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- W3015921112 endingPage "144655" @default.
- W3015921112 startingPage "144655" @default.
- W3015921112 abstract "MID1 is an E3 ubiquitin ligase of the Tripartite Motif (TRIM) subfamily of RING-containing proteins, hence also known as TRIM18. MID1 is a microtubule-binding protein found in complex with the catalytic subunit of PP2A (PP2Ac) and its regulatory subunit alpha 4 (α4). To date, several substrates and interactors of MID1 have been described, providing evidence for the involvement of MID1 in a plethora of essential biological processes, especially during embryonic development. Mutations in the MID1 gene are responsible of the X-linked form of Opitz syndrome (XLOS), a multiple congenital disease characterised by defects in the development of midline structures during embryogenesis. Here, we review MID1-related physiological mechanisms as well as the pathological implication of the MID1 gene in XLOS and in other clinical conditions." @default.
- W3015921112 created "2020-04-17" @default.
- W3015921112 creator A5011134047 @default.
- W3015921112 creator A5022321145 @default.
- W3015921112 creator A5083717579 @default.
- W3015921112 date "2020-07-01" @default.
- W3015921112 modified "2023-10-09" @default.
- W3015921112 title "The MID1 gene product in physiology and disease" @default.
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