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Title:	Loss of Omi mitochondrial protease activity causes the neuromuscular disorder of mnd2 mutant mice
Source:	Nature [0028-0836] Jones, Julie yr:2003

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description	1.	Takahashi, Y. "Accumulation of HtrA2/Omi in neuronal and glial inclusions in brains with alpha-synucleinopathies." Journal of Neuropathology and Experimental Neurology 67.10 (2008): 984-993.
description	2.	Bogaerts, V. "Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease." Human Mutation 29.6 (2008): 832-840.
description	3.	Liu, Ming-Jie J. "Transgenic mice with neuron-specific overexpression of HtrA2/Omi suggest a neuroprotective role for HtrA2/Omi." Biochemical and biophysical research communications 362.2 (2007): 295-300.
description	4.	Orrenius, S. "Reactive Oxygen Species in Mitochondria-Mediated Cell Death." Drug metabolism reviews 39.2 (2007): 443-455.
description	5.	Moore, Chris B B. "NLRX1 is a regulator of mitochondrial antiviral immunity." Nature 451.7178 (2007): 573-7.
description	6.	Orrenius S, S. "Mitochondrial oxidative stress: implications for cell death." Annual Review Of Pharmacology And Toxicology 47.1 (2007): 143-83.
description	7.	Park, H. "The serine protease HtrA2/Omi cleaves Parkin and irreversibly inactivates its E3 ubiquitin ligase activity." Biochemical and biophysical research communications 387.3 (2009): 537-542.
description	8.	Gandhi, A. "PINK1-associated Parkinson's disease is caused by neuronal vulnerability to calcium-induced cell death." Molecular cell 33.5 (2009): 627-38.
description	9.	Ehrmann, M. "A temperature-dependent switch from chaperone to protease in a widely conserved heat shock protein." Cell 97.3 (1999): 339-47.
description	10.	Ding, X. "Enhanced HtrA2/Omi Expression in Oxidative Injury to Retinal Pigment Epithelial Cells and Murine Models of Neurodegeneration." Investigative ophthalmology & visual science 50.10 (2009): 4957-4966.
description	11.	Gullotta, F. "Cell death mechanisms in multiple system atrophy." Journal of neuropathology and experimental neurology 57.9 (1998): 814-21.
description	12.	Vande, P L. "The mitochondrial serine protease HtrA2/Omi: an overview." Cell death and differentiation 15.3 (2008): 453-460.
description	13.	Alerte, Tshianda N M N. "alpha-Synuclein aggregation alters tyrosine hydroxylase phosphorylation and immunoreactivity: Lessons from viral transduction of knockout mice." Neuroscience Letters 435.1 (2008): 24-9.
description	14.	Lindholm, D. "Mitochondrial proteins in neuronal degeneration." Biochemical and biophysical research communications 321.4 (2004): 753-8.
description	15.	Eisenberg, T. "The mitochondrial pathway in yeast apoptosis." Apoptosis 12.5 (2007): 1011-1023.
description	16.	Petit, A W A. "Characterization of the double-stranded RNA responses in human liver progenitor cells." Biochemical and biophysical research communications 256.3 (2008): 549-56.
description	17.	Leber, Jess H H. "Distinct TLR- and NLR-mediated transcriptional responses to an intracellular pathogen." PLoS Pathogens 4.1 (2007): 12-95.
description	18.	Benedetti, M D D. "Hysterectomy, menopause, and estrogen use preceding Parkinson's disease: an exploratory case-control study." Movement disorders 16.5 (2001): 830-7.
description	19.	Higgs, Douglas R R. "A regulatory SNP causes a human genetic disease by creating a new transcriptional promoter." Science 312.5777 (2006): 1215-1217.
description	20.	Ye, Z. "NLR, the nucleotide-binding domain leucine-rich repeat containing gene family." Current opinion in immunology 20.1 (2008): 3-9.