Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients. (Q38267184)

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21 February 2020

title

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

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21 February 2020

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3

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21 February 2020

Yusuke Okuno

4

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21 February 2020

Keitaro Matsuo

12

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21 February 2020

Minoru Takata

13

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21 February 2020

author name string

Asuka Hira

1

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21 February 2020

Hiromasa Yabe

2

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21 February 2020

Yuichi Shiraishi

5

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21 February 2020

Kenichi Chiba

6

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21 February 2020

Hiroko Tanaka

7

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21 February 2020

Satoru Miyano

8

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21 February 2020

Jun Nakamura

9

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21 February 2020

Seiji Kojima

10

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21 February 2020

Seishi Ogawa

11

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21 February 2020

Miharu Yabe

14

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21 February 2020

language of work or name

English

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publication date

13 September 2013

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21 February 2020

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21 February 2020

volume

122

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21 February 2020

issue

18

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21 February 2020

page(s)

3206-3209

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Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.

21 February 2020

cites work

1 reference

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ACTN1 mutations cause congenital macrothrombocytopenia

6 September 2017

1 reference

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Fanconi anaemia and the repair of Watson and Crick DNA crosslinks

6 September 2017

1 reference

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Genotoxic consequences of endogenous aldehydes on mouse haematopoietic stem cell function

6 September 2017

1 reference

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Regulation of DNA cross-link repair by the Fanconi anemia/BRCA pathway

6 September 2017

1 reference

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Bone marrow failure in Fanconi anemia is triggered by an exacerbated p53/p21 DNA damage response that impairs hematopoietic stem and progenitor cells

6 September 2017

1 reference

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Fancd2 counteracts the toxic effects of naturally produced aldehydes in mice

6 September 2017

1 reference

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Mutations of the SLX4 gene in Fanconi anemia

6 September 2017

1 reference

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Fanconi anemia and its diagnosis

6 September 2017

1 reference

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Mouse models of Fanconi anemia

6 September 2017

1 reference

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Activation of aldehyde dehydrogenase-2 reduces ischemic damage to the heart

6 September 2017

1 reference

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Cells deficient in the FANC/BRCA pathway are hypersensitive to plasma levels of formaldehyde

6 September 2017

1 reference

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Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer

6 September 2017

1 reference

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Statistical methods for the analysis and presentation of the results of bone marrow transplants. Part I: unadjusted analysis

6 September 2017

1 reference

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Hematologic abnormalities in Fanconi anemia: an International Fanconi Anemia Registry study.

6 September 2017

1 reference

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International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity

6 September 2017

1 reference

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Genotypes for aldehyde dehydrogenase deficiency and alcohol sensitivity. The inactive ALDH2(2) allele is dominant

6 September 2017

1 reference

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The FANCA gene in Japanese Fanconi anemia: reports of eight novel mutations and analysis of sequence variability

6 September 2017

1 reference

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Whole exome sequencing reveals uncommon mutations in the recently identified Fanconi anemia gene SLX4/FANCP.

23 June 2018

1 reference

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SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype

31 August 2018

1 reference

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Gene-environment interaction between an aldehyde dehydrogenase-2 (ALDH2) polymorphism and alcohol consumption for the risk of esophageal cancer

31 August 2018

1 reference

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Alcohol Dehydrogenase 2 His47Arg Polymorphism Influences Drinking Habit Independently of Aldehyde Dehydrogenase 2 Glu487Lys Polymorphism: Analysis of 2,299 Japanese Subjects

31 August 2018

1 reference

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Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia

3 December 2018

1 reference

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Outcome of 69 allogeneic stem cell transplantations for Fanconi anemia using HLA-matched unrelated donors: a study on behalf of the European Group for Blood and Marrow Transplantation

3 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24037726

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1182/BLOOD-2013-06-507962

1 reference

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21 February 2020

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21 February 2020

1 reference

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