Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jana Michalova"'
Publikováno v:
Developmental & Comparative Immunology. 36:385-389
Adult B-lymphopoiesis is suppressed by the inhibitory effects of elevated estrogens during pregnancy. At the same time, hematopoietic cells in the fetal liver are resistant to this suppression by estrogens and ensure active production of B-cells. We
Autor:
Emanuel Necas, Katarina Forgacova, Katerina Faltusova, Filipp Savvulidi, Jana Michalova, Ludek Sefc
Publikováno v:
Biology of Blood and Marrow Transplantation. 17(9):1273-1281
Hematopoietic stem and progenitor cells (HSPC) for bone marrow transplantation are currently obtained directly from living voluntary donors or from cord blood units. However, a suitable donor is not always found. Because HSPC are known for their rela
Publikováno v:
Chimerism. 2:86-87
Every year, bone marrow transplantation saves many lives worldwide. Unfortunately, a suitable donor is not always available. Since organs are routinely harvested from cadaveric organ donors, we decided to assess such a possibility for bone marrow. We
Autor:
Emanuel Necas, Katarina Forgacova, Katerina Faltusova, Ludek Sefc, Filipp Savvulidi, Ko-Tung Chang, Jana Michalova
Publikováno v:
Blood. 116:4694-4694
Abstract 4694 Background: Quiescent hematopoietic stem cells (HSCs) located in stem cell niches are characterized by a relative resistance to hypoxia. This study is focused primarily on maintainance of the repopulating ability of HSCs in structurally
Autor:
Emanuel Necas, Filipp Savvulidi, Jana Michalova, Ludek Sefc, Forgacova Katarina, Ko-Tung Chang
Publikováno v:
ResearcherID
Abstract 3713 Introduction: Therapeutic bone marrow transplantation (BMT) is usually performed 0–2 days after a conditioning treatment. Our aim was to determine the „transplantation window“, i.e. for how long after conditioning by irradiation a
Autor:
Tomáš Zima, Gabriela Dostálová, Vladimír Tesař, Petr Přikryl, Lucie Vojtova, Jana Michalova, Aleš Linhart
Publikováno v:
ResearcherID
Anderson-Fabry disease (AFD) is an X-linked genetic disorder with deficient α-galactosidase A activity. The main aim of this work was to investigate possible differences in urine proteins between healthy controls and AFD patients and to identify abn
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