This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Adelman MW, Woodworth MH, Langelier C, Busch LM, Kempker JA, Kraft CS, Martin GS. The gut microbiome’s role in the development, maintenance, and outcomes of sepsis. Crit Care. 2020 Jun;24(1):278. https://doi.org/10.1186/s13054-020-02989-1AdelmanMWWoodworthMHLangelierCBuschLMKempkerJAKraftCSMartinGS.The gut microbiome’s role in the development, maintenance, and outcomes of sepsis. . 2020Jun;24(1):278. https://doi.org/10.1186/s13054-020-02989-1Search in Google Scholar
Anggraini D, Hasni D, Amelia R. Pathogenesis of sepsis. Sci J. 2022; 1(4):332–339. https://doi.org/10.56260/sciena.v1i4.63AnggrainiDHasniDAmeliaR.Pathogenesis of sepsis. . 2022; 1(4):332–339. https://doi.org/10.56260/sciena.v1i4.63Search in Google Scholar
Cai X, Deng L, Ma X, Guo Y, Feng Z, Liu M, Guan Y, Huang Y, Deng J, Li H, et al. Altered diversity and composition of gut microbiota in Wilson’s disease. Sci Rep. 2020 Dec;10(1):21825. https://doi.org/10.1038/s41598-020-78988-7CaiXDengLMaXGuoYFengZLiuMGuanYHuangYDengJLiHAltered diversity and composition of gut microbiota in Wilson’s disease. . 2020Dec;10(1):21825. https://doi.org/10.1038/s41598-020-78988-7Search in Google Scholar
Chancharoenthana W, Kamolratanakul S, Schultz MJ, Leela-havanichkul A. The leaky gut and the gut microbiome in sepsis – targets in research and treatment. Clin Sci (Lond). 2023 Apr; 137(8): 645–662. https://doi.org/10.1042/CS20220777ChancharoenthanaWKamolratanakulSSchultzMJLeela-havanichkulA.The leaky gut and the gut microbiome in sepsis – targets in research and treatment. . 2023Apr; 137(8): 645–662. https://doi.org/10.1042/CS20220777Search in Google Scholar
Choi SW, O’Reilly PF. PRSice-2: Polygenic Risk Score software for biobank-scale data. Gigascience. 2019 Jul;8(7):giz082. https://doi.org/10.1093/gigascience/giz082ChoiSWO’ReillyPF.PRSice-2: Polygenic Risk Score software for biobank-scale data. . 2019Jul;8(7):giz082. https://doi.org/10.1093/gigascience/giz082Search in Google Scholar
Di Gioia D, Bozzi Cionci N, Baffoni L, Amoruso A, Pane M, Mogna L, Gaggìa F, Lucenti MA, Bersano E, Cantello R, et al. A prospective longitudinal study on the microbiota composition in amyotrophic lateral sclerosis. BMC Med. 2020 Jun;18(1):153. https://doi.org/10.1186/s12916-020-01607-9Di GioiaDBozzi CionciNBaffoniLAmorusoAPaneMMognaLGaggìaFLucentiMABersanoECantelloRA prospective longitudinal study on the microbiota composition in amyotrophic lateral sclerosis. . 2020Jun;18(1):153. https://doi.org/10.1186/s12916-020-01607-9Search in Google Scholar
Di Rienzi SC, Sharon I, Wrighton KC, Koren O, Hug LA, Thomas BC, Goodrich JK, Bell JT, Spector TD, Banfield JF, et al. The human gut and groundwater harbor non-photosynthetic bacteria belonging to a new candidate phylum sibling to Cyanobacteria. Elife. 2013 Oct;2:e01102. https://doi.org/10.7554/eLife.01102Di RienziSCSharonIWrightonKCKorenOHugLAThomasBCGoodrichJKBellJTSpectorTDBanfieldJFThe human gut and groundwater harbor non-photosynthetic bacteria belonging to a new candidate phylum sibling to Cyanobacteria. . 2013Oct;2:e01102. https://doi.org/10.7554/eLife.01102Search in Google Scholar
Durazzi F, Sala C, Castellani G, Manfreda G, Remondini D, De Cesare A. Comparison between 16S rRNA and shotgun sequencing data for the taxonomic characterization of the gut microbiota. Sci Rep. 2021 Feb;11(1):3030. https://doi.org/10.1038/s41598-021-82726-yDurazziFSalaCCastellaniGManfredaGRemondiniDDe CesareA.Comparison between 16S rRNA and shotgun sequencing data for the taxonomic characterization of the gut microbiota. . 2021Feb;11(1):3030. https://doi.org/10.1038/s41598-021-82726-ySearch in Google Scholar
Evans L, Rhodes A, Alhazzani W, Antonelli M, Coopersmith CM, French C, Machado FR, Mcintyre L, Ostermann M, Prescott HC, et al. Executive summary: Surviving Sepsis Campaign: International Guidelines for the Management of Sepsis and Septic Shock 2021. Crit Care Med. 2021 Nov;49(11):1974–1982. https://doi.org/10.1097/CCM.0000000000005357EvansLRhodesAAlhazzaniWAntonelliMCoopersmithCMFrenchCMachadoFRMcintyreLOstermannMPrescottHCExecutive summary: Surviving Sepsis Campaign: International Guidelines for the Management of Sepsis and Septic Shock 2021. . 2021Nov;49(11):1974–1982. https://doi.org/10.1097/CCM.0000000000005357Search in Google Scholar
Fang H, Fang M, Wang Y, Zhang H, Li J, Chen J, Wu Q, He L, Xu J, Deng J, et al. Indole-3-propionic acid as a potential therapeutic agent for sepsis-induced gut microbiota disturbance. Microbiol Spectr. 2022 Jun;10(3):e0012522. https://doi.org/10.1128/spectrum.00125-22FangHFangMWangYZhangHLiJChenJWuQHeLXuJDengJIndole-3-propionic acid as a potential therapeutic agent for sepsis-induced gut microbiota disturbance. . 2022Jun;10(3):e0012522. https://doi.org/10.1128/spectrum.00125-22Search in Google Scholar
Hemani G, Zheng J, Elsworth B, Wade KH, Haberland V, Baird D, Laurin C, Burgess S, Bowden J, Langdon R, et al. The MR-Base platform supports systematic causal inference across the human phenome. Elife. 2018 May;7:e34408. https://doi.org/10.7554/eLife.34408HemaniGZhengJElsworthBWadeKHHaberlandVBairdDLaurinCBurgessSBowdenJLangdonRThe MR-Base platform supports systematic causal inference across the human phenome. . 2018May;7:e34408. https://doi.org/10.7554/eLife.34408Search in Google Scholar
Hu C, Rzymski P. Non-photosynthetic Melainabacteria (Cyanobacteria) in human gut: Characteristics and association with health. Life. 2022 Mar;12(4):476. https://doi.org/10.3390/life12040476HuCRzymskiP.Non-photosynthetic Melainabacteria (Cyanobacteria) in human gut: Characteristics and association with health. . 2022Mar;12(4):476. https://doi.org/10.3390/life12040476Search in Google Scholar
Huang ZB, Hu Z, Lu CX, Luo SD, Chen Y, Zhou ZP, Hu JJ, Zhang FL, Deng F, Liu KX. Gut microbiota-derived indole 3-pro-pionic acid partially activates aryl hydrocarbon receptor to promote macrophage phagocytosis and attenuate septic injury. Front Cell Infect Microbiol. 2022 Oct;12:1015386. https://doi.org/10.3389/fcimb.2022.1015386HuangZBHuZLuCXLuoSDChenYZhouZPHuJJZhangFLDengFLiuKX.Gut microbiota-derived indole 3-pro-pionic acid partially activates aryl hydrocarbon receptor to promote macrophage phagocytosis and attenuate septic injury. . 2022Oct;12:1015386. https://doi.org/10.3389/fcimb.2022.1015386Search in Google Scholar
Kang H, Thomas RM. Bacteria and sepsis: Microbiome to the rescue? J Clin Med. 2021 Aug;10(16):3578. https://doi.org/10.3390/jcm10163578KangHThomasRM.Bacteria and sepsis: Microbiome to the rescue?. 2021Aug;10(16):3578. https://doi.org/10.3390/jcm10163578Search in Google Scholar
Klingensmith NJ, Coopersmith CM. Gut microbiome in sepsis. Surg Infect. 2023 Apr;24(3):250–257. https://doi.org/10.1089/sur.2022.420KlingensmithNJCoopersmithCM.Gut microbiome in sepsis. . 2023Apr;24(3):250–257. https://doi.org/10.1089/sur.2022.420Search in Google Scholar
Kullberg RFJ, Wiersinga WJ, Haak BW. Gut microbiota and sepsis: from pathogenesis to novel treatments. Curr Opin Gastroenterol. 2021 Nov;37(6):578–585. https://doi.org/10.1097/MOG.0000000000000781KullbergRFJWiersingaWJHaakBW.Gut microbiota and sepsis: from pathogenesis to novel treatments. . 2021Nov;37(6):578–585. https://doi.org/10.1097/MOG.0000000000000781Search in Google Scholar
Kurilshikov A, Medina-Gomez C, Bacigalupe R, Radjabzadeh D, Wang J, Demirkan A, Le Roy CI, Raygoza Garay JA, Finnicum CT, Liu X, et al. Large-scale association analyses identify host factors influencing human gut microbiome composition. Nat Genet. 2021 Feb;53(2):156–165. https://doi.org/10.1038/s41588-020-00763-1KurilshikovAMedina-GomezCBacigalupeRRadjabzadehDWangJDemirkanALe RoyCIRaygoza GarayJAFinnicumCTLiuXLarge-scale association analyses identify host factors influencing human gut microbiome composition. . 2021Feb;53(2):156–165. https://doi.org/10.1038/s41588-020-00763-1Search in Google Scholar
Kurki MI, Karjalainen J, Palta P, Sipilä TP, Kristiansson K, Donner KM, Reeve MP, Laivuori H, Aavikko M, Kaunisto MA, et al. FinnGen provides genetic insights from a well-phenotyped isolated population. Nature. 2023 Jan;613(7944):508–518. https://doi.org/10.1038/s41586-022-05473-8KurkiMIKarjalainenJPaltaPSipiläTPKristianssonKDonnerKMReeveMPLaivuoriHAavikkoMKaunistoMAFinnGen provides genetic insights from a well-phenotyped isolated population. . 2023Jan;613(7944):508–518. https://doi.org/10.1038/s41586-022-05473-8Search in Google Scholar
Liu Y, Zhang H, Tang X, Jiang X, Yan X, Liu X, Gong J, Mew K, Sun H, Chen X, et al. Distinct metagenomic signatures in the SARS-CoV-2 infection. Front Cell Infect Microbiol. 2021 Dec;11:706970. https://doi.org/10.3389/fcimb.2021.706970LiuYZhangHTangXJiangXYanXLiuXGongJMewKSunHChenXDistinct metagenomic signatures in the SARS-CoV-2 infection. . 2021Dec;11:706970. https://doi.org/10.3389/fcimb.2021.706970Search in Google Scholar
Longhitano Y, Zanza C, Thangathurai D, Taurone S, Kozel D, Racca F, Audo A, Ravera E, Migneco A, Piccioni A, et al. Gut alterations in septic patients: A biochemical literature review. Rev Recent Clin Trials. 2020;15(4):289–297. https://doi.org/10.2174/1574887115666200811105251LonghitanoYZanzaCThangathuraiDTauroneSKozelDRaccaFAudoARaveraEMignecoAPiccioniAGut alterations in septic patients: A biochemical literature review. . 2020;15(4):289–297. https://doi.org/10.2174/1574887115666200811105251Search in Google Scholar
Mancino W, Lugli GA, Sinderen DV, Ventura M, Turroni F. Mobilome and resistome reconstruction from genomes belonging to members of the Bifidobacterium genus. Microorganisms. 2019 Dec; 7(12):638. https://doi.org/10.3390/microorganisms7120638MancinoWLugliGASinderenDVVenturaMTurroniF.Mobilome and resistome reconstruction from genomes belonging to members of the Bifidobacterium genus. . 2019Dec; 7(12):638. https://doi.org/10.3390/microorganisms7120638Search in Google Scholar
Manzanares W, Lemieux M, Langlois PL, Wischmeyer PE. Probiotic and synbiotic therapy in critical illness: A systematic review and meta-analysis. Crit Care. 2016 Aug;19:262. https://doi.org/10.1186/s13054-016-1434-yManzanaresWLemieuxMLangloisPLWischmeyerPE.Probiotic and synbiotic therapy in critical illness: A systematic review and meta-analysis. . 2016Aug;19:262. https://doi.org/10.1186/s13054-016-1434-ySearch in Google Scholar
Mbatchou J, Barnard L, Backman J, Marcketta A, Kosmicki JA, Ziyatdinov A, Benner C, O’Dushlaine C, Barber M, Boutkov B, et al. Computationally efficient whole-genome regression for quantitative and binary traits. Nat Genet. 2021 Jul;53(7):1097–1103. https://doi.org/10.1038/s41588-021-00870-7MbatchouJBarnardLBackmanJMarckettaAKosmickiJAZiyatdinovABennerCO’DushlaineCBarberMBoutkovBComputationally efficient whole-genome regression for quantitative and binary traits. . 2021Jul;53(7):1097–1103. https://doi.org/10.1038/s41588-021-00870-7Search in Google Scholar
Miller WD, Keskey R, Alverdy JC. Sepsis and the microbiome: A vicious cycle. J Infect Dis. 2021 Jun;223(Suppl_3):S264–S269. https://doi.org/10.1093/infdis/jiaa682MillerWDKeskeyRAlverdyJC.Sepsis and the microbiome: A vicious cycle. . 2021Jun;223(Suppl_3):S264–S269. https://doi.org/10.1093/infdis/jiaa682Search in Google Scholar
Murphy K, O’Donovan AN, Caplice NM, Ross RP, Stanton C. Exploring the gut microbiota and cardiovascular disease. Metabolites. 2021 Jul;11(8):493. https://doi.org/10.3390/metabo11080493MurphyKO’DonovanANCapliceNMRossRPStantonC.Exploring the gut microbiota and cardiovascular disease. . 2021Jul;11(8):493. https://doi.org/10.3390/metabo11080493Search in Google Scholar
Niu M, Chen P. Crosstalk between gut microbiota and sepsis. Burns Trauma. 2021 Oct;9:tkab036. https://doi.org/10.1093/burnst/tkab036NiuMChenP.Crosstalk between gut microbiota and sepsis. . 2021Oct;9:tkab036. https://doi.org/10.1093/burnst/tkab036Search in Google Scholar
Olaisen M, Flatberg A, Granlund AVB, Røyset ES, Martinsen TC, Sandvik AK, Fossmark R. Bacterial mucosa-associated micro-biome in inflamed and proximal noninflamed ileum of patients with Crohn’s disease. Inflamm Bowel Dis. 2021 Jan;27(1):12–24. https://doi.org/10.1093/ibd/izaa107OlaisenMFlatbergAGranlundAVBRøysetESMartinsenTCSandvikAKFossmarkR.Bacterial mucosa-associated microbiome in inflamed and proximal noninflamed ileum of patients with Crohn’s disease. . 2021Jan;27(1):12–24. https://doi.org/10.1093/ibd/izaa107Search in Google Scholar
Papadimitriou N, Dimou N, Tsilidis KK, Banbury B, Martin RM, Lewis SJ, Kazmi N, Robinson TM, Albanes D, Aleksandrova K, et al. Physical activity and risks of breast and colorectal cancer: A Mendelian randomisation analysis. Nat Commun. 2020 Jan; 11(1):597. https://doi.org/10.1038/s41467-020-14389-8PapadimitriouNDimouNTsilidisKKBanburyBMartinRMLewisSJKazmiNRobinsonTMAlbanesDAleksandrovaKPhysical activity and risks of breast and colorectal cancer: A Mendelian randomisation analysis. . 2020Jan; 11(1):597. https://doi.org/10.1038/s41467-020-14389-8Search in Google Scholar
Peng Y, Wei J, Jia X, Luan F, Man M, Ma X, Luo Y, Li Y, Li N, Wang Q, et al. Changes in the microbiota in different intestinal segments of mice with sepsis. Front Cell Infect Microbiol. 2023 Jan; 12:954347. https://doi.org/10.3389/fcimb.2022.954347PengYWeiJJiaXLuanFManMMaXLuoYLiYLiNWangQChanges in the microbiota in different intestinal segments of mice with sepsis. . 2023Jan; 12:954347. https://doi.org/10.3389/fcimb.2022.954347Search in Google Scholar
Prevel R, Enaud R, Orieux A, Camino A, Berger P, Boyer A, Delhaes L, Gruson D. Gut bacteriobiota and mycobiota are both associated with Day-28 mortality among critically ill patients. Crit Care. 2022 Apr;26(1):105. https://doi.org/10.1186/s13054-022-03980-8PrevelREnaudROrieuxACaminoABergerPBoyerADelhaesLGrusonD.Gut bacteriobiota and mycobiota are both associated with Day-28 mortality among critically ill patients. . 2022Apr;26(1):105. https://doi.org/10.1186/s13054-022-03980-8Search in Google Scholar
R Core Team. A language and environment for statistical computing. Vienna (Austria): R Foundation for Statistical Computing; 2020 [cited 2023 Oct 10]. Available from https://www.r-project.orgR Core Team. . Vienna (Austria): R Foundation for Statistical Computing; 2020 [cited 2023 Oct 10]. Available from https://www.r-project.orgSearch in Google Scholar
Robertson C, Savva GM, Clapuci R, Jones J, Maimouni H, Brown E, Minocha A, Hall LJ, Clarke P. Incidence of necrotis-ing enterocolitis before and after introducing routine prophylactic Lactobacillus and Bifidobacterium probiotics. Arch Dis Child Fetal Neonatal Ed. 2020 Jul;105(4):380–386. https://doi.org/10.1136/archdischild-2019-317346RobertsonCSavvaGMClapuciRJonesJMaimouniHBrownEMinochaAHallLJClarkeP.Incidence of necrotis-ing enterocolitis before and after introducing routine prophylactic Lactobacillus and Bifidobacterium probiotics. . 2020Jul;105(4):380–386. https://doi.org/10.1136/archdischild-2019-317346Search in Google Scholar
Rosario D, Bidkhori G, Lee S, Bedarf J, Hildebrand F, Le Chatelier E, Uhlen M, Ehrlich SD, Proctor G, Wüllner U, et al. Systematic analysis of gut microbiome reveals the role of bacterial folate and homocysteine metabolism in Parkinson’s disease. Cell Rep. 2021 Mar;34(9):108807. https://doi.org/10.1016/j.celrep.2021.108807RosarioDBidkhoriGLeeSBedarfJHildebrandFLe ChatelierEUhlenMEhrlichSDProctorGWüllnerUSystematic analysis of gut microbiome reveals the role of bacterial folate and homocysteine metabolism in Parkinson’s disease. . 2021Mar;34(9):108807. https://doi.org/10.1016/j.celrep.2021.108807Search in Google Scholar
Skrivankova VW, Richmond RC, Woolf BAR, Yarmolinsky J, Davies NM, Swanson SA, VanderWeele TJ, Higgins JPT, Timpson NJ, Dimou N, et al. Strengthening the Reporting of Observational Studies in Epidemiology using Mendelian randomization: The STROBE-MR Statement. JAMA. 2021 Oct;326(16):1614–1621. https://doi.org/10.1001/jama.2021.18236SkrivankovaVWRichmondRCWoolfBARYarmolinskyJDaviesNMSwansonSAVanderWeeleTJHigginsJPTTimpsonNJDimouNStrengthening the Reporting of Observational Studies in Epidemiology using Mendelian randomization: The STROBE-MR Statement. . 2021Oct;326(16):1614–1621. https://doi.org/10.1001/jama.2021.18236Search in Google Scholar
Sun S, Wang D, Dong D, Xu L, Xie M, Wang Y, Ni T, Jiang W, Zhu X, Ning N, et al. Altered intestinal microbiome and metabolome correspond to the clinical outcome of sepsis. Crit Care. 2023 Mar; 27(1):127. https://doi.org/10.1186/s13054-023-04412-xSunSWangDDongDXuLXieMWangYNiTJiangWZhuXNingNAltered intestinal microbiome and metabolome correspond to the clinical outcome of sepsis. . 2023Mar; 27(1):127. https://doi.org/10.1186/s13054-023-04412-xSearch in Google Scholar
Ventura M, Turroni F, Lugli GA, van Sinderen D. Bifidobacteria and humans: Our special friends, from ecological to genomics perspectives. J Sci Food Agric. 2014 Jan;94(2):163–168. https://doi.org/10.1002/jsfa.6356VenturaMTurroniFLugliGAvan SinderenD.Bifidobacteria and humans: Our special friends, from ecological to genomics perspectives. . 2014Jan;94(2):163–168. https://doi.org/10.1002/jsfa.6356Search in Google Scholar
Wei R, Chen X, Hu L, He Z, Ouyang X, Liang S, Dai S, Sha W, Chen C. Dysbiosis of intestinal microbiota in critically ill patients and risk of in-hospital mortality. Am J Transl Res. 2021 Mar;13(3): 1548–1557.WeiRChenXHuLHeZOuyangXLiangSDaiSShaWChenC.Dysbiosis of intestinal microbiota in critically ill patients and risk of in-hospital mortality. . 2021Mar;13(3): 1548–1557.Search in Google Scholar
Xiong L, Li Y, Li J, Yang J, Shang L, He X, Liu L, Luo Y, Xie X. Intestinal microbiota profiles in infants with acute gastroenteritis caused by rotavirus and norovirus infection: A prospective cohort study. Int J Infect Dis. 2021 Oct;111:76–84. https://doi.org/10.1016/j.ijid.2021.08.024XiongLLiYLiJYangJShangLHeXLiuLLuoYXieX.Intestinal microbiota profiles in infants with acute gastroenteritis caused by rotavirus and norovirus infection: A prospective cohort study. . 2021Oct;111:76–84. https://doi.org/10.1016/j.ijid.2021.08.024Search in Google Scholar
Xu AA, Kennedy LK, Hoffman K, White DL, Kanwal F, El-Serag HB, Petrosino JF, Jiao L. Dietary fatty acid intake and the colonic gut microbiota in humans. Nutrients. 2022 Jun;14(13):2722. https://doi.org/10.3390/nu14132722XuAAKennedyLKHoffmanKWhiteDLKanwalFEl-SeragHBPetrosinoJFJiaoL.Dietary fatty acid intake and the colonic gut microbiota in humans. . 2022Jun;14(13):2722. https://doi.org/10.3390/nu14132722Search in Google Scholar
Yutin N, Galperin MY. A genomic update on clostridial phylogeny: Gram-negative spore formers and other misplaced clostridia. Environ Microbiol. 2013 Oct;15(10):2631–2641. https://doi.org/10.1111/1462-2920.12173YutinNGalperinMY.A genomic update on clostridial phylogeny: Gram-negative spore formers and other misplaced clostridia. . 2013Oct;15(10):2631–2641. https://doi.org/10.1111/1462-2920.12173Search in Google Scholar
Zhang B, Jiang M, Zhao J, Song Y, Du W, Shi J. The mechanism underlying the influence of indole-3-propionic acid: A relevance to metabolic disorders. Front Endocrinol (Lausanne). 2022 Mar;13: 841703. https://doi.org/10.3389/fendo.2022.841703ZhangBJiangMZhaoJSongYDuWShiJ.The mechanism underlying the influence of indole-3-propionic acid: A relevance to metabolic disorders. . 2022Mar;13: 841703. https://doi.org/10.3389/fendo.2022.841703Search in Google Scholar
Zhang W, Sun Z, Zhang Q, Sun Z, Su Y, Song J, Wang B, Gao R. Preliminary evidence for an influence of exposure to polycyclic aromatic hydrocarbons on the composition of the gut microbiota and neurodevelopment in three-year-old healthy children. BMC Pediatr. 2021 Feb;21(1):86. https://doi.org/10.1186/s12887-021-02539-wZhangWSunZZhangQSunZSuYSongJWangBGaoR.Preliminary evidence for an influence of exposure to polycyclic aromatic hydrocarbons on the composition of the gut microbiota and neurodevelopment in three-year-old healthy children. . 2021Feb;21(1):86. https://doi.org/10.1186/s12887-021-02539-wSearch in Google Scholar
Zhu L, Xu F, Wan W, Yu B, Tang L, Yang Y, Du Y, Chen Z, Xu H. Gut microbial characteristics of adult patients with allergy rhinitis. Microb Cell Fact. 2020 Sep;19(1):171. https://doi.org/10.1186/s12934-020-01430-0ZhuLXuFWanWYuBTangLYangYDuYChenZXuH.Gut microbial characteristics of adult patients with allergy rhinitis. . 2020Sep;19(1):171. https://doi.org/10.1186/s12934-020-01430-0Search in Google Scholar
Zhu S, Han M, Liu S, Fan L, Shi H, Li P. Composition and diverse differences of intestinal microbiota in ulcerative colitis patients. Front Cell Infect Microbiol. 2022 Aug;12:953962. https://doi.org/10.3389/fcimb.2022.953962ZhuSHanMLiuSFanLShiHLiP.Composition and diverse differences of intestinal microbiota in ulcerative colitis patients. . 2022Aug;12:953962. https://doi.org/10.3389/fcimb.2022.953962Search in Google Scholar