The lysine demethylase LSD1 (KDM1) is required for maintenance of global DNA methylation (Q28304726)

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Language	Label	Description	Also known as
English	The lysine demethylase LSD1 (KDM1) is required for maintenance of global DNA methylation	scientific article

Statements

instance of

scholarly article

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title

The lysine demethylase LSD1 (KDM1) is required for maintenance of global DNA methylation (English)

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main subject

DNA methylation

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author name string

Jing Wang

series ordinal

1

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Sarah Hevi

series ordinal

2

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Julia K Kurash

series ordinal

3

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Hong Lei

series ordinal

4

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Frédérique Gay

series ordinal

5

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Jeffrey Bajko

series ordinal

6

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Hui Su

series ordinal

7

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Weitao Sun

series ordinal

8

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Hua Chang

series ordinal

9

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Guoliang Xu

series ordinal

10

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François Gaudet

series ordinal

11

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En Li

series ordinal

12

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Taiping Chen

series ordinal

13

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language of work or name

English

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publication date

January 2009

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published in

Nature Genetics

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volume

41

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issue

1

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page(s)

125-9

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cites work

Histone demethylation mediated by the nuclear amine oxidase homolog LSD1

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Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.268

retrieved

21 April 2017

LSD1 demethylates repressive histone marks to promote androgen-receptor-dependent transcription

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.268

retrieved

21 April 2017

Opposing LSD1 complexes function in developmental gene activation and repression programmes

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.268

retrieved

21 April 2017

Suv39h-mediated histone H3 lysine 9 methylation directs DNA methylation to major satellite repeats at pericentric heterochromatin

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.268

retrieved

21 April 2017

The Polycomb group protein EZH2 directly controls DNA methylation

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.268

retrieved

21 April 2017

Direct interaction between DNMT1 and G9a coordinates DNA and histone methylation during replication

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.268

retrieved

21 April 2017

Somatic mutations in the neurofibromatosis 1 gene in human tumors

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.268

retrieved

21 April 2017

DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.268

retrieved

21 April 2017

Gene-specific modulation of TAF10 function by SET9-mediated methylation

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.268

retrieved

21 April 2017

Regulation of p53 activity through lysine methylation

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.268

retrieved

21 April 2017

Repression of p53 activity by Smyd2-mediated methylation

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.268

retrieved

21 April 2017

p53 is regulated by the lysine demethylase LSD1

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.268

retrieved

21 April 2017

A novel Dnmt3a isoform produced from an alternative promoter localizes to euchromatin and its expression correlates with active de novo methylation

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG.268

retrieved

21 April 2017

Control of CpNpG DNA methylation by the KRYPTONITE histone H3 methyltransferase

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG.268

retrieved

21 April 2017

A histone H3 methyltransferase controls DNA methylation in Neurospora crassa

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG.268

retrieved

21 January 2018

Methylation of a histone mimic within the histone methyltransferase G9a regulates protein complex assembly

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG.268

retrieved

21 January 2018

trans-2-Phenylcyclopropylamine is a mechanism-based inactivator of the histone demethylase LSD1.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG.268

retrieved

21 January 2018

Methylation of p53 by Set7/9 mediates p53 acetylation and activity in vivo

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG.268

retrieved

21 January 2018

In vivo stabilization of the Dnmt1 (cytosine-5)- methyltransferase protein

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG.268

retrieved

21 January 2018

Increased protein stability causes DNA methyltransferase 1 dysregulation in breast cancer.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG.268

retrieved

21 January 2018

Phosphatidylinositol 3-kinase/protein kinase B pathway stabilizes DNA methyltransferase I protein and maintains DNA methylation.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG.268

retrieved

21 January 2018

Complete inactivation of DNMT1 leads to mitotic catastrophe in human cancer cells

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG.268

retrieved

21 January 2018

Establishment and maintenance of genomic methylation patterns in mouse embryonic stem cells by Dnmt3a and Dnmt3b.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG.268

retrieved

21 January 2018

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19098913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

De novo DNA cytosine methyltransferase activities in mouse embryonic stem cells

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19098913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1038/NG.268

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

686588

Fatcat ID

release_gu5paeipeza7lbp7ov2kvicecy

1 reference

stated in

Fatcat

reference URL

https://api.fatcat.wiki/v0/release/gu5paeipeza7lbp7ov2kvicecy

retrieved

24 November 2022

based on heuristic

mapped directly with Wikidata item

OpenCitations bibliographic resource ID

686588

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

686588

PubMed publication ID

19098913

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

686588

 

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