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The c20068t gene variant in the 3 ' end of the prothrombin gene and recurrent pregnancy loss: a pilot study
(Društvo genetičara Srbije, Beograd, 2015)
Recurrent pregnancy loss (RPL) is a health problem affecting up to 5% of women of reproductive age. Several thrombophilic risk factors might contribute to RPL. To investigate relationship between a novel C20068T gene variant ...
Molecular tools for utilization of mitochondrial diversity in faba bean (vicia faba)
(Društvo genetičara Srbije, Beograd, 2014)
We performed in silico PCR analyses utilizing complete mitochondrial (mtDNA) genome sequences of faba bean (Vicia faba) and two related species, Vigna angularis and Vigna radiata, currently available in GenBank, to infer ...
Genetičko predviđanje hemofilije analizom int18/BclI RFLP / Genetic prediction of hemophilia a by int18/BclI RFLP analysis
(Društvo genetičara Srbije, Beograd, 2000)
Hemofilija A je X vezana bolest, koja se javlja sa učestalošću od 1 do 2 na 10000 muškaraca. Ona predstavlja najčešći koagulacioni poremećaj i izazvana je mutacijama u genu koji kodira osmi faktor koagulacije (FVIII). Nakon ...
Mutacije FV Leiden, FII G20210A i MTHFR C677T kao faktori rizika za nastanak tromboze dubokih vena gornjih i donjih ekstremiteta / FV Leiden, FII G20210A and MTHFR C677T mutations in patients with lower or upper limb deep vein thrombosis
(Društvo genetičara Srbije, Beograd, 2011)
Tromboze dubokih vena (TDV) su multifaktorijalno oboljenje koje se javlja sa učestalošću 1/1000 stanovnika godišnje. Mutacije FV Leiden, FII G20210A i MTHFR C677T predstavljaju genetske faktore za nastanak venskih tromboza. ...
Molecular genetic strategy for diagnosis of congenital adrenal hyperplasia in Serbia
(Društvo genetičara Srbije, Beograd, 2017)
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is one of the most common endocrine diseases, yet genetic diagnosis is among the most complicated of all monogenic disorders. It has an overall incidence ...
Cross-species amplification of nuclear est-microsatellites developed for other pinus species in pinus nigra
(Društvo genetičara Srbije, Beograd, 2015)
Due to the current lack of nuclear microsatellites (simple sequence repeats SSRs) specifically developed for Pinus nigra, an important European coniferous species, we cross-species amplified 12 EST-SSRs (expressed sequence ...
Characterization of lactic acid bacteria isolated from Bosnian artisanal dry fermented sausage sudzuk) during fermentation
(Društvo genetičara Srbije, Beograd, 2015)
Bosnian sudzuk is a dry fermented sausage produced in a rural household near the town of Visoko in central Bosnia and Herzegovina. This kind of sausage was manufactured only from beef and spices in a traditional way without ...
The frequencies of fv leiden and fii g20210a mutations in patients with different clinical manifestations of venous thromboembolism: experience from large Serbian cohort
(Društvo genetičara Srbije, Beograd, 2016)
Venous thromboembolism is a multifactorial disorder with two manifestations: deep-vein thrombosis and pulmonary embolism. Pulmonary embolism is usually considered as the complication of deep-vein thrombosis, but there are ...
Physiological and gene expression changes during imbibition in maize seeds under low temperature conditions
(Društvo genetičara Srbije, Beograd, 2021)
Maize is one of the most important crop species worldwide, but also extremely susceptible to the effects of increasingly higher temperatures and drought during the summer and its flowering and grain filling stage. Different ...