Real-time polymerase chain reaction quantification of specific butyrate-producing bacteria, Desulfovibrio and Enterococcus faecalis in the feces of patients with colorectal cancer.
about
Gut microbiota: next frontier in understanding human health and development of biotherapeuticsAssociation of colorectal cancer with pathogenic Escherichia coli: Focus on mechanisms using optical imagingGut microbiota imbalance and colorectal cancerRelationship between intestinal microbiota and colorectal cancerMetagenomic surveys of gut microbiotaRole of the Microbiota in Colorectal Cancer: Updates on Microbial Associations and Therapeutic ImplicationsCurrent Hypothesis for the Relationship between Dietary Rice Bran Intake, the Intestinal Microbiota and Colorectal Cancer PreventionDiet, microbiota, and dysbiosis: a 'recipe' for colorectal cancer.Colon Macrophages Polarized by Commensal Bacteria Cause Colitis and Cancer through the Bystander Effect.Mucosa-associated Faecalibacterium prausnitzii phylotype richness is reduced in patients with inflammatory bowel disease.Dysbiosis of fecal microbiota in Crohn's disease patients as revealed by a custom phylogenetic microarray.Microbiota, Inflammation and Colorectal Cancer.Functional Characterization of Novel Faecalibacterium prausnitzii Strains Isolated from Healthy Volunteers: A Step Forward in the Use of F. prausnitzii as a Next-Generation Probiotic.Faecal microbiota of healthy adults in south India: Comparison of a tribal & a rural population.Structural segregation of gut microbiota between colorectal cancer patients and healthy volunteers.Gut microbes, diet, and cancer.Detection of human intestinal catalase-negative, Gram-positive cocci by rRNA-targeted reverse transcription-PCR.Impact of feed efficiency and diet on adaptive variations in the bacterial community in the rumen fluid of cattle.Cultured representatives of two major phylogroups of human colonic Faecalibacterium prausnitzii can utilize pectin, uronic acids, and host-derived substrates for growth.Gut microbiota, inflammation and colorectal cancer.Stool phospholipid signature is altered by diet and tumorsA gnotobiotic mouse model demonstrates that dietary fiber protects against colorectal tumorigenesis in a microbiota- and butyrate-dependent manner.Enterococcus faecalis infection causes inflammation, intracellular oxphos-independent ROS production, and DNA damage in human gastric cancer cells.Bacteroides thetaiotaomicron and Faecalibacterium prausnitzii influence the production of mucus glycans and the development of goblet cells in the colonic epithelium of a gnotobiotic model rodentDysbiosis signature of fecal microbiota in colorectal cancer patients.Understanding how commensal obligate anaerobic bacteria regulate immune functions in the large intestine.Emerging roles of the microbiome in cancer.Overestimation of the abundance of sulfate-reducing bacteria in human feces by quantitative PCR targeting the Desulfovibrio 16S rRNA geneQuantitative profiling of colorectal cancer-associated bacteria reveals associations between fusobacterium spp., enterotoxigenic Bacteroides fragilis (ETBF) and clinicopathological features of colorectal cancer.Microbial mucosal colonic shifts associated with the development of colorectal cancer reveal the presence of different bacterial and archaeal biomarkers.The gastrointestinal microbiome: a malleable, third genome of mammals.Gut microbiome, gut function, and probiotics: Implications for health.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 acidDifferential susceptibility to colorectal cancer due to naturally occurring gut microbiotaColorectal cancer: role of commensal bacteria and bystander effects.The Colonic Microbiome and Epithelial Transcriptome Are Altered in Rats Fed a High-Protein Diet Compared with a Normal-Protein Diet.Metagenomic evidence for taxonomic dysbiosis and functional imbalance in the gastrointestinal tracts of children with cystic fibrosis.Gut microbiota: an Indicator to Gastrointestinal Tract Diseases.Bacterially-Associated Transcriptional Remodelling in a Distinct Genomic Subtype of Colorectal Cancer Provides a Plausible Molecular Basis for Disease Development.Enterococcus faecalis enhances cell proliferation through hydrogen peroxide-mediated epidermal growth factor receptor activation
P2860
Q24617327-6EA745C3-A12B-4944-B991-A8D2B5B38F89Q24658471-C3022457-119D-4073-BDBE-4F7076BBE8E9Q26774708-2D8EC00E-B9DD-404D-9448-58238DFD55DEQ26781449-8C21FAEB-1CE3-4D8A-824C-0DF6146BE9D1Q26799820-9D0CCC69-691C-41FA-8536-1DF2725FAC39Q28073131-4A739FED-FFD8-4E96-A1AB-907EC4A1417BQ28080177-C756B334-F387-450A-A25E-2957FF97F5CDQ30384134-042FE047-DBD9-4EAB-8D3B-A0E65356E6D7Q30551486-8EC3C0ED-DB9A-418C-91E3-EE4463975F8EQ30988830-0C457DCA-7400-49A6-A02C-4C7C3F5470D1Q33694531-D88E9F47-3109-4FCD-BDF6-8A53B4578DF3Q33839116-5C95ED1B-29FA-4455-A894-29366EA715BAQ33857259-16FDD5F8-3AC0-48E8-91D7-88187AE7BD30Q33882796-8D9743AF-6982-4785-BD20-557C43E034D5Q33995488-02F12A79-14E7-450B-9F85-A3BD0D61FED1Q34000541-2038773E-E4C0-4557-BBAF-EC2BE5CA5A1CQ34055214-12FE6224-8AE8-4A5F-AEC2-995C463989F6Q34096117-C311A9E3-02A8-40C5-A7CF-BB7642F1D714Q34234386-F9393662-4600-499E-86B4-0BBB22F4FDD5Q34549031-EB94D1D5-1CD5-4C5A-8BD5-C862F75E2761Q34627630-DA81129C-4244-4453-A7F0-D936E0FE680BQ34644406-EEDFEC1D-8361-4E13-A2D3-8D5103A47159Q34707058-CB19A2E9-B4F6-4D81-BED2-0A5CF5E74348Q34732850-0EC44826-D77A-44F3-B050-911CBAD98992Q34754690-71B5E0B3-451D-469A-A745-98420E98E334Q35003724-BF10310C-9931-4895-8E1D-E8A0FA650099Q35058372-62371081-8474-4D17-BCAD-A5ADF53AE155Q35077359-673946AB-4C5F-41DD-A511-1E5747C3AACDQ35159162-1D03A156-20F0-460C-AE76-0769B791A4B4Q35165688-4C28BA1C-6CF2-4B16-ABF7-806A239C6CBBQ35214930-62EA99BB-0C50-4053-AD89-A8DEAA887C14Q35616074-947A69E5-0D71-4EC8-B282-1B2F1F4DFA1AQ35742145-5AC32DBB-F592-427C-AAC8-F21F73B6F1E9Q35778047-8B65D2EF-D30B-44B6-A7CA-5267EE9A025AQ35884122-AE802088-4FD2-4D0A-9750-C972C4EDB730Q35914215-49C5EB7C-B7D2-45E3-BE8F-E9C740CD2A43Q35945463-D020AEFA-02A9-4E53-9AEA-90CDDB86B812Q36002545-214E7D21-B0F5-49B2-BFD1-EBE3A6E9E1BFQ36192702-46F4C455-968F-4C0C-9C85-EDCFCD80C87BQ36277449-B737309F-A228-4631-995D-0FABD346A27C
P2860
Real-time polymerase chain reaction quantification of specific butyrate-producing bacteria, Desulfovibrio and Enterococcus faecalis in the feces of patients with colorectal cancer.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Real-time polymerase chain rea ...... tients with colorectal cancer.
@en
Real-time polymerase chain rea ...... tients with colorectal cancer.
@nl
type
label
Real-time polymerase chain rea ...... tients with colorectal cancer.
@en
Real-time polymerase chain rea ...... tients with colorectal cancer.
@nl
prefLabel
Real-time polymerase chain rea ...... tients with colorectal cancer.
@en
Real-time polymerase chain rea ...... tients with colorectal cancer.
@nl
P2093
P1476
Real-time polymerase chain rea ...... tients with colorectal cancer.
@en
P2093
Balakrishnan S Ramakrishna
Ethendhar Rajendiran
G Vijay Samuel
Ramadass Balamurugan
Sarah George
P2860
P304
P356
10.1111/J.1440-1746.2008.05490.X
P433
P577
2008-07-08T00:00:00Z