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6th Annual Conference of the Neuropathology Society of India (NPSICON) - Meeting Abstracts, February 23–25, 2023

open access: yesFree Neuropathology, 2023
The 6th Annual conference of the Neuropathology Society of India, (NPSICON 2023) was held in a virtual mode, from 23rd to 25th February 2023, hosted by the Division of Neuropathology, Department of Pathology, Christian Medical College Vellore.
Neuropathology Society of India
doaj   +1 more source

5th Asian Oceanian Congress of Neuropathology along with the 5th Annual Conference of the Neuropathology Society of India - Meeting Abstracts, September 24–26, 2021

open access: yesFree Neuropathology, 2022
The 5th Asian Oceanian Congress of Neuropathology along with the 5 th Annual Conference of the Neuropathology Society of India  (AOCN-NPSICON) was held in virtual mode on September 24–26, 2021, at National Institute of Mental Health and Neurosciences ...
Neuropathology Society of India
doaj   +1 more source

62nd Meeting of the French Society of Neuropathology - Meeting Abstracts , December 4th. 2020

open access: yesFree Neuropathology, 2020
The French Society of Neuropathology was created in 1989, succeeding the French Club of Neuropathology set up in 1965. The Society organizes two scientific meetings per year.
The French Society of Neuropathology
doaj   +1 more source

APOE genotype dependent molecular abnormalities in the cerebrovasculature of Alzheimer’s disease and age-matched non-demented brains

open access: yesMolecular Brain, 2021
Cerebrovascular dysfunction is a hallmark feature of Alzheimer's disease (AD). One of the greatest risk factors for AD is the apolipoprotein E4 (E4) allele.
Joseph O. Ojo   +11 more
doaj   +1 more source

YTHDF2 facilitates UBXN1 mRNA decay by recognizing METTL3-mediated m6A modification to activate NF-κB and promote the malignant progression of glioma

open access: yesJournal of Hematology & Oncology, 2021
Background The prognosis for diffuse gliomas is very poor and the mechanism underlying their malignant progression remains unclear. Here, we aimed to elucidate the role and mechanism of the RNA N6,2′-O-dimethyladenosine (m6A) reader, YTH N6 ...
Rui-Chao Chai   +8 more
doaj   +1 more source

Loss of PIKfyve drives the spongiform degeneration in prion diseases

open access: yesEMBO Molecular Medicine, 2021
Brain‐matter vacuolation is a defining trait of all prion diseases, yet its cause is unknown. Here, we report that prion infection and prion‐mimetic antibodies deplete the phosphoinositide kinase PIKfyve—which controls endolysosomal maturation—from mouse
Asvin K K Lakkaraju   +6 more
doaj   +1 more source

Monoaminergic Neuropathology in Alzheimer's disease [PDF]

open access: yes, 2016
Acknowledgments This work was supported by The Croatian Science Foundation grant. no. IP-2014-09-9730 (“Tau protein hyperphosphorylation, aggregation, and trans-synaptic transfer in Alzheimer’s disease: cerebrospinal fluid analysis and assessment of ...
Bažadona, Danira   +11 more
core   +1 more source

A case of recurrent epilepsy-associated rosette-forming glioneuronal tumor with anaplastic transformation in the absence of therapy. [PDF]

open access: yes, 2019
Rosette-forming glioneuronal tumor (RGNT) most commonly occurs adjacent to the fourth ventricle and therefore rarely presents with epilepsy. Recent reports describe RGNT occurrence in other anatomical locations with considerable morphologic and genetic ...
Corless, Christopher L   +14 more
core   +1 more source

Molecular and cellular pathogenesis of adamantinomatous craniopharyngioma. [PDF]

open access: yes, 2015
Adamantinomatous craniopharyngiomas (ACPs) are the most common pituitary tumours in children. Although histologically benign, these are clinically aggressive tumours, difficult to manage and associated with poor quality of life for the patients.
Martinez-Barbera, JP
core   +1 more source

Selective Loss of MATR3 in Spinal Interneurons, Upper Motor Neurons and Hippocampal CA1 Neurons in a MATR3 S85C Knock-In Mouse Model of Amyotrophic Lateral Sclerosis

open access: yesBiology, 2022
The neuropathological hallmark of amyotrophic lateral sclerosis (ALS) is motor neuron degeneration in the spinal cord and cortex. Accumulating studies report that other neurons in the central nervous system (CNS) are also affected in ALS.
Justin You   +5 more
doaj   +1 more source

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