Results 31 to 40 of about 93,399 (211)

Loss of Immunohistochemical Reactivity in Association With Handling-Induced Dark Neurons in Mouse Brains. [PDF]

open access: yes, 2020
The handling-induced dark neuron is a histological artifact observed in brain samples handled before fixation with aldehydes. To explore associations between dark neurons and immunohistochemical alterations in mouse brains, we examined protein products ...
Chang, Rachel C   +5 more
core  

Genetic background affects human glial fibrillary acidic protein promoter activity. [PDF]

open access: yesPLoS ONE, 2013
The human glial fibrillary acidic protein (hGFAP) promoter has been used to generate numerous transgenic mouse lines, which has facilitated the analysis of astrocyte function in health and disease.
Xianshu Bai   +5 more
doaj   +1 more source

Abnormal white matter tracts resembling pencil fibers involving prefrontal cortex (Brodmann area 47) in autism: a case report. [PDF]

open access: yes, 2016
BackgroundAutism is not correlated with any neuropathological hallmark as the brain of autistic individuals lack defined lesions. However, previous investigations have reported cortical heterotopias and local distortion of the cytoarchitecture of the ...
Ariza, Jeanelle   +4 more
core   +1 more source

Phosphorylation of GFAP is associated with injury in the neonatal pig hypoxic-ischemic brain [PDF]

open access: yes, 2012
Glial fibrillary acidic protein (GFAP) is an intermediate filament protein expressed in the astrocyte cytoskeleton that plays an important role in the structure and function of the cell.
A Lee   +53 more
core   +1 more source

Abnormal evoked potentials in autoimmune glial fibrillary acidic protein astrocytopathy

open access: yeseNeurologicalSci, 2020
Autoimmune GFAP astrocytopathy is a new clinical entity and only a limited number of cases have been reported. Here we report the results of multimodal central conduction studies performed in a case of this disorder.A 72-year-old woman developed gradual ...
Ryo Tokimura   +4 more
doaj   +1 more source

Maternal embryonic leucine zipper kinase (MELK) regulates multipotent neural progenitor proliferation. [PDF]

open access: yes, 2005
Maternal embryonic leucine zipper kinase (MELK) was previously identified in a screen for genes enriched in neural progenitors. Here, we demonstrate expression of MELK by progenitors in developing and adult brain and that MELK serves as a marker for self-
Bajpai, Ruchi   +17 more
core   +2 more sources

Serum glial fibrillary acidic protein and protein gene product 9.5 for predicting neurological outcomes in cardiac arrest patients with cortical response to somatosensory evoked potentials

open access: yesResuscitation Plus
Aim: Predicting neurological prognosis after cardiac arrest remains challenging. Somatosensory evoked potential N20 absence is highly specific but lacks sensitivity.
Chenchen Hang   +8 more
doaj   +1 more source

Extracellular vesicle-induced differentiation of neural stem progenitor cells [PDF]

open access: yes, 2019
Neural stem progenitor cells (NSPCs) from E13.5 mouse embryos can be maintained in culture under proliferating conditions. Upon growth-factor removal, they may differentiate toward either neuronal or glial phenotypes or both.
Biagioni, S.   +5 more
core   +1 more source

Glial Fibrillary Acidic Protein as a Biomarker in Acute Ischemic Stroke: Diagnostic Value and Prognostic Implications

open access: yesNamık Kemal Tıp Dergisi
Stroke is one of the leading causes of mortality and long-term disability worldwide, with ischemic stroke representing the most common subtype. Despite significant progress in neuroimaging and reperfusion therapies, rapid and accurate diagnosis remains a
Ümit ATASEVER
doaj   +1 more source

A Case of Adult-Onset Alexander Disease Featuring Severe Atrophy of the Medulla Oblongata and Upper Cervical Cord on Magnetic Resonance Imaging

open access: yesCase Reports in Neurology, 2012
Adult-onset Alexander disease (AOAD) has been increasingly recognized since the identification of the glial fibrillary acidic protein gene mutation in 2001.
Tadahiro Yonezu   +5 more
doaj   +1 more source

Home - About - Disclaimer - Privacy