Katalog GES



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
More Articles
Type of Publication: Article
Language: English
Published: 2011
Keywords: research-article
Online: Volltext
  Search for full text

Online

Volltext

Similar Items

Cannot find similar records

Library Services

Search Options

Quick links

Orientation