Showing results (331-340 of 401) with videos related to
Sort By:
Pageof 41
Genes, Brain, and Behavior|August 8, 2007
Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1-targeted miceE J Young, T Lipina, E Tam, et al.Scandinavian Journal of Immunology|April 21, 2007
The influence of MHC class II molecules containing the rheumatoid arthritis shared epitope on the immune response to aggrecan G1 and its peptidesW Brintnell, D A Bell, J A Hill, et al.Lancet (London, England)|February 3, 1996
Increased risk for myelodysplastic syndromes in individuals with glutathione transferase theta 1 (GSTT1) gene defectH Chen, D P Sandler, J A Taylor, et al.Environmental Health Perspectives|November 1, 1992
Genetic monitoring of human polymorphic cancer susceptibility genes by polymerase chain reaction: application to glutathione transferase muD A Bell, C L Thompson, J Taylor, et al.Diabetic Medicine : a Journal of the British Diabetic Association|August 1, 2019
Implementing simple algorithms to improve glucose and lipid management in people with diabetes and acute coronary syndromeN S R Lan, P G Fegan, J M Rankin, et al.International Journal of Cancer|August 5, 2000
A pilot study investigating the role of NAT1 and NAT2 polymorphisms in gastric adenocarcinomaR J Boissy, M A Watson, D M Umbach, et al.Journal of Cutaneous Pathology|August 1, 1991
Application of DNA flow cytometry from paraffin-embedded tissue to the diagnosis of mycosis fungoidesC Pastel-Levy, T J Flotte, F Preffer, et al.Genes, Brain, and Behavior|March 23, 2007
Forward genetic screen of mouse reveals dominant missense mutation in the P/Q-type voltage-dependent calcium channel, CACNA1AG Xie, S J Clapcote, B J Nieman, et al.Pharmacogenetics|March 25, 1998
Identification and characterization of variant alleles of human acetyltransferase NAT1 with defective function using p-aminosalicylate as an in-vivo and in-vitro probeN C Hughes, S A Janezic, K L McQueen, et al.Carcinogenesis|April 7, 2000
XPD polymorphisms: effects on DNA repair proficiencyR M Lunn, K J Helzlsouer, R Parshad, et al.Pageof 41