Developmental expression of ?4 protein phosphatase regulatory subunit in tissues affected by Opitz syndrome
Author:
Publisher
Wiley
Subject
Developmental Biology
Reference13 articles.
1. A gene for FG syndrome maps in the Xq12-q21.31 region
2. Functional Characterization of the Opitz Syndrome Gene Product (Midin): Evidence for Homodimerization and Association With Microtubules Throughout the Cell Cycle
3. New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome
4. The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region
5. Nutrients, via the Tor proteins, stimulate the association of Tap42 with type 2A phosphatases.
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1. MID1 Catalyzes the Ubiquitination of Protein Phosphatase 2A and Mutations within Its Bbox1 Domain Disrupt Polyubiquitination of Alpha4 but Not of PP2Ac;PLoS ONE;2014-09-10
2. α4 contributes to bladder urothelial carcinoma cell invasion and/or metastasis via regulation of E-cadherin and is a predictor of outcome in bladder urothelial carcinoma patients;European Journal of Cancer;2014-03
3. The MID1 E3 Ligase Catalyzes the Polyubiquitination of Alpha4 (α4), a Regulatory Subunit of Protein Phosphatase 2A (PP2A);Journal of Biological Chemistry;2013-07
4. NMR Studies of the C-Terminus of alpha4 Reveal Possible Mechanism of Its Interaction with MID1 and Protein Phosphatase 2A;PLoS ONE;2011-12-14
5. Overexpression of immunoglobulin (CD79a) binding protein1 (IGBP-1) in small lung adenocarcinomas and its clinicopathological significance;Pathology International;2011-03
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