Results 201 to 210 of about 681,467 (332)

Structure and Spectroscopic Characterisation of Phenanthroline‐Based Iodobismuthate(III) Complexes Utilised for Raw Acoustic Signal Classification

Advanced Intelligent Discovery, EarlyView.
Memristors based on trimethylsulfonium (phenanthroline)tetraiodobismuthate have been utilised as a nonlinear node in a delayed feedback reservoir. This system allowed an efficient classification of acoustic signals, namely differentiation of vocalisation of the brushtail possum (Trichosurus vulpecula).
Ewelina Cechosz, Gisya Abdi, Andrzej Sławek, Marlena Gryl, Konrad Szaciłowski   +4 more
wiley   +1 more source

Could dark energy be changing over time? [PDF]

Proc Natl Acad Sci U S A
Mann A.
europepmc   +1 more source

Disentangling complex relationships and disjunctions in western Camassia: Integrating multiple criteria to resolve taxonomic boundaries

American Journal of Botany, EarlyView.
Abstract Premise Understanding genetic and morphological variability helps efforts to sustain landscapes and develop effective species concepts for resolving difficult groups. To unravel puzzling relationships and range disjunctions, we applied morphometrics, phenology, phylogenetics and population genetics in Camassia species with cultural, ecological,
Susan R. Kephart, Theresa M. Culley, Jenny K. Archibald, Robert Tunison, Kathryn E. Theiss, James E. Kephart   +5 more
wiley   +1 more source

Neuropathological contributions to grey matter atrophy and white matter hyperintensities in amnestic dementia. [PDF]

Alzheimers Res Ther
Ortega-Cruz D, Rabano A, Strange BA.
europepmc   +1 more source

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim, Alexsandra Christianne Malaquias, Debora Romeo Bertola, Raissa Carneiro Rezende, Laurana De Polli Cellin, Lucas Vieira Lacerda Pires, Ana Maria Santillan‐Vasconez, Antônio Marcondes Lerario, Renata da Cunha Scalco, Alexander Augusto de Lima Jorge   +9 more
wiley   +1 more source

Artificial intelligence pioneers the double-strangeness factory. [PDF]

Nat Commun
He Y, Saito TR, Ekawa H, Kasagi A, Gao Y, Liu E, Nakazawa K, Rappold C, Taki M, Tanaka YK, Wang H, Yanai A, Yoshida J, Zhang H.   +13 more
europepmc   +1 more source

Strange hyperon and antihyperon production from quark and string-rope matter [PDF]

, 1999
Péter Csizmadia, P. Lévai, S. E. Vance, Tamás S. Bíró, Miklós Gyulassy, J. Zimányi   +5 more
openalex   +1 more source

Treg Cells Modulate Neuroinflammation and Behavioral Deficits in Autism: Evidence From MR‐Based Genetic Analyses and Experimental Models

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Autism spectrum disorder (ASD) is a neurodevelopmental condition that is increasingly linked to immune dysfunction and neuroinflammation. Regulatory T cells (Tregs), which are crucial in maintaining immune homeostasis, have been implicated in the pathogenesis of ASD.
Zuqing Nie, Xinyi Xu, Junhao Chen, Huiling Chen, Meng Li, Yang Zhang, Zhiwei Li, Chen Shen, Jie Wen, Xia Cao   +9 more
wiley   +1 more source

The Heart of Medicine: Healing Beyond Numbers. [PDF]

US Cardiol
Amir R.
europepmc   +1 more source

Strange and heavy mesons in hadronic matter [PDF]

, 2014
Daniel Cabrera, Luciano M. Abreu, Elena Bratkovskaya, Andrej Ilner, Felipe J. Llanes–Estrada, À. Ramos, Laura Tolós, Juan M. Torres-Rincón   +7 more
openalex