Acta Neuropathol; 2003 Aug; 106(2):112-20. PubMed ID: 12707786
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Redox system expression in the motor neurons in amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS, superoxide dismutase 1 (SOD1)-mutated familial ALS, and SOD1-mutated ALS animal models.
    Kato S; Kato M; Abe Y; Matsumura T; Nishino T; Aoki M; Itoyama Y; Asayama K; Awaya A; Hirano A; Ohama E
    Acta Neuropathol; 2005 Aug; 110(2):101-12. PubMed ID: 15983830
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Detection of N epsilon-(carboxymethyl)lysine (CML) and non-CML advanced glycation end-products in the anterior horn of amyotrophic lateral sclerosis spinal cord.
    Kikuchi S; Shinpo K; Ogata A; Tsuji S; Takeuchi M; Makita Z; Tashiro K
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2002 Jun; 3(2):63-8. PubMed ID: 12215227
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Relationship of oxygen radical-induced lipid peroxidative damage to disease onset and progression in a transgenic model of familial ALS.
    Hall ED; Andrus PK; Oostveen JA; Fleck TJ; Gurney ME
    J Neurosci Res; 1998 Jul; 53(1):66-77. PubMed ID: 9670993
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Advanced glycation endproducts in neurofilament conglomeration of motoneurons in familial and sporadic amyotrophic lateral sclerosis.
    Chou SM; Wang HS; Taniguchi A; Bucala R
    Mol Med; 1998 May; 4(5):324-32. PubMed ID: 9642682
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.