Results 141 to 150 of about 2,074,212 (425)

Reciprocity and rationality for the greedy normal form of a Coxeter group [PDF]

open access: yesarXiv, 2008
We show that the characteristic series for the greedy normal form of a Coxeter group is always a rational series, and prove a reciprocity formula for this series when the group is right-angled and the nerve is Eulerian. As corollaries we obtain many of the known rationality and reciprocity results for the growth series of Coxeter groups as well as some
arxiv  

Cytokines and neurotrophins in psychiatric disorders [PDF]

open access: yes, 1999
In addition to their immune cell origin and immunological effects, cytokines are produced by neuronal and glial cells and can influence nerve growth and plasticity.
Shintani, Futoshi
core   +2 more sources

Blood exosome connexins and small RNAs related to demyelinating disease activity

open access: yesAnnals of Clinical and Translational Neurology, Volume 12, Issue 3, Page 538-555, March 2025.
Abstract Objectives To assess blood exosome (Ex)‐connexin (Cx)43 (encoded by GJA1) and its truncated isoforms in multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD), which show distinct alterations in astroglial Cx43. Methods Serum Exs from 48 patients with MS (34 relapsing–remitting, 14 secondary‐progressive), 35 with NMOSD, 20 ...
Guzailiayi Maimaitijiang   +12 more
wiley   +1 more source

The genuine operadic nerve [PDF]

open access: yesTheory Appl. Categ. 34 (2019), 736-780, 2019
We construct a generalization of the operadic nerve, providing a translation between the equivariant simplicially enriched operadic world to the parametrized $\infty$-categorical perspective. This naturally factors through genuine equivariant operads, a model for "equivariant operads with norms up to homotopy".
arxiv  

Perspectives on the Trypanosoma cruzi-host cell receptor interaction [PDF]

open access: yes, 2009
Chagas disease is caused by the parasite Trypanosoma cruzi. The critical initial event is the interaction of the trypomastigote form of the parasite with host receptors. This review highlights recent observations concerning these interactions.
A Belley   +108 more
core   +1 more source

Ethnoracial disparities in gray matter atrophy are mediated by structural disconnectivity in multiple sclerosis

open access: yesAnnals of Clinical and Translational Neurology, Volume 12, Issue 3, Page 615-630, March 2025.
This study aimed to assess gray matter (GM) atrophy, the contribution of white matter (WM) lesions, and consequent structural disconnectivity in minority patients with multiple sclerosis (PwMS). Minority PwMS were found to have greater lesion burden and GM atrophy. Differences in GM atrophy were partially mediated by WM pathology. Abstract Objective To
Ahmed Bayoumi   +8 more
wiley   +1 more source

Continuous infusion of nerve growth factor prevents basal forebrain neuronal death after fimbria fornix transection.

open access: yesProceedings of the National Academy of Sciences of the United States of America, 1986
Neurons in the rat medial septum (MS) and vertical limb of the diagonal band of Broca (VDB) undergo a rapid and severe cell death after transection of their dorsal projection to the hippocampus by aspiration of the ipsilateral fimbria fornix and ...
L. R. Williams   +6 more
semanticscholar   +1 more source

Nerve growth factor nonresponsive pheochromocytoma cells: altered internalization results in signaling dysfunction. [PDF]

open access: yes, 1992
Variant rat pheochromocytoma (PC12) cells which fail to respond to nerve growth factor (NGF) (PC12nnr5) (Green, S. H., R. E. Rydel, J. L. Connoly, and L. A. Greene. 1986. J. Cell Biol. 102:830-843) bind NGF at both high and low affinity sites.
Bradshaw, RA, Eveleth, DD
core  

Novel pathogenic mtDNA variants in Chinese children with neurological mitochondrial disorders

open access: yesAnnals of Clinical and Translational Neurology, Volume 12, Issue 3, Page 586-601, March 2025.
Abstract Objective Pathogenic variations in the mitochondrial genome are tightly linked to neurological mitochondrial disorders in children. However, the mutation spectrum of mitochondrial DNA (mtDNA) in the Chinese population remains incomplete. Therefore, the primary objective of our study was to comprehensively characterize pathogenic mtDNA variants
Zhimei Liu   +15 more
wiley   +1 more source

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