Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Shaun Alexander"'
Publikováno v:
PLoS ONE, Vol 17, Iss 3, p e0264177 (2022)
BackgroundAtaxia-telangiectasia is an autosomal recessive, multi-system, and life-shortening disease caused by mutations in the ataxia-telangiectasia mutated gene. Although widely reported, there are no studies that give a comprehensive picture of th
Externí odkaz:
https://doaj.org/article/7cdc1f3759e74527a16647edf75b837a
Autor:
Ammar Al-Taie, Yasmeen Abdrabou, Shaun Alexander Macdonald, Frank Pollick, Stephen Anthony Brewster
Publikováno v:
Proceedings of the 2023 CHI Conference on Human Factors in Computing Systems.
Publikováno v:
THE INTERNATIONAL JOURNAL OF MANAGEMENT SCIENCE AND BUSINESS ADMINISTRATION. 8:15-23
This qualitative descriptive phenomenological study explored how business managers describe their lived experiences as a cyberloafer in the Southern United States. There were eight participants that supervised at least five employees, older than 24 y
Publikováno v:
Augmented Humans Conference.
Publikováno v:
Journal of Surgical Case Reports. 2022
Adrenal myelolipomas are rare, hormonally silent, adipose and myeloid-containing lesions that are mostly asymptomatic. If they do present it is usually with mass-related flank pain or spontaneous haemorrhage. A 55-year-old female presented with right
Publikováno v:
INTERNATIONAL CONFERENCE ON MULTIMODAL INTERACTION.
Publikováno v:
Anal Biochem
We compared the accuracy of three common methods of total protein normalization. The Stain-Free method was accurate across different types/brands of western blotting membrane and for various protein loads, unlike Ponceau S and Amido Black. Normalizin
Publikováno v:
ICMI
This paper presents a survey informing a user-first approach to designing calming affective haptic stimuli by eliciting user preferences in different social scenarios. Prior affective haptics research presented users with stimuli and recorded emotion
Publikováno v:
Abstracts.
Background Ataxia-telangiectasia (A-T) is a rare autosomal recessive, progressive, multi-system disease caused by mutations in the ataxia-telangiectasia mutated (ATM) gene on chromosome 11q.26. There are 2 types of A-T; the more severe phenotype of c
Publikováno v:
Abstracts.