Microcephaly models in the developing zebrafish retinal neuroepithelium point to an underlying defect in metaphase progression. (Q30556376)

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28 February 2020

title

Microcephaly models in the developing zebrafish retinal neuroepithelium point to an underlying defect in metaphase progression (English)

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28 February 2020

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0 references

Christopher J Wilkinson

9

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28 February 2020

author name string

Claire Novorol

1

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28 February 2020

Janina Burkhardt

2

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28 February 2020

Kirstin J Wood

3

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28 February 2020

Anila Iqbal

4

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28 February 2020

Claudio Roque

5

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28 February 2020

Nicola Coutts

6

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28 February 2020

Alexandra D Almeida

7

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28 February 2020

Jie He

8

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28 February 2020

William A Harris

10

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28 February 2020

language of work or name

English

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publication date

23 October 2013

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28 February 2020

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28 February 2020

volume

3

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28 February 2020

issue

10

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28 February 2020

page(s)

130065

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Mechanisms of cell competition: themes and variations

28 February 2020

cites work

1 reference

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How variable clones build an invariant retina

20 June 2018

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WD40-repeat protein 62 is a JNK-phosphorylated spindle pole protein required for spindle maintenance and timely mitotic progression

20 June 2018

1 reference

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A truncating mutation of CEP135 causes primary microcephaly and disturbed centrosomal function

20 June 2018

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Apical migration of nuclei during G2 is a prerequisite for all nuclear motion in zebrafish neuroepithelia

20 June 2018

1 reference

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The human microcephaly protein STIL interacts with CPAP and is required for procentriole formation

20 June 2018

1 reference

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A primary microcephaly protein complex forms a ring around parental centrioles.

20 June 2018

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MCPH1 regulates the neuroprogenitor division mode by coupling the centrosomal cycle with mitotic entry through the Chk1-Cdc25 pathway

20 June 2018

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The microcephaly gene aspm is involved in brain development in zebrafish

20 June 2018

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Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations

20 June 2018

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The Stil protein regulates centrosome integrity and mitosis through suppression of Chfr

20 June 2018

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CEP152 is a genome maintenance protein disrupted in Seckel syndrome

20 June 2018

1 reference

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Cep152 acts as a scaffold for recruitment of Plk4 and CPAP to the centrosome

20 June 2018

1 reference

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WDR62 is associated with the spindle pole and is mutated in human microcephaly

20 June 2018

1 reference

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Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture

20 June 2018

1 reference

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Asterless is a scaffold for the onset of centriole assembly

20 June 2018

1 reference

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Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

20 June 2018

1 reference

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Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4.

20 June 2018

1 reference

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Novel CENPJ mutation causes Seckel syndrome

20 June 2018

1 reference

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The zebrafish flotte lotte mutant reveals that the local retinal environment promotes the differentiation of proliferating precursors emerging from their stem cell niche

20 June 2018

1 reference

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Cdk5rap2 interacts with pericentrin to maintain the neural progenitor pool in the developing neocortex

20 June 2018

1 reference

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Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors

20 June 2018

1 reference

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Drosophila Ana2 is a conserved centriole duplication factor

20 June 2018

1 reference

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Illuminating cell-cycle progression in the developing zebrafish embryo

20 June 2018

1 reference

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Primary microcephaly: do all roads lead to Rome?

20 June 2018

1 reference

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Asymmetric centrosome inheritance maintains neural progenitors in the neocortex

20 June 2018

1 reference

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Actomyosin is the main driver of interkinetic nuclear migration in the retina.

20 June 2018

1 reference

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Plk1-dependent and -independent roles of an ODF2 splice variant, hCenexin1, at the centrosome of somatic cells

20 June 2018

1 reference

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Mutations in STIL, encoding a pericentriolar and centrosomal protein, cause primary microcephaly

20 June 2018

1 reference

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The molecular landscape of ASPM mutations in primary microcephaly

20 June 2018

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Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling

20 June 2018

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The zebra fish cassiopeia mutant reveals that SIL is required for mitotic spindle organization

20 June 2018

1 reference

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The SIL gene is essential for mitotic entry and survival of cancer cells.

20 June 2018

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Polarization and orientation of retinal ganglion cells in vivo

20 June 2018

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Microcephalin: a causal link between impaired damage response signalling and microcephaly

20 June 2018

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A novel deletion mutation in CENPJ gene in a Pakistani family with autosomal recessive primary microcephaly

20 June 2018

1 reference

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Aspm specifically maintains symmetric proliferative divisions of neuroepithelial cells

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

The microcephaly ASPM gene is expressed in proliferating tissues and encodes for a mitotic spindle protein

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

Microcephalin Is a DNA Damage Response Protein Involved in Regulation of CHK1 and BRCA1

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

A novel locus for autosomal recessive primary microcephaly (MCPH6) maps to 13q12.2

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

ASPM is a major determinant of cerebral cortical size

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

Identification of microcephalin, a protein implicated in determining the size of the human brain

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

The drosophila protein asp is involved in microtubule organization during spindle formation and cytokinesis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

Molecular genetics of human microcephaly

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

A fifth locus for primary autosomal recessive microcephaly maps to chromosome 1q31.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

Primary autosomal recessive microcephaly: MCPH5 maps to 1q25-q32

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1-13.2.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

Primary autosomal recessive microcephaly: homozygosity mapping of MCPH4 to chromosome 15.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

The SIL gene is required for mouse embryonic axial development and left-right specification

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

Neurogenesis in the visual system of embryonic and adult zebrafish (Danio rerio). off.

20 June 2018

1 reference

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Recessive (true) microcephaly: a case report with neuropathological observations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

Stages of embryonic development of the zebrafish

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

Mutations at the asp locus of Drosophila lead to multiple free centrosomes in syncytial embryos, but restrict centrosome duplication in larval neuroblasts

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

A proximal centriole-like structure is present in Drosophila spermatids and can serve as a model to study centriole duplication

20 June 2018

1 reference

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Insertional mutagenesis in zebrafish rapidly identifies genes essential for early vertebrate development

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

Nonradioactive in situ hybridization to xenopus tissue sections

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

p53-independent apoptosis and p53-dependent block of DNA rereplication following mitotic spindle inhibition in human cells.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3814721

Retroviral-mediated insertional mutagenesis in zebrafish

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24153002

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1098/RSOB.130065

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24153002 AND SRC:MED&resulttype=core&format=json

28 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24153002 AND SRC:MED&resulttype=core&format=json

28 February 2020

PubMed publication ID

24153002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24153002 AND SRC:MED&resulttype=core&format=json