Publications
600 results found
Davies JC, Cunningham S, Alton EWFW, et al., 2008, Lung clearance index in CF: a sensitive marker of lung disease severity, THORAX, Vol: 63, Pages: 96-97, ISSN: 0040-6376
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- Citations: 35
Horsley AR, Gustafsson PM, Macleod KA, et al., 2008, Lung clearance index is a sensitive, repeatable and practical measure of airways disease in adults with cystic fibrosis, THORAX, Vol: 63, Pages: 135-140, ISSN: 0040-6376
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- Citations: 179
Rakonczay Z, Hegyi P, Hasegawa M, et al., 2008, CFTR gene transfer to human cystic fibrosis pancreatic duct cells using a sendai virus vector, JOURNAL OF CELLULAR PHYSIOLOGY, Vol: 214, Pages: 442-455, ISSN: 0021-9541
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- Citations: 31
Green A, Alton E, 2008, Cardiac repair clinical trials, Advances in Tissue Engineering, Pages: 695-731, ISBN: 9781848161825
Cardiovascular disease is a major problem worldwide, and remains the leading cause of death within Europe. Clinical trials of stem cells have been conducted in the setting of acute myocardial infarction and chronic heart disease. At the time of writing there have been a number of different cell types, preparation and doses delivered by a number of different delivery routes to a variety of patients in small, mostly uncontrolled trials, generally with positive outcomes. Larger placebo-controlled trials are ongoing and we eagerly await their results. The challenges currently facing the field are to define the optimal target patient population, cell source, preparation, dose, delivery and retention of cells within the myocardium and the appropriate assays to detect meaningful clinical changes. Clearly not all of these questions can be answered in the clinical trial setting and it is imperative that basic science and translational research are conducted simultaneously to help guide clinical research. At present there appears to be no clear steer in answering these questions but we attempt to discuss the evidence to date and the future of stem cells in the management of cardiovascular disease.
Regamey N, Hilliard TN, Saglani S, et al., 2008, Endobronchial biopsy in childhood, CHEST, Vol: 133, Pages: 312-312, ISSN: 0012-3692
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- Citations: 3
Griesenbach U, Munkonge FM, Sumner-Jones S, et al., 2008, Assessment of CFTR function after gene transfer in vitro and in vivo., Methods Mol Biol, Vol: 433, Pages: 229-242, ISSN: 1064-3745
Cystic fibrosis (CF) a monogenic lethal disease and, therefore, ideally suited for the development of gene therapy. The first clinical trials were carried out shortly after cloning the CF gene in 1989. Since then, 25 trials have been carried out. Proof of principle for low-level airway gene transfer was established in most, but not all, trials. It is currently unclear whether current gene transfer efficiency will lead to improvements in clinically relevant endpoints such as inflammation or infection. In addition to addressing this important question, we and others are further improving airway gene transfer, by modifying existing and developing new gene transfer agents. Here, we describe pre-clinical methods related to assessing correction of the CF chloride transport defect.
Davies JC, Alton EWFW, Bush A, 2007, Cystic fibrosis, BMJ-BRITISH MEDICAL JOURNAL, Vol: 335, Pages: 1255-1259, ISSN: 1756-1833
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- Citations: 228
Aziz ZA, Wells A, Meister M, et al., 2007, Computed tomography in infective exacerbations in cystic fibrosis: Serial change and observer agreement, Winter Meeting of the British-Thoracic-Society, Publisher: B M J PUBLISHING GROUP, Pages: A30-A31, ISSN: 0040-6376
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- Citations: 1
Alexander BL, Ali RR, Alton EWFW, et al., 2007, Progress and prospects: gene therapy clinical trials (part 1) (vol 14, pg 1439, 2007), GENE THERAPY, Vol: 14, Pages: 1754-1754, ISSN: 0969-7128
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- Citations: 6
Xenariou S, Griesenbach U, Liang HD, et al., 2007, Assessing ultrasound as a method to enhance non-viral gene transfer to the lung, Winter Meeting of the British-Thoracic-Society, Publisher: B M J PUBLISHING GROUP, Pages: A105-A105, ISSN: 0040-6376
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- Citations: 1
Griesenbach U, Jeswiet SB, Larsen MDB, et al., 2007, UK cf gene therapy consortium tracking study: Change in sputum properties in response to IV antibiotics, Winter Meeting of the British-Thoracic-Society, Publisher: B M J PUBLISHING GROUP, Pages: A30-A30, ISSN: 0040-6376
Hilliard TN, Regamey N, Shute JK, et al., 2007, Airway remodelling in children with cystic fibrosis, THORAX, Vol: 62, Pages: 1074-1080, ISSN: 0040-6376
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- Citations: 109
Larsen MDB, Griesenbach U, Goussard S, et al., 2007, Bactofection into airway epithelial cells in vitro and in vivo using a genetically modified Escherichia coli, Winter Meeting of the British-Thoracic-Society, Publisher: B M J PUBLISHING GROUP, Pages: A105-A105, ISSN: 0040-6376
Horsley AR, Aziz Z, Macleod KA, et al., 2007, Functional and structural changes in the cystic fibrosis lung following antibiotic treatment for exacerbation, Winter Meeting of the British-Thoracic-Society, Publisher: B M J PUBLISHING GROUP, Pages: A31-A31, ISSN: 0040-6376
Ban H, Inoue M, Griesenbach U, et al., 2007, Expression and maturation of Sendai virus vector-derived CFTR protein: functional and biochemical evidence using a GFP-CFTR fusion protein, GENE THERAPY, Vol: 14, Pages: 1688-1694, ISSN: 0969-7128
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- Citations: 17
Davies JC, Voase N, Dewar M, et al., 2007, Uk CF gene therapy consortium tracking study: Response of clinically available assays to intravenous antibiotics, Winter Meeting of the British-Thoracic-Society, Publisher: B M J PUBLISHING GROUP, Pages: A30-A30, ISSN: 0040-6376
Alton E, Ferrari S, Griesenbach U, 2007, Progress and prospects: Gene therapy clinical trials (part 2), GENE THERAPY, Vol: 14, Pages: 1555-1563, ISSN: 0969-7128
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- Citations: 62
Alton E, 2007, Progress and prospects: Gene therapy clinical trials (part 1), GENE THERAPY, Vol: 14, Pages: 1439-1447, ISSN: 0969-7128
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- Citations: 73
Ferrari S, Griesenbach U, Iida A, et al., 2007, Sendai virus-mediated CFTR gene transfer to the airway epithelium, GENE THERAPY, Vol: 14, Pages: 1371-1379, ISSN: 0969-7128
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- Citations: 49
Regamey N, Hilliard TN, Saglani S, et al., 2007, Quality, size, and composition of pediatric endobronchial biopsies in cystic fibrosis, CHEST, Vol: 131, Pages: 1710-1717, ISSN: 0012-3692
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- Citations: 27
Xenariou S, Griesenbach U, Liang H-D, et al., 2007, Use of ultrasound to enhance nonviral lung gene transfer in vivo, GENE THERAPY, Vol: 14, Pages: 768-774, ISSN: 0969-7128
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- Citations: 59
Alton EWFW, Davies JC, Geddes DM, 2007, Biomarkers for cystic fibrosis - Are we progressing?, AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, Vol: 175, Pages: 750-751, ISSN: 1073-449X
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- Citations: 9
Aziz ZA, Davies JC, Alton EW, et al., 2007, Computed tomography and cystic fibrosis: promises and problems, THORAX, Vol: 62, Pages: 181-186, ISSN: 0040-6376
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- Citations: 21
McLachlan G, Baker A, Tennant P, et al., 2007, Optimizing aerosol gene delivery and expression in the ovine lung, MOLECULAR THERAPY, Vol: 15, Pages: 348-354, ISSN: 1525-0016
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- Citations: 43
Regamey N, Ochs M, Hilliard TN, et al., 2007, Airway smooth muscle remodeling in children with cystic fibrosis, PEDIATRIC PULMONOLOGY, Pages: 349-350, ISSN: 8755-6863
Alton E, 2007, Measures of CFTR molecular and clinical function, 21st Annual North American Cystic Fibrosis Conference, Publisher: WILEY-LISS, Pages: 178-179, ISSN: 8755-6863
Horsley A, Macleod K, Saunders C, et al., 2007, UKCF gene therapy consortium tracking study: Lung clearance index improves with treatment of an infective exacerbation, PEDIATRIC PULMONOLOGY, Pages: 335-336, ISSN: 8755-6863
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- Citations: 3
Gray RD, Horsley A, Macleod K, et al., 2007, UKCF gene therapy consortium tracking study: Sputum and serum calprotectin are useful novel measurements in CF exacerbation, PEDIATRIC PULMONOLOGY, Pages: 338-338, ISSN: 8755-6863
Reizarney N, Tsartsali L, Hilliard TN, et al., 2007, Airway mucosa inflammation in children with cystic fibrosis, PEDIATRIC PULMONOLOGY, Pages: 262-263, ISSN: 8755-6863
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- Citations: 1
Macleod K, Horsley A, Gray R, et al., 2007, UK cystic fibrosis gene therapy consortium tracking study: Exhaled breath condensate pH increases with treatment of an infective exacerbation, PEDIATRIC PULMONOLOGY, Pages: 343-344, ISSN: 8755-6863
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