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Carla M. Koehler - Publications

Affiliations: 
University of California, Los Angeles, Los Angeles, CA 
Area:
mitochondrial protein translocation
Website:
http://koehler.chem.ucla.edu/profile.html
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106 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Han M, Bushong EA, Segawa M, Tiard A, Wong A, Brady MR, Momcilovic M, Wolf DM, Zhang R, Petcherski A, Madany M, Xu S, Lee JT, Poyurovsky MV, Olszewski K, ... ... Koehler CM, et al. Spatial mapping of mitochondrial networks and bioenergetics in lung cancer. Nature. PMID 36922590 DOI: 10.1038/s41586-023-05793-3  0.342
2022 Liang WG, Wijaya J, Wei H, Noble AJ, Mancl JM, Mo S, Lee D, Lin King JV, Pan M, Liu C, Koehler CM, Zhao M, Potter CS, Carragher B, Li S, et al. Structural basis for the mechanisms of human presequence protease conformational switch and substrate recognition. Nature Communications. 13: 1833. PMID 35383169 DOI: 10.1038/s41467-022-29322-4  0.781
2021 Zhang D, Dailey OR, Simon DJ, Roca-Datzer K, Jami-Alahmadi Y, Hennen MS, Wolfschlegel JA, Koehler CM, Dabir DV. Aim32 is a dual-localized 2Fe-2S mitochondrial protein that functions in redox quality control. The Journal of Biological Chemistry. 101135. PMID 34461091 DOI: 10.1016/j.jbc.2021.101135  0.421
2020 Momcilovic M, Shirihai O, Murphy MP, Koehler CM, Sadeghi S, Shackelford DB. Reply to: In vivo quantification of mitochondrial membrane potential. Nature. 583: E19-E20. PMID 32641810 DOI: 10.1038/S41586-020-2367-9  0.526
2020 Momcilovic M, Jones A, Bailey ST, Waldmann CM, Li R, Lee JT, Abdelhady G, Gomez A, Holloway T, Schmid E, Stout D, Fishbein MC, Stiles L, Dabir DV, Dubinett SM, ... ... Koehler CM, et al. Publisher Correction: In vivo imaging of mitochondrial membrane potential in non-small-cell lung cancer. Nature. PMID 31896820 DOI: 10.1038/S41586-019-1890-Z  0.382
2020 Momcilovic M, Han M, Bushong E, Stiles L, Dubinett S, Christofk H, Shirihai O, Koehler C, Sadeghi S, Ellisman M, Shackelford D. IA08 Mapping Mitochondrial Heterogeneity in Lung Cancer Journal of Thoracic Oncology. 15: S4. DOI: 10.1016/J.Jtho.2019.12.009  0.334
2019 Momcilovic M, Jones A, Bailey ST, Waldmann CM, Li R, Lee JT, Abdelhady G, Gomez A, Holloway T, Schmid E, Stout D, Fishbein MC, Stiles L, Dabir DV, Dubinett SM, ... ... Koehler CM, et al. In vivo imaging of mitochondrial membrane potential in non-small-cell lung cancer. Nature. PMID 31666695 DOI: 10.1038/S41586-019-1715-0  0.48
2018 Yien YY, Shi J, Chen C, Cheung JT, Grillo AS, Shrestha R, Li L, Zhang X, Kafina MD, Kingsley PD, King MJ, Ablain J, Li H, Zon L, Palis J, ... ... Koehler CM, et al. FAM210B is an erythropoietin target and regulates erythroid heme synthesis by controlling mitochondrial iron import and ferrochelatase activity. The Journal of Biological Chemistry. PMID 30366982 DOI: 10.1074/Jbc.Ra118.002742  0.373
2018 Shimada E, Ahsan FM, Nili M, Huang D, Atamdede S, TeSlaa T, Case D, Yu X, Gregory BD, Perrin BJ, Koehler CM, Teitell MA. PNPase knockout results in mtDNA loss and an altered metabolic gene expression program. Plos One. 13: e0200925. PMID 30024931 DOI: 10.1371/Journal.Pone.0200925  0.38
2018 Steffen J, Koehler CM. ER-mitochondria contacts: Actin dynamics at the ER control mitochondrial fission via calcium release. The Journal of Cell Biology. 217: 15-17. PMID 29259094 DOI: 10.1083/Jcb.201711075  0.429
2018 Yien YY, Shi J, Chen C, Cheung J, Grillo A, Shrestha R, Li L, Zhang X, Kafina MD, Kingsley PD, King M, Ablain J, Zon LI, Palis J, Burke M, ... ... Koehler C, et al. Target of Erythropoietin, Fam210b, Regulates Erythroid Heme Synthesis By Control of Mitochondrial Iron Import and Regulation of Fech Activity Blood. 132: 849-849. DOI: 10.1182/Blood-2018-99-120299  0.391
2017 Filipuzzi I, Steffen J, Germain M, Goepfert L, Conti MA, Potting C, Cerino R, Pfeifer M, Krastel P, Hoepfner D, Bastien J, Koehler CM, Helliwell SB. Stendomycin selectively inhibits TIM23-dependent mitochondrial protein import. Nature Chemical Biology. PMID 28991239 DOI: 10.1038/Nchembio.2493  0.604
2017 Neal SE, Dabir DV, Wijaya J, Boon C, Koehler CM. Osm1 facilitates the transfer of electrons from Erv1 to fumarate in the redox-regulated import pathway in the mitochondrial intermembrane space. Molecular Biology of the Cell. PMID 28814504 DOI: 10.1091/Mbc.E16-10-0712  0.823
2017 Miyata N, Tang Z, Conti MA, Johnson ME, Douglas CJ, Hasson SA, Damoiseaux R, Chang CA, Koehler CM. Adaptation of a genetic screen reveals an inhibitor for mitochondrial protein import component Tim44. The Journal of Biological Chemistry. PMID 28167535 DOI: 10.1074/Jbc.M116.770131  0.852
2017 Thangamani S, Maland M, Mohammad H, Pascuzzi PE, Avramova L, Koehler CM, Hazbun TR, Seleem MN. Repurposing Approach Identifies Auranofin with Broad Spectrum Antifungal Activity That Targets Mia40-Erv1 Pathway. Frontiers in Cellular and Infection Microbiology. 7: 4. PMID 28149831 DOI: 10.3389/Fcimb.2017.00004  0.335
2017 Steffen J, Vashisht AA, Wan J, Jen JC, Claypool SM, Wohlschlegel JA, Koehler CM. Rapid degradation of mutant SLC25A46 by the ubiquitin-proteasome system results in MFN1/2 mediated hyperfusion of mitochondria. Molecular Biology of the Cell. PMID 28057766 DOI: 10.1091/Mbc.E16-07-0545  0.776
2016 Wan J, Steffen J, Yourshaw M, Mamsa H, Andersen E, Rudnik-Schöneborn S, Pope K, Howell KB, McLean CA, Kornberg AJ, Joseph J, Lockhart PJ, Zerres K, Ryan MM, Nelson SF, ... Koehler CM, et al. Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia. Brain : a Journal of Neurology. PMID 27543974 DOI: 10.1093/Brain/Aww212  0.496
2016 Wu TH, Sagullo E, Case D, Zheng X, Li Y, Hong JS, TeSlaa T, Patananan AN, McCaffery JM, Niazi K, Braas D, Koehler CM, Graeber TG, Chiou PY, Teitell MA. Mitochondrial Transfer by Photothermal Nanoblade Restores Metabolite Profile in Mammalian Cells. Cell Metabolism. 23: 921-929. PMID 27166949 DOI: 10.1016/J.Cmet.2016.04.007  0.375
2016 Lu YW, Galbraith L, Herndon JD, Lu YL, Pras-Raves M, Vervaart M, van Kampen A, Luyf A, Koehler CM, McCaffery JM, Gottlieb E, Vaz FM, Claypool SM. Defining functional classes of Barth syndrome mutation in humans. Human Molecular Genetics. PMID 26908608 DOI: 10.1093/Hmg/Ddw046  0.782
2016 Patananan AN, Wu T, Sagullo E, Case D, Zheng X, Li Y, Hong JS, TeSlaa T, McCaffery JM, Niazi K, Braas D, Koehler CM, Graeber TG, Chiou P, Teitell MA. Mitochondrial Transfer by Photothermal Nanoblade Restores Respiration in Mammalian Cells with Dysfunctional Mitochondria Biophysical Journal. 110: 471a-472a. DOI: 10.1016/J.Bpj.2015.11.2523  0.452
2015 Setoguchi K, TeSlaa T, Koehler CM, Teitell MA. P53 Regulates Rapid Apoptosis in Human Pluripotent Stem Cells. Journal of Molecular Biology. PMID 26239243 DOI: 10.1016/J.Jmb.2015.07.019  0.335
2015 Neal SE, Dabir DV, Tienson HL, Horn DM, Glaeser K, Ogozalek Loo RR, Barrientos A, Koehler CM. Mia40 serves as an electron sink in the Mia40-Erv1 import pathway. The Journal of Biological Chemistry. PMID 26085103 DOI: 10.1074/Jbc.M115.669440  0.812
2015 Wang G, Shimada E, Nili M, Koehler CM, Teitell MA. Mitochondria-targeted RNA import. Methods in Molecular Biology (Clifton, N.J.). 1264: 107-16. PMID 25631008 DOI: 10.1007/978-1-4939-2257-4_11  0.349
2015 Koehler C. Small molecule modulators for mitochondrial protein import Mitochondrion. 24: S5. DOI: 10.1016/J.Mito.2015.07.020  0.508
2015 Lu Y, Galbraith L, Herndon JD, Lu Y, Pras-Raves M, Vervaart M, van Kampen A, Luyf A, Koehler CM, Gottlieb E, Vaz FM, Claypool SM. Topological differences but dysfunctional conservation of cardiolipin remodeling in mammals and yeast Mitochondrion. 24: S4-S5. DOI: 10.1016/J.Mito.2015.07.019  0.769
2014 Steffen J, Koehler CM. The great escape: Mgr2 of the mitochondrial TIM23 translocon is a gatekeeper Tasked with releasing membrane proteins. Molecular Cell. 56: 613-4. PMID 25479635 DOI: 10.1016/J.Molcel.2014.11.022  0.502
2014 Miyata N, Steffen J, Johnson ME, Fargue S, Danpure CJ, Koehler CM. Pharmacologic rescue of an enzyme-trafficking defect in primary hyperoxaluria 1. Proceedings of the National Academy of Sciences of the United States of America. 111: 14406-11. PMID 25237136 DOI: 10.1073/Pnas.1408401111  0.698
2014 Yien YY, Robledo RF, Schultz IJ, Takahashi-Makise N, Gwynn B, Bauer DE, Dass A, Yi G, Li L, Hildick-Smith GJ, Cooney JD, Pierce EL, Mohler K, Dailey TA, Miyata N, ... ... Koehler CM, et al. TMEM14C is required for erythroid mitochondrial heme metabolism. The Journal of Clinical Investigation. 124: 4294-304. PMID 25157825 DOI: 10.1172/Jci76979  0.464
2013 Hildick-Smith GJ, Cooney JD, Garone C, Kremer LS, Haack TB, Thon JN, Miyata N, Lieber DS, Calvo SE, Akman HO, Yien YY, Huston NC, Branco DS, Shah DI, Freedman ML, ... Koehler CM, et al. Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4. American Journal of Human Genetics. 93: 906-14. PMID 24119684 DOI: 10.1016/J.Ajhg.2013.09.011  0.526
2013 Herndon JD, Claypool SM, Koehler CM. The Taz1p transacylase is imported and sorted into the outer mitochondrial membrane via a membrane anchor domain Eukaryotic Cell. 12: 1600-1608. PMID 24078306 DOI: 10.1128/Ec.00237-13  0.749
2013 Dabir DV, Hasson SA, Setoguchi K, Johnson ME, Wongkongkathep P, Douglas CJ, Zimmerman J, Damoiseaux R, Teitell MA, Koehler CM. A small molecule inhibitor of redox-regulated protein translocation into mitochondria. Developmental Cell. 25: 81-92. PMID 23597483 DOI: 10.1016/J.Devcel.2013.03.006  0.856
2013 Paw BH, Yien YY, Robledo RF, Schultz IJ, Takahashi-Makise N, Philllips J, Miyata N, Gwynn B, Dailey TA, Pierce E, Hildick-Smith GJ, Cooney JD, Chen W, Shah DI, Hattangadi SM, ... ... Koehler CM, et al. Tmem14c Plays An Essential Role In Mitochondrial Heme Metabolism Blood. 122: 427-427. DOI: 10.1182/Blood.V122.21.427.427  0.519
2012 von Ameln S, Wang G, Boulouiz R, Rutherford MA, Smith GM, Li Y, Pogoda HM, Nürnberg G, Stiller B, Volk AE, Borck G, Hong JS, Goodyear RJ, Abidi O, Nürnberg P, ... ... Koehler CM, et al. A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss. American Journal of Human Genetics. 91: 919-27. PMID 23084290 DOI: 10.1016/J.Ajhg.2012.09.002  0.495
2012 Bourens M, Dabir DV, Tienson HL, Sorokina I, Koehler CM, Barrientos A. Role of twin Cys-Xaa9-Cys motif cysteines in mitochondrial import of the cytochrome c oxidase biogenesis factor Cmc1 Journal of Biological Chemistry. 287: 31258-31269. PMID 22767599 DOI: 10.1074/Jbc.M112.383562  0.84
2012 Wang G, Shimada E, Zhang J, Hong JS, Smith GM, Teitell MA, Koehler CM. Correcting human mitochondrial mutations with targeted RNA import. Proceedings of the National Academy of Sciences of the United States of America. 109: 4840-5. PMID 22411789 DOI: 10.1073/Pnas.1116792109  0.482
2012 Wang G, Shimada E, Koehler CM, Teitell MA. PNPASE and RNA trafficking into mitochondria Biochimica Et Biophysica Acta - Gene Regulatory Mechanisms. 1819: 998-1007. PMID 22023881 DOI: 10.1016/J.Bbagrm.2011.10.001  0.464
2012 Claypool SM, Koehler CM. The complexity of cardiolipin in health and disease Trends in Biochemical Sciences. 37: 32-41. PMID 22014644 DOI: 10.1016/J.Tibs.2011.09.003  0.708
2012 Cooney JD, Hildick-Smith GJ, Garone C, Thon JN, Akman OH, Chen C, Shah DI, Branco DS, Miyata N, Freedman ML, Calvo SE, Mootha VK, Koehler CM, Italiano JE, Donati MA, et al. Megaloblastic Anemia and Mitochondriopathy Caused by a Homozygous Mutation in Sideroflexin-4. Blood. 120: 79-79. DOI: 10.1182/Blood.V120.21.79.79  0.486
2012 Claypool SM, Oktay Y, Boontheung P, Loo JA, Koehler CM. Cardiolipin defines the interactome of the major ADP/ATP carrier protein of the mitochondrial inner membrane Journal of Cell Biology. 197: 1029. DOI: 10.1083/jcb.2008011521977c  0.755
2011 Zhang J, Khvorostov I, Hong JS, Oktay Y, Vergnes L, Nuebel E, Wahjudi PN, Setoguchi K, Wang G, Do A, Jung HJ, McCaffery JM, Kurland IJ, Reue K, Lee WN, ... Koehler CM, et al. UCP2 regulates energy metabolism and differentiation potential of human pluripotent stem cells. The Embo Journal. 30: 4860-73. PMID 22085932 DOI: 10.1038/Emboj.2011.401  0.466
2011 Claypool SM, Whited K, Srijumnong S, Han X, Koehler CM. Barth syndrome mutations that cause tafazzin complex lability Journal of Cell Biology. 192: 447-462. PMID 21300850 DOI: 10.1083/Jcb.201008177  0.699
2011 Zhang J, Khvorostov I, Hong J, Oktay Y, Vergnes L, Nuebel E, Do A, Jung H, McCaffery M, Reue K, Koehler C, Teitell M. Abstract 4360: Distinct energy metabolism in human pluripotent stem cells and differentiated cells regulated by UCP2 Cancer Research. 71: 4360-4360. DOI: 10.1158/1538-7445.Am2011-4360  0.446
2011 Dabir⁎ D, Hasson SA, Damoiseaux R, Zimmerman J, Johnson ME, Koehler CM. Chemical inhibition of the Erv1 mitochondrial oxidative folding pathway by a small molecule inhibitor Mitochondrion. 11: 638. DOI: 10.1016/J.Mito.2011.03.015  0.814
2010 Wang G, Chen HW, Oktay Y, Zhang J, Allen EL, Smith GM, Fan KC, Hong JS, French SW, McCaffery JM, Lightowlers RN, Morse HC, Koehler CM, Teitell MA. PNPASE regulates RNA import into mitochondria. Cell. 142: 456-67. PMID 20691904 DOI: 10.1016/J.Cell.2010.06.035  0.386
2010 Curado S, Ober EA, Walsh S, Cortes-Hernandez P, Verkade H, Koehler CM, Stainier DY. The mitochondrial import gene tomm22 is specifically required for hepatocyte survival and provides a liver regeneration model. Disease Models & Mechanisms. 3: 486-95. PMID 20483998 DOI: 10.1242/Dmm.004390  0.405
2010 Hasson SA, Damoiseaux R, Glavin JD, Dabir DV, Walker SS, Koehler CM. Substrate specificity of the TIM22 mitochondrial import pathway revealed with small molecule inhibitor of protein translocation Proceedings of the National Academy of Sciences of the United States of America. 107: 9578-9583. PMID 20457929 DOI: 10.1073/Pnas.0914387107  0.832
2010 Zaltsman Y, Shachnai L, Yivgi-Ohana N, Schwarz M, Maryanovich M, Houtkooper RH, Vaz FM, De Leonardis F, Fiermonte G, Palmieri F, Gillissen B, Daniel PT, Jimenez E, Walsh S, Koehler CM, et al. MTCH2/MIMP is a major facilitator of tBID recruitment to mitochondria Nature Cell Biology. 12: 553-562. PMID 20436477 DOI: 10.1038/Ncb2057  0.521
2009 Area-Gomez E, de Groof AJ, Boldogh I, Bird TD, Gibson GE, Koehler CM, Yu WH, Duff KE, Yaffe MP, Pon LA, Schon EA. Presenilins are enriched in endoplasmic reticulum membranes associated with mitochondria. The American Journal of Pathology. 175: 1810-6. PMID 19834068 DOI: 10.2353/Ajpath.2009.090219  0.794
2009 Chacinska A, Koehler CM, Milenkovic D, Lithgow T, Pfanner N. Importing Mitochondrial Proteins: Machineries and Mechanisms Cell. 138: 628-644. PMID 19703392 DOI: 10.1016/J.Cell.2009.08.005  0.596
2009 Tienson HL, Dabir DV, Neal SE, Loo R, Hasson SA, Boontheung P, Kim SK, Loo JA, Koehler CM. Reconstitution of the mia40-erv1 oxidative folding pathway for the small tim proteins. Molecular Biology of the Cell. 20: 3481-90. PMID 19477928 DOI: 10.1091/Mbc.E08-10-1062  0.78
2009 Lu G, Sun H, Korge P, Koehler CM, Weiss JN, Wang Y. Functional characterization of a mitochondrial Ser/Thr protein phosphatase in cell death regulation. Methods in Enzymology. 457: 255-73. PMID 19426872 DOI: 10.1016/S0076-6879(09)05014-9  0.54
2009 Koehler CM, Tienson HL. Redox regulation of protein folding in the mitochondrial intermembrane space Biochimica Et Biophysica Acta - Molecular Cell Research. 1793: 139-145. PMID 18761382 DOI: 10.1016/J.Bbamcr.2008.08.002  0.851
2008 Claypool SM, Boontheung P, McCaffery JM, Loo JA, Koehler CM. The cardiolipin transacylase, tafazzin, associates with two distinct respiratory components providing insight into Barth syndrome. Molecular Biology of the Cell. 19: 5143-55. PMID 18799610 DOI: 10.1091/Mbc.E08-09-0896  0.736
2008 Claypool SM, Oktay Y, Boontheung P, Loo JA, Koehler CM. Cardiolipin defines the interactome of the major ADP/ATP carrier protein of the mitochondrial inner membrane. The Journal of Cell Biology. 182: 937-50. PMID 18779372 DOI: 10.1083/Jcb.200801152  0.782
2008 Beverly KN, Sawaya MR, Schmid E, Koehler CM. The Tim8-Tim13 Complex Has Multiple Substrate Binding Sites and Binds Cooperatively to Tim23 Journal of Molecular Biology. 382: 1144-1156. PMID 18706423 DOI: 10.1016/J.Jmb.2008.07.069  0.479
2008 Walsh S, Koehler CM. Gazing at Translocation in the Mitochondrion Cell. 134: 382-383. PMID 18692459 DOI: 10.1016/J.Cell.2008.07.024  0.523
2008 Gebert N, Chacinska A, Wagner K, Guiard B, Koehler CM, Rehling P, Pfanner N, Wiedemann N. Assembly of the three small Tim proteins precedes docking to the mitochondrial carrier translocase Embo Reports. 9: 548-554. PMID 18421298 DOI: 10.1038/Embor.2008.49  0.583
2007 Stuart RA, Koehler CM. In vitro analysis of yeast mitochondrial protein import. Current Protocols in Cell Biology / Editorial Board, Juan S. Bonifacino ... [Et Al.]. Unit 11.19. PMID 18228496 DOI: 10.1002/0471143030.Cb1119S34  0.567
2007 Chen HW, Koehler CM, Teitell MA. Human polynucleotide phosphorylase: location matters Trends in Cell Biology. 17: 600-608. PMID 17983748 DOI: 10.1016/J.Tcb.2007.09.006  0.451
2007 Dabir DV, Leverich EP, Kim SK, Tsai FD, Hirasawa M, Knaff DB, Koehler CM. A role for cytochrome c and cytochrome c peroxidase in electron shuttling from Erv1. The Embo Journal. 26: 4801-11. PMID 17972915 DOI: 10.1038/Sj.Emboj.7601909  0.8
2007 Hwang DK, Claypool SM, Leuenberger D, Tienson HL, Koehler CM. Tim54p connects inner membrane assembly and proteolytic pathways in the mitochondrion Journal of Cell Biology. 178: 1161-1175. PMID 17893242 DOI: 10.1083/Jcb.200706195  0.836
2007 Sedivá A, Smith CI, Asplund AC, Hadac J, Janda A, Zeman J, Hansíková H, Dvoráková L, Mrázová L, Velbri S, Koehler C, Roesch K, Sullivan KE, Futatani T, Ochs HD. Contiguous X-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes. Journal of Clinical Immunology. 27: 640-6. PMID 17851739 DOI: 10.1007/S10875-007-9123-X  0.742
2007 Lu G, Ren S, Korge P, Choi J, Dong Y, Weiss J, Koehler C, Chen JN, Wang Y. A novel mitochondrial matrix serine/threonine protein phosphatase regulates the mitochondria permeability transition pore and is essential for cellular survival and development. Genes & Development. 21: 784-96. PMID 17374715 DOI: 10.1101/Gad.1499107  0.527
2007 French SW, Dawson DW, Chen HW, Rainey RN, Sievers SA, Balatoni CE, Wong L, Troke JJ, Nguyen MT, Koehler CM, Teitell MA. The TCL1 oncoprotein binds the RNase PH domains of the PNPase exoribonuclease without affecting its RNA degrading activity. Cancer Letters. 248: 198-210. PMID 16934922 DOI: 10.1016/J.Canlet.2006.07.006  0.784
2007 Oktay Y, Rainey RN, Koehler CM. The Function of TIM22 in the Insertion of Inner Membrane Proteins in Mitochondria Enzymes. 25: 367-385. DOI: 10.1016/S1874-6047(07)25014-0  0.837
2006 Chen HW, Rainey RN, Balatoni CE, Dawson DW, Troke JJ, Wasiak S, Hong JS, McBride HM, Koehler CM, Teitell MA, French SW. Mammalian polynucleotide phosphorylase is an intermembrane space RNase that maintains mitochondrial homeostasis Molecular and Cellular Biology. 26: 8475-8487. PMID 16966381 DOI: 10.1128/Mcb.01002-06  0.851
2006 Rainey RN, Glavin JD, Chen HW, French SW, Teitell MA, Koehler CM. A new function in translocation for the mitochondrial i-AAA protease Yme1: Import of polynucleotide phosphorylase into the intermembrane space Molecular and Cellular Biology. 26: 8488-8497. PMID 16966379 DOI: 10.1128/Mcb.01006-06  0.807
2006 Claypool SM, McCaffery JM, Koehler CM. Mitochondrial mislocalization and altered assembly of a cluster of Barth syndrome mutant tafazzins Journal of Cell Biology. 174: 379-390. PMID 16880272 DOI: 10.1083/Jcb.200605043  0.739
2006 Koehler CM, Beverly KN, Leverich EP. Redox pathways of the mitochondrion Antioxidants and Redox Signaling. 8: 813-822. PMID 16771672 DOI: 10.1089/Ars.2006.8.813  0.829
2006 Lu G, Ren S, Korge P, Choi J, Dong Y, Weiss J, Koehler C, Chen J, Wang Y. A Novel Mitochondrial Matrix Serine/Threonine Protein Phosphatase Is Essential to Cardiomyocyte Survival and Cardiac Function by Regulating Mitochondrial Permeability Transition Journal of Cardiac Failure. 12: S42. DOI: 10.1016/J.Cardfail.2006.06.147  0.488
2006 Koehler CM, Hwang DK. Protein Translocation Across Membranes Reviews in Cell Biology and Molecular Medicine. DOI: 10.1002/3527600906.Mcb.200500069  0.622
2005 Claypool SM, Koehler CM. Hereditary spastic paraplegia: Respiratory choke or unactivated substrate? Cell. 123: 183-185. PMID 16239134 DOI: 10.1016/J.Cell.2005.10.006  0.727
2005 Liki? VA, Perry A, Hulett J, Derby M, Traven A, Waller RF, Keeling PJ, Koehler CM, Curran SP, Gooley PR, Lithgow T. Patterns that define the four domains conserved in known and novel isoforms of the protein import receptor Tom20 Journal of Molecular Biology. 347: 81-93. PMID 15733919 DOI: 10.1016/J.Jmb.2004.12.057  0.647
2004 Curran SP, Leverich EP, Koehler CM, Larsen PL. Defective mitochondrial protein translocation precludes normal Caenorhabditis elegans development Journal of Biological Chemistry. 279: 54655-54662. PMID 15485840 DOI: 10.1074/Jbc.M409618200  0.84
2004 Koehler CM. New developments in mitochondrial assembly Annual Review of Cell and Developmental Biology. 20: 309-335. PMID 15473843 DOI: 10.1146/Annurev.Cellbio.20.010403.105057  0.569
2004 Curran SP, Leuenberger D, Leverich EP, Hwang DK, Beverly KN, Koehler CM. The role of Hot13p and redox chemistry in the mitochondrial TIM22 import pathway Journal of Biological Chemistry. 279: 43744-43751. PMID 15294910 DOI: 10.1074/Jbc.M404878200  0.836
2004 Roesch K, Hynds PJ, Varga R, Tranebjaerg L, Koehler CM. The calcium-binding aspartate/glutamate carriers, citrin and aralar1, are new substrates for the DDP1/TIMM8a-TIMM13 complex Human Molecular Genetics. 13: 2101-2111. PMID 15254020 DOI: 10.1093/Hmg/Ddh217  0.842
2004 Koehler CM. The small Tim proteins and the twin Cx3C motif Trends in Biochemical Sciences. 29: 1-4. PMID 14729324 DOI: 10.1016/J.Tibs.2003.11.003  0.55
2003 van der Bliek AM, Koehler CM. A mitochondrial rhomboid protease Developmental Cell. 4: 769-770. PMID 12791261 DOI: 10.1016/S1534-5807(03)00167-9  0.594
2003 Dyall SD, Lester DC, Schneider RE, Delgadillo-Correa MG, Plümper E, Martinez A, Koehler CM, Johnson PJ. Trichomonas vaginalis Hmp35, a putative pore-forming hydrogenosomal membrane protein, can form a complex in yeast mitochondria Journal of Biological Chemistry. 278: 30548-30561. PMID 12766161 DOI: 10.1074/Jbc.M304032200  0.526
2003 Leuenberger D, Curran SP, Wong D, Koehler CM. The role of Tim9p in the assembly of the TIM22 import complexes Traffic. 4: 144-152. PMID 12656987 DOI: 10.1034/J.1600-0854.2003.00095.X  0.826
2002 Curran SP, Leuenberger D, Schmidt E, Koehler CM. The role of the Tim8p-Tim13p complex in a conserved import pathway for mitochondrial polytopic inner membrane proteins Journal of Cell Biology. 158: 1017-1027. PMID 12221072 DOI: 10.1083/Jcb.200205124  0.829
2002 Roesch K, Curran SP, Tranebjaerg L, Koehler CM. Human deafness dystonia syndrome is caused by a defect in assembly of the DDP1/TIMM8a-TIMM13 complex Human Molecular Genetics. 11: 477-486. PMID 11875042 DOI: 10.1093/Hmg/11.5.477  0.854
2002 Curran SP, Leuenberger D, Oppliger W, Koehler CM. The Tim9p-Tim10p complex binds to the transmembrane domains of the ADP/ATP carrier Embo Journal. 21: 942-953. PMID 11867522 DOI: 10.1093/Emboj/21.5.942  0.807
2001 Murphy MP, Leuenberger D, Curran SP, Oppliger W, Koehler CM. The essential function of the small tim proteins in the TIM22 import pathway does not depend on formation of the soluble 70-kilodalton complex Molecular and Cellular Biology. 21: 6132-6138. PMID 11509656 DOI: 10.1128/Mcb.21.18.6132-6138.2001  0.814
2000 Koehler CM. Protein translocation pathways of the mitochondrion Febs Letters. 476: 27-31. PMID 10878244 DOI: 10.1016/S0014-5793(00)01664-1  0.574
2000 Patterson SD, Spahr CS, Daugas E, Susin SA, Irinopoulou T, Koehler C, Kroemer G. Mass spectrometric identification of proteins released from mitochondria undergoing permeability transition Cell Death and Differentiation. 7: 137-144. PMID 10713728 DOI: 10.1038/Sj.Cdd.4400640  0.537
2000 Dyall SD, Koehler CM, Delgadillo-Correa MG, Bradley PJ, Plümper E, Leuenberger D, Turck CW, Johnson PJ. Presence of a member of the mitochondrial carrier family in hydrogenosomes: conservation of membrane-targeting pathways between hydrogenosomes and mitochondria. Molecular and Cellular Biology. 20: 2488-97. PMID 10713172 DOI: 10.1128/Mcb.20.7.2488-2497.2000  0.779
2000 Koehler CM, Murphy MP, Bally NA, Leuenberger D, Oppliger W, Dolfini L, Junne T, Schatz G, Or E. Tim18p, a new subunit of the TIM22 complex that mediates insertion of imported proteins into the yeast mitochondrial inner membrane. Molecular and Cellular Biology. 20: 1187-93. PMID 10648604 DOI: 10.1128/Mcb.20.4.1187-1193.2000  0.812
2000 Renold A, Koehler CM, Murphy MP. Mitochondrial import of the long and short isoforms of human uncoupling protein 3 Febs Letters. 465: 135-140. PMID 10631320 DOI: 10.1016/S0014-5793(99)01688-9  0.577
2000 Tranebjaerg L, Lindal S, Merchant S, Ingebretsen O, Hamel B, Fung V, Hayes M, Koehler C, Hilssen O, Ghelue MV. Mohr-Tranebjaerg Syndrome is an X-linked Recessive Disorder Characterized by Mitochondrial Dysfunction Associated with Neuronal Cell Death Genetics in Medicine. 2: 107-107. DOI: 10.1097/00125817-200001000-00206  0.353
2000 Curran S, Leuenberger D, Perrin B, Jordan C, Koehler CM. Biogenesis of the mitochondrial inner membrane Biochemical Society Transactions. 28: A127-A127. DOI: 10.1042/Bst028A127  0.817
1999 Koehler CM, Merchant S, Schatz G. How membrane proteins travel across the mitochondrial intermembrane space. Trends in Biochemical Sciences. 24: 428-32. PMID 10542408 DOI: 10.1016/S0968-0004(99)01462-0  0.702
1999 Leuenberger D, Bally NA, Schatz G, Koehler CM. Different import pathways through the mitochondrial intermembrane space for inner membrane proteins. The Embo Journal. 18: 4816-22. PMID 10469659 DOI: 10.1093/Emboj/18.17.4816  0.809
1999 Koehler CM, Leuenberger D, Merchant S, Renold A, Junne T, Schatz G. Human deafness dystonia syndrome is a mitochondrial disease. Proceedings of the National Academy of Sciences of the United States of America. 96: 2141-6. PMID 10051608 DOI: 10.1073/Pnas.96.5.2141  0.809
1998 Koehler CM, Merchant S, Oppliger W, Schmid K, Jarosch E, Dolfini L, Junne T, Schatz G, Tokatlidis K. Tim9p, an essential partner subunit of Tim10p for the import of mitochondrial carrier proteins. The Embo Journal. 17: 6477-86. PMID 9822593 DOI: 10.1093/Emboj/17.22.6477  0.703
1998 Komiya T, Rospert S, Koehler C, Looser R, Schatz G, Mihara K. Interaction of mitochondrial targeting signals with acidic receptor domains along the protein import pathway: evidence for the 'acid chain' hypothesis. The Embo Journal. 17: 3886-98. PMID 9670006 DOI: 10.1093/Emboj/17.14.3886  0.587
1998 Koehler CM, Jarosch E, Tokatlidis K, Schmid K, Schweyen RJ, Schatz G. Import of mitochondrial carriers mediated by essential proteins of the intermembrane space. Science (New York, N.Y.). 279: 369-73. PMID 9430585 DOI: 10.1126/Science.279.5349.369  0.691
1998 Koehler CM, Jarosch E, Tokatlidis K, Schmid K, Schweyen R, Schatz G. Import of membrane-multispanning proteins into the yeast mitochondrial inner membrane Biology of the Cell. 90: 116-116. DOI: 10.1016/S0248-4900(98)80277-3  0.675
1997 Koehler CM, Myers AM. Serine-threonine protein kinase activity of Elm1p, a regulator of morphologic differentiation in Saccharomyces cerevisiae. Febs Letters. 408: 109-14. PMID 9180279 DOI: 10.1016/S0014-5793(97)00401-8  0.68
1994 Schutz MM, Freeman AE, Lindberg GL, Koehler CM, Beitz DC. The effect of mitochondrial DNA on milk production and health of dairy cattle Livestock Production Science. 37: 283-295. DOI: 10.1016/0301-6226(94)90123-6  0.32
1993 Blacketer MJ, Koehler CM, Coats SG, Myers AM, Madaule P. Regulation of dimorphism in Saccharomyces cerevisiae: involvement of the novel protein kinase homolog Elm1p and protein phosphatase 2A. Molecular and Cellular Biology. 13: 5567-81. PMID 8395007 DOI: 10.1128/Mcb.13.9.5567  0.602
1992 Lindberg GL, Koehler CM, Mayfield JE, Myers AM, Beitz DC. Recovery of mitochondrial DNA from blood leukocytes using detergent lysis. Biochemical Genetics. 30: 27-33. PMID 1381581 DOI: 10.1007/Bf00554425  0.61
1991 Koehler CM, Lindberg GL, Brown DR, Beitz DC, Freeman AE, Mayfield JE, Myers AM. Replacement of bovine mitochondrial DNA by a sequence variant within one generation. Genetics. 129: 247-55. PMID 1682213  0.512
1989 Brown DR, Koehler CM, Lindberg GL, Freeman AE, Mayfield JE, Myers AM, Schutz MM, Beitz DC. Molecular analysis of cytoplasmic genetic variation in Holstein cows. Journal of Animal Science. 67: 1926-32. PMID 2571604 DOI: 10.2527/Jas1989.6781926X  0.564
1989 Lindberg GL, Shank BB, Rothschild MF, Mayfield JE, Freeman AE, Koehler CM, Beitz DC. Characteristics of mammary mitochondria in lines of mice genetically divergent for milk production. Journal of Dairy Science. 72: 1175-1181. PMID 2473102 DOI: 10.3168/Jds.S0022-0302(89)79221-3  0.325
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