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.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117 Mol+Cell+Neurosci
2016 ; 71
(ä): 34-45
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gab.com Text
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Expression of microRNAs in human post-mortem amyotrophic lateral sclerosis spinal
cords provides insight into disease mechanisms
#MMPMID26704906
Figueroa-Romero C
; Hur J
; Lunn JS
; Paez-Colasante X
; Bender DE
; Yung R
; Sakowski SA
; Feldman EL
Mol Cell Neurosci
2016[Mar]; 71
(ä): 34-45
PMID26704906
show ga
Amyotrophic lateral sclerosis is a late-onset and terminal neurodegenerative
disease. The majority of cases are sporadic with unknown causes and only a small
number of cases are genetically linked. Recent evidence suggests that
post-transcriptional regulation and epigenetic mechanisms, such as microRNAs,
underlie the onset and progression of neurodegenerative disorders; therefore,
altered microRNA expression may result in the dysregulation of key genes and
biological pathways that contribute to the development of sporadic amyotrophic
lateral sclerosis. Using systems biology analyses on postmortem human spinal cord
tissue, we identified dysregulated mature microRNAs and their potential targets
previously implicated in functional process and pathways associated with the
pathogenesis of ALS. Furthermore, we report a global reduction of mature
microRNAs, alterations in microRNA processing, and support for a role of the
nucleotide binding protein, TAR DNA binding protein 43, in regulating sporadic
amyotrophic lateral sclerosis-associated microRNAs, thereby offering a potential
underlying mechanism for sporadic amyotrophic lateral sclerosis.