| Year |
Citation |
Score |
| 2020 |
Verheijen BM, Vermulst M, van Leeuwen FW. Correction to: Somatic mutations in neurons during aging and neurodegeneration. Acta Neuropathologica. PMID 32632518 DOI: 10.1007/S00401-020-02186-Y |
0.437 |
|
| 2019 |
Haroon S, Vermulst M. Oxygen Consumption Measurements in Using the Seahorse XF24. Bio-Protocol. 9: e3288. PMID 33654802 DOI: 10.21769/BioProtoc.3288 |
0.367 |
|
| 2019 |
Kim MJ, Haroon S, Chen GD, Ding D, Wanagat J, Liu L, Zhang Y, White K, Park HJ, Han C, Boyd K, Caicedo I, Evans K, Linser PJ, Tanokura M, ... ... Vermulst M, et al. Increased burden of mitochondrial DNA deletions and point mutations in early-onset age-related hearing loss in mitochondrial mutator mice. Experimental Gerontology. 110675. PMID 31344454 DOI: 10.1016/J.Exger.2019.110675 |
0.566 |
|
| 2018 |
McManus MJ, Picard M, Chen HW, De Haas HJ, Potluri P, Leipzig J, Towheed A, Angelin A, Sengupta P, Morrow RM, Kauffman BA, Vermulst M, Narula J, Wallace DC. Mitochondrial DNA Variation Dictates Expressivity and Progression of Nuclear DNA Mutations Causing Cardiomyopathy. Cell Metabolism. PMID 30174309 DOI: 10.1016/J.Cmet.2018.08.002 |
0.596 |
|
| 2018 |
Verheijen BM, Vermulst M, van Leeuwen FW. Somatic mutations in neurons during aging and neurodegeneration. Acta Neuropathologica. PMID 29705908 DOI: 10.1007/S00401-018-1850-Y |
0.45 |
|
| 2018 |
Haroon S, Li A, Weinert JL, Fritsch C, Ericson NG, Alexander-Floyd J, Braeckman BP, Haynes CM, Bielas JH, Gidalevitz T, Vermulst M. Multiple Molecular Mechanisms Rescue mtDNA Disease in C. elegans. Cell Reports. 22: 3115-3125. PMID 29562168 DOI: 10.1016/J.Celrep.2018.02.099 |
0.469 |
|
| 2017 |
Someya S, Kujoth GC, Kim MJ, Hacker TA, Vermulst M, Weindruch R, Prolla TA. Effects of calorie restriction on the lifespan and healthspan of POLG mitochondrial mutator mice. Plos One. 12: e0171159. PMID 28158260 DOI: 10.1371/Journal.Pone.0171159 |
0.615 |
|
| 2016 |
Haroon S, Vermulst M. Linking mitochondrial dynamics to mitochondrial protein quality control. Current Opinion in Genetics & Development. 38: 68-74. PMID 27235806 DOI: 10.1016/J.Gde.2016.04.004 |
0.514 |
|
| 2012 |
Ericson NG, Kulawiec M, Vermulst M, Sheahan K, O'Sullivan J, Salk JJ, Bielas JH. Decreased mitochondrial DNA mutagenesis in human colorectal cancer. Plos Genetics. 8: e1002689. PMID 22685414 DOI: 10.1371/Journal.Pgen.1002689 |
0.594 |
|
| 2010 |
Chen H, Vermulst M, Wang YE, Chomyn A, Prolla TA, McCaffery JM, Chan DC. Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations. Cell. 141: 280-9. PMID 20403324 DOI: 10.1016/J.Cell.2010.02.026 |
0.508 |
|
| 2009 |
Vermulst M, Wanagat J, Loeb LA. On Mitochondria, Mutations, and Methodology Cell Metabolism. 10: 437. PMID 19945399 DOI: 10.1016/J.Cmet.2009.11.001 |
0.605 |
|
| 2009 |
Dai DF, Santana LF, Vermulst M, Tomazela DM, Emond MJ, MacCoss MJ, Gollahon K, Martin GM, Loeb LA, Ladiges WC, Rabinovitch PS. Overexpression of catalase targeted to mitochondria attenuates murine cardiac aging. Circulation. 119: 2789-97. PMID 19451351 DOI: 10.1161/Circulationaha.108.822403 |
0.555 |
|
| 2008 |
Vermulst M, Bielas JH, Loeb LA. Quantification of random mutations in the mitochondrial genome Methods. 46: 263-268. PMID 18948200 DOI: 10.1016/J.Ymeth.2008.10.008 |
0.611 |
|
| 2008 |
Vermulst M, Wanagat J, Kujoth GC, Bielas JH, Rabinovitch PS, Prolla TA, Loeb LA. DNA deletions and clonal mutations drive premature aging in mitochondrial mutator mice Nature Genetics. 40: 392-394. PMID 18311139 DOI: 10.1038/Ng.95 |
0.661 |
|
| 2007 |
Vermulst M, Bielas JH, Kujoth GC, Ladiges WC, Rabinovitch PS, Prolla TA, Loeb LA. Mitochondrial point mutations do not limit the natural lifespan of mice Nature Genetics. 39: 540-543. PMID 17334366 DOI: 10.1038/Ng1988 |
0.663 |
|
| Show low-probability matches. |