Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Linda Moses"'
Publikováno v:
Journal of Learning Development in Higher Education (2015)
Peer Assisted Study Sessions (PASS) is an established part of widening participation and retention activities at the University of Cumbria. In October 2013, the question of sustainability and growth of the scheme was addressed. The small team of PASS
Externí odkaz:
https://doaj.org/article/bc3342b78b9840bb8b1048b94f4de415
Autor:
Rebecca Wagner, Linda Moses
Publikováno v:
Journal of forensic sciencesREFERENCES. 66(3)
The proliferation of misuse of prescription and non-prescription opioids, in recent years, has caused an opioid epidemic in the United States. Forensic toxicology laboratories often encounter implications of abuse in both driving under the influence
Autor:
Joseph M. Devaney, Linda Moses, Eric P. Hoffman, Kristen C. Hoffbuhr, William A. Thistlethwaite
Publikováno v:
The Journal of Molecular Diagnostics. 5:121-126
Rett syndrome is a neurodevelopmental disorder that affects females almost exclusively, and in which eight common point mutations on the X-linked MeCP2 gene are knows to cause over 70% of mutation-positive cases. We explored the use of a novel platfo
Autor:
Ashley Harris, Jennifer Price, Kristie Ramser, Danielle L. Tate, Linda Moses-Simmons, April M. Miller, Luis M. Gomez
Publikováno v:
American Journal of Obstetrics and Gynecology. 218:S59
Autor:
Sisir K. Dutta, Yue Chen, Linda Moses, Akanchha Kesari, Supriyo De, Raghunath Chatterjee, Eric P. Hoffman, Somiranjan Ghosh
Publikováno v:
Environment International, Vol 36, Iss 8, Pp 907-917 (2010)
In this study we have examined the effect of exposure to different congeners of PCBs and their role in oxidative stress response. A metabolically competent human liver cell line (HepG2) was exposed with two prototype congeners of PCBs: coplanar PCB-7
Publikováno v:
Haematologica. 90(12)
Molecular screening for glucose-6-phosphate (G6PD) mutations in two Jordanian populations revealed six different mutations and higher incidences of G6PD deficiency and G6PD A- (376A--G + 202G--A) mutation in Jordan Valley than in the Amman area. Thes
Autor:
Gabriele V. Ronnett, Sakku Bai Naidu, Eric P. Hoffman, Kristen C. Hoffbuhr, Xiaohe Cai, Donald Leopold, Linda Moses
Publikováno v:
Annals of neurology. 54(2)
Rett's Syndrome (RTT) is a neurodevelopmental disorder resulting from mutation in the mecp2 gene that encodes methyl CpG binding protein 2, a transcriptional repressor. Because this disease primarily affects neurons, tissue is not available during ac
Publikováno v:
Mental retardation and developmental disabilities research reviews. 8(2)
Rett syndrome is a neurodevelopmental disorder of early postnatal brain growth in girls. Patients show a normal neonatal period with subsequent developmental regression and a loss of acquired skills (communication and motor skills), deceleration of h