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Peter B. Becker (1958-)

Biochemiker

Name	Peter B. Becker
Zeit	1958- (Lebensdaten)
Ort	Deutschland
Akademischer Grad bzw. Titel	Prof. Dr.
Beruf	Biochemiker (charakteristischer Beruf) Molekularbiologie
Beziehung	Deutsche Akademie der Naturforscher Leopoldina (Mitglied, Matrikelnummer 07150) (2007-)
Weitere Angaben	Dt. Biochemiker und Molekularbiologe ; Leibniz-Preis 2005, Zellbiologie/Biochemie, Univ. München
Quelle	LCAuth
Datensatztyp	Person
GND-Nummer	143078690
Datensatz-ID	143078690
Beteiligt an alle anzeigen ISWI catalyzes nucleosome sliding in condensed nucleosome arrays Progressive dosage compensation during Drosophila embryogenesis is reflected by gene arrangement Genome-wide measurement of local nucleosome array regularity and spacing by nanopore sequencing Chromosome topology guides the Drosophila Dosage Compensation Complex for target gene activation Life span extension by targeting a link between metabolism and histone acetylation in Drosophila Active promoters give rise to false positive 'Phantom Peaks' in ChIP-seq experiments Global Analysis of the Relationship between JIL-1 Kinase and Transcription Phosphorylation of SU(VAR)3-9 by the chromosomal kinase JIL-1 Chromodomains are protein-RNA interaction modules Chromatin-remodelling factor CHRAC contains the ATPases ISWI and topoisomerase II ATP-dependent nucleosome disruption at a heat-shock promoter mediated by binding of GAGA transcription factor ATP-dependent nucleosome disruption at a heat-shock promoter mediated by binding of GAGA transcription factor In vivo protein-DNA interactions in a glucocorticoid response element require the presence of the hormone In vivo protein-DNA interactions in a glucocorticoid response element require the presence of the hormone

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Peter B. Becker (1958-)

ISWI catalyzes nucleosome sliding in condensed nucleosome arrays

Progressive dosage compensation during Drosophila embryogenesis is reflected by gene arrangement

Genome-wide measurement of local nucleosome array regularity and spacing by nanopore sequencing

Chromosome topology guides the Drosophila Dosage Compensation Complex for target gene activation

Life span extension by targeting a link between metabolism and histone acetylation in Drosophila

Active promoters give rise to false positive 'Phantom Peaks' in ChIP-seq experiments

Global Analysis of the Relationship between JIL-1 Kinase and Transcription

Phosphorylation of SU(VAR)3-9 by the chromosomal kinase JIL-1

Chromodomains are protein-RNA interaction modules

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

ATP-dependent nucleosome disruption at a heat-shock promoter mediated by binding of GAGA transcription factor

ATP-dependent nucleosome disruption at a heat-shock promoter mediated by binding of GAGA transcription factor

In vivo protein-DNA interactions in a glucocorticoid response element require the presence of the hormone

In vivo protein-DNA interactions in a glucocorticoid response element require the presence of the hormone