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Control of mTORC1 signaling by the Opitz syndrome protein MID1

Mutations in the MID1 gene are causally linked to X-linked Opitz BBB/G syndrome (OS), a congenital disorder that primarily affects the formation of diverse ventral midline structures. The MID1 protein has been shown to function as an E3 ligase targeting the catalytic subunit of protein... Full description

1st Person: Liu, Enbo
Additional Persons: Knutzen, Christine A. verfasserin; Krauss, Sybille verfasserin; Schweiger, Susann verfasserin; Chiang, Gary G. verfasserin
Source: in Proceedings of the National Academy of Sciences of the United States of America Vol. 108, No. 21 (2011), p. 8680-8685
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Type of Publication: Article
Language: English
Published: 2011
Keywords: research-article
Online: Volltext
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