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141. Genetic variant PLCE1 rs2274223 and gastric cancer: more to be explored?

作者: Yazhou He.;Chengdi Wang.;Ziqiang Wang.;Zongguang Zhou.
来源: Gut. 2016年65卷2期359-60页

142. CD248/endosialin critically regulates hepatic stellate cell proliferation during chronic liver injury via a PDGF-regulated mechanism.

作者: Annika Wilhelm.;Victoria Aldridge.;Debashis Haldar.;Amy J Naylor.;Christopher J Weston.;Ditte Hedegaard.;Abhilok Garg.;Janine Fear.;Gary M Reynolds.;Adam P Croft.;Neil C Henderson.;Christopher D Buckley.;Philip N Newsome.
来源: Gut. 2016年65卷7期1175-85页
CD248 (endosialin) is a stromal cell marker expressed on fibroblasts and pericytes. During liver injury, myofibroblasts are the main source of fibrotic matrix.

143. Psychological comorbidity increases the risk for postinfectious IBS partly by enhanced susceptibility to develop infectious gastroenteritis.

作者: Mira M Wouters.;Sander Van Wanrooy.;Anh Nguyen.;James Dooley.;Javier Aguilera-Lizarraga.;Winde Van Brabant.;Josselyn E Garcia-Perez.;Lukas Van Oudenhove.;Marc Van Ranst.;Jan Verhaegen.;Adrian Liston.;Guy Boeckxstaens.
来源: Gut. 2016年65卷8期1279-88页
Psychological factors increase the risk to develop postinfectious IBS (PI-IBS), but the mechanisms involved are unclear. As stress affects the immune system, we investigated the potential interaction between psychological factors, the immune response against infectious gastroenteritis (IGE) and the development of IGE and PI-IBS in a large cohort exposed to contaminated drinking water.

144. Carbonic anhydrase IV inhibits colon cancer development by inhibiting the Wnt signalling pathway through targeting the WTAP-WT1-TBL1 axis.

作者: Jingwan Zhang.;Ho Tsoi.;Xiaoxing Li.;Hua Wang.;Jing Gao.;Kunning Wang.;Minnie Yy Go.;Siew C Ng.;Francis Kl Chan.;Joseph Jy Sung.;Jun Yu.
来源: Gut. 2016年65卷9期1482-93页
We found that carbonic anhydrase IV (CA4), a member of the carbonic anhydrases, is silenced in colorectal cancer (CRC). We analysed its epigenetic inactivation, biological effects and prognostic significance in CRC.

145. Mechanism of mitochondrial permeability transition pore induction and damage in the pancreas: inhibition prevents acute pancreatitis by protecting production of ATP.

作者: Rajarshi Mukherjee.;Olga A Mareninova.;Irina V Odinokova.;Wei Huang.;John Murphy.;Michael Chvanov.;Muhammad A Javed.;Li Wen.;David M Booth.;Matthew C Cane.;Muhammad Awais.;Bruno Gavillet.;Rebecca M Pruss.;Sophie Schaller.;Jeffery D Molkentin.;Alexei V Tepikin.;Ole H Petersen.;Stephen J Pandol.;Ilya Gukovsky.;David N Criddle.;Anna S Gukovskaya.;Robert Sutton.; .
来源: Gut. 2016年65卷8期1333-46页
Acute pancreatitis is caused by toxins that induce acinar cell calcium overload, zymogen activation, cytokine release and cell death, yet is without specific drug therapy. Mitochondrial dysfunction has been implicated but the mechanism not established.

146. Pancreatic epithelial fluid and bicarbonate secretion is significantly elevated in the absence of peripheral serotonin.

作者: József Maléth.;Tamara Madácsy.;Petra Pallagi.;Anita Balázs.;Viktória Venglovecz.;Zoltán Rakonczay.;Péter Hegyi.
来源: Gut. 2015年64卷9期1497-8页

147. Stool consistency is strongly associated with gut microbiota richness and composition, enterotypes and bacterial growth rates.

作者: Doris Vandeputte.;Gwen Falony.;Sara Vieira-Silva.;Raul Y Tito.;Marie Joossens.;Jeroen Raes.
来源: Gut. 2016年65卷1期57-62页
The assessment of potentially confounding factors affecting colon microbiota composition is essential to the identification of robust microbiome based disease markers. Here, we investigate the link between gut microbiota variation and stool consistency using Bristol Stool Scale classification, which reflects faecal water content and activity, and is considered a proxy for intestinal colon transit time.

148. The value of models in informing resource allocation in colorectal cancer screening: the case of The Netherlands.

作者: Frank van Hees.;Ann G Zauber.;Harriët van Veldhuizen.;Marie-Louise A Heijnen.;Corine Penning.;Harry J de Koning.;Marjolein van Ballegooijen.;Iris Lansdorp-Vogelaar.
来源: Gut. 2015年64卷12期1985-97页
In May 2011, the Dutch government decided to implement a national programme for colorectal cancer (CRC) screening using biennial faecal immunochemical test screening between ages 55 and 75. Decision modelling played an important role in informing this decision, as well as in the planning and implementation of the programme afterwards. In this overview, we illustrate the value of models in informing resource allocation in CRC screening using the role that decision modelling has played in the Dutch CRC screening programme as an example.

149. ABO blood type B and fucosyltransferase 2 non-secretor status as genetic risk factors for chronic pancreatitis.

作者: Frank Ulrich Weiss.;Claudia Schurmann.;Alexander Teumer.;Julia Mayerle.;Peter Simon.;Henry Völzke.;Andreas Greinacher.;Jens-Peter Kuehn.;Martin Zenker.;Uwe Völker.;Georg Homuth.;Markus M Lerch.
来源: Gut. 2016年65卷2期353-4页

150. Magnetic compression for treatment of large oesophageal diverticula: a new endoscopic approach for a risky surgical disease?

作者: Simon Bouchard.;Vincent Huberty.;Daniel Blero.;Jacques Devière.
来源: Gut. 2015年64卷11期1678-9页

151. Pathogenesis of pancreatic cancer exosome-induced lipolysis in adipose tissue.

作者: Gunisha Sagar.;Raghuwansh P Sah.;Naureen Javeed.;Shamit K Dutta.;Thomas C Smyrk.;Julie S Lau.;Nino Giorgadze.;Tamar Tchkonia.;James L Kirkland.;Suresh T Chari.;Debabrata Mukhopadhyay.
来源: Gut. 2016年65卷7期1165-74页
New-onset diabetes and concomitant weight loss occurring several months before the clinical presentation of pancreatic cancer (PC) appear to be paraneoplastic phenomena caused by tumour-secreted products. Our recent findings have shown exosomal adrenomedullin (AM) is important in development of diabetes in PC. Adipose tissue lipolysis might explain early onset weight loss in PC. We hypothesise that lipolysis-inducing cargo is carried in exosomes shed by PC and is responsible for the paraneoplastic effects. Therefore, in this study we investigate if exosomes secreted by PC induce lipolysis in adipocytes and explore the role of AM in PC-exosomes as the mediator of this lipolysis.

152. Optimising colorectal cancer screening acceptance: a review.

作者: Carlo Senore.;John Inadomi.;Nereo Segnan.;Cristina Bellisario.;Cesare Hassan.
来源: Gut. 2015年64卷7期1158-77页
The study aims to review available evidence concerning effective interventions to increase colorectal cancer (CRC) screening acceptance. We performed a literature search of randomised trials designed to increase individuals' use of CRC screening on PubMed, Embase, Cochrane Database of Systematic Reviews and Database of Abstracts of Reviews of Effects. Small (≤ 100 subjects per arm) studies and those reporting results of interventions implemented before publication of the large faecal occult blood test trials were excluded. Interventions were categorised following the Continuum of Cancer Care and the PRECEDE-PROCEED models and studies were grouped by screening model (opportunistic vs organised). Multifactor interventions targeting multiple levels of care and considering factors outside the individual clinician control, represent the most effective strategy to enhance CRC screening acceptance. Removing financial barriers, implementing methods allowing a systematic contact of the whole target population, using personal invitation letters, preferably signed by the reference care provider, and reminders mailed to all non-attendees are highly effective in enhancing CRC screening acceptance. Physician reminders may support the diffusion of screening, but they can be effective only for individuals who have access to and make use of healthcare services. Educational interventions for patients and providers are effective, but the implementation of organisational measures may be necessary to favour their impact. Available evidence indicates that organised programmes allow to achieve an extensive coverage and to enhance equity of access, while maximising the health impact of screening. They provide at the same time an infrastructure allowing to achieve a more favourable cost-effectiveness profile of potentially effective strategies, which would not be sustainable in opportunistic settings.

153. HBV cccDNA: viral persistence reservoir and key obstacle for a cure of chronic hepatitis B.

作者: Michael Nassal.
来源: Gut. 2015年64卷12期1972-84页
At least 250 million people worldwide are chronically infected with HBV, a small hepatotropic DNA virus that replicates through reverse transcription. Chronic infection greatly increases the risk for terminal liver disease. Current therapies rarely achieve a cure due to the refractory nature of an intracellular viral replication intermediate termed covalently closed circular (ccc) DNA. Upon infection, cccDNA is generated as a plasmid-like episome in the host cell nucleus from the protein-linked relaxed circular (RC) DNA genome in incoming virions. Its fundamental role is that as template for all viral RNAs, and in consequence new virions. Biosynthesis of RC-DNA by reverse transcription of the viral pregenomic RNA is now understood in considerable detail, yet conversion of RC-DNA to cccDNA is still obscure, foremostly due to the lack of feasible, cccDNA-dependent assay systems. Conceptual and recent experimental data link cccDNA formation to cellular DNA repair, which is increasingly appreciated as a critical interface between cells and viruses. Together with new in vitro HBV infection systems, based on the identification of the bile acid transporter sodium taurocholate cotransporting polypeptide as an HBV entry receptor, this offers novel opportunities to decipher, and eventually interfere with, formation of the HBV persistence reservoir. After a brief overview of the role of cccDNA in the HBV infectious cycle, this review aims to summarise current knowledge on cccDNA molecular biology, to highlight the experimental restrictions that have hitherto hampered faster progress and to discuss cccDNA as target for new, potentially curative therapies of chronic hepatitis B.

154. Serous cystic neoplasm of the pancreas: a multinational study of 2622 patients under the auspices of the International Association of Pancreatology and European Pancreatic Club (European Study Group on Cystic Tumors of the Pancreas).

作者: B Jais.;V Rebours.;G Malleo.;R Salvia.;M Fontana.;L Maggino.;C Bassi.;R Manfredi.;R Moran.;A M Lennon.;A Zaheer.;C Wolfgang.;R Hruban.;G Marchegiani.;C Fernández Del Castillo.;W Brugge.;Y Ha.;M H Kim.;D Oh.;I Hirai.;W Kimura.;J Y Jang.;S W Kim.;W Jung.;H Kang.;S Y Song.;C M Kang.;W J Lee.;S Crippa.;M Falconi.;I Gomatos.;J Neoptolemos.;A C Milanetto.;C Sperti.;C Ricci.;R Casadei.;M Bissolati.;G Balzano.;I Frigerio.;R Girelli.;M Delhaye.;B Bernier.;H Wang.;K T Jang.;D H Song.;M T Huggett.;K W Oppong.;L Pererva.;K V Kopchak.;M Del Chiaro.;R Segersvard.;L S Lee.;D Conwell.;A Osvaldt.;V Campos.;G Aguero Garcete.;B Napoleon.;I Matsumoto.;M Shinzeki.;F Bolado.;J M Urman Fernandez.;M G Keane.;S P Pereira.;I Araujo Acuna.;E C Vaquero.;M R Angiolini.;A Zerbi.;J Tang.;R W Leong.;A Faccinetto.;G Morana.;M C Petrone.;P G Arcidiacono.;J H Moon.;H J Choi.;R S Gill.;D Pavey.;M Ouaïssi.;B Sastre.;M Spandre.;C G De Angelis.;M A Rios-Vives.;M Concepcion-Martin.;T Ikeura.;K Okazaki.;L Frulloni.;O Messina.;P Lévy.
来源: Gut. 2016年65卷2期305-12页
Serous cystic neoplasm (SCN) is a cystic neoplasm of the pancreas whose natural history is poorly known. The purpose of the study was to attempt to describe the natural history of SCN, including the specific mortality.

155. Serum viral duplex-linear DNA proportion increases with the progression of liver disease in patients infected with HBV.

作者: Xing-Liang Zhao.;Jian-Rong Yang.;Sheng-Zhang Lin.;Hui Ma.;Fang Guo.;Rui-Feng Yang.;Heng-Hui Zhang.;Jin-Chao Han.;Lai Wei.;Xiao-Ben Pan.
来源: Gut. 2016年65卷3期502-11页
HBV has two forms of genomic DNA, relaxed-circular DNA (rcDNA) and duplex-linear DNA (dlDNA). Compared to rcDNA, dlDNA has been demonstrated to integrate more frequently into host cellular chromosomes, which may have oncogenic consequences. However, the dlDNA proportion relative to total HBV DNA and its clinical significance in patients remain to be investigated.

156. Antibiotics promote inflammation through the translocation of native commensal colonic bacteria.

作者: Kathryn A Knoop.;Keely G McDonald.;Devesha H Kulkarni.;Rodney D Newberry.
来源: Gut. 2016年65卷7期1100-9页
Antibiotic use is associated with an increased risk of developing multiple inflammatory disorders, which in turn are linked to alterations in the intestinal microbiota. How these alterations in the intestinal microbiota translate into an increased risk for inflammatory responses is largely unknown. Here we investigated whether and how antibiotics promote inflammation via the translocation of live native gut commensal bacteria.

157. A hepatic stellate cell gene expression signature associated with outcomes in hepatitis C cirrhosis and hepatocellular carcinoma after curative resection.

作者: David Y Zhang.;Nicolas Goossens.;Jinsheng Guo.;Ming-Chao Tsai.;Hsin-I Chou.;Civan Altunkaynak.;Angelo Sangiovanni.;Massimo Iavarone.;Massomo Colombo.;Masahiro Kobayashi.;Hiromitsu Kumada.;Augusto Villanueva.;Josep M Llovet.;Yujin Hoshida.;Scott L Friedman.
来源: Gut. 2016年65卷10期1754-64页
We used an informatics approach to identify and validate genes whose expression is unique to hepatic stellate cells and assessed the prognostic capability of their expression in cirrhosis.

158. A new instrumental platform for Trans-Anal Submucosal Endoscopic Resection (TASER).

作者: Zacharias P Tsiamoulos.;Janindra Warusavitarne.;Omar Faiz.;Andrew Castello-Cortes.;Timothy Elliott.;Simon T Peake.;Paul Bassett.;Brian P Saunders.
来源: Gut. 2015年64卷12期1844-6页

159. Monocyte-derived hepatocyte-like cells for causality assessment of idiosyncratic drug-induced liver injury.

作者: Andreas Benesic.;Alexandra Leitl.;Alexander L Gerbes.
来源: Gut. 2016年65卷9期1555-63页
Idiosyncratic drug-induced liver injury (iDILI) is a frequent cause of acute liver injury and a serious problem in late stage drug-development. Its diagnosis is one of the most challenging in hepatology, since it is done by exclusion and relies on expert opinion. Until now no reliable in vitro test exists to support the diagnosis of iDILI. In some instances it is impossible to determine the causative drug in polymedicated patients.

160. Identification of an anti-inflammatory protein from Faecalibacterium prausnitzii, a commensal bacterium deficient in Crohn's disease.

作者: E Quévrain.;M A Maubert.;C Michon.;F Chain.;R Marquant.;J Tailhades.;S Miquel.;L Carlier.;L G Bermúdez-Humarán.;B Pigneur.;O Lequin.;P Kharrat.;G Thomas.;D Rainteau.;C Aubry.;N Breyner.;C Afonso.;S Lavielle.;J-P Grill.;G Chassaing.;J M Chatel.;G Trugnan.;R Xavier.;P Langella.;H Sokol.;P Seksik.
来源: Gut. 2016年65卷3期415-425页
Crohn's disease (CD)-associated dysbiosis is characterised by a loss of Faecalibacterium prausnitzii, whose culture supernatant exerts an anti-inflammatory effect both in vitro and in vivo. However, the chemical nature of the anti-inflammatory compounds has not yet been determined.
共有 16045 条符合本次的查询结果, 用时 4.5995542 秒