The C. elegans protein EGL-1 is required for programmed cell death and interacts with the Bcl-2–like protein CED-9 B Conradt, HR Horvitz Cell 93 (4), 519-529, 1998 | 892 | 1998 |
DRP-1-mediated mitochondrial fragmentation during EGL-1-induced cell death in C. elegans R Jagasia, P Grote, B Westermann, B Conradt Nature 433 (7027), 754-760, 2005 | 383 | 2005 |
Translocation of C. elegans CED-4 to nuclear membranes during programmed cell death F Chen, BM Hersh, B Conradt, Z Zhou, D Riemer, Y Gruenbaum, ... Science 287 (5457), 1485-1489, 2000 | 304 | 2000 |
The TRA-1A sex determination protein of C. elegans regulates sexually dimorphic cell deaths by repressing the egl-1 cell death activator gene B Conradt, HR Horvitz Cell 98 (3), 317-327, 1999 | 289 | 1999 |
C. elegans ced-13 can promote apoptosis and is induced in response to DNA damage B Schumacher, C Schertel, N Wittenburg, S Tuck, S Mitani, A Gartner, ... Cell Death & Differentiation 12 (2), 153-161, 2005 | 210 | 2005 |
Genetic control of programmed cell death during animal development B Conradt Annual review of genetics 43, 493-523, 2009 | 203 | 2009 |
G-protein ligands inhibit in vitro reactions of vacuole inheritance. A Haas, B Conradt, W Wickner The Journal of cell biology 126 (1), 87-97, 1994 | 192 | 1994 |
Programmed cell death B Conradt, D Xue WormBook: The Online Review of C. elegans Biology [Internet], 2005 | 167 | 2005 |
The Snail-like CES-1 protein of C. elegans can block the expression of theBH3-only cell-death activator gene egl-1 by antagonizing the function of bHLH proteins M Thellmann, J Hatzold, B Conradt Oxford University Press for The Company of Biologists Limited 130 (17), 4057 …, 2003 | 155 | 2003 |
In vitro reactions of vacuole inheritance in Saccharomyces cerevisiae. B Conradt, J Shaw, T Vida, S Emr, W Wickner The Journal of cell biology 119 (6), 1469-1479, 1992 | 150 | 1992 |
Compromised mitochondrial protein import acts as a signal for UPRmt SG Rolland, S Schneid, M Schwarz, E Rackles, C Fischer, S Haeussler, ... Cell reports 28 (7), 1659-1669. e5, 2019 | 136 | 2019 |
Age-dependent changes in mitochondrial morphology and volume are not predictors of lifespan SG Regmi, SG Rolland, B Conradt Aging (Albany NY) 6 (2), 118, 2014 | 119 | 2014 |
A conserved RhoGAP limits M phase contractility and coordinates with microtubule asters to confine RhoA during cytokinesis E Zanin, A Desai, I Poser, Y Toyoda, C Andree, C Moebius, M Bickle, ... Developmental Cell 26 (5), 496-510, 2013 | 115 | 2013 |
Programmed Cell Death During Caenorhabditis elegans Development B Conradt, YC Wu, D Xue Genetics 203 (4), 1533-1562, 2016 | 112 | 2016 |
The BCL-2–like protein CED-9 of C. elegans promotes FZO-1/Mfn1,2– and EAT-3/Opa1–dependent mitochondrial fusion SG Rolland, Y Lu, CN David, B Conradt Journal of cell biology 186 (4), 525-540, 2009 | 106 | 2009 |
New role of the BCL2 family of proteins in the regulation of mitochondrial dynamics SG Rolland, B Conradt Current opinion in cell biology 22 (6), 852-858, 2010 | 102 | 2010 |
Determination of four biochemically distinct, sequential stages during vacuole inheritance in vitro. B Conradt, A Haas, W Wickner The Journal of cell biology 126 (1), 99-110, 1994 | 97 | 1994 |
Control of apoptosis by asymmetric cell division J Hatzold, B Conradt PLoS biology 6 (4), e84, 2008 | 96 | 2008 |
Impaired complex IV activity in response to loss of LRPPRC function can be compensated by mitochondrial hyperfusion SG Rolland, E Motori, N Memar, J Hench, S Frank, KF Winklhofer, ... Proceedings of the National Academy of Sciences 110 (32), E2967-E2976, 2013 | 87 | 2013 |
C. elegans orthologs of components of the RB tumor suppressor complex have distinct pro-apoptotic functions C Schertel, B Conradt Oxford University Press for The Company of Biologists Limited 134 (20), 3691 …, 2007 | 82 | 2007 |