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Disruption of the gene regulatory programme in neurodevelopmental disorders.
Griffin, Aoife; Mahesh, Arun; Tiwari, Vijay K.
Afiliação
  • Griffin A; Wellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry & Biomedical Science, Queens University, Belfast BT9 7BL, United Kingdom.
  • Mahesh A; Wellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry & Biomedical Science, Queens University, Belfast BT9 7BL, United Kingdom.
  • Tiwari VK; Wellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry & Biomedical Science, Queens University, Belfast BT9 7BL, United Kingdom. Electronic address: v.tiwari@qub.ac.uk.
Biochim Biophys Acta Gene Regul Mech ; 1865(7): 194860, 2022 10.
Article em En | MEDLINE | ID: mdl-36007842
ABSTRACT
Cortical development consists of a series of synchronised events, including fate transition of cortical progenitors, neuronal migration, specification and connectivity. It is becoming clear that gene expression programs governing these events rely on the interplay between signalling molecules, transcription factors and epigenetic mechanisms. When genetic or environmental factors disrupt expression of genes involved in important brain development processes, neurodevelopmental disorders can occur. This review aims to highlight how recent advances in technologies have helped uncover and imitate the gene regulatory mechanisms commonly disrupted in neurodevelopmental disorders.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epigênese Genética / Transtornos do Neurodesenvolvimento Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epigênese Genética / Transtornos do Neurodesenvolvimento Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article