Electron and Hole Doping Effects on the Magnetic Properties and Band Gap Energy of Ba<sub>2</sub>FeMoO<sub>6</sub> and Sr<sub>2</sub>FeMoO<sub>6</sub>. [PDF]
Apostolov AT+2 more
europepmc +1 more source
The cochaperone BAG3 promotes the stabilization of p53 under heat stress conditions
Under heat stress, BAG3 translocates to the nucleus and forms a complex with Hsp70 and p53, thereby promoting p53 stabilization and enhancing its transcriptional activity. These findings suggest that BAG3 functions as a cochaperone that supports p53‐mediated stress responses in cooperation with Hsp70.
Ngoc Nguyen Thi Minh+2 more
wiley +1 more source
Impact of electric field and strain on the electronic thermal conductivity of topological crystalline insulator SnTe (001). [PDF]
Gholami E+3 more
europepmc +1 more source
Mitochondrial DNA disorders in neuromuscular diseases in diverse populations
Abstract Neuromuscular features are common in mitochondrial DNA (mtDNA) disorders. The genetic architecture of mtDNA disorders in diverse populations is poorly understood. We analysed mtDNA variants from whole‐exome sequencing data in neuromuscular patients from South Africa, Brazil, India, Turkey and Zambia. In 998 individuals, there were two definite
Fei Gao+34 more
wiley +1 more source
Assessment of hydrological loading displacement from GNSS and GRACE data using deep learning algorithms. [PDF]
Wei C, Zhou M, Du Z, Han L, Gao H.
europepmc +1 more source
ABSTRACT C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who
Sara Rubio‐Guerra+17 more
wiley +1 more source
Dynamical Characteristics of Isolated Donors, Acceptors, and Complex Defect Centers in Novel ZnO. [PDF]
Talwar DN, Becla P.
europepmc +1 more source
Time-domain Green’s functions for unsaturated soils. Part I: Two-dimensional solution
Behrouz Gatmiri, Ehsan Jabbari
openalex +1 more source
Compound Heterozygous MRPS14 Variants Associated With Leigh Syndrome
ABSTRACT MRPS14 (uS14m) is a nuclear‐encoded ribosomal protein important for mitochondria‐specific translation. To date, only a single individual with a recessive MRPS14‐related disorder (also known as COXPD38) has been reported. We report an additional subject possessing novel compound heterozygous MRPS14 variants (p.Asp37Asn, p.Asn60Asp). The subject
Maria Gabriela Otero+15 more
wiley +1 more source