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Epigenetic alterations and advancement of treatment in peripheral T-cell lymphoma.
Zhang P, Zhang M. Zhang P, et al. Clin Epigenetics. 2020 Nov 7;12(1):169. doi: 10.1186/s13148-020-00962-x. Clin Epigenetics. 2020. PMID: 33160401 Free PMC article. Review.
Genetic studies have also shown that some recurrent mutations in genes involved in the epigenetic machinery, including TET2, IDH2-R172, DNMT3A, RHOA, CD28, IDH2, TET2, MLL2, KMT2A, KDM6A, CREBBP, and EP300, have been observed in cases of PTCL. ...
Genetic studies have also shown that some recurrent mutations in genes involved in the epigenetic machinery, including TET2, IDH2-R172, DNMT …
The cancer driver genes IDH1/2, JARID1C/ KDM5C, and UTX/ KDM6A: crosstalk between histone demethylation and hypoxic reprogramming in cancer metabolism.
Chang S, Yim S, Park H. Chang S, et al. Exp Mol Med. 2019 Jun 20;51(6):1-17. doi: 10.1038/s12276-019-0230-6. Exp Mol Med. 2019. PMID: 31221981 Free PMC article. Review.
Table 1 Cancer driver genes involved in epigenetics Pathways involved in epigenetics Driver genes Tumor suppressor/oncogene prediction (by 20/20+(a)) Approved name Activity Cancer type(b) Other driver genes in this pathways Histone modification KDM6A tsg Lysine demethylase 6A, UT …
Table 1 Cancer driver genes involved in epigenetics Pathways involved in epigenetics Driver genes Tumor suppressor/oncogene prediction (by 2 …
Phenotypes of Cornelia de Lange syndrome caused by non-cohesion genes: Novel variants and literature review.
Shangguan H, Chen R. Shangguan H, et al. Front Pediatr. 2022 Jul 22;10:940294. doi: 10.3389/fped.2022.940294. eCollection 2022. Front Pediatr. 2022. PMID: 35935361 Free PMC article.
RESULTS: Variants in non-cohesion genes were found in six patients [KMT2A (n = 2), KMT2D, ANKRD11, KDM6A, and UBE2A]. Of them, four variants (KMT2A c.7789C > T, ANKRD11 c.1757_1776del, KDM6A c.655-1G > A, and UBE2A c.439C > T) were novel. ...From this total …
RESULTS: Variants in non-cohesion genes were found in six patients [KMT2A (n = 2), KMT2D, ANKRD11, KDM6A, and UBE2A]. Of them, four v …
BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome.
García-Gutiérrez P, García-Domínguez M. García-Gutiérrez P, et al. Front Mol Biosci. 2021 Jul 27;8:709232. doi: 10.3389/fmolb.2021.709232. eCollection 2021. Front Mol Biosci. 2021. PMID: 34386522 Free PMC article. Review.
Actually, CdLS-like phenotypes have been associated to mutations in chromatin-associated proteins, as KMT2A, AFF4, EP300, TAF6, SETD5, SMARCB1, MAU2, ZMYND11, MED13L, PHIP, ARID1B, NAA10, BRD4 or ANKRD11, most of which have no known direct association with cohesin. …
Actually, CdLS-like phenotypes have been associated to mutations in chromatin-associated proteins, as KMT2A, AFF4, EP300, TAF6 …
Longitudinal genetic studies of cognitive characteristics.
Mustafin RN, Kazantseva AV, Enikeeva RF, Malykh SB, Khusnutdinova EK. Mustafin RN, et al. Vavilovskii Zhurnal Genet Selektsii. 2020 Feb;24(1):87-95. doi: 10.18699/VJ20.599. Vavilovskii Zhurnal Genet Selektsii. 2020. PMID: 33659785 Free PMC article.
The present review describes longitudinal studies of cognitive traits and functions determining the causes of their variations and their possible correction to prevent cognitive impairment. ...The genes involved in DNA methylation (DNMT1, DNMT3B, and FTO), histone modifica …
The present review describes longitudinal studies of cognitive traits and functions determining the causes of their variations and th …