Mu A - Search Results

1

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

Mori T, Okamoto Y, Mu A, Ide Y, Yoshimura A, Senda N, Inagaki-Kawata Y, Kawashima M, Kitao H, Tokunaga E, Miyoshi Y, Ohsumi S, Tsugawa K, Ohta T, Katagiri T, Ohtsuru S, Koike K, Ogawa S, Toi M, Iwata H, Nakamura S, Matsuo K, Takata M. Mori T, et al. Among authors: mu a. Cancer Med. 2023 Mar;12(6):6594-6602. doi: 10.1002/cam4.5430. Epub 2022 Nov 7. Cancer Med. 2023. PMID: 36345163 Free PMC article.

2

p53 directly regulates the transcription of the human frataxin gene and its lack of regulation in tumor cells decreases the utilization of mitochondrial iron.

Shimizu R, Lan NN, Tai TT, Adachi Y, Kawazoe A, Mu A, Taketani S. Shimizu R, et al. Among authors: mu a. Gene. 2014 Nov 1;551(1):79-85. doi: 10.1016/j.gene.2014.08.043. Epub 2014 Aug 23. Gene. 2014. PMID: 25158131

3

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

Mu A, Li M, Tanaka M, Adachi Y, Tai TT, Liem PH, Izawa S, Furuyama K, Taketani S. Mu A, et al. FEBS Lett. 2016 May;590(10):1447-54. doi: 10.1002/1873-3468.12178. Epub 2016 May 18. FEBS Lett. 2016. PMID: 27087140 Free article.

4

A simple and highly sensitive method of measuring heme oxygenase activity.

Liem PH, Mu A, Kikuta S, Ohta K, Kitajima S, Taketani S. Liem PH, et al. Among authors: mu a. Biol Chem. 2015 Nov;396(11):1265-8. doi: 10.1515/hsz-2015-0176. Biol Chem. 2015. PMID: 26040009

5

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

Okamoto Y, Abe M, Mu A, Tempaku Y, Rogers CB, Mochizuki AL, Katsuki Y, Kanemaki MT, Takaori-Kondo A, Sobeck A, Bielinsky AK, Takata M. Okamoto Y, et al. Among authors: mu a. Blood. 2021 Jan 21;137(3):336-348. doi: 10.1182/blood.2019003782. Blood. 2021. PMID: 32735670 Free PMC article.

6

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

Dingler FA, Wang M, Mu A, Millington CL, Oberbeck N, Watcham S, Pontel LB, Kamimae-Lanning AN, Langevin F, Nadler C, Cordell RL, Monks PS, Yu R, Wilson NK, Hira A, Yoshida K, Mori M, Okamoto Y, Okuno Y, Muramatsu H, Shiraishi Y, Kobayashi M, Moriguchi T, Osumi T, Kato M, Miyano S, Ito E, Kojima S, Yabe H, Yabe M, Matsuo K, Ogawa S, Göttgens B, Hodskinson MRG, Takata M, Patel KJ. Dingler FA, et al. Among authors: mu a. Mol Cell. 2020 Dec 17;80(6):996-1012.e9. doi: 10.1016/j.molcel.2020.10.012. Epub 2020 Nov 3. Mol Cell. 2020. PMID: 33147438 Free PMC article.

7

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

Mu A, Hira A, Niwa A, Osawa M, Yoshida K, Mori M, Okamoto Y, Inoue K, Kondo K, Kanemaki MT, Matsuda T, Ito E, Kojima S, Nakahata T, Ogawa S, Tanaka K, Matsuo K, Saito MK, Takata M. Mu A, et al. Blood. 2021 Apr 15;137(15):2021-2032. doi: 10.1182/blood.2020009111. Blood. 2021. PMID: 33512438 Free article.

8

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

Mu A, Hira A, Matsuo K, Takata M. Mu A, et al. Rinsho Ketsueki. 2021;62(6):547-553. doi: 10.11406/rinketsu.62.547. Rinsho Ketsueki. 2021. PMID: 34219079 Japanese.

9

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

Qi F, Alvi E, Ogawa M, Kobayashi J, Mu A, Takata M. Qi F, et al. Among authors: mu a. Genes Cells. 2023 Sep;28(9):663-673. doi: 10.1111/gtc.13056. Epub 2023 Jul 19. Genes Cells. 2023. PMID: 37469008 Free article.

10

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

Mu A, Hira A, Mori M, Okamoto Y, Takata M. Mu A, et al. DNA Repair (Amst). 2023 Oct;130:103546. doi: 10.1016/j.dnarep.2023.103546. Epub 2023 Aug 1. DNA Repair (Amst). 2023. PMID: 37572579

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