Lack of Mid1, the mouse ortholog of the Opitz syndrome gene, causes abnormal development of the anterior cerebellar vermis. (Q48295006)

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18 January 2020

title

Lack of Mid1, the mouse ortholog of the Opitz syndrome gene, causes abnormal development of the anterior cerebellar vermis (English)

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Luisa Maria Rosaria Napolitano

18 January 2020

author

5

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18 January 2020

author name string

Alessio Lancioni

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18 January 2020

Mariateresa Pizzo

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18 January 2020

Bianca Fontanella

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18 January 2020

Rosa Ferrentino

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18 January 2020

Elvira De Leonibus

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18 January 2020

Germana Meroni

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18 January 2020

language of work or name

English

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publication date

1 February 2010

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18 January 2020

published in

Journal of Neuroscience

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18 January 2020

volume

30

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issue

8

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18 January 2020

page(s)

2880-2887

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18 January 2020

ImageJ

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11 June 2022

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inferred from PubMed Central ID database lookup

cites work

FGF8 induces formation of an ectopic isthmic organizer and isthmocerebellar development via a repressive effect on Otx2 expression.

1 reference

12 December 2020

The Opitz syndrome gene product, MID1, associates with microtubules

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12 December 2020

Genomic structure, mapping, activity and expression of fibroblast growth factor 17

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12 December 2020

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

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12 December 2020

MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development

1 reference

12 December 2020

The caudal limit of Otx2 expression positions the isthmic organizer

1 reference

12 December 2020

FGF8 can activate Gbx2 and transform regions of the rostral mouse brain into a hindbrain fate.

1 reference

12 December 2020

Temporal and spatial gradients of Fgf8 and Fgf17 regulate proliferation and differentiation of midline cerebellar structures

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12 December 2020

Effects of early midline cerebellar lesion on cognitive and emotional functions in the rat.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

12 December 2020

Genetic regulation of cerebellar development

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12 December 2020

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

1 reference

12 December 2020

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

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

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12 December 2020

Development and malformations of the cerebellum in mice

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Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome.

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Bilateral lesion of the cerebellar-dentate nucleus impairs egocentric sequential learning but not egocentric navigation in the rat.

1 reference

12 December 2020

Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations

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12 December 2020

Evidence of functional redundancy between MID proteins: implications for the presentation of Opitz syndrome

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12 December 2020

Spatial navigation impairment in mice lacking cerebellar LTD: a motor adaptation deficit?

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12 December 2020

TRIM/RBCC, a novel class of 'single protein RING finger' E3 ubiquitin ligases

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12 December 2020

What you can learn from one gene: GLI3

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12 December 2020

FGF signalling pathways in development of the midbrain and anterior hindbrain

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Cytokine activation of p38 mitogen-activated protein kinase and apoptosis is opposed by alpha-4 targeting of protein phosphatase 2A for site-specific dephosphorylation of MEK3.

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Morphology, molecular codes, and circuitry produce the three-dimensional complexity of the cerebellum

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12 December 2020

Habit learning dissociation in rats with lesions to the vermis and the interpositus of the cerebellum

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12 December 2020

Disorders of cognitive and affective development in cerebellar malformations.

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12 December 2020

Analysis of the midbrain-hindbrain boundary cell fate using a boundary cell-specific Cre-mouse strain

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12 December 2020

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

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12 December 2020

Gli3 coordinates three-dimensional patterning and growth of the tectum and cerebellum by integrating Shh and Fgf8 signaling.

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12 December 2020

Protein phosphatase 2A and rapamycin regulate the nuclear localization and activity of the transcription factor GLI3

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12 December 2020

G syndrome (hypertelorism with esophageal abnormality and hypospadias, or hypospadias-dysphagia, or "Opitz-Frias" or "Opitz-G" syndrome)--perspective in 1987 and bibliography

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12 December 2020

Cerebellar vermis: essential for long-term habituation of the acoustic startle response

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Effects of midline and lateral cerebellar lesions on motor coordination and spatial orientation

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12 December 2020

A gene spans the pseudoautosomal boundary in mice

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12 December 2020

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

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12 December 2020

Cerebellum and procedural learning: evidence from focal cerebellar lesions

1 reference

12 December 2020

Cerebellar Contribution to Spatial Event Processing: Right/Left Discrimination Abilities in Rats

1 reference

12 December 2020

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

1 reference

12 December 2020

The cerebellum in the spatial problem solving: a co-star or a guest star?

1 reference

12 December 2020

10.1523/JNEUROSCI.4196-09.2010

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20181585 AND SRC:MED&resulttype=core&format=json

18 January 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20181585 AND SRC:MED&resulttype=core&format=json

18 January 2020

PubMed publication ID

20181585

1 reference