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See also: KAT6B lysine acetyltransferase 6B in the Gene database

kat6b in Homo sapiensMus musculusRattus norvegicusAll 283 Gene records

Search results

Items: 1 to 20 of 86

1.

Inhibition of histone acetylation and deacetylation enzymes affects longevity, development, and fecundity in the pea aphid (Acyrthosiphon pisum).

Kirfel P, Skaljac M, Grotmann J, Kessel T, Seip M, Michaelis K, Vilcinskas A.

Arch Insect Biochem Physiol. 2019 Sep 9:e21614. doi: 10.1002/arch.21614. [Epub ahead of print]

PMID:
31498475
2.

De novo KAT6B mutation, Say-Barber-Biesecker-Young-Simpson syndrome, and specific language impairment.

Fernández-Mayoralas DM, Calleja-Pérez B, Álvarez S, Fernández-Jaén A.

Neurologia. 2019 Jul 17. pii: S0213-4853(19)30085-4. doi: 10.1016/j.nrl.2019.05.006. [Epub ahead of print] English, Spanish. No abstract available.

3.

MicroRNA-4513 Promotes Gastric Cancer Cell Proliferation and Epithelial-Mesenchymal Transition Through Targeting KAT6B.

Ding H, Shi Y, Liu X, Qiu A.

Hum Gene Ther Clin Dev. 2019 Sep;30(3):142-148. doi: 10.1089/humc.2019.094.

PMID:
31310159
4.

[A case of SBBYSS syndrome caused by KAT6B gene variant].

Lyu N, Shang Q, Li J, Ma C, Li D.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jul 10;36(7):727-730. doi: 10.3760/cma.j.issn.1003-9406.2019.07.018. Chinese.

PMID:
31302922
5.

Clinical and molecular cytogenetic characterization of a novel 10q interstitial deletion: a case report and review of the literature.

Herriges JC, Dugan SL, Lamb AN.

Mol Cytogenet. 2019 May 17;12:20. doi: 10.1186/s13039-019-0430-8. eCollection 2019.

6.

Leiomyoma with KAT6B-KANSL1 fusion: case report of a rapidly enlarging uterine mass in a postmenopausal woman.

Ainsworth AJ, Dashti NK, Mounajjed T, Fritchie KJ, Davila J, Mopuri R, Jackson RA, Halling KC, Bakkum-Gamez JN, Schoolmeester JK.

Diagn Pathol. 2019 Apr 25;14(1):32. doi: 10.1186/s13000-019-0809-1.

7.

A novel pathogenic frameshift variant of KAT6B identified by clinical exome sequencing in a newborn with the Say-Barber-Biesecker-Young-Simpson syndrome.

Mendez R, Delea M, Dain L, Rittler M.

Clin Dysmorphol. 2019 Mar 26. doi: 10.1097/MCD.0000000000000270. [Epub ahead of print] No abstract available.

PMID:
30921092
8.

Genitopatellar Syndrome Secondary to De Novo KAT6B Mutation: The First Genetically Confirmed Case in South Korea.

Kim BR, Han JH, Shin JE, Park MS, Park KI, Namgung R, Lee HJ, Lee JS, Eun HS.

Yonsei Med J. 2019 Apr;60(4):395-398. doi: 10.3349/ymj.2019.60.4.395.

9.

Kat6b Modulates Oct4 and Nanog Binding to Chromatin in Embryonic Stem Cells and Is Required for Efficient Neural Differentiation.

Cosentino MS, Oses C, Vázquez Echegaray C, Solari C, Waisman A, Álvarez Y, Petrone MV, Francia M, Schultz M, Sevlever G, Miriuka S, Levi V, Guberman A.

J Mol Biol. 2019 Mar 15;431(6):1148-1159. doi: 10.1016/j.jmb.2019.02.012. Epub 2019 Feb 18.

PMID:
30790630
10.

Novel truncating variants expand the phenotypic spectrum of KAT6B-related disorders.

Brea-Fernández A, Dacruz D, Eirís J, Barros F, Carracedo Á.

Am J Med Genet A. 2019 Feb;179(2):290-294. doi: 10.1002/ajmg.a.60689. Epub 2018 Dec 20.

PMID:
30569622
11.

New KAT6 inhibitors induce senescence and arrest cancer growth.

Huang F.

Synth Syst Biotechnol. 2018 Nov 2;3(4):244-245. doi: 10.1016/j.synbio.2018.10.006. eCollection 2018 Dec.

12.

Novel KAT6B proximal familial variant expands genotypic and phenotypic spectrum.

Yates TM, Langley CLM; DDD Study, Grozeva D, Raymond FL, Johnson DS.

Clin Genet. 2019 Feb;95(2):334-335. doi: 10.1111/cge.13456. Epub 2018 Oct 24. No abstract available.

PMID:
30353918
13.

Genitopatellar syndrome and neuroblastoma: The multidisciplinary management of a previously unreported association.

Knight S, VanHouwelingen L, Cervi D, Clay MR, Corkins M, Hines-Dowell S, Hamilton KV, Mostafavi R, Ward J, Furman WL, Murphy AJ.

Pediatr Blood Cancer. 2018 Dec;65(12):e27373. doi: 10.1002/pbc.27373. Epub 2018 Aug 7. No abstract available.

PMID:
30084242
14.

Inhibitors of histone acetyltransferases KAT6A/B induce senescence and arrest tumour growth.

Baell JB, Leaver DJ, Hermans SJ, Kelly GL, Brennan MS, Downer NL, Nguyen N, Wichmann J, McRae HM, Yang Y, Cleary B, Lagiakos HR, Mieruszynski S, Pacini G, Vanyai HK, Bergamasco MI, May RE, Davey BK, Morgan KJ, Sealey AJ, Wang B, Zamudio N, Wilcox S, Garnham AL, Sheikh BN, Aubrey BJ, Doggett K, Chung MC, de Silva M, Bentley J, Pilling P, Hattarki M, Dolezal O, Dennis ML, Falk H, Ren B, Charman SA, White KL, Rautela J, Newbold A, Hawkins ED, Johnstone RW, Huntington ND, Peat TS, Heath JK, Strasser A, Parker MW, Smyth GK, Street IP, Monahan BJ, Voss AK, Thomas T.

Nature. 2018 Aug;560(7717):253-257. doi: 10.1038/s41586-018-0387-5. Epub 2018 Aug 1.

PMID:
30069049
15.

miR-22/KAT6B axis is a chemotherapeutic determiner via regulation of PI3k-Akt-NF-kB pathway in tongue squamous cell carcinoma.

Gu Y, Liu H, Kong F, Ye J, Jia X, Zhang Z, Li N, Yin J, Zheng G, He Z.

J Exp Clin Cancer Res. 2018 Jul 24;37(1):164. doi: 10.1186/s13046-018-0834-z.

16.

The Kat in the HAT: The Histone Acetyl Transferase Kat6b (MYST4) Is Downregulated in Murine Macrophages in Response to LPS.

Shukla S, Levine C, Sripathi RP, Elson G, Lutz CS, Leibovich SJ.

Mediators Inflamm. 2018 Jun 6;2018:7852742. doi: 10.1155/2018/7852742. eCollection 2018.

17.

Genitopatellar syndrome: the first reported case in Japan.

Okano S, Miyamoto A, Fukuda I, Tanaka H, Hata K, Kaname T, Matsubara Y, Makita Y.

Hum Genome Var. 2018 May 28;5:8. doi: 10.1038/s41439-018-0010-1. eCollection 2018.

18.

[KAT6B promotes LPS-triggered IL-6 production via enhancing recruitment of H3K23 acetylation to IL-6 promoter region].

Sun D, Wen Q, Wang C.

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2017 Nov;33(11):1441-147. Chinese.

PMID:
29268844
19.

A novel truncating variant within exon 7 of KAT6B associated with features of both Say-Barber-Bieseker-Young-Simpson syndrome and genitopatellar syndrome: Further evidence of a continuum in the clinical spectrum of KAT6B-related disorders.

Marangi G, Di Giacomo MC, Lattante S, Orteschi D, Patrizi S, Doronzio PN, Riviello FN, Vaisfeld A, Frangella S, Zollino M.

Am J Med Genet A. 2018 Feb;176(2):455-459. doi: 10.1002/ajmg.a.38571. Epub 2017 Dec 11.

PMID:
29226580
20.

Syndromic Craniosynostosis Can Define New Candidate Genes for Suture Development or Result from the Non-specifc Effects of Pleiotropic Genes: Rasopathies and Chromatinopathies as Examples.

Zollino M, Lattante S, Orteschi D, Frangella S, Doronzio PN, Contaldo I, Mercuri E, Marangi G.

Front Neurosci. 2017 Oct 18;11:587. doi: 10.3389/fnins.2017.00587. eCollection 2017. Review.

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