Results 131 to 140 of about 4,657 (257)

Mechanisms for the Modulation of Dopamine D1 Receptor Signaling in Striatal Neurons [PDF]

open access: yes, 2011
In the striatum, dopamine D1 receptors are preferentially expressed in striatonigral neurons, and increase the neuronal excitability, leading to the increase in GABAergic inhibitory output to substantia nigra pars reticulata.
Akinori eNishi   +5 more
core   +3 more sources

Quantitative metrics for drug-target ligandability. [PDF]

open access: yes, 2018
Ligandability is a prerequisite for druggability and is a much easier concept to understand, model and predict because it does not depend on the complex pharmacodynamic and pharmacokinetic mechanisms in the human body.
Huggins, David J, Vukovic, Sinisa
core   +1 more source

Additional file 1 of Phosphodiesterase 10A (PDE10A) as a novel target to suppress β-catenin and RAS signaling in epithelial ovarian cancer

open access: gold, 2022
Rebecca M. Borneman   +16 more
openalex   +2 more sources

MODL-41. LOSS OF DISTAL CHROMOSOME 6Q AND ASSOCIATED PDE10A INDUCES AN AGGRESSIVE GLIOMA PHENOTYPE BY FACILITATING PRONEURAL TO MESENCHYMAL TRANSITION

open access: green, 2023
Nicholas Nuechterlein   +19 more
openalex   +2 more sources

A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.

open access: yesPLoS Genetics, 2013
Thyroid hormone is essential for normal metabolism and development, and overt abnormalities in thyroid function lead to common endocrine disorders affecting approximately 10% of individuals over their life span.
Eleonora Porcu   +93 more
doaj   +1 more source

Expression analysis of novel striatal-enriched genes in Huntington disease [PDF]

open access: yes, 2017
Selective degeneration of striatal neurons is a pathologic hallmark of Huntington disease (HD). The exact mechanism(s) behind this specific neurodegeneration is still unknown.
Becanovic, Kristina   +5 more
core  

Striatal Vulnerability in Huntington’s Disease : Neuroprotection Versus Neurotoxicity [PDF]

open access: yes, 2020
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disease caused by the expansion of a CAG trinucleotide repeat encoding an abnormally long polyglutamine tract (PolyQ) in the huntingtin (Htt) protein.
Goto, Satoshi, Morigaki, Ryoma
core  

The human phosphodiesterase PDE10A gene [PDF]

open access: bronze, 2000
Kotomi Fujishige   +3 more
openalex   +1 more source

MOESM3 of Computer-aided design of multi-target ligands at A1R, A2AR and PDE10A, key proteins in neurodegenerative diseases

open access: gold, 2017
Leen Kalash   +11 more
openalex   +2 more sources

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