Results 61 to 70 of about 13,038 (207)

Transcriptional and translational differences of microglia from male and female brains [PDF]

open access: yes, 2019
Sex differences in brain structure and function are of substantial scientific interest because of sex-related susceptibility to psychiatric and neurological disorders. Neuroinflammation is a common denominator of many of these diseases and thus microglia
Güneykaya, Dilansu
core   +1 more source

Discovery of prognostic biomarker candidates of lacunar infarction by quantitative proteomics of microvesicles enriched plasma. [PDF]

open access: yesPLoS ONE, 2014
Lacunar infarction (LACI) is a subtype of acute ischemic stroke affecting around 25% of all ischemic stroke cases. Despite having an excellent recovery during acute phase, certain LACI patients have poor mid- to long-term prognosis due to the recurrence ...
Arnab Datta   +2 more
doaj   +1 more source

Deep proteome profiling reveals signatures of age and sex differences in paw skin and sciatic nerve of naïve mice

open access: yeseLife, 2022
The age and sex of studied animals profoundly impact experimental outcomes in biomedical research. However, most preclinical studies in mice use a wide-spanning age range from 4 to 20 weeks and do not assess male and female mice in parallel.
Feng Xian   +3 more
doaj   +1 more source

White matter injury restoration after stem cell administration in subcortical ischemic stroke [PDF]

open access: yes, 2015
This is an Open Access article distributed under the terms of the Creative Commons Attribution License.-- et al.[Introduction]: An animal model of subcortical ischemic stroke with white matter affectation was induced in rats by injection of endothelin-1.
C Matute   +26 more
core   +2 more sources

Quantitative profiling of brain lipid raft proteome in a mouse model of fragile X syndrome. [PDF]

open access: yesPLoS ONE, 2015
Fragile X Syndrome, a leading cause of inherited intellectual disability and autism, arises from transcriptional silencing of the FMR1 gene encoding an RNA-binding protein, Fragile X Mental Retardation Protein (FMRP).
Magdalena Kalinowska   +2 more
doaj   +1 more source

Bod1, a novel kinetochore protein required for chromosome biorientation [PDF]

open access: yes, 2007
We have combined the proteomic analysis of Xenopus laevis in vitro–assembled chromosomes with RNA interference and live cell imaging in HeLa cells to identify novel factors required for proper chromosome segregation. The first of these is Bod1, a protein
Andersen, Jens S.   +7 more
core   +4 more sources

Immunodominant fragments of myelin basic protein initiate T cell-dependent pain

open access: yesJournal of Neuroinflammation, 2012
Background The myelin sheath provides electrical insulation of mechanosensory Aβ-afferent fibers. Myelin-degrading matrix metalloproteinases (MMPs) damage the myelin sheath.
Liu Huaqing   +9 more
doaj   +1 more source

S-nitrosation of proteins relevant to Alzheimer's disease during early stages of neurodegeneration [PDF]

open access: yes, 2016
Protein S-nitrosation (SNO-protein), the nitric oxide-mediated posttranslational modification of cysteine thiols, is an important regulatory mechanism of protein function in both physiological and pathological pathways.
Bhat, Vadiraja B.   +6 more
core   +1 more source

Inhibition of SLC11A1‐Mediated Lysosomal Iron Accumulation in Microglia Promotes Repair Following White Matter Stroke

open access: yesAdvanced Science, EarlyView.
Genetic and pharmacological inhibition of SLC11A1 functioning as an H+/Fe2+ antiporter–mediated lysosomal iron accumulation in microglia promotes lysosomal lumen acidification, increases CTSD expression, enhances lysosomal myelin debris uptake and degradation, and promotes repair following white matter stroke. ABSTRACT White matter stroke (WMS) results
Lingling Qiu   +11 more
wiley   +1 more source

Proteomics‐level analysis of myelin formation and regeneration in a mouse model for Vanishing White Matter disease [PDF]

open access: yesJournal of Neurochemistry, 2015
AbstractVanishing white matter (VWM) is a recessive neurodegenerative disease caused by mutations in translation initiation factor eIF2B and leading to progressive brain myelin deterioration, secondary axonal damage, and death in early adolescence. Eif2b5R132H/R132H mice exhibit delayed developmental myelination, mild early neurodegeneration and a ...
Irit, Gat-Viks   +4 more
openaire   +2 more sources

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