Common variants within MECP2 confer risk of systemic lupus erythematosus (Q21144341)

inferred from title

author

Marta E Alarcón-Riquelme

7

object named as

Marta E Alarcón-Riquelme

Marta E

Alarcón-Riquelme

1 reference

16 August 2022

Jennifer A Kelly

4

Jennifer A

Kelly

1 reference

16 August 2022

Robert P Kimberly

6

Robert P

Kimberly

1 reference

16 August 2022

Sang-Cheol Bae

13

Sang-Cheol

Bae

1 reference

16 August 2022

9

Timothy J Vyse

Timothy J

Vyse

1 reference

16 August 2022

15

John B Harley

John B

Harley

1 reference

16 August 2022

8

Judith A James

Judith A

James

1 reference

16 August 2022

10

Gary S Gilkeson

Gary S

Gilkeson

1 reference

16 August 2022

Amr H Sawalha

1

Amr H

Sawalha

1 reference

16 August 2022

Ryan Webb

2

Ryan

Webb

1 reference

16 August 2022

Shizhong Han

3

Shizhong

Han

1 reference

16 August 2022

Kenneth M Kaufman

5

Kenneth M

Kaufman

1 reference

16 August 2022

Chan-Bum Choi

11

Chan-Bum

Choi

1 reference

16 August 2022

R Hal Scofield

12

R Hal

Scofield

1 reference

16 August 2022

Swapan K Nath

14

Swapan K

Nath

1 reference

Creative Commons CC0 License

16 August 2022

language of work or name

English

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publication date

2008

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published in

PLOS One

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volume

3

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issue

3

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page(s)

e1727

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copyright license

start time

5 March 2008

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted, dedicated to the public domain by copyright holder

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cites work

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

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Mechanisms of disease: neurogenetics of MeCP2 deficiency

19 March 2017

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Mutations and polymorphisms in the human methyl CpG-binding protein MECP2

19 March 2017

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A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

19 March 2017

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Methyl-CpG-binding protein, MeCP2, is a target molecule for maintenance DNA methyltransferase, Dnmt1

19 March 2017

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Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

19 March 2017

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Reversal of neurological defects in a mouse model of Rett syndrome

7 April 2017

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Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

7 April 2017

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Regulations and roles of the interleukin-1 receptor associated kinases (IRAKs) in innate and adaptive immunity

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Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.

12 September 2017

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DNA binding selectivity of MeCP2 due to a requirement for A/T sequences adjacent to methyl-CpG.

12 September 2017

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Mechanism of drug-induced lupus. I. Cloned Th2 cells modified with DNA methylation inhibitors in vitro cause autoimmunity in vivo

27 September 2017

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Overexpression of CD70 and overstimulation of IgG synthesis by lupus T cells and T cells treated with DNA methylation inhibitors

27 September 2017

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Demethylation of promoter regulatory elements contributes to perforin overexpression in CD4 lupus T cells

21 January 2018

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MECP2 structural and 3'-UTR variants in schizophrenia, autism and other psychiatric diseases: a possible association with autism

21 January 2018

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Demethylation of CD40LG on the inactive X in T cells from women with lupus

21 January 2018

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Functions for DNA Methylation in Vertebrates

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Reactivation of an inactive human X chromosome: evidence for X inactivation by DNA methylation

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Effect of an inhibitor of DNA methylation on T cells. II. 5-Azacytidine induces self-reactivity in antigen-specific T4 cells

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Phenotypic and functional similarities between 5-azacytidine-treated T cells and a T cell subset in patients with active systemic lupus erythematosus

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Decreased Ras-mitogen-activated protein kinase signaling may cause DNA hypomethylation in T lymphocytes from lupus patients

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10.1371/JOURNAL.PONE.0001727

Identifiers

DOI

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