(Q33435460)

26 July 2017

title

Patterns of expression of Bardet-Biedl syndrome proteins in the mammalian cochlea suggest noncentrosomal functions (English)

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26 July 2017

main subject

Bardet-Biedl syndrome

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Daniel J Jagger

6

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author name string

Helen L May-Simera

1

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26 July 2017

Alison Ross

2

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26 July 2017

Suzanne Rix

3

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26 July 2017

Andrew Forge

4

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26 July 2017

Philip L Beales

5

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26 July 2017

language of work or name

English

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publication date

1 May 2009

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The Journal of Comparative Neurology

26 July 2017

published in

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26 July 2017

volume

514

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26 July 2017

issue

2

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26 July 2017

page(s)

174-188

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Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome

26 July 2017

cites work

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7 January 2021

Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2.

1 reference

7 January 2021

Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet-Biedl patients with two mutations at a second BBS locus

1 reference

7 January 2021

Microtubule cold stability in supporting cells of the gerbil auditory sensory epithelium: correlation with tubulin post-translational modifications

1 reference

7 January 2021

Bardet-Biedl syndrome: an emerging pathomechanism of intracellular transport.

1 reference

7 January 2021

Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport

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7 January 2021

Assembly of centrosomal proteins and microtubule organization depends on PCM-1

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7 January 2021

Dynactin is required for bidirectional organelle transport

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7 January 2021

Establishment of hair bundle polarity and orientation in the developing vestibular system of the mouse

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7 January 2021

Mkks-null mice have a phenotype resembling Bardet-Biedl syndrome

1 reference

7 January 2021

Genetic insights into the morphogenesis of inner ear hair cells.

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7 January 2021

Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response

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7 January 2021

Loss of alpha-tubulin polyglutamylation in ROSA22 mice is associated with abnormal targeting of KIF1A and modulated synaptic function

1 reference

7 January 2021

Compartmentalized and signal-selective gap junctional coupling in the hearing cochlea.

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7 January 2021

The oligogenic properties of Bardet-Biedl syndrome

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7 January 2021

Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder

1 reference

7 January 2021

The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression

1 reference

7 January 2021

MKKS/BBS6, a divergent chaperonin-like protein linked to the obesity disorder Bardet-Biedl syndrome, is a novel centrosomal component required for cytokinesis

1 reference

7 January 2021

Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse

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7 January 2021

Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development

1 reference

7 January 2021

Initial characterization of kinocilin, a protein of the hair cell kinocilium

1 reference

7 January 2021

Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene

1 reference

7 January 2021

Microtubule actin crosslinking factor 1b: a novel plakin that localizes to the Golgi complex

1 reference

7 January 2021

Centrosomal deployment of gamma-tubulin and pericentrin: evidence for a microtubule-nucleating domain and a minus-end docking domain in certain mouse epithelial cells

1 reference

7 January 2021

The adenomatous polyposis coli protein unambiguously localizes to microtubule plus ends and is involved in establishing parallel arrays of microtubule bundles in highly polarized epithelial cells

1 reference

7 January 2021

Ninein is released from the centrosome and moves bi-directionally along microtubules

1 reference

7 January 2021

Identification of the gene that, when mutated, causes the human obesity syndrome BBS4.

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7 January 2021

Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly

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7 January 2021

A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis

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7 January 2021

Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin

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7 January 2021

Novel interaction partners of Bardet-Biedl syndrome proteins

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7 January 2021

The neuron-specific kinesin superfamily protein KIF1A is a unique monomeric motor for anterograde axonal transport of synaptic vesicle precursors

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7 January 2021

Functional coordination of intraflagellar transport motors.

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7 January 2021

Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates

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7 January 2021

Post-translational modifications of tubulin suggest that dynamic microtubules are present in sensory cells and stable microtubules are present in supporting cells of the mammalian cochlea

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7 January 2021

BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus

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7 January 2021

Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome

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7 January 2021

Bardet-Biedl syndrome: beyond the cilium.

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7 January 2021

Microtubule rearrangement and bending during assembly of large curved microtubule bundles in mouse cochlear epithelial cells.

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7 January 2021

Structure and function of a protein folding machine: the eukaryotic cytosolic chaperonin CCT.

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7 January 2021

Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function

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7 January 2021

Defect in synaptic vesicle precursor transport and neuronal cell death in KIF1A motor protein-deficient mice.

1 reference

7 January 2021

Identifiers

DOI

10.1002/CNE.22001

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26 July 2017

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