(Q29143437)

protein heterodimerization activity

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Beta-tubulin YFL037W

1 reference

GOA release 2020-03-11

1 reference

1 reference

Martin W. Breuss

1

0 references

Anjana Srivatsan

Anjana Srivatsan

3

0 references

David Keays

David A. Keays

16

0 references

Joseph G Gleeson

17

Joseph G. Gleeson

1 reference

4 April 2017

Jennifer McEvoy-Venneri

9

Jennifer McEvoy-Venneri

1 reference

4 April 2017

Thai Nguyen

2

1 reference

4 April 2017

Ines Leca

4

1 reference

4 April 2017

Guoling Tian

5

1 reference

4 April 2017

Tanja Fritz

6

1 reference

4 April 2017

Andi H. Hansen

7

1 reference

4 April 2017

Damir Musaev

8

1 reference

4 April 2017

Kiely N. James

10

1 reference

4 April 2017

Rasim O. Rosti

11

1 reference

4 April 2017

Eric Scott

12

1 reference

4 April 2017

Uner Tan

13

1 reference

4 April 2017

Richard D. Kolodner

14

1 reference

4 April 2017

Nicholas J. Cowan

describes a project that uses

15

1 reference

4 April 2017

15 January 2017

1 reference

4 April 2017

Human Molecular Genetics

1 reference

4 April 2017

26

1 reference

4 April 2017

258–269

1 reference

4 April 2017

2

1 reference

4 April 2017

ImageJ

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC6075555/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

Centrosomes, microtubules and neuronal development

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Microtubules and neurodevelopmental disease: the movers and the makers

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Neuronal migration disorders: from genetic diseases to developmental mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

The diverse genetic landscape of neurodevelopmental disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Cytoskeletal genes regulating brain size

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Mutations in TUBB8 and Human Oocyte Meiotic Arrest

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

De novo mutations in the beta-tubulin gene TUBB2A cause simplified gyral patterning and infantile-onset epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

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%2FDDW383

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Mutation of the beta1-tubulin gene associated with congenital macrothrombocytopenia affecting microtubule assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Overlapping cortical malformations and mutations in TUBB2B and TUBA1A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Tuba8 is expressed at low levels in the developing mouse and human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

CA8 mutations cause a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gait

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Two families with quadrupedalism, mental retardation, no speech, and infantile hypotonia (Uner Tan Syndrome Type-II); a novel theory for the evolutionary emergence of human bipedalism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Reference Values for Weight, Height, Head Circumference, and Body Mass Index in Turkish Children

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Exome sequencing can improve diagnosis and alter patient management

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

HomozygosityMapper2012--bridging the gap between homozygosity mapping and deep sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

HomozygosityMapper--an interactive approach to homozygosity mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

MutationTaster evaluates disease-causing potential of sequence alterations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Refined structure of alpha beta-tubulin at 3.5 A resolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

A new tubulin-binding site and pharmacophore for microtubule-destabilizing anticancer drugs

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

The alpha- and beta-tubulin folding pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Mutagenesis of beta-tubulin cysteine residues in Saccharomyces cerevisiae: mutation of cysteine 354 results in cold-stable microtubules

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Designer deletion strains derived from Saccharomyces cerevisiae S288C: a useful set of strains and plasmids for PCR-mediated gene disruption and other applications

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Construction of a set of convenient Saccharomyces cerevisiae strains that are isogenic to S288C

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

The Expression of Tubb2b Undergoes a Developmental Transition in Murine Cortical Neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Reeler/Disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Mutations in a P-type ATPase gene cause axonal degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Carbonic anhydrase-related protein VIII deficiency is associated with a distinctive lifelong gait disorder in waddles mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Localization, purification, and functional reconstitution of the P4-ATPase Atp8a2, a phosphatidylserine flippase in photoreceptor disc membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

WDR81 is necessary for purkinje and photoreceptor cell survival

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Mice deficient in carbonic anhydrase type 8 exhibit motor dysfunctions and abnormal calcium dynamics in the somatic region of cerebellar granule cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Distinct alpha- and beta-tubulin isotypes are required for the positioning, differentiation and survival of neurons: new support for the 'multi-tubulin' hypothesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

A pachygyria-causing alpha-tubulin mutation results in inefficient cycling with CCT and a deficient interaction with TBCB.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

TUBB5 and its disease-associated mutations influence the terminal differentiation and dendritic spine densities of cerebral cortical neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

The Molecular Biology Toolkit (MBT): a modular platform for developing molecular visualization applications

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383

beta-Tubulin mutation suppresses microtubule dynamics in vitro and slows mitosis in vivo.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW383