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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1999 | 1 |
2005 | 1 |
2018 | 1 |
2020 | 1 |
2021 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 10943
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Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder.
Genet Med. 2021 Feb;23(2):384-395. doi: 10.1038/s41436-020-00993-y. Epub 2020 Nov 11.
Genet Med. 2021.
PMID: 33173220
Free PMC article.
De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation.
Basilicata MF, Bruel AL, Semplicio G, Valsecchi CIK, Aktaş T, Duffourd Y, Rumpf T, Morton J, Bache I, Szymanski WG, Gilissen C, Vanakker O, Õunap K, Mittler G, van der Burgt I, El Chehadeh S, Cho MT, Pfundt R, Tan TY, Kirchhoff M, Menten B, Vergult S, Lindstrom K, Reis A, Johnson DS, Fryer A, McKay V; DDD Study; Fisher RB, Thauvin-Robinet C, Francis D, Roscioli T, Pajusalu S, Radtke K, Ganesh J, Brunner HG, Wilson M, Faivre L, Kalscheuer VM, Thevenon J, Akhtar A.
Basilicata MF, et al.
Nat Genet. 2018 Oct;50(10):1442-1451. doi: 10.1038/s41588-018-0220-y. Epub 2018 Sep 17.
Nat Genet. 2018.
PMID: 30224647
Free PMC article.
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A human protein complex homologous to the Drosophila MSL complex is responsible for the majority of histone H4 acetylation at lysine 16.
Smith ER, Cayrou C, Huang R, Lane WS, Côté J, Lucchesi JC.
Smith ER, et al.
Mol Cell Biol. 2005 Nov;25(21):9175-88. doi: 10.1128/MCB.25.21.9175-9188.2005.
Mol Cell Biol. 2005.
PMID: 16227571
Free PMC article.
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Characterization of a novel chromo domain gene in xp22.3 with homology to Drosophila msl-3.
Prakash SK, Van den Veyver IB, Franco B, Volta M, Ballabio A, Zoghbi HY.
Prakash SK, et al.
Genomics. 1999 Jul 1;59(1):77-84. doi: 10.1006/geno.1999.5844.
Genomics. 1999.
PMID: 10395802
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