Molecular cloning of YinP gene from Leishmania major using two red fluorescent pXG-mCherry plasmids. Valuable tools for gene expression location.

Charles University in Prague Faculty of Pharmacy in Hradec Králové Department of Biochemical Sciences Candidate: Kateřina Musilová Supervisor: Prof. Ing. Vladimír Wsól, Ph.D. Tutor: Prof. Paul Nguewa, Ph.D. Title of diploma thesis: Molecular cloning of YinP gene from Leishmania major using two red f...

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Main Author: Musilová, Kateřina
Other Authors: Wsól, Vladimír
Format: Dissertation
Language:English
Published: 2016
Online Access:http://www.nusl.cz/ntk/nusl-344048
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spelling ndltd-nusl.cz-oai-invenio.nusl.cz-3440482017-06-28T04:20:27Z Molecular cloning of YinP gene from Leishmania major using two red fluorescent pXG-mCherry plasmids. Valuable tools for gene expression location. Musilová, Kateřina Wsól, Vladimír Štambergová, Hana Charles University in Prague Faculty of Pharmacy in Hradec Králové Department of Biochemical Sciences Candidate: Kateřina Musilová Supervisor: Prof. Ing. Vladimír Wsól, Ph.D. Tutor: Prof. Paul Nguewa, Ph.D. Title of diploma thesis: Molecular cloning of YinP gene from Leishmania major using two red fluorescent pXG-mCherry plasmids. Valuable tools for gene expression location. In the 21st century, leishmaniasis remains a major health problem in numerous de- veloping countries. Around 2 million cases of leishmaniasis are reported every year and estimated mortality is over 20,000 deaths annually. Antileishmanial drugs are often unaf- fordable for affected people and display severe toxic side effects. Potent human vaccines are not available. This, together with increasing resistance, is a reason why new effective, safe, and affordable medicines are greatly needed. Leishmaniasis is caused by Leishmania species. These parasites are transmitted by phlebotomine sand flies, which also provide to the leishmania environment necessary for their development into infective forms. The process of transformation into a stage in- fective for vertebrate hosts is called metacyclogenesis. Nowadays, genes, enzymes, and proteins possibly exhibiting a function in the metacyclogenesis are extensively examined. One of the... 2016 info:eu-repo/semantics/masterThesis http://www.nusl.cz/ntk/nusl-344048 eng info:eu-repo/semantics/restrictedAccess
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language English
format Dissertation
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description Charles University in Prague Faculty of Pharmacy in Hradec Králové Department of Biochemical Sciences Candidate: Kateřina Musilová Supervisor: Prof. Ing. Vladimír Wsól, Ph.D. Tutor: Prof. Paul Nguewa, Ph.D. Title of diploma thesis: Molecular cloning of YinP gene from Leishmania major using two red fluorescent pXG-mCherry plasmids. Valuable tools for gene expression location. In the 21st century, leishmaniasis remains a major health problem in numerous de- veloping countries. Around 2 million cases of leishmaniasis are reported every year and estimated mortality is over 20,000 deaths annually. Antileishmanial drugs are often unaf- fordable for affected people and display severe toxic side effects. Potent human vaccines are not available. This, together with increasing resistance, is a reason why new effective, safe, and affordable medicines are greatly needed. Leishmaniasis is caused by Leishmania species. These parasites are transmitted by phlebotomine sand flies, which also provide to the leishmania environment necessary for their development into infective forms. The process of transformation into a stage in- fective for vertebrate hosts is called metacyclogenesis. Nowadays, genes, enzymes, and proteins possibly exhibiting a function in the metacyclogenesis are extensively examined. One of the...
author2 Wsól, Vladimír
author_facet Wsól, Vladimír
Musilová, Kateřina
author Musilová, Kateřina
spellingShingle Musilová, Kateřina
Molecular cloning of YinP gene from Leishmania major using two red fluorescent pXG-mCherry plasmids. Valuable tools for gene expression location.
author_sort Musilová, Kateřina
title Molecular cloning of YinP gene from Leishmania major using two red fluorescent pXG-mCherry plasmids. Valuable tools for gene expression location.
title_short Molecular cloning of YinP gene from Leishmania major using two red fluorescent pXG-mCherry plasmids. Valuable tools for gene expression location.
title_full Molecular cloning of YinP gene from Leishmania major using two red fluorescent pXG-mCherry plasmids. Valuable tools for gene expression location.
title_fullStr Molecular cloning of YinP gene from Leishmania major using two red fluorescent pXG-mCherry plasmids. Valuable tools for gene expression location.
title_full_unstemmed Molecular cloning of YinP gene from Leishmania major using two red fluorescent pXG-mCherry plasmids. Valuable tools for gene expression location.
title_sort molecular cloning of yinp gene from leishmania major using two red fluorescent pxg-mcherry plasmids. valuable tools for gene expression location.
publishDate 2016
url http://www.nusl.cz/ntk/nusl-344048
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