BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 11874201)

  • 41. 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]  

  • 42. Prominent expression of glial cell line-derived neurotrophic factor in human skeletal muscle.
    Suzuki H; Hase A; Miyata Y; Arahata K; Akazawa C
    J Comp Neurol; 1998 Dec; 402(3):303-12. PubMed ID: 9853901
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Delayed disease onset and extended survival in the SOD1G93A rat model of amyotrophic lateral sclerosis after suppression of mutant SOD1 in the motor cortex.
    Thomsen GM; Gowing G; Latter J; Chen M; Vit JP; Staggenborg K; Avalos P; Alkaslasi M; Ferraiuolo L; Likhite S; Kaspar BK; Svendsen CN
    J Neurosci; 2014 Nov; 34(47):15587-600. PubMed ID: 25411487
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Focal transplantation-based astrocyte replacement is neuroprotective in a model of motor neuron disease.
    Lepore AC; Rauck B; Dejea C; Pardo AC; Rao MS; Rothstein JD; Maragakis NJ
    Nat Neurosci; 2008 Nov; 11(11):1294-301. PubMed ID: 18931666
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Additivity and potentiation of IGF-I and GDNF in the complete rescue of postnatal motor neurons.
    Bilak MM; Corse AM; Kuncl RW
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2001 Jun; 2(2):83-91. PubMed ID: 11675876
    [TBL] [Abstract][Full Text] [Related]  

  • 46. 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]  

  • 47. Overexpression of metallothionein-I, a copper-regulating protein, attenuates intracellular copper dyshomeostasis and extends lifespan in a mouse model of amyotrophic lateral sclerosis caused by mutant superoxide dismutase-1.
    Tokuda E; Okawa E; Watanabe S; Ono S
    Hum Mol Genet; 2014 Mar; 23(5):1271-85. PubMed ID: 24163136
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Overexpressed wild-type superoxide dismutase 1 exhibits amyotrophic lateral sclerosis-related misfolded conformation in induced pluripotent stem cell-derived spinal motor neurons.
    Komatsu K; Imamura K; Yamashita H; Julien JP; Takahashi R; Inoue H
    Neuroreport; 2018 Jan; 29(1):25-29. PubMed ID: 29140847
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Amyloid precursor protein (APP) contributes to pathology in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Bryson JB; Hobbs C; Parsons MJ; Bosch KD; Pandraud A; Walsh FS; Doherty P; Greensmith L
    Hum Mol Genet; 2012 Sep; 21(17):3871-82. PubMed ID: 22678056
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Gene transfer for neuroprotection in animal models of Parkinson's disease and amyotrophic lateral sclerosis.
    Bohn MC; Connor B; Kozlowski DA; Mohajeri MH
    Novartis Found Symp; 2000; 231():70-89; discussion 89-93. PubMed ID: 11131547
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice.
    Clement AM; Nguyen MD; Roberts EA; Garcia ML; Boillée S; Rule M; McMahon AP; Doucette W; Siwek D; Ferrante RJ; Brown RH; Julien JP; Goldstein LS; Cleveland DW
    Science; 2003 Oct; 302(5642):113-7. PubMed ID: 14526083
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Gene transfer of glial cell line-derived neurotrophic factor promotes functional recovery following spinal cord contusion.
    Tai MH; Cheng H; Wu JP; Liu YL; Lin PR; Kuo JS; Tseng CJ; Tzeng SF
    Exp Neurol; 2003 Oct; 183(2):508-15. PubMed ID: 14552891
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A glial cell line-derived neurotrophic factor (GDNF):tetanus toxin fragment C protein conjugate improves delivery of GDNF to spinal cord motor neurons in mice.
    Larsen KE; Benn SC; Ay I; Chian RJ; Celia SA; Remington MP; Bejarano M; Liu M; Ross J; Carmillo P; Sah D; Phillips KA; Sulzer D; Pepinsky RB; Fishman PS; Brown RH; Francis JW
    Brain Res; 2006 Nov; 1120(1):1-12. PubMed ID: 17020749
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Gene therapy and neurotrophic factor treatment for amyotrophic lateral sclerosis].
    Abe K; Manabe Y; Murakami T
    Rinsho Shinkeigaku; 2001 Dec; 41(12):1160-1. PubMed ID: 12235826
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Amyotrophic lateral sclerosis-related mutant superoxide dismutase 1 aggregates inhibit 14-3-3-mediated cell survival by sequestration into the JUNQ compartment.
    Park JH; Jang HR; Lee IY; Oh HK; Choi EJ; Rhim H; Kang S
    Hum Mol Genet; 2017 Sep; 26(18):3615-3629. PubMed ID: 28666328
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Analysis of neurotrophic factors in limb and extraocular muscles of mouse model of amyotrophic lateral sclerosis.
    Harandi VM; Lindquist S; Kolan SS; Brännström T; Liu JX
    PLoS One; 2014; 9(10):e109833. PubMed ID: 25334047
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A commentary on glial cell line-derived neurotrophic factor (GDNF). From a glial secreted molecule to gene therapy.
    Bohn MC
    Biochem Pharmacol; 1999 Jan; 57(2):135-42. PubMed ID: 9890561
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Rescue of lesioned adult rat spinal motoneurons by adenoviral gene transfer of glial cell line-derived neurotrophic factor.
    Watabe K; Ohashi T; Sakamoto T; Kawazoe Y; Takeshima T; Oyanagi K; Inoue K; Eto Y; Kim SU
    J Neurosci Res; 2000 May; 60(4):511-9. PubMed ID: 10797554
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Motor neuron-astrocyte interactions and levels of Cu,Zn superoxide dismutase in sporadic amyotrophic lateral sclerosis.
    O'Reilly SA; Roedica J; Nagy D; Hallewell RA; Alderson K; Marklund SL; Kuby J; Kushner PD
    Exp Neurol; 1995 Feb; 131(2):203-10. PubMed ID: 7895821
    [TBL] [Abstract][Full Text] [Related]  

  • 60. The in vivo contribution of motor neuron TrkB receptors to mutant SOD1 motor neuron disease.
    Zhai J; Zhou W; Li J; Hayworth CR; Zhang L; Misawa H; Klein R; Scherer SS; Balice-Gordon RJ; Kalb RG
    Hum Mol Genet; 2011 Nov; 20(21):4116-31. PubMed ID: 21816949
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.