(Q36920886)

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BBS7 is required for BBSome formation and its absence in mice results in Bardet-Biedl syndrome phenotypes and selective abnormalities in membrane protein trafficking

scientific article published on 09 April 2013

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

BBS7 is required for BBSome formation and its absence in mice results in Bardet-Biedl syndrome phenotypes and selective abnormalities in membrane protein trafficking (English)

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

membrane protein

1 reference

based on heuristic

inferred from title

Bardet-Biedl syndrome

1 reference

based on heuristic

inferred from title

object named as

Edwin M Stone

11

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author name string

Qihong Zhang

1

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Darryl Nishimura

2

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Tim Vogel

3

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Jianqiang Shao

4

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Ruth Swiderski

5

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Terry Yin

6

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Charles Searby

7

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Calvin S Carter

8

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Gunhee Kim

9

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Kevin Bugge

10

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Europe PubMed Central

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17 August 2017

Val C Sheffield

12

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Europe PubMed Central

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17 August 2017

language of work or name

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publication date

9 April 2013

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Europe PubMed Central

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17 August 2017

Journal of Cell Science

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Europe PubMed Central

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17 August 2017

126

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Europe PubMed Central

PMC publication ID

17 August 2017

Pt 11

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Europe PubMed Central

PMC publication ID

17 August 2017

2372-2380

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Abnormal development of NG2+PDGFR-α+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse model

1 reference

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Association of a bitter taste receptor mutation with Balkan Endemic Nephropathy (BEN).

1 reference

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29 September 2017

T2R38 taste receptor polymorphisms underlie susceptibility to upper respiratory infection

1 reference

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29 September 2017

The BBSome controls IFT assembly and turnaround in cilia

1 reference

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29 September 2017

Intrinsic protein-protein interaction-mediated and chaperonin-assisted sequential assembly of stable bardet-biedl syndrome protein complex, the BBSome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes

1 reference

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29 September 2017

Hyperactive neuroendocrine secretion causes size, feeding, and metabolic defects of C. elegans Bardet-Biedl syndrome mutants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

The ciliopathies in neuronal development: a clinical approach to investigation of Joubert syndrome and Joubert syndrome-related disorders

1 reference

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29 September 2017

Patients with Bardet-Biedl syndrome have hyperleptinemia suggestive of leptin resistance

1 reference

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29 September 2017

Dopamine receptor 1 localizes to neuronal cilia in a dynamic process that requires the Bardet-Biedl syndrome proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

The conserved Bardet-Biedl syndrome proteins assemble a coat that traffics membrane proteins to cilia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

The Chlamydomonas reinhardtii BBSome is an IFT cargo required for export of specific signaling proteins from flagella

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

The planar cell polarity effector Fuz is essential for targeted membrane trafficking, ciliogenesis and mouse embryonic development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

Motile cilia of human airway epithelia are chemosensory

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle trafficking

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

Requirement of Bardet-Biedl syndrome proteins for leptin receptor signaling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

Bardet-Biedl syndrome proteins are required for the localization of G protein-coupled receptors to primary cilia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

Leptin resistance contributes to obesity and hypertension in mouse models of Bardet-Biedl syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

Identification of ciliary localization sequences within the third intracellular loop of G protein-coupled receptors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

Gene expression analysis of photoreceptor cell loss in bbs4-knockout mice reveals an early stress gene response and photoreceptor cell damage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity

1 reference

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29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

Phenotypic differences among patients with Bardet-Biedl syndrome linked to three different chromosome loci.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

29 September 2017

Behavioural phenotype of Bardet-Biedl syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679484

4 September 2018

A functional role for dopamine transmission in the amygdala during conditioned fear

1 reference

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4 September 2018

Amygdaloid D1 dopamine receptor involvement in Pavlovian fear conditioning

1 reference

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4 September 2018

Identifiers

10.1242/JCS.111740

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

ResearchGate publication ID

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