Genomic Diversity and Versatility of Lactobacillus plantarum, a Natural Metabolic Engineer

Random Forests

Breiman, L. (2001) · Machine Learning · doi:10.1023/a:1010933404324 · Cited by 133,538 · see citing works

Classification and Regression by randomForest

Liaw, A. I., & Wiener, M. C. (2007) · Cited by 18,594 · see citing works

Food microbiology : fundamentals and frontiers

Doyle, M. P., Beuchat, L. R., & Montville, T. J. (2013) · doi:10.1128/9781555819972 · Cited by 3,589 · see citing works

Complete genome sequence of <i>Lactobacillus plantarum</i> WCFS1

Kleerebezem, M., Boekhorst, J., van Kranenburg, R., Molenaar, D., Kuipers, O. P., Leer, R., Tarchini, R., Peters, S. A., Sandbrink, H. M., Fiers, M. W. E. J., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0337704100 · Cited by 1,472 · see citing works

Probiotics and the gut microbiota in intestinal health and disease

Gareau, M. G., Sherman, P. M., & Walker, W. A. (2010) · Nature Reviews Gastroenterology &amp; Hepatology · doi:10.1038/nrgastro.2010.117 · Cited by 907 · see citing works

Differentiation of Lactobacillus plantarum, L. pentosus, and L. paraplantarum by recA Gene Sequence Analysis and Multiplex PCR Assay with recA Gene-Derived Primers

Torriani, S., Felis, G. E., & Dellaglio, F. (2001) · Applied and Environmental Microbiology · doi:10.1128/aem.67.8.3450-3454.2001 · Cited by 626 · see citing works

Artemis and ACT: viewing, annotating and comparing sequences stored in a relational database

Carver, T. J., Berriman, M., Tivey, A. R., Patel, C., Böhme, U., BARRELL, B. G., Parkhill, J., & Rajandream, M. (2008) · Bioinformatics · doi:10.1093/bioinformatics/btn529 · Cited by 572 · see citing works

The normal Lactobacillus flora of healthy human rectal and oral mucosa

Ahrné, Nobaek, Jeppsson, Adlerberth, Wold, A. E., & Molin (1998) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.1998.00480.x · Cited by 439 · see citing works

Engineering for biofuels: exploiting innate microbial capacity or importing biosynthetic potential?

Alper, H. S., & Stephanopoulos, G. N. (2009) · Nature Reviews Microbiology · doi:10.1038/nrmicro2186 · Cited by 384 · see citing works

Differential NF-κB pathways induction by Lactobacillus plantarum in the duodenum of healthy humans correlating with immune tolerance

van Baarlen, P., Troost, F. J., van Hemert, S., van Kraaij, C., de Vos, W. M., de Groot, P. J., Hooiveld, G. J. E. J., Brummer, R. J., & Kleerebezem, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809919106 · Cited by 384 · see citing works

The extracellular biology of the lactobacilli

Kleerebezem, M., Pascal Hols, A., Bernard, E., Rolain, T., Zhou, M., Siezen, R. J., & Bron, P. A. (2009) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2009.00208.x · Cited by 381 · see citing works

Carbohydrate, peptide and lipid metabolism of lactic acid bacteria in sourdough

Gänzle, M. G., Vermeulen, N., & Vogel, R. F. (2006) · Food Microbiology · doi:10.1016/j.fm.2006.07.006 · Cited by 367 · see citing works

Taxonomy of Lactobacilli and Bifidobacteria.

Felis, G. E., & Dellaglio, F. (2007) · PubMed · Cited by 326 · see citing works

Taxonomy of lactobacilli and bifidobacteria.

Dellaglio, F., & Felis, G. E. (2005) · Cited by 319 · see citing works

Biodiversity, ecological determinants, and metabolic exploitation of sourdough microbiota

Vuyst, L. D., Vrancken, G., Ravyts, F., Rimaux, T., & Weckx, S. (2009) · Food Microbiology · doi:10.1016/j.fm.2009.07.012 · Cited by 310 · see citing works

Phenotypic and genomic diversity of Lactobacillus plantarum strains isolated from various environmental niches

Siezen, R. J., Tzeneva, V. A., Castioni, A., Wels, M., Phan, H. T. K., Rademaker, J. L. W., Starrenburg, M. J. C., Kleerebezem, M., Douwe Molenaar, B., & Vlieg, J. E. T. V. H. (2009) · Environmental Microbiology · doi:10.1111/j.1462-2920.2009.02119.x · Cited by 293 · see citing works

Analysis of Growth of Lactobacillus plantarum WCFS1 on a Complex Medium Using a Genome-scale Metabolic Model

Teusink, B., Wiersma, A., Douwe Molenaar, B., Francke, C., de Vos, W. M., Siezen, R. J., & Smid, E. J. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m606263200 · Cited by 283 · see citing works

Bacterial Community Structure and Location in Stilton Cheese

Ercolini, D., Hill, P. J., & Dodd, C. E. R. (2003) · Applied and Environmental Microbiology · doi:10.1128/aem.69.6.3540-3548.2003 · Cited by 280 · see citing works

Biochemistry, Genetics, and Applications of Exopolysaccharide Production in Streptococcus thermophilus: A Review

Broadbent, J. R., McMahon, D. J., Welker, D. L., Oberg, C. J., & Moineau, S. (2003) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(03)73619-4 · Cited by 271 · see citing works

Structure-Function Relationships of the Non-Lanthionine-Containing Peptide (class II) Bacteriocins Produced by Gram-Positive Bacteria

Nissen-Meyer, J., Rogne, P., Oppegård, C., Haugen, H., & Kristiansen, P. E. (2009) · Current Pharmaceutical Biotechnology · doi:10.2174/138920109787048661 · Cited by 256 · see citing works

Selection and characterization of mixed starter cultures for lactic acid fermentation of carrot, cabbage, beet and onion vegetable mixtures

Gardner, N. J., Savard, T., Obermeier, P., Caldwell, G., & Champagne, C. P. (2001) · International Journal of Food Microbiology · doi:10.1016/s0168-1605(00)00461-x · Cited by 255 · see citing works

Microbial Quality and Direct PCR Identification of Lactic Acid Bacteria and Nonpathogenic Staphylococci from Artisanal Low-Acid Sausages

Aymerich, T., Martín, B., Garriga, M., et al. (2003) · Applied and Environmental Microbiology · doi:10.1128/aem.69.8.4583-4594.2003 · Cited by 252 · see citing works

ExploringLactobacillus plantarumGenome Diversity by Using Microarrays

Molenaar, D., Bringel, F., Schuren, F. H. J., de Vos, W. M., Siezen, R. J., & Kleerebezem, M. (2005) · Journal of Bacteriology · doi:10.1128/jb.187.17.6119-6127.2005 · Cited by 252 · see citing works

Reconstructing the metabolic network of a bacterium from its genome

Francke, C., Siezen, R. J., & Teusink, B. (2005) · Trends in Microbiology · doi:10.1016/j.tim.2005.09.001 · Cited by 239 · see citing works

At the crossroads of vaginal health and disease, the genome sequence of Lactobacillus iners AB-1

Macklaim, J. M., Gloor, G. B., Anukam, K. C., Cribby, S., & Reid, G. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000086107 · Cited by 217 · see citing works

DNA Fingerprinting of Lactic Acid Bacteria in Sauerkraut Fermentations

Plengvidhya, V., Breidt, F., Lu, Z., & Fleming, H. P. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.01342-07 · Cited by 214 · see citing works

Structure and Mode-of-Action of the Two-Peptide (Class-IIb) Bacteriocins

Nissen-Meyer, J., Oppegård, C., Rogne, P., Haugen, H. S., & Kristiansen, P. E. (2009) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-009-9021-z · Cited by 199 · see citing works

In Silico Reconstruction of the Metabolic Pathways of Lactobacillus plantarum : Comparing Predictions of Nutrient Requirements with Those from Growth Experiments

Teusink, B., van Enckevort, F. H. J., Francke, C., Wiersma, A., Wegkamp, A., Smid, E. J., & Siezen, R. J. (2005) · Applied and Environmental Microbiology · doi:10.1128/aem.71.11.7253-7262.2005 · Cited by 180 · see citing works

An overview of the mosaic bacteriocin pln loci from Lactobacillus plantarum

Diep, D. B., Straume, D., Kjos, M., Torres, C., & Nes, I. F. (2009) · Peptides · doi:10.1016/j.peptides.2009.05.014 · Cited by 177 · see citing works

The microbial ecology of a typical Italian salami during its natural fermentation

Aquilanti, L., Santarelli, S., Silvestri, G., Osimani, A., Petruzzelli, A., & Clementi, F. (2007) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2007.06.010 · Cited by 150 · see citing works

Understanding the Adaptive Growth Strategy of Lactobacillus plantarum by In Silico Optimisation

Teusink, B., Wiersma, A., Jacobs, L., Notebaart, R. A., & Smid, E. J. (2009) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000410 · Cited by 143 · see citing works

Lactobacillus plantarum subsp. argentoratensis subsp. nov., isolated from vegetable matrices

Bringel, F., Castioni, A., Olukoya, D. K., et al. (2005) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.63333-0 · Cited by 131 · see citing works

The predicted secretome of Lactobacillus plantarum WCFS1 sheds light on interactions with its environment

Boekhorst, J., Wels, M., Kleerebezem, M., & Siezen, R. J. (2006) · Microbiology · doi:10.1099/mic.0.29217-0 · Cited by 114 · see citing works

Lactobacillus plantarum gene clusters encoding putative cell-surface protein complexes for carbohydrate utilization are conserved in specific gram-positive bacteria

Siezen, R. J., Boekhorst, J., Muscariello, L., Molenaar, D., Renckens, B., & Kleerebezem, M. (2006) · BMC Genomics · doi:10.1186/1471-2164-7-126 · Cited by 112 · see citing works

Similarity and Differences in the Lactobacillus acidophilus Group Identified by Polyphasic Analysis and Comparative Genomics

Berger, B. W., Pridmore, R. D., Barretto, C., Delmas-Julien, F., Schreiber, K., Arigoni, F., & Brüssow, H. (2006) · Journal of Bacteriology · doi:10.1128/jb.01393-06 · Cited by 108 · see citing works

Development of a multilocus sequence typing method for analysis of Lactobacillus plantarum strains

Rivas, B. D. L., Marcobal, A. M., & Múñoz, R. (2005) · Microbiology · doi:10.1099/mic.0.28482-0 · Cited by 106 · see citing works

Convergence in probiotic Lactobacillus gut-adaptive responses in humans and mice

Marco, M. L., de Vries, M. C., Wels, M., Douwe Molenaar, B., Mangell, P., Ahrné, S., de Vos, W. M., Vaughan, E. E., & Kleerebezem, M. (2010) · The ISME Journal · doi:10.1038/ismej.2010.61 · Cited by 105 · see citing works

The complete genomes of Lactobacillus plantarum and Lactobacillus johnsonii reveal extensive differences in chromosome organization and gene content

Boekhorst, J., Siezen, R. J., Zwahlen, M.-C., Vilanova, D., Pridmore, R. D., Mercenier, A., Kleerebezem, M., de Vos, W. M., Brüssow, H., & Desiere, F. (2004) · Microbiology · doi:10.1099/mic.0.27392-0 · Cited by 105 · see citing works

Use of the probiotic Lactobacillus plantarum 299 to reduce pathogenic bacteria in the oropharynx of intubated patients: a randomised controlled open pilot study

Klarin, B., Molin, G., Jeppsson, B. W., & Larsson, A. (2008) · Critical Care · doi:10.1186/cc7109 · Cited by 104 · see citing works

Streptococcus thermophilus Core Genome: Comparative Genome Hybridization Study of 47 Strains

Rasmussen, T. B., Danielsen, M., Valina, O., Garrigues, C., Johansen, E., & Pedersen, M. B. (2008) · Applied and Environmental Microbiology · doi:10.1128/aem.00132-08 · Cited by 102 · see citing works

Complete Genome Sequence of Lactobacillus plantarum JDM1

Zhang, Z. Y., Liu, C., Zhu, Y., Zhong, Y., Zhu, Y., Zheng, H., Zhao, G., Wang, S., & Guo, X. (2009) · Journal of Bacteriology · doi:10.1128/jb.00587-09 · Cited by 93 · see citing works

Complete Genome Sequence of the Probiotic Lactobacillus plantarum ST-III

Wang, Y., Chen, C., Ai, L., et al. (2010) · Journal of Bacteriology · doi:10.1128/jb.01159-10 · Cited by 93 · see citing works

LAB-Secretome: a genome-scale comparative analysis of the predicted extracellular and surface-associated proteins of Lactic Acid Bacteria

Zhou, M., Theunissen, D. H. J., Wels, M., & Siezen, R. J. (2010) · BMC Genomics · doi:10.1186/1471-2164-11-651 · Cited by 90 · see citing works

Genome‐scale diversity and niche adaptation analysis of Lactococcus lactis by comparative genome hybridization using multi‐strain arrays

Siezen, R. J., Bayjanov, J. R., Felis, G. E., van der Sijde, M. R., Starrenburg, M. J. C., Douwe Molenaar, B., Wels, M., van Hijum, S. A. F. T., & Vlieg, J. E. T. V. H. (2011) · Microbial Biotechnology · doi:10.1111/j.1751-7915.2011.00247.x · Cited by 89 · see citing works

Genomic Diversity of Lactobacillus salivarius

Raftis, E. J., Salvetti, E., Torriani, S., Felis, G. E., & O’Toole, P. W. (2010) · Applied and Environmental Microbiology · doi:10.1128/aem.01687-10 · Cited by 85 · see citing works

Differentiation of Lactobacillus plantarum, L. pentosus and L. paraplantarum Species by RAPD-PCR and AFLP

Torriani, S., Clementi, F., Vancanneyt, M., Hoste, B., Dellaglio, F., & Kersters, K. (2001) · Systematic and Applied Microbiology · doi:10.1078/0723-2020-00071 · Cited by 84 · see citing works

Community Dynamics of Bacteria in Sourdough Fermentations as Revealed by Their Metatranscriptome

Weckx, S., der Meulen, R. V., Allemeersch, J., Huys, G. R. B., Vandamme, P. A. R., Hummelen, P. V., & Vuyst, L. D. (2010) · Applied and Environmental Microbiology · doi:10.1128/aem.00570-10 · Cited by 82 · see citing works

Visualization for genomics: the Microbial Genome Viewer

Kerkhoven, R., van Enckevort, F. H. J., Boekhorst, J., et al. (2004) · Bioinformatics · doi:10.1093/bioinformatics/bth159 · Cited by 80 · see citing works

Are horizontal transfers involved in the evolution of the Streptococcus thermophilus exopolysaccharide synthesis loci?

Charron-Bourgoin, F., Pluvinet, A., Gintz, B., Decaris, B., & Guédon, G. (1999) · Gene · doi:10.1016/s0378-1119(99)00144-4 · Cited by 76 · see citing works

Lactobacilli on Plants

Mundt, J. O., & Hammer, J. L. (1968) · Applied Microbiology · doi:10.1128/am.16.9.1326-1330.1968 · Cited by 72 · see citing works

Genome data mining of lactic acid bacteria: the impact of bioinformatics

Siezen, R. J., van Enckevort, F. H. J., Kleerebezem, M., & Teusink, B. (2004) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2004.02.002 · Cited by 68 · see citing works

Lactobacillus fabifermentans sp. nov. and Lactobacillus cacaonum sp. nov., isolated from Ghanaian cocoa fermentations

Bruyne, K. D., Camu, N., Vuyst, L. D., & Vandamme, P. A. R. (2009) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.001172-0 · Cited by 65 · see citing works

Genetic diversity of the pln locus among oenological Lactobacillus plantarum strains

Sáenz, Y., Rojo‐Bezares, B., Navarro, L., Díez, L., Somalo, S., Zarazaga, M., Ruiz‐Larrea, F., & Torres, C. (2009) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2009.06.004 · Cited by 61 · see citing works

The occurrence and growth of microorganisms during the fermentation of fish sausage

Aryanta, R. W., Fleet, G. H., & Buckle, K. A. (1991) · International Journal of Food Microbiology · doi:10.1016/0168-1605(91)90056-u · Cited by 59 · see citing works

Cell–cell communication in sourdough lactic acid bacteria: A proteomic study in Lactobacillus sanfranciscensis CB1

Cagno, R. D., Angelis, M. D., Limitone, A., Minervini, F., Simonetti, M. C., Buchin, S., & Gobbetti, M. (2007) · PROTEOMICS · doi:10.1002/pmic.200700143 · Cited by 58 · see citing works

A generic approach to identify Transcription Factor-specific operator motifs; Inferences for LacI-family mediated regulation in Lactobacillus plantarum WCFS1

Francke, C., Kerkhoven, R., Wels, M., & Siezen, R. J. (2008) · BMC Genomics · doi:10.1186/1471-2164-9-145 · Cited by 51 · see citing works

Polyphasic Investigation of the Diversity within Lactobacillus plantarum Related Strains Revealed Two L. plantarum subgroups

Bringel, F., Quénée, P., & Tailliez, P. (2001) · Systematic and Applied Microbiology · doi:10.1078/0723-2020-00061 · Cited by 50 · see citing works

Biodiversity of mannose-specific adhesion in Lactobacillus plantarum revisited: strain-specific domain composition of the mannose-adhesin

Gross, G., Snel, J., Boekhorst, J., Smits, M. A., & Kleerebezem, M. (2009) · Beneficial Microbes · doi:10.3920/bm2008.1006 · Cited by 50 · see citing works

Predicting cis-acting elements of Lactobacillus plantarum by comparative genomics with different taxonomic subgroups

Wels, M. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl138 · Cited by 44 · see citing works

Metatranscriptome Analysis for Insight into Whole-Ecosystem Gene Expression during Spontaneous Wheat and Spelt Sourdough Fermentations

Weckx, S., Allemeersch, J., der Meulen, R. V., Vrancken, G., Huys, G. R. B., Vandamme, P. A. R., Hummelen, P. V., & Vuyst, L. D. (2010) · Applied and Environmental Microbiology · doi:10.1128/aem.02028-10 · Cited by 43 · see citing works

Molecular Description and Industrial Potential of Tn <i>6098</i> Conjugative Transfer Conferring Alpha-Galactoside Metabolism in <i>Lactococcus lactis</i>

Machielsen, R., Siezen, R. J., van Hijum, S. A. F. T., & van Hylckama Vlieg, J. E. T. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.02283-10 · Cited by 34 · see citing works

Comparison of Components and Synthesis Genes of Cell Wall Teichoic Acid amongLactobacillus plantarumStrains

Tomita, S., Irisawa, T., Tanaka, N., Nukada, T., Satoh, E., Uchimura, T., & Okada, S. (2010) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.90736 · Cited by 30 · see citing works

Monitoring Lactobacillus plantarum BCC 9546 starter culture during fermentation of Nham, a traditional Thai pork sausage

Luxananil, P., Promchai, R., Wanasen, S., et al. (2008) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2008.12.011 · Cited by 29 · see citing works

Reconstruction of the regulatory network of Lactobacillus plantarum WCFS1 on basis of correlated gene expression and conserved regulatory motifs

Wels, M., Overmars, L., Francke, C., Kleerebezem, M., & Siezen, R. J. (2010) · Microbial Biotechnology · doi:10.1111/j.1751-7915.2010.00217.x · Cited by 28 · see citing works

Probiotics genomics

Siezen, R. J., & Wilson, G. (2009) · Microbial Biotechnology · doi:10.1111/j.1751-7915.2009.00159.x · Cited by 26 · see citing works

Development and Validation of a Species-Independent Functional Gene Microarray That Targets Lactic Acid Bacteria

Weckx, S., Allemeersch, J., der Meulen, R. V., Vrancken, G., Huys, G. R. B., Vandamme, P. A. R., Hummelen, P. V., & Vuyst, L. D. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01055-09 · Cited by 25 · see citing works

Stress Physiology of Lactic Acid Bacteria.

Papadimitriou, K., Alegría, Á., Bron, P. A., de Angelis, M., Gobbetti, M., Kleerebezem, M., Lemos, J. A., Linares, D. M., Ross, P., Stanton, C., et al. (2016) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00076-15 · Cited by 914 · see citing works

Fate, activity, and impact of ingested bacteria within the human gut microbiota

Derrien, M., & van Hylckama Vlieg, J. E. T. (2015) · Trends in Microbiology · doi:10.1016/j.tim.2015.03.002 · Cited by 605 · see citing works

Nitrate reduction to nitrite, nitric oxide and ammonia by gut bacteria under physiological conditions

Tiso, M., & Schechter, A. N. (2015) · PLOS ONE · doi:10.1371/journal.pone.0119712 · Cited by 311 · see citing works

Lactic Acid Bacteria Exopolysaccharides Producers: A Sustainable Tool for Functional Foods

Prete, R., Alam, M. K., Perpetuini, G., Perla, C., Pittia, P., & Corsetti, A. (2021) · Foods · doi:10.3390/foods10071653 · Cited by 194 · see citing works

Comparative Genome Analysis of Lactococcus lactis Indicates Niche Adaptation and Resolves Genotype/Phenotype Disparity

Wels, M., Siezen, R., van Hijum, S., Kelly, W. J., & Bachmann, H. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00004 · Cited by 181 · see citing works

Unconventional microbial systems for the cost-efficient production of high-quality protein therapeutics

Corchero, J. L., Gasser, B., Resina, D., Smith, W., Parrilli, E., Vázquez, F., Abasolo, I., Giuliani, M., Jäntti, J., Ferrer, P., et al. (2013) · Biotechnology Advances · doi:10.1016/j.biotechadv.2012.09.001 · Cited by 133 · see citing works

Impact of 4 Lactobacillus plantarum Capsular Polysaccharide Clusters on Surface Glycan Composition and Host Cell Signaling

Remus, D. M., van Kranenburg, R., van Swam, I. I., Taverne, N., Bongers, R. S., Wels, M., Wells, J. M., Bron, P. A., & Kleerebezem, M. (2012) · Microbial Cell Factories · doi:10.1186/1475-2859-11-149 · Cited by 131 · see citing works

Insights into the completely annotated genome of Lactobacillus buchneri CD034, a strain isolated from stable grass silage.

Heinl, S., Wibberg, D., Eikmeyer, F., Szczepanowski, R., Blom, J., Linke, B., Goesmann, A., Grabherr, R., Schwab, H., Pühler, A., et al. (2012) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2012.03.007 · Cited by 102 · see citing works

Complete Genome Sequence of Bacteriocin-Producing Lactobacillus plantarum KLDS1.0391, a Probiotic Strain with Gastrointestinal Tract Resistance and Adhesion to the Intestinal Epithelial Cells

Jia, F.-F., Zhang, L.-J., Pang, X.-H., Gu, X.-X., Abdelazez, A., Liang, Y., Sun, S.-R., & Meng, X.-C. (2017) · Genomics · doi:10.1016/j.ygeno.2017.06.008 · Cited by 82 · see citing works

Feasibility of genome-wide screening for biosafety assessment of probiotics: A case study of Lactobacillus helveticus MTCC 5463

Senan, S., Prajapati, J. B., & Joshi, C. G. (2015) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-015-9199-1 · Cited by 46 · see citing works

Bile salt hydrolase activity is present in nonintestinal lactic acid bacteria at an intermediate level

Ru, X., Zhang, C.-C., Yuan, Y.-H., Yue, T.-L., & Guo, C.-F. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-018-9492-5 · Cited by 45 · see citing works

New insights into the role of plasmids from probiotic Lactobacillus pentosus MP-10 in Aloreña table olive brine fermentation

Abriouel, H., Pérez Montoro, B., de la Fuente Ordoñez, J. J., Lavilla Lerma, L., Knapp, C. W., & Benomar, N. (2019) · Scientific Reports · doi:10.1038/s41598-019-47384-1 · Cited by 22 · see citing works

Strain-specific metabolomic diversity of Lactiplantibacillus plantarum under aerobic and anaerobic conditions

Kim, S.-H., Singh, D., Kim, S.-A., Kwak, M. J., Cho, D., Kim, J., Roh, J.-H., Kim, W.-G., Han, N. S., & Lee, C. H. (2023) · Food Microbiology · doi:10.1016/j.fm.2023.104364 · Cited by 12 · see citing works

Functional Genomics and the Comparative Physiology of Hypoxia

Powell, F. L. (2003) · Annual Review of Physiology · doi:10.1146/annurev.physiol.65.092101.142711 · Cited by 47 · see citing works

Functional genomics of microbial pathogens

Lazarević, V., & François, P. (2013) · Briefings in Functional Genomics · doi:10.1093/bfgp/elt032 · Cited by 4 · see citing works

Human-Mouse Comparative Genomics: Successes and Failures to Reveal Functional Regions of the Human GenomePreprint

Pennacchio, L. A., Baroukh, N., & Rubin, E. M. (2003) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2003.68.303 · Cited by 10 · see citing works

Comparative population genomics: power and principles for the inference of functionality

Lawrie, D. S., & Petrov, D. A. (2014) · Trends in Genetics · doi:10.1016/j.tig.2014.02.002 · Cited by 52 · see citing works

A powerful tool for functional genomics research——Comparative genomics

Zhi-gang, G. (2005) · Dongbei Nongye Daxue xuebao · Cited by 1 · see citing works