Results 151 to 160 of about 20,395,316 (257)
Rare‐Variant Burden Analysis of Dystonia Genes in Parkinson's Disease
Abstract Background Dystonia frequently coexists with Parkinson's disease (PD), yet the extent of genetic overlap remains insufficiently explored. Objective The aim was to examine whether rare variants in dystonia‐related genes are associated with PD or early‐onset PD (EOPD).
Sajanth Kanagasingam +4 more
wiley +1 more source
c-Maf Deletion in Cortical Somatostatin, But Not Parvalbumin, Interneurons Leads to Absence-Like Epileptiform Activity in Mice. [PDF]
Leroux MA +7 more
europepmc +1 more source
GCH1 p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations
Abstract Introduction GCH1 has been implicated in Parkinson's disease (PD), but its risks variants and associations are not well defined. Objectives Our goal was to investigate the clinical relevance and PD risk associated with the GCH1 p.Ser80Asn variant.
Yi Wen Tay +37 more
wiley +1 more source
USP5-C-MAF Axis Regulates Autophagy-Dependent Neuronal Ferroptosis in Spinal Cord Injury Therapeutics. [PDF]
Weng S, Wu K, Huang Y, Cao L, Fu H.
europepmc +1 more source
Abstract The prognostic and predictive impact of TP53 variants in leukemia led to their inclusion in diagnostic and treatment guidelines, increasing the demand for rapid, reliable laboratory analysis, interpretation, and reporting. While most TP53 variants identified in tumor samples can be interpreted using data from large‐scale functional studies ...
Šárka Pavlová +28 more
wiley +1 more source
c-Maf nuclear oncoprotein is frequently expressed in multiple myeloma [PDF]
Hong, Chang, Q, Qi, W, Xu, B, Patterson
openaire +2 more sources
c-MAF Transcriptionally Activates Slc40a1 to Repress Ferroptosis in Sepsis-Associated Encephalopathy. [PDF]
Song W +5 more
europepmc +1 more source
TrGO–Ni/Co Hybrid Nanocomposites: From Hydrothermal Synthesis to Melt Processing. ABSTRACT Polymeric nanocomposites have attracted significant interest for their low density, processability, and multifunctional properties, making them suitable for applications such as flexible electronics, sensors, biomedical devices, and functional coatings.
Bruno B. Storte +8 more
wiley +1 more source
Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis
ABSTRACT Hereditary pyropoikilocytosis (HPP) is a severe hemolytic anemia caused by variants in SPTA1, SPTB, and EPB41. These weaken horizontal interactions in the erythrocyte cytoskeleton, causing membrane fragmentation and splenic sequestration. It will readily cause fetal anemia and often hydrops fetalis. Prenatal diagnosis requires first ruling out
Connor Hartzell +6 more
wiley +1 more source

