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共有 3503 条符合本次的查询结果, 用时 3.240801 秒

3381. Functional annotation of high-quality SNP biomarkers of gastric cancer susceptibility: the Yin Yang of PSCA rs2294008.

作者: Hyuna Sung.;Howard H Yang.;Nan Hu.;Hua Su.;Philip R Taylor.;Paula L Hyland.
来源: Gut. 2016年65卷2期361-4页

3382. The gamma-glutamyl transpeptidase to platelet ratio (GPR) predicts significant liver fibrosis and cirrhosis in patients with chronic HBV infection in West Africa.

作者: Maud Lemoine.;Yusuke Shimakawa.;Shevanthi Nayagam.;Mustapha Khalil.;Penda Suso.;Jo Lloyd.;Robert Goldin.;Harr-Freeya Njai.;Gibril Ndow.;Makie Taal.;Graham Cooke.;Umberto D'Alessandro.;Muriel Vray.;Papa Saliou Mbaye.;Ramou Njie.;Vincent Mallet.;Mark Thursz.
来源: Gut. 2016年65卷8期1369-76页
Simple and inexpensive non-invasive fibrosis tests are highly needed but have been poorly studied in sub-Saharan Africa.

3383. Derivation of genetic biomarkers for cancer risk stratification in Barrett's oesophagus: a prospective cohort study.

作者: Margriet R Timmer.;Pierre Martinez.;Chiu T Lau.;Wytske M Westra.;Silvia Calpe.;Agnieszka M Rygiel.;Wilda D Rosmolen.;Sybren L Meijer.;Fiebo J W Ten Kate.;Marcel G W Dijkgraaf.;Rosalie C Mallant-Hent.;Anton H J Naber.;Arnoud H A M van Oijen.;Lubbertus C Baak.;Pieter Scholten.;Clarisse J M Böhmer.;Paul Fockens.;Carlo C Maley.;Trevor A Graham.;Jacques J G H M Bergman.;Kausilia K Krishnadath.
来源: Gut. 2016年65卷10期1602-10页
The risk of developing adenocarcinoma in non-dysplastic Barrett's oesophagus is low and difficult to predict. Accurate tools for risk stratification are needed to increase the efficiency of surveillance. We aimed to develop a prediction model for progression using clinical variables and genetic markers.

3384. Akkermansia muciniphila and improved metabolic health during a dietary intervention in obesity: relationship with gut microbiome richness and ecology.

作者: Maria Carlota Dao.;Amandine Everard.;Judith Aron-Wisnewsky.;Nataliya Sokolovska.;Edi Prifti.;Eric O Verger.;Brandon D Kayser.;Florence Levenez.;Julien Chilloux.;Lesley Hoyles.; .;Marc-Emmanuel Dumas.;Salwa W Rizkalla.;Joel Doré.;Patrice D Cani.;Karine Clément.
来源: Gut. 2016年65卷3期426-36页
Individuals with obesity and type 2 diabetes differ from lean and healthy individuals in their abundance of certain gut microbial species and microbial gene richness. Abundance of Akkermansia muciniphila, a mucin-degrading bacterium, has been inversely associated with body fat mass and glucose intolerance in mice, but more evidence is needed in humans. The impact of diet and weight loss on this bacterial species is unknown. Our objective was to evaluate the association between faecal A. muciniphila abundance, faecal microbiome gene richness, diet, host characteristics, and their changes after calorie restriction (CR).

3385. Hepatitis C: new clues to better vaccines?

作者: Marian E Major.
来源: Gut. 2016年65卷1期4-5页

3386. The broad assessment of HCV genotypes 1 and 3 antigenic targets reveals limited cross-reactivity with implications for vaccine design.

作者: Annette von Delft.;Isla S Humphreys.;Anthony Brown.;Katja Pfafferott.;Michaela Lucas.;Paul Klenerman.;Georg M Lauer.;Andrea L Cox.;Silvana Gaudieri.;Eleanor Barnes.
来源: Gut. 2016年65卷1期112-23页
Developing a vaccine that is cross-reactive between HCV genotypes requires data on T cell antigenic targets that extends beyond genotype-1. We characterised T cell immune responses against HCV genotype-3, the most common infecting genotype in the UK and Asia, and assessed within genotype and between genotype cross-reactivity.

3387. Clinical profiles and outcomes in idiopathic duct-centric chronic pancreatitis (type 2 autoimmune pancreatitis): the Mayo Clinic experience.

作者: Phil A Hart.;Michael J Levy.;Thomas C Smyrk.;Naoki Takahashi.;Barham K Abu Dayyeh.;Jonathan E Clain.;Ferga C Gleeson.;Randall K Pearson.;Bret T Petersen.;Mark D Topazian.;Santhi S Vege.;Lizhi Zhang.;Suresh T Chari.
来源: Gut. 2016年65卷10期1702-9页
Idiopathic duct-centric chronic pancreatitis (IDCP), also known as type 2 autoimmune pancreatitis (AIP), is an uncommon subtype of AIP. International Consensus Diagnostic Criteria for IDCP propose that the diagnosis requires pancreatic histology and/or concurrent IBD. We examined our experience with IDCP (type 2 AIP) to assess the appropriateness of these criteria, and identify unique characteristics in patients presenting with acute pancreatitis.

3388. Prevalent low-grade dysplasia: the strongest predictor of malignant progression in Barrett's columnar-lined oesophagus.

作者: Lisa H Moyes.;Karin A Oien.;Alan K Foulis.;Grant M Fullarton.;James J Going.
来源: Gut. 2016年65卷2期360-1页

3389. Ribavirin restores IFNα responsiveness in HCV-infected livers by epigenetic remodelling at interferon stimulated genes.

作者: Barbara Testoni.;David Durantel.;Fanny Lebossé.;Judith Fresquet.;François Helle.;Francesco Negro.;Maria Francesca Donato.;Massimo Levrero.;Fabien Zoulim.
来源: Gut. 2016年65卷4期672-82页
Caveats in the understanding of ribavirin (RBV) mechanisms of action has somehow prevented the development of better analogues able to further improve its therapeutic contribution in interferon (IFN)-based and direct antiviral agent-based regimens for chronic HCV or other indications. Here, we describe a new mechanism by which RBV modulates IFN-stimulated genes (ISGs) and contributes to restore hepatic immune responsiveness.

3390. The MUC1 mucin protects against Helicobacter pylori pathogenesis in mice by regulation of the NLRP3 inflammasome.

作者: Garrett Z Ng.;Trevelyan R Menheniott.;Alison L Every.;Andrew Stent.;Louise M Judd.;Yok Teng Chionh.;Poshmaal Dhar.;Jasper C Komen.;Andrew S Giraud.;Timothy C Wang.;Michael A McGuckin.;Philip Sutton.
来源: Gut. 2016年65卷7期1087-99页
The mucin MUC1, best known for providing an epithelial barrier, is an important protective host factor in both humans and mice during Helicobacter pylori pathogenesis. This study aimed to identify the long-term consequences of MUC1 deficiency on H. pylori pathogenesis and the mechanism by which MUC1 protects against H. pylori gastritis.

3391. Sensitivity to wheat, gluten and FODMAPs in IBS: facts or fiction?

作者: Roberto De Giorgio.;Umberto Volta.;Peter R Gibson.
来源: Gut. 2016年65卷1期169-78页
IBS is one of the most common types of functional bowel disorder. Increasing attention has been paid to the causative role of food in IBS. Food ingestion precipitates or exacerbates symptoms, such as abdominal pain and bloating in patients with IBS through different hypothesised mechanisms including immune and mast cell activation, mechanoreceptor stimulation and chemosensory activation. Wheat is regarded as one of the most relevant IBS triggers, although which component(s) of this cereal is/are involved remain(s) unknown. Gluten, other wheat proteins, for example, amylase-trypsin inhibitors, and fructans (the latter belonging to fermentable oligo-di-mono-saccharides and polyols (FODMAPs)), have been identified as possible factors for symptom generation/exacerbation. This uncertainty on the true culprit(s) opened a scenario of semantic definitions favoured by the discordant results of double-blind placebo-controlled trials, which have generated various terms ranging from non-coeliac gluten sensitivity to the broader one of non-coeliac wheat or wheat protein sensitivity or, even, FODMAP sensitivity. The role of FODMAPs in eliciting the clinical picture of IBS goes further since these short-chain carbohydrates are found in many other dietary components, including vegetables and fruits. In this review, we assessed current literature in order to unravel whether gluten/wheat/FODMAP sensitivity represent 'facts' and not 'fiction' in IBS symptoms. This knowledge is expected to promote standardisation in dietary strategies (gluten/wheat-free and low FODMAP) as effective measures for the management of IBS symptoms.

3392. 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

3393. 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.

3394. 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.

3395. 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.

3396. 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.

3397. 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.

3398. 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

3399. 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.

3400. 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.
共有 3503 条符合本次的查询结果, 用时 3.240801 秒