Results 191 to 200 of about 8,272 (249)
Interplay between CARD9 genetic variants and fungal colonization patterns among patients with diabetes. [PDF]
Khateb AM +8 more
europepmc +1 more source
The study outlines the tectono‐sedimentary evolution of the İnegöl Basin in north‐western Anatolia. Basin formation was controlled by interacting extensional and strike‐slip fault systems linked to uplift of the Uludağ Massif. Terrestrial sedimentation from the Miocene to Pleistocene is reconstructed using abundant fossil mammal assemblages that ...
M. Cihat Alçiçek +2 more
wiley +1 more source
Kinship verification via correlation calculation-based multi-task learning. [PDF]
Qin X, Liu D, Gui B.
europepmc +1 more source
U–Pb isotope and trace element geochemistry of apatite from carbonatites of Peshawar Plain Alkaline Igneous Province, western Himalaya shows Permo‐Carboniferous magmatism, an additional magmatic pulse during Cretaceous, and post‐magmatic hydrothermal/metasomatism during Oligocene. ABSTRACT U–Pb isotope and trace element geochemistry of apatite combined
Mehboob ur Rashid +9 more
wiley +1 more source
Deficiency in homozygous haplotypes reveals recessive lethal variants affecting fertility and viability in the Friesian horse. [PDF]
Steensma MJ +5 more
europepmc +1 more source
This review systematically summarizes two‐dimensional layered and nonlayered oxides, focusing on their synthesis, properties, and post‐Moore applications in transistors, gate dielectrics, optoelectronics, and ferroelectric/magnetic devices. It also discusses challenges including scalable growth and interface engineering, along with future industrial ...
Xinjie Hou +5 more
wiley +1 more source
Automatic diagnosis of heating in oil-filled terminals of cables. [PDF]
Yao S, Liu Z, Zhao Y, Ni S.
europepmc +1 more source
Whole exome sequencing in a consanguineous Iranian family with autosomal recessive non‐syndromic hearing loss revealed a novel homozygous frameshift mutation, c.3713dupA (p.Asp1238Glufs*10), in the LOXHD1 gene. This mutation, located in exon 24, results in a premature stop codon and a truncated protein. Sanger sequencing confirmed co‐segregation of the
Solmaz Hassani Fard Katiraei +4 more
wiley +1 more source
Dystonia as an early and prominent feature in a patient with CYP2U1 gene mutation: expanding the phenotype of SPG56-a case report. [PDF]
Alhamwy Z +3 more
europepmc +1 more source
Anti‐inflammatory and cytotoxic properties of kānuka (Kunzea ericoides) subcritical water extract
Abstract BACKGROUND Kānuka (Kunzea ericoides) is a medicinal plant native to New Zealand with numerous therapeutic benefits due to its rich bioactive profile. Although several in vitro studies have shown promising anti‐inflammatory activity, substantial evidence elucidating its underlying inflammatory regulatory mechanism and evaluating its cytotoxic ...
Indhuja Devadass +2 more
wiley +1 more source

