Bibliography
Li, J. B., Gerdes, J. M., Haycraft, C. J., Fan, Y., Teslovich, T. M., May-Simera, H., Li, H., Blacque, O. E., Li, L., Leitch, C. C., Lewis, R. A., Green, J. S., Parfrey, P. S., Leroux, M. R., Davidson, W. S., Beales, P. L., Guay-Woodford, L. M., Yoder, B. K., Stormo, G. D., ⦠Dutcher, S. K. (2004). Comparative Genomics Identifies a Flagellar and Basal Body Proteome that Includes the BBS5 Human Disease Gene. Cell, 117(4), 541â552.
Authors
21
- Jin Billy Li (first)
- Jantje M Gerdes (additional)
- Courtney J Haycraft (additional)
- Yanli Fan (additional)
- Tanya M Teslovich (additional)
- Helen May-Simera (additional)
- Haitao Li (additional)
- Oliver E Blacque (additional)
- Linya Li (additional)
- Carmen C Leitch (additional)
- Richard Allan Lewis (additional)
- Jane S Green (additional)
- Patrick S Parfrey (additional)
- Michel R Leroux (additional)
- William S Davidson (additional)
- Philip L Beales (additional)
- Lisa M Guay-Woodford (additional)
- Bradley K Yoder (additional)
- Gary D Stormo (additional)
- Nicholas Katsanis (additional)
- Susan K Dutcher (additional)
References
72
Referenced
632
10.1021/bi00469a004
/ Biochemistry / Olfactory transduction by Anholt (1990)10.1038/nature02030
/ Nature / Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome by Ansley (2003)10.1086/368204
/ Am. J. Hum. Genet. / Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2 by Badano (2003)10.1093/hmg/ddg188
/ Hum. Mol. Genet. / Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet-Biedl patients with two mutations at a second BBS locus by Badano (2003)10.1093/nar/gkh121
/ Nucleic Acids Res. / The Pfam protein families database by Bateman (2004)10.1086/318794
/ Am. J. Hum. Genet. / 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 by Beales (2001)10.1086/375178
/ Am. J. Hum. Genet. / Genetic interaction of BBS1 mutations with alleles at other BBS loci can result in non-Mendelian Bardet-Biedl syndrome by Beales (2003)10.1016/S0171-9335(99)80053-3
/ Eur. J. Cell Biol. / Microtubule polyglutamylation in Drosophila melanogaster brain and testis by Bobinnec (1999)10.1093/genetics/77.1.71
/ Genetics / The genetics of Caenorhabditis elegans by Brenner (1974)10.1034/j.1600-0854.2003.t01-1-00103.x
/ Traffic / The intraflagellar transport machinery of Chlamydomonas reinhardtii by Cole (2003)10.1083/jcb.141.4.993
/ J. Cell Biol. / Chlamydomonas kinesin-II-dependent intraflagellar transport (IFT) by Cole (1998)10.1093/hmg/ddg122
/ Hum. Mol. Genet. / Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin, a large novel gene by Davy (2003)10.1016/S0168-9525(00)89123-4
/ Trends Genet. / Flagellar assembly in two hundred and fifty easy-to-follow steps by Dutcher (1995)10.1016/S0091-679X(08)60826-2
/ Methods Cell Biol. / Purification of basal bodies and basal body complexes from Chlamydomonas reinhardtii by Dutcher (1995)10.1034/j.1600-0854.2003.00104.x
/ Traffic / Elucidation of basal body and centriole functions in Chlamydomonas reinhardtii by Dutcher (2003)10.1016/j.mib.2003.10.016
/ Curr. Opin. Microbiol. / Long-lost relatives reappear by Dutcher (2003){'key': '10.1016/S0092-8674(04)00450-7_BIB17', 'series-title': 'Dissection of Basal Body and Centriole Function in the Unicellular Green Alga Chlamydomonas Reinhardtii', 'year': '2004'}
/ Dissection of Basal Body and Centriole Function in the Unicellular Green Alga Chlamydomonas Reinhardtii (2004)10.1093/genetics/141.3.945
/ Genetics / Loss of spatial control of the mitotic spindle apparatus in a Chlamydomonas reinhardtii mutant strain lacking basal bodies by Ehler (1995)10.1038/418037a
/ Nature / Conserved function for embryonic nodal cilia by Essner (2002)10.1046/j.1365-313X.1999.00526.x
/ Plant J. / A synthetic gene coding for the green fluorescent protein (GFP) is a versatile reporter in Chlamydomonas reinhardtii by Fuhrmann (1999)10.1242/dev.126.21.4839
/ Development / A novel WD40 protein, CHE-2, acts cell-autonomously in the formation of C. elegans sensory cilia by Fujiwara (1999)10.1016/S0306-4522(98)00354-6
/ Neuroscience / Selective targeting of somatostatin receptor 3 to neuronal cilia by Handel (1999)10.1242/dev.128.9.1493
/ Development / The C. elegans homolog of the murine cystic kidney disease gene Tg737 functions in a ciliogenic pathway and is disrupted in osm-5 mutant worms by Haycraft (2001)10.1093/bioinformatics/15.7.563
/ Bioinformatics. / Identifying DNA and protein patterns with statistically significant alignments of multiple sequences by Hertz (1999)10.1126/science.1056866
/ Science / Requirement of a centrosomal activity for cell cycle progression through G1 into S phase by Hinchcliffe (2001)10.1073/pnas.0931459100
/ Proc. Natl. Acad. Sci. USA / Phototropin is the blue-light receptor that controls multiple steps in the sexual life cycle of the green alga Chlamydomonas reinhardtii by Huang (2003)10.1038/nature02061
/ Nature / Hedgehog signalling in the mouse requires intraflagellar transport proteins by Huangfu (2003)10.1038/79201
/ Nat. Genet. / Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome by Katsanis (2000)10.1126/science.1063525
/ Science / Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder by Katsanis (2001)10.1086/341031
/ Am. J. Hum. Genet. / BBS4 is a minor contributor to Bardet-Biedl syndrome and may also participate in triallelic inheritance by Katsanis (2002)10.1083/jcb.153.1.237
/ J. Cell Biol. / Centrosomes enhance the fidelity of cytokinesis in vertebrates and are required for cell cycle progression by Khodjakov (2001)10.1016/0092-8674(80)90633-9
/ Cell / Increased levels of mRNAs for tubulin and other flagellar proteins after amputation or shortening of Chlamydomonas flagella by Lefebvre (1980)10.1016/S0378-1119(01)00582-0
/ Gene / Molecular cloning and characterization of the mouse and human TUSP gene, a novel member of the tubby superfamily by Li (2001)10.1111/j.1550-7408.2003.tb00109.x
/ J. Eukaryot. Microbiol. / Analysis of Chlamydomonas reinhardtii genome structure using large-scale sequencing of regions on linkage groups I and III by Li (2003)10.1016/S0002-9440(10)65513-7
/ Am. J. Pathol. / Altered centrosome structure is associated with abnormal mitoses in human breast tumors by Lingle (1999)10.1093/nar/gkg573
/ Nucleic Acids Res. / WU-Blast2 server at the European Bioinformatics Institute by Lopez (2003)10.1016/S0167-4889(00)00015-X
/ Biochim. Biophys. Acta / Understanding the functions of kinesin-II by Marszalek (2000)10.1002/j.1460-2075.1991.tb04966.x
/ EMBO J. / Efficient gene transfer in C.elegans by Mello (1991)10.1242/jcs.114.20.3749
/ J. Cell Sci. / Centrosome cohesion is regulated by a balance of kinase and phosphatase activities by Meraldi (2001)10.1038/ng996
/ Nat. Genet. / The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin by Mollet (2002)10.1038/88925
/ Nat. Genet. / Identification of the gene that, when mutated, causes the human obesity syndrome BBS4 by Mykytyn (2001)10.1038/ng935
/ Nat. Genet. / Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome by Mykytyn (2002)10.1093/hmg/10.8.865
/ Hum. Mol. Genet. / Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2) by Nishimura (2001)10.1083/jcb.105.5.2279
/ J. Cell Biol. / Cyclic AMP functions as a primary sexual signal in gametes of Chlamydomonas reinhardtii by Pasquale (1987)10.1016/S0962-8924(02)02410-8
/ Trends Cell Biol. / Intraflagellar transport and cilia-dependent diseases by Pazour (2002)10.1016/S0955-0674(02)00012-1
/ Curr. Opin. Cell Biol. / The vertebrate primary cilium is a sensory organelle by Pazour (2003)10.1083/jcb.151.3.709
/ J. Cell Biol. / Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella by Pazour (2000)10.1016/S0960-9822(02)00877-1
/ Curr. Biol. / Polycystin-2 localizes to kidney cilia and the ciliary level is elevated in orpk mice with polycystic kidney disease by Pazour (2002)10.1091/mbc.E02-10-0682
/ Mol. Biol. Cell / A novel Dynein light intermediate chain colocalizes with the retrograde motor for intraflagellar transport at sites of axoneme assembly in chlamydomonas and Mammalian cells by Perrone (2003)10.1242/jcs.00337
/ J. Cell Sci. / Chlamydomonas DIP13 and human NA14 by Pfannenschmid (2003){'key': '10.1016/S0092-8674(04)00450-7_BIB51', 'first-page': '205', 'article-title': 'The autonomy of the centriole', 'volume': '3', 'author': 'Pickett-Heaps', 'year': '1971', 'journal-title': 'Cytobios'}
/ Cytobios / The autonomy of the centriole by Pickett-Heaps (1971)10.1073/pnas.94.9.4457
/ Proc. Natl. Acad. Sci. USA / Transport of a novel complex in the cytoplasmic matrix of Chlamydomonas flagella by Piperno (1997)10.1073/pnas.74.4.1600
/ Proc. Natl. Acad. Sci. USA / Two-dimensional analysis of flagellar proteins from wild-type and paralyzed mutants of Chlamydomonas reinhardtii by Piperno (1977)10.1091/mbc.E02-10-0677
/ Mol. Biol. Cell / XBX-1 encodes a dynein light intermediate chain required for retrograde intraflagellar transport and cilia assembly in Caenorhabditis elegans by Schafer (2003)10.1073/pnas.122243399
/ Proc. Natl. Acad. Sci. USA / Two rhodopsins mediate phototaxis to low- and high-intensity light in Chlamydomonas reinhardtii by Sineshchekov (2002)10.1016/S0378-1119(01)00616-3
/ Gene / A Streptomyces rimosus aphVIII gene coding for a new type phosphotransferase provides stable antibiotic resistance to Chlamydomonas reinhardtii by Sizova (2001)10.1038/79116
/ Nat. Genet. / Mutations in MKKS cause Bardet-Biedl syndrome by Slavotinek (2000){'key': '10.1016/S0092-8674(04)00450-7_BIB58', 'first-page': '457', 'article-title': 'Cystic fibrosis transmembrane conductance regulator (CFTR) and renal function', 'volume': '109', 'author': 'Stanton', 'year': '1997', 'journal-title': 'Wien. Klin. Wochenschr.'}
/ Wien. Klin. Wochenschr. / Cystic fibrosis transmembrane conductance regulator (CFTR) and renal function by Stanton (1997)10.1016/S1097-2765(00)80436-0
/ Mol. Cell / The RFX-type transcription factor DAF-19 regulates sensory neuron cilium formation in C. elegans by Swoboda (2000)10.1101/gad.1053803
/ Genes Dev. / A two-cilia model for vertebrate left-right axis specification by Tabin (2003)10.1083/jcb.145.4.825
/ J. Cell Biol. / Left-right asymmetry and kinesin superfamily protein KIF3A by Takeda (1999)10.1091/mbc.12.3.589
/ Mol. Biol. Cell / Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia by Taulman (2001)10.1097/01.ASN.0000113793.12558.1D
/ J. Am. Soc. Nephrol. / The autosomal recessive polycystic kidney disease protein is localized to primary cilia, with concentration in the basal body area by Wang (2004)10.1002/cne.901600305
/ J. Comp. Neurol. / Electron microscopical reconstruction of the anterior sensory anatomy of the nematode Caenorhabditis elegans by Ward (1975)10.1038/ng833
/ Nat. Genet. / The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein by Ward (2002)10.1098/rstb.1976.0086
/ Philos. Trans. R. Soc. Lond. B Biol. Sci. / The structure of the ventral nerve cord of Caenorhabditis elegans by White (1976)10.1006/dbio.2000.9686
/ Dev. Biol. / CHE-3, a cytosolic dynein heavy chain, is required for sensory cilia structure and function in Caenorhabditis elegans by Wicks (2000)10.1083/jcb.54.3.507
/ J. Cell Biol. / Chlamydomonas flagella. I. Isolation and electrophoretic analysis of microtubules, matrix, membranes, and mastigonemes by Witman (1972)10.1016/S0896-6273(00)00060-X
/ Neuron / Disruption of the type III adenylyl cyclase gene leads to peripheral and behavioral anosmia in transgenic mice by Wong (2000)10.1126/science.290.5494.1159
/ Science / Transgene and transposon silencing in Chlamydomonas reinhardtii by a DEAH-box RNA helicase by Wu-Scharf (2000)10.1097/01.ASN.0000029587.47950.25
/ J. Am. Soc. Nephrol. / The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia by Yoder (2002)10.1002/(SICI)1096-8628(19980806)78:5<461::AID-AJMG12>3.0.CO;2-D
/ Am. J. Med. Genet. / Canadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype by Young (1998)
Dates
Type | When |
---|---|
Created | 21 years, 3 months ago (May 14, 2004, 6:34 a.m.) |
Deposited | 4 years, 2 months ago (June 17, 2021, 11:37 a.m.) |
Indexed | 18 hours, 10 minutes ago (Aug. 23, 2025, 1 a.m.) |
Issued | 21 years, 3 months ago (May 1, 2004) |
Published | 21 years, 3 months ago (May 1, 2004) |
Published Print | 21 years, 3 months ago (May 1, 2004) |
@article{Li_2004, title={Comparative Genomics Identifies a Flagellar and Basal Body Proteome that Includes the BBS5 Human Disease Gene}, volume={117}, ISSN={0092-8674}, url={http://dx.doi.org/10.1016/s0092-8674(04)00450-7}, DOI={10.1016/s0092-8674(04)00450-7}, number={4}, journal={Cell}, publisher={Elsevier BV}, author={Li, Jin Billy and Gerdes, Jantje M and Haycraft, Courtney J and Fan, Yanli and Teslovich, Tanya M and May-Simera, Helen and Li, Haitao and Blacque, Oliver E and Li, Linya and Leitch, Carmen C and Lewis, Richard Allan and Green, Jane S and Parfrey, Patrick S and Leroux, Michel R and Davidson, William S and Beales, Philip L and Guay-Woodford, Lisa M and Yoder, Bradley K and Stormo, Gary D and Katsanis, Nicholas and Dutcher, Susan K}, year={2004}, month=may, pages={541–552} }