Last Updated: 09/26/2026
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Found 7 publications
A homozygous missense variant in UBE2T is associated with a mild Fanconi anemia phenotype.
Journal: Haematologica
Published: July 11, 2020
Esophageal cancer as initial presentation of Fanconi anemia in patients with a hypomorphic FANCA variant.
Journal: Cold Spring Harbor molecular case studies
Published: May 20, 2020
Advances in understanding DNA processing and protection at stalled replication forks.
Journal: The Journal of cell biology
Published: September 04, 2018
S. pombe Uba1-Ubc15 Structure Reveals a Novel Regulatory Mechanism of Ubiquitin E2 Activity.
Journal: Molecular cell
Published: August 23, 2016
Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia.
Journal: Cell reports
Published: May 05, 2015
Showing 1-7 of 7
Last Updated: 09/26/2026