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Oncogene|May 12, 2015
USP7 is essential for maintaining Rad18 stability and DNA damage toleranceA Zlatanou, S Sabbioneda, E S Miller, et al.Genomics|February 1, 1993
Irradiation hybrids for human chromosome 11: characterization and use for generating region-specific markers in 11q14-q23G T Gillett, C M McConville, P J Byrd, et al.Oncogene|August 19, 2014
The dual-acting chemotherapeutic agent Alchemix induces cell death independently of ATM and p53A Thomas, T Perry, S Berhane, et al.Cell|December 28, 1999
The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorderG S Stewart, R S Maser, T Stankovic, et al.Human Molecular Genetics|May 24, 2001
hMRE11: genomic structure and a null mutation identified in a transcript protected from nonsense-mediated mRNA decayS A Pitts, H S Kullar, T Stankovic, et al.Blood Cancer Journal|July 23, 2013
BET inhibition as a single or combined therapeutic approach in primary paediatric B-precursor acute lymphoblastic leukaemiaD Da Costa, A Agathanggelou, T Perry, et al.The Journal of Pathology|September 19, 2007
Down-regulation of ATM protein in HRS cells of nodular sclerosis Hodgkin's lymphoma in children occurs in the absence of ATM gene inactivationS Bose, J Starczynski, M Chukwuma, et al.American Journal of Human Genetics|April 16, 1998
ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancerT Stankovic, A M Kidd, A Sutcliffe, et al.Genomics|March 1, 1997
Construction of a transcription map around the gene for ataxia telangiectasia: identification of at least four novel genesT Stankovic, P J Byrd, P R Cooper, et al.Cell Death & Disease|August 7, 2015
Assessment of p53 and ATM functionality in chronic lymphocytic leukemia by multiplex ligation-dependent probe amplificationG D te Raa, P D Moerland, A C Leeksma, et al.Pageof 4