Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates (Q28506652)

24 January 2017

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7 January 2020

title

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

2 references

24 January 2017

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Bardet-Biedl syndrome 1 (human)

7 January 2020

main subject

1 reference

VANGL planar cell polarity 2

1 reference

Bardet-Biedl syndrome 4 (human)

1 reference

McKusick-Kaufman syndrome

1 reference

Bardet-Biedl syndrome

1 reference

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

inferred from title

corrigendum / erratum

0 references

author

Daniel J Jagger

6

1 reference

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7 January 2020

Paul Chapple

8

1 reference

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7 January 2020

Helen M. Phillips

12

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7 January 2020

Deborah Henderson

14

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7 January 2020

Andrew Copp

16

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7 January 2020

Nicholas Katsanis

22

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18

James R Lupski

1 reference

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7 January 2020

13

Michel R Leroux

1 reference

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7 January 2020

20

Hélène Dollfus

2 references

24 January 2017

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7 January 2020

21

Masazumi Tada

2 references

24 January 2017

7 January 2020

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author name string

Helen May-Simera

2

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24 January 2017

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7 January 2020

Masatake Kai

4

2 references

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7 January 2020

Josephine Hill

5

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7 January 2020

Shannon Fisher

10

2 references

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Marie-Madeleine Eliot

17

2 references

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7 January 2020

Andrew Forge

23

2 references

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7 January 2020

Alison J Ross

1

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Erica R Eichers

3

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Carmen C Leitch

7

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7 January 2020

Peter M Munro

9

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Perciliz L Tan

11

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Jennifer N Murdoch

15

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David T Kemp

19

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Philip L Beales

24

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language of work or name

English

0 references

publication date

18 September 2005

1 reference

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7 January 2020

number of pages

6

1 reference

inferred from page(s)

2 references

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volume

37

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issue

10

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page(s)

1135-1140

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

7 January 2020

cites work

1 reference

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

21 April 2017

1 reference

PTK7/CCK-4 is a novel regulator of planar cell polarity in vertebrates

21 April 2017

1 reference

Identification of Vangl2 and Scrb1 as planar polarity genes in mammals

21 April 2017

1 reference

Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse

21 April 2017

1 reference

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

21 April 2017

1 reference

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

21 April 2017

1 reference

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

21 April 2017

1 reference

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

21 April 2017

1 reference

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

21 April 2017

1 reference

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

21 April 2017

1 reference

Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification

21 April 2017

1 reference

Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways

21 April 2017

1 reference

Van Gogh-like2 (Strabismus) and its role in planar cell polarity and convergent extension in vertebrates

21 April 2017

1 reference

7 January 2021

Shaping the vertebrate body plan by polarized embryonic cell movements

1 reference

7 January 2021

Lifting the lid on Pandora's box: the Bardet-Biedl syndrome

1 reference

7 January 2021

Decoding cilia function: defining specialized genes required for compartmentalized cilia biogenesis

1 reference

7 January 2021

Antenatal presentation of Bardet-Biedl syndrome may mimic Meckel syndrome

1 reference

7 January 2021

Genetic insights into the morphogenesis of inner ear hair cells.

1 reference

7 January 2021

Otoacoustic emissions, travelling waves and cochlear mechanisms

1 reference

7 January 2021

Prickle 1 regulates cell movements during gastrulation and neuronal migration in zebrafish

1 reference

7 January 2021

Zebrafish trilobite identifies new roles for Strabismus in gastrulation and neuronal movements.

1 reference

7 January 2021

The Zebrafish trilobite gene is essential for tangential migration of branchiomotor neurons

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

Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells

1 reference

7 January 2021

Age- and gender-specific reference ranges for hearing level and longitudinal changes in hearing level

1 reference

7 January 2021

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

1 reference

7 January 2021

Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy.

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG1644

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16170314%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017