Genetically dictated change in host mucus carbohydrate landscape exerts a diet-dependent effect on the gut microbiota

QIIME allows analysis of high-throughput community sequencing data

Caporaso, J. G., Kuczynski, J., Stombaugh, J., Bittinger, K., Bushman, F. D., Costello, E. K., Fierer, N., Peña, A. G., Goodrich, J. K., Gordon, J. I., et al. (2010) · Nature Methods · doi:10.1038/nmeth.f.303 · Cited by 34,887

Human gut microbiome viewed across age and geography

Yatsunenko, T., Rey, F. E., Manary, M. J., Trehan, I., Dominguez-Bello, M. G., Contreras, M., Magris, M., Hidalgo, G., Baldassano, R. N., Anokhin, A. P., et al. (2012) · Nature · doi:10.1038/nature11053 · Cited by 7,815

Linking long-term dietary patterns with gut microbial enterotypes

Wu, G. D., Chen, J., Hoffmann, C., Bittinger, K., Chen, Y.-Y., Keilbaugh, S. A., Bewtra, M., Knights, D., Walters, W. A., Knight, R., et al. (2011) · Science · doi:10.1126/science.1208344 · Cited by 6,513

The Carbohydrate-Active EnZymes database (CAZy): an expert resource for Glycogenomics

Cantarel, B. L., Coutinho, P. M., Rancurel, C., Bernard, T., Lombard, V., & Henrissat, B. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn663 · Cited by 6,108

Unravelling the pathogenesis of inflammatory bowel disease

Xavier, R. J., & Podolsky, D. K. (2007) · Nature · doi:10.1038/nature06005 · Cited by 4,364

Interactions Between the Microbiota and the Immune System

Hooper, L. V., Littman, D. R., & Macpherson, A. J. (2012) · Science · doi:10.1126/science.1223490 · Cited by 4,173

The Effect of Diet on the Human Gut Microbiome: A Metagenomic Analysis in Humanized Gnotobiotic Mice

Turnbaugh, P. J., Ridaura, V. K., Faith, J. J., Rey, F. E., Knight, R., & Gordon, J. I. (2009) · Science Translational Medicine · doi:10.1126/scitranslmed.3000322 · Cited by 3,058 · cited 1×

Dysfunction of the intestinal microbiome in inflammatory bowel disease and treatment

Morgan, X. C., Tickle, T. L., Sokol, H., Gevers, D., Devaney, K. L., Ward, D. V., Reyes, J. A., Shah, S. A., LeLeiko, N., Snapper, S. B., et al. (2012) · Genome Biology · doi:10.1186/gb-2012-13-9-r79 · Cited by 2,713

dbCAN: a web resource for automated carbohydrate-active enzyme annotation

Yin, Y.-B., Mao, X., Yang, J., Chen, X., Mao, F., & Xu, Y. (2012) · Nucleic Acids Res. · doi:10.1093/nar/gks479 · Cited by 1,666

UniFrac – An online tool for comparing microbial community diversity in a phylogenetic context

Lozupone, C., Hamady, M., & Knight, R. D. (2006) · BMC Bioinformatics · doi:10.1186/1471-2105-7-371 · Cited by 1,454

Fut2 deficiency aggravates chronic colitis through 2-oxindole-AHR mediated cGAS-STING pathway

Hong, G., Zhao, Y., Li, Q., & Liu, S. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.112512 · Cited by 7

Electroacupuncture Alleviates Brain Injury Through Vagus Nerve Activation and Gut Microbiota in a Rat Model of Ischemic Stroke

Zhao, Q., Ning, Y., Xu, T., Zhao, Z., Pei, Y., Niu, J., Li, X., & Chen, D. (2025) · Journal of the American Heart Association · doi:10.1161/jaha.125.045929 · Cited by 9

Exercise and the Gut Microbiome: From Mechanisms to Clinical Applications

AL-Sinani, Y., Rostamkhani, F., & Shirvani, H. (2026) · Nutrients · doi:10.3390/nu18101565 · Cited by 8

Translational evaluation of Gelsectan ® effects on gut barrier dysfunction and visceral pain in animal models and irritable bowel syndrome with diarrhoea

Inczefi, O., Eutamène, H., Placide, F., Tondereau, V., Pallagi, P., Bagyánszki, M., Bódi, N., Gémes, N., Szebeni, G. J., Molnár, T., et al. (2024) · United European Gastroenterology Journal · doi:10.1002/ueg2.12625 · Cited by 6

Mice deficient in intestinal γδ intraepithelial lymphocytes display an altered intestinal O-glycan profile compared with wild-type littermates

Fuell, C., Coleman, O. I., Hautefort, I., & Juge, N. (2014) · Glycobiology · doi:10.1093/glycob/cwu088 · Cited by 7

Blood group O expression in normal tissues and tumors

Tulin, E. K. C., Muerner, L., McKitrick, T. R., Tilton, C. A., Pepi, L. E., Jia, T., Noël, M., Zheng, L., Stowell, S. R., von Gunten, S., et al. (2025) · FEBS Journal · doi:10.1111/febs.70172 · Cited by 6

The Research Progress on the Interaction between Mammalian Gut Microbiota and the Host’s Metabolism Homeostasis during Hibernation

Zhang, Z., Song, F., Wang, L., & Yuan, Z. (2024) · Metabolites · doi:10.3390/metabo14030134 · Cited by 5

Resistance is futile? Mucosal immune mechanisms in the context of microbial ecology and evolution

Slack, E. M. C., & Diard, M. (2022) · Mucosal Immunology · doi:10.1038/s41385-022-00574-z · Cited by 6

The Gut Microbiome in Inflammatory Bowel Disease

Lavelle, A., & Sokol, H. (2019) · Springer eBooks · doi:10.1007/978-3-030-28703-0_16 · Cited by 6

Bacteriophage Adaptation to a Mammalian Mucosa Reveals a Trans-Domain Evolutionary AxisPreprint

Chin, W. H., Kett, C., Cooper, O., Müseler, D., Zhang, Y., Bamert, R. S., Patwa, R. R., Woods, L. C., Devendran, C., Tiralongo, J., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.05.11.443681 · Cited by 6

A type 4 resistant potato starch alters the cecal microbiome, gene expression and resistance to colitis in mice fed a Western diet based on NHANES data

Pletsch, E. A., Dawson, H. D., Cheung, L., Ragonese, J., Chen, C. T., & Smith, A. D. (2025) · Food & Function · doi:10.1039/d4fo04697h · Cited by 5

Intestinal Fut2 deficiency exacerbated alcohol‐related liver disease by disrupting nicotinamide metabolism

Chen, L., Yin, Z., Shang, L., Yuan, H., Gao, W., Wang, S., Wang, S., Hou, X., Yang, S., & Chu, H. (2025) · Clinical and Translational Medicine · doi:10.1002/ctm2.70447 · Cited by 5

Nutrient encryption and the diversity of cobamides, siderophores, and glycans

Taga, M. E., & Ludington, W. B. (2022) · Trends in Microbiology · doi:10.1016/j.tim.2022.11.011 · Cited by 4

Fucosylated TLR4 mediates communication between mutualist fucotrophic microbiota and mammalian gut mucosa

Nanthakumar, N. N., Meng, D., & Newburg, D. S. (2023) · Frontiers in Medicine · doi:10.3389/fmed.2023.1070734 · Cited by 5

Diet Effects on Gut Microbiome Composition, Function, and Host Physiology

Battaglioli, E. J., & Kashyap, P. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809954-4.00033-5 · Cited by 6

Toxigenic gut bacteria, diet and colon carcinogenesis

Keenan, J. I., & Frizelle, F. (2019) · Journal of the Royal Society of New Zealand · doi:10.1080/03036758.2019.1695636 · Cited by 6

481 Individualized Responses of Gut Microbiota to Dietary Intervention Modeled in Humanized Mice

Kashyap, P., Marcobal, A. M., Higginbottom, S. K., Smits, S. A., & Sonnenburg, J. L. (2013) · Gastroenterology · doi:10.1016/s0016-5085(13)60325-x · Cited by 5

The Cholesterol-Lowering Effects of Probiotic Bacteria on Lipid Metabolism

Aydaş, S. B., & Aslım, B. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-802189-7.00054-x · Cited by 5

Mucins: Progress in Understanding Physiological Functions and Involvement in Pathological Processes and Prospects for Use (A Review)

Георгиевна, Б. Н. (2025) · Applied Biochemistry and Microbiology · doi:10.1134/s0003683825600046 · Cited by 4

Human Milk Oligosaccharides as Modulators of Intestinal and Systemic Immunity

Comstock, S. S., & Donovan, S. M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802725-7.00008-7 · Cited by 4

Host immunity alters successional ecology and stability of the microbiome in a C. elegans modelPreprint

Taylor, M. N., & Vega, N. M. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.26.174706 · Cited by 4

Diet Leaves a Genetic Signature in a Keystone Member of the Gut MicrobiotaPreprint

Đapa, T., Pedro, M. F., Ramiro, R. S., Gordo, I., & Xavier, K. B. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3907580 · Cited by 4

Seasonal changes in gut microbiota of sea cucumber over natural aestivation cycle

Zhao, Y., Wang, H., Wang, H., Zhang, L., Sun, H., & Zhang, Y. (2024) · Journal of Oceanology and Limnology · doi:10.1007/s00343-023-3077-6 · Cited by 3

Commensal bacteria prevent pathogenic bacterial infection by inducing of activation of host immune system

Goto, Y. (2020) · Nippon Saikingaku Zasshi · doi:10.3412/jsb.75.185 · Cited by 3

Secretory Defense Response in the Bird’s Gastro-Intestinal Tract and Nutritional Strategies to Modulate It

Gómez-Osorio, L.-M., Jiang, Z., Zhang, Q., Yan, H., Villegas, A.-M., & Applegate, T. J. (2021) · IntechOpen eBooks · doi:10.5772/intechopen.95952 · Cited by 3

Host gene effects on gut microbiota in type 1 diabetes

Guo, K., Huang, J., & Zhou, Z. (2022) · Biochemical Society Transactions · doi:10.1042/bst20220004 · Cited by 3

Ileal mucosal response to the same probiotic Lactobacillus strains is markedly different between suckling and adult mice

Inoüe, R., Fujiwara, S., & Tsukahara, T. (2018) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2017.1422387 · Cited by 3

Glycoproteomic analysis identifies cryptdin-related sequence 1 as O-glycosylated protein modified with α1,2-fucose in the small intestine

Hashiguchi, H., Tsukamoto, Y., Ogawa, M., Tashima, Y., Takeuchi, H., Nakamura, M., Kawashima, H., Fujishiro, M., & Okajima, T. (2020) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2020.108653 · Cited by 3

Mucin Type Drives Composition and Mucin Glycan Degradation of an In Vitro Synthetic Microbial Community

Berkhout, M. D., de Ram, C., van Gaal, M. P., Schols, H. A., Belzer, C., & Plugge, C. M. (2026) · Environmental Microbiology · doi:10.1111/1462-2920.70288 · Cited by 2

Potential Public Health Impact of Human Milk Oligosaccharides

Morrow, A. L., & Yu, Y. Q. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802725-7.00007-5 · Cited by 2

Variation in Holobionts

ROSENBERG, E. B., & Zilber‐Rosenberg, I. (2013) · Springer eBooks · doi:10.1007/978-3-319-04241-1_6 · Cited by 3

Host mucin glycosylation and gut symbiosis

Juge, N., Latousakis, D., & Crost, E. H. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-819655-7.00018-7 · Cited by 2

Cloacal Microbiota of Captive-bred and Wild Attwater’s Prairie-chicken, Tympanuchus Cupido Attwateri

Simon, S. E. (2014) · doi:10.12794/metadc699867 · Cited by 2

Mucin and human milk oligosaccharides utilization: a strategy of Akkermansia muciniphila to ensure survival in the human gut

Kostopoulos, I. (2021) · doi:10.18174/531651 · Cited by 2

SRS-FISH: High-Throughput Platform Linking Microbiome Function to Identity at the Single Cell LevelPreprint

Ge, X., Pereira, F. C., Mitteregger, M., Berry, D., Zhang, M., Wagner, M., & Cheng, J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.23.453601 · Cited by 2

A genetic locus in the gut microbe Bacteroides thetaiotaomicron encodes activities consistent with mucin-O-glycoprotein processing and plays a critical role in N -acetylgalactosamine metabolismPreprint

Ndeh, D. A., Nakjang, S., Kwiatkowski, K. J., Koropatkin, N. M., Hirt, R. P., & Bolam, D. N. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.01.578401 · Cited by 2

Living Computers

Brāzma, A. (2023) · doi:10.1093/oso/9780192871947.001.0001 · Cited by 1

Gut Microbiome Composition as the Key Factor for Immunomodulation in the Host

Bhat, M. I., Kumari, A., Kapila, S., & Kapila, R. (2022) · Springer eBooks · doi:10.1007/978-981-16-1626-6_7 · Cited by 1

Vibrio cholerae Gut Colonization of Zebrafish Larvae Induces a Dampened Sensorimotor Response

Cubillejo, I., Theis, K. R., Panzer, J. J., Luo, X., Banerjee, S., Thummel, R., & Withey, J. H. (2025) · Biomedicines · doi:10.3390/biomedicines13010226 · Cited by 1

Molecular systems in inflammatory bowel disease

Pathan, S. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-809356-6.00021-6 · Cited by 1

Genetic Variation in Holobionts

ROSENBERG, E. B. (2021) · The microbiomes of humans, animals, plants, and the environment · doi:10.1007/978-3-030-65317-0_8 · Cited by 1

Dysbiosis in Microbiome Leading to Colitis-Associated Cancer

Priyamvada, P. (2021) · Advances in medical diagnosis, treatment, and care (AMDTC) book series · doi:10.4018/978-1-7998-3580-6.ch007 · Cited by 1

Characterization and Profiling of Gut Bacterial Microbiome and Pathobionts among HIV-negative and HIV-infected Individuals in Cameroon

Ako, S. E., Nkenfou, C. N., Assob, J. N., Pokam, T. B., Ngemenya, M. N., Ndip, R. N., Anong, D. N., Tongo, M., Njopin, C., Eteneneng, E. J., et al. (2023) · International Journal of TROPICAL DISEASE & Health · doi:10.9734/ijtdh/2023/v44i91431 · Cited by 1

Characterization of Intestinal Microbiota in Healthy Adults and the Effect of Perturbations

Jalanka, J. (2014) · Työväentutkimus Vuosikirja · Cited by 1

A Low FUT(2) Diet For a High-Fat World: Connecting Intestinal Fucosylation With Western Diet–Driven Liver Disease

Stine, R. R. (2021) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2021.05.005 · Cited by 1

Intermittent fasting has a diet-specific impact on the gut microbiota and colonic mucin O -glycosylation of micePreprint

Gamage, H. K. A. H., Shathili, A. M. M., Nishtala, K., Chong, R. W. W., Packer, N. H., & Paulsen, I. T. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.15.508181 · Cited by 1

Vibrio cholerae Gut Colonization of Zebrafish Larvae Induces Differential Behavior ResponsesPreprint

Cubillejo, I., Theis, K. R., Panzer, J. J., Luo, X., Banerjee, S., Thummel, R., & Withey, J. H. (2024) · Preprints.org · doi:10.20944/preprints202408.1167.v1 · Cited by 1

Temporal Associations Between Human Milk Metabolites and the Infant Gut Microbiome and metabolomePreprint

Isokääntä, H., Perasto, L., Lamichhane, S., Ovaska, M., Kallonen, T., Munukka, E., Kråkström, M., Karlsson, H., Karlsson, L., Kailanto, H.-M., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.28.681130 · Cited by 1

Impact of polyphenols and feeding rhythms on the immunomodulation properties of the probiotic bacteria in the gastro-intestinal tract

Tarraf, A. A. (2021) · theses.fr (ABES) · doi:10.70675/545bd347z20bcz444cza534z622ac595baf9 · Cited by 1

Technology Advances in Medical Microbiology

Tang, Y. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.07827-2

What's bugging you and your diet?

Yeomans, B. L., & Bello, N. T. (2015) · Journal of Food & Nutritional Disorders · doi:10.4172/2324-9323.1000e110

Not Got Milk? The Effect on the Gut Microbiome of Removing Dairy from the Diet

Stovall, P. T. (2015)

Dietary Impacts on the Composition of Microbiota in Human Health and Disease

Verma, A. K., Kumari, R., Bhattacharya, A., & Paul, J. (2017) · Springer eBooks · doi:10.1007/978-981-10-5708-3_21

Modulating the immune system and intestinal barrier integrity with functional oligosaccharides

Figueroa‐Lozano, S. (2021) · University of Groningen research database (University of Groningen / Centre for Information Technology) · doi:10.33612/diss.151659844

Gut Microbiota and the Liver: Interaction Shaping Interactome

Devi, P., Khan, A., Chattopadhyay, P., Garg, A., & Pandey, R. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819265-8.00080-2

La compraventa de vivienda con préstamo hipotecario

Gil, F. J. G., García, J. L., & García, M. Á. G. (2005) · Dialnet (Universidad de la Rioja)

Faculty Opinions recommendation of Phylosymbiosis: Relationships and Functional Effects of Microbial Communities across Host Evolutionary History.

Morris, J. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.726993863.793551603

Fucosyltransferases Regulated by Fusobacterium Nucleatum Promote the Progression of Colon AdenocarcinomaPreprint

Wang, P., Liu, X., Yu, J., Meng, Z., Lv, Z., Shang, C., Geng, Q., Wang, D., Xue, D., & Li, L. (2022) · Research Square · doi:10.21203/rs.3.rs-1920071/v1

Adaptation of Gut Microbiota to Modern Dietary Sugars and Sweeteners

李, 梦. (2022) · Advances in Clinical Medicine · doi:10.12677/acm.2022.1291193

Dietary L-arabinose-induced gut dysbiosis exacerbates bacterial infectionPreprint

Yu, J., Tang, H., Zhou, N., Wang, Z., Huang, W., Wang, D., Ni, J., Lu, J. L., & Yao, Y. (2023) · Research Square · doi:10.21203/rs.3.rs-3245490/v1

Evolving Replicators

Brāzma, A. (2023) · Oxford University Press eBooks · doi:10.1093/oso/9780192871947.003.0006

Dedication

(2023) · Oxford University Press eBooks · doi:10.1093/oso/9780192871947.002.0004

Introduction

Brāzma, A. (2023) · Oxford University Press eBooks · doi:10.1093/oso/9780192871947.003.0001

Life on Earth

Brāzma, A. (2023) · Oxford University Press eBooks · doi:10.1093/oso/9780192871947.003.0007

Epilogue

Brāzma, A. (2023) · Oxford University Press eBooks · doi:10.1093/oso/9780192871947.003.0010

The Simplest Life

Brāzma, A. (2023) · Oxford University Press eBooks · doi:10.1093/oso/9780192871947.003.0005

How to Clone Oneself?

Brāzma, A. (2023) · Oxford University Press eBooks · doi:10.1093/oso/9780192871947.003.0002

From DNA to Language

Brāzma, A. (2023) · Oxford University Press eBooks · doi:10.1093/oso/9780192871947.003.0009

Preface

(2023) · Oxford University Press eBooks · doi:10.1093/oso/9780192871947.002.0005

Notes

(2023) · Oxford University Press eBooks · doi:10.1093/oso/9780192871947.002.0008

Informed Self-organization

Brāzma, A. (2023) · Oxford University Press eBooks · doi:10.1093/oso/9780192871947.003.0004

Evolution as a Ratchet of Information

Brāzma, A. (2023) · Oxford University Press eBooks · doi:10.1093/oso/9780192871947.003.0008

Copyright Page

(2023) · Oxford University Press eBooks · doi:10.1093/oso/9780192871947.002.0003

Self-organizing Molecules

Brāzma, A. (2023) · Oxford University Press eBooks · doi:10.1093/oso/9780192871947.003.0003

Efeito da cocção úmida, germinação e extrusão de milheto (Pennisetum glaucum (L.) R. Br.) na qualidade proteica, saúde intestinal, controle glicêmico e saciedade, in vivo

Magalhães, T. L. S. (2023) · doi:10.47328/ufvbbt.2023.636

N -Glycans as fundamental immune-checkpoints at the frontiers of inflammation, autoimmunity and cancer

Azevedo, C. M., Santos‐Pereira, B., Leite-Gomes, E., Rodrigues, C. T., Dantas, C. S., Faria, G., Nogueira, R., Almeida, P., Tavares-Gomes, L., Gaifem, J., et al. (2025) · Royal Society of Chemistry eBooks · doi:10.1039/9781837676101-00001

Rôle de la pantéthéinase épithéliale Vanin-1 dans l'inflammation intestinale

Gensollen, T. (2014) · theses.fr (ABES) · doi:10.70675/4525dc6dz222cz40b2za3b8z6077ea8bed51

Le porc européen CF : un modèle unique pour décrypter les altérations de glycosylation des mucines pulmonaires

Ringot-Destrez, B. (2018) · theses.fr (ABES) · doi:10.70675/f7ae5fcfz9161z42f4zaafez00d9e3f000ad

Modulatory properties of dietary fiber and role of intestinal mucus on Enterotoxigenic Escherichia coli (ETEC) pathogenicity

Sauvaitre, T. (2022) · theses.fr (ABES) · doi:10.70675/004c1986z8392z4e4bzb718zacdeca62f6a7

Antibiotic tolerance and biofilm formation in the anaerobic intestinal symbiont, bacteroides thetaiotaomicron

Lopes, A. (2022) · theses.fr (ABES) · doi:10.70675/04693f9dze3abz4646z9e5az23de057e2d4e

Contribution de la virulence de Listeria monocytogenes à sa dissémination dans l'hôte et l'environnement

Gaillard, J. (2023) · theses.fr (ABES) · doi:10.70675/8c3e1078zf49ez4662z893ezbf256ef32bc5

Organ‐Specific Human Microbiomes and Dysbiosis: Mechanistic Links to Disease and Emerging Therapeutic Strategies

Alanazi, A. (2026) · Journal of Clinical Laboratory Analysis · doi:10.1002/jcla.70307

Sulfate Groups Modulate the Protective Effects of Laminaria japonica Fucoidan against High-Fat Diet-Induced Intestinal Mucus Layer Injury via Gut Microbiota Regulation and Metabolic Profiling

Li, H., Chen, J., Zhang, C., Cai, W., Che, H., & Li, H. (2026) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.6c08201

Determination of Gene‐Level Fitness Contributions Across the Mucin‐Utilization Network of Bacteroides thetaiotaomicro n

Kim, K., Lee, J., 강민정, Yim, S. S., Choe, D., & Cho, B. (2026) · Advanced Science · doi:10.1002/advs.78118

Sedentary behavior as a gut-brain metabolic state

Yu, Q., Zhang, Z., Tian, Z., Kuang, J., Corbin, K. D., Oberlin, L. E., Collins, A. M., Goodpaster, B. H., Erickson, K. I., Owen, N. G., et al. (2026) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2026.107068

Effects of Diet on Resource Utilization by a Model Human Gut Microbiota Containing Bacteroides cellulosilyticus WH2, a Symbiont with an Extensive Glycobiome

McNulty, N. P., Wu, M., Erickson, A. R., Pan, C., Erickson, B. K., Martens, E. C., Pudlo, N. A., Muegge, B. D., Henrissat, B., Hettich, R. L., et al. (2013) · PLoS Biology · doi:10.1371/journal.pbio.1001637 · Cited by 298

Data from: Effects of diet on resource utilization by a model human gut microbiota containing Bacteroides cellulosilyticus WH2, a symbiont with an extensive glycobiome

McNulty, N. P., Meng, W., Erickson, A. R., Pan, C., Erickson, B. K., Martens, E. C., Pudlo, N. A., Muegge, B. D., Henrissat, B., Hettich, R. L., et al. (2013) · Data Archiving and Networked Services (DANS) · doi:10.5061/dryad.7fj1k

Characterization of Human Gut Microbiota Dynamics Using Model Communities in Gnotobiotic Mice

McNulty, N. P. (2013) · Open Scholarship Institutional Repository (Washington University in St. Louis) · doi:10.7936/k7m61h82

A Continuous Battle for Host-Derived Glycans Between a Mucus Specialist and a Glycan Generalist in vitro and in vivo

Kostopoulos, I., Aalvink, S., Kovatcheva‐Datchary, P., Nijsse, B., Bäckhed, F., Knol, J., de Vos, W. M., & Belzer, C. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.632454 · Cited by 40

Adaptive foraging of a prominent human intestinal symbiont in gnotobiotic mice

Sonnenburg, J. L., Xu, J., Leip, D., & Chen, W. B. (2005) · Institutional knowledge base (Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences) · Cited by 8