R01HD04260/HD/NICHD NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2006	2
2008	2
2009	9
2010	8
2011	5
2012	5
2013	4
2014	2
2015	1
2024	0

1

Ciliary function and Wnt signal modulation.

Gerdes JM, Katsanis N. Gerdes JM, et al. Curr Top Dev Biol. 2008;85:175-95. doi: 10.1016/S0070-2153(08)00807-7. Curr Top Dev Biol. 2008. PMID: 19147006 Review.

2

Thermosensory and mechanosensory perception in human genetic disease.

Tan PL, Katsanis N. Tan PL, et al. Hum Mol Genet. 2009 Oct 15;18(R2):R146-55. doi: 10.1093/hmg/ddp412. Hum Mol Genet. 2009. PMID: 19808790 Free PMC article. Review.

3

Context-dependent regulation of Wnt signaling through the primary cilium.

Oh EC, Katsanis N. Oh EC, et al. J Am Soc Nephrol. 2013 Jan;24(1):10-8. doi: 10.1681/ASN.2012050526. Epub 2012 Nov 2. J Am Soc Nephrol. 2013. PMID: 23123400 Review.

4

The ciliopathies: an emerging class of human genetic disorders.

Badano JL, Mitsuma N, Beales PL, Katsanis N. Badano JL, et al. Annu Rev Genomics Hum Genet. 2006;7:125-48. doi: 10.1146/annurev.genom.7.080505.115610. Annu Rev Genomics Hum Genet. 2006. PMID: 16722803 Review.

5

Functional modules, mutational load and human genetic disease.

Zaghloul NA, Katsanis N. Zaghloul NA, et al. Trends Genet. 2010 Apr;26(4):168-76. doi: 10.1016/j.tig.2010.01.006. Epub 2010 Mar 11. Trends Genet. 2010. PMID: 20226561 Free PMC article. Review.

6

The emerging complexity of the vertebrate cilium: new functional roles for an ancient organelle.

Davis EE, Brueckner M, Katsanis N. Davis EE, et al. Dev Cell. 2006 Jul;11(1):9-19. doi: 10.1016/j.devcel.2006.06.009. Dev Cell. 2006. PMID: 16824949 Free article. Review.

7

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

Gerdes JM, Davis EE, Katsanis N. Gerdes JM, et al. Cell. 2009 Apr 3;137(1):32-45. doi: 10.1016/j.cell.2009.03.023. Cell. 2009. PMID: 19345185 Free PMC article. Review.

8

The ciliopathies: a transitional model into systems biology of human genetic disease.

Davis EE, Katsanis N. Davis EE, et al. Curr Opin Genet Dev. 2012 Jun;22(3):290-303. doi: 10.1016/j.gde.2012.04.006. Epub 2012 May 23. Curr Opin Genet Dev. 2012. PMID: 22632799 Free PMC article. Review.

9

Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophy.

Riazuddin SA, Vithana EN, Seet LF, Liu Y, Al-Saif A, Koh LW, Heng YM, Aung T, Meadows DN, Eghrari AO, Gottsch JD, Katsanis N. Riazuddin SA, et al. Hum Mutat. 2010 Nov;31(11):1261-8. doi: 10.1002/humu.21356. Epub 2010 Oct 14. Hum Mutat. 2010. PMID: 20848555 Free PMC article.

10

Direct role of Bardet-Biedl syndrome proteins in transcriptional regulation.

Gascue C, Tan PL, Cardenas-Rodriguez M, Libisch G, Fernandez-Calero T, Liu YP, Astrada S, Robello C, Naya H, Katsanis N, Badano JL. Gascue C, et al. J Cell Sci. 2012 Jan 15;125(Pt 2):362-75. doi: 10.1242/jcs.089375. Epub 2012 Feb 2. J Cell Sci. 2012. PMID: 22302990 Free PMC article.

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