Reactome: A Curated Pathway Database

Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

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Pathways authored by Reinberg, Danny (75947)

DB_ID Name
73779 RNA Polymerase II Transcription Pre-Initiation And Promoter Opening
74160 Gene expression (Transcription)

Details on Person Reinberg, Danny

_displayNameReinberg, Danny
_timestamp2017-08-22 20:36:52
affiliation[Affiliation:69324] NYU School of Medicine, Department of Biochemistry
created[InstanceEdit:75936] Joshi-Tope, G, 2003-09-11 07:35:00
modified[InstanceEdit:1237444] D'Eustachio, P, 2011-03-30
[InstanceEdit:8932050] D'Eustachio, Peter, 2016-07-20
(author)[LiteratureReference:110385] The general transcription factors of RNA polymerase II.
[LiteratureReference:110389] Recycling of the general transcription factors during RNA polymerase II transcription.
[LiteratureReference:113810] FCP1, a phosphatase specific for the heptapeptide repeat of the largest subunit of RNA polymerase II, stimulates transcription elongation.
[LiteratureReference:212244] Histone methyltransferase activity associated with a human multiprotein complex containing the Enhancer of Zeste protein
[LiteratureReference:212305] Composition and histone substrates of polycomb repressive group complexes change during cellular differentiation
[LiteratureReference:212880] A unified nomenclature for protein subunits of mediator complexes linking transcriptional regulators to RNA polymerase II
[LiteratureReference:1022081] Different EZH2-containing complexes target methylation of histone H1 or nucleosomal histone H3
[LiteratureReference:1226039] Inhibition of excess nodal signaling during mouse gastrulation by the transcriptional corepressor DRAP1
[LiteratureReference:1605418] SirT3 is a nuclear NAD+-dependent histone deacetylase that translocates to the mitochondria upon cellular stress
[LiteratureReference:2301212] PR-Set7 is a nucleosome-specific methyltransferase that modifies lysine 20 of histone H4 and is associated with silent chromatin
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