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41. Real friends: Faecalibacterium prausnitzii supports mucosal immune homeostasis.

作者: Mathias W Hornef.;Oliver Pabst.
来源: Gut. 2016年65卷3期365-7页

42. Gut to lung.

作者: Sylvia Knapp.
来源: Gut. 2016年65卷4期544-5页

43. Dense genotyping of immune-related loci identifies HLA variants associated with increased risk of collagenous colitis.

作者: Helga Westerlind.;Marie-Rose Mellander.;Francesca Bresso.;Andreas Munch.;Ferdinando Bonfiglio.;Ghazaleh Assadi.;Joseph Rafter.;Matthias Hübenthal.;Wolfgang Lieb.;Henrik Källberg.;Boel Brynedal.;Leonid Padyukov.;Jonas Halfvarson.;Leif Törkvist.;Jan Bjork.;Anna Andreasson.;Lars Agreus.;Sven Almer.;Stephan Miehlke.;Ahmed Madisch.;Bodil Ohlsson.;Robert Löfberg.;Rolf Hultcrantz.;Andre Franke.;Mauro D'Amato.
来源: Gut. 2017年66卷3期421-428页
Collagenous colitis (CC) is a major cause of chronic non-bloody diarrhoea, particularly in the elderly female population. The aetiology of CC is unknown, and still poor is the understanding of its pathogenesis. This possibly involves dysregulated inflammation and immune-mediated reactions in genetically predisposed individuals, but the contribution of genetic factors to CC is underinvestigated. We systematically tested immune-related genes known to impact the risk of several autoimmune diseases for their potential CC-predisposing role.

44. Faecal haemoglobin concentration influences risk prediction of interval cancers resulting from inadequate colonoscopy quality: analysis of the Taiwanese Nationwide Colorectal Cancer Screening Program.

作者: Sherry Yueh-Hsia Chiu.;Shu-Ling Chuang.;Sam Li-Sheng Chen.;Amy Ming-Fang Yen.;Jean Ching-Yuan Fann.;Dun-Cheng Chang.;Yi-Chia Lee.;Ming-Shiang Wu.;Chu-Kuang Chou.;Wen-Feng Hsu.;Shu-Ti Chiou.;Han-Mo Chiu.
来源: Gut. 2017年66卷2期293-300页
Interval colorectal cancer (CRC) after colonoscopy may affect effectiveness and cost-effectiveness of screening programmes. We aimed to investigate whether and how faecal haemoglobin concentration (FHbC) of faecal immunochemical testing (FIT) affected the risk prediction of interval cancer (IC) caused by inadequate colonoscopy quality in a FIT-based population screening programme.

45. A 50-year-old woman with a recurrent oesophageal stricture.

作者: Tahir Akbar.;Adnan Al Badri.;John N Gordon.
来源: Gut. 2016年65卷4期615, 646页

46. Bacterial infection in compensated viral cirrhosis impairs 5-year survival (ANRS CO12 CirVir prospective cohort).

作者: Pierre Nahon.;Mathilde Lescat.;Richard Layese.;Valérie Bourcier.;Nabila Talmat.;Setty Allam.;Patrick Marcellin.;Dominique Guyader.;Stanislas Pol.;Dominique Larrey.;Victor De Lédinghen.;Denis Ouzan.;Fabien Zoulim.;Dominique Roulot.;Albert Tran.;Jean-Pierre Bronowicki.;Jean-Pierre Zarski.;Odile Goria.;Paul Calès.;Jean-Marie Péron.;Laurent Alric.;Marc Bourlière.;Philippe Mathurin.;Jean-Frédéric Blanc.;Armand Abergel.;Lawrence Serfaty.;Ariane Mallat.;Jean-Didier Grangé.;Pierre Attali.;Yannick Bacq.;Claire Wartelle.;Thông Dao.;Yves Benhamou.;Christophe Pilette.;Christine Silvain.;Christos Christidis.;Dominique Capron.;Brigitte Bernard-Chabert.;Sophie Hillaire.;Vincent Di Martino.;Jean-Claude Trinchet.;Richard Moreau.;Françoise Roudot-Thoraval.; .
来源: Gut. 2017年66卷2期330-341页
To assess incidence and prognostic significance of bacterial infections (BIs) occurring in compensated viral cirrhosis.

47. A rare cause of upper GI bleeding and wasting disease.

作者: Rene J van Erp.;Bernd Schröppel.;Thomas F Barth.;Thomas Seufferlein.;Stefan A Schmidt.;Alexander Meining.;Alexander Kleger.
来源: Gut. 2016年65卷5期787, 881页

48. The gut microbiota plays a protective role in the host defence against pneumococcal pneumonia.

作者: Tim J Schuijt.;Jacqueline M Lankelma.;Brendon P Scicluna.;Felipe de Sousa e Melo.;Joris J T H Roelofs.;J Daan de Boer.;Arjan J Hoogendijk.;Regina de Beer.;Alex de Vos.;Clara Belzer.;Willem M de Vos.;Tom van der Poll.;W Joost Wiersinga.
来源: Gut. 2016年65卷4期575-83页
Pneumonia accounts for more deaths than any other infectious disease worldwide. The intestinal microbiota supports local mucosal immunity and is increasingly recognised as an important modulator of the systemic immune system. The precise role of the gut microbiota in bacterial pneumonia, however, is unknown. Here, we investigate the function of the gut microbiota in the host defence against Streptococcus pneumoniae infections.

49. TGR5 contributes to glucoregulatory improvements after vertical sleeve gastrectomy in mice.

作者: Anne K McGavigan.;Darline Garibay.;Zachariah M Henseler.;Jack Chen.;Ahmed Bettaieb.;Fawaz G Haj.;Ruth E Ley.;Michael L Chouinard.;Bethany P Cummings.
来源: Gut. 2017年66卷2期226-234页
Vertical sleeve gastrectomy (VSG) produces high rates of type 2 diabetes remission; however, the mechanisms responsible remain incompletely defined. VSG increases circulating bile acid concentrations and bile acid signalling through TGR5 improves glucose homeostasis. Therefore, we investigated the role of TGR5 signalling in mediating the glucoregulatory benefits of VSG.

50. Targeting TGR5 in cholangiocyte proliferation: default topic.

作者: Cecília M P Rodrigues.;Han Moshage.
来源: Gut. 2016年65卷3期369-70页

51. Dual role of Helicobacter and Campylobacter species in IBD: a systematic review and meta-analysis.

作者: Natalia Castaño-Rodríguez.;Nadeem O Kaakoush.;Way Seah Lee.;Hazel M Mitchell.
来源: Gut. 2017年66卷2期235-249页
To conduct a comprehensive global systematic review and meta-analysis on the association between Helicobacter pylori infection and IBD. As bacterial antigen cross-reactivity has been postulated to be involved in this association, published data on enterohepatic Helicobacter spp (EHS) and Campylobacter spp and IBD was also analysed.

52. Spectral biomarkers for chemoprevention of colonic neoplasia: a placebo-controlled double-blinded trial with aspirin.

作者: Hemant K Roy.;Vladimir Turzhitsky.;Ramesh Wali.;Andrew J Radosevich.;Borko Jovanovic.;Gary Della'Zanna.;Asad Umar.;David T Rubin.;Michael J Goldberg.;Laura Bianchi.;Mart De La Cruz.;Andrej Bogojevic.;Irene B Helenowski.;Luz Rodriguez.;Robert Chatterton.;Silvia Skripkauskas.;Katherine Page.;Christopher R Weber.;Xiaoke Huang.;Ellen Richmond.;Raymond C Bergan.;Vadim Backman.
来源: Gut. 2017年66卷2期285-292页
A major impediment to translating chemoprevention to clinical practice has been lack of intermediate biomarkers. We previously reported that rectal interrogation with low-coherence enhanced backscattering spectroscopy (LEBS) detected microarchitectural manifestations of field carcinogenesis. We now wanted to ascertain if reversion of two LEBS markers spectral slope (SPEC) and fractal dimension (FRAC) could serve as a marker for chemopreventive efficacy.

53. Development and validation of a histological index for UC.

作者: Mahmoud H Mosli.;Brian G Feagan.;Guangyong Zou.;William J Sandborn.;Geert D'Haens.;Reena Khanna.;Lisa M Shackelton.;Christopher W Walker.;Sigrid Nelson.;Margaret K Vandervoort.;Valerie Frisbie.;Mark A Samaan.;Vipul Jairath.;David K Driman.;Karel Geboes.;Mark A Valasek.;Rish K Pai.;Gregory Y Lauwers.;Robert Riddell.;Larry W Stitt.;Barrett G Levesque.
来源: Gut. 2017年66卷1期50-58页
Although the Geboes score (GS) and modified Riley score (MRS) are commonly used to evaluate histological disease activity in UC, their operating properties are unknown. Accordingly, we developed an alternative instrument.

54. Clinicopathological and molecular features of sessile serrated adenomas with dysplasia or carcinoma.

作者: Mark Bettington.;Neal Walker.;Christophe Rosty.;Ian Brown.;Andrew Clouston.;Diane McKeone.;Sally-Ann Pearson.;Barbara Leggett.;Vicki Whitehall.
来源: Gut. 2017年66卷1期97-106页
Sessile serrated adenomas (SSAs) are the precursors of at least 15% of colorectal carcinomas, but their biology is incompletely understood. We performed a clinicopathological and molecular analysis of a large number of the rarely observed SSAs with dysplasia/carcinoma to better define their features and the pathways by which they progress to carcinoma.

55. Managing HBV in pregnancy. Prevention, prophylaxis, treatment and follow-up: position paper produced by Australian, UK and New Zealand key opinion leaders.

作者: Kumar Visvanathan.;Geoff Dusheiko.;Michelle Giles.;May-Ling Wong.;Nghi Phung.;Susan Walker.;Suong Le.;Seng Gee Lim.;Ed Gane.;Meng Ngu.;Winita Hardikar.;Ben Cowie.;Scott Bowden.;Simone Strasser.;Miriam Levy.;Joe Sasaduesz.
来源: Gut. 2016年65卷2期340-50页
Hepatitis B during pregnancy presents unique management issues for both the mother and fetus. These include the lack of a current cohesive strategy for treatment and follow-up of mothers and their babies; the uncertain risk of postpartum HBV flares; the lack of randomised trial data on the safety and efficacy of antiviral treatment in pregnancy; the lack of head-to-head studies comparing different antivirals in pregnancy; and the lack of epidemiologic information regarding infection across different populations globally. This position paper provides a comprehensive review of the management of women with HBV infection prior to conception, throughout each stage of pregnancy and postpartum, as well as recommendations and clinical approaches for the follow-up of children born to infected mothers, based on available evidence in the literature and recommendations from international experts. Prevention of perinatal transmission is an important component of global efforts to reduce the burden of chronic HBV since vertical transmission is responsible for most of the chronic infection worldwide.

56. Clinical significance of SNORA42 as an oncogene and a prognostic biomarker in colorectal cancer.

作者: Yoshinaga Okugawa.;Yuji Toiyama.;Shusuke Toden.;Hiroki Mitoma.;Takeshi Nagasaka.;Koji Tanaka.;Yasuhiro Inoue.;Masato Kusunoki.;C Richard Boland.;Ajay Goel.
来源: Gut. 2017年66卷1期107-117页
Despite recent advances in colorectal cancer (CRC) treatment, the prognosis of patients suffering from this malignancy still remains substandard, and metastatic recurrence following curative surgery is the leading cause of mortality. Therefore, it is imperative to identify prognostic markers to predict the clinical outcome of CRC patients. Recent evidence revealed the new role of small nucleolar RNAs (snoRNAs) in oncogenesis. Herein, we systematically evaluated dysregulation of snoRNAs in CRC and clarified their biomarker potential and biological significance in CRC.

57. Development and validation of the Nancy histological index for UC.

作者: Aude Marchal-Bressenot.;Julia Salleron.;Camille Boulagnon-Rombi.;Claire Bastien.;Virginie Cahn.;Guillaume Cadiot.;Marie-Danièle Diebold.;Silvio Danese.;Walter Reinisch.;Stefan Schreiber.;Simon Travis.;Laurent Peyrin-Biroulet.
来源: Gut. 2017年66卷1期43-49页
We developed a validated index for assessing histological disease activity in UC and established its responsiveness.

58. Next-generation metabolic imaging in pancreatic cancer.

作者: Rickmer F Braren.;Jens T Siveke.
来源: Gut. 2016年65卷3期367-9页

59. Targeting of tumour-infiltrating macrophages via CCL2/CCR2 signalling as a therapeutic strategy against hepatocellular carcinoma.

作者: Xiaoguang Li.;Wenbo Yao.;Ya Yuan.;Peizhan Chen.;Bin Li.;Jingquan Li.;Ruiai Chu.;Haiyun Song.;Dong Xie.;Xiaoqing Jiang.;Hui Wang.
来源: Gut. 2017年66卷1期157-167页
Hepatocellular carcinoma (HCC) is an aggressive malignancy with limited effective treatment options. An alternative strategy is to target cells, such as tumour-infiltrating macrophages, in the HCC tumour microenvironment. The CCL2/CCR2 axis is required for recruitment of monocytes/macrophages and is implicated in various aspects of liver pathology, including HCC. We investigated the feasibility of CCL2/CCR2 as a therapeutic target against HCC.

60. Hepatitis C virus treatment in the real world: optimising treatment and access to therapies.

作者: Fabien Zoulim.;T Jake Liang.;Alexander L Gerbes.;Alessio Aghemo.;Sylvie Deuffic-Burban.;Geoffrey Dusheiko.;Michael W Fried.;Stanislas Pol.;Jürgen Kurt Rockstroh.;Norah A Terrault.;Stefan Wiktor.
来源: Gut. 2015年64卷11期1824-33页
Chronic HCV infections represent a major worldwide public health problem and are responsible for a large proportion of liver related deaths, mostly because of HCV-associated hepatocellular carcinoma and cirrhosis. The treatment of HCV has undergone a rapid and spectacular revolution. In the past 5 years, the launch of direct acting antiviral drugs has seen sustained virological response rates reach 90% and above for many patient groups. The new treatments are effective, well tolerated, allow for shorter treatment regimens and offer new opportunities for previously excluded groups. This therapeutic revolution has changed the rules for treatment of HCV, moving the field towards an interferon-free era and raising the prospect of HCV eradication. This manuscript addresses the new challenges regarding treatment optimisation in the real world, improvement of antiviral efficacy in 'hard-to-treat' groups, the management of patients whose direct acting antiviral drug treatment was unsuccessful, and access to diagnosis and treatment in different parts of the world.
共有 16045 条符合本次的查询结果, 用时 3.3510843 秒