Coscattering/coannihilation dark matter in a fraternal twin Higgs model
Sign Up to like & getrecommendations! Published in 2018 at "Journal of High Energy Physics"
DOI: 10.1007/jhep09(2018)098
Abstract: A bstractDark matter candidates arise naturally in many models that address the hierarchy problem. In the fraternal twin Higgs model which could explain the absence of the new physics signals at the Large Hadron Collider… read more here.
Keywords: matter; dark matter; coannihilation; fraternal twin ... See more keywords
Exploiting the fraternal twin nature of thermoelectrics and topological insulators in Zintl phases as a tool for engineering new efficient thermoelectric generators
Sign Up to like & getrecommendations! Published in 2023 at "Journal of Materials Chemistry C"
DOI: 10.1039/d3tc00556a
Abstract: This review article presents a radical overview of the rich chemistry and physics of Zintl phases as it relates to their interesting structure-property relationships. In particular, it unveils the evolution... read more here.
Keywords: twin nature; zintl phases; chemistry; exploiting fraternal ... See more keywords
Case Report: Desmoglein-3 Gene Mutation Leading to Airway Compromise in Fraternal Twin Infants.
Sign Up to like & getrecommendations! Published in 2022 at "A&A practice"
DOI: 10.1213/xaa.0000000000001584
Abstract: The desmoglein 3 18q11 gene mutation has not been well described in humans, except for a few case reports. The desmoglein 3 gene controls a transmembrane component of the desmosome complex that mediates epidermal cell… read more here.
Keywords: gene mutation; desmoglein gene; fraternal twin; mutation ... See more keywords
Crouzon syndrome in a fraternal twin: A case report and review of the literature
Sign Up to like & getrecommendations! Published in 2022 at "World Journal of Clinical Cases"
DOI: 10.12998/wjcc.v10.i16.5317
Abstract: BACKGROUND Crouzon syndrome (CS; OMIM 123500) is an autosomal dominant inherited craniofacial disorder caused by mutations in the fibroblast growth factor receptor 2 (FGFR2) gene. CS is characterized by craniofacial dysostosis, exophthalmos, and facial anomalies… read more here.
Keywords: twin; crouzon syndrome; report; fraternal twin ... See more keywords
Comparison of Treadmill Gait Between a Pediatric-Aged Individual With SYNGAP1-Related Intellectual Disability and a Fraternal Twin
Sign Up to like & getrecommendations! Published in 2022 at "Frontiers in Human Neuroscience"
DOI: 10.3389/fnhum.2022.918918
Abstract: SYNGAP1-related Intellectual Disability (SYNGAP1-ID) is a rare neurodevelopmental condition characterized by profound intellectual disability, gross motor delays, and behavioral issues. Ataxia and gait difficulties are often observed but have not yet been characterized by laboratory-based… read more here.
Keywords: intellectual disability; syngap1; individual syngap1; fraternal twin ... See more keywords