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International Journal of Radiation Oncology, Biology, Physics|October 15, 2017
Identification of ATIC as a Novel Target for ChemoradiosensitizationXiangfei Liu, Uma Devi Paila, Sharon N Teraoka, et al.Journal of the Neurological Sciences|January 23, 2017
Cardiac transplantation in Friedreich Ataxia: Extended follow-upAshley McCormick, Julianna Shinnick, Kim Schadt, et al.Journal of Immunology (Baltimore, Md. : 1950)|March 21, 2003
ATM is not required in somatic hypermutation of VH, but is involved in the introduction of mutations in the switch mu regionQiang Pan-Hammarström, Shujing Dai, Yaofeng Zhao, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 23, 2005
Clinical feature profile of spinocerebellar ataxia type 1-8 predicts genetically defined subtypesMatthias Maschke, Gary Oehlert, Ting-Dong Xie, et al.Journal of Clinical Immunology|February 14, 2015
Nijmegen breakage syndrome detected by newborn screening for T cell receptor excision circles (TRECs)Jay P Patel, Jennifer M Puck, Rajgopal Srinivasan, et al.Proceedings of the National Academy of Sciences of the United States of America|February 4, 2015
Aberrant recombination and repair during immunoglobulin class switching in BRCA1-deficient human B cellsAndrea Björkman, Per Qvist, Likun Du, et al.International Journal of Radiation Biology|March 16, 2011
High throughput screening of small molecule libraries for modifiers of radiation responsesKwanghee Kim, Robert Damoiseaux, Andrew J Norris, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|June 19, 2013
A new series of small molecular weight compounds induce read through of all three types of nonsense mutations in the ATM geneLiutao Du, Michael E Jung, Robert Damoiseaux, et al.The Journal of Pediatrics|April 16, 2002
Nijmegen breakage syndrome: clinical characteristics and mutation analysis in eight unrelated Russian familiesIgor B Resnick, Irina Kondratenko, Oleg Togoev, et al.Plos One|August 20, 2015
Evaluation of Aminoglycoside and Non-Aminoglycoside Compounds for Stop-Codon Readthrough Therapy in Four Lysosomal Storage DiseasesMarta Gómez-Grau, Elena Garrido, Mónica Cozar, et al.Pageof 19