Depreux FF - Search Results

1

Rescue of Outer Hair Cells with Antisense Oligonucleotides in Usher Mice Is Dependent on Age of Treatment.

Ponnath A, Depreux FF, Jodelka FM, Rigo F, Farris HE, Hastings ML, Lentz JJ. Ponnath A, et al. Among authors: depreux ff. J Assoc Res Otolaryngol. 2018 Feb;19(1):1-16. doi: 10.1007/s10162-017-0640-x. Epub 2017 Oct 12. J Assoc Res Otolaryngol. 2018. PMID: 29027038 Free PMC article.

2

Antisense oligonucleotides delivered to the amniotic cavity in utero modulate gene expression in the postnatal mouse.

Depreux FF, Wang L, Jiang H, Jodelka FM, Rosencrans RF, Rigo F, Lentz JJ, Brigande JV, Hastings ML. Depreux FF, et al. Nucleic Acids Res. 2016 Nov 16;44(20):9519-9529. doi: 10.1093/nar/gkw867. Epub 2016 Sep 28. Nucleic Acids Res. 2016. PMID: 27683224 Free PMC article.

3

Rescue of peripheral vestibular function in Usher syndrome mice using a splice-switching antisense oligonucleotide.

Vijayakumar S, Depreux FF, Jodelka FM, Lentz JJ, Rigo F, Jones TA, Hastings ML. Vijayakumar S, et al. Among authors: depreux ff. Hum Mol Genet. 2017 Sep 15;26(18):3482-3494. doi: 10.1093/hmg/ddx234. Hum Mol Genet. 2017. PMID: 28633508 Free PMC article.

4

Antisense oligonucleotide therapy rescues disruptions in organization of exploratory movements associated with Usher syndrome type 1C in mice.

Donaldson TN, Jennings KT, Cherep LA, McNeela AM, Depreux FF, Jodelka FM, Hastings ML, Wallace DG. Donaldson TN, et al. Among authors: depreux ff. Behav Brain Res. 2018 Feb 15;338:76-87. doi: 10.1016/j.bbr.2017.10.012. Epub 2017 Oct 14. Behav Brain Res. 2018. PMID: 29037661 Free PMC article.

5

Gene expression, chromosome position and lamin A/C mutations.

Puckelwartz MJ, Depreux FF, McNally EM. Puckelwartz MJ, et al. Among authors: depreux ff. Nucleus. 2011 May-Jun;2(3):162-7. doi: 10.4161/nucl.2.3.16003. Nucleus. 2011. PMID: 21818408 Free PMC article.

6

Hearing differences in Hartley guinea pig stocks from two breeders.

Whitlon DS, Young H, Barna M, Depreux F, Richter CP. Whitlon DS, et al. Hear Res. 2019 Aug;379:69-78. doi: 10.1016/j.heares.2019.04.016. Epub 2019 May 1. Hear Res. 2019. PMID: 31103815

7

Disruption of the lamin A and matrin-3 interaction by myopathic LMNA mutations.

Depreux FF, Puckelwartz MJ, Augustynowicz A, Wolfgeher D, Labno CM, Pierre-Louis D, Cicka D, Kron SJ, Holaska J, McNally EM. Depreux FF, et al. Hum Mol Genet. 2015 Aug 1;24(15):4284-95. doi: 10.1093/hmg/ddv160. Epub 2015 May 6. Hum Mol Genet. 2015. PMID: 25948554 Free PMC article.

8

Nesprin-1 mutations in human and murine cardiomyopathy.

Puckelwartz MJ, Kessler EJ, Kim G, Dewitt MM, Zhang Y, Earley JU, Depreux FF, Holaska J, Mewborn SK, Pytel P, McNally EM. Puckelwartz MJ, et al. Among authors: depreux ff. J Mol Cell Cardiol. 2010 Apr;48(4):600-8. doi: 10.1016/j.yjmcc.2009.11.006. Epub 2009 Nov 24. J Mol Cell Cardiol. 2010. PMID: 19944109 Free PMC article.

9

Sex Genotyping of Archival Fixed and Immunolabeled Guinea Pig Cochleas.

Depreux FF, Czech L, Whitlon DS. Depreux FF, et al. Sci Rep. 2018 Mar 26;8(1):5156. doi: 10.1038/s41598-018-23491-3. Sci Rep. 2018. PMID: 29581456 Free PMC article.

10

Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss.

Schönberger J, Wang L, Shin JT, Kim SD, Depreux FF, Zhu H, Zon L, Pizard A, Kim JB, Macrae CA, Mungall AJ, Seidman JG, Seidman CE. Schönberger J, et al. Among authors: depreux ff. Nat Genet. 2005 Apr;37(4):418-22. doi: 10.1038/ng1527. Epub 2005 Feb 27. Nat Genet. 2005. PMID: 15735644

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