| scholarly article | Q13442814 |
| P2093 | author name string | David L Brautigan | |
| Allen D Everett | |||
| P2860 | cites work | MID1 and MID2 homo- and heterodimerise to tether the rapamycin-sensitive PP2A regulatory subunit, alpha 4, to microtubules: implications for the clinical variability of X-linked Opitz GBBB syndrome and other developmental disorders | Q21284182 |
| The Opitz syndrome gene product, MID1, associates with microtubules | Q22009027 | ||
| Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22 | Q24323194 | ||
| Phosphorylation and microtubule association of the Opitz syndrome protein mid-1 is regulated by protein phosphatase 2A via binding to the regulatory subunit alpha 4. | Q24601712 | ||
| Nutrients, via the Tor proteins, stimulate the association of Tap42 with type 2A phosphatases | Q27932611 | ||
| Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle | Q28139334 | ||
| New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome | Q28141107 | ||
| MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation | Q28202743 | ||
| Expression and chromosomal localization of the human alpha 4/IGBP1 gene, the structure of which is closely related to the yeast TAP42 protein of the rapamycin-sensitive signal transduction pathway | Q34453498 | ||
| Opitz G/BBB syndrome: clinical comparisons of families linked to Xp22 and 22q, and a review of the literature | Q41178545 | ||
| The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region | Q48038871 | ||
| Studies of malformation syndromes of man XXXIII: The FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardation | Q56001488 | ||
| A gene for FG syndrome maps in the Xq12-q21.31 region | Q57720321 | ||
| P433 | issue | 4 | |
| P304 | page(s) | 461-464 | |
| P577 | publication date | 2002-08-01 | |
| P1433 | published in | Developmental Dynamics | Q59752 |
| P1476 | title | Developmental expression of alpha4 protein phosphatase regulatory subunit in tissues affected by Opitz syndrome | |
| P478 | volume | 224 |
| Q35245786 | MID1 catalyzes the ubiquitination of protein phosphatase 2A and mutations within its Bbox1 domain disrupt polyubiquitination of alpha4 but not of PP2Ac |
| Q28478425 | NMR studies of the C-terminus of alpha4 reveal possible mechanism of its interaction with MID1 and protein phosphatase 2A |
| Q37175200 | The MID1 E3 ligase catalyzes the polyubiquitination of Alpha4 (α4), a regulatory subunit of protein phosphatase 2A (PP2A): novel insights into MID1-mediated regulation of PP2A. |
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