Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene (Q28590359)

31 January 2017

title

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

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Bardet-Biedl syndrome 5 (human)

31 January 2017

main subject

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Bardet-Biedl syndrome 5 protein homolog CELE_R01H10.6

GOA release 2020-03-11

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GOA release 2020-03-11

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Jantje M. Gerdes

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31 January 2017

Nicholas Katsanis

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Tanya M. Teslovich

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31 January 2017

Michel R. Leroux

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31 January 2017

Jin Billy Li

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31 January 2017

Courtney J. Haycraft

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31 January 2017

Yanli Fan

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31 January 2017

Helen May-Simera

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31 January 2017

Haitao Li

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31 January 2017

Oliver E. Blacque

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31 January 2017

Linya Li

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31 January 2017

Carmen C. Leitch

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31 January 2017

Richard Allan Lewis

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31 January 2017

Jane S. Green

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31 January 2017

Patrick S. Parfrey

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31 January 2017

William S. Davidson

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31 January 2017

Philip L. Beales

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31 January 2017

Lisa M. Guay-Woodford

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31 January 2017

Bradley K. Yoder

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31 January 2017

Gary D. Stormo

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31 January 2017

Susan K. Dutcher

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31 January 2017

language of work or name

English

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publication date

14 May 2004

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31 January 2017

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31 January 2017

volume

117

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31 January 2017

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31 January 2017

page(s)

541–552

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Olfactory transduction: cross-talk between second-messenger systems

31 January 2017

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7 January 2021

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

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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

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

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7 January 2021

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7 January 2021

Genetic and mutational analyses of a large multiethnic Bardet-Biedl cohort reveal a minor involvement of BBS6 and delineate the critical intervals of other loci

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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

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Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin, a large novel gene

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7 January 2021

Flagellar assembly in two hundred and fifty easy-to-follow steps

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7 January 2021

Purification of basal bodies and basal body complexes from Chlamydomonas reinhardtii.

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7 January 2021

Elucidation of basal body and centriole functions in Chlamydomonas reinhardtii

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7 January 2021

Long-lost relatives reappear: identification of new members of the tubulin superfamily

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7 January 2021

Conserved function for embryonic nodal cilia.

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7 January 2021

A synthetic gene coding for the green fluorescent protein (GFP) is a versatile reporter in Chlamydomonas reinhardtii

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7 January 2021

Selective targeting of somatostatin receptor 3 to neuronal cilia

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7 January 2021

Identifying DNA and protein patterns with statistically significant alignments of multiple sequences

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7 January 2021

Requirement of a centrosomal activity for cell cycle progression through G1 into S phase

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7 January 2021

Phototropin is the blue-light receptor that controls multiple steps in the sexual life cycle of the green alga Chlamydomonas reinhardtii

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7 January 2021

Hedgehog signalling in the mouse requires intraflagellar transport proteins

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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

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

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7 January 2021

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

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7 January 2021

Centrosomes enhance the fidelity of cytokinesis in vertebrates and are required for cell cycle progression

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7 January 2021

Increased levels of mRNAs for tubulin and other flagellar proteins after amputation or shortening of Chlamydomonas Flagella

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7 January 2021

Molecular cloning and characterization of the mouse and human TUSP gene, a novel member of the tubby superfamily

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7 January 2021

Analysis of Chlamydomonas reinhardtii genome structure using large-scale sequencing of regions on linkage groups I and III.

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7 January 2021

Altered centrosome structure is associated with abnormal mitoses in human breast tumors

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7 January 2021

WU-Blast2 server at the European Bioinformatics Institute

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7 January 2021

Understanding the functions of kinesin-II.

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7 January 2021

The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin

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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

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

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7 January 2021

Cyclic AMP functions as a primary sexual signal in gametes of Chlamydomonas reinhardtii

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7 January 2021

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7 January 2021

The vertebrate primary cilium is a sensory organelle

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7 January 2021

Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella

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7 January 2021

Polycystin-2 localizes to kidney cilia and the ciliary level is elevated in orpk mice with polycystic kidney disease

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7 January 2021

A novel dynein light intermediate chain colocalizes with the retrograde motor for intraflagellar transport at sites of axoneme assembly in chlamydomonas and Mammalian cells

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7 January 2021

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7 January 2021

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7 January 2021

Two rhodopsins mediate phototaxis to low- and high-intensity light in Chlamydomonas reinhardtii

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7 January 2021

A Streptomyces rimosus aphVIII gene coding for a new type phosphotransferase provides stable antibiotic resistance to Chlamydomonas reinhardtii.

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7 January 2021

Mutations in MKKS cause Bardet-Biedl syndrome

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7 January 2021

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

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7 January 2021

A two-cilia model for vertebrate left-right axis specification.

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7 January 2021

Left-right asymmetry and kinesin superfamily protein KIF3A: new insights in determination of laterality and mesoderm induction by kif3A-/- mice analysis

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7 January 2021

Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia

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7 January 2021

The autosomal recessive polycystic kidney disease protein is localized to primary cilia, with concentration in the basal body area

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7 January 2021

Electron microscopical reconstruction of the anterior sensory anatomy of the nematodecaenorhabditis elegans

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7 January 2021

The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein

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7 January 2021

The structure of the ventral nerve cord of Caenorhabditis elegans

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7 January 2021

CHE-3, a cytosolic dynein heavy chain, is required for sensory cilia structure and function in Caenorhabditis elegans

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7 January 2021

Chlamydomonas flagella. I. Isolation and electrophoretic analysis of microtubules, matrix, membranes, and mastigonemes

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7 January 2021

Disruption of the type III adenylyl cyclase gene leads to peripheral and behavioral anosmia in transgenic mice

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7 January 2021

Transgene and transposon silencing in Chlamydomonas reinhardtii by a DEAH-box RNA helicase

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7 January 2021

The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia

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7 January 2021

Canadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype.

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7 January 2021