279 related articles for article (PubMed ID: 24037726)
1. Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients.
Hira A; Yabe H; Yoshida K; Okuno Y; Shiraishi Y; Chiba K; Tanaka H; Miyano S; Nakamura J; Kojima S; Ogawa S; Matsuo K; Takata M; Yabe M
Blood; 2013 Oct; 122(18):3206-9. PubMed ID: 24037726
[TBL] [Abstract][Full Text] [Related]
2. Associations of complementation group, ALDH2 genotype, and clonal abnormalities with hematological outcome in Japanese patients with Fanconi anemia.
Yabe M; Koike T; Ohtsubo K; Imai E; Morimoto T; Takakura H; Koh K; Yoshida K; Ogawa S; Ito E; Okuno Y; Muramatsu H; Kojima S; Matsuo K; Mori M; Hira A; Takata M; Yabe H
Ann Hematol; 2019 Feb; 98(2):271-280. PubMed ID: 30368588
[TBL] [Abstract][Full Text] [Related]
3. The phenotype and clinical course of Japanese Fanconi Anaemia infants is influenced by patient, but not maternal ALDH2 genotype.
Yabe M; Yabe H; Morimoto T; Fukumura A; Ohtsubo K; Koike T; Yoshida K; Ogawa S; Ito E; Okuno Y; Muramatsu H; Kojima S; Matsuo K; Hira A; Takata M
Br J Haematol; 2016 Nov; 175(3):457-461. PubMed ID: 27377053
[TBL] [Abstract][Full Text] [Related]
4. 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
Cancer Med; 2023 Mar; 12(6):6594-6602. PubMed ID: 36345163
[TBL] [Abstract][Full Text] [Related]
5. Functional analysis of Fanconi anemia mutations in China.
Li N; Ding L; Li B; Wang J; D'Andrea AD; Chen J
Exp Hematol; 2018 Oct; 66():32-41.e8. PubMed ID: 30031030
[TBL] [Abstract][Full Text] [Related]
6. Genetic Study of Fanconi Anemia in Infancy Revealed FANCI Mutations and Defective ALDH2 Variant: A Case Report.
Urata T; Imamura T; Osone S; Muramatsu H; Takahashi Y; Hosoi H
J Pediatr Hematol Oncol; 2022 Mar; 44(2):e438-e441. PubMed ID: 34310468
[TBL] [Abstract][Full Text] [Related]
7. Maternal aldehyde elimination during pregnancy preserves the fetal genome.
Oberbeck N; Langevin F; King G; de Wind N; Crossan GP; Patel KJ
Mol Cell; 2014 Sep; 55(6):807-817. PubMed ID: 25155611
[TBL] [Abstract][Full Text] [Related]
8. FANCA and FANCG are the major Fanconi anemia genes in the Korean population.
Park J; Chung NG; Chae H; Kim M; Lee S; Kim Y; Lee JW; Cho B; Jeong DC; Park IY
Clin Genet; 2013 Sep; 84(3):271-5. PubMed ID: 23067021
[TBL] [Abstract][Full Text] [Related]
9. ALDH2 polymorphism in patients with Diamond-Blackfan anemia in Japan.
Ikeda F; Toki T; Kanezaki R; Terui K; Yoshida K; Kanno H; Ohga S; Ohara A; Kojima S; Ogawa S; Ito E
Int J Hematol; 2016 Jan; 103(1):112-4. PubMed ID: 26608366
[No Abstract] [Full Text] [Related]
10. Founder haplotype analysis of Fanconi anemia in the Korean population finds common ancestral haplotypes for a FANCG variant.
Park J; Kim M; Jang W; Chae H; Kim Y; Chung NG; Lee JW; Cho B; Jeong DC; Park IY; Park MS
Ann Hum Genet; 2015 May; 79(3):153-61. PubMed ID: 25703136
[TBL] [Abstract][Full Text] [Related]
11. 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
Blood; 2021 Apr; 137(15):2021-2032. PubMed ID: 33512438
[TBL] [Abstract][Full Text] [Related]
12. Current knowledge on the pathophysiology of Fanconi anemia: from genes to phenotypes.
Yamashita T; Nakahata T
Int J Hematol; 2001 Jul; 74(1):33-41. PubMed ID: 11530803
[TBL] [Abstract][Full Text] [Related]
13. Aldehyde dehydrogenase 2 in aplastic anemia, Fanconi anemia and hematopoietic stem cells.
Van Wassenhove LD; Mochly-Rosen D; Weinberg KI
Mol Genet Metab; 2016 Sep; 119(1-2):28-36. PubMed ID: 27650066
[TBL] [Abstract][Full Text] [Related]
14. Comprehensive analysis on phenotype and genetic basis of Chinese Fanconi anemia patients: dismal outcomes call for nationwide studies.
Nie D; Zhang J; Wang F; Zhang W; Liu L; Chen X; Zhang Y; Cao P; Xiong M; Wang T; Wu P; Ma X; Tian W; Wang M; Chen KN; Liu H
BMC Med Genet; 2020 Jun; 21(1):118. PubMed ID: 32487094
[TBL] [Abstract][Full Text] [Related]
15. Compromised repair of radiation-induced DNA double-strand breaks in Fanconi anemia fibroblasts in G2.
Zahnreich S; Weber B; Rösch G; Schindler D; Schmidberger H
DNA Repair (Amst); 2020 Dec; 96():102992. PubMed ID: 33069004
[TBL] [Abstract][Full Text] [Related]
16. Severe telomere shortening in Fanconi anemia complementation group L.
Shah A; George M; Dhangar S; Rajendran A; Mohan S; Vundinti BR
Mol Biol Rep; 2021 Jan; 48(1):585-593. PubMed ID: 33394227
[TBL] [Abstract][Full Text] [Related]
17. Genotoxic consequences of endogenous aldehydes on mouse haematopoietic stem cell function.
Garaycoechea JI; Crossan GP; Langevin F; Daly M; Arends MJ; Patel KJ
Nature; 2012 Sep; 489(7417):571-5. PubMed ID: 22922648
[TBL] [Abstract][Full Text] [Related]
18. [A new Fanconi anemia-like disorder, aldehyde degradation deficiency syndrome: two defense mechanisms working together for the genome and hematopoiesis].
Takata M
Rinsho Ketsueki; 2023; 64(7):639-645. PubMed ID: 37544724
[TBL] [Abstract][Full Text] [Related]
19. Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
Chandrasekharappa SC; Lach FP; Kimble DC; Kamat A; Teer JK; Donovan FX; Flynn E; Sen SK; Thongthip S; Sanborn E; Smogorzewska A; Auerbach AD; Ostrander EA;
Blood; 2013 May; 121(22):e138-48. PubMed ID: 23613520
[TBL] [Abstract][Full Text] [Related]
20. In silico study of missense variants of FANCA, FANCC and FANCG genes reveals high risk deleterious alleles predisposing to Fanconi anemia pathogenesis.
Shahid M; Azfaralariff A; Zubair M; Abdulkareem Najm A; Khalili N; Law D; Firasat S; Fazry S
Gene; 2022 Feb; 812():146104. PubMed ID: 34864095
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]