Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 18

1.

Protein coding mitochondrial-targeted RNAs rescue mitochondrial disease in vivo.

Markantone DM, Towheed A, Crain AT, Collins JM, Celotto AM, Palladino MJ.

Neurobiol Dis. 2018 Sep;117:203-210. doi: 10.1016/j.nbd.2018.06.009. Epub 2018 Jun 13.

2.

A conserved polybasic domain mediates plasma membrane targeting of Lgl and its regulation by hypoxia.

Dong W, Zhang X, Liu W, Chen YJ, Huang J, Austin E, Celotto AM, Jiang WZ, Palladino MJ, Jiang Y, Hammond GR, Hong Y.

J Cell Biol. 2015 Oct 26;211(2):273-86. doi: 10.1083/jcb.201503067. Epub 2015 Oct 19.

3.

Small mitochondrial-targeted RNAs modulate endogenous mitochondrial protein expression in vivo.

Towheed A, Markantone DM, Crain AT, Celotto AM, Palladino MJ.

Neurobiol Dis. 2014 Sep;69:15-22. doi: 10.1016/j.nbd.2014.04.017. Epub 2014 May 5.

4.

Evidence of a triosephosphate isomerase non-catalytic function crucial to behavior and longevity.

Roland BP, Stuchul KA, Larsen SB, Amrich CG, Vandemark AP, Celotto AM, Palladino MJ.

J Cell Sci. 2013 Jul 15;126(Pt 14):3151-8. doi: 10.1242/jcs.124586. Epub 2013 May 2.

5.

A novel Drosophila SOD2 mutant demonstrates a role for mitochondrial ROS in neurodevelopment and disease.

Celotto AM, Liu Z, Vandemark AP, Palladino MJ.

Brain Behav. 2012 Jul;2(4):424-34. doi: 10.1002/brb3.73. Epub 2012 Jun 25.

6.

Modes of metabolic compensation during mitochondrial disease using the Drosophila model of ATP6 dysfunction.

Celotto AM, Chiu WK, Van Voorhies W, Palladino MJ.

PLoS One. 2011;6(10):e25823. doi: 10.1371/journal.pone.0025823. Epub 2011 Oct 3.

7.

Genetically encoded redox sensor identifies the role of ROS in degenerative and mitochondrial disease pathogenesis.

Liu Z, Celotto AM, Romero G, Wipf P, Palladino MJ.

Neurobiol Dis. 2012 Jan;45(1):362-8. doi: 10.1016/j.nbd.2011.08.022. Epub 2011 Aug 25.

8.

Degradation of functional triose phosphate isomerase protein underlies sugarkill pathology.

Seigle JL, Celotto AM, Palladino MJ.

Genetics. 2008 Jun;179(2):855-62. doi: 10.1534/genetics.108.087551. Epub 2008 May 5.

9.

Drosophila model of human inherited triosephosphate isomerase deficiency glycolytic enzymopathy.

Celotto AM, Frank AC, Seigle JL, Palladino MJ.

Genetics. 2006 Nov;174(3):1237-46. Epub 2006 Sep 15.

10.

Mitochondrial encephalomyopathy in Drosophila.

Celotto AM, Frank AC, McGrath SW, Fergestad T, Van Voorhies WA, Buttle KF, Mannella CA, Palladino MJ.

J Neurosci. 2006 Jan 18;26(3):810-20.

11.

Drosophila: a "model" model system to study neurodegeneration.

Celotto AM, Palladino MJ.

Mol Interv. 2005 Oct;5(5):292-303. Review.

PMID:
16249525
12.
13.

Identification of alternative splicing regulators by RNA interference in Drosophila.

Park JW, Parisky K, Celotto AM, Reenan RA, Graveley BR.

Proc Natl Acad Sci U S A. 2004 Nov 9;101(45):15974-9. Epub 2004 Oct 18.

14.

RNA interference of mRNA processing factors in Drosophila S2 cells.

Celotto AM, Graveley BR.

Methods Mol Biol. 2004;257:245-54.

16.

Arginine/serine repeats are sufficient to constitute a splicing activation domain.

Philipps D, Celotto AM, Wang QQ, Tarng RS, Graveley BR.

Nucleic Acids Res. 2003 Nov 15;31(22):6502-8.

17.
18.

Supplemental Content

Loading ...
Support Center