Novel interaction partners of Bardet-Biedl syndrome proteins (Q24300396)

aldolase, fructose-bisphosphate B

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Keratin 18

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Flotillin 1

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Paired box 2

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Bardet-Biedl syndrome

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F Oeffner

1

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C Moch

2

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A Neundorf

3

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J Hofmann

4

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M Koch

5

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K H Grzeschik

Basic local alignment search tool

6

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language of work or name

English

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publication date

February 2008

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published in

Cytoskeleton

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volume

65

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page(s)

143-55

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issue

2

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cites work

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

21 January 2018

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7 January 2021

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

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7 January 2021

Dissection of epistasis in oligogenic Bardet-Biedl syndrome

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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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

Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.

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7 January 2021

Formins regulate actin filament flexibility through long range allosteric interactions

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7 January 2021

Characterization of an aldolase-binding site in the Wiskott-Aldrich syndrome protein

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7 January 2021

Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3)

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7 January 2021

Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)

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7 January 2021

Enzymes with extra talents: moonlighting functions and catalytic promiscuity

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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

Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome

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7 January 2021

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

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7 January 2021

Coassembly of flotillins induces formation of membrane microdomains, membrane curvature, and vesicle budding

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7 January 2021

FHOD1 coordinates actin filament and microtubule alignment to mediate cell elongation

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7 January 2021

Dual role of the exocyst in AMPA receptor targeting and insertion into the postsynaptic membrane

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7 January 2021

The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome

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7 January 2021

Compartmentalization of the exocyst complex in lipid rafts controls Glut4 vesicle tethering

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7 January 2021

The oligogenic properties of Bardet-Biedl syndrome

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7 January 2021

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

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7 January 2021

Exploring the molecular basis of Bardet-Biedl syndrome

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7 January 2021

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

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7 January 2021

Pitfalls of homozygosity mapping: an extended consanguineous Bardet-Biedl syndrome family with two mutant genes (BBS2, BBS10), three mutations, but no triallelism

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7 January 2021

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

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7 January 2021

Disruption of formin-encoding transcripts in two mutant limb deformity alleles

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7 January 2021

Establishing a connection between cilia and Bardet-Biedl Syndrome

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7 January 2021

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

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7 January 2021

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

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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

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

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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

Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome gene

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7 January 2021

Sensory ciliogenesis in Caenorhabditis elegans: assignment of IFT components into distinct modules based on transport and phenotypic profiles

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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

Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.

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7 January 2021

Biochemical characterization of the diaphanous autoregulatory interaction in the formin homology protein FHOD1

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7 January 2021

Multiple organ pathology, metabolic abnormalities and impaired homeostasis of reactive oxygen species in Epas1-/- mice

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7 January 2021

Mutations in MKKS cause Bardet-Biedl syndrome

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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

Cytoplasmic dynein binds dynactin through a direct interaction between the intermediate chains and p150Glued

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7 January 2021

The mammalian exocyst, a complex required for exocytosis, inhibits tubulin polymerization

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7 January 2021

The p150Glued component of the dynactin complex binds to both microtubules and the actin-related protein centractin (Arp-1)

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7 January 2021

Cortactin localization to sites of actin assembly in lamellipodia requires interactions with F-actin and the Arp2/3 complex

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7 January 2021

Interaction of BIG2, a brefeldin A-inhibited guanine nucleotide-exchange protein, with exocyst protein Exo70

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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