Results 81 to 90 of about 3,294 (160)

Organization of Astrocytic GLT‐1 at Cortical Inhibitory Synapses

open access: yesGlia, Volume 74, Issue 8, August 2026.
GLT‐1+ ALs frequently juxtapose symmetric synapses. Distance‐based phenotyping identifies symmetric‐ and asymmetric‐associated GLT‐1+ ALs. Distal inhibitory synapses show enriched GLT‐1/α2 couples in ALs within 1000 nm, conserved in human cortex. ABSTRACT Glutamate spillover from excitatory synapses modulates neighboring inhibitory synapses, yet the ...
Marcello Melone   +3 more
wiley   +1 more source

Japanese Women's Attitudes Toward Learning Languages Other Than English in the Era of Global English

open access: yesInternational Journal of Applied Linguistics, Volume 36, Issue 3, Page 2298-2308, August 2026.
ABSTRACT This study on female Japanese learners of the Korean language is situated in the centuries‐long anti‐Korean sentiments in Japan, the global popularity of the Korean Wave, particularly among women, and the essentialized image of socially marginalized young Japanese women who study English with romantic desires for Western men.
Yoko Kobayashi
wiley   +1 more source

List of overlapping genes in spinal cord from Atp1a2 ASO1 and ASO3 treated SOD1*G93A mice.

open access: yes, 2023
77 commonly differentially expressed genes between Atp1a2 ASO1 and ASO3 treatments as shown in Fig 8C. (XLSX)
Azad Bonni (221908)   +9 more
core   +1 more source

ATP1A2 is a differentially expressed gene in human metastatic breast cancer, in the brain and in the lymph nodes.

open access: yes, 2021
Metastasis to the brain is a clinical problem in patients with breast cancer (1-3). We mined published microarray data (4, 5) to compare primary and metastatic tumor transcriptomes for the discovery of genes associated with brain metastasis in humans ...
Shahan Mamoor
core   +1 more source

Validation of strain variation in Atp1a2 expression in the BXD population by RNA-seq.

open access: yes, 2013
Normalized (RPKM) values in whole brain are shown for the B (N = 20) and D allele (N = 11) for each feature of Atp1a2 RefSeq transcript model. “Transcript level” (far right on X-axis) measures expression for the entire Atp1a2 transcript based on the NCBI
Detlef H. Heck (320756)   +6 more
core   +1 more source

Abnormal expression of ATP1A1 and ATP1A2 in breast cancer [version 1; referees: 2 approved]

open access: yesF1000Research, 2017
Breast cancer is the first in incidence and the second in death among all solid tumors occurring in women. The identification of molecular genetic abnormalities in breast cancer is important to improve the results of treatment.
Alexey Bogdanov   +2 more
doaj   +1 more source

The influence of Na+,K+-ATPase on glutamate signaling in neurodegenerative diseases and senescence

open access: yesFrontiers in Physiology, 2016
Decreased Na+,K+-ATPase (NKA) activity causes energy deficiency, which is commonly observed in neurodegenerative diseases. The NKA is constituted of three subunits: α, β and γ, with four distinct isoforms of the catalytic α subunit (α1-4).
Paula Fernanda Kinoshita   +6 more
doaj   +1 more source

A new approach in association study of single nucleotide polymorphism of genes for carcass and meat quality traits in commercial pigs

open access: yesItalian Journal of Animal Science, 2010
Six batches of four commercial hybrids of heavy pigs, reared for the production of Italian dry-cured hams, were identifiedfor having homogeneous feeding and farm conditions.
Vincenzo Russo   +8 more
doaj   +1 more source

Clinical Benefit of NMDA Receptor Antagonists in a Patient With ATP1A2 Gene Mutation

open access: yes, 2018
Mutations in the ATP1A2 gene cause familial hemiplegic migraine type 2, alternating hemiplegia of childhood, and cerebellar function deficits, epilepsy, and mental retardation. These symptoms are likely related to glutamatergic hyperexcitability.
Fatema Serajee, Ahm M. Huq, Keisuke Ueda
core   +1 more source

MECCANISMI PATOGENETICI NELLA EMICRANIA EMIPLEGICA FAMILIARE E SPORADICA:DESCRIZIONE DI TRE NUOVE MUTAZIONI DEL GENE ATP1A2 [PDF]

open access: yes, 2010
Familial hemiplegic migraine (FHM) is a rare, autosomal-dominant, form of migraine with aura. Sporadic hemiplegic migraine (SHM) is a heterogeneous disorder, where some patients may have a pathophysiology identical to FHM, with a mutation in one of the ...
V. Cardin
core   +1 more source

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