Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 104

1.

Ofd1 is required in limb bud patterning and endochondral bone development.

Bimonte S, De Angelis A, Quagliata L, Giusti F, Tammaro R, Dallai R, Ascenzi MG, Diez-Roux G, Franco B.

Dev Biol. 2011 Jan 15;349(2):179-91. doi: 10.1016/j.ydbio.2010.09.020. Epub 2010 Oct 14.

2.

The primary cilium in different tissues-lessons from patients and animal models.

D'Angelo A, Franco B.

Pediatr Nephrol. 2011 May;26(5):655-62. doi: 10.1007/s00467-010-1650-7. Epub 2010 Oct 3. Review.

PMID:
20890766
3.

Quantitative analyses link modulation of sonic hedgehog signaling to continuous variation in facial growth and shape.

Young NM, Chong HJ, Hu D, Hallgrímsson B, Marcucio RS.

Development. 2010 Oct;137(20):3405-9. doi: 10.1242/dev.052340. Epub 2010 Sep 8.

4.

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

Jin H, White SR, Shida T, Schulz S, Aguiar M, Gygi SP, Bazan JF, Nachury MV.

Cell. 2010 Jun 25;141(7):1208-19. doi: 10.1016/j.cell.2010.05.015.

5.

Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.

Walczak-Sztulpa J, Eggenschwiler J, Osborn D, Brown DA, Emma F, Klingenberg C, Hennekam RC, Torre G, Garshasbi M, Tzschach A, Szczepanska M, Krawczynski M, Zachwieja J, Zwolinska D, Beales PL, Ropers HH, Latos-Bielenska A, Kuss AW.

Am J Hum Genet. 2010 Jun 11;86(6):949-56. doi: 10.1016/j.ajhg.2010.04.012. Epub 2010 May 20.

6.

The primary cilium: a signalling centre during vertebrate development.

Goetz SC, Anderson KV.

Nat Rev Genet. 2010 May;11(5):331-44. doi: 10.1038/nrg2774. Review.

7.

Isolation of primary cilia for morphological analysis.

Huang B, Masyuk T, LaRusso N.

Methods Cell Biol. 2009;94:103-15. doi: 10.1016/S0091-679X(08)94005-X. Epub 2009 Dec 23.

PMID:
20362087
8.

The output of Hedgehog signaling is controlled by the dynamic association between Suppressor of Fused and the Gli proteins.

Humke EW, Dorn KV, Milenkovic L, Scott MP, Rohatgi R.

Genes Dev. 2010 Apr 1;24(7):670-82. doi: 10.1101/gad.1902910.

9.

Functional modules, mutational load and human genetic disease.

Zaghloul NA, Katsanis N.

Trends Genet. 2010 Apr;26(4):168-76. doi: 10.1016/j.tig.2010.01.006. Epub 2010 Mar 11. Review.

10.

Directional cell migration and chemotaxis in wound healing response to PDGF-AA are coordinated by the primary cilium in fibroblasts.

Schneider L, Cammer M, Lehman J, Nielsen SK, Guerra CF, Veland IR, Stock C, Hoffmann EK, Yoder BK, Schwab A, Satir P, Christensen ST.

Cell Physiol Biochem. 2010;25(2-3):279-92. doi: 10.1159/000276562. Epub 2010 Jan 12.

11.

A primary cilia-dependent etiology for midline facial disorders.

Brugmann SA, Allen NC, James AW, Mekonnen Z, Madan E, Helms JA.

Hum Mol Genet. 2010 Apr 15;19(8):1577-92. doi: 10.1093/hmg/ddq030. Epub 2010 Jan 27.

12.

Making sense of cilia in disease: the human ciliopathies.

Baker K, Beales PL.

Am J Med Genet C Semin Med Genet. 2009 Nov 15;151C(4):281-95. doi: 10.1002/ajmg.c.30231. Review.

PMID:
19876933
13.

A mouse model for Meckel syndrome reveals Mks1 is required for ciliogenesis and Hedgehog signaling.

Weatherbee SD, Niswander LA, Anderson KV.

Hum Mol Genet. 2009 Dec 1;18(23):4565-75. doi: 10.1093/hmg/ddp422. Epub 2009 Sep 22.

14.

Cranioectodermal dysplasia: a probable ciliopathy.

Konstantinidou AE, Fryssira H, Sifakis S, Karadimas C, Kaminopetros P, Agrogiannis G, Velonis S, Nikkels PG, Patsouris E.

Am J Med Genet A. 2009 Oct;149A(10):2206-11. doi: 10.1002/ajmg.a.33013.

PMID:
19760621
15.

Primary cilia are not required for normal canonical Wnt signaling in the mouse embryo.

Ocbina PJ, Tuson M, Anderson KV.

PLoS One. 2009 Aug 31;4(8):e6839. doi: 10.1371/journal.pone.0006839.

16.

Lrp6-mediated canonical Wnt signaling is required for lip formation and fusion.

Song L, Li Y, Wang K, Wang YZ, Molotkov A, Gao L, Zhao T, Yamagami T, Wang Y, Gan Q, Pleasure DE, Zhou CJ.

Development. 2009 Sep;136(18):3161-71. doi: 10.1242/dev.037440.

17.

Dampened Hedgehog signaling but normal Wnt signaling in zebrafish without cilia.

Huang P, Schier AF.

Development. 2009 Sep;136(18):3089-98. doi: 10.1242/dev.041343.

18.

Zebrafish ift57, ift88, and ift172 intraflagellar transport mutants disrupt cilia but do not affect hedgehog signaling.

Lunt SC, Haynes T, Perkins BD.

Dev Dyn. 2009 Jul;238(7):1744-59. doi: 10.1002/dvdy.21999.

19.

A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies.

Khanna H, Davis EE, Murga-Zamalloa CA, Estrada-Cuzcano A, Lopez I, den Hollander AI, Zonneveld MN, Othman MI, Waseem N, Chakarova CF, Maubaret C, Diaz-Font A, MacDonald I, Muzny DM, Wheeler DA, Morgan M, Lewis LR, Logan CV, Tan PL, Beer MA, Inglehearn CF, Lewis RA, Jacobson SG, Bergmann C, Beales PL, Attié-Bitach T, Johnson CA, Otto EA, Bhattacharya SS, Hildebrandt F, Gibbs RA, Koenekoop RK, Swaroop A, Katsanis N.

Nat Genet. 2009 Jun;41(6):739-45. doi: 10.1038/ng.366. Epub 2009 May 10.

20.

The vertebrate primary cilium in development, homeostasis, and disease.

Gerdes JM, Davis EE, Katsanis N.

Cell. 2009 Apr 3;137(1):32-45. doi: 10.1016/j.cell.2009.03.023. Review.

Supplemental Content

Support Center