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Results 1 - 20 of 23  for All Library Resources

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Refined by: Database: Wiley Open Access remove
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1
FXR an emerging therapeutic target for the treatment of atherosclerosis
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Article
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FXR an emerging therapeutic target for the treatment of atherosclerosis

Journal of cellular and molecular medicine, 2010-01, Vol.14 (1‐2), p.79-92 [Peer Reviewed Journal]

2009 The Authors Journal compilation © 2010 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd ;Copyright Blackwell Publishing Ltd. Jan/Feb 2010 ;Copyright John Wiley & Sons, Inc. Jan 2010 ;2009 The Authors Journal compilation © 2010 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd 2009 ;ISSN: 1582-1838 ;EISSN: 1582-4934 ;DOI: 10.1111/j.1582-4934.2009.00997.x ;PMID: 20041971

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2
Defective Bile Acid Signaling Promotes Vascular Dysfunction, Supporting a Role for G-Protein Bile Acid Receptor 1/Farnesoid X Receptor Agonism and Statins in the Treatment of Nonalcoholic Fatty Liver Disease
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Defective Bile Acid Signaling Promotes Vascular Dysfunction, Supporting a Role for G-Protein Bile Acid Receptor 1/Farnesoid X Receptor Agonism and Statins in the Treatment of Nonalcoholic Fatty Liver Disease

Journal of the American Heart Association, 2023-12, Vol.12 (23), p.e031241-e031241 [Peer Reviewed Journal]

2023 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. ;ISSN: 2047-9980 ;EISSN: 2047-9980 ;DOI: 10.1161/JAHA.123.031241 ;PMID: 37996988

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3
Activation of the bile acid receptor GPBAR1 protects against gastrointestinal injury caused by non‐steroidal anti‐inflammatory drugs and aspirin in mice
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Activation of the bile acid receptor GPBAR1 protects against gastrointestinal injury caused by non‐steroidal anti‐inflammatory drugs and aspirin in mice

British journal of pharmacology, 2013-01, Vol.168 (1), p.225-237 [Peer Reviewed Journal]

2012 The Authors. British Journal of Pharmacology © 2012 The British Pharmacological Society ;2012 The Authors. British Journal of Pharmacology © 2012 The British Pharmacological Society. ;British Journal of Pharmacology © 2013 The British Pharmacological Society ;ISSN: 0007-1188 ;EISSN: 1476-5381 ;DOI: 10.1111/j.1476-5381.2012.02128.x ;PMID: 22881598

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4
Galectin‐1 exerts immunomodulatory and protective effects on concanavalin a–induced hepatitis in mice
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Galectin‐1 exerts immunomodulatory and protective effects on concanavalin a–induced hepatitis in mice

Hepatology (Baltimore, Md.), 2000-02, Vol.31 (2), p.399-406 [Peer Reviewed Journal]

Copyright © 2000 American Association for the Study of Liver Diseases ;2000 INIST-CNRS ;ISSN: 0270-9139 ;EISSN: 1527-3350 ;DOI: 10.1002/hep.510310220 ;PMID: 10655263 ;CODEN: HPTLD9

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5
Atorvastatin protects against liver and vascular damage in a model of diet induced steatohepatitis by resetting FXR and GPBAR1 signaling
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Article
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Atorvastatin protects against liver and vascular damage in a model of diet induced steatohepatitis by resetting FXR and GPBAR1 signaling

The FASEB journal, 2022-01, Vol.36 (1), p.e22060-n/a [Peer Reviewed Journal]

2021 The Authors. published by Wiley Periodicals LLC on behalf of Federation of American Societies for Experimental Biology. ;2021 The Authors. The FASEB Journal published by Wiley Periodicals LLC on behalf of Federation of American Societies for Experimental Biology. ;ISSN: 0892-6638 ;EISSN: 1530-6860 ;DOI: 10.1096/fj.202101397R ;PMID: 34862975

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6
TRPM8 indicates poor prognosis in colorectal cancer patients and its pharmacological targeting reduces tumour growth in mice by inhibiting Wnt/β‐catenin signalling
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TRPM8 indicates poor prognosis in colorectal cancer patients and its pharmacological targeting reduces tumour growth in mice by inhibiting Wnt/β‐catenin signalling

British journal of pharmacology, 2023-01, Vol.180 (2), p.235-251 [Peer Reviewed Journal]

2022 The Authors. published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. ;2022 The Authors. British Journal of Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. ;2022. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0007-1188 ;EISSN: 1476-5381 ;DOI: 10.1111/bph.15960 ;PMID: 36168728

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7
Activation of the farnesoid‐X receptor protects against gastrointestinal injury caused by non‐steroidal anti‐inflammatory drugs in mice
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Activation of the farnesoid‐X receptor protects against gastrointestinal injury caused by non‐steroidal anti‐inflammatory drugs in mice

British journal of pharmacology, 2011-12, Vol.164 (8), p.1929-1938 [Peer Reviewed Journal]

2011 The Authors. British Journal of Pharmacology © 2011 The British Pharmacological Society ;2015 INIST-CNRS ;2011 The Authors. British Journal of Pharmacology © 2011 The British Pharmacological Society. ;British Journal of Pharmacology © 2011 The British Pharmacological Society 2011 ;ISSN: 0007-1188 ;EISSN: 1476-5381 ;DOI: 10.1111/j.1476-5381.2011.01481.x ;PMID: 21564085 ;CODEN: BJPCBM

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8
Activation of the bile acid receptor GPBAR 1 protects against gastrointestinal injury caused by non‐steroidal anti‐inflammatory drugs and aspirin in mice
Material Type:
Article
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Activation of the bile acid receptor GPBAR 1 protects against gastrointestinal injury caused by non‐steroidal anti‐inflammatory drugs and aspirin in mice

British journal of pharmacology, 2013-01, Vol.168 (1), p.225-237 [Peer Reviewed Journal]

ISSN: 0007-1188 ;EISSN: 1476-5381 ;DOI: 10.1111/j.1476-5381.2012.02128.x

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9
Activation of the bile acid receptor GPBAR1 protects against gastrointestinal injury caused by nonsteroidal anti-inflammatory drugs and aspirin in mice
Material Type:
Article
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Activation of the bile acid receptor GPBAR1 protects against gastrointestinal injury caused by nonsteroidal anti-inflammatory drugs and aspirin in mice

British journal of pharmacology, 2012-12, Vol.168 (1), p.225-237 [Peer Reviewed Journal]

British Journal of Pharmacology © 2013 The British Pharmacological Society 2013 ;ISSN: 0007-1188 ;EISSN: 1476-5381 ;DOI: 10.1111/j.1476-5381.2012.02128.x ;PMID: 22881598

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10
Activation of the farnesoid-X receptor protects against gastrointestinal injury caused by non-steroidal anti-inflammatory drugs in mice: FXR and NSAID gastro-enteropathy
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Article
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Activation of the farnesoid-X receptor protects against gastrointestinal injury caused by non-steroidal anti-inflammatory drugs in mice: FXR and NSAID gastro-enteropathy

British journal of pharmacology, 2011-12, Vol.164 (8), p.1929-1938 [Peer Reviewed Journal]

ISSN: 0007-1188 ;EISSN: 1476-5381 ;DOI: 10.1111/j.1476-5381.2011.01481.x

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11
Liver delivery of NO by NCX‐1000 protects against acute liver failure and mitochondrial dysfunction induced by APAP in mice 
THIS ARTICLE HAS BEEN RETRACTED
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Article
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Liver delivery of NO by NCX‐1000 protects against acute liver failure and mitochondrial dysfunction induced by APAP in mice 
THIS ARTICLE HAS BEEN RETRACTED

British journal of pharmacology, 2009-02, Vol.143 (1), p.33-42 [Peer Reviewed Journal]

2004 British Pharmacological Society ;ISSN: 0007-1188 ;EISSN: 1476-5381 ;DOI: 10.1038/sj.bjp.0705780

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12
Evidence that 5‐lipoxygenase and acetylated cyclooxygenase 2‐derived eicosanoids regulate leukocyte–endothelial adherence in response to aspirin
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Article
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Evidence that 5‐lipoxygenase and acetylated cyclooxygenase 2‐derived eicosanoids regulate leukocyte–endothelial adherence in response to aspirin

British journal of pharmacology, 2003-08, Vol.139 (7), p.1351-1359 [Peer Reviewed Journal]

2003 British Pharmacological Society ;2004 INIST-CNRS ;Copyright Nature Publishing Group Aug 2003 ;Copyright 2003, Nature Publishing Group 2003 Nature Publishing Group ;ISSN: 0007-1188 ;EISSN: 1476-5381 ;DOI: 10.1038/sj.bjp.0705356 ;PMID: 12890715 ;CODEN: BJPCBM

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13
A NO‐releasing derivative of acetaminophen spares the liver by acting at several checkpoints in the Fas pathway 
THIS ARTICLE HAS BEEN RETRACTED
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Article
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A NO‐releasing derivative of acetaminophen spares the liver by acting at several checkpoints in the Fas pathway 
THIS ARTICLE HAS BEEN RETRACTED

British journal of pharmacology, 2009-02, Vol.135 (3), p.589-599 [Peer Reviewed Journal]

2002 British Pharmacological Society ;ISSN: 0007-1188 ;EISSN: 1476-5381 ;DOI: 10.1038/sj.bjp.0704500

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14
Liver delivery of NO by NCX-1000 protects against acute liver failure and mitochondrial dysfunction induced by APAP in mice
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Article
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Liver delivery of NO by NCX-1000 protects against acute liver failure and mitochondrial dysfunction induced by APAP in mice

British journal of pharmacology, 2004-09, Vol.143 (1), p.33-42 [Peer Reviewed Journal]

Copyright Nature Publishing Group Sep 2004 ;Copyright 2004, Nature Publishing Group 2004 Nature Publishing Group ;ISSN: 0007-1188 ;EISSN: 1476-5381 ;DOI: 10.1038/sj.bjp.0705780 ;PMID: 15345658

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15
NO‐naproxen modulates inflammation, nociception and downregulates T cell response in rat Freund's adjuvant arthritis
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Article
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NO‐naproxen modulates inflammation, nociception and downregulates T cell response in rat Freund's adjuvant arthritis

British journal of pharmacology, 2000-07, Vol.130 (6), p.1399-1405 [Peer Reviewed Journal]

2000 British Pharmacological Society ;2000 INIST-CNRS ;Copyright Nature Publishing Group Jul 2000 ;Copyright 2000, Nature Publishing Group 2000 Nature Publishing Group ;ISSN: 0007-1188 ;EISSN: 1476-5381 ;DOI: 10.1038/sj.bjp.0703449 ;PMID: 10903982 ;CODEN: BJPCBM

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16
21‐NO‐prednisolone is a novel nitric oxide‐releasing derivative of prednisolone with enhanced anti‐inflammatory properties
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Article
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21‐NO‐prednisolone is a novel nitric oxide‐releasing derivative of prednisolone with enhanced anti‐inflammatory properties

British journal of pharmacology, 2000-12, Vol.131 (7), p.1345-1354 [Peer Reviewed Journal]

2000 British Pharmacological Society ;2001 INIST-CNRS ;Copyright Nature Publishing Group Dec 2000 ;Copyright 2000, Nature Publishing Group 2000 Nature Publishing Group ;ISSN: 0007-1188 ;EISSN: 1476-5381 ;DOI: 10.1038/sj.bjp.0703704 ;PMID: 11090106 ;CODEN: BJPCBM

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17
A NO-releasing derivative of acetaminophen spares the liver by acting at several checkpoints in the Fas pathway
Material Type:
Article
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A NO-releasing derivative of acetaminophen spares the liver by acting at several checkpoints in the Fas pathway

British journal of pharmacology, 2002-02, Vol.135 (3), p.589-599 [Peer Reviewed Journal]

2002 INIST-CNRS ;Copyright Nature Publishing Group Feb 2002 ;Copyright 2002, Nature Publishing Group 2002 Nature Publishing Group ;ISSN: 0007-1188 ;EISSN: 1476-5381 ;DOI: 10.1038/sj.bjp.0704500 ;PMID: 11834606 ;CODEN: BJPCBM

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18
Liver delivery of NO by NCX-1000 protects against acute liver failure and mitochondrial dysfunction induced by APAP in mice. Commentary
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Article
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Liver delivery of NO by NCX-1000 protects against acute liver failure and mitochondrial dysfunction induced by APAP in mice. Commentary

British journal of pharmacology, 2004, Vol.143 (1), p.33-2 [Peer Reviewed Journal]

2004 INIST-CNRS ;ISSN: 0007-1188 ;EISSN: 1476-5381 ;CODEN: BJPCBM

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19
Involvement of CD44 variant isoforms in hyaluronate adhesion by human activated T cells
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Involvement of CD44 variant isoforms in hyaluronate adhesion by human activated T cells

European journal of immunology, 1995-10, Vol.25 (10), p.2932-2939 [Peer Reviewed Journal]

Copyright © 1995 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 0014-2980 ;EISSN: 1521-4141 ;DOI: 10.1002/eji.1830251033 ;PMID: 7589094

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20
Emerging trends and hotspots in the links between the bile acids and NAFLD from 2002 to 2022: A bibliometric analysis
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Article
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Emerging trends and hotspots in the links between the bile acids and NAFLD from 2002 to 2022: A bibliometric analysis

Endocrinology, diabetes & metabolism, 2024-01, Vol.7 (1), p.e460-n/a [Peer Reviewed Journal]

2023 The Authors. published by John Wiley & Sons Ltd. ;2023 The Authors. Endocrinology, Diabetes & Metabolism published by John Wiley & Sons Ltd. ;2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2398-9238 ;EISSN: 2398-9238 ;DOI: 10.1002/edm2.460 ;PMID: 37941122

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