Zobrazeno 1 - 10 of 102 pro vyhledávání: '"Munye, M. M."'
1
Dissertation/ Thesis
Towards gene therapy for primary ciliary dyskinesia
Autor: Munye, M. M.
Primary ciliary dyskinesia is a genetic disorder where patients develop lung disease as they are unable to clear airway infections effectively. There is currently no treatment for the underlying genetic defect. This thesis describes advances towards
Externí odkaz: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.631947
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2
Akademický článek
Achieving Endo/Lysosomal Escape Using Smart Nanosystems for Efficient Cellular Delivery.
Autor: Desai, Nimeet1 (AUTHOR) nimeet.desai@gmail.com, Rana, Dhwani2 (AUTHOR) dhwanirana73@gmail.com, Salave, Sagar2 (AUTHOR) sagarsalave1994@gmail.com, Benival, Derajram2 (AUTHOR) derajram@niperahm.res.in, Khunt, Dignesh3 (AUTHOR) digneshkhunt80@gmail.com, Prajapati, Bhupendra G.4,5 (AUTHOR) bhupen27@gmail.com
Publikováno v: Molecules. Jul2024, Vol. 29 Issue 13, p1-28. 28p. 2 Diagrams, 2 Charts, 4 Graphs.
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3
Akademický článek
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4
Akademický článek
Blood-brain barrier disruption in dementia: Nano-solutions as new treatment options.
Autor: Cooper CG; Department of Biology, Edge Hill University, Ormskirk, UK., Kafetzis KN; Department of Biology, Edge Hill University, Ormskirk, UK., Patabendige A; Department of Biology, Edge Hill University, Ormskirk, UK.; Liverpool Centre for Cardiovascular Science, University of Liverpool, Liverpool, UK., Tagalakis AD; Department of Biology, Edge Hill University, Ormskirk, UK.; UCL Great Ormond Street Institute of Child Health, University College London, London, UK.
Publikováno v: The European journal of neuroscience [Eur J Neurosci] 2024 Mar; Vol. 59 (6), pp. 1359-1385. Date of Electronic Publication: 2023 Dec 28.
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5
Akademický článek
Mutations in CFAP47, a previously reported MMAF causative gene, also contribute to the respiratory defects in patients with PCD.
Autor: Ge, Haijun1 (AUTHOR), Zhou, Wangji2 (AUTHOR), He, Miao1 (AUTHOR), Zheng, Haixia1 (AUTHOR), Zhao, Xinyue1 (AUTHOR), Zhang, Ting2 (AUTHOR), Zhang, Ying2 (AUTHOR), Shao, Chi2 (AUTHOR), Cheng, Chongsheng2 (AUTHOR), Liu, Yaping1 (AUTHOR) ypliu_pumc@163.com, Tian, Xinlun2 (AUTHOR) tianxl@pumch.cn, Xu, Kai‐Feng2 (AUTHOR), Zhang, Xue1 (AUTHOR) xuezhang@pumc.edu.cn
Publikováno v: Molecular Genetics & Genomic Medicine. Jan2024, Vol. 12 Issue 1, p1-10. 10p.
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6
Akademický článek
Functions of cilia in cardiac development and disease.
Autor: Shaikh Qureshi, Wasay Mohiuddin1 (AUTHOR), Hentges, Kathryn E.1 (AUTHOR) Kathryn.hentges@manchester.ac.uk
Publikováno v: Annals of Human Genetics. Jan2024, Vol. 88 Issue 1, p4-26. 23p.
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8
Akademický článek
A novel heterozygous variant of FOXJ1 in a Chinese female with primary ciliary dyskinesia and hydrocephalus: A case report and literature review.
Autor: Gao, Shiyang1 (AUTHOR) g13898199031@163.com, Zhang, Qianwen1 (AUTHOR), Feng, Biyun1 (AUTHOR), Gu, Shili1 (AUTHOR), Li, Zhiying1 (AUTHOR), Sun, Lianping2 (AUTHOR), Yao, Ru‐en3 (AUTHOR), Yu, Tingting3 (AUTHOR), Ding, Yu1 (AUTHOR) dingyuscmc@sohu.com, Wang, Xiumin1 (AUTHOR) wangxiumin1019@126.com
Publikováno v: Molecular Genetics & Genomic Medicine. Sep2023, Vol. 11 Issue 9, p1-9. 9p.
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10
Akademický článek
Minicircle Delivery to the Neural Retina as a Gene Therapy Approach.
Autor: Staurenghi, Federica1 (AUTHOR), McClements, Michelle E.1 (AUTHOR), Salman, Ahmed1 (AUTHOR), MacLaren, Robert E.1,2 (AUTHOR) enquiries@eye.ox.ac.uk
Publikováno v: International Journal of Molecular Sciences. Oct2022, Vol. 23 Issue 19, p11673. 11p.
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