(Q28292823)

17

0 references

Karine Poirier

1

0 references

Nadia Bahi-Buisson

3

0 references

Nathalie Boddaert

15

object named as

Nathalie Boddaert

0 references

Tania Attié-Bitach

object named as

Tania Attie-Bitach

9

0 references

Catherine Fallet-Bianco

5

object named as

Catherine Fallet-Bianco

0 references

author name string

Yoann Saillour

2

0 references

Xavier H Jaglin

4

0 references

Rima Nabbout

6

0 references

Laetitia Castelnau-Ptakhine

7

0 references

Agathe Roubertie

8

0 references

Isabelle Desguerre

10

0 references

David Genevieve

11

0 references

Christine Barnerias

12

0 references

Boris Keren

13

0 references

Nicolas Lebrun

14

0 references

Féréchté Encha-Razavi

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

16

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language of work or name

English

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publication date

15 November 2010

0 references

published in

Human Molecular Genetics

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volume

19

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issue

22

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page(s)

4462-73

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cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3298850

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3298850

Structure of the alpha beta tubulin dimer by electron crystallography

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3298850

Tubulin subunits exist in an activated conformational state generated and maintained by protein cofactors

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3298850

Pathway leading to correctly folded beta-tubulin

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3298850

Diffusion imaging and tractography of congenital brain malformations

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3298850

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3298850

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3298850

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3298850

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3298850

A panel of monoclonal antibodies against reelin, the extracellular matrix protein defective in reeler mutant mice.

29 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ377

Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ377

21 January 2018

Identifiers

DOI

10.1093/HMG/DDQ377

1 reference

1247646

1247646

1 reference

1 reference

1 reference