Cold Spring Harbor Laboratory

Mitochondrial remnant organelles of Giardia function in iron-sulphur protein maturation

Tovar, J., León-Avila, G., Sánchez, L. B., Sutak, R., Tachezy, J., van der Giezen, M., Hernández, M., Müller, M., & Lucocq, J. M. (2003) · Nature · doi:10.1038/nature01945 · Cited by 608

TGF-β – an excellent servant but a bad master

Kubiczkova, L., Sedlarikova, L., Hajek, R., & Sevcikova, S. (2012) · Journal of Translational Medicine · doi:10.1186/1479-5876-10-183 · Cited by 511

Antibiotic Resistance Genes in the Bacteriophage DNA Fraction of Environmental Samples

Colomer-Lluch, M., Jofre, J., & Muniesa, M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017549 · Cited by 353

Oestrogen exposure and breast cancer risk

Travis, R. C., & Key, T. J. (2003) · Breast Cancer Research · doi:10.1186/bcr628 · Cited by 346

Effects of Multiple Deletions of Murein Hydrolases on Viability, Septum Cleavage, and Sensitivity to Large Toxic Molecules in Escherichia coli

Heidrich, C., Ursinus, A., Berger, J., Schwarz, H., & Höltje, J.-V. (2002) · Journal of Bacteriology · doi:10.1128/jb.184.22.6093-6099.2002 · Cited by 272

COSA-1 Reveals Robust Homeostasis and Separable Licensing and Reinforcement Steps Governing Meiotic Crossovers

Yokoo, R., Zawadzki, K. A., Nabeshima, K., Drake, M., Arur, S., & Villeneuve, A. M. (2012) · Cell · doi:10.1016/j.cell.2012.01.052 · Cited by 256

Biofilm-Grown Burkholderia cepacia Complex Cells Survive Antibiotic Treatment by Avoiding Production of Reactive Oxygen Species

Van Acker, H., Sass, A., Bazzini, S., De Roy, K., Udine, C., Messiaen, T., Riccardi, G., Boon, N., Nelis, H. J., Mahenthiralingam, E., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058943 · Cited by 135

The current status of primary hepatocyte culture

Mitaka, T. (1998) · International Journal of Experimental Pathology · doi:10.1046/j.1365-2613.1998.00083.x · Cited by 115

Mutation rates, spectra, and genome-wide distribution of spontaneous mutations in mismatch repair deficient yeast.

Lang, G. I., Parsons, L., & Gammie, A. E. (2013) · G3 Genes Genomes Genetics · doi:10.1534/g3.113.006429 · Cited by 107

Functional gene groups are concentrated within chromosomes, among chromosomes and in the nuclear space of the human genome

Thévenin, A., Ein-Dor, L., Ozery-Flato, M., & Shamir, R. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku667 · Cited by 84

Pilus Biogenesis in Lactococcus lactis: Molecular Characterization and Role in Aggregation and Biofilm Formation

Oxaran, V., Ledue-Clier, F., Dieye, Y., Herry, J.-M., Péchoux, C., Meylheuc, T., Briandet, R., Juillard, V., & Piard, J.-C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0050989 · Cited by 73

ArgR is an essential local transcriptional regulator of the arcABC operon in Streptococcus suis and is crucial for biological fitness in an acidic environment

Fulde, M., Willenborg, J., de Greeff, A., Benga, L., Smith, H. E., Valentin-Weigand, P., & Goethe, R. (2011) · Microbiology · doi:10.1099/mic.0.043067-0 · Cited by 70

Expression and Activation of Matrix Metalloproteinases in Wounds: Modulation by the Tripeptide–Copper Complex Glycyl-L-Histidyl-L-Lysine-Cu2+

Siméon, A., Monier, F., Emonard, H., Gillery, P., Hornebeck, W., Maquart, F.-X., & Birembaut, P. (1999) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.1999.00606.x · Cited by 68

Functional Characterization of the Bacterial iac Genes for Degradation of the Plant Hormone Indole-3-Acetic Acid

Scott, J. C., Greenhut, I. V., & Leveau, J. H. J. (2013) · Journal of Chemical Ecology · doi:10.1007/s10886-013-0324-x · Cited by 67

The iCRISPR Platform for Rapid Genome Editing in Human Pluripotent Stem Cells

Zhu, Z., González, F., & Huangfu, D. (2014) · Methods in Enzymology · doi:10.1016/b978-0-12-801185-0.00011-8 · Cited by 66

Modelling the Regulation of Thermal Adaptation in Candida albicans, a Major Fungal Pathogen of Humans

Leach, M. D., Tyc, K. M., Brown, A. J. P., & Klipp, E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032467 · Cited by 61

Mechanisms Employed by Escherichia coli to Prevent Ribonucleotide Incorporation into Genomic DNA by Pol V

McDonald, J. P., Vaisman, A., Kuban, W., Goodman, M. F., & Woodgate, R. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1003030 · Cited by 38

ERG2 and ERG24 Are Required for Normal Vacuolar Physiology as Well as Candida albicans Pathogenicity in a Murine Model of Disseminated but Not Vaginal Candidiasis

Luna-Tapia, A., Peters, B. M., Eberle, K. E., Kerns, M. E., Foster, T. P., Marrero, L., Noverr, M. C., Fidel, P. L., & Palmer, G. E. (2015) · Eukaryotic Cell · doi:10.1128/ec.00116-15 · Cited by 35

Spontaneous mutation in Escherichia coli containing the dnaE911 DNA polymerase antimutator allele

Oller, A. R., & Schaaper, R. M. (1994) · Genetics · doi:10.1093/genetics/138.2.263 · Cited by 33

Sub-diffraction Limit Localization of Proteins in Volumetric Space Using Bayesian Restoration of Fluorescence Images from Ultrathin Specimens

Wang, G., & Smith, S. J. (2012) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002671 · Cited by 27

Endosomal Trafficking Defects Can Induce Calcium-Dependent Azole Tolerance in Candida albicans

Luna-Tapia, A., Tournu, H., Peters, T. L., & Palmer, G. E. (2016) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01034-16 · Cited by 12

Early Systems Biology and Prebiotic Networks

Shenhav, B., Solomon, A., Lancet, D., & Kafri, R. (2005) · Lecture Notes in Computer Science · doi:10.1007/978-3-540-32126-2_2 · Cited by 13