当前位置: 首页 >> 检索结果
共有 16360 条符合本次的查询结果, 用时 3.9648316 秒

1021. Variation in referral practice and differential cancer outcome: a strong reason to reflect on whether current guidelines are fit for purpose or implemented effectively in primary care.

作者: Keith Bodger.;Mustafa Shawihdi.
来源: Gut. 2014年63卷4期703-4页

1022. Obese patients after gastric bypass surgery have lower brain-hedonic responses to food than after gastric banding.

作者: Samantha Scholtz.;Alexander D Miras.;Navpreet Chhina.;Christina G Prechtl.;Michelle L Sleeth.;Norlida M Daud.;Nurhafzan A Ismail.;Giuliana Durighel.;Ahmed R Ahmed.;Torsten Olbers.;Royce P Vincent.;Jamshid Alaghband-Zadeh.;Mohammad A Ghatei.;Adam D Waldman.;Gary S Frost.;Jimmy D Bell.;Carel W le Roux.;Anthony P Goldstone.
来源: Gut. 2014年63卷6期891-902页
Roux-en-Y gastric bypass (RYGB) has greater efficacy for weight loss in obese patients than gastric banding (BAND) surgery. We hypothesise that this may result from different effects on food hedonics via physiological changes secondary to distinct gut anatomy manipulations.

1023. Genomic ATG16L1 risk allele-restricted Paneth cell ER stress in quiescent Crohn's disease.

作者: J Jasper Deuring.;Gwenny M Fuhler.;Sergey R Konstantinov.;Maikel P Peppelenbosch.;Ernst J Kuipers.;Colin de Haar.;C Janneke van der Woude.
来源: Gut. 2014年63卷7期1081-91页
Although genome wide association studies have partly uncovered the genetic basis of Crohn's disease (CD), it remains a challenge to link genetic polymorphisms to functional intestinal phenotypes. Paneth cells are specialised antimicrobial epithelial cells localised to the small-intestinal crypt-base. Here, we investigate whether genomic variations in ATG16L1 affect Paneth cell function.

1024. Combining risk factors with faecal immunochemical test outcome for selecting CRC screenees for colonoscopy.

作者: Inge Stegeman.;Thomas R de Wijkerslooth.;Esther M Stoop.;Monique E van Leerdam.;Evelien Dekker.;Marjolein van Ballegooijen.;Ernst J Kuipers.;Paul Fockens.;Roderik A Kraaijenhagen.;Patrick M Bossuyt.
来源: Gut. 2014年63卷3期466-71页
Faecal immunochemical testing (FIT) is increasingly used in colorectal cancer (CRC) screening but has a less than perfect sensitivity. Combining risk stratification, based on established risk factors for advanced neoplasia, with the FIT result for allocating screenees to colonoscopy could increase the sensitivity and diagnostic yield of FIT-based screening. We explored the use of a risk prediction model in CRC screening.

1025. Keratin 19: a key role player in the invasion of human hepatocellular carcinomas.

作者: Olivier Govaere.;Mina Komuta.;Johannes Berkers.;Bart Spee.;Carl Janssen.;Francesca de Luca.;Aezam Katoonizadeh.;Jasper Wouters.;Léon C van Kempen.;Anne Durnez.;Chris Verslype.;Joery De Kock.;Vera Rogiers.;Leo A van Grunsven.;Baki Topal.;Jacques Pirenne.;Hugo Vankelecom.;Frederik Nevens.;Joost van den Oord.;Massimo Pinzani.;Tania Roskams.
来源: Gut. 2014年63卷4期674-85页
Keratin (K)19, a biliary/hepatic progenitor cell (HPC) marker, is expressed in a subset of hepatocellular carcinomas (HCC) with poor prognosis. The underlying mechanisms driving this phenotype of K19-positive HCC remain elusive.

1026. Evaluation of disease extent with the Crohn's disease endoscopic index of severity.

作者: Philippe Marteau.
来源: Gut. 2013年62卷12期1819-20页

1027. Use of CT colonography in the English Bowel Cancer Screening Programme.

作者: Andrew A Plumb.;Steve Halligan.;Claire Nickerson.;Paul Bassett.;Andrew F Goddard.;Stuart A Taylor.;Julietta Patnick.;David Burling.
来源: Gut. 2014年63卷6期964-73页
To examine use of CT colonography (CTC) in the English Bowel Cancer Screening Programme (BCSP) and investigate detection rates.

1028. The learning curve for detection of non-polypoid (flat and depressed) colorectal neoplasms.

作者: Sarah K McGill.;Tonya Kaltenbach.;Shai Friedland.;Roy Soetikno.
来源: Gut. 2015年64卷1期184-5页

1029. Genetic variants associated with colorectal cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence.

作者: Xiangyu Ma.;Ben Zhang.;Wei Zheng.
来源: Gut. 2014年63卷2期326-36页
In the past two decades, approximately 1000 reports have been published regarding associations between genetic variants in candidate genes and risk of colorectal cancer (CRC). Study results are inconsistent. We aim to provide a synopsis of the current understanding of genetic factors for CRC risk through systematically evaluating results from previous studies.

1030. Shanghai fever: a distinct Pseudomonas aeruginosa enteric disease.

作者: Chih-Hsien Chuang.;Yi-Hsin Wang.;Hsin-Ju Chang.;Hsiu-Ling Chen.;Yhu-Chering Huang.;Tzou-Yien Lin.;Egon A Ozer.;Jonathan P Allen.;Alan R Hauser.;Cheng-Hsun Chiu.
来源: Gut. 2014年63卷5期736-43页
Shanghai fever, a community-acquired enteric illness associated with sepsis caused by Pseudomonas aeruginosa, was first described in 1918. The understanding of Shanghai fever is incomplete.

1031. Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia.

作者: Iona Cheng.;Jonathan M Kocarnik.;Logan Dumitrescu.;Noralane M Lindor.;Jenny Chang-Claude.;Christy L Avery.;Christian P Caberto.;Shelly-Ann Love.;Martha L Slattery.;Andrew T Chan.;John A Baron.;Lucia A Hindorff.;Sungshim Lani Park.;Fredrick R Schumacher.;Michael Hoffmeister.;Peter Kraft.;Anne M Butler.;David J Duggan.;Lifang Hou.;Chris S Carlson.;Kristine R Monroe.;Yi Lin.;Cara L Carty.;Sue Mann.;Jing Ma.;Edward L Giovannucci.;Charles S Fuchs.;Polly A Newcomb.;Mark A Jenkins.;John L Hopper.;Robert W Haile.;David V Conti.;Peter T Campbell.;John D Potter.;Bette J Caan.;Robert E Schoen.;Richard B Hayes.;Stephen J Chanock.;Sonja I Berndt.;Sebastien Küry.;Stephane Bézieau.;Jose Luis Ambite.;Gowri Kumaraguruparan.;Danielle M Richardson.;Robert J Goodloe.;Holli H Dilks.;Paxton Baker.;Brent W Zanke.;Mathieu Lemire.;Steven Gallinger.;Li Hsu.;Shuo Jiao.;Tabitha A Harrison.;Daniela Seminara.;Christopher A Haiman.;Charles Kooperberg.;Lynne R Wilkens.;Carolyn M Hutter.;Emily White.;Dana C Crawford.;Gerardo Heiss.;Thomas J Hudson.;Hermann Brenner.;William S Bush.;Graham Casey.;Loïc Le Marchand.;Ulrike Peters.
来源: Gut. 2014年63卷5期800-7页
Genome-wide association studies have identified a large number of single nucleotide polymorphisms (SNPs) associated with a wide array of cancer sites. Several of these variants demonstrate associations with multiple cancers, suggesting pleiotropic effects and shared biological mechanisms across some cancers. We hypothesised that SNPs previously associated with other cancers may additionally be associated with colorectal cancer. In a large-scale study, we examined 171 SNPs previously associated with 18 different cancers for their associations with colorectal cancer.

1032. Comparison of MRI with liver-specific contrast agents and multidetector row CT for the detection of hepatocellular carcinoma: a meta-analysis of 15 direct comparative studies.

作者: Lihua Chen.;Lin Zhang.;Jing Bao.;Jiuquan Zhang.;Chuanming Li.;Yunbao Xia.;Xuequan Huang.;Jian Wang.
来源: Gut. 2013年62卷10期1520-1页

1033. Newly diagnosed diabetes mellitus after acute pancreatitis: a systematic review and meta-analysis.

作者: Stephanie L M Das.;Primal P Singh.;Anthony R J Phillips.;Rinki Murphy.;John A Windsor.;Maxim S Petrov.
来源: Gut. 2014年63卷5期818-31页
Diabetes mellitus (DM) is common in the general population and it poses a heavy burden to society in the form of long-term disability, healthcare use and costs. The pancreas is a key player in glucose homeostasis, but the occurrence of newly diagnosed DM after acute pancreatitis (AP), the most frequent disease of the pancreas, has never been assessed systematically. The aim of this study was to conduct a systematic literature review to determine the prevalence and time course of DM and related conditions after the first attack of AP as well as the impact of covariates.

1034. A distinct vagal anti-inflammatory pathway modulates intestinal muscularis resident macrophages independent of the spleen.

作者: Gianluca Matteoli.;Pedro J Gomez-Pinilla.;Andrea Nemethova.;Martina Di Giovangiulio.;Cathy Cailotto.;Sjoerd H van Bree.;Klaus Michel.;Kevin J Tracey.;Michael Schemann.;Werend Boesmans.;Pieter Vanden Berghe.;Guy E Boeckxstaens.
来源: Gut. 2014年63卷6期938-48页
The cholinergic anti-inflammatory pathway (CAIP) has been proposed as a key mechanism by which the brain, through the vagus nerve, modulates the immune system in the spleen. Vagus nerve stimulation (VNS) reduces intestinal inflammation and improves postoperative ileus. We investigated the neural pathway involved and the cells mediating the anti-inflammatory effect of VNS in the gut. The effect of VNS on intestinal inflammation and transit was investigated in wild-type, splenic denervated and Rag-1 knockout mice. To define the possible role of α7 nicotinic acetylcholine receptor (α7nAChR), we used knockout and bone marrow chimaera mice. Anterograde tracing of vagal efferents, cell sorting and Ca(2+) imaging were used to reveal the intestinal cells targeted by the vagus nerve. VNS attenuates surgery-induced intestinal inflammation and improves postoperative intestinal transit in wild-type, splenic denervated and T-cell-deficient mice. In contrast, VNS is ineffective in α7nAChR knockout mice and α7nAChR-deficient bone marrow chimaera mice. Anterograde labelling fails to detect vagal efferents contacting resident macrophages, but shows close contacts between cholinergic myenteric neurons and resident macrophages expressing α7nAChR. Finally, α7nAChR activation modulates ATP-induced Ca(2+) response in small intestine resident macrophages. We show that the anti-inflammatory effect of the VNS in the intestine is independent of the spleen and T cells. Instead, the vagus nerve interacts with cholinergic myenteric neurons in close contact with the muscularis macrophages. Our data suggest that intestinal muscularis resident macrophages expressing α7nAChR are most likely the ultimate target of the gastrointestinal CAIP.

1035. Interval cancer: nightmare of colonoscopists.

作者: Ulrike Haug.;Jaroslaw Regula.
来源: Gut. 2014年63卷6期865-6页

1036. Decreased gut microbiota diversity, delayed Bacteroidetes colonisation and reduced Th1 responses in infants delivered by caesarean section.

作者: Hedvig E Jakobsson.;Thomas R Abrahamsson.;Maria C Jenmalm.;Keith Harris.;Christopher Quince.;Cecilia Jernberg.;Bengt Björkstén.;Lars Engstrand.;Anders F Andersson.
来源: Gut. 2014年63卷4期559-66页
The early intestinal microbiota exerts important stimuli for immune development, and a reduced microbial exposure as well as caesarean section (CS) has been associated with the development of allergic disease. Here we address how microbiota development in infants is affected by mode of delivery, and relate differences in colonisation patterns to the maturation of a balanced Th1/Th2 immune response.

1037. Treatment of patients with dual hepatitis B and C: a step in the right direction.

作者: Alessio Aghemo.;Massimo Colombo.
来源: Gut. 2014年63卷3期380-1页

1038. Correctness is mandatory in science: response to 'Correct determination of critical flicker frequency is mandatory when comparisons to other tests are made'.

作者: Anita Blanka Tryc.;Karin Weissenborn.
来源: Gut. 2014年63卷4期702-3页

1039. Update from EIC 2013.

作者: Emad El-Omar.
来源: Gut. 2013年62卷9期1233页

1040. Farnesoid X receptor agonists attenuate colonic epithelial secretory function and prevent experimental diarrhoea in vivo.

作者: Magdalena S Mroz.;Niamh Keating.;Joseph B Ward.;Rafiquel Sarker.;Silvie Amu.;Gabriella Aviello.;Mark Donowitz.;Padraic G Fallon.;Stephen J Keely.
来源: Gut. 2014年63卷5期808-17页
Bile acids are important regulators of intestinal physiology, and the nuclear bile acid receptor, farnesoid X receptor (FXR), is emerging as a promising therapeutic target for several intestinal disorders. Here, we investigated a role for FXR in regulating intestinal fluid and electrolyte transport and the potential for FXR agonists in treating diarrhoeal diseases.
共有 16360 条符合本次的查询结果, 用时 3.9648316 秒