Anfeng Mu

Kyoto, Japan

Last Updated: 09/26/2026

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Found 17 publications

The role of SLFN11 in DNA replication stress response and its implications for the Fanconi anemia pathway.

The role of SLFN11 in DNA replication stress response and its implications for the Fanconi anemia pathway.

Journal: DNA repair

Published: January 23, 2024

SLFN11 inhibition rescues the Fanconi anemia phenotype by stabilizing stalled replication forks

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

The ribonuclease domain function is dispensable for SLFN11 to mediate cell fate decision during replication stress response.

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

Fanconi anemia and Aldehyde Degradation Deficiency Syndrome: Metabolism and DNA repair protect the genome and hematopoiesis from endogenous DNA damage.

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.

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.

Mouse Slfn8 and Slfn9 genes complement human cells lacking SLFN11 during the replication stress response.

Journal: Communications biology

Published: February 15, 2023

Lack of impact of the ALDH2 rs671 variant on breast cancer development in Japanese BRCA1/2-mutation carriers.

Lack of impact of the ALDH2 rs671 variant on breast cancer development in Japanese BRCA1/2-mutation carriers.

Journal: Cancer medicine

Published: May 12, 2022

Aldehyde degradation deficiency (ADD) syndrome: discovery of a novel fanconi anemia-like inherited BMF syndrome due to combined ADH5/ALDH2 deficiency

Aldehyde degradation deficiency (ADD) syndrome: discovery of a novel fanconi anemia-like inherited BMF syndrome due to combined ADH5/ALDH2 deficiency

Journal: [Rinsho ketsueki] The Japanese journal of clinical hematology

Published: July 05, 2021

Analysis of disease model iPSCs derived from patients with a novel Fanconi anemia-like IBMFS ADH5/ALDH2 deficiency.

Analysis of disease model iPSCs derived from patients with a novel Fanconi anemia-like IBMFS ADH5/ALDH2 deficiency.

Journal: Blood

Published: September 14, 2020

Two Aldehyde Clearance Systems Are Essential to Prevent Lethal Formaldehyde Accumulation in Mice and Humans.

Two Aldehyde Clearance Systems Are Essential to Prevent Lethal Formaldehyde Accumulation in Mice and Humans.

Journal: Molecular cell

Published: June 15, 2020

SLFN11 promotes stalled fork degradation that underlies the phenotype in Fanconi anemia cells.

SLFN11 promotes stalled fork degradation that underlies the phenotype in Fanconi anemia cells.

Journal: Blood

Published: October 18, 2019

Enhancements of the production of bilirubin and the expression of β-globin by carbon monoxide during erythroid differentiation.

Enhancements of the production of bilirubin and the expression of β-globin by carbon monoxide during erythroid differentiation.

Journal: FEBS letters

Published: February 25, 2016

Showing 1-12 of 17

Last Updated: 09/26/2026