| scholarly article | Q13442814 |
| P50 | author | Brian M M Ahmer | Q73087808 |
| Peter White | Q39600851 | ||
| P2093 | author name string | Tony Romeo | |
| Jenee N Smith | |||
| Jessica L Dyszel | |||
| Prosper N Boyaka | |||
| Yakhya Dieye | |||
| David L Newsom | |||
| Steven Krakowka | |||
| Anice Sabag-Daigle | |||
| Edward J Behrman | |||
| Juan F González | |||
| Mohamed M Ali | |||
| Razvan Arsenescu | |||
| Brandi Steidley | |||
| Christopher Stahl | |||
| Judith Dubena | |||
| P2860 | cites work | Acrylamide: A Cooking Carcinogen? | Q56115376 |
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| Normalization of cDNA microarray data | Q28181692 | ||
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| Gut inflammation provides a respiratory electron acceptor for Salmonella | Q29615318 | ||
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| Identification of a pathway for the utilization of the Amadori product fructoselysine in Escherichia coli | Q30708333 | ||
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| Statistical Issues in cDNA Microarray Data Analysis | Q30788312 | ||
| A model of Salmonella colitis with features of diarrhea in SLC11A1 wild-type mice | Q33319574 | ||
| Perturbation of the small intestine microbial ecology by streptomycin alters pathology in a Salmonella enterica serovar typhimurium murine model of infection | Q33443646 | ||
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| The physiological stimulus for the BarA sensor kinase. | Q33725412 | ||
| Identifying genetic determinants needed to establish a human gut symbiont in its habitat | Q33955014 | ||
| The alternative electron acceptor tetrathionate supports B12-dependent anaerobic growth of Salmonella enterica serovar typhimurium on ethanolamine or 1,2-propanediol | Q33995982 | ||
| Genetic and functional analysis of a PmrA-PmrB-regulated locus necessary for lipopolysaccharide modification, antimicrobial peptide resistance, and oral virulence of Salmonella enterica serovar typhimurium | Q34004929 | ||
| Analysis of acrylamide, a carcinogen formed in heated foodstuffs | Q34143312 | ||
| Acrylamide is formed in the Maillard reaction | Q34153328 | ||
| Fructoselysine 3-epimerase, an enzyme involved in the metabolism of the unusual Amadori compound psicoselysine in Escherichia coli | Q34279306 | ||
| High-throughput comparison of gene fitness among related bacteria | Q34286388 | ||
| Advanced protein glycosylation in diabetes and aging | Q34298835 | ||
| Ethanolamine utilization in Salmonella typhimurium: nucleotide sequence, protein expression, and mutational analysis of the cchA cchB eutE eutJ eutG eutH gene cluster | Q34319376 | ||
| In-depth mechanistic study on the formation of acrylamide and other vinylogous compounds by the maillard reaction | Q34341651 | ||
| Robust Salmonella metabolism limits possibilities for new antimicrobials. | Q34502598 | ||
| Salmonella SPI-1-mediated neutrophil recruitment during enteric colitis is associated with reduction and alteration in intestinal microbiota | Q34558189 | ||
| Parallel exploitation of diverse host nutrients enhances Salmonella virulence. | Q34697874 | ||
| Gac/Rsm signal transduction pathway of gamma-proteobacteria: from RNA recognition to regulation of social behaviour | Q34719736 | ||
| Pretreatment of mice with streptomycin provides a Salmonella enterica serovar Typhimurium colitis model that allows analysis of both pathogen and host | Q34935646 | ||
| Circuitry linking the Csr and stringent response global regulatory systems | Q35046553 | ||
| Integration of a complex regulatory cascade involving the SirA/BarA and Csr global regulatory systems that controls expression of the Salmonella SPI-1 and SPI-2 virulence regulons through HilD | Q35049823 | ||
| Intestinal inflammation allows Salmonella to use ethanolamine to compete with the microbiota | Q35409022 | ||
| A Comprehensive Subcellular Proteomic Survey of Salmonella Grown under Phagosome-Mimicking versus Standard Laboratory Conditions | Q36135035 | ||
| Gut immune maturation depends on colonization with a host-specific microbiota | Q36235223 | ||
| The intestinal fatty acid propionate inhibits Salmonella invasion through the post-translational control of HilD | Q36636799 | ||
| The preparation and characterization of some Amadori compounds (1-amino-1-deoxy-D-fructose derivatives) derived from a series of aliphatic omega-amino acids | Q36729038 | ||
| Formate acts as a diffusible signal to induce Salmonella invasion | Q36747272 | ||
| HilD-mediated transcriptional cross-talk between SPI-1 and SPI-2. | Q36936468 | ||
| A perspective on the Maillard reaction and the analysis of protein glycation by mass spectrometry: probing the pathogenesis of chronic disease | Q37097143 | ||
| Microbiota-liberated host sugars facilitate post-antibiotic expansion of enteric pathogens | Q37302434 | ||
| In silico identification and experimental characterization of regulatory elements controlling the expression of the Salmonella csrB and csrC genes | Q37545958 | ||
| The Maillard reaction in the human body. The main discoveries and factors that affect glycation | Q37629139 | ||
| Comparative analysis of Salmonella genomes identifies a metabolic network for escalating growth in the inflamed gut. | Q37667983 | ||
| 1-Amino-1-deoxy-D-fructose ("fructosamine") and its derivatives. | Q37788385 | ||
| The streptomycin mouse model for Salmonella diarrhea: functional analysis of the microbiota, the pathogen's virulence factors, and the host's mucosal immune response | Q37968294 | ||
| Post-transcriptional regulation on a global scale: form and function of Csr/Rsm systems. | Q38016604 | ||
| Advanced glycation end products: role in pathology of diabetic cardiomyopathy | Q38081119 | ||
| Global regulation by CsrA in Salmonella typhimurium | Q38353868 | ||
| Intestinal short-chain fatty acids alter Salmonella typhimurium invasion gene expression and virulence through BarA/SirA. | Q40687509 | ||
| Why asparagine needs carbohydrates to generate acrylamide. | Q44344770 | ||
| Effects of asparagine, fructose, and baking conditions on acrylamide content in yeast-leavened wheat bread | Q44821502 | ||
| Characterization of two novel regulatory genes affecting Salmonella invasion gene expression | Q44872560 | ||
| The Salmonella pathogenicity island (SPI)-2 and SPI-1 type III secretion systems allow Salmonella serovar typhimurium to trigger colitis via MyD88-dependent and MyD88-independent mechanisms. | Q45232038 | ||
| Increased pentosidine, an advanced glycation end-product, in urine and tissue reflects disease activity in inflammatory bowel diseases | Q46176631 | ||
| Transcriptional activation of Salmonella typhimurium invasion genes by a member of the phosphorylated response-regulator superfamily. | Q48058213 | ||
| Contribution of the SirA regulon to biofilm formation in Salmonella enterica serovar Typhimurium | Q50075877 | ||
| Catabolite repression of the SirA regulatory cascade in Salmonella enterica. | Q50077366 | ||
| Salmonella SirA is a global regulator of genes mediating enteropathogenesis | Q50127381 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P4510 | describes a project that uses | limma | Q112236343 |
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | e1004209 | |
| P577 | publication date | 2014-06-26 | |
| P1433 | published in | PLOS Pathogens | Q283209 |
| P1476 | title | Fructose-asparagine is a primary nutrient during growth of Salmonella in the inflamed intestine | |
| P478 | volume | 10 |
| Q35913824 | A Mannose Family Phosphotransferase System Permease and Associated Enzymes Are Required for Utilization of Fructoselysine and Glucoselysine in Salmonella enterica Serovar Typhimurium. |
| Q37701371 | A Salmonella Regulator Modulates Intestinal Colonization and Use of Phosphonoacetic Acid |
| Q37086779 | A metabolic intermediate of the fructose-asparagine utilization pathway inhibits growth of a Salmonella fraB mutant |
| Q49943064 | An Oxidative Central Metabolism Enables Salmonella to Utilize Microbiota-Derived Succinate. |
| Q49955801 | Characterization of a Salmonella sugar kinase essential for the utilization of fructose-asparagine |
| Q36340549 | Colonization resistance: The deconvolution of a complex trait. |
| Q37611979 | Contribution of Asparagine Catabolism to Salmonella Virulence |
| Q35989778 | Depletion of Butyrate-Producing Clostridia from the Gut Microbiota Drives an Aerobic Luminal Expansion of Salmonella |
| Q49587782 | Dysbiosis-Associated Change in Host Metabolism Generates Lactate to Support Salmonella Growth |
| Q35355392 | Glyphosate, pathways to modern diseases III: Manganese, neurological diseases, and associated pathologies |
| Q49928270 | Identification of bacterial species that can utilize fructose-asparagine |
| Q35650976 | Identification of sdiA-regulated genes in a mouse commensal strain of Enterobacter cloacae. |
| Q48133744 | Measurement of Fructose-Asparagine Concentrations in Human and Animal Foods. |
| Q38763262 | Metabolic crosstalk between host and pathogen: sensing, adapting and competing |
| Q92652196 | Multicentered hydrogen bonding in 1-[(1-de-oxy-β-d-fructo-pyranos-1-yl)aza-nium-yl]cyclo-pentane-carboxyl-ate ('d-fructose-cyclo-leucine') |
| Q61809795 | Role of CsrA in stress responses and metabolism important for Salmonella virulence revealed by integrated transcriptomics |
| Q40077267 | Salmonella FraE, an asparaginase homolog, contributes to fructose-asparagine but not asparagine utilization |
| Q41907191 | Salmonella Mitigates Oxidative Stress and Thrives in the Inflamed Gut by Evading Calprotectin-Mediated Manganese Sequestration. |
| Q42694341 | Salmonella enterica Serovar Typhimurium Strategies for Host Adaptation |
| Q54266197 | Salmonella-Mediated Inflammation Eliminates Competitors for Fructose-Asparagine in the Gut. |
| Q41972545 | Synthesis of 6-phosphofructose aspartic acid and some related Amadori compounds. |
| Q41845880 | The Periplasmic Nitrate Reductase NapABC Supports Luminal Growth of Salmonella enterica Serovar Typhimurium during Colitis |
| Q26801079 | Understanding the complexities of Salmonella-host crosstalk as revealed by in vivo model organisms |
| Q40105597 | Use of Attenuated but Metabolically Competent Salmonella as a Probiotic To Prevent or Treat Salmonella Infection |
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