Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Kamila Reblova"'
Autor:
Martina Réblová, Miroslav Kolařík, Jana Nekvindová, Kamila Réblová, František Sklenář, Andrew N. Miller, Margarita Hernández-Restrepo
Publikováno v:
Journal of Fungi, Vol 7, Iss 12, p 1097 (2021)
The genus Codinaea is a phialidic, dematiaceous hyphomycete known for its intriguing morphology and turbulent taxonomic history. This polyphasic study represents a new, comprehensive view on the taxonomy, systematics, and biogeography of Codinaea and
Externí odkaz:
https://doaj.org/article/33e4b904040f4e01bfd501bab6db5c61
Autor:
Terezia Kurucova, Kamila Reblova, Pavlina Janovska, Jakub Pawel Porc, Veronika Navrkalova, Sarka Pavlova, Jitka Malcikova, Karla Plevova, Boris Tichy, Michael Doubek, Vitezslav Bryja, Jana Kotaskova, Sarka Pospisilova
Publikováno v:
Molecular Oncology, Vol 18, Iss 10, Pp 2541-2553 (2024)
Early identification of resistant cancer cells is currently a major challenge, as their expansion leads to refractoriness. To capture the dynamics of these cells, we made a comprehensive analysis of disease progression and treatment response in a chr
Externí odkaz:
https://doaj.org/article/c833416f75ab4151874dbe6f3b782ba0
Autor:
Daniela Skálová, Jana Zídková, Stanislav Voháňka, Radim Mazanec, Zuzana Mušová, Petr Vondráček, Lenka Mrázová, Josef Kraus, Kamila Réblová, Lenka Fajkusová
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e82549 (2013)
Myotonia congenita (MC) is a genetic disease caused by mutations in the skeletal muscle chloride channel gene (CLCN1) encoding the skeletal muscle chloride channel (ClC-1). Mutations of CLCN1 result in either autosomal dominant MC (Thomsen disease) o
Externí odkaz:
https://doaj.org/article/9653d61cf48c46f79d6d9e29cb829433
Autor:
Katerina Stano Kozubik, Lenka Radova, Kamila Reblova, Michal Smida, Marketa Zaliova Kubricanova, Jiri Baloun, Michaela Pesova, Zuzana Vrzalova, Frantisek Folber, Sona Mejstrikova, Sarka Pospisilova, Michael Doubek
Publikováno v:
Platelets, Vol 32, Iss 6, Pp 838-841 (2021)
Germline mutations in ETV6 gene cause inherited thrombocytopenia with leukemia predisposition. Here, we report on functional validation of ETV6 W380R mutation segregating with thrombocytopenia in a family where two family members also suffered from a
Externí odkaz:
https://doaj.org/article/df06206cdabd4b8b86d66e3bdd0b8058
Autor:
Veronika Kanderova, Hana Grombirikova, Irena Zentsova, Kamila Reblova, Adam Klocperk, Martina Fejtkova, Marketa Bloomfield, Barbora Ravcukova, Tomas Kalina, Tomas Freiberger, Anna Sediva
Publikováno v:
Haematologica, Vol 104, Iss 1 (2019)
Externí odkaz:
https://doaj.org/article/e499ab134e854d8c9b7d672745285506
Publikováno v:
The Scientific World Journal, Vol 1, Pp 122-122 (2001)
Externí odkaz:
https://doaj.org/article/f0f9f99df26c4a9bb1fdceef020eb3eb
Autor:
Katerina Stano, Kozubik, Lenka, Radova, Kamila, Reblova, Michal, Smida, Marketa, Zaliova Kubricanova, Jiri, Baloun, Michaela, Pesova, Zuzana, Vrzalova, Frantisek, Folber, Sona, Mejstrikova, Sarka, Pospisilova, Michael, Doubek
Publikováno v:
Platelets. 32(6)
Germline mutations in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::38169227838a163812f7506f59fdcaab
https://pubmed.ncbi.nlm.nih.gov/32819174
https://pubmed.ncbi.nlm.nih.gov/32819174
Autor:
Terézia Kurucová, Kamila Réblová, Martina Vališová, Jakub Paweł Porc, Veronika Navrkalová, Šárka Pavlová, Jitka Malčíková, Karla Plevová, Boris Tichý, Michael Doubek, Jana Kotašková, Šárka Pospíšilová
Publikováno v:
HemaSphere, Vol 7, p e16660f0 (2023)
Externí odkaz:
https://doaj.org/article/fbb3849734a54002a8a3828164028c77
Autor:
Lucie Ballonová, Přemysl Souček, Peter Slanina, Kamila Réblová, Ondřej Zapletal, Marcela Vlková, Roman Hakl, Viktor Bíly, Hana Grombiříková, Eliška Svobodová, Petra Kulíšková, Julie Štíchová, Marta Sobotková, Radana Zachová, Jana Hanzlíková, Martina Vachová, Pavlína Králíčková, Irena Krčmová, Miloš Jeseňák, Tomáš Freiberger
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Hereditary angioedema (HAE) is a rare genetic disorder with variable expressivity even in carriers of the same underlying genetic defect, suggesting other genetic and epigenetic factors participate in modifying HAE severity. Recent knowledge indicate
Externí odkaz:
https://doaj.org/article/1d1b0d48084f450184f9a098e21c6523
Publikováno v:
SPIE Proceedings.
Photodynamic therapy is a treatment that is used for destruction of certain tumors. The treatment is performed with photosensitizers that generate reactive oxygen species in the presence of light and oxygen. The absorption and fluorescence spectra of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6dda243a157a05cfb636b7e072c837e8
https://doi.org/10.1117/12.446710
https://doi.org/10.1117/12.446710