Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Michaela Pesova"'
Autor:
Veronika Mancikova, Michaela Pesova, Sarka Pavlova, Robert Helma, Kristyna Zavacka, Vaclav Hejret, Petr Taus, Jakub Hynst, Karla Plevova, Jitka Malcikova, Sarka Pospisilova
Publikováno v:
Molecular Oncology, Vol 17, Iss 1, Pp 82-97 (2023)
TP53 gene abnormalities represent the most important biomarker in chronic lymphocytic leukemia (CLL). Altered protein modifications could also influence p53 function, even in the wild‐type protein. We assessed the impact of p53 protein phosphorylat
Externí odkaz:
https://doaj.org/article/d23f7fd800de4b44a79aa2866eceb35e
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 Mancikova, Michaela Pesova, Sarka Pavlova, Robert Helma, Kristyna Zavacka, Vaclav Hejret, Petr Taus, Jakub Hynst, Karla Plevova, Jitka Malcikova, Sarka Pospisilova
Publikováno v:
MOLECULAR ONCOLOGY
TP53 gene abnormalities represent the most important biomarker in chronic lymphocytic leukemia (CLL). Altered protein modifications could also influence p53 function, even in the wild-type protein. We assessed the impact of p53 protein phosphorylatio
Autor:
null Veronika Mancikova, null Michaela Pesova, null Sarka Pavlova, null Robert Helma, null Kristyna Zavacka, null Vaclav Hejret, null Petr Taus, null Jakub Hynst, null Karla Plevova, null Jitka Malcikova, null Sarka Pospisilova
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c701c231e672495f249bb95db5df114
https://doi.org/10.1002/1878-0261.13337/v2/response1
https://doi.org/10.1002/1878-0261.13337/v2/response1
Autor:
Šárka Pospíšilová, Jiri Baloun, Sona Mejstrikova, Marketa Zaliova Kubricanova, František Folber, Michael Doubek, Lenka Radová, Zuzana Vrzalová, Katerina Stano Kozubik, Michal Šmída, Michaela Pesova, Kamila Réblová
Publikováno v:
Platelets. 32:838-841
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
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
Autor:
Jakub Trizuljak, Kateřina Staňo Kozubík, Lenka Radová, Michaela Pešová, Karol Pál, Kamila Réblová, Olga Stehlíková, Petr Smejkal, Jiřina Zavřelová, Milan Pacejka, Jiří Mayer, Šárka Pospíšilová, Michael Doubek
Publikováno v:
Platelets, Vol 29, Iss 8, Pp 827-833 (2018)
Mutations in the GP1BA gene have been associated with platelet-type von Willebrand disease and Bernard-Soulier syndrome. Here, we report a novel GP1BA mutation in a family with autosomal dominant macrothrombocytopenia and mild bleeding. We performed
Externí odkaz:
https://doaj.org/article/5689635ac7c94c4a9194ae805cf5ba1d