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Cited by 39

The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.

Mutant Twinkle increases dopaminergic neurodegeneration, mtDNA deletions and modulates Parkin expression

Song, Lanying, Shan, Yuxi, Lloyd, K.C. Kent, Cortopassi, Gino A.·2012·Human Molecular Genetics
DOI 10.1093/hmg/dds365
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Crossref · 10.1093/hmg/dds365

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  • Mouse models have been used to study comparable phenotypes due to mutations in nuclear-encoded proteins involved in mitochondrial biogenesis, such as TFAM, PolG, Twinkle, and SURF-1.

    “Mouse models have further been used to study comparable phenotypes due to mutations in nuclear-encoded proteins involved in mitochondrial biogenesis, such as TFAM [152], PolG [153], Twinkle [154,155,156], and SURF-1 [157].”

    From The Mitochondrial Genome in Aging and Disease and the Future of Mitochondrial Therapeutics (2022) · cites this paper as [155]

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Research works printed but not linked: 37

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  4. Serikawa, 2011, Successful twin pregnancy in a patient with parkin-associated autosomal recessive juvenile parkinsonism, BMC Neurol., 11, 72, 10.1186/1471-2377-11-72 · DOI
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  7. Cortopassi, 1992, A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues, Proc. Natl Acad. Sci. USA., 89, 7370, 10.1073/pnas.89.16.7370 · DOI
  8. Soong, 1992, Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain, Nat. Genet., 2, 318, 10.1038/ng1292-318 · DOI
  9. Trifunovic, 2004, Premature ageing in mice expressing defective mitochondrial DNA polymerase, Nature, 429, 417, 10.1038/nature02517 · DOI · Paper page
  10. Luoma, 2004, Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study, Lancet, 364, 875, 10.1016/S0140-6736(04)16983-3 · DOI · Paper page
  11. Baloh, 2007, Familial Parkinsonism and ophthalmoplegia from a mutation in the mitochondrial DNA helicase twinkle, Arch. Neurol., 64, 998, 10.1001/archneur.64.7.998 · DOI
  12. Rothfuss, 2009, Parkin protects mitochondrial genome integrity and supports mitochondrial DNA repair, Hum. Mol. Genet., 18, 3832, 10.1093/hmg/ddp327 · DOI
  13. Glauser, 2011, Parkin promotes the ubiquitination and degradation of the mitochondrial fusion factor mitofusin 1, J. Neurochem., 118, 636, 10.1111/j.1471-4159.2011.07318.x · DOI · Paper page
  14. Um, 2010, Parkin directly modulates 26S proteasome activity, J. Neurosci., 30, 11805, 10.1523/JNEUROSCI.2862-09.2010 · DOI
  15. Hara, 2006, Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice, Nature, 441, 885, 10.1038/nature04724 · DOI · Paper page
  16. Cotan, 2011, Secondary coenzyme Q10 deficiency triggers mitochondria degradation by mitophagy in MELAS fibroblasts, FASEB J., 25, 2669, 10.1096/fj.10-165340 · DOI
  17. Archer, 2010, Syrbactin class proteasome inhibitor-induced apoptosis and autophagy occurs in association with p53 accumulation and Akt/PKB activation in neuroblastoma, Biochem. Pharmacol., 80, 170, 10.1016/j.bcp.2010.03.031 · DOI
  18. Casarejos, 2009, Parkin deficiency increases the resistance of midbrain neurons and glia to mild proteasome inhibition: the role of autophagy and glutathione homeostasis, J. Neurochem., 110, 1523, 10.1111/j.1471-4159.2009.06248.x · DOI
  19. Fukui, 2009, Mechanisms of formation and accumulation of mitochondrial DNA deletions in aging neurons, Hum. Mol. Genet., 18, 1028, 10.1093/hmg/ddn437 · DOI
  20. Deng, 2008, The Parkinson's disease genes pink1 and parkin promote mitochondrial fission and/or inhibit fusion in Drosophila, Proc. Natl Acad. Sci. USA., 105, 14503, 10.1073/pnas.0803998105 · DOI
  21. Yang, 2011, Mitochondrial dysfunction induced by knockdown of mortalin is rescued by Parkin, Biochem. Biophys. Res. Commun., 410, 114, 10.1016/j.bbrc.2011.05.116 · DOI
  22. Greenwood, 2010, Astrocytic activation and an inhibition of MAP kinases are required for proteinase-activated receptor-2-mediated protection from neurotoxicity, J. Neurochem., 113, 1471, 10.1111/j.1471-4159.2010.06737.x · DOI
  23. Stichel, 2007, Mono- and double-mutant mouse models of Parkinson's disease display severe mitochondrial damage, Hum. Mol. Genet., 16, 2377, 10.1093/hmg/ddm083 · DOI
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  30. Lee, 2010, Disease-causing mutations in parkin impair mitochondrial ubiquitination, aggregation, and HDAC6-dependent mitophagy, J. Cell Biol., 189, 671, 10.1083/jcb.201001039 · DOI
  31. Matsushita, 2002, Dynamics of tyrosine hydroxylase promoter activity during midbrain dopaminergic neuron development, J. Neurochem., 82, 295, 10.1046/j.1471-4159.2002.00972.x · DOI
  32. Fleming, 2004, Early and progressive sensorimotor anomalies in mice overexpressing wild-type human alpha-synuclein, J. Neurosci., 24, 9434, 10.1523/JNEUROSCI.3080-04.2004 · DOI
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  34. Zhang, 2000, Parkin functions as an E2-dependent ubiquitin- protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1, Proc. Natl Acad. Sci. USA., 97, 13354, 10.1073/pnas.240347797 · DOI · Paper page
  35. Goydos, 2003, Vascular endothelial growth factor C mRNA expression correlates with stage of progression in patients with melanoma, Clin. Cancer Res., 9, 5962
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  37. Shan, 2007, Mitochondrial frataxin interacts with ISD11 of the NFS1/ISCU complex and multiple mitochondrial chaperones, Hum. Mol. Genet., 16, 929, 10.1093/hmg/ddm038 · DOI

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Metadata

Authors
Song, L., Shan, Y., Lloyd, K. C. K., & Cortopassi, G. A.
Venue
Human Molecular Genetics
Publisher
Oxford University Press (OUP)
Published
2012-09-04
Volume
21
Issue
23
Pages
5147-5158
ISSN
  • 1460-2083
  • 0964-6906
DOI
10.1093/hmg/dds365
Cited by
39
References
8
Language
en

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