Katsanis N - Search Results

1

Small molecule inhibition of RAS/MAPK signaling ameliorates developmental pathologies of Kabuki Syndrome.

Tsai IC, McKnight K, McKinstry SU, Maynard AT, Tan PL, Golzio C, White CT, Price DJ, Davis EE, Amrine-Madsen H, Katsanis N. Tsai IC, et al. Among authors: katsanis n. Sci Rep. 2018 Jul 17;8(1):10779. doi: 10.1038/s41598-018-28709-y. Sci Rep. 2018. PMID: 30018450 Free PMC article.

2

In vivo modeling of the morbid human genome using Danio rerio.

Niederriter AR, Davis EE, Golzio C, Oh EC, Tsai IC, Katsanis N. Niederriter AR, et al. Among authors: katsanis n. J Vis Exp. 2013 Aug 24;(78):e50338. doi: 10.3791/50338. J Vis Exp. 2013. PMID: 23995499 Free PMC article.

3

Dissecting intraflagellar transport, one molecule at a time.

Davis EE, Katsanis N. Davis EE, et al. Among authors: katsanis n. Dev Cell. 2014 Nov 10;31(3):263-264. doi: 10.1016/j.devcel.2014.10.021. Epub 2014 Nov 10. Dev Cell. 2014. PMID: 25453827 Free article.

4

Unique among ciliopathies: primary ciliary dyskinesia, a motile cilia disorder.

Praveen K, Davis EE, Katsanis N. Praveen K, et al. Among authors: katsanis n. F1000Prime Rep. 2015 Mar 10;7:36. doi: 10.12703/P7-36. eCollection 2015. F1000Prime Rep. 2015. PMID: 25926987 Free PMC article. Review.

5

Genome-wide suppressor screen identifies USP35/USP38 as therapeutic candidates for ciliopathies.

Tsai IC, Adams KA, Tzeng JA, Shennib O, Tan PL, Katsanis N. Tsai IC, et al. Among authors: katsanis n. JCI Insight. 2019 Nov 14;4(22):e130516. doi: 10.1172/jci.insight.130516. JCI Insight. 2019. PMID: 31723061 Free PMC article.

6

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

Davis EE, Katsanis N. Davis EE, et al. Among authors: katsanis n. 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.

7

Genetic architecture of reciprocal CNVs.

Golzio C, Katsanis N. Golzio C, et al. Among authors: katsanis n. Curr Opin Genet Dev. 2013 Jun;23(3):240-8. doi: 10.1016/j.gde.2013.04.013. Epub 2013 Jun 5. Curr Opin Genet Dev. 2013. PMID: 23747035 Free PMC article. Review.

8

Interpreting human genetic variation with in vivo zebrafish assays.

Davis EE, Frangakis S, Katsanis N. Davis EE, et al. Among authors: katsanis n. Biochim Biophys Acta. 2014 Oct;1842(10):1960-1970. doi: 10.1016/j.bbadis.2014.05.024. Epub 2014 Jun 2. Biochim Biophys Acta. 2014. PMID: 24887202 Free PMC article. Review.

9

A novel ribosomopathy caused by dysfunction of RPL10 disrupts neurodevelopment and causes X-linked microcephaly in humans.

Brooks SS, Wall AL, Golzio C, Reid DW, Kondyles A, Willer JR, Botti C, Nicchitta CV, Katsanis N, Davis EE. Brooks SS, et al. Among authors: katsanis n. Genetics. 2014 Oct;198(2):723-33. doi: 10.1534/genetics.114.168211. Genetics. 2014. PMID: 25316788 Free PMC article.

10

Mitochondrial Copy Number as a Biomarker for Autism?

Golzio C, Katsanis N. Golzio C, et al. Among authors: katsanis n. Pediatrics. 2016 Apr;137(4):e20160049. doi: 10.1542/peds.2016-0049. Epub 2016 Mar 31. Pediatrics. 2016. PMID: 27033113 Free PMC article. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

311 results

Search Page

Filters