131 related articles for article (PubMed ID: 9875737)
21. Mice overexpressing the human neurofilament heavy gene as a model of ALS.
Julien JP; Côté F; Collard JF
Neurobiol Aging; 1995; 16(3):487-90; discussion 490-2. PubMed ID: 7566355
[TBL] [Abstract][Full Text] [Related]
22. A 14-3-3 mRNA is up-regulated in amyotrophic lateral sclerosis spinal cord.
Malaspina A; Kaushik N; de Belleroche J
J Neurochem; 2000 Dec; 75(6):2511-20. PubMed ID: 11080204
[TBL] [Abstract][Full Text] [Related]
23. Focal accumulation of phosphorylated neurofilaments within anterior horn cell in familial amyotrophic lateral sclerosis.
Mizusawa H; Matsumoto S; Yen SH; Hirano A; Rojas-Corona RR; Donnenfeld H
Acta Neuropathol; 1989; 79(1):37-43. PubMed ID: 2511732
[TBL] [Abstract][Full Text] [Related]
24. Neurofilament light and polyadenylated mRNA levels are decreased in amyotrophic lateral sclerosis motor neurons.
Bergeron C; Beric-Maskarel K; Muntasser S; Weyer L; Somerville MJ; Percy ME
J Neuropathol Exp Neurol; 1994 May; 53(3):221-30. PubMed ID: 7909836
[TBL] [Abstract][Full Text] [Related]
25. Altered ionic conductances in axons of transgenic mouse expressing the human neurofilament heavy gene: A mouse model of amyotrophic lateral sclerosis.
Kriz J; Meier J; Julien JP; Padjen AL
Exp Neurol; 2000 Jun; 163(2):414-21. PubMed ID: 10833316
[TBL] [Abstract][Full Text] [Related]
26. A simple test to monitor the motor dysfunction in a transgenic mouse model of amyotrophic lateral sclerosis.
Collard JF; Julien JP
J Psychiatry Neurosci; 1995 Jan; 20(1):80-2. PubMed ID: 7865504
[TBL] [Abstract][Full Text] [Related]
27. Variation of the neurofilament medium KSP repeat sub-domain across mammalian species: implications for altering axonal structure.
Barry DM; Carpenter C; Yager C; Golik B; Barry KJ; Shen H; Mikse O; Eggert LS; Schulz DJ; Garcia ML
J Exp Biol; 2010 Jan; 213(1):128-36. PubMed ID: 20008369
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. CSF neurofilament proteins as diagnostic and prognostic biomarkers for amyotrophic lateral sclerosis.
Rossi D; Volanti P; Brambilla L; Colletti T; Spataro R; La Bella V
J Neurol; 2018 Mar; 265(3):510-521. PubMed ID: 29322259
[TBL] [Abstract][Full Text] [Related]
30. Amyotrophic lateral sclerosis associated with genetic abnormalities in the gene encoding Cu/Zn superoxide dismutase: molecular pathology of five new cases, and comparison with previous reports and 73 sporadic cases of ALS.
Ince PG; Tomkins J; Slade JY; Thatcher NM; Shaw PJ
J Neuropathol Exp Neurol; 1998 Oct; 57(10):895-904. PubMed ID: 9786240
[TBL] [Abstract][Full Text] [Related]
31. Tar DNA binding protein of 43 kDa (TDP-43), 14-3-3 proteins and copper/zinc superoxide dismutase (SOD1) interact to modulate NFL mRNA stability. Implications for altered RNA processing in amyotrophic lateral sclerosis (ALS).
Volkening K; Leystra-Lantz C; Yang W; Jaffee H; Strong MJ
Brain Res; 2009 Dec; 1305():168-82. PubMed ID: 19815002
[TBL] [Abstract][Full Text] [Related]
32. Ultrastructural evidence of neurofilament involvement in immune-mediated motor neuron injury.
Liu YL; Guo YS; Xu L; Wu SY; Wu DX; Yang C; Li CY
Neurol Res; 2008 Nov; 30(9):990-4. PubMed ID: 18662498
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Allelic variants of the canine heavy neurofilament (NFH) subunit and extensive phosphorylation in dogs with motor neuron disease.
Green SL; Westendorf JM; Jaffe H; Pant HC; Cork LC; Ostrander EA; Vignaux F; Ferrell JE
J Comp Pathol; 2005 Jan; 132(1):33-50. PubMed ID: 15629478
[TBL] [Abstract][Full Text] [Related]
35. The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy.
Bomont P; Cavalier L; Blondeau F; Ben Hamida C; Belal S; Tazir M; Demir E; Topaloglu H; Korinthenberg R; Tüysüz B; Landrieu P; Hentati F; Koenig M
Nat Genet; 2000 Nov; 26(3):370-4. PubMed ID: 11062483
[TBL] [Abstract][Full Text] [Related]
36. Cerebrospinal fluid neurofilament light levels in amyotrophic lateral sclerosis: impact of SOD1 genotype.
Zetterberg H; Jacobsson J; Rosengren L; Blennow K; Andersen PM
Eur J Neurol; 2007 Dec; 14(12):1329-33. PubMed ID: 17903209
[TBL] [Abstract][Full Text] [Related]
37. Humoral response to neurofilaments and dipeptide repeats in ALS progression.
Puentes F; Lombardi V; Lu CH; Yildiz O; Fratta P; Isaacs A; Bobeva Y; Wuu J; ; ; Benatar M; Malaspina A
Ann Clin Transl Neurol; 2021 Sep; 8(9):1831-1844. PubMed ID: 34318620
[TBL] [Abstract][Full Text] [Related]
38. Neurofilament levels as biomarkers in asymptomatic and symptomatic familial amyotrophic lateral sclerosis.
Weydt P; Oeckl P; Huss A; Müller K; Volk AE; Kuhle J; Knehr A; Andersen PM; Prudlo J; Steinacker P; Weishaupt JH; Ludolph AC; Otto M
Ann Neurol; 2016 Jan; 79(1):152-8. PubMed ID: 26528863
[TBL] [Abstract][Full Text] [Related]
39. Diagnostic and prognostic significance of neurofilament light chain NF-L, but not progranulin and S100B, in the course of amyotrophic lateral sclerosis: Data from the German MND-net.
Steinacker P; Huss A; Mayer B; Grehl T; Grosskreutz J; Borck G; Kuhle J; Lulé D; Meyer T; Oeckl P; Petri S; Weishaupt J; Ludolph AC; Otto M
Amyotroph Lateral Scler Frontotemporal Degener; 2017 Feb; 18(1-2):112-119. PubMed ID: 27819158
[TBL] [Abstract][Full Text] [Related]
40. A novel TARDBP mutation in an Australian amyotrophic lateral sclerosis kindred.
Williams KL; Durnall JC; Thoeng AD; Warraich ST; Nicholson GA; Blair IP
J Neurol Neurosurg Psychiatry; 2009 Nov; 80(11):1286-8. PubMed ID: 19864664
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
