BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 33402700)

  • 1. Positional cloning and comprehensive mutation analysis identified a novel KDM2B mutation in a Japanese family with minor malformations, intellectual disability, and schizophrenia.
    Yokotsuka-Ishida S; Nakamura M; Tomiyasu Y; Nagai M; Kato Y; Tomiyasu A; Umehara H; Hayashi T; Sasaki N; Ueno SI; Sano A
    J Hum Genet; 2021 Jun; 66(6):597-606. PubMed ID: 33402700
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Linkage and exome analysis implicate multiple genes in non-syndromic intellectual disability in a large Swedish family.
    Lindholm Carlström E; Halvardson J; Etemadikhah M; Wetterberg L; Gustavson KH; Feuk L
    BMC Med Genomics; 2019 Nov; 12(1):156. PubMed ID: 31694657
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability.
    Labonne JD; Lee KH; Iwase S; Kong IK; Diamond MP; Layman LC; Kim CH; Kim HG
    Hum Genet; 2016 Jul; 135(7):757-71. PubMed ID: 27106595
    [TBL] [Abstract][Full Text] [Related]  

  • 4. KDM2B is a histone H3K79 demethylase and induces transcriptional repression via sirtuin-1-mediated chromatin silencing.
    Kang JY; Kim JY; Kim KB; Park JW; Cho H; Hahm JY; Chae YC; Kim D; Kook H; Rhee S; Ha NC; Seo SB
    FASEB J; 2018 Oct; 32(10):5737-5750. PubMed ID: 29763382
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation and expression alterations of histone methylation-related NSD2, KDM2B and SETMAR genes in colon cancers.
    Moon SW; Son HJ; Mo HY; Choi EJ; Yoo NJ; Lee SH
    Pathol Res Pract; 2021 Mar; 219():153354. PubMed ID: 33621919
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Interplay between the Epigenetic Enzyme Lysine (K)-Specific Demethylase 2B and Epstein-Barr Virus Infection.
    Vargas-Ayala RC; Jay A; Manara F; Maroui MA; Hernandez-Vargas H; Diederichs A; Robitaille A; Sirand C; Ceraolo MG; Romero-Medina MC; Cros MP; Cuenin C; Durand G; Le Calvez-Kelm F; Mundo L; Leoncini L; Manet E; Herceg Z; Gruffat H; Accardi R
    J Virol; 2019 Jul; 93(13):. PubMed ID: 30996097
    [TBL] [Abstract][Full Text] [Related]  

  • 7. SRF is a nonhistone methylation target of KDM2B and SET7 in the regulation of skeletal muscle differentiation.
    Kwon DH; Kang JY; Joung H; Kim JY; Jeong A; Min HK; Shin S; Lee YG; Kim YK; Seo SB; Kook H
    Exp Mol Med; 2021 Feb; 53(2):250-263. PubMed ID: 33564100
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Biological Functions of the KDM2 Family of Histone Demethylases.
    Andricovich J; Tzatsos A
    Adv Exp Med Biol; 2023; 1433():51-68. PubMed ID: 37751135
    [TBL] [Abstract][Full Text] [Related]  

  • 9. KDM2B, an H3K36-specific demethylase, regulates apoptotic response of GBM cells to TRAIL.
    Kurt IC; Sur I; Kaya E; Cingoz A; Kazancioglu S; Kahya Z; Toparlak OD; Senbabaoglu F; Kaya Z; Ozyerli E; Karahüseyinoglu S; Lack NA; Gümüs ZH; Onder TT; Bagci-Onder T
    Cell Death Dis; 2017 Jun; 8(6):e2897. PubMed ID: 28661478
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder.
    Kato H; Kushima I; Mori D; Yoshimi A; Aleksic B; Nawa Y; Toyama M; Furuta S; Yu Y; Ishizuka K; Kimura H; Arioka Y; Tsujimura K; Morikawa M; Okada T; Inada T; Nakatochi M; Shinjo K; Kondo Y; Kaibuchi K; Funabiki Y; Kimura R; Suzuki T; Yamakawa K; Ikeda M; Iwata N; Takahashi T; Suzuki M; Okahisa Y; Takaki M; Egawa J; Someya T; Ozaki N
    Transl Psychiatry; 2020 Dec; 10(1):421. PubMed ID: 33279929
    [TBL] [Abstract][Full Text] [Related]  

  • 11. KDM2B is involved in the epigenetic regulation of TGF-β-induced epithelial-mesenchymal transition in lung and pancreatic cancer cell lines.
    Wanna-Udom S; Terashima M; Suphakhong K; Ishimura A; Takino T; Suzuki T
    J Biol Chem; 2021; 296():100213. PubMed ID: 33779563
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Tip60-dependent acetylation of KDM2B promotes osteosarcoma carcinogenesis.
    Shi X; Fan M
    J Cell Mol Med; 2019 Sep; 23(9):6154-6163. PubMed ID: 31218831
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Histone demethylase KDM2B promotes triple negative breast cancer proliferation by suppressing p15INK4B, p16INK4A, and p57KIP2 transcription.
    Zheng Q; Fan H; Meng Z; Yuan L; Liu C; Peng Y; Zhao W; Wang L; Li J; Feng J
    Acta Biochim Biophys Sin (Shanghai); 2018 Sep; 50(9):897-904. PubMed ID: 30060056
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Depletion of histone demethylase KDM2A inhibited cell proliferation of stem cells from apical papilla by de-repression of p15INK4B and p27Kip1.
    Gao R; Dong R; Du J; Ma P; Wang S; Fan Z
    Mol Cell Biochem; 2013 Jul; 379(1-2):115-22. PubMed ID: 23559091
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The KDM2B- let-7b -EZH2 axis in myelodysplastic syndromes as a target for combined epigenetic therapy.
    Karoopongse E; Yeung C; Byon J; Ramakrishnan A; Holman ZJ; Jiang PY; Yu Q; Deeg HJ; Marcondes AM
    PLoS One; 2014; 9(9):e107817. PubMed ID: 25225797
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lysine demethylase 2B regulates angiogenesis via Jumonji C dependent suppression of angiogenic transcription factors.
    Sasaki Y; Higashijima Y; Suehiro JI; Sugasawa T; Oguri-Nakamura E; Fukuhara S; Nagai N; Hirakawa Y; Wada Y; Nangaku M; Kanki Y
    Biochem Biophys Res Commun; 2022 May; 605():16-23. PubMed ID: 35306360
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Disrupted intricacy of histone H3K4 methylation in neurodevelopmental disorders.
    Vallianatos CN; Iwase S
    Epigenomics; 2015; 7(3):503-19. PubMed ID: 26077434
    [TBL] [Abstract][Full Text] [Related]  

  • 18. KDM5C mutational screening among males with intellectual disability suggestive of X-Linked inheritance and review of the literature.
    Gonçalves TF; Gonçalves AP; Fintelman Rodrigues N; dos Santos JM; Pimentel MM; Santos-Rebouças CB
    Eur J Med Genet; 2014 Mar; 57(4):138-44. PubMed ID: 24583395
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel KDM5B splice variants identified in patients with developmental disorders: Functional consequences.
    Lebrun N; Mehler-Jacob C; Poirier K; Zordan C; Lacombe D; Carion N; Billuart P; Bienvenu T
    Gene; 2018 Dec; 679():305-313. PubMed ID: 30217758
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A genome-wide DNA methylation signature for SETD1B-related syndrome.
    Krzyzewska IM; Maas SM; Henneman P; Lip KVD; Venema A; Baranano K; Chassevent A; Aref-Eshghi E; van Essen AJ; Fukuda T; Ikeda H; Jacquemont M; Kim HG; Labalme A; Lewis SME; Lesca G; Madrigal I; Mahida S; Matsumoto N; Rabionet R; Rajcan-Separovic E; Qiao Y; Sadikovic B; Saitsu H; Sweetser DA; Alders M; Mannens MMAM
    Clin Epigenetics; 2019 Nov; 11(1):156. PubMed ID: 31685013
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.