It takes guts to grow a brain: Increasing evidence of the important role of the intestinal microflora in neuro‐ and immune‐modulatory functions during development and adulthood
Open accessAbstract
A new study entitled “Normal gut microbiota modulates brain development and behavior”, published in the Proceedings of the National Academy of Sciences, requires that we reconsider the notion that the brain is an immune‐privileged site. The authors demonstrate that intestinal microbiota must be present within a set time‐frame for normal synaptogenesis to occur in the brain. In the absence of intestinal microbiota, histopathological and behavioral abnormalities arise. These observations necessitate a new look at the many interconnections of the immune system and the brain, suggesting new frontiers for research and new therapeutic strategies for neurodevelopmental diseases.
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Rodents lacking all gut bacteria from birth have memory deficits and behavioral abnormalities compared to animals with normal gut microbiota.
“These studies show that rodents lacking all gut bacteria from birth (germ-free animals) have memory deficits28 and behavioral abnormalities29, 30 when compared to animals with normal gut microbiota.”
From The relation between cesarean birth and child cognitive development (2017) · cites this paper as [29]
These cognitive deficits in rodents can be corrected through colonization of the intestine via a fecal transplant from the control group, but only if it occurs early in life.
“Interestingly, these cognitive deficits in rodents can be corrected through the colonization of the intestine via a fecal transplant from the control group, but only if it occurs early in life.”
From The relation between cesarean birth and child cognitive development (2017) · cites this paper as [29]
Developmental abnormalities found in germ-free mice are totally reversible by colonization with intestinal bacteria early in life but not in adulthood, suggesting that the microbiome influences brain development.
“The developmental abnormalities found in GF mice are totally reversible by colonization with intestinal bacteria early in life but not in adulthood, suggesting that the microbiome influences brain development.9,10”
From The Gut Microbiome and the Brain (2014) · cites this paper as [10]
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Cites
Induction of Intestinal Th17 Cells by Segmented Filamentous Bacteria
Ivanov, I. I., Atarashi, K., Manel, N., Brodie, E. L., Shima, T., Karaoz, U., Wei, D., Goldfarb, K. C., Santee, C. A., Lynch, S. V., et al. (2009) · Cell · doi:10.1016/j.cell.2009.09.033 · Cited by 4,554 · see citing works
Tracey, K. J. (2002) · Nature · doi:10.1038/nature01321 · Cited by 3,728 · see citing works
Self-citationThe Classical Complement Cascade Mediates CNS Synapse Elimination
Stevens, B., Allen, N. J., Vazquez, L. E., Howell, G. R., Christopherson, K. S., Nouri, N., Micheva, K. D., Mehalow, A. K., Huberman, A. D., Stafford, B., et al. (2007) · Cell · doi:10.1016/j.cell.2007.10.036 · Cited by 3,313 · see citing works
Normal gut microbiota modulates brain development and behavior
Heijtz, R. D., Wang, S., Anuar, F., Qian, Y., Björkholm, B., Samuelsson, A., Hibberd, M. L., Forssberg, H., & Pettersson, S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1010529108 · Cited by 3,228 · see citing works
Synaptic scaling mediated by glial TNF-α
Stellwagen, D., & Malenka, R. C. (2006) · Nature · doi:10.1038/nature04671 · Cited by 1,715 · see citing works
Maternal Immune Activation Alters Fetal Brain Development through Interleukin-6
Smith, S. E. P., Li, J., Garbett, K., Mirnics, K., & Patterson, P. H. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2178-07.2007 · Cited by 1,605 · see citing works
Gut-Residing Segmented Filamentous Bacteria Drive Autoimmune Arthritis via T Helper 17 Cells
Wu, H.-J., Ivanov, I. I., Darce, J., Hattori, K., Shima, T., Umesaki, Y., Littman, D. R., Benoist, C., & Mathis, D. (2010) · Immunity · doi:10.1016/j.immuni.2010.06.001 · Cited by 1,577 · see citing works
PDZ domain proteins of synapses
Kim, E., & Sheng, M. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1517 · Cited by 1,565 · see citing works
Gaboriau-Routhiau, V., Rakotobe, S., Lécuyer, E., Mulder, I., Lan, A., Bridonneau, C., Rochet, V., Pisi, A., De Paepe, M., Brandi, G., et al. (2009) · Immunity · doi:10.1016/j.immuni.2009.08.020 · Cited by 1,452 · see citing works
Proinflammatory T-cell responses to gut microbiota promote experimental autoimmune encephalomyelitis
Lee, Y. K., Menezes, J. S., Umesaki, Y., & Mazmanian, S. K. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000082107 · Cited by 1,323 · see citing works
Tracey, K. J. (2009) · Nature Reviews Immunology · doi:10.1038/nri2566 · Cited by 1,154 · cited 1× · see citing works
“The afferent pathways that sense inflammation and activate the efferent responses in brain are under study, but extensive data indicate that cytokine receptors in both the peripheral and the central nervous system activate sensory pathways in the vagus nerve [31].”
Self-citationATP drives lamina propria TH17 cell differentiation
Atarashi, K., Nishimura, J., Shima, T., Umesaki, Y., Yamamoto, M., Onoue, M., Yagita, H., Ishii, N., Evans, R., Honda, K., et al. (2008) · Nature · doi:10.1038/nature07240 · Cited by 1,089 · see citing works
Deverman, B. E., & Patterson, P. H. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.002 · Cited by 865 · see citing works
Functional requirement for class I MHC in CNS development and plasticity
Huh, G. S., Boulanger, L. M., Du, H., Riquelme, P. A., Brotz, T. M., & Shatz, C. J. (2000) · Science · doi:10.1126/science.290.5499.2155 · Cited by 828 · see citing works
Immune proteins in brain development and synaptic plasticity
Boulanger, L. M. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.001 · Cited by 555 · see citing works
Interleukin 1β inhibits synaptic strength and long-term potentiation in the rat CA1 hippocampus
Bellinger, F. P., Madamba, S. G., & Siggins, G. R. (1993) · Brain Research · doi:10.1016/0006-8993(93)90959-q · Cited by 388 · see citing works
MHC Class I: An Unexpected Role in Neuronal Plasticity
Shatz, C. J. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.044 · Cited by 369 · see citing works
Synaptophysin: leading actor or walk‐on role in synaptic vesicle exocytosis?
Valtorta, F., Pennuto, M., Bonanomi, D., & Benfenati, F. (2004) · BioEssays · doi:10.1002/bies.20012 · Cited by 346 · see citing works
Greenwood, J., Heasman, S. J., Alvarez, J. I., Prat, A., Lyck, R., & Engelhardt, B. (2011) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.2010.01140.x · Cited by 240 · see citing works
The Neurology of the Immune System: Neural Reflexes Regulate Immunity
Rosas‐Ballina, M., & Tracey, K. J. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.039 · Cited by 226 · see citing works
Self-citationClassical MHCI Molecules Regulate Retinogeniculate Refinement and Limit Ocular Dominance Plasticity
Datwani, A., McConnell, M. J., Kanold, P. O., Micheva, K. D., Busse, B., Shamloo, M., Smith, S. J., & Shatz, C. J. (2009) · Neuron · doi:10.1016/j.neuron.2009.10.015 · Cited by 212 · see citing works
Transcranial magnetic stimulation, synaptic plasticity and network oscillations
Huerta, P. T., & Volpe, B. T. (2009) · Journal of NeuroEngineering and Rehabilitation · doi:10.1186/1743-0003-6-7 · Cited by 204 · see citing works
Self-citationModulation of immune homeostasis by commensal bacteria
Ivanov, I. I., & Littman, D. R. (2011) · Current Opinion in Microbiology · doi:10.1016/j.mib.2010.12.003 · Cited by 183 · see citing works
Innate and Adaptive Autoimmunity Directed to the Central Nervous System
Bhat, R., & Steinman, L. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.015 · Cited by 166 · see citing works
Neurotoxic autoantibodies mediate congenital cortical impairment of offspring in maternal lupus
Lee, J. Y., Huerta, P. T., Zhang, J., Kowal, C., Bertini, E., Volpe, B. T., & Diamond, B. (2009) · Nature Medicine · doi:10.1038/nm.1892 · Cited by 163 · see citing works
Self-citationUnderstanding immunity requires more than immunology
Tracey, K. J. (2010) · Nature Immunology · doi:10.1038/ni0710-561 · Cited by 160 · see citing works
Self-citationUeda, Y., Kayama, H., Jeon, S. G., Kusu, T., Isaka, Y., Rakugi, H., Yamamoto, M., & Takeda, K. (2010) · International Immunology · doi:10.1093/intimm/dxq449 · Cited by 138 · see citing works
TLR8: An Innate Immune Receptor in Brain, Neurons and Axons
Ma, Y., Haynes, R., Sidman, R., & Vartanian, T. (2007) · Cell Cycle · doi:10.4161/cc.6.23.5018 · Cited by 104 · see citing works
How cytokines can influence the brain: A role for chemokines?
Guyon, A., Massa, F., Rovère, C., & Nahon, J. (2008) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2008.04.009 · Cited by 57 · see citing works
The Human Brain: Prenatal Development and Structure
Marín‐Padilla, M. (2010) · Medical Entomology and Zoology · Cited by 47 · see citing works
Role of immune molecules in the establishment and plasticity of glutamatergic synapses
Fourgeaud, L., & Boulanger, L. M. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07342.x · Cited by 44 · see citing works
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The gut microbiota--masters of host development and physiology
Sommer, F., & Bäckhed, F. (2013) · Nature Reviews Microbiology · doi:10.1038/nrmicro2974 · Cited by 3,681 · see citing works
The role of microbiome in central nervous system disorders
Wang, Y., & Kasper, L. H. (2014) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2013.12.015 · Cited by 803 · see citing works
Liang, S., Wang, T., Hu, X., Luo, J., Li, W., Wu, X., Duan, Y., & Jin, F. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.09.033 · Cited by 651 · see citing works
The Gut Microbiome and the Brain
Galland, L. (2014) · Journal of Medicinal Food · doi:10.1089/jmf.2014.7000 · Cited by 648 · see citing works
The Gut Microbiota and Autism Spectrum Disorders
Li, Q., Han, Y., Dy, A. B. C., & Hagerman, R. J. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00120 · Cited by 462 · see citing works
Dysbiosis of gut microbiota and microbial metabolites in Parkinson's disease
Sun, M.-F., & Shen, Y.-Q. (2018) · Ageing Research Reviews · doi:10.1016/j.arr.2018.04.004 · Cited by 445 · see citing works
The microbiome: stress, health and disease
Moloney, R. D., Desbonnet, L., Clarke, G., Dinan, T. G., & Cryan, J. F. (2014) · Mammalian Genome · doi:10.1007/s00335-013-9488-5 · Cited by 430 · see citing works
Neural reflexes in inflammation and immunity
Andersson, U., & Tracey, K. J. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20120571 · Cited by 379 · see citing works
Self-citationThe Impact of Microbiota on Brain and Behavior: Mechanisms & Therapeutic Potential
Borre, Y. E., Moloney, R. D., Clarke, G., Dinan, T. G., & Cryan, J. F. (2014) · Advances in Experimental Medicine and Biology · doi:10.1007/978-1-4939-0897-4_17 · Cited by 329 · see citing works
O’Mahony, S. M., Felice, V. D., Nally, K., Savignac, H. M., Claesson, M. J., Scully, P., Woznicki, J., Hyland, N. P., Shanahan, F., Quigley, E. M., et al. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.07.054 · Cited by 272 · see citing works
Antibiotics in early life: dysbiosis and the damage done
Neuman, H., Forsythe, P., Uzan-Yulzari, A., Avni, O., & Koren, O. (2018) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuy018 · Cited by 258 · see citing works
Microbial ecology and host-microbiota interactions during early life stages
Collado, M. C., Cernada, M., Bäuerl, C., Vento, M., & Pérez‐Martínez, G. (2012) · Gut Microbes · doi:10.4161/gmic.21215 · Cited by 254 · see citing works
Dehhaghi, M., Panahi, H. K. S., & Guillemin, G. J. (2019) · International Journal of Tryptophan Research · doi:10.1177/1178646919852996 · Cited by 245 · see citing works
An epigenetic framework for neurodevelopmental disorders: From pathogenesis to potential therapy
Millan, M. J. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.11.015 · Cited by 229 · see citing works
Mind-altering with the gut: Modulation of the gut-brain axis with probiotics
Kim, N., Yun, M., Oh, Y. J., & Choi, H.-J. (2018) · Journal of Microbiology · doi:10.1007/s12275-018-8032-4 · Cited by 210 · see citing works
Tipping the balance of autism risk: potential mechanisms linking pesticides and autism
Shelton, J. F., Hertz-Picciotto, I., & Pessah, I. N. (2012) · Environmental Health Perspectives · doi:10.1289/ehp.1104553 · Cited by 164 · see citing works
Environmental Mechanisms of Neurodevelopmental Toxicity
Rock, K. D., & Patisaul, H. B. (2018) · Current Environmental Health Reports · doi:10.1007/s40572-018-0185-0 · Cited by 124 · see citing works
The relation between cesarean birth and child cognitive development
Polidano, C., Zhu, A., & Bornstein, J. C. (2017) · Scientific Reports · doi:10.1038/s41598-017-10831-y · Cited by 119 · see citing works
Gut microbial communities modulating brain development and function
Al‐Asmakh, M., Anuar, F., Zadjali, F., Rafter, J. J., & Pettersson, S. (2012) · Gut Microbes · doi:10.4161/gmic.21287 · Cited by 117 · see citing works
Gut Vibes in Parkinson's Disease: The Microbiota‐Gut‐Brain Axis
Bullich‐Vilarrubias, C., Keshavarzian, A., Garssen, J., Kraneveld, A. D., & Perez‐Pardo, P. (2019) · Movement Disorders Clinical Practice · doi:10.1002/mdc3.12840 · Cited by 116 · see citing works
Early-Life Sugar Consumption Affects the Rat Microbiome Independently of Obesity
Noble, E. E., Hsu, T. M., Jones, R. B., Fodor, A. A., Goran, M. I., & Kanoski, S. E. (2016) · Journal of Nutrition · doi:10.3945/jn.116.238816 · Cited by 111 · see citing works
The Promising Role of Probiotics in Managing the Altered Gut in Autism Spectrum Disorders
Abdellatif, B., McVeigh, C., Bendriss, G., & Châari, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21114159 · Cited by 84 · see citing works
Kaur, H., Golovko, S. A., Golovko, M. Y., Singh, S., Darland, D. C., & Combs, C. K. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-200436 · Cited by 77 · see citing works
Zhong, H., Xu, J., Yang, M., Hussain, M., Liu, X., Feng, F., & Guan, R. (2023) · Nutrients · doi:10.3390/nu15030496 · Cited by 77 · see citing works
Perioperative neurocognitive dysfunction: thinking from the gut?
Xu, X., Hu, Y., Yan, E., Zhan, G., Liu, C., & Yang, C. (2020) · Aging · doi:10.18632/aging.103738 · Cited by 69 · see citing works
Gut-Brain Axis a Key Player to Control Gut Dysbiosis in Neurological Diseases
Pan, I., Issac, P. K., Rahman, M. M., Guru, A., & Arockiaraj, J. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03691-3 · Cited by 60 · see citing works
Neurodevelopment of Preterm Infants at 24 Months After Neonatal Supplementation of a Prebiotic Mix
van den Berg, J. P., Westerbeek, E. A. M., Bröring, T., Garssen, J., & van Elburg, R. M. (2016) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0000000000001148 · Cited by 57 · see citing works
Kaur, G., Behl, T., BUNGAU, S. G., Kumar, A., Uddin, M. S., Mehta, V., Zengin, G., Mathew, B., Shah, M. A., & Arora, S. (2020) · Current Neuropharmacology · doi:10.2174/1570159x18666200606233050 · Cited by 56 · see citing works
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y. H., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Microbiome · doi:10.1186/s40168-024-01795-z · Cited by 56 · see citing works
Murakami, K., Habukawa, C., Nobuta, Y., Moriguchi, N., & Takemura, T. (2012) · BioPsychoSocial Medicine · doi:10.1186/1751-0759-6-16 · Cited by 52 · see citing works
Yadav, H., Jaldhi, Bhardwaj, R., Anamika, A., Bakshi, A., Gupta, S., & Maurya, S. K. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.122022 · Cited by 46 · see citing works
Tyagi, P., Tasleem, M., Prakash, S., & Chouhan, G. (2020) · Food Research International · doi:10.1016/j.foodres.2020.109489 · Cited by 42 · see citing works
Salivary proteomics and biomarkers in neurology and psychiatry
Wormwood, K. L., Aslebagh, R., Channaveerappa, D., Dupree, E. J., Borland, M. M., Ryan, J. P., Darie, C. C., & Woods, A. G. (2015) · PROTEOMICS - CLINICAL APPLICATIONS · doi:10.1002/prca.201400153 · Cited by 36 · see citing works
Two faces of microbiota in inflammatory and autoimmune diseases: triggers and drugs
Kverka, M., & Tlaskalová‐Hogenová, H. (2012) · Apmis · doi:10.1111/apm.12007 · Cited by 30 · see citing works
Lotan, D., Cunningham, M. W., & Joel, D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0101257 · Cited by 30 · see citing works
Dominy, S. S., Brown, J. N., Ryder, M. I., Gritsenko, M., Jacobs, J., & Smith, R. D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0089366 · Cited by 29 · see citing works
Blake, J. A., Gardner, M., Najman, J. M., & Scott, J. G. (2021) · Social Psychiatry and Psychiatric Epidemiology · doi:10.1007/s00127-020-02008-2 · Cited by 23 · see citing works
Microbiota Involvement in the Gut–Brain Axis
Indrio, F., Riezzo, G., Raimondi, F., Mauro, A. D., & Francavilla, R. (2013) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/01.mpg.0000441927.20931.d6 · Cited by 22 · see citing works
Pathogenesis from the microbial-gut-brain axis in white matter injury in preterm infants: A review
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Indrio, F., Dargenio, V. N., Giordano, P., & Francavilla, R. (2019) · Advances in experimental medicine and biology · doi:10.1007/5584_2018_315 · Cited by 15 · see citing works
Kazem, Y. I., Mahmoud, M. H., Essa, H. A., Azmy, O. M., Kandeel, W. A., Al‐Moghazy, M., El-Attar, I., Hashish, A. F., & Mehanna, N. S. (2021) · Journal of Complementary and Integrative Medicine · doi:10.1515/jcim-2021-0351 · Cited by 15 · see citing works
Liu, Z., Wei, S., Chen, X., Liu, L., Wei, Z., Liao, Z., Wu, J., Li, Z., Zhou, H., & Wang, D. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.833365 · Cited by 10 · see citing works
Dachew, B. A., Tessema, G. A., & Alati, R. (2022) · Social Psychiatry and Psychiatric Epidemiology · doi:10.1007/s00127-022-02374-z · Cited by 8 · see citing works
Microbiota in healthy term infant
Indrio, F., Mauro, A. D., Riezzo, G., Mauro, F. D., & Francavilla, R. (2013) · Early Human Development · doi:10.1016/s0378-3782(13)70083-5 · Cited by 8 · see citing works
Probiotic Mechanism to Modulate the Gut-Brain Axis (GBA)
Samtiya, M., Dhewa, T., & Puniya, A. K. (2022) · Springer eBooks · doi:10.1007/978-981-16-1626-6_10 · Cited by 6 · see citing works
Consequences of Gut Dysbiosis on the Human Brain
Hickman, R. A., Hussein, M. A., & Pei, Z. (2016) · InTech eBooks · doi:10.5772/64690 · Cited by 4 · see citing works
Importance of gut microbiota in health and diseases of new born infants
Gao, J., WU, H., & Liu, J. (2016) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2016.3253 · Cited by 2 · see citing works
Schaly, S., & Prakash, S. (2023) · Healthy ageing and longevity · doi:10.1007/978-3-031-14023-5_10 · Cited by 1 · see citing works
Thyroid Dysfunction in Pregnancy: Comparison of Outcomes in Infants
Koroljević, Z. D. (2022) · Acta Clinica Croatica · doi:10.20471/acc.2022.61.02.11 · Cited by 1 · see citing works
Tungland, B. C. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-814649-1.00012-0 · Cited by 1 · see citing works
Autonomous or Integrated Immune System is Right for Biology?
Berczi, I. (2014) · Advances in Neuroimmune Biology · doi:10.3233/nib-140098
Moore, A. (2011) · BioEssays · doi:10.1002/bies.201190036
Probiotics in Functional Gastrointestinal Disorders in Children: Therapy and Prevention
Indrio, F., Riezzo, G., & Mauro, A. D. (2015) · CRC Press eBooks · doi:10.1201/b19308-56
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Indrio, F., & Cristofori, F. (2017) · Springer eBooks · doi:10.1007/978-3-319-60678-1_22
Indrio, F., & Cristofori, F. (2022) · Springer eBooks · doi:10.1007/978-3-030-99067-1_15
Kırmızıbekmez, A. M., Önder, A., Ozdemir, M. Y., Gurerk, G., Aydın, S., Eryiğit, Ö. Y., Güloğlu, M. O., & Kara, İ. (2025) · Scientific Reports · doi:10.1038/s41598-025-29256-z · Cited by 1 · see citing works
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716846
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716825
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716858
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716867
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716834
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Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716831
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716879
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716849
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716828
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716855
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716870
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.25770353
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716873
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716840
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716843
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716876
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.25770461
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716864
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716837
Hong, Y., Li, H., Chen, L., Su, H., Zhang, B., Luo, Y., Li, C., Zhao, Z., Shao, Y., & Guo, L. (2024) · Figshare · doi:10.6084/m9.figshare.26716822
Fischer, N. (2014) · theses.fr (ABES) · doi:10.70675/7ecf88e2z7851z4354zb134z317e666a94cb
- Authors
- Diamond, B., Huerta, P. T., Tracey, K., & Volpe, B. T.
- Affiliations
- Northwell Health (US)
- Cornell University (US)
- Corresponding author
- Diamond, Betty
- Venue
- BioEssays
- Publisher
- Wiley
- Published
- 2011-06-16
- Volume
- 33
- Issue
- 8
- Pages
- 588-591
- ISSN
- 0265-9247 (ISSN-L)
- 1521-1878
- PMC
- PMC4532368
- OpenAlex
- W1892012164
- Cited by
- 69
- References
- 31
- Citations by year
- 2025: 1 · 2024: 12 · 2023: 5 · 2022: 5 · 2021: 2 · 2020: 6 · 2019: 3 · 2018: 5 · 2017: 3 · 2016: 4 · 2015: 3 · 2014: 7 · 2013: 5 · 2012: 7
- FWCI
- 0.58
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- BioEssays (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of General Medical Sciences (R01GM089807, R01GM057226)
- National Institute of Allergy and Infectious Diseases (P01AI073693)
- National Center for Research Resources (M01RR018535)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- gut microbiota, brain development, synaptogenesis, neurodevelopmental disorders, immune privilege, gut-brain axis, behavioral abnormalities, histopathology, microbiota depletion
- MeSH terms
- Animals, Behavior, Brain, Humans, Immunologic Factors, Intestines, Synaptic Transmission, Receptors, Immunologic, Synapses, Neuroimmunomodulation, Histocompatibility Antigens Class I, Cytokines, Long-Term Potentiation, Metagenome
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