Revealing Localized Dark‐Exciton Populations in 2D Perovskites via Magneto‐Optical Microscopy
Magneto‐optical microscopy is used on metal halide perovskites for the first time to reveal the heterogenous nature of exciton emission in 2D perovskites. The study reveals that the morphology of 2D perovskite thin films has a crucial impact on localisation of bright and dark excitons.
Christopher G. Bailey+7 more
wiley +1 more source
L-RCA (ligation-rolling circle amplification): a general method for genotyping of single nucleotide polymorphisms (SNPs) [PDF]
Xiaoquan Qi
openalex +1 more source
Mainstream Artificial Intelligence Technologies in Contemporary Ophthalmology
This review explores the latest artificial intelligence (AI) technologies in ophthalmology, focusing on four key data types: medical imaging, electronic health records, robotic‐assisted surgery, and genomics. It examines the structural features, use cases, clinical goals, and evaluation metrics of various AI algorithms, while also introducing emerging ...
Shiqi Yin+9 more
wiley +1 more source
Allele-specific binding of the ubiquitous transcription factor OCT-1 to the functional single nucleotide polymorphism (SNP) sites in the tumor necrosis factor-alpha gene (TNFA) promoter [PDF]
Hirohiko Hohjoh, Katsushi Tokunaga
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The unique morphological basis and repeated evolutionary origins of personate flowers in Penstemon
Abstract Premise Adaptive radiation in ecologically and morphologically diverse plant lineages presents an opportunity to investigate the rapid evolution of novel floral traits. While some types of floral traits, such as flower color, are well characterized, other types of complex morphologies remain understudied.
Trinity H. Depatie, Carolyn A. Wessinger
wiley +1 more source
Catalog of 258 single-nucleotide polymorphisms (SNPs) in genes encoding three organic anion transporters, three organic anion-transporting polypeptides, and three NADH:ubiquinone oxidoreductase flavoproteins [PDF]
Aritoshi Iida+8 more
openalex +1 more source
ABSTRACT Inherited retinal dystrophies (IRDs) inherited are visually disabling monogenic diseases with remarkable genetic and phenotypic heterogeneity. Mutations in more than 300 different genes have been identified as disease‐causing. The genetic diagnosis of IRDs has significantly advanced with the integration of Next Generation Sequencing (NGS ...
Gerardo E. Fabian‐Morales+6 more
wiley +1 more source
Catalog of 320 single nucleotide polymorphisms (SNPs) in 20 quinone oxidoreductase and sulfotransferase genes [PDF]
Aritoshi Iida+7 more
openalex +1 more source