Auswahl der wissenschaftlichen Literatur zum Thema „Cystic fibrosis Gene therapy“
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Zeitschriftenartikel zum Thema "Cystic fibrosis Gene therapy":
Griesenbach, Uta, Jane C. Davies und Eric Alton. „Cystic fibrosis gene therapy“. Current Opinion in Pulmonary Medicine 22, Nr. 6 (November 2016): 602–9. http://dx.doi.org/10.1097/mcp.0000000000000327.
Colledge, W. H., und M. J. Evans. „Cystic fibrosis gene therapy“. British Medical Bulletin 51, Nr. 1 (Januar 1995): 82–90. http://dx.doi.org/10.1093/oxfordjournals.bmb.a072955.
Colledge, William H. „Cystic fibrosis gene therapy“. Current Opinion in Genetics & Development 4, Nr. 3 (Juni 1994): 466–71. http://dx.doi.org/10.1016/0959-437x(94)90037-x.
Prickett, Michelle, und Manu Jain. „Gene therapy in cystic fibrosis“. Translational Research 161, Nr. 4 (April 2013): 255–64. http://dx.doi.org/10.1016/j.trsl.2012.12.001.
Colledge, WH. „Gene therapy for cystic fibrosis“. Lancet 349, Nr. 9060 (April 1997): 1249. http://dx.doi.org/10.1016/s0140-6736(97)26017-4.
Dodge, J. A. „Gene therapy for cystic fibrosis“. Nature Medicine 1, Nr. 3 (März 1995): 182. http://dx.doi.org/10.1038/nm0395-182a.
Armstrong, D. K., S. Cunningham, J. C. Davies und E. W. F. Alton. „Gene therapy in cystic fibrosis“. Archives of Disease in Childhood 99, Nr. 5 (24.01.2014): 465–68. http://dx.doi.org/10.1136/archdischild-2012-302158.
Wagner, MD, PhD, John A., und Phyllis Gardner, MD. „TOWARD CYSTIC FIBROSIS GENE THERAPY“. Annual Review of Medicine 48, Nr. 1 (Februar 1997): 203–16. http://dx.doi.org/10.1146/annurev.med.48.1.203.
Flotte, Terence R., und Beth L. Laube. „Gene Therapy in Cystic Fibrosis“. Chest 120, Nr. 3 (September 2001): 124S—131S. http://dx.doi.org/10.1378/chest.120.3_suppl.124s.
Alton, Eric, Stephen Smith und Duncan Geddes. „Gene therapy for cystic fibrosis“. Lancet 349, Nr. 9060 (April 1997): 1249–50. http://dx.doi.org/10.1016/s0140-6736(05)62441-5.
Dissertationen zum Thema "Cystic fibrosis Gene therapy":
Davies, Gwyneth. „Outcome measures for cystic fibrosis gene therapy clinical trials“. Thesis, Imperial College London, 2013. http://hdl.handle.net/10044/1/28414.
Rose, Andrew C. „Studies on the expression of the murine CFTR gene : implications for gene therapy“. Thesis, University of Oxford, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.365354.
Dragomir, Anca. „Approaches to Pharmacological Treatment and Gene Therapy of Cystic Fibrosis“. Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3845.
McKay, Tristan Rowntree. „Investigations toward gene therapy for hepatobiliary disease in cystic fibrosis“. Thesis, Imperial College London, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.392184.
Cooney, Ashley L. „Integrating viral vectors as a gene therapy approach for cystic fibrosis“. Diss., University of Iowa, 2018. https://ir.uiowa.edu/etd/6083.
Scott, Emily Siân. „Improving the efficiency of liposome-mediated gene transfer for cystic fibrosis gene therapy“. Thesis, University of Cambridge, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.624332.
Jannetta, Evelyn Elena. „Qualitative study of cystic fibrosis (CF) patients' expectations of gene therapy“. Thesis, University of Edinburgh, 2009. http://hdl.handle.net/1842/8745.
Jaffe, Adam. „Assessment and feasibility of gene therapy for cystic fibrosis in children“. Thesis, Imperial College London, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.589769.
Middleton, Peter Gordon. „Cystic fibrosis ion transport and the effect of CFTR gene transfer“. Thesis, Imperial College London, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307399.
Kwilas, Anna R. „Respiratory Syncytial Virus Based Vectors for the Treatment of Cystic Fibrosis“. The Ohio State University, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=osu1284384649.
Bücher zum Thema "Cystic fibrosis Gene therapy":
Love, Cynthia B. Genetic testing for cystic fibrosis: January 1989 through February 1997 : 1224 citations. Bethesda, Md. (8600 Rockville Pike, Bethesda 20894): U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, National Library of Medicine, Reference Section, 1997.
United States. Congress. Senate. Committee on Small Business. Research on childhood diseases by entrepreneurs: Hearing before the Committee on Small Business, United States Senate, One Hundred Third Congress, second session ... Thursday, May 26, 1994. Washington: U.S. G.P.O., 1995.
United States. Congress. Senate. Committee on Small Business. Research on childhood diseases by entrepreneurs: Hearing before the Committee on Small Business, United States Senate, One Hundred Third Congress, second session ... Thursday, May 26, 1994. Washington: U.S. G.P.O., 1995.
Skypala, Isabel. Eating well with cystic fibrosis. Bromley: Cystic Fibrosis Trust, 1994.
Tsui, Lap-Chee, Giovanni Romeo, Rainer Greger und Sergio Gorini, Hrsg. The Identification of the CF (Cystic Fibrosis) Gene. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4684-5934-0.
Ferguson, Kate. The physical treatment of cystic fibrosis. Bromley: Cystic Fibrosis Trust, 1995.
Mofford, K. A. Preclinical studies in DNA/liposome gene transfer for cystic fibrosis. Oxford: Oxford Brookes University, 1996.
MacDonald, Anita. Eating well with cystic fibrosis: A guide for children and parents. Bromley: Cystic Fibrosis Trust, 1996.
Genetic Analysis Workshop (6th 1988 Long Beach, Miss.). Multipoint mapping and linkage based upon affected pedigree members: Genetic Analysis Workshop 6, proceedings of a workshop held at Gulf Park, Long Beach, Mississippi, October 10-12, 1988. Herausgegeben von Elston Robert C. 1932-. New York: Liss, 1988.
Duguay, François. Use of the Xenopus oocyte as a potential expression system for the cystic fibrosis gene. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1991.
Buchteile zum Thema "Cystic fibrosis Gene therapy":
Porteous, D. J., und J. A. Innes. „Gene Therapy for Cystic Fibrosis“. In Gene Therapy, 137–49. Basel: Birkhäuser Basel, 1999. http://dx.doi.org/10.1007/978-3-0348-7011-5_10.
Boyd, A. Christopher. „Gene and Stem Cell Therapy“. In Cystic Fibrosis in the 21st Century, 221–29. Basel: KARGER, 2005. http://dx.doi.org/10.1159/000088601.
Sumner-Jones, Stephanie G., Deborah R. Gill und Stephen C. Hyde. „Gene therapy for cystic fibrosis lung disease“. In Gene Therapy for Autoimmune and Inflammatory Diseases, 47–64. Basel: Springer Basel, 2010. http://dx.doi.org/10.1007/978-3-0346-0165-8_4.
Trapnell, Bruce C. „Gene Therapy for Cystic Fibrosis Lung Disease“. In The Pediatric Lung, 229–58. Basel: Birkhäuser Basel, 1997. http://dx.doi.org/10.1007/978-3-0348-8960-5_10.
Alton, Eric W. F. W. „Gene Delivery and Therapy: The Case for Cystic Fibrosis“. In Targeting of Drugs 5, 15–19. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4615-6405-8_2.
Carter, B. J., und T. R. Flotte. „Development of Adeno-associated Virus Vectors for Gene Therapy of Cystic Fibrosis“. In Adeno-Associated Virus (AAV) Vectors in Gene Therapy, 119–44. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-80207-2_8.
Bruzzese, Eugenia, Vittoria Buccigrossi, Giusy Ranucci und Alfredo Guarino. „Microbial therapy for cystic fibrosis“. In The Human Microbiota and Chronic Disease, 497–506. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781118982907.ch32.
Wadsworth, Samuel C., und Alan E. Smith. „Cystic fibrosis and lung diseases“. In Molecular and Cell Biology of Human Gene Therapeutics, 237–51. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0547-7_12.
Schnabel, Dirk. „Cystic Fibrosis – Growth Hormone Treatment“. In Growth Hormone Therapy in Pediatrics - 20 Years of KIGS, 296–303. Basel: KARGER, 2007. http://dx.doi.org/10.1159/000101859.
Gajbhiye, Rahul, und Avinash Gaikwad. „Cystic Fibrosis, CFTR Gene, and Male Infertility“. In Male Infertility: Understanding, Causes and Treatment, 131–50. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-4017-7_9.
Konferenzberichte zum Thema "Cystic fibrosis Gene therapy":
Sinadinos, AJ, A. Sergijenko, AD Saleh, NAM Nafchi, JW Hickmott, T. Gamlen, DR Gill, SC Hyde, EWFW Alton und U. Griesenbach. „S82 Quantification of mRNA and protein from single cells for cystic fibrosis gene therapy“. In British Thoracic Society Winter Meeting, Wednesday 17 to Friday 19 February 2021, Programme and Abstracts. BMJ Publishing Group Ltd and British Thoracic Society, 2021. http://dx.doi.org/10.1136/thorax-2020-btsabstracts.87.
Saleh, AD, NK Clarke, C. Meng, MR Jacobson, JC Davies, SR Durham, EWFW Alton und U. Griesenbach. „S94 Development of assays to assess safety and efficacy of lentiviral gene therapy for cystic fibrosis“. In British Thoracic Society Winter Meeting 2017, QEII Centre Broad Sanctuary Westminster London SW1P 3EE, 6 to 8 December 2017, Programme and Abstracts. BMJ Publishing Group Ltd and British Thoracic Society, 2017. http://dx.doi.org/10.1136/thoraxjnl-2017-210983.100.
Collie, David, Peter Tennant, Catherine Gordon, Christina Vrettou, Alison Baker, Eilidh Baker, David Porteous et al. „The Uk Cystic Fibrosis Gene Therapy Consortium: Normal Values And Reproducibility Of Forced Expiratory Flow Volume Curves In Sheep“. In American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a2176.
Saleh, AD, SR Durham, MH Shamji, U. Griesenbach und EWFW Alton. „S19 Peak nasal inspiratory flow and nasal cytokines are useful biomarkers of nasal inflammation in cystic fibrosis gene therapy“. In British Thoracic Society Winter Meeting 2019, QEII Centre, Broad Sanctuary, Westminster, London SW1P 3EE, 4 to 6 December 2019, Programme and Abstracts. BMJ Publishing Group Ltd and British Thoracic Society, 2019. http://dx.doi.org/10.1136/thorax-2019-btsabstracts2019.25.
Coleman, Phoebe, und Bill Elder. „The journey of the Cystic Fibrosis gene“. In SIGGRAPH '09: Posters. New York, New York, USA: ACM Press, 2009. http://dx.doi.org/10.1145/1599301.1599395.
Nguyen, J. P., M. Bianca, R. D. Huff, N. Tiessen, Y. Kim, V. Hou, M. Heller, M. D. Inman und J. A. Hirota. „Development of a Novel Combinatorial Therapy for Cystic Fibrosis“. In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a2580.
Tymchuk, I. V., M. A. Panas, Yu T. Konechnyi, O. P. Korniychuk und V. V. Danyleichenko. „Pseudomonadaceae as vancomycin resistance gene reservoir in patients with cystic fibrosis“. In NEW TRENDS AND UNRESOLVED ISSUES OF PREVENTIVE AND CLINICAL MEDICINE. Baltija Publishing, 2020. http://dx.doi.org/10.30525/978-9934-588-81-5-2.40.
Yoshimura, K., C. Anzai, A. Miyamoto, H. Uruga, Y. Beika, N. Morokawa und K. Kishi. „Analysis of CFTR Gene Mutations in Japanese Individuals with Cystic Fibrosis.“ In American Thoracic Society 2009 International Conference, May 15-20, 2009 • San Diego, California. American Thoracic Society, 2009. http://dx.doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a1201.
Einhorn, Klaus, und Manfred Ballmann. „Pseudomonas aeruginosa eradication therapy on Cystic Fibrosis- Guideline and clinical routine“. In ERS International Congress 2018 abstracts. European Respiratory Society, 2018. http://dx.doi.org/10.1183/13993003.congress-2018.pa1330.
Mitchelmore, Philip, Louise Anning, Victoria Carnell, Sarah Jephcote, Pia Charters, Tim Crowe, Christopher Dean, Anna Lowdon, Christopher Sheldon und Nicholas Withers. „Azithromycin therapy andpseudomonas aeruginosaisolation in a non-cystic fibrosis bronchiectasis cohort“. In Annual Congress 2015. European Respiratory Society, 2015. http://dx.doi.org/10.1183/13993003.congress-2015.oa470.