Mid1/Mid2expression in craniofacial development and a literature review of X-linked Opitz syndrome

A novel mutation in MID1 in a patient with X-linked Opitz G/BBB syndrome

(2014) Xing Ji et al.   GENE

MID1 Catalyzes the Ubiquitination of Protein Phosphatase 2A and Mutations within Its Bbox1 Domain Disrupt Polyubiquitination of Alpha4 but Not of PP2Ac

(2014) Haijuan Du et al.   PLoS One

Exon 2 duplication of the MID1 gene in a patient with a mild phenotype of Opitz G/BBB syndrome

(2013) Irina Hüning et al.   European Journal of Medical Genetics

Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations

(2013) Chiara Migliore et al.   European Journal of Medical Genetics

Targeted Deep Resequencing IdentifiesMID2Mutation for X-Linked Intellectual Disability with Varied Disease Severity in a Large Kindred from India

(2013) Thenral S. Geetha et al.   HUMAN MUTATION

A MID1 gene mutation in a patient with Opitz G/BBB syndrome that altered the 3D structure of SPRY domain

(2012) Ching-Hsuan Hu et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Regulation of PP2A activity by Mid1 controls cranial neural crest speed and gangliogenesis

(2012) Elizabeth J. Latta et al.   MECHANISMS OF DEVELOPMENT

The E3 Ubiquitin Ligase- and Protein Phosphatase 2A (PP2A)-binding Domains of the Alpha4 Protein Are Both Required for Alpha4 to Inhibit PP2A Degradation

(2011) Michele LeNoue-Newton et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Detection and Characterization of the In Vitro E3 Ligase Activity of the Human MID1 Protein

(2011) Xiaofeng Han et al.   JOURNAL OF MOLECULAR BIOLOGY

Alpha4 Is a Ubiquitin-Binding Protein That Regulates Protein Serine/Threonine Phosphatase 2A Ubiquitination

(2010) Jamie L. McConnell et al.   BIOCHEMISTRY

MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization

(2010) M. Suzuki et al.   DEVELOPMENT

Clinical and molecular studies of patients with characteristics of Opitz G/BBB syndrome shows a novelMID1mutation

(2008) Elena W.Y. Hsieh et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

MID1 mutations in patients with X-linked Opitz G/BBB syndrome

(2008) Bianca Fontanella et al.   HUMAN MUTATION

Active Transport of the Ubiquitin Ligase MID1 along the Microtubules Is Regulated by Protein Phosphatase 2A

(2008) Beatriz Aranda-Orgillés et al.   PLoS One

Diagnosis of a terminal deletion of 4p with duplication of Xp22.31 in a patient with findings of Opitz G/BBB syndrome and Wolf-Hirschhorn syndrome

(2007) Joyce So et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A