Showing results (91-100 of 127) with videos related to

Sort By:
Pageof 13
Scientific Reports|April 30, 2026
Differential regulation of retinoic acid metabolism in Fanconi anemiaJustin L Blaize, Bahaa M Noori, Kelsey P Hunter, et al.
Plos Genetics|April 13, 2011
Roles of brca2 (fancd1) in oocyte nuclear architecture, gametogenesis, gonad tumors, and genome stability in zebrafishAdriana Rodríguez-Marí, Catherine Wilson, Tom A Titus, et al.
Cancer Research|October 3, 2007
Genetic heterogeneity among Fanconi anemia heterozygotes and risk of cancerMarianne Berwick, Jaya M Satagopan, Leah Ben-Porat, et al.
Human Mutation|July 3, 2010
Clinical variability and novel mutations in the NHEJ1 gene in patients with a Nijmegen breakage syndrome-like phenotypeVéronique Dutrannoy, Ilja Demuth, Ulrich Baumann, et al.
Molecular Cancer|June 1, 2010
Genetic inactivation of the Fanconi anemia gene FANCC identified in the hepatocellular carcinoma cell line HuH-7 confers sensitivity towards DNA-interstrand crosslinking agentsAndreas Palagyi, Kornelia Neveling, Ursula Plinninger, et al.
Orphanet Journal of Rare Diseases|October 22, 2014
Combined immunodeficiency develops with age in Immunodeficiency-centromeric instability-facial anomalies syndrome 2 (ICF2)Horst von Bernuth, Ethiraj Ravindran, Hang Du, et al.
Scientific Reports|November 15, 2018
Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutationBeate Hagl, Benedikt D Spielberger, Silvia Thoene, et al.
Cellular Oncology : the Official Journal of the International Society for Cellular Oncology|April 25, 2007
Identification of the Fanconi anemia complementation group I gene, FANCIJosephine C Dorsman, Marieke Levitus, Davy Rockx, et al.
Plos Genetics|April 29, 2017
Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformationEthiraj Ravindran, Hao Hu, Scott A Yuzwa, et al.
Molecular Cell|June 19, 2012
A ubiquitin-binding protein, FAAP20, links RNF8-mediated ubiquitination to the Fanconi anemia DNA repair networkZhijiang Yan, Rong Guo, Manikandan Paramasivam, et al.
Pageof 13