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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 8, 2020
RAD50 regulates mitotic progression independent of DNA repair functionsLea Völkening, Anna Vatselia, Girmay Asgedom, et al.
American Journal of Human Genetics|February 22, 2002
Premature chromosome condensation in humans associated with microcephaly and mental retardation: a novel autosomal recessive conditionHeidemarie Neitzel, Luitgard M Neumann, Detlev Schindler, et al.
Plos One|September 7, 2012
A novel MCPH1 isoform complements the defective chromosome condensation of human MCPH1-deficient cellsIoannis Gavvovidis, Isabell Rost, Marc Trimborn, et al.
Cell Cycle (Georgetown, Tex.)|December 15, 2010
MCPH1 patient cells exhibit delayed release from DNA damage-induced G2/M checkpoint arrestIoannis Gavvovidis, Charlotte Pöhlmann, Juan Alberto Marchal, et al.
Human Mutation|October 4, 2012
Whole exome sequencing reveals uncommon mutations in the recently identified Fanconi anemia gene SLX4/FANCPBeatrice Schuster, Kerstin Knies, Chantal Stoepker, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 6, 2013
Visualization of local DNA unwinding by Mre11/Rad50/Nbs1 using single-molecule FRETBrian Cannon, Jeffrey Kuhnlein, Soo-Hyun Yang, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 9, 2010
Hepatoblastoma in a 4-year-old girl with Fanconi anaemiaSascha Kopic, Katharina Eirich, Beatrice Schuster, et al.
Environmental and Molecular Mutagenesis|February 14, 2006
Radiation-induced DNA damage and repair in peripheral blood mononuclear cells from Nijmegen breakage syndrome patients and carriers assessed by the Comet assaySusann Bürger, Detlev Schindler, Martin Fehn, et al.
Blood Cells, Molecules & Diseases|December 20, 2011
Treatment of the bone marrow failure in Fanconi anemia patients with danazolKathrin Scheckenbach, Mary Morgan, Judith Filger-Brillinger, et al.
International Journal of Molecular Sciences|July 29, 2025
BRCA2 Pre-mRNA Differential 5' Splicing: A Rescue of Functional Protein Properties from Pathogenic Gene Variants and a Lifeline for Fanconi Anemia D1 PatientsRoberto Paredes, Kiran Batta, Daniel H Wiseman, et al.
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