Results 71 to 80 of about 777,747 (311)

An Analysis of Functional Differences in Implicit Learning

open access: yes, 2010
This thesis analysed whether functional implicit learning differences existed in two areas that have produced promising, but equivocal, findings: individual differences in typical populations (e.g., Gebauer & Mackintosh, 2010) and group differences ...
Brown, Jamie
core   +1 more source

Development of autobiographical memory in children with autism spectrum disorders : deficits, gains, and predictors of performance [PDF]

open access: yes, 2014
Autobiographical memory (AM) was assessed in 63 children (aged 8-17 years) with an autism spectrum disorder (ASD) and compared with 63 typically developing children matched for age, gender, IQ, and verbal ability.
Goddard, L.   +7 more
core   +1 more source

Spatiotemporal and quantitative analyses of phosphoinositides – fluorescent probe—and mass spectrometry‐based approaches

open access: yesFEBS Letters, EarlyView.
Fluorescent probes allow dynamic visualization of phosphoinositides in living cells (left), whereas mass spectrometry provides high‐sensitivity, isomer‐resolved quantitation (right). Their synergistic use captures complementary aspects of lipid signaling. This review illustrates how these approaches reveal the spatiotemporal regulation and quantitative
Hiroaki Kajiho   +3 more
wiley   +1 more source

Unified Functional Spectrum Analysis: A Framework for Understanding Nonverbal Multimodal Multifunctional Interactions in Multiparty Conversations

open access: yesIEEE Access
An analytic framework called unified functional spectrum analysis (U-FSA) to reveal the multimodal multifunctional interplay that emerges and comprises interpersonal interactions in multiparty conversations is proposed.
Momoka Tajima   +3 more
doaj   +1 more source

Structural instability impairs function of the UDP‐xylose synthase 1 Ile181Asn variant associated with short‐stature genetic syndrome in humans

open access: yesFEBS Letters, EarlyView.
The Ile181Asn variant of human UDP‐xylose synthase (hUXS1), associated with a short‐stature genetic syndrome, has previously been reported as inactive. Our findings demonstrate that Ile181Asn‐hUXS1 retains catalytic activity similar to the wild‐type but exhibits reduced stability, a looser oligomeric state, and an increased tendency to precipitate ...
Tuo Li   +2 more
wiley   +1 more source

Facial motion perception in autism spectrum disorder and neurotypical controls [PDF]

open access: yes, 2015
This thesis was submitted for the degree of Doctor of Philosophy and was awarded by Brunel University LondonFacial motion provides an abundance of information necessary for mediating social communication.
Girges, Christine, Christine Girges
core  

Extensions of the multicentric functional calculus

open access: yes, 2021
In operator theory, one of the central concepts is the spectrum of an operator and if one knows how to separate the spectrum into components, then the multicentric calculus is a useful tool, introduced by Olavi Nevanlinna in 2011.
Andrei, Diana
core   +1 more source

A novel FAM83H variant causes familial amelogenesis imperfecta with incomplete penetrance

open access: yesMolecular Genetics & Genomic Medicine, 2022
Background Amelogenesis imperfecta (AI) is known to be a monogenic genetic disease caused by a variety of genes demonstrating a wide spectrum of penetrance.
Rui‐Qi Bai   +8 more
doaj   +1 more source

The (Glg)ABCs of cyanobacteria: modelling of glycogen synthesis and functional divergence of glycogen synthases in Synechocystis sp. PCC 6803

open access: yesFEBS Letters, EarlyView.
We reconstituted Synechocystis glycogen synthesis in vitro from purified enzymes and showed that two GlgA isoenzymes produce glycogen with different architectures: GlgA1 yields denser, highly branched glycogen, whereas GlgA2 synthesizes longer, less‐branched chains.
Kenric Lee   +3 more
wiley   +1 more source

Why are autism spectrum conditions more prevalent in males? [PDF]

open access: yes, 2011
Autism Spectrum Conditions (ASC) are much more common in males, a bias that may offer clues to the etiology of this condition. Although the cause of this bias remains a mystery, we argue that it occurs because ASC is an extreme manifestation of the male ...
Simon Baron-Cohen   +21 more
core   +1 more source

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