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    Results: 1 to 20 of 46

    1.

    Novel homozygous mutations in the genes ARL6 and BBS10 underlying Bardet-Biedl syndrome.

    Khan S, Ullah I, Irfanullah, Touseef M, Basit S, Khan MN, Ahmad W.

    Gene. 2013 Feb 15;515(1):84-8. doi: 10.1016/j.gene.2012.11.023. Epub 2012 Dec 6.

    PMID:
    23219996
    [PubMed - indexed for MEDLINE]
    2.

    BBS1 mutations in a wide spectrum of phenotypes ranging from nonsyndromic retinitis pigmentosa to Bardet-Biedl syndrome.

    Estrada-Cuzcano A, Koenekoop RK, Senechal A, De Baere EB, de Ravel T, Banfi S, Kohl S, Ayuso C, Sharon D, Hoyng CB, Hamel CP, Leroy BP, Ziviello C, Lopez I, Bazinet A, Wissinger B, Sliesoraityte I, Avila-Fernandez A, Littink KW, Vingolo EM, Signorini S, Banin E, Mizrahi-Meissonnier L, Zrenner E, Kellner U, Collin RW, den Hollander AI, Cremers FP, Klevering BJ.

    Arch Ophthalmol. 2012 Nov;130(11):1425-32. doi: 10.1001/archophthalmol.2012.2434.

    PMID:
    23143442
    [PubMed - indexed for MEDLINE]
    3.

    Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström syndromes.

    Redin C, Le Gras S, Mhamdi O, Geoffroy V, Stoetzel C, Vincent MC, Chiurazzi P, Lacombe D, Ouertani I, Petit F, Till M, Verloes A, Jost B, Chaabouni HB, Dollfus H, Mandel JL, Muller J.

    J Med Genet. 2012 Aug;49(8):502-12. doi: 10.1136/jmedgenet-2012-100875. Epub 2012 Jul 7.

    PMID:
    22773737
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    4.

    A role for the vesicle-associated tubulin binding protein ARL6 (BBS3) in flagellum extension in Trypanosoma brucei.

    Price HP, Hodgkinson MR, Wright MH, Tate EW, Smith BA, Carrington M, Stark M, Smith DF.

    Biochim Biophys Acta. 2012 Jul;1823(7):1178-91. doi: 10.1016/j.bbamcr.2012.05.007. Epub 2012 May 15.

    PMID:
    22609302
    [PubMed - indexed for MEDLINE]
    5.

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

    Zhang Q, Yu D, Seo S, Stone EM, Sheffield VC.

    J Biol Chem. 2012 Jun 8;287(24):20625-35. doi: 10.1074/jbc.M112.341487. Epub 2012 Apr 12.

    PMID:
    22500027
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    6.

    Genotype-phenotype correlations in Bardet-Biedl syndrome.

    Daniels AB, Sandberg MA, Chen J, Weigel-DiFranco C, Fielding Hejtmancic J, Berson EL.

    Arch Ophthalmol. 2012 Jul 1;130(7):901-7. doi: 10.1001/archophthalmol.2012.89.

    PMID:
    22410627
    [PubMed - indexed for MEDLINE]
    7.

    Differentiating Alström from Bardet-Biedl syndrome (BBS) using systematic ciliopathy genes sequencing.

    Aliferis K, Hellé S, Gyapay G, Duchatelet S, Stoetzel C, Mandel JL, Dollfus H.

    Ophthalmic Genet. 2012 Mar;33(1):18-22. doi: 10.3109/13816810.2011.620055. Epub 2011 Oct 17.

    PMID:
    22004009
    [PubMed - indexed for MEDLINE]
    8.

    U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutation.

    Schmid F, Glaus E, Barthelmes D, Fliegauf M, Gaspar H, Nürnberg G, Nürnberg P, Omran H, Berger W, Neidhardt J.

    Hum Mutat. 2011 Jul;32(7):815-24. doi: 10.1002/humu.21509.

    PMID:
    21520335
    [PubMed - indexed for MEDLINE]
    9.

    DISC1-dependent switch from progenitor proliferation to migration in the developing cortex.

    Ishizuka K, Kamiya A, Oh EC, Kanki H, Seshadri S, Robinson JF, Murdoch H, Dunlop AJ, Kubo K, Furukori K, Huang B, Zeledon M, Hayashi-Takagi A, Okano H, Nakajima K, Houslay MD, Katsanis N, Sawa A.

    Nature. 2011 May 5;473(7345):92-6. doi: 10.1038/nature09859. Epub 2011 Apr 6.

    PMID:
    21471969
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    10.

    BBS mutational analysis: a strategic approach.

    Billingsley G, Deveault C, Héon E.

    Ophthalmic Genet. 2011 Sep;32(3):181-7. doi: 10.3109/13816810.2011.567319. Epub 2011 Apr 4.

    PMID:
    21463199
    [PubMed - indexed for MEDLINE]
    11.

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

    Feuillan PP, Ng D, Han JC, Sapp JC, Wetsch K, Spaulding E, Zheng YC, Caruso RC, Brooks BP, Johnston JJ, Yanovski JA, Biesecker LG.

    J Clin Endocrinol Metab. 2011 Mar;96(3):E528-35. doi: 10.1210/jc.2010-2290. Epub 2011 Jan 5.

    PMID:
    21209035
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    12.

    DJ-1 enhances cell survival through the binding of Cezanne, a negative regulator of NF-kappaB.

    McNally RS, Davis BK, Clements CM, Accavitti-Loper MA, Mak TW, Ting JP.

    J Biol Chem. 2011 Feb 11;286(6):4098-106. doi: 10.1074/jbc.M110.147371. Epub 2010 Nov 19.

    PMID:
    21097510
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    13.

    Mutation analysis in Bardet-Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individuals.

    Janssen S, Ramaswami G, Davis EE, Hurd T, Airik R, Kasanuki JM, Van Der Kraak L, Allen SJ, Beales PL, Katsanis N, Otto EA, Hildebrandt F.

    Hum Genet. 2011 Jan;129(1):79-90. doi: 10.1007/s00439-010-0902-8. Epub 2010 Oct 30.

    PMID:
    21052717
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    14.

    BBS10 mutations are common in 'Meckel'-type cystic kidneys.

    Putoux A, Mougou-Zerelli S, Thomas S, Elkhartoufi N, Audollent S, Le Merrer M, Lachmeijer A, Sigaudy S, Buenerd A, Fernandez C, Delezoide AL, Gubler MC, Salomon R, Saad A, Cordier MP, Vekemans M, Bouvier R, Attie-Bitach T.

    J Med Genet. 2010 Dec;47(12):848-52. doi: 10.1136/jmg.2010.079392. Epub 2010 Aug 30.

    PMID:
    20805367
    [PubMed - indexed for MEDLINE]
    15.

    Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population.

    Billingsley G, Bin J, Fieggen KJ, Duncan JL, Gerth C, Ogata K, Wodak SS, Traboulsi EI, Fishman GA, Paterson A, Chitayat D, Knueppel T, Millán JM, Mitchell GA, Deveault C, Héon E.

    J Med Genet. 2010 Jul;47(7):453-63. doi: 10.1136/jmg.2009.073205. Epub 2010 May 14.

    PMID:
    20472660
    [PubMed - indexed for MEDLINE]
    16.

    Identification of 28 novel mutations in the Bardet-Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease.

    Muller J, Stoetzel C, Vincent MC, Leitch CC, Laurier V, Danse JM, Hellé S, Marion V, Bennouna-Greene V, Vicaire S, Megarbane A, Kaplan J, Drouin-Garraud V, Hamdani M, Sigaudy S, Francannet C, Roume J, Bitoun P, Goldenberg A, Philip N, Odent S, Green J, Cossée M, Davis EE, Katsanis N, Bonneau D, Verloes A, Poch O, Mandel JL, Dollfus H.

    Hum Genet. 2010 Mar;127(5):583-93. doi: 10.1007/s00439-010-0804-9. Epub 2010 Feb 23.

    PMID:
    20177705
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    17.

    New mutations in BBS genes in small consanguineous families with Bardet-Biedl syndrome: detection of candidate regions by homozygosity mapping.

    Pereiro I, Valverde D, Piñeiro-Gallego T, Baiget M, Borrego S, Ayuso C, Searby C, Nishimura D.

    Mol Vis. 2010 Feb 1;16:137-43.

    PMID:
    20142850
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    18.

    Bardet-Biedl syndrome in Denmark--report of 13 novel sequence variations in six genes.

    Hjortshøj TD, Grønskov K, Philp AR, Nishimura DY, Riise R, Sheffield VC, Rosenberg T, Brøndum-Nielsen K.

    Hum Mutat. 2010 Apr;31(4):429-36. doi: 10.1002/humu.21204.

    PMID:
    20120035
    [PubMed - indexed for MEDLINE]
    19.

    BBS7 and TTC8 (BBS8) mutations play a minor role in the mutational load of Bardet-Biedl syndrome in a multiethnic population.

    Bin J, Madhavan J, Ferrini W, Mok CA, Billingsley G, Héon E.

    Hum Mutat. 2009 Jul;30(7):E737-46. doi: 10.1002/humu.21040.

    PMID:
    19402160
    [PubMed - indexed for MEDLINE]
    20.

    Antibiotic susceptibility patterns in Helicobacter pylori strains from patients with upper gastrointestinal pathology in western Nigeria.

    Oyedeji KS, Smith SI, Coker AO, Arigbabu AO.

    Br J Biomed Sci. 2009;66(1):10-3.

    PMID:
    19348120
    [PubMed - indexed for MEDLINE]

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