Showing results (81-90 of 127) with videos related to

Sort By:
Pageof 13
Biorxiv : the Preprint Server for Biology|April 17, 2023
Differential Regulation of Retinoic Acid Metabolism in Fanconi AnemiaJustin L Blaize, Bahaa M Noori, Kelsey P Hunter, et al.
Cell Death and Differentiation|October 6, 2021
Inhibition of USP28 overcomes Cisplatin-resistance of squamous tumors by suppression of the Fanconi anemia pathwayCristian Prieto-Garcia, Oliver Hartmann, Michaela Reissland, et al.
BMC Medical Genetics|January 13, 2018
Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPFIsabell Popp, Maqsood Punekar, Nick Telford, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 9, 2005
A rapid method for retrovirus-mediated identification of complementation groups in Fanconi anemia patientsSaurabh Chandra, Orna Levran, Ingrid Jurickova, et al.
The British Journal of Radiology|September 16, 2015
Central nervous system abnormalities in Fanconi anaemia: patterns and frequency on magnetic resonance imagingStavros M Stivaros, Robert Alston, Neville B Wright, et al.
Journal of Lipid Research|July 2, 2002
Defects in degradation of blood group A and B glycosphingolipids in Schindler and Fabry diseasesBefekadu Asfaw, Jana Ledvinová, Robert Dobrovolńy, et al.
BMC Cancer|March 10, 2012
Analysis of SLX4/FANCP in non-BRCA1/2-mutated breast cancer familiesJuana Fernández-Rodríguez, Francisco Quiles, Ignacio Blanco, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|May 17, 2013
Living related liver transplantation in an adult patient with hepatocellular adenoma and carcinoma 13 years after bone marrow transplantation for Fanconi anemia: A case reportIsabelle Colle, Geneviève Laureys, Sarah Raevens, et al.
Cell Cycle (Georgetown, Tex.)|August 23, 2011
Misregulation of mitotic chromosome segregation in a new type of autosomal recessive primary microcephalyJuan Alberto Marchal, Mahdi Ghani, Detlev Schindler, et al.
Cell Reports|June 30, 2015
Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi AnemiaKimberly A Rickman, Francis P Lach, Avinash Abhyankar, et al.
Pageof 13