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Приказ резултата 41-50 од 436
Prognostic Impact of NPM1 Mutations in Serbian Adult Patients with Acute Myeloid Leukemia
(Karger, Basel, 2012)
Based on current findings, the presence of NPM1 mutations in acute myeloid leukemia (AML) patients is associated with an increased probability of complete remission (CR) and better overall survival (OS). We determined the ...
Interaction between insulin and estradiol in regulation of cardiac glucose and free fatty acid transporters
(Hormone and Metabolic Research, 2011)
The estrogen binding to specific extranuclear receptors (ER) activates several intracellular pathways that are activated by insulin as well. Moreover, insulin and estradiol (E2) influence cardiac energy substrates, blood ...
Analiza sekundarne strukture u okviru sgm i kgmB mRNA / Analysis of secondary structure within sgm and kgmB mRNA
(Srpsko biološko društvo, Beograd, i dr., 2010)
Sgm metiltransferaza iz soja Micromonospora zionensis i KgmB metiltransferaza iz soja Streptoalloteichus tenebrarius ostvaruju rezistenciju na aminoglikozidne antibiotike metilacijom nukleotida na poziciji G1405 u okviru ...
Inherited Thrombophilia is Associated With Pregnancy Losses That Occur After 12th Gestational Week in Serbian Population
(Sage Publications Inc, Thousand Oaks, 2010)
Recurrent fetal loss (RFL) is a significant clinical problem, occurring in 1% to 5% of reproductive females. Inherited or acquired thrombophilia has been diagnosed in 50% to 65% of women with history of unexplained fetal ...
A note on the earliest distribution, cultivation and genetic changes in bitter vetch (vicia ervilia) in ancient Europe
(Društvo genetičara Srbije, Beograd, 2015)
Bitter vetch (Vicia ervilia (L.) Willd.) was a part of the everyday diet of the Eurasian Neanderthal population and the modern human Palaeolithic hunter-gatherers at the end of the last Ice Age. The major criteria to ...
Acute myeloid leukemia with NUP98-HOXC13 fusion and FLT3 internal tandem duplication mutation: case report and literature review
(Elsevier Science Inc, New York, 2009)
The NUP98 gene at chromosome band 11p15 is known to be fused to a number of different partners in various hematological malignancies. The most frequently observed fusion partners of NUP98 are the homeobox family of ...
Type and Location of Venous Thromboembolism in Carriers of Factor V Leiden or Prothrombin G20210A Mutation Versus Patients With No Mutation
(Sage Publications Inc, Thousand Oaks, 2010)
Factor V Leiden (FVLeiden) and prothrombin G20210A are the most common genetic causes of thrombophilia and established risk factors for different clinical manifestations of venous thromboembolism (VTE). This study investigated ...
Extreme sensitivity to acenocoumarol therapy in patient with both VKORC.-1639 A/A and CYP2C9*1/*3 genotypes
(Springer, Dordrecht, 2011)
The initiation phase of vitamin K antagonist (VKA) is a challenging and demanding process that can result in adverse event such as bleeding. Dosing is influenced by a variety of acquired factors, while another factor that ...
Alpha-1-Antitrypsin Deficiency in Serbian Adults with Lung Diseases
(Mary Ann Liebert, Inc, New Rochelle, 2012)
Aim: Alpha-1-antitrypsin (A1AT) is the main inhibitor of neutrophil elastase, and severe alpha-1-antitrypsin deficiency (A1ATD) is a genetic risk factor for early-onset emphysema. Despite the relatively high prevalence of ...
The presence of prothrombotic mutations and a higher FVIII activity contribute to thrombosis development during the breast cancer treatment
(Pergamon-Elsevier Science Ltd, Oxford, 2014)