Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Lucie Piterkova"'
Autor:
Nikica Ljubas Tomasic, Lucie Piterkova, Chad Huff, Ernest Bilic, Donghoon Yoon, Galina Y. Miasnikova, Adelina I. Sergueeva, Xiaomei Niu, Sergei Nekhai, Victor Gordeuk, Josef T. Prchal
Publikováno v:
Haematologica, Vol 98, Iss 4 (2013)
Mutations of VHL (a negative regulator of hypoxia-inducible factors) have position-dependent distinct cancer phenotypes. Only two known inherited homozygous VHL mutations exist and they cause polycythemia: Chuvash R200W and Croatian H191D. We report
Externí odkaz:
https://doaj.org/article/adef9eac38274f7f83d77908abbec6d2
Publikováno v:
Czech Journal of Food Sciences. 22:1-8
The growth kinetics of thermophilic bacteria Bacillus acidocaldarius (CCM 3497), Bacillus stearothermophilus (CCMI 237), Thermus aquaticus (CCM 3488), Thermus ruber (CCM 4212), and Thermus species (CCM 4199) on solid media were studied in the tempera
Autor:
Lucie Piterkova, Nikica Ljubas Tomasic, Adelina I. Sergueeva, Chad D. Huff, Victor R. Gordeuk, Xiaomei Niu, Galina Y. Miasnikova, Josef T. Prchal, Sergei Nekhai, Donghoon Yoon, Ernest Bilić
Mutations of VHL (a negative regulator of hypoxia-inducible factors) have position-dependent distinct cancer phenotypes. Only two known inherited homozygous VHL mutations exist and they cause polycythemia: Chuvash R200W and Croatian H191D. We report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e65d848d14cd59d969b9a93c21b8f5f0
https://doi.org/10.3324/haematol.2012.070508
https://doi.org/10.3324/haematol.2012.070508
Autor:
Charles J. Parker, Kimberly Hickman, Sue Hammoud, Andrew Wilson, Neeraj Agarwal, Josef T. Prchal, Bradley R. Cairns, Sabina Swierczek, Lucie Piterkova, Jaroslav Jelinek
Publikováno v:
Blood. 119(13)
Clonality can be established by a lack of mosaicism in a female because of random inactivation of either the maternal or paternal X chromosome early in embryogenesis. The methylation status of CpG sites close to the trinucleotide repeats in exon 1 of
Autor:
Sabina Swierczek, Lucie Piterkova, Linghua Wang, Kimberly Hickman, Josef T. Prchal, David A. Wheeler
Publikováno v:
Blood. 120:705-705
Abstract 705 Polycythemia vera (PV) is a clonally derived hematopoietic malignancy arising from a multipotent hematopoietic stem cell (HSC). Almost all patients have the acquired somatic mutation, JAK2V617F. There is strong evidence suggesting that t
Autor:
Richard A. Drachtman, Lucie Piterkova, Josef T. Prchal, Felipe R. Lorenzo, Hari Vankalayapati
Publikováno v:
Blood. 120:2081-2081
Abstract 2081 There are two known homozygous VHL gene mutations causing polycythemia that are not associated with a VHL cancer syndrome - an R200W mutation endemic in Chuvashia causing the first recognized disorder of augmented hypoxia sensing in nor
Autor:
Linzhao Cheng, Zhaohui Ye, Linghua Wang, Hakon Hakonarson, Lifeng Tian, Lucie Piterkova, Josef T. Prchal, David A. Wheeler
Publikováno v:
Blood. 120:1755-1755
Abstract 1755 Polycythemia vera (PV) is an acquired clonal hematopoietic disorder characterized by the JAK2V617F somatic mutation, which, however, constitutes only a variable part of the PV clone. Even within the JAK2V617F subclone, heterozygous and
Autor:
Sabina Swierczek, Bin Kuan Chou, Sarah N. Dowey, Zhaohui Ye, Linzhao Cheng, Jerry L. Spivak, Xiaosong Huang, Lucie Piterkova, Cyndi F. Liu, Alison R. Moliterno, Josef T. Prchal
Publikováno v:
Blood. 118:2826-2826
Abstract 2826 Polycythemia vera (PV) is a clonal blood disorder arising from a multipotent hematopoietic stem cell (HSC) associated in ∼95% of patients with the acquired somatic mutation, JAK2 V617F. Although important for the PV phenotype, we and
Autor:
Lucie Piterkova, Martina Partschova, Karel Indrak, Renata Mojzikova, Monika Horvathova, Vladimir Divoky, Dagmar Pospisilova, Pavla Pospisilova, Zuzana Laluhova Striezencova, Martina Divoka, Jaroslav Cermak
Publikováno v:
Blood. 118:5307-5307
Abstract 5307 Background: Thalassemias are rare disorders in Middle Europe. However, as a result of historical and recent migration, thalassemias became common cause of congenital anemia in the Czech and Slovak populations. Abnormal hemoglobin varian
Publikováno v:
Blood. 116:2073-2073
Abstract 2073 We have previously described a unique etiology of β-thalassemia due retrotransposon LINE-1 (L1) insertion into the intron-2 of the β-globin gene in a mother and daughter of Ukrainian descent who exhibited typical laboratory features o