(Q24803465)

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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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scholarly article

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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 (English)

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GOA release 2020-03-11

Mid1 interacting protein 1 (gastrulation specific G12-like (zebrafish))

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GOA release 2020-03-11

author name string

Caterina Berti

1

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Bianca Fontanella

2

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Rosa Ferrentino

3

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Germana Meroni

4

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language of work or name

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publication date

29 February 2004

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BMC Cell Biology

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5

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1

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9

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PRC1 is a microtubule binding and bundling protein essential to maintain the mitotic spindle midzone

1 reference

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7 April 2017

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

1 reference

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7 April 2017

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.

1 reference

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7 April 2017

The tripartite motif family identifies cell compartments

1 reference

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Clasps are CLIP-115 and -170 associating proteins involved in the regional regulation of microtubule dynamics in motile fibroblasts

1 reference

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7 April 2017

The Opitz syndrome gene product, MID1, associates with microtubules

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385223

7 April 2017

Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385223

7 April 2017

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

1 reference

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7 April 2017

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1 reference

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7 April 2017

X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385223

7 April 2017

The Opitz syndrome gene MID1 is essential for establishing asymmetric gene expression in Hensen's node

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385223

7 April 2017

Duplication of the MID1 first exon in a patient with Opitz G/BBB syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385223

7 April 2017

Direct binding of NuMA to tubulin is mediated by a novel sequence motif in the tail domain that bundles and stabilizes microtubules

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385223

7 April 2017

Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385223

7 April 2017

MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385223

7 April 2017

New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385223

7 April 2017

Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385223

7 April 2017

Characterization and physical mapping in human and mouse of a novel RING finger gene in Xp22

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385223

7 April 2017

Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385223

7 April 2017

The MID1/PP2A complex: a key to the pathogenesis of Opitz BBB/G syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385223

28 September 2017

Identification of a novel microtubule-associated protein that regulates microtubule organization and cytokinesis by using a GFP-screening strategy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385223

28 September 2017

A novel centrosome-associated protein with affinity for microtubules

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385223

28 September 2017

Evolutionary conservation of microtubule-capture mechanisms

1 reference

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28 September 2017

Early eye development in vertebrates

1 reference

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28 September 2017

Genetics of craniofacial development and malformation

1 reference

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Expression pattern of the ocular albinism type 1 (Oa1) gene in the murine retinal pigment epithelium.

1 reference

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28 September 2017

Cellular Samurai: katanin and the severing of microtubules

1 reference

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28 September 2017

"Spot 14" protein: a metabolic integrator in normal and neoplastic cells

1 reference

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A gene spans the pseudoautosomal boundary in mice

1 reference

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28 September 2017

Molecular cloning of a cDNA clone encoding a phosphoprotein component related to the Ig receptor-mediated signal transduction

1 reference

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Interaction mating reveals binary and ternary connections between Drosophila cell cycle regulators.

1 reference

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28 September 2017

Microtubules and microtubule-associated proteins

1 reference

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28 September 2017

Phenotypic overlap of the BBB and G syndromes

1 reference

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28 September 2017

Opitz G/BBB syndrome: clinical comparisons of families linked to Xp22 and 22q, and a review of the literature

1 reference

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28 September 2017

Direct evidence for a role of the "spot 14" protein in the regulation of lipid synthesis

1 reference

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28 September 2017

The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region

1 reference

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30 May 2018

The Opitz syndrome: a new designation for the clinically indistinguishable BBB and G syndromes.

1 reference

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30 May 2018

Microtubules are acetylated in domains that turn over slowly

1 reference

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30 May 2018

Isolation and characterisation of the chick orthologue of the Opitz syndrome gene, Mid1, supports a conserved role in vertebrate development

1 reference

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A novel gene expressed during zebrafish gastrulation identified by differential RNA display

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28 November 2018

Identifiers

10.1186/1471-2121-5-9

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