Isolation and characterization of a new gene encoding a member of the HIRA family of proteins from Drosophila melanogaster (Q42678537)

4 November 2017

title

Isolation and characterization of a new gene encoding a member of the HIRA family of proteins from Drosophila melanogaster (English)

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4 November 2017

main subject

Drosophila melanogaster

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1 reference

Kirov N

1

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4 November 2017

Shtilbans A

series ordinal

2

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4 November 2017

Rushlow C

series ordinal

3

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4 November 2017

language of work or name

English

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publication date

1 June 1998

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4 November 2017

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4 November 2017

volume

212

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4 November 2017

issue

2

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4 November 2017

page(s)

323-332

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Isolation of a zinc finger gene consistently deleted in DiGeorge syndrome

4 November 2017

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Functional cDNA libraries from Drosophila embryos

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Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene

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7 January 2021

Comparison of the consensus sequence flanking translational start sites in Drosophila and vertebrates

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7 January 2021

Nuclear targeting sequences--a consensus?

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Comparative analysis of the beta transducin family with identification of several new members including PWP1, a nonessential gene of Saccharomyces cerevisiae that is divergently transcribed from NMT1

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7 January 2021

Repetitive segmental structure of the transducin beta subunit: homology with the CDC4 gene and identification of related mRNAs

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7 January 2021

A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11.

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7 January 2021

Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2

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7 January 2021

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

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7 January 2021

Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome

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7 January 2021

The p150 and p60 subunits of chromatin assembly factor I: a molecular link between newly synthesized histones and DNA replication

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Ultraviolet radiation sensitivity and reduction of telomeric silencing in Saccharomyces cerevisiae cells lacking chromatin assembly factor-I.

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7 January 2021

A human homolog of the S.cerevisiae HIR1 and HIR2 transcriptional repressors cloned from the DiGeorge syndrome critical region

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7 January 2021

A transcription map in the CATCH22 critical region: identification, mapping, and ordering of four novel transcripts expressed in heart.

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7 January 2021

Genomic organization of TUPLE1/HIRA: a gene implicated in DiGeorge syndrome

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7 January 2021

Structural Organization of the WD repeat protein-encoding gene HIRA in the DiGeorge syndrome critical region of human chromosome 22.

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The ancient regulatory-protein family of WD-repeat proteins

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G protein heterodimers: new structures propel new questions

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Trans-acting regulatory mutations that alter transcription of Saccharomyces cerevisiae histone genes

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7 January 2021

Cloning and developmental expression analysis of chick Hira (Chira), a candidate gene for DiGeorge syndrome

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7 January 2021

The HIR protein family: isolation and characterization of a complete murine cDNA.

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7 January 2021

Characterization of HIR1 and HIR2, two genes required for regulation of histone gene transcription in Saccharomyces cerevisiae

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7 January 2021

Isolation of a new clathrin heavy chain gene with muscle-specific expression from the region commonly deleted in velo-cardio-facial syndrome

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7 January 2021

Hir1p and Hir2p function as transcriptional corepressors to regulate histone gene transcription in the Saccharomyces cerevisiae cell cycle

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7 January 2021

A non-radioactive in situ hybridization method for the localization of specific RNAs in Drosophila embryos reveals translational control of the segmentation gene hunchback

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7 January 2021

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The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients

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Identifiers

DOI

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4 November 2017

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