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Identification of FMRP target genes expressed in corticogenesis: implication for common phenotypes a...

Identification of FMRP target genes expressed in corticogenesis: implication for common phenotypes a...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2292429513

Identification of FMRP target genes expressed in corticogenesis: implication for common phenotypes among neurodevelopmental disorders

About this item

Full title

Identification of FMRP target genes expressed in corticogenesis: implication for common phenotypes among neurodevelopmental disorders

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

Journal title

bioRxiv, 2019-09

Language

English

Formats

Publication information

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

More information

Scope and Contents

Contents

Fragile X mental retardation protein (FMRP) is encoded by FMR1 gene that is responsible for Fragile X Syndrome (FXS) showing intellectual disability and autism spectrum disorder. FMRP is an RNA binding protein highly expressed in the brain. Although several target genes for FMRP have been identified, limited studies have suggested the role of FMRP...

Alternative Titles

Full title

Identification of FMRP target genes expressed in corticogenesis: implication for common phenotypes among neurodevelopmental disorders

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_2292429513

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2292429513

Other Identifiers

E-ISSN

2692-8205

DOI

10.1101/769026