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Identification of miRNAs and their potential targets in halophyte plant Thellungiella halophila

100%

Panahi B., Mohammadi S. A., Ebrahimie E.

BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology

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2013

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tom 94

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nr 3

2

Improvement of the strain for the rapid identification of genes encoding restriction and modification enzymes

100%

Piekarowicz A., Weglenska A.

Acta Microbiologica Polonica

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1994

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tom 43

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nr 2

3

Effect of acute exercise on mRNA and protein expression of main components of the lipolytic complex in different skeletal muscle types in the rat

84%

Miklosz A., Baranowski M., Lukaszuk B., Zabielski P., Chabowski A., Gorski J.

Journal of Physiology and Pharmacology

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2019

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tom 70

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nr 3

4

Gene expression profiling in peripheral blood nuclear cells in patients with refractory ischaemic end-stage heart failure

84%

Szmit S., Jank M., Maciejewski H., Grabowski M., Glowczynska R., Majewska A., Filipiak K. J., Motyl T., Opolski G.

Journal of Applied Genetics

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2010

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tom 51

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nr 3

Functional analysis of up- and down-regulated genes might reveal whether peripheral blood cells may be considered as a material of diagnostic or prognostic value in patients with end-stage heart failure (HF). The aim of the present study was to compare the transcriptomic profile of peripheral blood nuclear cells from 6 male patients with ischaemic end-stage HF with those of 6 male patients with asymptomatic cardiac dysfunction. The expression of genes in peripheral blood nuclear cells in both groups of patients was measured using whole-genome oligonucleotide microarrays utilizing 35 035 oligonucleotide probes. Microarray analyses revealed 130 down-regulated genes and 15 up-regulated genes in the patients with end-stage HF. Some of the down-regulated genes belonged to the pathways that other studies have shown to be down-regulated in cardiomyopathy. We also identified up-regulated genes that have been correlated with HF severity (CXCL16) and genes involved in the regulation of expression of platelet activation factor receptor (PTAFR, RBPSUH, MCC, and PSMA7). In conclusion, the identification of genes that are differentially expressed in peripheral blood nuclear cells of patients with HF supports the suggestion that this diagnostic approach may be useful in searching for the molecular predisposition for development of severe refractory HF in patients with post-infarction asymptomatic abnormalities and remodelling of the left ventricle. These results need further investigation and validation.

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Genetic associations of reproductive traits in pigs

67%

Kumalska M., Terman A.

Annals of Warsaw University of Life Sciences - SGGW. Animal Science

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2017

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tom 56[2]

Genetic associations of reproductive traits in pigs. In the field of genetics, one of the main research area in relation to animal reproduction is the identification of genes or genomic regions influencing reproductive phenotypes. The genes analysed for the determinants of their fertility are among other: LEP, PRL, PRLR, RBP4. With the use of genetic markers, it is possible to identify of both males and females carrying beneficial alleles, and choose reproduce high-quality individuals, which in turn accelerates the genetic improvement of the examined feature. According to literature, about 30% of culling in pig production systems has been primarily due to reproductive problems. Litter size is very important and easily measured reproductive trait, and often included in scientific researches, and defined as the total number of piglets born (TNB) and the number of piglets born alive (NBA). Selection of individuals carrying favourable alleles has the potential to improve reproductive traits and in this connection also sow productive life (SPL). SLP is a measure of the longevity and reproductive performance of a sow and is directly related to the number of viable piglets produced during its lifespan. Because reproductive traits are so multifaceted, researchers are able to consider many different facets of the organism biology to come up with candidate genes and QTLs genes.

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Identyfikacja genow karlowatosci w polskich odmianach pszenicy jarej

67%

Kowalczyk K., Chrzastek M., Miazga D.

Biuletyn Instytutu Hodowli i Aklimatyzacji Roślin

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1999

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nr 211

35-38

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Identifying the grain chalkiness gene using molecular marker techniques in rice (Oryza sativa L.)

67%

Thi Lang N., Ho Truc Giang P., Thi Thu Ha P., Bao Toan T., Anh Phuong T., Chi Buu B.

International Letters of Natural Sciences

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2017

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tom 63

Chalkiness is a major constraint on rice production because it is one of the key factors determining grain quality (appearance, processing, milling, storing, eating, and cooking quality) and price. In this study, we conducted grain chalkiness gene identification using co-dominant insertion/deletion (INDEL) markers and SSR marker combination on 50 different varieties. The application results in 7 InDel markers and SSR marker on chromosome 7 were recorded. Three primers, InDel 5, InDel 14 and RM21938, associated with grain chalkiness. For the InDel 5 primer, the amplification product was 100%. Use of primer InDel 5 in detection and evaluation of genotype to the chalkiness trait of rice grain on 50 rice varieties indicated the suitability level with phenotypic evaluation was 86% and the unsuitability level was 14%. For the InDel 14 primer, the amplification products were 100%. The suitability with phenotypic assessment was 84% and the unsuitability was 16%. For the RM21938 primer, the amplification product was 94%. The suitability with phenotypic assessment was 76% and the unsuitability was 24%. Thirteen of the selected varieties had grain chalkiness gene both InDel 5, InDel 14 and RM21938. Total 13 varieties were detected from InDel 5, InDel 14 and RM12938 primer combinations also showed high efficiency of the InDel technique in identifying chalkiness gene in rice grain. A cluster analysis was performed and a dendrogram was constructed which evinced the nature of phylogenetic classification among the genotypes of the varieties. These markers could be used for developing quality of rice in breeding program.

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Identyfikacja genow karlowatosci niewrazliwych na egzogenny kwas giberelinowy w polskich odmianach i rodach pszenicy ozimej oraz karlowych mutantach pszenzyta ozimego

59%

Kowalczyk K., Miazga D., Grzesik H.

Biuletyn Instytutu Hodowli i Aklimatyzacji Roślin

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1997

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nr 203

31-36

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Identyfikacja genu odpornosci na rdze zolta Yr9 za pomoca testu zywiciel-patogen i markerow DNA w polskich odmianach pszenicy zwyczajnej

51%

Kowalczyk K., Hsam S. L. K., Zeller F. J.

Zeszyty Problemowe Postępów Nauk Rolniczych

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2007

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tom 517

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nr 1

439-446

W pracy inokulowano dwoma izolatami rdzy żółtej (Puccinia striiformis Westend f. sp. tritici) GR2 i GR5, 70 polskich odmian pszenicy zwyczajnej. Jako formy kontrolne zastosowano odmiany: Vuka (podatna na porażenie) oraz Disponent zawierającą geny Yr9. Na podstawie przeprowadzonych badań wykazano, że odmiany: Aleta, Jubilatka, Lama, Lanca, Olma, Weneda, Wilga oraz odmiana kontrolna Disponent były odporne na porażenie przez izolaty GR2 i GR5. Za pomocą markerów STS-PCR stwierdzono obecność translokacji 1BL/1RS w tych odmianach. Na podstawie przeprowadzonych badań wykazano, że polskie odmiany pszenicy zwyczajnej: Aleta, Jubilatka, Lama, Lanca, Olma, Weneda oraz Wilga zawierają geny odporności na rdzę żółtą Yr9.

Ograniczanie wyników

Identification of miRNAs and their potential targets in halophyte plant Thellungiella halophila

Improvement of the strain for the rapid identification of genes encoding restriction and modification enzymes

Effect of acute exercise on mRNA and protein expression of main components of the lipolytic complex in different skeletal muscle types in the rat

Gene expression profiling in peripheral blood nuclear cells in patients with refractory ischaemic end-stage heart failure

Genetic associations of reproductive traits in pigs

Identyfikacja genow karlowatosci w polskich odmianach pszenicy jarej

Identifying the grain chalkiness gene using molecular marker techniques in rice (Oryza sativa L.)

Identyfikacja genow karlowatosci niewrazliwych na egzogenny kwas giberelinowy w polskich odmianach i rodach pszenicy ozimej oraz karlowych mutantach pszenzyta ozimego

Identyfikacja genu odpornosci na rdze zolta Yr9 za pomoca testu zywiciel-patogen i markerow DNA w polskich odmianach pszenicy zwyczajnej