Results 211 to 220 of about 79,800 (306)

Cell-type-specific profiling of alternative translation identifies regulated protein isoform variation in the mouse brain [PDF]

open access: yes, 2019
Dalal, Jasbir S   +12 more
core   +1 more source

Defining the Intestinal eCBome and Oxylipin Signaling Systems in a TDP‐43 Mouse Model of Frontotemporal Dementia

open access: yesThe FASEB Journal, Volume 40, Issue 2, 31 January 2026.
TDP‐43 overexpressing mice, a genetic model of frontotemporal dementia, exhibit dramatic changes in their small intestinal endocannabinoidome members, in terms of both altered concentrations of lipid mediators and expression of some of their receptors (Cnr1, Gpr119, Gpr55, Pparg) and metabolic enzymes (Napepld, Faah). Also, the levels of some oxylipins
Hayatte‐Dounia Mir   +9 more
wiley   +1 more source

Anti-toxoplasma effect of <i>Moringa oleifera</i> leaves in a rat model of toxoplasmosis-induced pregnancy. [PDF]

open access: yesOpen Vet J
Nurinasari H   +8 more
europepmc   +1 more source

Corrigendum: Oligodendrocyte precursor cell-derived exosomes combined with cell therapy promote clinical recovery by immunomodulation and gliosis attenuation [PDF]

open access: gold
Sarah Ingrid Pinto Santos   +9 more
openalex   +1 more source

Review of published research on primary dysautonomia of domestic animals

open access: yesVeterinary Record, Volume 198, Issue 1, Page e30-e40, 3/10 January 2026.
Abstract An article published in 1992 by Marion M. Pollin and I.R. Griffiths reviewed the topic of primary dysautonomias of the autonomic nervous system of unidentified origin in multiple domestic species, specifically cats, dogs and horses. Thirty‐one years later, we appear no closer to identifying the causal agents of these strikingly similar ...
Tanith Harte   +3 more
wiley   +1 more source

Proliferative reactive gliosis is compatible with glial metabolic support and neuronal function [PDF]

open access: gold, 2011
Felix Vázquez-Chona   +8 more
openalex   +1 more source

Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics

open access: yesAnnals of Clinical and Translational Neurology, Volume 13, Issue 1, Page 108-121, January 2026.
ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco   +18 more
wiley   +1 more source

Is intrapleural sericin administration toxic to the nervous system of rats? [PDF]

open access: yesTurk Gogus Kalp Damar Cerrahisi Derg
Yazıcıoğlu A   +4 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy