BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 17482163)

  • 41. Early upregulation of cytosolic phospholipase A
    Malada Edelstein YF; Solomonov Y; Hadad N; Alfahel L; Israelson A; Levy R
    J Neuroinflammation; 2021 Nov; 18(1):274. PubMed ID: 34823547
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Alteration of familial ALS-linked mutant SOD1 solubility with disease progression: its modulation by the proteasome and Hsp70.
    Koyama S; Arawaka S; Chang-Hong R; Wada M; Kawanami T; Kurita K; Kato M; Nagai M; Aoki M; Itoyama Y; Sobue G; Chan PH; Kato T
    Biochem Biophys Res Commun; 2006 May; 343(3):719-30. PubMed ID: 16563356
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Aggregation of ubiquitin and a mutant ALS-linked SOD1 protein correlate with disease progression and fragmentation of the Golgi apparatus.
    Stieber A; Gonatas JO; Gonatas NK
    J Neurol Sci; 2000 Feb; 173(1):53-62. PubMed ID: 10675580
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Complement upregulation and activation on motor neurons and neuromuscular junction in the SOD1 G93A mouse model of familial amyotrophic lateral sclerosis.
    Heurich B; El Idrissi NB; Donev RM; Petri S; Claus P; Neal J; Morgan BP; Ramaglia V
    J Neuroimmunol; 2011 Jun; 235(1-2):104-9. PubMed ID: 21501881
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Ammonium tetrathiomolybdate delays onset, prolongs survival, and slows progression of disease in a mouse model for amyotrophic lateral sclerosis.
    Tokuda E; Ono S; Ishige K; Watanabe S; Okawa E; Ito Y; Suzuki T
    Exp Neurol; 2008 Sep; 213(1):122-8. PubMed ID: 18617166
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Isoform-selective as opposed to complete depletion of fibroblast growth factor 2 (FGF-2) has no major impact on survival and gene expression in SOD1
    Kefalakes E; Sarikidi A; Bursch F; Ettcheto M; Schmuck M; Rumpel R; Grothe C; Petri S
    Eur J Neurosci; 2019 Sep; 50(6):3028-3045. PubMed ID: 30883949
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Insoluble mutant SOD1 is partly oligoubiquitinated in amyotrophic lateral sclerosis mice.
    Basso M; Massignan T; Samengo G; Cheroni C; De Biasi S; Salmona M; Bendotti C; Bonetto V
    J Biol Chem; 2006 Nov; 281(44):33325-35. PubMed ID: 16943203
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Co-chaperone CHIP associates with mutant Cu/Zn-superoxide dismutase proteins linked to familial amyotrophic lateral sclerosis and promotes their degradation by proteasomes.
    Choi JS; Cho S; Park SG; Park BC; Lee DH
    Biochem Biophys Res Commun; 2004 Aug; 321(3):574-83. PubMed ID: 15358145
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Immunohistochemical study on the distribution of glycogen synthase kinase 3alpha in the central nervous system of SOD1(G93A) transgenic mice.
    Chung YH; Joo KM; Kim DJ; Kim SS; Kim KY; Lee WB; Cha CI
    Neurol Res; 2008 Nov; 30(9):926-31. PubMed ID: 18671898
    [TBL] [Abstract][Full Text] [Related]  

  • 50. SQSTM1, a protective factor of SOD1-linked motor neuron disease, regulates the accumulation and distribution of ubiquitinated protein aggregates in neuron.
    Mitsui S; Otomo A; Sato K; Ishiyama M; Shimakura K; Okada-Yamaguchi C; Warabi E; Yanagawa T; Aoki M; Shang HF; Hadano S
    Neurochem Int; 2022 Sep; 158():105364. PubMed ID: 35640762
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Disease-dependent reciprocal phosphorylation of serine and tyrosine residues of c-Met/HGF receptor contributes disease retardation of a transgenic mouse model of ALS.
    Kadoyama K; Funakoshi H; Ohya-Shimada W; Nakamura T; Matsumoto K; Matsuyama S; Nakamura T
    Neurosci Res; 2009 Oct; 65(2):194-200. PubMed ID: 19595710
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Mutation of the caspase-3 cleavage site in the astroglial glutamate transporter EAAT2 delays disease progression and extends lifespan in the SOD1-G93A mouse model of ALS.
    Rosenblum LT; Shamamandri-Markandaiah S; Ghosh B; Foran E; Lepore AC; Pasinelli P; Trotti D
    Exp Neurol; 2017 Jun; 292():145-153. PubMed ID: 28342750
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Enhanced Function and Overexpression of Metabotropic Glutamate Receptors 1 and 5 in the Spinal Cord of the SOD1
    Bonifacino T; Rebosio C; Provenzano F; Torazza C; Balbi M; Milanese M; Raiteri L; Usai C; Fedele E; Bonanno G
    Int J Mol Sci; 2019 Sep; 20(18):. PubMed ID: 31540330
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Increased autophagy in transgenic mice with a G93A mutant SOD1 gene.
    Morimoto N; Nagai M; Ohta Y; Miyazaki K; Kurata T; Morimoto M; Murakami T; Takehisa Y; Ikeda Y; Kamiya T; Abe K
    Brain Res; 2007 Sep; 1167():112-7. PubMed ID: 17689501
    [TBL] [Abstract][Full Text] [Related]  

  • 55. ACTH (Acthar Gel) Reduces Toxic SOD1 Protein Linked to Amyotrophic Lateral Sclerosis in Transgenic Mice: A Novel Observation.
    Arrat H; Lukas TJ; Siddique T
    PLoS One; 2015; 10(5):e0125638. PubMed ID: 25955410
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Mutation of SOD1 in ALS: a gain of a loss of function.
    Sau D; De Biasi S; Vitellaro-Zuccarello L; Riso P; Guarnieri S; Porrini M; Simeoni S; Crippa V; Onesto E; Palazzolo I; Rusmini P; Bolzoni E; Bendotti C; Poletti A
    Hum Mol Genet; 2007 Jul; 16(13):1604-18. PubMed ID: 17504823
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. Fatigability of spinal reflex transmission in a mouse model (SOD1(G93A) ) of amyotrophic lateral sclerosis.
    Schomburg ED; Steffens H; Zschüntzsch J; Dibaj P; Keller BU
    Muscle Nerve; 2011 Feb; 43(2):230-6. PubMed ID: 21254088
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Sex specific activation of the ERα axis of the mitochondrial UPR (UPRmt) in the G93A-SOD1 mouse model of familial ALS.
    Riar AK; Burstein SR; Palomo GM; Arreguin A; Manfredi G; Germain D
    Hum Mol Genet; 2017 Apr; 26(7):1318-1327. PubMed ID: 28186560
    [TBL] [Abstract][Full Text] [Related]  

  • 60. C1q induction and global complement pathway activation do not contribute to ALS toxicity in mutant SOD1 mice.
    Lobsiger CS; Boillée S; Pozniak C; Khan AM; McAlonis-Downes M; Lewcock JW; Cleveland DW
    Proc Natl Acad Sci U S A; 2013 Nov; 110(46):E4385-92. PubMed ID: 24170856
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.