(Q47595186)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29077851%20AND%20SRC:MED&resulttype=core&format=json

8 April 2020

title

Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical development (English)

1 reference

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8 April 2020

0 references

13

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8 April 2020

Juliette D Godin

18

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8 April 2020

Johan G Gilet

6

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8 April 2020

Alexandre Benmerah

14

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8 April 2020

Nadia Bahi-Buisson

15

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8 April 2020

Laurent Nguyen

17

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8 April 2020

author name string

Loïc Broix

1

1 reference

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8 April 2020

Laure Asselin

2

1 reference

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8 April 2020

Carla G Silva

3

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8 April 2020

Ekaterina L Ivanova

4

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8 April 2020

Peggy Tilly

5

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8 April 2020

Nicolas Lebrun

7

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8 April 2020

Hélène Jagline

8

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8 April 2020

Giuseppe Muraca

9

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8 April 2020

Yoann Saillour

10

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8 April 2020

Nathalie Drouot

11

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8 April 2020

Madeline Louise Reilly

12

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8 April 2020

Richard Belvindrah

16

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8 April 2020

Jamel Chelly

19

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8 April 2020

Maria-Victoria Hinckelmann

20

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8 April 2020

publication date

1 January 2018

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8 April 2020

published in

Human Molecular Genetics

1 reference

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8 April 2020

volume

27

1 reference

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8 April 2020

issue

2

1 reference

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8 April 2020

page(s)

224-238

1 reference

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doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)

8 April 2020

cites work

1 reference

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Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats

21 January 2018

1 reference

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Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

21 January 2018

1 reference

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New insights into genotype-phenotype correlations for the doublecortin-related lissencephaly spectrum

21 January 2018

1 reference

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Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans

21 January 2018

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21 January 2018

1 reference

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Mutations in the neuronal ß-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX384

Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities

21 January 2018

1 reference

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Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly

21 January 2018

1 reference

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The wide spectrum of tubulinopathies: what are the key features for the diagnosis?

21 January 2018

1 reference

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Phenotypic spectrum of the tubulin-related disorders and functional implications of disease-causing mutations.

21 January 2018

1 reference

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Mutations in the murine homologue of TUBB5 cause microcephaly by perturbing cell cycle progression and inducing p53-associated apoptosis

21 January 2018

1 reference

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Beta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdown

21 January 2018

1 reference

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Recurrent KIF2A mutations are responsible for classic lissencephaly

21 January 2018

1 reference

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A patient with lissencephaly, developmental delay, and infantile spasms, due to de novo heterozygous mutation of KIF2A.

21 January 2018

1 reference

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Kin I kinesins are microtubule-destabilizing enzymes

21 January 2018

1 reference

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Kinesin-13s in mitosis: Key players in the spatial and temporal organization of spindle microtubules

21 January 2018

1 reference

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DDA3 recruits microtubule depolymerase Kif2a to spindle poles and controls spindle dynamics and mitotic chromosome movement

21 January 2018

1 reference

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Efficient mitosis in human cells lacking poleward microtubule flux

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX384

Aurora B and Kif2A control microtubule length for assembly of a functional central spindle during anaphase

21 January 2018

1 reference

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DDA3 and Mdp3 modulate Kif2a recruitment onto the mitotic spindle to control minus-end spindle dynamics.

21 January 2018

1 reference

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The kinesin-13 proteins Kif2a, Kif2b, and Kif2c/MCAK have distinct roles during mitosis in human cells.

21 January 2018

1 reference

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Kinesin superfamily protein 2A (KIF2A) functions in suppression of collateral branch extension

21 January 2018

1 reference

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KIF2 is a new microtubule-based anterograde motor that transports membranous organelles distinct from those carried by kinesin heavy chain or KIF3A/B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX384

The Microtubule-Depolymerizing Activity of a Mitotic Kinesin Protein KIF2A Drives Primary Cilia Disassembly Coupled with Cell Proliferation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX384

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX384

Radial glial cells: key organisers in CNS development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX384

Cortical progenitor expansion, self-renewal and neurogenesis-a polarized perspective

21 January 2018

1 reference

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Control of asymmetric cell division of mammalian neural progenitors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX384

The KinI kinesin Kif2a is required for bipolar spindle assembly through a functional relationship with MCAK

21 January 2018

1 reference

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Primary cilia in neurodevelopmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX384

DOCK7 interacts with TACC3 to regulate interkinetic nuclear migration and cortical neurogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX384

Myosin II is required for interkinetic nuclear migration of neural progenitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX384

Lucky 13-microtubule depolymerisation by kinesin-13 motors

21 January 2018

1 reference

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Cellular and molecular introduction to brain development

21 January 2018

1 reference

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Patterns of neuronal migration in the embryonic cortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX384

Nucleokinesis in neuronal migration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX384

Molecular layers underlying cytoskeletal remodelling during cortical development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX384

RNAi reveals doublecortin is required for radial migration in rat neocortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX384

Dual subcellular roles for LIS1 and dynein in radial neuronal migration in live brain tissue

21 January 2018

1 reference

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Molecular logic of neocortical projection neuron specification, development and diversity

21 January 2018

1 reference

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Current topics of functional links between primary cilia and cell cycle

21 January 2018

1 reference

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Ciliary transition zone activation of phosphorylated Tctex-1 controls ciliary resorption, S-phase entry and fate of neural progenitors

21 January 2018

1 reference

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Microcephaly Proteins Wdr62 and Aspm Define a Mother Centriole Complex Regulating Centriole Biogenesis, Apical Complex, and Cell Fate

21 January 2018

1 reference

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CPAP promotes timely cilium disassembly to maintain neural progenitor pool

21 January 2018

1 reference

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Proteomics of Primary Cilia by Proximity Labeling

21 January 2018

1 reference

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A Dynamic Protein Interaction Landscape of the Human Centrosome-Cilium Interface

21 January 2018

1 reference

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An organelle-specific protein landscape identifies novel diseases and molecular mechanisms

21 January 2018

1 reference

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21 January 2018

Identifiers

DOI

10.1093/HMG/DDX384

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29077851%20AND%20SRC:MED&resulttype=core&format=json

8 April 2020

1 reference