211 related articles for article (PubMed ID: 9804382)
1. Transgenic mice in the study of ALS: the role of neurofilaments.
Julien JP; Couillard-Després S; Meier J
Brain Pathol; 1998 Oct; 8(4):759-69. PubMed ID: 9804382
[TBL] [Abstract][Full Text] [Related]
2. The neuronal Golgi apparatus is fragmented in transgenic mice expressing a mutant human SOD1, but not in mice expressing the human NF-H gene.
Stieber A; Gonatas JO; Collard J; Meier J; Julien J; Schweitzer P; Gonatas NK
J Neurol Sci; 2000 Feb; 173(1):63-72. PubMed ID: 10675581
[TBL] [Abstract][Full Text] [Related]
3. Protective effect of neurofilament heavy gene overexpression in motor neuron disease induced by mutant superoxide dismutase.
Couillard-Després S; Zhu Q; Wong PC; Price DL; Cleveland DW; Julien JP
Proc Natl Acad Sci U S A; 1998 Aug; 95(16):9626-30. PubMed ID: 9689131
[TBL] [Abstract][Full Text] [Related]
4. Overexpression of neurofilament subunit NF-L and NF-H extends survival of a mouse model for amyotrophic lateral sclerosis.
Kong J; Xu Z
Neurosci Lett; 2000 Mar; 281(1):72-4. PubMed ID: 10686419
[TBL] [Abstract][Full Text] [Related]
5. Absence of neurofilaments reduces the selective vulnerability of motor neurons and slows disease caused by a familial amyotrophic lateral sclerosis-linked superoxide dismutase 1 mutant.
Williamson TL; Bruijn LI; Zhu Q; Anderson KL; Anderson SD; Julien JP; Cleveland DW
Proc Natl Acad Sci U S A; 1998 Aug; 95(16):9631-6. PubMed ID: 9689132
[TBL] [Abstract][Full Text] [Related]
6. Extra axonal neurofilaments do not exacerbate disease caused by mutant Cu,Zn superoxide dismutase.
Couillard-Després S; Meier J; Julien JP
Neurobiol Dis; 2000 Aug; 7(4):462-70. PubMed ID: 10964615
[TBL] [Abstract][Full Text] [Related]
7. Cytoskeletal abnormalities in amyotrophic lateral sclerosis: beneficial or detrimental effects?
Julien JP; Beaulieu JM
J Neurol Sci; 2000 Nov; 180(1-2):7-14. PubMed ID: 11090858
[TBL] [Abstract][Full Text] [Related]
8. Neurofilaments in health and disease.
Julien JP; Mushynski WE
Prog Nucleic Acid Res Mol Biol; 1998; 61():1-23. PubMed ID: 9752717
[TBL] [Abstract][Full Text] [Related]
9. Neurofilaments and orthograde transport are reduced in ventral root axons of transgenic mice that express human SOD1 with a G93A mutation.
Zhang B; Tu P; Abtahian F; Trojanowski JQ; Lee VM
J Cell Biol; 1997 Dec; 139(5):1307-15. PubMed ID: 9382875
[TBL] [Abstract][Full Text] [Related]
10. Oxidative stress, mutant SOD1, and neurofilament pathology in transgenic mouse models of human motor neuron disease.
Tu PH; Gurney ME; Julien JP; Lee VM; Trojanowski JQ
Lab Invest; 1997 Apr; 76(4):441-56. PubMed ID: 9111507
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions.
Tu PH; Raju P; Robinson KA; Gurney ME; Trojanowski JQ; Lee VM
Proc Natl Acad Sci U S A; 1996 Apr; 93(7):3155-60. PubMed ID: 8610185
[TBL] [Abstract][Full Text] [Related]
13. Altered axonal architecture by removal of the heavily phosphorylated neurofilament tail domains strongly slows superoxide dismutase 1 mutant-mediated ALS.
Lobsiger CS; Garcia ML; Ward CM; Cleveland DW
Proc Natl Acad Sci U S A; 2005 Jul; 102(29):10351-6. PubMed ID: 16002469
[TBL] [Abstract][Full Text] [Related]
14. A role for neurofilaments in the pathogenesis of amyotrophic lateral sclerosis.
Julien JP
Biochem Cell Biol; 1995; 73(9-10):593-7. PubMed ID: 8714677
[TBL] [Abstract][Full Text] [Related]
15. Reduction of axonal caliber does not alleviate motor neuron disease caused by mutant superoxide dismutase 1.
Nguyen MD; Larivière RC; Julien JP
Proc Natl Acad Sci U S A; 2000 Oct; 97(22):12306-11. PubMed ID: 11050249
[TBL] [Abstract][Full Text] [Related]
16. Early and selective pathology of light chain neurofilament in the spinal cord and sciatic nerve of G86R mutant superoxide dismutase transgenic mice.
Morrison BM; Shu IW; Wilcox AL; Gordon JW; Morrison JH
Exp Neurol; 2000 Oct; 165(2):207-20. PubMed ID: 10993681
[TBL] [Abstract][Full Text] [Related]
17. Transgenic mouse model for familial amyotrophic lateral sclerosis with superoxide dismutase-1 mutation.
Shibata N
Neuropathology; 2001 Mar; 21(1):82-92. PubMed ID: 11304046
[TBL] [Abstract][Full Text] [Related]
18. Extra neurofilament NF-L subunits rescue motor neuron disease caused by overexpression of the human NF-H gene in mice.
Meier J; Couillard-Després S; Jacomy H; Gravel C; Julien JP
J Neuropathol Exp Neurol; 1999 Oct; 58(10):1099-110. PubMed ID: 10515233
[TBL] [Abstract][Full Text] [Related]
19. The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the disease.
Mourelatos Z; Gonatas NK; Stieber A; Gurney ME; Dal Canto MC
Proc Natl Acad Sci U S A; 1996 May; 93(11):5472-7. PubMed ID: 8643599
[TBL] [Abstract][Full Text] [Related]
20. Sequence variants in human neurofilament proteins: absence of linkage to familial amyotrophic lateral sclerosis.
Vechio JD; Bruijn LI; Xu Z; Brown RH; Cleveland DW
Ann Neurol; 1996 Oct; 40(4):603-10. PubMed ID: 8871580
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
