Results 241 to 250 of about 43,167 (288)
A novel splice site mutation in the UBE2A gene leads to aberrant mRNA splicing in a Chinese patient with X-linked intellectual disability type Nascimento. [PDF]
Mol Genet Genomic Med, 2019 Ma D +8 more
europepmc +1 more source
Virtuous Organizations in the Age of AI: Relational Goods and Human Flourishing
Business Ethics, the Environment &Responsibility, EarlyView.ABSTRACT The integration of AI‐based systems in everyday work has given rise to augmented organizations, transforming traditional work paradigms and prompting new research questions concerning augmented work processes and their related ethical issues. Drawing upon the practice‐institution framework proposed by Alasdair MacIntyre, integrated with Donati'
Francesco Vincenzo Giarmoleo +3 more
wiley +1 more source
A novel PAK3 pathogenic variant identified in two siblings from a Japanese family with X-linked intellectual disability: case report and review of the literature. [PDF]
Cold Spring Harb Mol Case Stud, 2019 Iida A +12 more
europepmc +1 more source
From Inaction to Action: The Cognitive Liberation of Amazon Workers in North Carolina
British Journal of Industrial Relations, EarlyView.ABSTRACT We examine the mechanism by which workers move from inaction to collective action, focusing on cognitive liberation, the awareness that change is possible, as it unfolded among workers at an Amazon warehouse in North Carolina who contributed to the emergence of an independent, worker‐led union during a period of renewed growth in organising ...
Carla Lima Aranzaes, Destiny Blackwell
wiley +1 more source
A novel UBE2A mutation causes X-linked intellectual disability type Nascimento. [PDF]
Hum Genome Var, 2017 Tsurusaki Y +6 more
europepmc +1 more source
British Journal of Psychology, EarlyView.Abstract Working memory updating is a crucial cognitive function for learning and academic achievement that develops significantly throughout childhood and adolescence. Despite the varieties of existing tasks to measure children's working memory updating, its overall developmental trajectory and task‐specific developmental patterns remain inadequately ...
Ye Song, Chen Cheng
wiley +1 more source
ARHGEF9 mutations cause a specific recognizable X-linked intellectual disability syndrome. [PDF]
Neurol Genet, 2017 Striano P, Zara F.
europepmc +1 more source