(Q24296493)

Tetratricopeptide repeat domain 8

1 reference

sensory processing

1 reference

Tetratricopeptide repeat domain 8

1 reference

Tetratricopeptide repeat protein 8 CELE_T25F10.5

1 reference

Bardet-Biedl syndrome 2 protein homolog CELE_F20D12.3

1 reference

Uncharacterized protein CELE_Y41G9A.1

1 reference

Bardet-Biedl syndrome 7 protein homolog CELE_Y75B8A.12

1 reference

Bardet-Biedl syndrome 1 protein homolog CELE_Y105E8A.5

1 reference

Bardet-Biedl syndrome

1 reference

1 reference

17

0 references

Oliver E Blacque

Oliver E Blacque

3

0 references

Jose Badano

Jose L Badano

2

0 references

Tanya M Teslovich

10

Tanya M Teslovich

0 references

Michel R Leroux

15

Michel R Leroux

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author name string

Stephen J Ansley

1

0 references

Josephine Hill

4

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Bethan E Hoskins

5

0 references

Carmen C Leitch

6

0 references

Jun Chul Kim

7

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Alison J Ross

8

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Erica R Eichers

9

0 references

Allan K Mah

11

0 references

Robert C Johnsen

12

0 references

John C Cavender

13

0 references

Richard Alan Lewis

14

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Philip L Beales

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

16

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language of work or name

English

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publication date

9 October 2003

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published in

Nature

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volume

425

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page(s)

628-33

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issue

6958

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cites work

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

Mutations in MKKS cause Bardet-Biedl syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

Genetic interaction of BBS1 mutations with alleles at other BBS loci can result in non-Mendelian Bardet-Biedl syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

Beyond Mendel: an evolving view of human genetic disease transmission

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

BBS4 is a minor contributor to Bardet-Biedl syndrome and may also participate in triallelic inheritance

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

Identification and characterization of genes determining receptor binding and pilus length of Escherichia coli type 1 pili

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

Pilus retraction powers bacterial twitching motility

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

Centriolar satellites: molecular characterization, ATP-dependent movement toward centrioles and possible involvement in ciliogenesis

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

Intraflagellar transport

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

The RFX-type transcription factor DAF-19 regulates sensory neuron cilium formation in C. elegans

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

Abnormal nodal flow precedes situs inversus in iv and inv mice

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

The intraflagellar transport protein, IFT88, is essential for vertebrate photoreceptor assembly and maintenance

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

Genetic evidence for selective transport of opsin and arrestin by kinesin-II in mammalian photoreceptors

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

Expression analyses and interaction with the anaphase promoting complex protein Apc2 suggest a role for inversin in primary cilia and involvement in the cell cycle

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

The left-right determinant Inversin is a component of node monocilia and other 9+0 cilia.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

PCR fusion-based approach to create reporter gene constructs for expression analysis in transgenic C. elegans

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02030

7 January 2021

Identifiers

DOI

10.1038/NATURE02030

1 reference

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

1899778

1016900691

0 references

1899778

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference