Editorial: Epigenetic Mechanisms and Their Involvement in Rare Diseases. | Front Genet;12: 755076, 2021. | MEDLINE

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Editorial: Epigenetic Mechanisms and Their Involvement in Rare Diseases.

Rastegar, Mojgan; Yasui, Dag H.

Afiliação

Rastegar M; Department of Biochemistry and Medical Genetics, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.
Yasui DH; Department of Medical Microbiology and Immunology, University of California Davis School of Medicine, Davis, CA, United States.

Front Genet ; 12: 755076, 2021.

Article em En | MEDLINE | ID: mdl-34539761

Palavras-chave

ATRX and gene regulatory mechanisms; Beckwith-Wiedemann Syndrome (BWS) and Prader-Willi Syndrome (PWS); DNA methylation and histone modifications; MYCN-related epigenetic factors and non-coding regulatory RNAs; MeCP2 isoforms and rett syndrome (RTT); O-linked-D-N-acetylglucosamine (O-GlcNAc); activity dependent neuroprotective protein (ADNP) and chromatin remodeling; epigenetics and rare diseases

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article