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The Journal of International Medical Research|January 18, 2005
Fresh homografts obtained through a national organ-sharing programme for repair of congenital heart diseaseS K Metin, B S Uğurlu, O Oto, et al.Neurogenetics|November 2, 2004
Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3AAnnette Abel, Nuria Fonknechten, Anne Hofer, et al.Breast Cancer Research and Treatment|November 1, 2005
N-cadherin expression in breast cancer: correlation with an aggressive histologic variant--invasive micropapillary carcinomaChandandeep Nagi, Mitchell Guttman, Shabnam Jaffer, et al.The Journal of Thoracic and Cardiovascular Surgery|March 1, 1983
Tricuspid atresia. Results of treatment in 115 childrenJ L de Brux, L Zannini, J P Binet, et al.Journal of Assisted Reproduction and Genetics|November 14, 2018
Time-lapse imaging reveals delayed development of embryos carrying unbalanced chromosomal translocationsHadar Amir, Shiri Barbash-Hazan, Yael Kalma, et al.Oncotarget|July 25, 2016
PreImplantation factor (PIF) therapy provides comprehensive protection against radiation induced pathologiesReut Shainer, Osnat Almogi-Hazan, Arye Berger, et al.Genomics|March 1, 1994
Genetic mapping of the human growth hormone-releasing factor gene (GHRF) using two intragenic polymorphisms detected by PCR amplificationL A Pérez Jurado, J A Phillips, M L Summar, et al.Oncogene|March 14, 2012
N-cadherin regulates mammary tumor cell migration through Akt3 suppressionS Chung, J Yao, K Suyama, et al.The Journal of Clinical Investigation|April 13, 2023
Biological rhythms in COVID-19 vaccine effectiveness in an observational cohort study of 1.5 million patientsGuy Hazan, Or A Duek, Hillel Alapi, et al.Cell|December 24, 1987
Overexpression of the human EGF receptor confers an EGF-dependent transformed phenotype to NIH 3T3 cellsP P Di Fiore, J H Pierce, T P Fleming, et al.Pageof 123