Minoru Takata
Kyoto, 6068501, Japan
Last Updated: 09/26/2026
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Found 91 publications
SLFN11 inhibition rescues the Fanconi anemia phenotype by stabilizing stalled replication forks
Journal: [Rinsho ketsueki] The Japanese journal of clinical hematology
Published: January 01, 2024
A new Fanconi anemia-like disorder, aldehyde degradation deficiency syndrome: two defense mechanisms working together for the genome and hematopoiesis
Journal: [Rinsho ketsueki] The Japanese journal of clinical hematology
Published: August 06, 2023
The ribonuclease domain function is dispensable for SLFN11 to mediate cell fate decision during replication stress response.
Journal: Genes to cells : devoted to molecular & cellular mechanisms
Published: June 01, 2023
Meeting report: AT workshop 2023-A platform for discussing cutting-edge science in DNA damage signaling, repair, and human disorders.
Journal: Genes to cells : devoted to molecular & cellular mechanisms
Published: May 22, 2023
Fanconi anemia and Aldehyde Degradation Deficiency Syndrome: Metabolism and DNA repair protect the genome and hematopoiesis from endogenous DNA damage.
Journal: DNA repair
Published: May 12, 2023
Effects of the major formaldehyde catalyzer ADH5 on phenotypes of fanconi anemia zebrafish model.
Journal: Molecular biology reports
Published: March 23, 2023
Mouse Slfn8 and Slfn9 genes complement human cells lacking SLFN11 during the replication stress response.
Journal: Communications biology
Published: February 15, 2023
RFWD3 and translesion DNA polymerases contribute to PCNA modification-dependent DNA damage tolerance.
Journal: Life science alliance
Published: June 29, 2022
Preoperative evaluation of pleural adhesions with dynamic chest radiography: a retrospective study of 146 patients with lung cancer.
Journal: Clinical radiology
Published: September 28, 2021
Last Updated: 09/26/2026