These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 37544724)

  • 1. [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]  

  • 2. 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
    DNA Repair (Amst); 2023 Oct; 130():103546. PubMed ID: 37572579
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [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
    Rinsho Ketsueki; 2021; 62(6):547-553. PubMed ID: 34219079
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. ALDH2 mutations and defense against genotoxic aldehydes in cancer and inherited bone marrow failure syndromes.
    Woo AY; Jia L
    Mutat Res; 2024; 829():111870. PubMed ID: 38944932
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Digenic mutations in
    Oka Y; Hamada M; Nakazawa Y; Muramatsu H; Okuno Y; Higasa K; Shimada M; Takeshima H; Hanada K; Hirano T; Kawakita T; Sakaguchi H; Ichimura T; Ozono S; Yuge K; Watanabe Y; Kotani Y; Yamane M; Kasugai Y; Tanaka M; Suganami T; Nakada S; Mitsutake N; Hara Y; Kato K; Mizuno S; Miyake N; Kawai Y; Tokunaga K; Nagasaki M; Kito S; Isoyama K; Onodera M; Kaneko H; Matsumoto N; Matsuda F; Matsuo K; Takahashi Y; Mashimo T; Kojima S; Ogi T
    Sci Adv; 2020 Dec; 6(51):. PubMed ID: 33355142
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Effects of the major formaldehyde catalyzer ADH5 on phenotypes of fanconi anemia zebrafish model.
    Mu A; Cao Z; Huang D; Hosokawa H; Maegawa S; Takata M
    Mol Biol Rep; 2023 Oct; 50(10):8385-8395. PubMed ID: 37615925
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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
    Mol Cell; 2020 Dec; 80(6):996-1012.e9. PubMed ID: 33147438
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. A Surge of DNA Damage Links Transcriptional Reprogramming and Hematopoietic Deficit in Fanconi Anemia.
    Shen X; Wang R; Kim MJ; Hu Q; Hsu CC; Yao J; Klages-Mundt N; Tian Y; Lynn E; Brewer TF; Zhang Y; Arun B; Gan B; Andreeff M; Takeda S; Chen J; Park JI; Shi X; Chang CJ; Jung SY; Qin J; Li L
    Mol Cell; 2020 Dec; 80(6):1013-1024.e6. PubMed ID: 33338401
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Formaldehyde catabolism is essential in cells deficient for the Fanconi anemia DNA-repair pathway.
    Rosado IV; Langevin F; Crossan GP; Takata M; Patel KJ
    Nat Struct Mol Biol; 2011 Nov; 18(12):1432-4. PubMed ID: 22081012
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [New insights into inherited bone marrow failure syndrome].
    Ito E; Toki T; Kamio T; Terui K
    Rinsho Ketsueki; 2021; 62(10):1455-1464. PubMed ID: 34732617
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Genotoxic aldehydes in the hematopoietic system.
    Wang M; Dingler FA; Patel KJ
    Blood; 2022 Apr; 139(14):2119-2129. PubMed ID: 35148375
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.