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Cancer Research|January 15, 1996
Expression of the human mismatch repair gene hMSH2 in normal and neoplastic tissuesF S Leach, K Polyak, M Burrell, et al.Proceedings of the National Academy of Sciences of the United States of America|April 29, 2015
Multiple functional variants in long-range enhancer elements contribute to the risk of SNP rs965513 in thyroid cancerHuiling He, Wei Li, Sandya Liyanarachchi, et al.Annales De Dermatologie Et De Venereologie|November 23, 2007
[Stress and seborrheic dermatitis]L Misery, S Touboul, C Vinçot, et al.Human Mutation|March 17, 2004
Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle EastStephan M Tanner, Zhongyuan Li, Ryan Bisson, et al.The American Journal of Psychiatry|March 3, 2005
A concordance study of three electrophysiological measures in schizophreniaSandrine Louchart-de la Chapelle, Irène Nkam, Emmanuelle Houy, et al.Gastroenterology|November 15, 2006
Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated proteinSaara Ollila, Laura Sarantaus, Reetta Kariola, et al.Cancer|December 15, 2005
American founder mutation for Lynch syndrome. Prevalence estimates and implicationsHenry T Lynch, Albert de la Chapelle, Heather Hampel, et al.Nanoscale|July 12, 2021
New insight into the aptamer conformation and aptamer/protein interaction by surface-enhanced Raman scattering and multivariate statistical analysisWafa Safar, Andra-Sorina Tatar, Aymeric Leray, et al.JAMA|February 12, 2004
A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United StatesHenry T Lynch, Stephanie M Coronel, Ross Okimoto, et al.Journal of Medical Genetics|September 9, 2000
Recurrent germline mutation in MSH2 arises frequently de novoD C Desai, J C Lockman, R B Chadwick, et al.Pageof 61