BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 8786408)

  • 21. 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]  

  • 22. Accumulation of neurofilaments and SOD1-immunoreactive products in a patient with familial amyotrophic lateral sclerosis with I113T SOD1 mutation.
    Kokubo Y; Kuzuhara S; Narita Y; Kikugawa K; Nakano R; Inuzuka T; Tsuji S; Watanabe M; Miyazaki T; Murayama S; Ihara Y
    Arch Neurol; 1999 Dec; 56(12):1506-8. PubMed ID: 10593307
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.
    Mackenzie IR; Bigio EH; Ince PG; Geser F; Neumann M; Cairns NJ; Kwong LK; Forman MS; Ravits J; Stewart H; Eisen A; McClusky L; Kretzschmar HA; Monoranu CM; Highley JR; Kirby J; Siddique T; Shaw PJ; Lee VM; Trojanowski JQ
    Ann Neurol; 2007 May; 61(5):427-34. PubMed ID: 17469116
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Expression of an endoplasmic reticulum-resident chaperone, glucose-regulated stress protein 78, in the spinal cord of a mouse model of amyotrophic lateral sclerosis.
    Wate R; Ito H; Zhang JH; Ohnishi S; Nakano S; Kusaka H
    Acta Neuropathol; 2005 Dec; 110(6):557-62. PubMed ID: 16231159
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Familial amyotrophic lateral sclerosis with an I104F mutation in the SOD1 gene: Multisystem degeneration with neurofilamentous aggregates and SOD1 inclusions.
    Jiang H; Shimizu H; Shiga A; Tanaka M; Onodera O; Kakita A; Takahashi H
    Neuropathology; 2017 Feb; 37(1):69-77. PubMed ID: 27444855
    [TBL] [Abstract][Full Text] [Related]  

  • 26. An autopsy case of sporadic amyotrophic lateral sclerosis associated with the I113T SOD1 mutation.
    Nakamura S; Wate R; Kaneko S; Ito H; Oki M; Tsuge A; Nagashima M; Asayama S; Fujita K; Nakamura M; Maruyama H; Kawakami H; Kusaka H
    Neuropathology; 2014 Feb; 34(1):58-63. PubMed ID: 23773010
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Amyotrophic lateral sclerosis is a non-amyloid disease in which extensive misfolding of SOD1 is unique to the familial form.
    Kerman A; Liu HN; Croul S; Bilbao J; Rogaeva E; Zinman L; Robertson J; Chakrabartty A
    Acta Neuropathol; 2010 Mar; 119(3):335-44. PubMed ID: 20111867
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mutant SOD1.
    Jaarsma D; Haasdijk ED; Grashorn JA; Hawkins R; van Duijn W; Verspaget HW; London J; Holstege JC
    Neurobiol Dis; 2000 Dec; 7(6 Pt B):623-43. PubMed ID: 11114261
    [TBL] [Abstract][Full Text] [Related]  

  • 30. FALS with Gly72Ser mutation in SOD1 gene: report of a family including the first autopsy case.
    Kobayashi Z; Tsuchiya K; Kubodera T; Shibata N; Arai T; Miura H; Ishikawa C; Kondo H; Ishizu H; Akiyama H; Mizusawa H
    J Neurol Sci; 2011 Jan; 300(1-2):9-13. PubMed ID: 21084099
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Nuclear TAR DNA binding protein 43 expression in spinal cord neurons correlates with the clinical course in amyotrophic lateral sclerosis.
    Sumi H; Kato S; Mochimaru Y; Fujimura H; Etoh M; Sakoda S
    J Neuropathol Exp Neurol; 2009 Jan; 68(1):37-47. PubMed ID: 19104447
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. 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]  

  • 35. Cu/Zn superoxide dismutase-like immunoreactivity in Lewy body-like inclusions of sporadic amyotrophic lateral sclerosis.
    Shibata N; Hirano A; Kobayashi M; Sasaki S; Kato T; Matsumoto S; Shiozawa Z; Komori T; Ikemoto A; Umahara T
    Neurosci Lett; 1994 Sep; 179(1-2):149-52. PubMed ID: 7845611
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Immunodetection of disease-associated conformers of mutant cu/zn superoxide dismutase 1 selectively expressed in degenerating neurons in amyotrophic lateral sclerosis.
    Sábado J; Casanovas A; Hernández S; Piedrafita L; Hereu M; Esquerda JE
    J Neuropathol Exp Neurol; 2013 Jul; 72(7):646-61. PubMed ID: 23771221
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Lack of evidence of monomer/misfolded superoxide dismutase-1 in sporadic amyotrophic lateral sclerosis.
    Liu HN; Sanelli T; Horne P; Pioro EP; Strong MJ; Rogaeva E; Bilbao J; Zinman L; Robertson J
    Ann Neurol; 2009 Jul; 66(1):75-80. PubMed ID: 19670443
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Immunohistochemical analysis of sympathetic involvement in the SOD1-G93A transgenic mouse model of amyotrophic lateral sclerosis.
    Kandinov B; Grigoriadis NC; Touloumi O; Drory VE; Offen D; Korczyn AD
    Amyotroph Lateral Scler Frontotemporal Degener; 2013 Sep; 14(5-6):424-33. PubMed ID: 23607704
    [TBL] [Abstract][Full Text] [Related]  

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