Katsanis N - Search Results

1

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. Among authors: katsanis n. 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.

2

MKKS/BBS6, a divergent chaperonin-like protein linked to the obesity disorder Bardet-Biedl syndrome, is a novel centrosomal component required for cytokinesis.

Kim JC, Ou YY, Badano JL, Esmail MA, Leitch CC, Fiedrich E, Beales PL, Archibald JM, Katsanis N, Rattner JB, Leroux MR. Kim JC, et al. Among authors: katsanis n. J Cell Sci. 2005 Mar 1;118(Pt 5):1007-20. doi: 10.1242/jcs.01676. J Cell Sci. 2005. PMID: 15731008

3

Life without centrioles: cilia in the spotlight.

Badano JL, Katsanis N. Badano JL, et al. Among authors: katsanis n. Cell. 2006 Jun 30;125(7):1228-30. doi: 10.1016/j.cell.2006.06.013. Cell. 2006. PMID: 16814708 Free article.

4

Cystic diseases of the kidney: ciliary dysfunction and cystogenic mechanisms.

Gascue C, Katsanis N, Badano JL. Gascue C, et al. Among authors: katsanis n. Pediatr Nephrol. 2011 Aug;26(8):1181-95. doi: 10.1007/s00467-010-1697-5. Epub 2010 Nov 27. Pediatr Nephrol. 2011. PMID: 21113628 Free PMC article. Review.

5

The Bardet-Biedl syndrome-related protein CCDC28B modulates mTORC2 function and interacts with SIN1 to control cilia length independently of the mTOR complex.

Cardenas-Rodriguez M, Irigoín F, Osborn DP, Gascue C, Katsanis N, Beales PL, Badano JL. Cardenas-Rodriguez M, et al. Among authors: katsanis n. Hum Mol Genet. 2013 Oct 15;22(20):4031-42. doi: 10.1093/hmg/ddt253. Epub 2013 May 31. Hum Mol Genet. 2013. PMID: 23727834 Free PMC article.

6

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

Katsanis N, Ansley SJ, Badano JL, Eichers ER, Lewis RA, Hoskins BE, Scambler PJ, Davidson WS, Beales PL, Lupski JR. Katsanis N, et al. Science. 2001 Sep 21;293(5538):2256-9. doi: 10.1126/science.1063525. Science. 2001. PMID: 11567139

7

Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet-Biedl syndrome.

Zaghloul NA, Liu Y, Gerdes JM, Gascue C, Oh EC, Leitch CC, Bromberg Y, Binkley J, Leibel RL, Sidow A, Badano JL, Katsanis N. Zaghloul NA, et al. Among authors: katsanis n. Proc Natl Acad Sci U S A. 2010 Jun 8;107(23):10602-7. doi: 10.1073/pnas.1000219107. Epub 2010 May 24. Proc Natl Acad Sci U S A. 2010. PMID: 20498079 Free PMC article.

8

BBS4 regulates the expression and secretion of FSTL1, a protein that participates in ciliogenesis and the differentiation of 3T3-L1.

Prieto-Echagüe V, Lodh S, Colman L, Bobba N, Santos L, Katsanis N, Escande C, Zaghloul NA, Badano JL. Prieto-Echagüe V, et al. Among authors: katsanis n. Sci Rep. 2017 Aug 29;7(1):9765. doi: 10.1038/s41598-017-10330-0. Sci Rep. 2017. PMID: 28852127 Free PMC article.

9

Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2.

Badano JL, Ansley SJ, Leitch CC, Lewis RA, Lupski JR, Katsanis N. Badano JL, et al. Among authors: katsanis n. Am J Hum Genet. 2003 Mar;72(3):650-8. doi: 10.1086/368204. Epub 2003 Feb 3. Am J Hum Genet. 2003. PMID: 12567324 Free PMC article.

10

Genetic interaction of BBS1 mutations with alleles at other BBS loci can result in non-Mendelian Bardet-Biedl syndrome.

Beales PL, Badano JL, Ross AJ, Ansley SJ, Hoskins BE, Kirsten B, Mein CA, Froguel P, Scambler PJ, Lewis RA, Lupski JR, Katsanis N. Beales PL, et al. Among authors: katsanis n. Am J Hum Genet. 2003 May;72(5):1187-99. doi: 10.1086/375178. Epub 2003 Apr 3. Am J Hum Genet. 2003. PMID: 12677556 Free PMC article.

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