| scholarly article | Q13442814 |
| P2093 | author name string | B Goodwin | |
| B Hopwood | |||
| T C Cox | |||
| L L Cox | |||
| G K Suthers | |||
| E Haan | |||
| L R Allen | |||
| P433 | issue | 17 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 2553-62 | |
| P577 | publication date | 2000-10-12 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome | |
| P478 | volume | 9 |
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| Q36891185 | Contribution of polymorphisms in genes associated with craniofacial development to the risk of nonsyndromic cleft lip and/or palate in the Brazilian population. |
| Q21092361 | DEAR1 is a dominant regulator of acinar morphogenesis and an independent predictor of local recurrence-free survival in early-onset breast cancer |
| Q30309870 | Developmental expression of alpha4 protein phosphatase regulatory subunit in tissues affected by Opitz syndrome |
| Q41834429 | Different subcellular localisations of TRIM22 suggest species-specific function |
| Q28204904 | Duplication of the MID1 first exon in a patient with Opitz G/BBB syndrome |
| Q30661538 | Enterophilins, a new family of leucine zipper proteins bearing a b30.2 domain and associated with enterocyte differentiation |
| Q52061727 | Evidence of functional redundancy between MID proteins: implications for the presentation of Opitz syndrome. |
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| Q30310233 | Identification of a novel microtubule-associated protein that regulates microtubule organization and cytokinesis by using a GFP-screening strategy |
| Q84231252 | Identification of novel transcription-regulating genes expressed during murine molar development |
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| Q21284182 | 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 |
| Q35245786 | MID1 catalyzes the ubiquitination of protein phosphatase 2A and mutations within its Bbox1 domain disrupt polyubiquitination of alpha4 but not of PP2Ac |
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| Q41929459 | Methylome repatterning in a mouse model of Maternal PKU Syndrome. |
| Q36447391 | Mid1/Mid2 expression in craniofacial development and a literature review of X-linked opitz syndrome. |
| Q24803465 | Mig12, a novel Opitz syndrome gene product partner, is expressed in the embryonic ventral midline and co-operates with Mid1 to bundle and stabilize microtubules |
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| Q24601712 | 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. |
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| Q30650786 | The Challenge of Prenatal Diagnostic Work-Up of Maternally Inherited X-Linked Opitz G/BBB: Case Report and Literature Review |
| 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. |
| Q28178134 | The Opitz syndrome gene MID1 is essential for establishing asymmetric gene expression in Hensen's node |
| Q49885121 | Two Novel Pathogenic MID1 Variants and Genotype-Phenotype Correlation Reanalysis in X-Linked Opitz G/BBB Syndrome |
| Q38537596 | Ubiquitin in regulation of spindle apparatus and its positioning: implications in development and disease |
| Q37462351 | Ubiquitous SPRY domains and their role in the skeletal type ryanodine receptor. |
| Q40366211 | Validation of mRNA/EST-based gene predictions in human Xp11.4 revealed differences to the organization of the orthologous mouse locus |
| Q37292238 | X-linked Opitz G/BBB syndrome: identification of a novel mutation and prenatal diagnosis in a Korean family |
| Q28183393 | X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum |
| Q37340680 | X-linked microtubule-associated protein, Mid1, regulates axon development |
| Q30366739 | XLOS-observed mutations of MID1 Bbox1 domain cause domain unfolding. |
| Q37178223 | aura (mid1ip1l) regulates the cytoskeleton at the zebrafish egg-to-embryo transition |
| Q30852257 | bloodthirsty, an RBCC/TRIM gene required for erythropoiesis in zebrafish |
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