Disease
Microbiota ☳
Metabolome
Factor
Lactobacillaceae ⇒ Lactobacillus {10000118}
Record Keys
Parent:
Definition: Lactobacillus
Details
Initialisation date: 2019-06-23
Meta Information
Rank:
Domain:
Zone: [ ]
Enzyme: [ ]
Function: [ ]
Notes: - Lactubacillus are reduced in chronic stress conditions, Can Lactobacillus probiotics relieve chronic stress?
Shared Reference Notes
[1.1 ] Lactobacillus genus ( Lactobacillus johnsonii, Lactobacillus gasseri) act upon mitochondria in the liver leading to the improvement of lipid metabolism.
- Metabolomics analyses revealed that reduced glutathione may mediate these effects.
- The mice receiving those Lactobacilli also had a lower fat mass index than those fed only a western diet
[1.2 ]
[1.3 ] Lactobacillus can resist the antimicrobial activity of bile salts.
[1.4 ] #Cancer chemo/immunotherapy in mice
- Smectite with LABs activates dendritic cells via TLR2 signaling
[1.5 ] [#Probiotic (Bifidobacter and Lactobacilus) ] Lactobacillus rhamnosus and Lactobacillus helveticus, reduced the symptoms of #Depression and anxiety
- Following an extremely stressful period, fewer species of Lactobacillus are present in the stool.
- Lactobacillus can produce #Acetylcholine
- Lactobacillus can produce #GABA
[1.6 ] [#Polycystic ovary syndrome ] Lactobacillus given to letrozole-treated (induces PCOS) rats reduced androgen levels, improved estrous cyclicity, normalized ovarian morphology, as well as increased Lactobacillus and #Clostridium species and decreased #Prevotella .
[1.7 ] #High salt diet , or HSD) for instance, can result in depletion of the gut bacteria Lactobacillus spp., which results in T helper cell-mediated immune dysregulation and cognitive dysfunction.
- A diet rich do not increase the serum concentration of proinflammatory molecules.
- Adult male offspring from HSD-fed mice show hyperactivity, reduced sociability and increased repetitive behaviors
[1.8 ] [#Fermented food ]
[1.9 ] #Acetylcholine is produced from Lactobacillus
[#Vaginally delivery ] - Gamma aminobutyrate (#GABA ), a major CNS inhibitory neurotransmitter, is produced from Lactobacillus and is the first bacterium that is colonized with most vaginally born infants.
[#Diabetes Type 2 ] - Lactobacillus > positively correlated with fasting glucose and HbA1c levels > increased insulin resistance.
[1.11 ] [#Fermented food ]
[1.12 ] [#Lactoferrin ] Lactobacillus sp. or #Bifidobacterium sp.
[1.13 ] [#Parkinson’s Disease ] [#Bifidobacterium adolescentis ] #Akkermansia , Bifidobacterium, and Lactobacillus and a decrease in #Prevotella
[1.14 ] [#Antibiotic Therapy ] #Bifidobacteria (5 studies) and Lactobacillus (2 studies), and significant increases in #Proteobacteria such as E. coli (4 studies).
[1.15 ] [#Pancreatic Cancer ] [#Indole , #Tryptophan ] [#Probiotic ]
[1.16 ] [#Ulcerative Colitis ] Lactobacillus and #Pediococcus acidilactici were absent in fecal samples
[1.17 ] [#Hypertension ] [#High salt diet ] Lactobacillus abundance, which was linked to increased T helper 17 cell numbers in murine small intestinal lamina propria lymphocytes and human peripheral blood lymphocytes, as well as higher blood pressure.
- a high-salt diet reduced Lactobacillus abundance, increased proinflammatory gene expression, and exacerbated #Colitis in two separate disease models
[1.18 ] [#Inflamatory bowel disease ] #Bifidobacterium , Lactobacillus , and #Akkermansia .
- the microbial community composition is different between ileal luminal samples from colonic and fecal samples, as well along the length of the colon itself.
[1.19 ] #Allicin (diallylthiosulfinate) is a natural food compound with multiple biological and pharmacological functions.
- #Allicin treatment significantly improved GM composition and induced the most significant alteration enrichment of #Bifidobacterium and Lactobacillus .
- #Allicin -induced GM to HFD mice (AGMT) significantly increased Blautia [short-chain fatty acids (SCFAs)-producing microbiota] and #Bifidobacterium in HFD mice, also increased the SCFAs in the cecum,
[#Parkinson’s Disease ] - most PD patients (about 70% of patients) develop gastrointestinal disorders such as constipation, dysphagia, and gastroesophageal reflux. Strikingly, these gastrointestinal dysfunctions (particularly constipation and delayed gastric emptying) can be detected up to 20 years prior to PD diagnosis.
- reduction in their number of #Prevotellaceae bacteria compared to controls. Strikingly, this alteration was associated with the severity of the motor symptoms.
- PD patients may exhibit not only a decreased abundance of Prevotella but also an increased abundance of Lactobacilliceae.
- These alterations may be associated with reduced levels of #Ghrelin , an important gut hormone involved in the survival and efficacy of dopaminergic neurons.
[1.21 ] [#Natural Skin Microbiome ] [#Gender ] Lactobacillus .
[1.22 ] [#Culinary herbs and spices ] #Bifidobacterium spp. in vitro, whereas turmeric was not.
- stimulation of Lactobacillus spp. and inhibition of certain #Clostridium spp. by all seven spices.
- increase in most #Clostridium spp. after turmeric and curcumin intervention in a human study.
- high consumption compared to low consumption of #Cocoa derived flavanols, significantly stimulated growth of #Bifidobacterium spp. and Lactobacillus spp.
[1.23 ] Lactobacillus are also “psychobiotics” and can modulate the gut–brain connection via neuroactive molecules (GABA, glutamate)
[1.24 ] [#Parkinson’s Disease ] #Bifidobacterium and Lactobacillus species, which are common constituents of commercial probiotics, were more abundant in PD than NHC metagenomes.
[1.25 ] [#Parkinson’s Disease ] #Akkermansia , Lactobacillus , #Bifidobacterium .
- PD > decreased relative abundance of family #Lachnospiraceae , #Faecalibacterium
[1.26 ] [#Polyphenol-rich supplementation ] Lactobacillus by 220% and #Bifidobacterium by 56% (mostly anthocyanins). -
[1.27 ] Lactobacillus and #Bifidobacterium counts with #Sleep and cortisol levels respectively
[#Bipolar disorder , #Major depressive disorder , #Schizophrenia ] - Gut microbiota in BD, MDD and SZ > increase in #Eggerthella and Lactobacillus , together with a decrease in #Coprococcus was common for the three conditions in comparison to controls.
[1.28 ] [#Vaginal microbiota , #Vulvovaginal candidiasis ] [#Candida albicans ] Lactobacillus spp. produces lactic and other organic acids that contribute to the low pH within the vaginal cavity.
- Low pH (< 4.5) inhibits C. albicans yeast-to-hypha transition.
[1.29 ] [#High-protein diet ] #Clostridium , #Desulfovibrio , #Peptostreptococcus , #Acidaminococcus , #Veillonella , #Propionibacterium , Bacillus, #Bacteroides , #Staphylococcus , and other species of the #Proteobacteria family, and the loss of carbohydrate fermenting bacteria such as #Bacteroides , Lactobacillus , #Bifidobacterium , #Prevotella , #Ruminococcus , #Roseburia , and #Faecalibacterium .
[#Infants ] - Bacterial genera commonly found in the infant small intestine include Lactobacillus , #Clostridium , #Staphylococcus , #Streptococcus , #Bacteroides , and #Bifidobacterium
[#Infants ] Greater proportions of #Palmitic acid in the pool of triacylglycerides, for instance > higher levels of fecal Lactobacillus and #Bifidobacterium in neonates.
- #Oleic acid is beneficial for Lactobacillus spp.
[1.31 ] [#Rheumatoid Arthritis ] #Prevotella copri in early RA patients
- proliferation of the genus Collinsela and some Lactobacillus species.
- Three mechanisms by which microbiota may contribute to RA pathogenesis were proposed: inflammatory responses (#Prevotella copri and Lactobacillus ), molecular mimicry (#Prevotella copri ) and loss of intestinal barrier integrity (#Collinsella ).
[1.32 ] #Akkermansia , #Christensenellaceae , and Lactobacillus , were higher in #Centenarians than in other groups
[#Aging ] - the loss of Lactobacillus and #Faecalibacterium , as well as the abundance of #Oscillibacter and #Alistipes genera along with the #Eubacteriaceae family is linked to #Frailty in elderly people.
[1.33 ] #Bifidobacteria and Lactobacillus spp. can produce micromolar concentrations of #GABA .
- #Grape seed > the growth of Lactobacillus and #Enterococcus spp. were elevated.
- These changes in the gut microbiota were associated with increases in #4-hydroxyphenylacetic acid , #Phenylpropionic acid , #Phenylacetic acid and #4-hydroxybenzoic acid
- #Ferulic acid is a #Hydroxycinnaminic acid produced as a microbial metabolite from several Lactobacillus species and the production of many of its bioactive metabolic products (#Dihydroferulic acid or #Vanillic acid ) is dependent on the gut microbiota.
[1.34 ] [#Anorexia nervosa ] Lactobacillus counts were observed in the AN microbiota.
[1.35 ] #Vaginal microbiota and reduced abundance of Lactobacillus spp. contribute to #HPV acquisition, persistence, and development of #Cervical cancer .
[1.36 ] #Bilophila , Butryicicoccus, #Alistipes , #Enterococcus , Lactobacillus , #Streptococcus , #Shigella , and #Desulfovibrio , have the metabolic capability to produce #Putrescine majorly by the #Putrescine III biosynthesis pathway.
- In neurodegenerative diseases > #Histamine and other important #Neurotransmitters were synthesized in reduced amounts by the microbes with an elevated population in the diseased state.
- Most of the microbes, except #Desulfovibrio , Lactobacillus , and #Streptococcus , showed no annotation in their #Genome to synthesize #Histamine .
- #Enterococcus and Lactobacillus had the highest PS for #Butyrate formation through the fermentation of #Pyruvate .
- in neurodegenerative disease > #Shigella , Lactobacillus , and #Streptococcus are such microbes with elevated populations and the highest PS for the #Putrescine III biosynthetic pathway.
[1.37 ] [#Natural Small intestine Microbiome ] [#Escherichia coli ] Lactobacillus , #Veillonella , #Streptococcus , #Gemella , #Actinomyces , and E. coli.
[#Natural Small intestine Microbiome ] - Only select bacteria, including #Clostridium , Lactobacillus , and #Enterococcus species, are able to penetrate, or attach to, the mucus layer at the epithelium and use the mucus as an energy source
[1.38 ] [#humanized Galactooligosaccharides ] Lactobacillus and #Bifidobacterium specialize in oligosaccharide fermentation, utilizing galactooligosaccharides (GOS), #Fructooligosaccharides (FOS), and #Polysaccharide #Inulin
[1.39 ] [#Bladder cancer ] [#Lactobacillus crispatus ] Lactobacillus spp were significantly enriched in the #BCG responders. Co-culture with increasing concentrations of Lactobacillus crispatus resulted in increased #BCG -GFP internalization in UCC when compared to controls
[#Short peptide bacteriocins ] - #Lactocillin , a thiopeptide SPB isolated from a vaginal commensal lactobacillus was shown to inhibit several pathogens colonising skin or vagina and showed no antimicrobial activity against other #Lactobacilli species
[1.41 ] [#Cognitive impairment , #Mild Cognitive Impairment ] [#Bacteriophage ] Lactobacillus phages (family #Siphoviridae of the order #Caudovirales positively associated with better cognitive function; and transplantation of these phages from humans to mice and Drosophila showed increased memory scores and upregulation of memory-involved brain genes.
[1.42 ] #Olive oil ingestion in rodents also can promote the growth of certain types of beneficial #Bacteria including species of Lactobacillus , #Bifidobacterium , #Bacteroides , and #Clostridium , and members of the Erysipelotrichaeae.
[#Short Chain Fatty Acid ] [#Olive ] - SCFAs, produced by a number of bacteria, such as #Bacteroides and Lactobacillus , which are often elevated with EVOO consumption, are also potent activators for GPR43
- Lactobacillus to lower plasma #Cholesterol levels may be due partly to the enhanced #Bile Salt hydrolase activity this genus exhibits, as well as the ability to convert #Cholesterol to #Coprostanol , both leading to an impairment of #Cholesterol absorption in the intestine.
[#Olive ] - Lactobacillus , also elevated with EVOO consumption25,29 when administered in #Probiotic form, promoted a significant reduction in plasma total #Cholesterol levels in mice as well as human patients with hypercholesterolemia.
[#Obesity ] [#Olive ] - in humans, EVOO has prebiotic effects, promoting the growth of beneficial bacteria such as Lactobacillus and #Bifidobacterium . Specifically, a #Mediterranean diet supplemented with 40 g/day EVOO for 3 months administered to 18 overweight/obese participants resulted in significantly increased levels of #Lactic acid bacteria compared to baseline.
[1.43 ] [#Polysaccharide ] #Cessation of breastfeeding initiates the transition towards an #Adult -like gut microbiome composition, which is characterized by expansion of #Roseburia spp. and #Anaerostipes spp., restriction of Lactobacillus spp. and a functional shift towards an increased capacity to degrade complex polysaccharides
[1.44 ] [#Celiac Disease ] #Bacillus subtilis LZU-GM was isolated from Pakistani traditional fermented sourdough and could degrade 73.7% of #Gluten in 24 h in vitro.
- The #Gluten degradation was 3-fold higher in the small intestine of the strain LZU-GM treated mice group.
- #Gluten -treated mice established positive antigliadin antibodies (AGA) in serum (IgA, IgG, and anti-TG2 antibodies) as compared to the strain LZU-GM treatment group.
- the number of IFN-γ, TNF-α, #IL-10 , and COX-2 cells decrease in the lamina propria of the strain LZU-GM treatment group.
- Microbial community bar plot analysis showed that Lactobacillus , #Dubosiella , and #Enterococcus genera were restored and stabilized in the LZU-GM treatment group while #Blautia and #Ruminococcus were found lower.
[1.45 ] #Firmicutes phylum comprises Gram-positive bacteria with low G + C DNA content and is composed of more than 200 different genera, such as Lactobacillus , #Bacillus , #Clostridium , #Enterococcus , and Ruminicoccus.
[#Diabetes Type 1 ] - Studies have reported an increased quantity of #Villanella , #Clostridium , and #Bacteroides and a decreased quantity of Lactobacillus , #Eubacterium rectale , #Blautia coccoides , and #Bifidobacterium in #Children with type 1 diabetes.
- #Diabetes Type 1 > negative correlation has been reported between plasma #Glucose level and #Bifidobacterium , Lactobacillus spp., and #Firmicutes and #Bacteroidetes spp., while there has been positive correlation between #Clostridium and plasma #Glucose level.
[1.46 ] [#Non-alcoholic fatty liver disease ] #Dorea , Lactobacillus and #Megasphaera are enriched in MAFLD group.
[1.47 ] [#Candida albicans , #Streptococcus mutans ] #Streptococcus (particularly S. mutans), certain Lactobacillus species, and salivary #Veillonella and #Prevotella , and also increase the cariogenic virulence of biofilms
[1.48 ] [#Postmenopausal osteoporosis ] Lactobacillus sp. in non-PMO and the increased abundances of #Peptoniphilus sp., #Propionic acid bacteria, and members of the #Galicola genus in PMO
[1.49 ] #Leptin serum level was positively correlated with the abundance of #Bifidobacterium and #Lactobacillus whereas #Leptin serum level was negatively correlated with #Clostridium , #Bacteroides and, #Prevotella
[#Postmenopausal ] - Gut #Bacteria that possess β-glucuronidase and/or β-galactosidase activity can metabolize #Estrogen including #Bifidobacterium , #Faecalibacterium , Lactobacillus , #Veillonella
[#Diabetes Type 2 , #Peripheral neuropathy ] [#Sphingomyelin ] [#High Fat Diet ] - Lactobacillus , #Lachnoclostridium , and #Anaerotruncus taxa variants positively correlated with several lipid species, particularly elevated plasma sphingomyelins and sciatic nerve triglycerides.
[#Peripheral neuropathy ] - Lactobacillus , #Lachnoclostridium , and #Anaerotruncus , correlated negatively with several free fatty acid and complex lipid species, including LysoPC 16:1, in both plasma and sciatic nerve.
[1.51 ] [#Systemic lupus erythematosus ] Lactobacillus treatment decreased #IL-6 and increased #IL-10 production in the gut contributing to an anti-inflammatory environment.
[1.52 ] [#Colorectal cancer ] [#Short Chain Fatty Acid ] [#Zizyphus jujuba cv. Muzao ] #Bifidobacterium , #Bacteroides and Lactobacillus .
[1.53 ] #Bacteroides , #Bifidobacterium , #Escherichia , #Faecalibacterium , and Lactobacillus ,) > encode β-glucuronidase and/or β-galactosidase > impacting endogenous #Estrogen metabolism
[1.54 ] #Bifidobacterium , #Bacteroides , and Lactobacillus species that have high activities of #Bile Salt hydrolase, the enzyme responsible for the deconjugation of #Bile Acids .
[1.55 ] Lactobacillus spp., which was prevalent in healthy controls’ microbiota, splitted #Gluten peptides, thus reducing their immunogenicity
[1.56 ] [#Spondyloarthritis ] #Bacilli , order #Lactobacillales , families #Lactobacillaceae and #Clostridiaceae , and genera Lactobacillus and #Clostridium in non-colonized SpA patients.
[1.57 ] [#Alzheimer’s disease ] Lactobacillus and #Bifidobacterium restored these changes in the wild-type mice.
[1.58 ] [#Escherichia coli ] #Vitamin B12 supplementation in mice significantly decreased #Parabacteroides and Lactobacillus and increased E. coli and #Enterococcus abundances in a murine model of #Colitis
[1.59 ] [#Attention Deficit Hyperactivity Disorder ] Lactobacillus and #Bifidobacterium producers of #GABA , which is known to decrease in patients with ADHD > Ameliorate ADHD
[#Autism ] - the levels of #Bifidobacterium (known as beneficial bacteria, such as Lactobacillus species) were significantly lower in the stool of #Children with ASD
- After probiotic supplementation, there was a significant increase in the colony counts of #Bifidobacterium and Lactobacillus with significant improvement in the severity of ASD and gastrointestinal symptoms.
- Lactobacillus species produce #Acetylcholine and #GABA
- enterobacterial metabolite #Norharman , which was partly exogenous and generated from #Tryptophan metabolism regulated by Lactobacillus , showed the strongest inhibitory effect on M1 macrophage activation.
- As a neuroactive β-carboline, #Norharman is a pyridoindole alkaloid that is naturally occurring, is plant-derived or in thermally processed foods, and is formed by the condensation of indoleamine (such as #Tryptamine ) and formaldehyde, showing antioxidant, anti-inflammatory, and antitumor activities
[1.61 ] [#Flavonoid ] #Lactic acid bacteria.
[1.62 ] #Bifidobacterium , #Clostridium , and Lactobacillus , can produce enzymes such as β-glucuronidases that modify excreted estrogens, causing them to be retained in the body via reabsorption into circulation. This leads to increased #Estrogen levels which can cause several hormone-linked diseases.
[1.63 ] Lactobacillus , #Lactococcus , #Bifidobacterium , #Streptococcus , #Leuconostoc , and #Pediococcus produce #Lactic acid
[1.64 ] #Celiac Disease showed the abundance of #Streptococcus , Lactobacillus , #Veillonella , and #Allisonella species, while the abundance of #Ruminococcus , #Faecalibacterium , #Blautia , #Gemmiger , and #Anaerostipes was decreased.
[1.65 ] #Ginger essential oil supplementation in PL mice enhanced the relative abundance of Lactobacillus , #Alistipes , and #Olsenella , which are considered beneficial bacteria.
[#Non-alcoholic fatty liver disease ] - Lactobacillus may be used as a #Probiotic to improve #Steatohepatitis through the gut microbiota–liver axis by modulating gut microbiota composition and the inflammatory pathway in NAFLD
[1.66 ] #Bifidobacterium and Lactobacillus , and #Wheat consumption has also been linked to their enrichment.
[#Genome ] - In addition to #Bifidobacterium and Lactobacillus , our study found a significant enrichment of #Streptococcus , a #Lactic acid -producing bacteria, in patients with #Ulcerative Colitis (UC).
- This is in contrast to the majority of earlier studies from west.
- This increase in #Streptococcus abundance has also been observed in UC patients from different populations.
[#Ulcerative Colitis ] - increased abundance of #Nitrate -reducing bacteria in UC patients.
- persistent inflammation in UC patients accumulates nonfermentable #Nitrate .
- #Bifidobacterium and Lactobacillus can utilize nonfermentable forms of #Nitrate .
[1.67 ] [#Indole-3-acetic acid ] Lactobacillus can use #Tryptophan instead of #Glucose as a source of energy, and produce #AHR ligands such as #Indole -3-acetic acid (IAA), #Tryptamine (TA) and 3-methyl #Indole
[1.68 ] #Sulfur -metabolism pathways were found to be one of the frequent pathways among certain member of #Cancer -increased taxa such as #Aquabacterium , #Bilophila wadsworthia , #Delftia , #Desulfovibrio , #Escherichia coli , #Fusobacterium , #Klebsiella , Lactobacillus , #Morganella , #Odoribacter , and #Proteus .
[1.69 ] [#Bacteroides-Prevotella group , #Ruminococcus gauvreauii ] [#Keto diet ] #Bacteroides , #Bifidobacterium , and #Blautia significantly increased, whereas that of Lactobacillus , #Romboutsia , #Facklamia , and #Turicibacter significantly declined in the KD group compared with the ND group.
[#Alzheimer’s disease ] - co-housing wild-type mice with AD transgenic mice or giving them AD transgenic mice feces caused AD-associated gut microbiota dysbiosis, #Tau phosphorylation, and #Cognitive impairment .
- Gavage with Lactobacillus and #Bifidobacterium restored these changes.
[1.71 ] [#Lachnospiraceae ] [#Fiber-free diet ] #Butyrate -producing genera Lachnospiraceaea NK4A136 and #Roseburia . Additionally, Lactobacillus , which was also reduced in Fibre deprived mice
[1.72 ] [#Osteopontin ] Lactobacillus in the intestine of mice and promote the abundance of #Dorea , which could further regulate metabolic disorders
[1.73 ] [#Parkinson’s Disease ] Lactobacillus and #Bifidobacterium genus were most abundant in PD patients. #Prevotella VZCB and other #Faecalibacterium were most abundant in controls.
[1.74 ] [#Non alcoholic steatohepatitis ] [#Probiotic ] #Bifidobacterium and Lactobacillus strains, have been shown to reduce oxidative and inflammatory liver damage while also decreasing hepatic triglycerides (TG) and hepatic steatosis.
[1.75 ] Lactobacillus was demonstrated to enhance antigen-specific IgA secretion and induce Tfh cells in mice
[#Primary immune thrombocytopenia ] - fecal bacteria such as #Actinomycetaceae , #Blautia , #Streptococcus , and Lactobacillus are enriched, whereas bacteria such as #Bacteroides are depleted in ITP patients.
[#Primary immune thrombocytopenia ] - lactobacillus might indeed play a key role in the progression of ITP.
[#Primary immune thrombocytopenia ] [#Streptococcus anginosus , #Streptococcus parasanguinis , #Streptococcus salivarius ] - Lactobacillus and #Streptococcus (including S. anginosus, #Streptococcus sp., S. parasanguinis, and S. salivarius) were enriched in ITP patients.
Intervention in Disease
Author: MetaBiomIdentifier: 10000118URL: https://www.metabiom.org/microbiota/17/lactobacillusKeywords: Microbiome, Dysbiosis, Microbiota, Organism, Bacteria
Common References
[1.1 ] Transkingdom interactions between Lactobacilli and hepatic mitochondria attenuate western diet-induced diabetes 80001503 ]
[1.2 ] Functional Properties and Sustainability Improvement of Sourdough Bread by Lactic Acid Bacteria 80001555 ]
[1.3 ] Bile resistance mechanisms in Lactobacillus and Bifidobacterium 80001642 ]
[1.4 ] Smectite promotes probiotic biofilm formation in the gut for cancer immunotherapy 80001709 ]
[1.5 ] The Contribution of Gut Microbiota–Brain Axis in the Development of Brain Disorders 80001732 ]
[1.6 ] Polycystic Ovary Syndrome and the Gut Microbiome 80001774 ]
[1.7 ] Altered gut microbiome and autism like behavior are associated with parental high salt diet in male mice 80001781 ]
[1.8 ] Anti-Inflammatory and Immunomodulatory Properties of Fermented Plant Foods 80001873 ]
[1.9 ] Probiotics: A potential immunotherapeutic approach for the treatment of schizophrenia 80001875 ]
[1.10 ] Insights into the role of gut microbiota in obesity: pathogenesis, mechanisms, and therapeutic perspectives 80002107 ]
[1.11 ] Bioaccessibility and Bioavailability of Minerals in Relation to a Healthy Gut Microbiome 80002142 ]
[1.12 ] The Functional Role of Lactoferrin in Intestine Mucosal Immune System and Inflammatory Bowel Disease 80002175 ]
[1.13 ] Composition of intestinal flora affects the risk relationship between Alzheimer’s disease/Parkinson’s disease and cancer 80002199 ]
[1.14 ] Association between antibiotics and gut microbiome dysbiosis in children: systematic review and meta-analysis 80002271 ]
[1.15 ] Tryptophan-derived microbial metabolites activate the aryl hydrocarbon receptor in tumor-associated macrophages to suppress anti-tumor immunity 80002298 ]
[1.16 ] The Efficacy of Probiotics, Prebiotic Inulin-Type Fructans, and Synbiotics in Human Ulcerative Colitis: A Systematic Review and Meta-Analysis 80002431 ]
[1.17 ] Rethinking healthy eating in light of the gut microbiome 80002441 ]
[1.18 ] Metabolomics: The Key to Unraveling the Role of the Microbiome in Visceral Pain Neurotransmission 80002461 ]
[1.19 ] Allicin‐induced host‐gut microbe interactions improves energy homeostasis 80002476 ]
[1.20 ] Nutrition and Gut–Brain Pathways Impacting the Onset of Parkinson’s Disease 80002546 ]
[1.21 ] Characteristics of the Skin Microbiome in Selected Dermatological Conditions: A Narrative Review 80002602 ]
[1.22 ] Gut microbial modulation by culinary herbs and spices 80002681 ]
[1.23 ] Shotgun Metagenomics Study Suggests Alteration in Sulfur Metabolism and Oxidative Stress in Children with Autism and Improvement after Microbiota Transfer Therapy 80002687 ]
[1.24 ] Metagenomics of Parkinson’s disease implicates the gut microbiome in multiple disease mechanisms 80002696 ]
[1.25 ] An open label, non-randomized study assessing a prebiotic fiber intervention in a small cohort of Parkinson’s disease participants 80002769 ]
[1.26 ] Dietary Polyphenol, Gut Microbiota, and Health Benefits 80002820 ]
[1.27 ] Microbiota–gut–brain axis mechanisms in the complex network of bipolar disorders: potential clinical implications and translational opportunities 80002837 ]
[1.28 ] The Role of Host and Fungal Factors in the Commensal-to-Pathogen Transition of Candida albicans 80002841 ]
[1.29 ] Gut-Muscle Axis Exists and May Affect Skeletal Muscle Adaptation to Training 80002842 ]
[1.30 ] The role of human milk fats in shaping neonatal development and the early life gut microbiota 80002843 ]
[1.31 ] The role of the microbiome in rheumatoid arthritis: a review 80002845 ]
[1.32 ] How Microbiomes Affect Skin Aging: The Updated Evidence and Current Perspectives 80002854 ]
[1.33 ] The Gut Microbiota Links Dietary Polyphenols With Management of Psychiatric Mood Disorders 80002856 ]
[1.34 ] The gut microbiota contributes to the pathogenesis of anorexia nervosa in humans and mice 80002863 ]
[1.35 ] The interplay between human papillomavirus and vaginal microbiota in cervical cancer development 80002867 ]
[1.36 ] Comparative in-silico analysis of microbial dysbiosis discern potential metabolic link in neurodegenerative diseases 80002870 ]
[1.37 ] The emerging role of the small intestinal microbiota in human health and disease 80002887 ]
[1.38 ] Gut Microbiome: Profound Implications for Diet and Disease 80002909 ]
[1.39 ] PD25-08 THE BLADDER TUMOR MICROBIOME MAY AUGMENT RESPONSE TO BCG IN NON-MUSCLE INVASIVE BLADDER CANCER 80002930 ]
[1.40 ] Microbial derived antimicrobial peptides as potential therapeutics in atopic dermatitis 80002951 ]
[1.41 ] Unique trans-kingdom microbiome structural and functional signatures predict cognitive decline in older adults 80002973 ]
[1.42 ] Extra-virgin olive oil and the gut-brain axis: influence on gut microbiota, mucosal immunity, and cardiometabolic and cognitive health 80002976 ]
[1.43 ] Gut microbiome immaturity and childhood acute lymphoblastic leukaemia 80003007 ]
[1.44 ] A gluten degrading probiotic Bacillus subtilis LZU-GM relieve adverse effect of gluten additive food and balances gut microbiota in mice 80003030 ]
[1.45 ] Gut Microbiome–Brain Alliance: A Landscape View into Mental and Gastrointestinal Health and Disorders 80003039 ]
[1.46 ] Characteristics of gut microbiota in patients with metabolic associated fatty liver disease 80003040 ]
[1.47 ] High-Throughput Sequencing of Oral Microbiota in Candida Carriage Sjögren’s Syndrome Patients: A Pilot Cross-Sectional Study 80003046 ]
[1.48 ] Gut microbiota signatures and fecal metabolites in postmenopausal women with osteoporosis 80003077 ]
[1.49 ] Targeting gut microbiota in osteoporosis: impact of the microbial based functional food ingredients 80003111 ]
[1.50 ] Gut microbiota in a mouse model of obesity and peripheral neuropathy associated with plasma and nerve lipidomics and nerve transcriptomics 80003115 ]
[1.51 ] Gut microbiota: a newly identified environmental factor in systemic lupus erythematosus 80003157 ]
[1.52 ] Microbiome-metabolomic analysis of the impact of Zizyphus jujuba cv. Muzao polysaccharides consumption on colorectal cancer mice fecal microbiota and metabolites 80003193 ]
[1.53 ] Perturbations in gut microbiota composition in patients with polycystic ovary syndrome: a systematic review and meta-analysis 80003217 ]
[1.54 ] Relationship between Oat Consumption, Gut Microbiota Modulation, and Short-Chain Fatty Acid Synthesis: An Integrative Review 80003252 ]
[1.55 ] The Role of Gluten in Gastrointestinal Disorders: A Review 80003268 ]
[1.56 ] Differential gut microbiome in spondyloarthritis patients associated to Blastocystis colonization 80003286 ]
[1.57 ] Transmission of Alzheimer’s disease-associated microbiota dysbiosis and its impact on cognitive function: evidence from mice and patients 80003288 ]
[1.58 ] B Vitamins and Their Roles in Gut Health 80003304 ]
[1.59 ] Psychobiotics and fecal microbial transplantation for autism and attention-deficit/hyperactivity disorder: microbiome modulation and therapeutic mechanisms 80003318 ]
[1.60 ] Tryptophan metabolite norharman secreted by cultivated Lactobacillus attenuates acute pancreatitis as an antagonist of histone deacetylases 80003321 ]
[1.61 ] Prebiotics: Definition, Types, Sources, Mechanisms, and Clinical Applications 80003325 ]
[1.62 ] Never fear, the gut bacteria are here: Estrogen and gut microbiome-brain axis interactions in fear extinction 80003326 ]
[1.63 ] Role of Oral Microbiota in Cancer Development 80003331 ]
[1.64 ] Microbiome Metabolites in Health and Disease 80003332 ]
[1.65 ] Ginger essential oil prevents NASH progression by blocking the NLRP3 inflammasome and remodeling the gut microbiota-LPS-TLR4 pathway 80003336 ]
[1.66 ] Enrichment of Lactic Acid-Producing Bacteria in the Fecal Microbiota of Patients with Ulcerative Colitis in North India 80003339 ]
[1.67 ] Modulation of Immune Responses by Nutritional Ligands of Aryl Hydrocarbon Receptor 80003354 ]
[1.68 ] Reproducible and opposing gut microbiome signatures distinguish autoimmune diseases and cancers: a systematic review and meta-analysis 80003358 ]
[1.69 ] Ketogenic diet ameliorates attention deficit hyperactivity disorder in rats via regulating gut microbiota 80003382 ]
[1.70 ] Transmission of Alzheimer’s Disease-Associated Microbiota Dysbiosis and its Impact on Cognitive Function: Evidence from Mouse Models and Human Patients 80003400 ]
[1.71 ] Fiber deprivation and microbiome-borne curli shift gut bacterial populations and accelerate disease in a mouse model of Parkinson’s disease 80003413 ]
[1.72 ] Functional proteins in breast milk and their correlation with the development of the infant gut microbiota: a study of mother-infant pairs 80003433 ]
[1.73 ] Dietary quality and the gut microbiome in early-stage Parkinson’s disease patients 80003439 ]
[1.74 ] Dietary Patterns, Foods, and Nutrients to Ameliorate Non-Alcoholic Fatty Liver Disease: A Scoping Review 80003456 ]
[1.75 ] Gut Microbiome and Metabolome Were Altered and Strongly Associated With Platelet Count in Adult Patients With Primary Immune Thrombocytopenia 80003463 ]
[1.76 ] Alterations in the gut microbiota of patients with acquired immune deficiency syndrome 80000714 ]
[1.77 ] Characterization of intestinal microbiota in alcoholic patients with and without alcoholic hepatitis or chronic alcoholic pancreatitis 80000689 ]
[1.78 ] Gut microbiota compositional and functional fingerprint in patients with alcohol use disorder and alcohol-associated liver disease 80001386 ]
[1.79 ] Mild cognitive impairment has similar alterations as Alzheimer’s disease in gut microbiota 80001081 ]
[1.80 ] Dysbiosis of saliva microbiome in patients with oral lichen planus 80001332 ]
[1.81 ] Microbial communities in the upper respiratory tract of patients with asthma and chronic obstructive pulmonary disease. 80000380 ]
[1.82 ] Fecal microbiota profile in atopic asthmatic adult patients 80000672 ]
[1.83 ] Distinct pattern of commensal gut microbiota in toddlers with eczema 80000546 ]
[1.84 ] Gastrointestinal microbiota in children with autism in Slovakia. 80000232 ]
[1.85 ] Alterations of gut microbiome in autoimmune hepatitis 80001159 ]
[1.86 ] Gut microbial profile in biliary atresia: a case-control study 80001225 ]
[1.87 ] The intestinal microbiota associated with cardiac valve calcification differs from that of coronary artery disease 80000915 ]
[1.88 ] Metagenomic investigation of bacteria associated with dental lesions: a cross-sectional study 80001389 ]
[1.89 ] Metagenomic and metatranscriptomic analysis of saliva reveals disease-associated microbiota in patients with periodontitis and dental caries 80000615 ]
[1.90 ] Salivary Gluten Degradation and Oral Microbial Profiles in Healthy Individuals and Celiac Disease Patients. 80000398 ]
[1.91 ] Comositional and functional differences between microbiota and cervical carcinogenesis as identified by shotgun metagenomic sequencing 80000960 ]
[1.92 ] Larger amounts of nitrite and nitrate-reducing bacteria in megaesophagus of Chagas’ disease than in controls. 80000549 ]
[1.93 ] Gut microbiota composition and frailty in elderly patients with Chronic Kidney Disease 80001402 ]
[1.94 ] The lung tissue microbiome in chronic obstructive pulmonary disease. 80000384 ]
[1.95 ] Alterations of Bacteroides sp., Neisseria sp., Actinomyces sp., and Streptococcus sp. populations in the oropharyngeal microbiome are associated with liver cirrhosis and pneumonia. 80000609 ]
[1.96 ] Hepatocellular carcinoma is associated with gut microbiota profile and inflammation in nonalcoholic fatty liver disease 80000791 ]
[1.97 ] Characterization of gut microbiota in hospitalized patients with Clostridium difficile infection 80001410 ]
[1.98 ] Increased rectal microbial richness is associated with the presence of colorectal adenomas in humans. 80000304 ]
[1.99 ] Dysbiosis signatures of gut microbiota in coronary artery disease 80000879 ]
[1.100 ] A pyrosequencing study in twins shows that gastrointestinal microbial profiles vary with inflammatory bowel disease phenotypes 80000284 ]
[1.101 ] Effect of gut microbiota on depressive-like behaviors in mice is mediated by the endocannabinoid system 80001488 ]
[1.102 ] Gut dysbiosis and detection of "live gut bacteria" in blood of Japanese patients with type 2 diabetes 80000309 ]
[1.103 ] Metagenomic analysis of duodenal microbiota reveals a potential biomarker of dysbiosis in the course of obesity and type 2 diabetes: a pilot study 80001381 ]
[1.104 ] Dysbiosis of urinary microbiota is positively correlated with type 2 diabetes mellitus 80000429 ]
[1.105 ] Intestinal microbiota is altered in patients with gastric cancer from Shanxi Province, China 80001028 ]
[1.106 ] Gastric microbial community profiling reveals a dysbiotic cancer-associated microbiota 80000711 ]
[1.107 ] Dysbiosis of fecal microbiota and high frequency of Citrobacter, Klebsiella spp., and Actinomycetes in patients with irritable bowel syndrome and gastroenteritis 80000589 ]
[1.108 ] Synchronous genitourinary lichen sclerosus signals a distinct urinary microbiome profile in men with urethral stricture disease 80001356 ]
[1.109 ] Hepatic glycogen storage diseases are associated to microbial dysbiosis 80001020 ]
[1.110 ] Metagenomic and metabolomic analyses unveil dysbiosis of gut microbiota in chronic heart failure patients 80000686 ]
[1.111 ] Featured gut microbiomes associated with the progression of chronic hepatitis B disease 80001369 ]
[1.112 ] Intestinal microbiota in patients with chronic hepatitis C with and without cirrhosis compared with healthy controls 80000712 ]
[1.113 ] Altered immunity and microbial dysbiosis in aged individuals with long-term controlled HIV infection 80000974 ]
[1.114 ] Hypertension is associated with intestinal microbiota dysbiosis and inflammation in a Brazilian population 80001373 ]
[1.115 ] Distinct nasopharyngeal and oropharyngeal microbiota of children with influenza A virus compared with healthy children 80000961 ]
[1.116 ] Characterization of gut microbiota, bile acid metabolism, and cytokines in intrahepatic cholangiocarcinoma 80001173 ]
[1.117 ] Comparative analysis of the oral microbiota between iron-deficiency anaemia (IDA) patients and healthy individuals by high-throughput sequencing 80001259 ]
[1.118 ] Molecular characterization of the intestinal microbiota in patients with and without abdominal bloating 80000352 ]
[1.119 ] Characteristics of the urinary microbiome in kidney stone patients with hypertension 80001334 ]
[1.120 ] Multiple sclerosis patients have a distinct gut microbiota compared to healthy controls_DUBLICATE 80000891 ]
[1.121 ] Fecal and blood microbial 16S rRNA gene alteration in Chinese patients with multiple system atrophy and its subtypes 80001176 ]
[1.122 ] Microbiome signatures associated with steatohepatitis and moderate to severe fibrosis in children with nonalcoholic fatty liver disease 80001063 ]
[1.123 ] Dysbiosis gut microbiota associated with inflammation and impaired mucosal immune function in intestine of humans with non-alcoholic fatty liver disease 80000572 ]
[1.124 ] Salivary cariogenic bacteria counts are associated with obesity in student women at a Malaysian university 80000682 ]
[1.125 ] Differences in gut microbiota composition between obese and lean children: a cross-sectional study 80000241 ]
[1.126 ] Microbial diversity in saliva of oral squamous cell carcinoma 80000786 ]
[1.127 ] Gut microbiota alterations associated with reduced bone mineral density in older adults 80001175 ]
[1.128 ] Gut microbial profile analysis by MiSeq sequencing of pancreatic carcinoma patients in China 80000728 ]
[1.129 ] Parkinson’s Disease and Parkinson’s Disease medications have distinct signatures of the gut microbiome. 80000277 ]
[1.130 ] Inflammatory microbes and genes as potential biomarkers of Parkinson’s disease 80002678 ]
[1.131 ] Characterization of pelvic and cervical microbiotas from patients with pelvic inflammatory disease 80000794 ]
[1.132 ] Obese adolescents with PCOS have altered biodiversity and relative abundance in Gastrointestinal microbiota 80001360 ]
[1.133 ] A complete guide to human microbiomes: Body niches, transmission, development, dysbiosis, and restoration 80002487 ]
[1.134 ] Gut microbial profile is altered in primary biliary cholangitis and partially restored after UDCA therapy 80000594 ]
[1.135 ] Characterization of intestinal microbiota in ulcerative colitis patients with and without primary sclerosing cholangitis 80000753 ]
[1.136 ] Primary sclerosing cholangitis is characterised by intestinal dysbiosis independent from IBD 80000513 ]
[1.137 ] Alveolar microbiota profile in patients with human pulmonary tuberculosis and interstitial pneumonia 80001312 ]
[1.138 ] Analysis of fecal lactobacillus community structure in patients with early rheumatoid arthritis 80000537 ]
[1.139 ] Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia 80002671 ]
[1.140 ] Analysis of microbiota in first episode psychosis identifies preliminary associations with symptom severity and treatment response 80000754 ]
[1.141 ] Alterations of gut microbiome in the patients with severe fever with thrombocytopenia syndrome 80000848 ]
[1.142 ] Fecal microbiota signatures of adult patients with different types of short bowel syndrome 80000662 ]
[1.143 ] Dysbiosis of the buccal mucosa microbiome in primary Sjögren’s syndrome patients 80000861 ]
[1.144 ] Saliva microbiome in primary Sjogren’s syndrome reveals distinct set of disease associated microbes 80001246 ]
[1.145 ] Connection between the Gut Microbiome, Systemic Inflammation, Gut Permeability and FOXP3 Expression in Patients with Primary Sjögren’s Syndrome 80001479 ]
[1.146 ] Dysbiosis in the oral bacterial and fungal microbiome of HIV-infected subjects is associated with clinical and immunologic variables of HIV infection 80000883 ]
[1.147 ] Comparison of the ocular microbiome between chronic Stevens-Johnson syndrome patients and healthy subjects 80001339 ]
[1.148 ] Association of systemic sclerosis with a unique colonic microbial consortium 80000333 ]
[1.149 ] Alterations in the gut microbiota and metabolite profiles of thyroid carcinoma patients 80000975 ]
[1.150 ] Dysbiosis of gut microbiota with reduced tremethylamine-N-oxide level in patients with large-artery atherosclerotic stroke or transient ischemic attack._DUBLICATE 80000456 ]
[1.151 ] Analysis of endoscopic brush samples identified mucosa-associated dysbiosis in inflammatory bowel disease 80000679 ]
[1.152 ] Alterations of mucosal microbiota in the colon of patients with inflammatory bowel disease revealed by real time polymerase chain reaction amplification of 16S ribosomal ribonucleic acid. 80000597 ]
[1.153 ] The microbiome in urogenital schistosomiasis and induced bladder pathologies 80001012 ]
[1.154 ] Diversity of endocervical microbiota associated with genital Chlamydia trachomatis infection and infertility among women visiting obstetrics and gynecology clinics in Malaysia 80001294 ]
[1.155 ] Gut microbiota alterations in moderate to severe acne vulgaris patients 80001044 ]
[1.156 ] Molecular diagnosis of vaginitis: comparing quantitative PCR and microbiome profiling approaches to current microscopy scoring 80001177 ]
[1.157 ] Temporal and long-term gut microbiota variation in allergic disease: a prospective study from infancy to school age 80001034 ]
[1.158 ] Microbiome-host interplay in atopic dermatitis and psoriasis 80001261 ]
[1.159 ] Gut microbiota and dietary patterns in children with attention-deficit/hyperactivity disorder 80001226 ]
[1.160 ] Altered gut microbiota in Chinese children with autism spectrum disorders 80000976 ]
[1.161 ] Abnormal intestinal permeability and microbiota in patients with autoimmune hepatitis 80000353 ]
[1.162 ] Study Of The Gut Microbiome In Egyptian Patients With Autoimmune Thyroid Diseases 80001587 ]
[1.163 ] Comparison of the diversity of the vaginal microbiota in HIV-infected and uninfected women with and without bacterial vaginosis. 80000370 ]
[1.164 ] Molecular analysis of the diversity of vaginal microbiota associated with bacterial vaginosis. 80000373 ]
[1.165 ] Dysbiosis signatures of the microbial profile in tissue from bladder cancer 80001272 ]
[1.166 ] Urinary microbiota - a potential biomarker and therapeutic target for bladder cancer 80001050 ]
[1.167 ] Duodenal and faecal microbiota of celiac children: molecular, phenotype and metabolome characterization. 80000529 ]
[1.168 ] Lactobacilli Have a Niche in the Human Nose 80001688 ]
[1.169 ] Gut microbiome and serum metabolome analyses identify unsaturated fatty acids and butanoate metabolism induced by gut microbiota in patients with chronic spontaneous urticaria 80001363 ]
[1.170 ] Intestinal floras of populations that have a high risk of colon cancer 80001116 ]
[1.171 ] Alterations of the predominant fecal microbiota and disruption of the gut mucosal barrier in patients with early-stage colorectal cancer 80001354 ]
[1.172 ] Reduced abundance of butyrate-producing bacteria species in the fecal microbial community in Crohn’s Disease. 80000250 ]
[1.173 ] Microbiota profile in new-onset pediatric Crohn’s disease: data from a non-Western population 80000941 ]
[1.174 ] Cutaneous burn injury modulates urinary antimicrobial peptide responses and the urinary microbiome 80000424 ]
[1.175 ] Gut microbiota in children with type 1 diabetes differs from that in healthy children: a case-control study 80000311 ]
[1.176 ] The salivary microbiome is altered in children with eosinophilic esophagitis and correlates with disease activity 80001126 ]
[1.177 ] Gallstone Disease and Bacterial Metabolic Performance of Gut Microbiota in Middle-Aged and Older Patients 80002433 ]
[1.178 ] The placental microbiota is altered among subjects with gestational diabetes mellitus: a pilot study 80000654 ]
[1.179 ] Molecular alteration analysis of human gut microbial composition in Graves’ disease patients 80000858 ]
[1.180 ] Molecular estimation of alteration in intestinal microbial composition in Hashimoto’s thyroiditis patients 80000607 ]
[1.181 ] Gut microbiome analysis as a tool towards targeted non-invasive biomarkers for early hepatocellular carcinoma 80000859 ]
[1.182 ] Gut microbe analysis between hyperthyroid and healthy individuals_DUBLICATE 80000655 ]
[1.183 ] Altered gut microbiota composition associated with eczema in infants 80000741 ]
[1.184 ] Alterations of microbiota in urine from women with interstitial cystitis 80000409 ]
[1.185 ] Microbiota profile is different for early and invasive colorectal cancer and is consistent throughout the colon 80001383 ]
[1.186 ] Functional dysbiosis within the gut microbiota of patients with constipated-irritable bowel syndrome 80000623 ]
[1.187 ] Profiling the urinary microbiome in men with calcium-based kidney stones 80001327 ]
[1.188 ] Possible association of Bifidobacterium and Lactobacillus in the gut microbiota of patients with major depressive disorder 80000768 ]
[1.189 ] The association between vaginal bacterial composition and miscarriage: a nested case-control study 80001270 ]
[1.190 ] Conjuctival dysbiosis in mucosa-associated lyphoid tissue lymphoma 80001109 ]
[1.191 ] Altered gut microbiota in myasthenia gravis 80000850 ]
[1.192 ] Altered fecal microbiota correlates with liver biochemistry in nonobese patients with non-alcoholic fatty liver disease. 80000569 ]
[1.193 ] Metagenome of gut microbiota of children with nonalcoholic fatty liver disease 80001279 ]
[1.194 ] Comparative study of vulva and abdominal skin microbiota of healthy females with high and average BMI 80000935 ]
[1.195 ] Characterization of microbiota in male infertility cases uncovers differences in seminal hyperviscosity and oligoasthenoteratozoospermia possibly correlated with increased prevalence of infectious bacteria 80000723 ]
[1.196 ] A case controlled study examining the bladder microbiome in women with overactive bladder (OAB) and healthy controls 80000805 ]
[1.197 ] Alteration of the fecal microbiota in Chinese patients with Parkinson’s disease 80000645 ]
[1.198 ] Characteristic gut microbiota and predicted metabolic functions in women with PCOS 80001274 ]
[1.199 ] Changes in the composition of gut and vaginal microbiota in patients with postmenopausal osteoporosis 80002530 ]
[1.200 ] Age, menopausal status and the bladder microbiome 80000804 ]
[1.201 ] Qualitative and semiquantitative analysis of Lactobacillus species in the vaginas of healthy fertile and postmenopausal Chinese women 80000503 ]
[1.202 ] Distinct microbiome in pouchitis compared to healthy pouches in ulcerative colitis and familial adenomatous polyposis. 80000242 ]
[1.203 ] Bronchoalveolar lavage fluid microbiota dysbiosis in infants with protracted bacterial bronchitis 80000720 ]
[1.204 ] Tissue-Associated Bacterial Alterations in Rectal Carcinoma Patients Revealed by 16S rRNA Community Profiling 80000432 ]
[1.205 ] Alteration of vaginal microbiota in patients with unexplained recurrent miscarriage 80000972 ]
[1.206 ] The bacterial communities of the small intestine and stool in children with short bowel syndrome 80001208 ]
[1.207 ] Association between cigarette smoking and the vaginal microbiota: a pilot study 80000639 ]
[1.208 ] Alterations in the Genital Microbiota in Women With Spinal Cord Injury 80000468 ]
[1.209 ] Alterations of urinary microbiota in type 2 Diabetes Mellitus with hypertension and/or hyperlipidemia 80000661 ]
[1.210 ] Altered fecal microbiota in paediatric inflammatory bowel disease 80000564 ]
[1.211 ] The female urinary microbiome: a comparison of women with and without urgency urinary incontinence 80000787 ]
[1.212 ] Defining dysbiosis in patients with urolithiasis_DUBLICATE 80000950 ]
[1.213 ] Molecular characterization of fecal microbiota in patients with viral diarrhea. 80000437 ]
[1.214 ] Gut Microbiota-Derived Tryptophan Metabolites Maintain Gut and Systemic Homeostasis 80002575 ]
[1.215 ] Maternal exposures and the infant gut microbiome: a systematic review with meta-analysis 80001848 ]
[1.216 ] Resistant starch type 2 and whole grain maize flours enrich different intestinal bacteria and metatranscriptomes 80002313 ]
[1.217 ] Beef, Casein, and Soy Proteins Differentially Affect Lipid Metabolism, Triglycerides Accumulation and Gut Microbiota of High-Fat Diet-Fed C57BL/6J Mice 80002362 ]
[1.218 ] Separating the Empirical Wheat From the Pseudoscientific Chaff: A Critical Review of the Literature Surrounding Glyphosate, Dysbiosis and Wheat-Sensitivity 80001476 ]
[1.219 ] Effects of Heat Stress on Gut Microbiome in Rats 80002087 ]
[1.220 ] Beneficial reconstitution of gut microbiota and control of alpha-synuclein and curli-amyloids-producing enterobacteria, by beta 1,3-1,6 glucans in a clinical pilot study of autism and potentials in neurodegenerative diseases 80002371 ]
[1.221 ] Metformin Reduces Aging-Related Leaky Gut and Improves Cognitive Function by Beneficially Modulating Gut Microbiome/Goblet Cell/Mucin Axis 80000214 ]
[1.222 ] Alterations of the Gut Microbiota in Response to Total Sleep Deprivation and Recovery Sleep in Rats 80002274 ]
[1.223 ] Sleep and the Gut Microbiome in Psoriasis: Clinical Implications for Disease Progression and the Development of Cardiometabolic Comorbidities 80002413 ]
[1.224 ] Dietary simple sugars alter microbial ecology in the gut and promote colitis in mice 80001430 ]
[1.225 ] Next Generation Microbiome Research: Identification of Keystone Species in the Metabolic Regulation of Host-Gut Microbiota Interplay 80002163 ]
[1.226 ] Role of Human Milk Bioactives on Infants’ Gut and Immune Health 80001660 ]
[1.227 ] Neurotransmitter and Intestinal Interactions: Focus on the Microbiota-Gut-Brain Axis in Irritable Bowel Syndrome 80002354 ]
