Beta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdown (Q28301198)

9

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Jamel Chelly

10

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Karine Poirier

7

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author name string

Yoann Saillour

1

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Loïc Broix

2

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Elodie Bruel-Jungerman

3

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Nicolas Lebrun

4

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Giuseppe Muraca

5

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Julien Rucci

6

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Richard Belvindrah

Life is a journey: a genetic look at neocortical development

8

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language of work or name

English

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publication date

15 March 2014

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published in

Human Molecular Genetics

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volume

23

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issue

6

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page(s)

1516-26

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cites work

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

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

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

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

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

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

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Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A).

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Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria

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Mutation of the variant alpha-tubulin TUBA8 results in polymicrogyria with optic nerve hypoplasia

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

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

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An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation

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Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance

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Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia

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A de novo mutation in the β-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellum

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Complex regulation and functional versatility of mammalian alpha- and beta-tubulin isotypes during the differentiation of testis and muscle cells

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Dcx reexpression reduces subcortical band heterotopia and seizure threshold in an animal model of neuronal migration disorder

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Efficient in utero gene transfer system to the developing mouse brain using electroporation: visualization of neuronal migration in the developing cortex

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β-Tubulin mutations that cause severe neuropathies disrupt axonal transport

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