(Q52562207)

3 May 2018

title

Targeting of MOF, a putative histone acetyl transferase, to the X chromosome of Drosophila melanogaster. (English)

1 reference

3 May 2018

main subject

Drosophila melanogaster

0 references

author name string

W Gu

series ordinal

1

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3 May 2018

P Szauter

series ordinal

2

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3 May 2018

J C Lucchesi

series ordinal

3

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3 May 2018

publication date

1 January 1998

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3 May 2018

published in

Genesis

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3 May 2018

volume

22

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3 May 2018

issue

1

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3 May 2018

page(s)

56-64

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3 May 2018

Binding of disparate transcriptional activators to nucleosomal DNA is inherently cooperative

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21 January 2018

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The CBP co-activator is a histone acetyltransferase

21 January 2018

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Acetylated histone H4 on the male X chromosome is associated with dosage compensation in Drosophila

21 January 2018

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Special HATs for special occasions: linking histone acetylation to chromatin assembly and gene activation

21 January 2018

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Sfh1p, a component of a novel chromatin-remodeling complex, is required for cell cycle progression

21 January 2018

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A male-specific lethal mutation in Drosophila melanogaster that transforms sex

21 January 2018

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Vive la différence: males vs females in flies vs worms

21 January 2018

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Contacts in context: promoter specificity and macromolecular interactions in transcription

21 January 2018

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Yeast Gcn5 functions in two multisubunit complexes to acetylate nucleosomal histones: characterization of an Ada complex and the SAGA (Spt/Ada) complex

21 January 2018

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RNA polymerase II holoenzyme and transcriptional regulation

21 January 2018

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mof, a putative acetyl transferase gene related to the Tip60 and MOZ human genes and to the SAS genes of yeast, is required for dosage compensation in Drosophila

21 January 2018

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ACF, an ISWI-containing and ATP-utilizing chromatin assembly and remodeling factor

21 January 2018

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Expression of msl-2 causes assembly of dosage compensation regulators on the X chromosomes and female lethality in Drosophila

21 January 2018

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Sex lethal controls dosage compensation in Drosophila by a non-splicing mechanism.

21 January 2018

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napts, a mutation affecting sodium channel activity in Drosophila, is an allele of mle, a regulator of X chromosome transcription

21 January 2018

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The maleless protein associates with the X chromosome to regulate dosage compensation in drosophila

21 January 2018

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Dosage compensation in Drosophila: the X chromosome binding of MSL-1 and MSL-2 in female embryos is prevented by the early expression of the Sxl gene.

21 January 2018

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roX1 RNA paints the X chromosome of male Drosophila and is regulated by the dosage compensation system

21 January 2018

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The TAF(II)250 subunit of TFIID has histone acetyltransferase activity

21 January 2018

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The transcriptional coactivators p300 and CBP are histone acetyltransferases

21 January 2018

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Sex-specific regulation of the male-specific lethal-1 dosage compensation gene in Drosophila.

21 January 2018

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Histone acetylation and chromatin assembly: a single escort, multiple dances?

21 January 2018

1 reference

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ISWI, a member of the SWI2/SNF2 ATPase family, encodes the 140 kDa subunit of the nucleosome remodeling factor

21 January 2018

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Histone acetylation in chromatin and chromosomes

21 January 2018

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Histone H4 isoforms acetylated at specific lysine residues define individual chromosomes and chromatin domains in Drosophila polytene nuclei

21 January 2018

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Chromatin-remodelling factor CHRAC contains the ATPases ISWI and topoisomerase II.

21 January 2018

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Targeting chromatin disruption: Transcription regulators that acetylate histones

21 January 2018

1 reference

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A p300/CBP-associated factor that competes with the adenoviral oncoprotein E1A

21 January 2018

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A growing coactivator network

21 January 2018

1 reference

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The link between dosage compensation and sex differentiation in Drosophila melanogaster

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291520-6408%281998%2922%3A1%3C56%3A%3AAID-DVG6%3E3.0.CO%3B2-6

10.1002/(SICI)1520-6408(1998)22:1<56::AID-DVG6>3.0.CO;2-6

21 January 2018

Identifiers

DOI

1 reference

3 May 2018

1 reference

3 May 2018