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1. Full Text In this issue – June 2018: Diversity of Haemophilus parasuis isolates from Australian piggeries · Detection of bovine noroviruses in Australian dairy cattle · Myocardial adenomatoid tumour in a calf · Hypertrophic cardiomyopathy in a horse  · A history of veterinary education  · Review of Q fever notifications in Victoria
by Jackson, AE
Australian Veterinary Journal, ISSN 0005-0423, 06/2018, Volume 96, Issue 6, pp. 193 - 194
Q fever | Cardiomyopathy | Fever | Tumors
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2. Full Text Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis
by Hobbs, Brian D and de Jong, Kim and Lamontagne, Maxime and Bosse, Yohan and Shrine, Nick and Artigas, Maria Soler and Wain, Louise V and Hall, Ian P and Jackson, Victoria E and Wyss, Annah B and London, Stephanie J and North, Kari E and Franceschini, Nora and Strachan, David P and Beaty, Terri H and Hokanson, John E and Crapo, James D and Castaldi, Peter J and Chase, Robert P and Bartz, Traci M and Heckbert, Susan R and Psaty, Bruce M and Gharib, Sina A and Zanen, Pieter and Lammers, Jan W and Oudkerk, Matthijs and Groen, H. J and Locantore, Nicholas and Tal-Singer, Ruth and Rennard, Stephen I and Vestbo, Jurgen and Timens, Wim and Pare, Peter D and Latourelle, Jeanne C and Dupuis, Josee and O'Connor, George T and Wilk, Jemma B and Kim, Woo Jin and Lee, Mi Kyeong and Oh, Yeon-Mok and Vonk, Judith M and de Koning, Harry J and Leng, Shuguang and Belinsky, Steven A and Tesfaigzi, Yohannes and Manichaikul, Ani and Wang, Xin-Qun and Rich, Stephen S and Barr, R. Graham and Sparrow, David and Litonjua, Augusto A and Bakke, Per and Gulsvik, Amund and Lahousse, Lies and Brusselle, Guy G and Stricker, Bruno H and Uitterlinden, Ane G and Ampleford, Elizabeth J and Bleecker, Eugene R and Woouff, Prescott G and Meyers, Deborah A and Qiao, Dandi and Lomas, David A and Yim, Jae-Joon and Kim, Deog Kyeom and Hawrylkiewicz, Iwona and Sliwinski, Pawel and Hardin, Megan and Fingerlin, Tasha E and Schwartz, David A and Postma, Dirkje S and MacNee, William and Tobin, Martin D and Silverman, Edwin K and Boezen, H. Marike and Cho, Michael H and UK BiLEVE Investigators and COPDGene Investigators and ECLIPSE Investigators and SPIROMICS Res Grp and Int COPD Genetics Network and LifeLines Investigators and Int COPD Genetics Consortium and SPIROMICS Research Group and International COPD Genetics Network Investigators and International COPD Genetics Consortium
Nature Genetics, ISSN 1061-4036, 03/2017, Volume 49, Issue 3, pp. 426 - 432
Chronic obstructive pulmonary disease (COPD) is a leading cause of mortality worldwide(1). We performed a genetic association study in 15,256 cases and 47,936... 
SURFACTANT PROTEIN-D | NLRX1 | VARIANTS | MICROTUBULES | SUSCEPTIBILITY | GENETICS & HEREDITY | DESMOPLAKIN | COMPLEX TRAITS | GENOME-WIDE ASSOCIATION | I INTERFERON | COPD | Genetic Predisposition to Disease - genetics | Humans | Middle Aged | Risk Factors | Genetic Loci - genetics | Male | Smoking - genetics | Pulmonary Fibrosis - genetics | Lung - physiology | Asthma - genetics | Phenotype | Alleles | Aged, 80 and over | Polymorphism, Single Nucleotide - genetics | Adult | Female | Aged | Genome-Wide Association Study - methods | Pulmonary Disease, Chronic Obstructive - genetics | Quantitative trait loci | Complications and side effects | Lung diseases, Obstructive | Care and treatment | Pulmonary fibrosis | Genetic aspects | Health aspects | Risk factors | Data analysis | Genomes | Cigarettes | Surfactants | Asthma | Proteins | Studies | Airway management | Data collection | Gene loci | Chronic obstructive pulmonary disease | Smoking | Index Medicus
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3. Full Text Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
by Wain, Louise V and Shrine, Nick R. G and Artigas, Maria Soler and Erzurumluoglu, A Mesut and Noyvert, Boris and Bossini-Castillo, Lara and Obeidat, Ma'en and Henrys, Amanda P and Portelli, Michael A and Hall, Robert J and Billington, Charlotte K and Rimington, Tracy L and Fenech, Anthony G and John, Catherine and Blake, Tineka and Jackson, Victoria E and Allen, Richard J and Prins, Bram P and Campbell, Archie and Porteous, David J and Jarvelin, Marjo-Riitta and Wielscher, Matthias and Jamess, Alan L and Hui, Jennie and Wareham, Nicholas J and Zhao, Jing Hua and Wilson, James F and Joshi, Peter K and Stubbe, Beate and Rawal, Rajesh and Schulz, Holger and Imboden, Medea and Probst-Hensch, Nicole M and Karrasch, Stefan and Gieger, Christian and Deary, Ian J and Harris, Sarah E and Marten, Jonathan and Rudan, Igor and Enroth, Stefan and Gyllensten, Ulf and Kerr, Shona M and Polasek, Ozren and Kahonen, Mika and Surakka, Ida and Vitart, Veronique and Hayward, Caroline and Lehtimaki, Terho and Raitakari, Olli T and Evans, David M and Henderson, A. John and Pennell, Craig E and Wang, Carol A and Sly, Peter D and Wan, Emily S and Busch, Robert and Hobbs, Brian D and Litonjua, Augusto and Sparrow, David W and Gulsvik, Amund and Bakke, Per S and Crapo, James D and Beaty, Terri H and Hansel, Nadia N and Mathias, Rasika A and Ruczinski, Ingo and Barnes, Kathleen C and Bosse, Yohan and Joubert, Philippe and van den Berge, Maarten and Brandsma, Corry-Anke and Pare, Peter D and Sin, Don and Nickle, David C and Hao, Ke and Gottesman, Omri and Dewey, Frederick E and Bruse, Shannon E and Carey, David J and Kirchner, H Lester and Jonsson, Stefan and Thorleifsson, Gudmar and Jonsdottir, Ingileif and Gislason, Thorarinn and Stefansson, Kari and Schurmann, Claudia and Nadkarni, Girish N and Bottinger, Erwin P and Loos, Ruth J. F and Walters, Robin G and Chen, Zhengming and Millwood, Iona Y and Vaucher, Julien and Kurmi, Om P and Li, Liming and Hansell, Anna L and Brightling, Chris and Zeggini, Eleftheria and Cho, Michael H and Silverman, Edwin K and ... and Geisinger-Regeneron DiscovEHR and Understanding Soc Sci Grp and Understanding Society Scientific Group and Geisinger-Regeneron DiscovEHR Collaboration and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Uppsala universitet
Nature Genetics, ISSN 1061-4036, 03/2017, Volume 49, Issue 3, pp. 416 - 425
Chronic obstructive pulmonary disease (COPD) is characterized by reduced lung function and is the third leading cause of death globally. Through genome-wide... 
VARIANTS | GENETICS | SUSCEPTIBILITY | FAM13A | GENETICS & HEREDITY | RISK | EPIDEMIOLOGY | HISTORY | Genetic Predisposition to Disease - genetics | Humans | Middle Aged | Risk Factors | Genetic Loci - genetics | Male | Lung - physiopathology | Asthma - genetics | Epigenesis, Genetic - genetics | Alleles | Aged, 80 and over | Polymorphism, Single Nucleotide - genetics | Adult | Female | Aged | Genome-Wide Association Study - methods | Pulmonary Disease, Chronic Obstructive - genetics | Quantitative trait loci | Molecular targeted therapy | Lung diseases, Obstructive | Care and treatment | Innovations | Development and progression | Genetic aspects | Health aspects | Studies | Chronic obstructive pulmonary disease | Genomes | Health risk assessment | Index Medicus | Medical and Health Sciences | Medicin och hälsovetenskap
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4. Full Text Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank
by Wain, Louise V, PhD and Shrine, Nick, PhD and Miller, Suzanne, PhD and Jackson, Victoria E, MSc and Ntalla, Ioanna, PhD and Artigas, María Soler, PhD and Billington, Charlotte K, PhD and Kheirallah, Abdul Kader, BSc and Allen, Richard, MSc and Cook, James P, PhD and Probert, Kelly, BSc and Obeidat, Ma'en, PhD and Bossé, Yohan, PhD and Hao, Ke, ScD and Postma, Dirkje S, Prof and Paré, Peter D, MD and Ramasamy, Adaikalavan, DPhil and Mägi, Reedik, PhD and Mihailov, Evelin, MSc and Reinmaa, Eva, MSc and Melén, Erik, MD and O'Connell, Jared, DPhil and Frangou, Eleni, MSc[Res] and Delaneau, Olivier, PhD and Freeman, Colin, PhD and Petkova, Desislava, PhD and McCarthy, Mark, Prof and Sayers, Ian, PhD and Deloukas, Panos, Prof and Hubbard, Richard, Prof and Pavord, Ian, FMedSci and Hansell, Anna L, MBBChir and Thomson, Neil C, Prof and Zeggini, Eleftheria, PhD and Morris, Andrew P, Prof and Marchini, Jonathan, Prof and Strachan, David P, Prof and Tobin, Martin D, Prof and Hall, Ian P, Prof and OxGSK Consortium and UKBEC and UK Brain Expression Consortium (UKBEC)
Lancet Respiratory Medicine, The, ISSN 2213-2600, 2015, Volume 3, Issue 10, pp. 769 - 781
Summary Background Understanding the genetic basis of airflow obstruction and smoking behaviour is key to determining the pathophysiology of chronic... 
Pulmonary/Respiratory | IMPUTATION | METAANALYSIS | VARIANTS | RESPIRATORY SYSTEM | SUSCEPTIBILITY LOCI | KANSL1 CAUSE | HAPLOTYPE | MUTATIONS | EXPRESSION | JOINT | GENOME-WIDE ASSOCIATION | CRITICAL CARE MEDICINE | Forced Expiratory Volume - genetics | Genetic Association Studies | Humans | Middle Aged | Risk Factors | Male | Smoking - genetics | United Kingdom | Lung - physiopathology | Case-Control Studies | Young Adult | Biological Specimen Banks | Adolescent | Aged, 80 and over | Adult | Female | Aged | Polymorphism, Single Nucleotide | Pulmonary Disease, Chronic Obstructive - genetics | Index Medicus
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5. The Victoria & Albert Museum's textile collection
: woven textile design in Britain from 1750 to 1850
by Rothstein, Natalie, 1930-2010 and Victoria and Albert Museum
1994, ISBN 1558598502, 112
Textile fabrics | History | Victoria and Albert Museum | Textile design
Book
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6. Full Text Vandetanib plus gemcitabine versus placebo plus gemcitabine in locally advanced or metastatic pancreatic carcinoma (ViP): a prospective, randomised, double-blind, multicentre phase 2 trial
by Middleton, Gary, Prof and Palmer, Daniel H, Prof and Greenhalf, William, PhD and Ghaneh, Paula, Prof and Jackson, Richard, PhD and Cox, Trevor, PhD and Evans, Anthony, PhD and Shaw, Victoria E, PhD and Wadsley, Jonathan, MA and Valle, Juan W, Prof and Propper, David, MD and Wasan, Harpreet, MD and Falk, Stephen, MD and Cunningham, David, Prof and Coxon, Fareeda, MBBS and Ross, Paul, PhD and Madhusudan, Srinivasan, Prof and Wadd, Nick, MBBS and Corrie, Pippa, FRCP and Hickish, Tamas, MD and Costello, Eithne, PhD and Campbell, Fiona, MD and Rawcliffe, Charlotte, MSc and Neoptolemos, John P, Prof
Lancet Oncology, The, ISSN 1470-2045, 2017, Volume 18, Issue 4, pp. 486 - 499
Summary Background Erlotinib is an EGFR tyrosine kinase inhibitor that has shown a significant but only marginally improved median overall survival when... 
Hematology, Oncology and Palliative Medicine | ONCOLOGY | BEVACIZUMAB | NEUROTROPHIC FACTOR | TYROSINE KINASE | ANTITUMOR-ACTIVITY | INHIBITOR | FACTOR RECEPTOR | III TRIAL | ZD6474 | ENDOTHELIAL GROWTH-FACTOR | CANCER CELL INVASION | Carcinoma, Pancreatic Ductal - secondary | Piperidines - administration & dosage | Prognosis | Double-Blind Method | Follow-Up Studies | Deoxycytidine - administration & dosage | Humans | Middle Aged | Pancreatic Neoplasms - pathology | Male | Survival Rate | Lymphatic Metastasis | Pancreatic Neoplasms - drug therapy | Carcinoma, Pancreatic Ductal - drug therapy | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Adult | Female | Quinazolines - administration & dosage | Aged | Neoplasm Staging | Deoxycytidine - analogs & derivatives | Antimitotic agents | Tyrosine | Hospitals | Oncology, Experimental | Pancreatic cancer | Clinical trials | Product development | Research | Metastasis | Antineoplastic agents | Cancer | Index Medicus
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7. Full Text Phenotypic and pharmacogenetic evaluation of patients with thiazide-induced hyponatremia
by Ware, James S and Wain, Louise V and Channavajjhala, Sarath K and Jackson, Victoria E and Edwards, Elizabeth and Lu, Run and Siew, Keith and Jia, Wenjing and Shrine, Nick and Kinnear, Sue and Jalland, Mahli and Henry, Amanda P and Clayton, Jenny and O'Shaughnessy, Kevin M and Tobin, Martin D and Schuster, Victor L and Cook, Stuart and Hall, Ian P and Glover, Mark
Journal of Clinical Investigation, ISSN 0021-9738, 09/2017, Volume 127, Issue 9, pp. 3367 - 3374
Thiazide diuretics are among the most widely used treatments for hypertension, but thiazide-induced hyponatremia (TIH), a clinically significant adverse... 
PATHOGENESIS | MEDICINE, RESEARCH & EXPERIMENTAL | SODIUM | PROSTAGLANDIN TRANSPORTER | DIURETIC-INDUCED HYPONATREMIA | COLLECTING DUCTS | RELEASE | HYPERTENSION | EXCRETION | ASSOCIATION | CELL | Hyponatremia - chemically induced | Hyponatremia - genetics | Genome-Wide Association Study | Pharmacogenetics | Humans | Middle Aged | Male | Sodium Chloride Symporter Inhibitors - adverse effects | United Kingdom | Aquaporin 1 - genetics | Dinoprostone - metabolism | Organic Anion Transporters - genetics | Phenotype | Thiazides - adverse effects | Water - chemistry | Aged, 80 and over | Female | Aged | Polymorphism, Single Nucleotide | Aquaporin 2 - genetics | Nephrons - metabolism | Cohort Studies | Prostaglandins - metabolism | Genetic aspects | Hyponatremia | Observations | Hypertension | Complications and side effects | Analysis | Vasopressin | Urine | Plasma | Excretion | Pathogenesis | Prostaglandin E2 | Reabsorption | Single-nucleotide polymorphism | Uric acid | Blood | Chloride | Sodium | Metabolites | Rodents | Diuretics | Magnesium | Potassium | Drug dosages | Index Medicus | Abridged Index Medicus
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8. Full Text Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
by Sakornsakolpat, Phuwanat and Prokopenko, Dmitry and Lamontagne, Maxime and Reeve, Nicola F and Guyatt, Anna L and Jackson, Victoria E and Shrine, Nick and Qiao, Dandi and Bartz, Traci M and Kim, Deog Kyeom and Lee, Mi Kyeong and Latourelle, Jeanne C and Li, Xingnan and Morrow, Jarrett D and Obeidat, Ma’en and Wyss, Annah B and Bakke, Per and Barr, R. Graham and Beaty, Terri H and Belinsky, Steven A and Brusselle, Guy G and Crapo, James D and de Jong, Kim and DeMeo, Dawn L and Fingerlin, Tasha E and Gharib, Sina A and Gulsvik, Amund and Hall, Ian P and Hokanson, John E and Kim, Woo Jin and Lomas, David A and London, Stephanie J and Meyers, Deborah A and O’Connor, George T and Rennard, Stephen I and Schwartz, David A and Sliwinski, Pawel and Sparrow, David and Strachan, David P and Tal-Singer, Ruth and Tesfaigzi, Yohannes and Vestbo, Jørgen and Vonk, Judith M and Yim, Jae-Joon and Zhou, Xiaobo and Bossé, Yohan and Manichaikul, Ani and Lahousse, Lies and Silverman, Edwin K and Boezen, H. Marike and Wain, Louise V and Tobin, Martin D and Hobbs, Brian D and Cho, Michael H and Shrine, Nick and Guyatt, Anna L and Batini, Chiara and Zhao, Jing Hua and Wielscher, Matthias and Weiss, Stefan and Kentistou, Katherine A and Cook, James P and Hui, Jennie and Karrasch, Stefan and Imboden, Medea and Harris, Sarah E and Marten, Jonathan and Enroth, Stefan and Kerr, Shona M and Surakka, Ida and Vitart, Veronique and Lehtimäki, Terho and Ewert, Ralf and Gieger, Christian and Homuth, Georg and Joshi, Peter K and Langenberg, Claudia and Lind, Lars and Luan, Jian’an and Mahajan, Anubha and Murray, Alison and Porteous, David J and Rawal, Rajesh and Smith, Blair H and Timmers, Paul R. H. J and Raitakari, Olli T and Kähönen, Mika and Polasek, Ozren and Gyllensten, Ulf and Rudan, Igor and Deary, Ian J and Probst-Hensch, Nicole M and Schulz, Holger and James, Alan L and Wilson, James F and Stubbe, Beate and Zeggini, Eleftheria and Jarvelin, Marjo-Riitta and Wareham, Nick and Hayward, Caroline and ... and SpiroMeta Consortium and Understanding Soc Sci Grp and Int COPD Genetics Consortium and International COPD Genetics Consortium
Nature Genetics, ISSN 1061-4036, 03/2019, Volume 51, Issue 3, pp. 494 - 505
Chronic obstructive pulmonary disease (COPD) is the leading cause of respiratory mortality worldwide. Genetic risk loci provide new insights into disease... 
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