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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 ...
Est-ssrs developed for other picea species amplify in picea omorika and reveal high genetic variation in two natural populations
(Soc Royal Botan Belgique, Meise, 2009)
Picea omorika (Pane.) Purk. is a relict and an endemic species found exclusively in the Balkan, within an area of ca. 10 000 km(2). Marker-based genetic diversity data in this conifer are very limited and partially ...
Response to salbutamol in children with acute asthma exacerbations
(Paediatria Croatica, 2012)
The aim of this study was to investigate response to salbutamol in children with acute asthma exacerbations in order to estimate the efficiency and safety of its administration in pediatric population. The study included ...
Molecular and biochemical characterization of Pseudomonas putida isolated from bottled uncarbonated mineral drinking water (vol 66, pg 23, 2014)
(Srpsko biološko društvo, Beograd, i dr., 2016)
Functional and structural characterisation of 5 missense mutations of the phenylalanine hydroxylase
(General Physiol And Biophysics, Bratislava, 2017)
Phenylketonuria (PKU) and hyperphenylalaninemia (HPA) are a group of genetic disorders predominantly caused by mutations in the phenylalanine hydroxylase (PAH) gene. To date, more than 950 variants have been identified, ...
Ankrd1-mediated signaling is supported by its interaction with zonula occludens-1
(Srpsko biološko društvo, Beograd, i dr., 2014)
The muscle ankyrin repeat protein Ankrd1 is localized in a mechanosensory complex of the sarcomeric I-band. It is involved in signaling pathways activated in response to mechanical stretch. It also acts as a transcriptional ...
Analysis of CFTR Gene Variants in Idiopathic Bronchiectasis in Serbian Children
(Mary Ann Liebert, Inc, New Rochelle, 2013)
This study has investigated a potential role of common Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene variants in the etiology of noncystic fibrosis bronchiectasis in Serbian children. The study has ...
Hirurško lečenje kolorektalnog karcinoma u Srbiji od 2010. do 2014. godine - procena registara više centara / Colorectal cancer surgery in Serbia 2010-2014: An evaluation of a multicenter registry
(Vojnomedicinska akademija - Institut za naučne informacije, Beograd, 2021)
Uvod/Cilj. Hirurški registri i baze podataka su posebno vredni za praćenje karakteristika lečenja i otkrivanje potencijalnih problema kod karcinoma. Za bolesnike sa kolorektalnim karcinomom (KRK) u Srbiji, podaci o primljenoj ...
JAK2V617F mutacija kod bolesnika sa B ćelijskom hroničnom limfocitnom leukemijom i prefibrotičkom primarnom mijelofibrozom / JAK2V617F mutation in a patient with B-cell chronic lymphocytic leukemia and prefibrotic primary myelofibrosis
(Srpsko lekarsko društvo, Beograd, 2015)
Uvod Sekundarni maligniteti, naročito solidni tumori, česti su kod bolesnika s hroničnom limfocitnom leukemijom (HLL), ali retko se sreće udruženost mijeloproliferativnih neoplazmi i HLL. Prikaz bolesnika Prikazujemo ...