Try a new search

Format these results:

Searched for:

person:lewisr02

in-biosketch:yes

Total Results:

6


Rough sets: Visually discerning neurological functionality during thought processes

Lewis, R; Mello, CA; Zhuang, Y; Yeh, MK-C; Yan, Y; Gopstein, D
The central aim of this paper is to test and illustrate the viability of utilizing Rough Set Theory to visualize neurological events that occur when a human is thinking very intensely to solve a problem or, conversely, solving a trivial problem with little to no effort. Since humans solve complex problems by leveraging synapses from a distributed neural network in the frontal and parietal lobe, which is a difficult portion of the brain to research, it has been a challenge for the neuroscience community to functionally measure how intensely a subject is thinking while trying to solve a problem. Herein, we present our research of optimizing machine intelligence to visually illustrate when members of our cohort experienced misunderstandings and challenges during periods where they read and comprehended short code snippets. This research is a continuation of the authors’ research efforts to use Rough Sets and artificial intelligence to deliver a system that will eventually visually illustrate deception
SCOPUS:85055867169
ISSN: 0302-9743
CID: 3527492

Forensic issues

Chapter by: Mathur, Jennifer A; Bielska, Wiktoria; Lewis, Rebecca; Subedi, Bipin
in: A Case-Based Approach to Emergency Psychiatry by Maloy, Katherine, Dr [Eds]
Oxford : Oxford University Press, 2016
pp. ?-?
ISBN: 0190250852
CID: 2332632

Evaluating and treating the forensic patient

Chapter by: Mathur, Jennifer A; Bielska, Wiktoria; Lewis, Rebecca; Subedi, Bipin
in: A case-based approach to emergency psychiatry by Maloy, Katherine [Eds]
New York, NY, US: Oxford University Press, 2016
pp. 139-151
ISBN: 978-0-19-025084-3
CID: 2523152

Right to refuse treatment

Chapter by: Lewis, Rebecca
in: Landmark cases in forensic psychiatry by Ford, Elizabeth; Rotter, Merrill [Eds]
New York, NY, US: Oxford University Press; US, 2014
pp. 54-58
ISBN: 978-0-19-934465-9
CID: 1153092

Prisoners' rights

Chapter by: Khan, Omar; Lewis, Rebecca; Subedi, Bipin
in: Landmark cases in forensic psychiatry by Ford, Elizabeth; Rotter, Merrill [Eds]
New York, NY, US: Oxford University Press; US, 2014
pp. 151-156
ISBN: 978-0-19-934465-9
CID: 1153032

Regular exercise enhances insulin activation of IRS-1-associated PI3-kinase in human skeletal muscle

Kirwan, J P; del Aguila, L F; Hernandez, J M; Williamson, D L; O'Gorman, D J; Lewis, R; Krishnan, R K
Insulin action in skeletal muscle is enhanced by regular exercise. Whether insulin signaling in human skeletal muscle is affected by habitual exercise is not well understood. Phosphatidylinositol 3-kinase (PI3-kinase) activation is an important step in the insulin-signaling pathway and appears to regulate glucose metabolism via GLUT-4 translocation in skeletal muscle. To examine the effects of regular exercise on PI3-kinase activation, 2-h hyperinsulinemic (40 mU. m(-2). min(-1))-euglycemic (5.0 mM) clamps were performed on eight healthy exercise-trained [24 +/- 1 yr, 71.8 +/- 2.0 kg, maximal O(2) uptake (VO(2 max)) of 56.1 +/- 2.5 ml. kg(-1). min(-1)] and eight healthy sedentary men and women (24 +/- 1 yr, 64.7 +/- 4.4 kg, VO(2 max) of 44.4 +/- 2.7 ml. kg(-1). min(-1)). A [6, 6-(2)H]glucose tracer was used to measure hepatic glucose output. A muscle biopsy was obtained from the vastus lateralis muscle at basal and at 2 h of hyperinsulinemia to measure insulin receptor substrate-1(IRS-1)-associated PI3-kinase activation. Insulin concentrations during hyperinsulinemia were similar for both groups (293 +/- 22 and 311 +/- 22 pM for trained and sedentary, respectively). Insulin-mediated glucose disposal rates (GDR) were greater (P < 0.05) in the exercise-trained compared with the sedentary control group (9.22 +/- 0.95 vs. 6.36 +/- 0.57 mg. kg fat-free mass(-1). min(-1)). Insulin-stimulated PI3-kinase activation was also greater (P < 0.004) in the trained compared with the sedentary group (3.8 +/- 0.5- vs. 1.8 +/- 0.2-fold increase from basal). Endurance capacity (VO(2 max)) was positively correlated with PI3-kinase activation (r = 0.53, P < 0.04). There was no correlation between PI3-kinase and muscle morphology. However, increases in GDR were positively related to PI3-kinase activation (r = 0.60, P < 0.02). We conclude that regular exercise leads to greater insulin-stimulated IRS-1-associated PI3-kinase activation in human skeletal muscle, thus facilitating enhanced insulin-mediated glucose uptake.
PMID: 10658053
ISSN: 8750-7587
CID: 3866172