Author

Asuka Hira

Observed name: Hira, Asuka

Institution: Kyoto University

Observed institution: Kyoto University

OpenAlex ID: A5009803907

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

2020 · Felix A. Dingler, Meng Wang, et al. · Molecular Cell · 187

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Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients

2013 · Asuka Hira, Hiromasa Yabe, et al. · Blood · 172

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Mutations in the Gene Encoding the E2 Conjugating Enzyme UBE2T Cause Fanconi Anemia

2015 · Asuka Hira, Kenichi Yoshida, et al. · The American Journal of Human Genetics · 114

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

2021 · Anfeng Mu, Asuka Hira, et al. · Blood · 41

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Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients

2019 · Minako Mori, Asuka Hira, et al. · Haematologica · 34

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Pluripotent Cell Models of Fanconi Anemia Identify the Early Pathological Defect in Human Hemoangiogenic Progenitors

2015 · Naoya M. Suzuki, Akira Niwa, et al. · Stem Cells Translational Medicine · 34

Common Variable Immunodeficiency Caused by FANC Mutations

2017 · Yujin Sekinaka, Noriko Mitsuiki, et al. · Journal of Clinical Immunology · 23

Associations of complementation group, ALDH2 genotype, and clonal abnormalities with hematological outcome in Japanese patients with Fanconi anemia

2018 · Miharu Yabe, Takashi Koike, et al. · Annals of Hematology · 19

The phenotype and clinical course of Japanese Fanconi Anaemia infants is influenced by patient, but not maternal ALDH2 genotype

2016 · Miharu Yabe, Hiromasa Yabe, et al. · British Journal of Haematology · 11

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

2023 · Anfeng Mu, Asuka Hira, et al. · DNA repair · 8

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

2021 · Anfeng Mu, Asuka Hira, et al. · PubMed · 5

Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients

2020 · Minako Mori, Asuka Hira, et al. · Haematologica · 4

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Characterization of Pathogenic Variants and Clinical Phenotypes in 117 Japanese Fanconi Anemia Patients

2018 · Minako Mori, Asuka Hira, et al. · Blood · 1

Aldehyde degradation deficiency（ADD）症候群 --アルデヒド代謝酵素欠損によるファンコニ貧血症類似の新たな遺伝性骨髄不全症候群の発見--

2021 · Mu, Anfeng, Hira, Asuka, et al. · Institutional Repositories DataBase (IRDB)

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Fanconi anemia-like genome instability syndrome caused by combined mutations in ADH5 and ALDH2 genes

2019 · Anfeng Mu, Asuka Hira, et al. · The Molecular Biology Society of Japan

ユビキチン結合e2酵素ube2t遺伝子変異を原因としたファンコニ貧血の発症

2015 · Hira, Asuka · Institutional Repositories DataBase (IRDB)

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[Fanconi anemia and the molecular mechanism of the repair of DNA crosslinks].

2013 · Asuka Hira, Minoru Takata · PubMed

Mesodermal Development From Reprogrammed Fanconi Anemia Cells Is Affected by ALDH2 Enzymatic Activity

2012 · Naoya Suzuki, Asuka Hira, et al. · Blood

Works count: 18

Citation count: 653

H-index: 9

I10-index: 9