Výsledky vyhledávání - "Bunjevački Vera"

Akademický článek

The level of knowledge retention and the attitude of students towards traditional and combined human genetics teaching

Autor: Petrušić Igor D., Radin Sonja P., Savković Zorica M., Bunjevački Vera I., Bajčetić Miloš I.

Publikováno v: Nastava i Vaspitanje, Vol 65, Iss 2, Pp 439-449 (2016)

The aim of this research was to compare knowledge retention and course satisfaction among the students who attended a combined teaching course (traditional form and online course) and those who attended only the traditional course in human genetics.

Externí odkaz: https://doaj.org/article/27952bf018bd4366bd915687885f6b1e

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Akademický článek

Possible influence of MTHFR C677T polymorphism on serum lipid levels in Serbian school children

Autor: Damnjanović Tatjana, Luković Ljiljana, Cvetković Dragana, Jekić Biljana, Bunjevački Vera, Maksimović Nela, Cvjetićanin Suzana, Majkić-Singh Nada, Slavko S., Novaković Ivana

Publikováno v: Archives of Biological Sciences, Vol 66, Iss 2, Pp 729-734 (2014)

The effect of 5,10-methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism on serum lipid profiles is controversial. We randomly selected 530 healthy schoolchildren that were included in the Yugoslav Study of the Precursors of Atherosc

Externí odkaz: https://doaj.org/article/e90020c868a04e52ab66f879d5677bfe

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Akademický článek

NPM1 gene mutations in children with Myelodysplastic syndromes

Autor: Jekić Biljana, Bunjevački Vera, Dobričić Valerija, Novaković Ivana, Milašin Jelena, Popović Branka, Damnjanović Tatjana, Maksimović Nela, Perović V., Luković Ljiljana

Publikováno v: Archives of Biological Sciences, Vol 63, Iss 3, Pp 649-653 (2011)

Myelodysplastic syndromes (MDS) are rare in children and only a few studies have analyzed their molecular mechanisms. The NPM1 gene encodes for nucleophosmin (NPM) which regulates hematopoiesis. Mutations in exon 12 of the NPM1 cause the nucleophosmi

Externí odkaz: https://doaj.org/article/f32720d0efec44eb89b664bb3e6228d8

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Akademický článek

Y chromosome microdeletions in infertile male candidates for microfertilization

Autor: Ristanović Momčilo, Bunjevački Vera, Tulić Cane, Novaković Ivana, Ille Tatjana, Radojković Dragica, Nikolić Aleksandra

Publikováno v: Srpski Arhiv za Celokupno Lekarstvo, Vol 136, Iss 3-4, Pp 126-130 (2008)

Introduction Y chromosome microdeletions are the second most frequent genetic cause of male infertility after Klinefelter's syndrome. Objective The aim of the study was to determine the frequency of Y chromosome microdeletions in a group of infertile

Externí odkaz: https://doaj.org/article/97b10bef63734130a60d66e765abd1ad

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