| Year |
Citation |
Score |
| 2023 |
Morava E, Oglesbee D. Laboratory and metabolic investigations. Handbook of Clinical Neurology. 194: 167-172. PMID 36813311 DOI: 10.1016/B978-0-12-821751-1.00012-9 |
0.32 |
|
| 2022 |
Sabharwal A, Wishman MD, Cervera RL, Serres MR, Anderson JL, Holmberg SR, Kar B, Treichel AJ, Ichino N, Liu W, Yang J, Ding Y, Deng Y, Lacey JM, Laxen WJ, ... ... Oglesbee D, et al. Genetic therapy in a mitochondrial disease model suggests a critical role for liver dysfunction in mortality. Elife. 11. PMID 36408801 DOI: 10.7554/eLife.65488 |
0.333 |
|
| 2021 |
Sharma R, Reinstadler B, Engelstad K, Skinner OS, Stackowitz E, Haller RG, Clish CB, Pierce K, Walker MA, Fryer R, Oglesbee D, Mao X, Shungu DC, Khatri A, Hirano M, et al. Circulating markers of NADH-reductive stress correlate with mitochondrial disease severity. The Journal of Clinical Investigation. 131. PMID 33463549 DOI: 10.1172/JCI136055 |
0.376 |
|
| 2020 |
Klein Gunnewiek TM, Van Hugte EJH, Frega M, Guardia GS, Foreman K, Panneman D, Mossink B, Linda K, Keller JM, Schubert D, Cassiman D, Rodenburg R, Vidal Folch N, Oglesbee D, Perales-Clemente E, et al. m.3243A > G-Induced Mitochondrial Dysfunction Impairs Human Neuronal Development and Reduces Neuronal Network Activity and Synchronicity. Cell Reports. 31: 107538. PMID 32320658 DOI: 10.1016/j.celrep.2020.107538 |
0.347 |
|
| 2016 |
Perales-Clemente E, Cook AN, Evans JM, Roellinger S, Secreto F, Emmanuele V, Oglesbee D, Mootha VK, Hirano M, Schon EA, Terzic A, Nelson TJ. Natural underlying mtDNA heteroplasmy as a potential source of intra-person hiPSC variability. The Embo Journal. PMID 27436875 DOI: 10.15252/Embj.201694892 |
0.408 |
|
| 2013 |
Folmes CD, Martinez-Fernandez A, Perales-Clemente E, Li X, McDonald A, Oglesbee D, Hrstka SC, Perez-Terzic C, Terzic A, Nelson TJ. Disease-causing mitochondrial heteroplasmy segregated within induced pluripotent stem cell clones derived from a patient with MELAS. Stem Cells (Dayton, Ohio). 31: 1298-308. PMID 23553816 DOI: 10.1002/Stem.1389 |
0.427 |
|
| 2006 |
Oglesbee D, Freedenberg D, Kramer KA, Anderson BD, Hahn SH. Normal muscle respiratory chain enzymes can complicate mitochondrial disease diagnosis. Pediatric Neurology. 35: 289-92. PMID 16996407 DOI: 10.1016/j.pediatrneurol.2006.05.007 |
0.412 |
|
| 2005 |
Kramer KA, Oglesbee D, Hartman SJ, Huey J, Anderson B, Magera MJ, Matern D, Rinaldo P, Robinson BH, Cameron JM, Hahn SH. Automated spectrophotometric analysis of mitochondrial respiratory chain complex enzyme activities in cultured skin fibroblasts. Clinical Chemistry. 51: 2110-6. PMID 16141288 DOI: 10.1373/Clinchem.2005.050146 |
0.304 |
|
| 2004 |
Hanson GT, Aggeler R, Oglesbee D, Cannon M, Capaldi RA, Tsien RY, Remington SJ. Investigating mitochondrial redox potential with redox-sensitive green fluorescent protein indicators. The Journal of Biological Chemistry. 279: 13044-53. PMID 14722062 DOI: 10.1074/Jbc.M312846200 |
0.561 |
|
| 2003 |
Murray J, Zhang B, Taylor SW, Oglesbee D, Fahy E, Marusich MF, Ghosh SS, Capaldi RA. The subunit composition of the human NADH dehydrogenase obtained by rapid one-step immunopurification. The Journal of Biological Chemistry. 278: 13619-22. PMID 12611891 DOI: 10.1074/Jbc.C300064200 |
0.596 |
|
| 2002 |
Capaldi RA, Aggeler R, Gilkerson R, Hanson G, Knowles M, Marcus A, Margineantu D, Marusich M, Murray J, Oglesbee D, Remington SJ, Rossignol R. A replicating module as the unit of mitochondrial structure and functioning. Biochimica Et Biophysica Acta. 1555: 192-5. PMID 12206914 DOI: 10.1016/S0005-2728(02)00277-3 |
0.304 |
|
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