Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jurgen Meier"'
Publikováno v:
Brain and Spine, Vol 3, Iss , Pp 101790- (2023)
Externí odkaz:
https://doaj.org/article/a3f629d8a4b04b94b0afed18db8cc954
Publikováno v:
Brain Pathol
Amyotrophic lateral sclerosis (ALS) is an adult-onset neurological disorder of multiple etiologies that affects primarily motor neurons in the brain and spinal cord. Abnormal accumulations of neurofilaments (NFs) in motor neurons and a down-regulatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b788eb270398f3f097de2a266053ab08
https://doi.org/10.1111/j.1750-3639.1998.tb00199.x
https://doi.org/10.1111/j.1750-3639.1998.tb00199.x
Autor:
Anna Stieber, Jacqueline O. Gonatas, Jean-Pierre Julien, Nicholas K. Gonatas, Peter Schweitzer, Jurgen Meier, Jean-Francois Collard
Publikováno v:
Journal of the neurological sciences. 173(1)
Fragmentation of the Golgi apparatus (GA) of motor neurons was first described in sporadic amyotrophic lateral sclerosis (ALS) and later confirmed in transgenic mice expressing the G93A mutation of the gene encoding the enzyme Cu,Zn superoxide dismut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fc62170608f09b8a1bc51f81c1d2a71
https://pubmed.ncbi.nlm.nih.gov/10675581
https://pubmed.ncbi.nlm.nih.gov/10675581
Publikováno v:
Journal of neuropathology and experimental neurology. 58(10)
Previous studies demonstrated that transgenic mice overexpressing human neurofilament heavy (hNF-H) protein develop a progressive motor neuron disease characterized by the perikaryal accumulations of neurofilaments resembling those found in amyotroph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85f3ec78e0223a2e3bf3191f49bd8787
https://pubmed.ncbi.nlm.nih.gov/10515233
https://pubmed.ncbi.nlm.nih.gov/10515233
Publikováno v:
ECS Meeting Abstracts. :294-294
not Available.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d50c57c9dc51c20372d6b1011f0f62e1
https://doi.org/10.1149/ma2005-01/5/294
https://doi.org/10.1149/ma2005-01/5/294
Publikováno v:
Neurobiology of Disease, Vol 7, Iss 4, Pp 462-470 (2000)
A recent report by T. L. Williamson et al. (1998, Proc. Natl. Acad. Sci. USA 95, 9631–9636) showed that disease caused by expression of mutant Cu,Zn superoxide dismutase (SOD1) in mice was slowed down by disruption of the neurofilament light (NF-L)
Externí odkaz:
https://doaj.org/article/d23737e94d9242019bba5236cea4c6f1