100 related articles for article (PubMed ID: 16456939)
1. SOD1 mutant protein gets loose in ALS.
McCaffrey P
Lancet Neurol; 2006 Feb; 5(2):119. PubMed ID: 16456939
[No Abstract] [Full Text] [Related]
2. [Molecular mechanisms of ALS-linked mutant SOD1-induced motor neuron death].
Nishitoh H; Ichijo H
Tanpakushitsu Kakusan Koso; 2009 Mar; 54(3):237-44. PubMed ID: 19288861
[No Abstract] [Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. Ablation of proliferating microglia does not affect motor neuron degeneration in amyotrophic lateral sclerosis caused by mutant superoxide dismutase.
Gowing G; Philips T; Van Wijmeersch B; Audet JN; Dewil M; Van Den Bosch L; Billiau AD; Robberecht W; Julien JP
J Neurosci; 2008 Oct; 28(41):10234-44. PubMed ID: 18842883
[TBL] [Abstract][Full Text] [Related]
7. Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis.
Urushitani M; Sik A; Sakurai T; Nukina N; Takahashi R; Julien JP
Nat Neurosci; 2006 Jan; 9(1):108-18. PubMed ID: 16369483
[TBL] [Abstract][Full Text] [Related]
8. Complete dissociation of motor neuron death from motor dysfunction by Bax deletion in a mouse model of ALS.
Gould TW; Buss RR; Vinsant S; Prevette D; Sun W; Knudson CM; Milligan CE; Oppenheim RW
J Neurosci; 2006 Aug; 26(34):8774-86. PubMed ID: 16928866
[TBL] [Abstract][Full Text] [Related]
9. From Charcot to SOD1: mechanisms of selective motor neuron death in ALS.
Cleveland DW
Neuron; 1999 Nov; 24(3):515-20. PubMed ID: 10595505
[No Abstract] [Full Text] [Related]
10. Early decrease of redox factor-1 in spinal motor neurons of presymptomatic transgenic mice with a mutant SOD1 gene.
Manabe Y; Warita H; Murakami T; Shiote M; Hayashi T; Nagano I; Shoji M; Abe K
Brain Res; 2001 Oct; 915(1):104-7. PubMed ID: 11578626
[TBL] [Abstract][Full Text] [Related]
11. Death signalling pathway in mice motoneurons is unique and sensitive in those expressing ALS mutant SOD1.
Reilly CE
J Neurol; 2002 Dec; 249(12):1756-8. PubMed ID: 12683398
[No Abstract] [Full Text] [Related]
12. Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loading.
Subramaniam JR; Lyons WE; Liu J; Bartnikas TB; Rothstein J; Price DL; Cleveland DW; Gitlin JD; Wong PC
Nat Neurosci; 2002 Apr; 5(4):301-7. PubMed ID: 11889469
[TBL] [Abstract][Full Text] [Related]
13. Zinc in the spinal cord of a mutant SOD1 mouse model of ALS.
Pamphlett R; Kum-Jew S
Neuroreport; 2003 Mar; 14(4):547-9. PubMed ID: 12657882
[TBL] [Abstract][Full Text] [Related]
14. Prion-like propagation of mutant SOD1 misfolding and motor neuron disease spread along neuroanatomical pathways.
Ayers JI; Fromholt SE; O'Neal VM; Diamond JH; Borchelt DR
Acta Neuropathol; 2016 Jan; 131(1):103-14. PubMed ID: 26650262
[TBL] [Abstract][Full Text] [Related]
15. New Model System Offers Clues to ALS.
Kuehn BM
JAMA; 2011 Oct; 306(14):1534. PubMed ID: 21990293
[No Abstract] [Full Text] [Related]
16. GAB(A) receptors present higher affinity and modified subunit composition in spinal motor neurons from a genetic model of amyotrophic lateral sclerosis.
Carunchio I; Mollinari C; Pieri M; Merlo D; Zona C
Eur J Neurosci; 2008 Oct; 28(7):1275-85. PubMed ID: 18973555
[TBL] [Abstract][Full Text] [Related]
17. Neuregulin 1 confers neuroprotection in SOD1-linked amyotrophic lateral sclerosis mice via restoration of C-boutons of spinal motor neurons.
Lasiene J; Komine O; Fujimori-Tonou N; Powers B; Endo F; Watanabe S; Shijie J; Ravits J; Horner P; Misawa H; Yamanaka K
Acta Neuropathol Commun; 2016 Feb; 4():15. PubMed ID: 26891847
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Wild-type superoxide dismutase acquires binding and toxic properties of ALS-linked mutant forms through oxidation.
Ezzi SA; Urushitani M; Julien JP
J Neurochem; 2007 Jul; 102(1):170-8. PubMed ID: 17394546
[TBL] [Abstract][Full Text] [Related]
20. Fas(t) balls and Lou Gehrig disease. A clue to selective vulnerability of motor neurons?
Xiong ZQ; McNamara JO
Neuron; 2002 Sep; 35(6):1011-3. PubMed ID: 12354390
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]