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Tytuł:
Genetic variability and host specialization in Alternaria alternata colonizing Solanaceous crops in Sudan
Autorzy:
Abbo, A.S.
Idris, M.O.
Elballa, M.A.
Hammad, A.M.
El Sidding, M.A.R.
Karlovsky, P.
Powiązania:
https://bibliotekanauki.pl/articles/66044.pdf
Data publikacji:
2018
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
plant disease
early blight
genetic variability
host
Alternaria alternata
diversity
Solanaceae
crop
amplified fragment length polymorphism
Sudan
Opis:
Early blight disease caused by Alternaria sp. is one of the most devastating diseases of Solanaceous crops widely distributed in Sudan. The aim of this study was to determine the genetic variation among different Alternaria isolates recovered from different Solanaceae crops showing typical symptoms of early blight disease. Infected leaves of tomato, potato, eggplant and pepper were collected from different geographical zones in Sudan. The recovered fungal isolates were identified to the genus level based on cultural and morphological characteristics. Five representative isolates were sent to the CABI Bioscience, U.K. for confirmation. The genetic relationship among the isolates was determined using the amplified fragments length polymorphism (AFLP) technique and the generated data were used to create similarity matrices using the PAST 3.01 software package. Dendrograms were constructed based on Jaccard’s similarity coefficients. A total of 70 fungal isolates was recovered from the tested plants and all of them showed morphological characteristics typical of Alternaria spp. The conidia appeared in multiple-branched chains with spore sizes in the range of 2.38−13.09 μm × 12.30−43.63 μm. Therefore, the isolates were identified as Alternaria alternata (Fr.) Keissl. The identification was then confirmed by CABI.AFLPbased dendrogram which revealed five clusters with a significant cophenetic correlation coefficient (r = 0.834) between the dendrogram and the original similarity matrix irrespective of their geographical origins. Eighteen (75%) of the Alternaria isolated from tomato leaves were clustered together in cluster I and five isolates formed two separate clusters, viz. cluster IV (T-Kh5 and T-H1) and cluster V (T-H4 and T-Med2). The remaining isolate, T-Am5, grouped with one of the potato isolates in cluster III. The other isolates which were recovered from potato, pepper and eggplants were all separated from the tomato isolates in the largest cluster.
Źródło:
Journal of Plant Protection Research; 2018, 58, 3
1427-4345
Pojawia się w:
Journal of Plant Protection Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Polimorfizm genu PPARA u polskich sportowców z grup dyscyplin siłowych
PPARA gene polymorphism in Polish strength athletes
Autorzy:
Ahmetov, I.
Maciejewska-Karlowska, A.
Buryta, M.
Grenda, A.
Wiazewicz, A.
Powiązania:
https://bibliotekanauki.pl/articles/790151.pdf
Data publikacji:
2012
Wydawca:
Uniwersytet Szczeciński. Wydawnictwo Naukowe Uniwersytetu Szczecińskiego
Tematy:
sport
dyscypliny sportowe
sporty silowe
Polska
sportowcy
polimorfizm genow
gen PPAR
genetyka czlowieka
sprawnosc fizyczna
Źródło:
Zeszyty Naukowe. Prace Instytutu Kultury Fizycznej. Uniwersytet Szczeciński; 2012, 28
1640-6818
Pojawia się w:
Zeszyty Naukowe. Prace Instytutu Kultury Fizycznej. Uniwersytet Szczeciński
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The PPARA gene polymorphism in team sports athletes
Autorzy:
Ahmetov, Ildus I.
Egorova, Emiliya S.
Mustafina, Leysan J.
Powiązania:
https://bibliotekanauki.pl/articles/1054633.pdf
Data publikacji:
2013
Wydawca:
Uniwersytet Szczeciński. Wydawnictwo Naukowe Uniwersytetu Szczecińskiego
Tematy:
PARA
game performance
gene polymorphism
sport selection
team sports
Opis:
Peroxisome proliferator-activated receptor α (PPARα) is a transcription factor that regulates lipid and glucose metabolism. Accumulating evidence suggests that the intron 7 C allele of the PPARA gene rs4253778 G/C polymorphism has an advantage for power-oriented athletes, presumably due to the hypertrophic effects on skeletal muscle and increase in glucose utilization in response to anaerobic exercise. The G allele, however, is said to be favorable for the endurance-oriented athletes. The metabolic demands of team sports involve aerobic and anaerobic energy pathways, as a result of the intermittent physical activity. The aim of the present study was to investigate the association between the PPARA gene polymorphism and team-sport athletic status. A total of 665 Russian athletes from 14 team sports and 1,706 controls were involved in the case-control study. We found that the frequency of the PPARA C allele was significantly higher in athletes compared to controls (20.5 vs. 16.4%, P = 0.0009), suggesting that anaerobic rather than aerobic metabolism may be crucial to the game performance in team sports. This means that our study indicates the association between the PPARA gene G/C polymorphism and team-sport athletic status. Although more replication studies are needed, the preliminary data suggest an opportunity to use the analysis of PPARA polymorphism, along with other gene variations and standard phenotypic assessment in team sports selection.
Źródło:
Central European Journal of Sport Sciences and Medicine; 2013, 1, 1; 19-24
2300-9705
2353-2807
Pojawia się w:
Central European Journal of Sport Sciences and Medicine
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Genetic diversity in Vernonia amygdalina Delile accessions revealed by random amplified polymorphic DNAs (RAPDs)
Autorzy:
Aikpokpodion, P.
Abebe, J.
Igwe, D.
Powiązania:
https://bibliotekanauki.pl/articles/79809.pdf
Data publikacji:
2018
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
genetic diversity
Vernonia amygdalina
random amplified polymorphic DNA
polymorphism
molecular characteristics
single-nucleotide polymorphism
geographic differentiation
Źródło:
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology; 2018, 99, 2
0860-7796
Pojawia się w:
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Molecular identification of blast resistance genes in rice genotypes using gene-specific markers
Autorzy:
Al-Daej, M.I.
Ismail, M.
Rezk, A.A.
El-Malky, M.M.
Powiązania:
https://bibliotekanauki.pl/articles/80189.pdf
Data publikacji:
2019
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
molecular identification
resistance gene
rice genotype
Oryza sativa
DNA marker
single-nucleotide polymorphism
simple sequence repeat
Źródło:
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology; 2019, 100, 3
0860-7796
Pojawia się w:
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
A comprehensive in silico prediction of the most deleterious missense variants in the bovine LEP gene
Autorzy:
Al-Shuhaib, M.B.S.
Powiązania:
https://bibliotekanauki.pl/articles/80824.pdf
Data publikacji:
2019
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
LEP gene
leptin
biological activity
bovine gene
single nucleotide polymorphism
coding sequence
cattle
Źródło:
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology; 2019, 100, 4
0860-7796
Pojawia się w:
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Badanie polimorfizmu rzepakochwastow za pomoca markerow RAPD
Autorzy:
Aleksandrzak, L
Broda, Z.
Powiązania:
https://bibliotekanauki.pl/articles/832682.pdf
Data publikacji:
2004
Wydawca:
Instytut Hodowli i Aklimatyzacji Roślin
Tematy:
polimorfizm DNA
rosliny oleiste
metoda RAPD
rzepakochwasty
rzepak ozimy
DNA polymorphism
oil plant
RAPD method
rapeseed-like weed
winter rape
Źródło:
Rośliny Oleiste - Oilseed Crops; 2004, 25, 1; 61-66
1233-8273
Pojawia się w:
Rośliny Oleiste - Oilseed Crops
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Lack of association between UBE2E2 gene polymorphism (rs7612463) and type 2 diabetes mellitus in a Saudi population
Autorzy:
Alharbi, Khalid
Khan, Imran
Al-Sheikh, Yazeed
Alharbi, Fawiziah
Alharbi, Fahad
Al-Nbaheen, May
Powiązania:
https://bibliotekanauki.pl/articles/1039212.pdf
Data publikacji:
2014
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
T2DM
UBE2E2
PCR-RFLP
Saudi population
Opis:
The ubiquitin-conjugating enzyme E2E 2 (UBE2E2) gene plays an important role in insulin synthesis and secretion under conditions in which stress to the endoplasmic reticulum is increased in β-cells. In this case-control study, we have selected rs7612462 polymorphism within UBE2E2 gene to identify in a Saudi population the type 2 diabetes mellitus (T2DM) subjects. In total, 376 subjects with T2DM and 380 controls were enrolled in this study. We have collected 5 mL of peripheral blood from each participant for biochemical and molecular analyses. PCR-RFLP was used to generate genotypes at rs7612462 in all of the study subjects. Clinical data and anthropometric measurements of the patients were significantly different from those of the controls (p<0.05). All of the subjects used in this study were non-obese (25
Źródło:
Acta Biochimica Polonica; 2014, 61, 4; 769-772
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The genetic polymorphism in the STK11 does not affect gestational diabetes
Autorzy:
Alharbi, Khalid
Khan, Imran
Eldesouky, Malek
Al-Hakeem, Malak
Abotalib, Zeinab
Powiązania:
https://bibliotekanauki.pl/articles/1039007.pdf
Data publikacji:
2015
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
gestational diabetes
STK11
rs8111699 polymorphism
Saudi women
Opis:
Gestational diabetes mellitus (GDM) is defined as carbohydrate intolerance of variable severity that develops during pregnancy. Recent studies indicate that GDM onset is rapid, and that women with GDM will develop other metabolic disorders such as obesity, type 2 diabetes, and cardiovascular disease in their future. Serine/threonine kinase 11 (STK11) is engaged in the insulin signaling pathway and encoded protein is an important activator of adenosine monophosphate activated protein kinase. Based on the previously reported association between the STK11 gene and diabetes, we aimed to investigate whether the rs8111699 polymorphism in STK11 has any role in gestation diabetes in Saudi women. In this case-control study, we recruited pregnant Saudi women based on biochemical analysis of their blood samples. Genomic DNA was obtained from confirmed subjects (200 GDM cases and 300 non-GDM). PCR-RFLP analysis was performed to detect the C528G polymorphism in the STK11 gene. The anthropometric and clinical data were similar between the GDM and non-GDM subjects (p > 0.05), whereas the biochemical analysis was significantly different between the cases and controls (p < 0.05). The genotype and allele frequencies between of the STK11 gene were not statistically significant difference between the GDM and non-GDM groups (OR=0.82; 95% CI:=0.6-1.0; p=0.12). Our study suggests that the rs8111699 polymorphism has no role in the development of GDM in pregnant Saudi women.
Źródło:
Acta Biochimica Polonica; 2015, 62, 3; 569-572
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The mRNA sequence polymorphisms of flowering key genes in bolting sensitive or tolerant sugar beet genotypes
Autorzy:
Alimirzaee, M.
Mirzaie-Asl, A.
Abdollahi, M.R.
Kolaei, H.E.
Fasahat, P.
Powiązania:
https://bibliotekanauki.pl/articles/79841.pdf
Data publikacji:
2017
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
sugar-beet
Beta vulgaris ssp.maritima
mRNA
polymorphism
flowering
single nucleotide polymorphism
genetic control
RNA extraction
protein structure prediction
Źródło:
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology; 2017, 98, 3
0860-7796
Pojawia się w:
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Role of Apolipoprotein E gene polymorphism in the risk of familial hypercholesterolemia: a case-control study
Autorzy:
Almigbal, Turky
Batais, Mohammed
Hasanato, Rana
Alharbi, Fawaziah
Khan, Imran
Alharbi, Khalid
Powiązania:
https://bibliotekanauki.pl/articles/1038371.pdf
Data publikacji:
2018
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
familial hypercholesterolemia
ApoE gene
TaqMan assay
Saudi population.
Opis:
Familial Hypercholesterolemia (FH) is characterized by elevated cholesterol and based on biochemical, clinical, and genetic studies and FH disease, which was documented even with limited mutations. Earlier studies focused on Apolipoprotein E (ApoE) in variable diseases. The current study aimed to investigate the genetic association between FH disease and ApoE gene polymorphisms (rs429358 and rs7412) in the Saudi population. This case-control study was a hospital-based study performed in Saudi Arabia. Two hundred and four subjects in total were recruited and consisted of FH participants (n=104) and the controls (n=100). Common polymorphisms of ApoE gene (rs429358 and rs7412) were chosen and subjected to the genotyping using the TaqMan assay. Moreover, the ApoE risk allele E4 was proved significantly associated with FH cases when compared with controls (OR-2.24 (95%CI: 1.06-4.70); p=0.02). Lipid profile parameters were significantly associated (p<0.05); however, the ApoE alleles and lipid profiles were not correlated (p>0.05). In conclusion, the FH case-control study was associated with the E4 allele in the Saudi population. However, E4 allele was appeared as a reliable risk marker for lipid profiles, but not for ApoE alleles.
Źródło:
Acta Biochimica Polonica; 2018, 65, 3; 415-420
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Comparative stability analysis of D23N mutated Aβ
Autorzy:
Alred, E. J.
Scheele, E. G.
Berhanu, W. M.
Hansmann, U. H. E.
Powiązania:
https://bibliotekanauki.pl/articles/1935815.pdf
Data publikacji:
2014
Wydawca:
Politechnika Gdańska
Tematy:

structural polymorphism
molecular dynamics
parallel and anti-parallel β sheets
Iowa mutant
Opis:
Amyloid β (Aβ) is the subject of numerous studies due to its link to the devastating Alzheimer’s disease and it exists in a parallel structure in fibril aggregate. The Iowa mutant (D 23 N) Aβ posses a unique antiparallel fibril aggregate structure and can also form parallel structure. This structural difference, coupled with the fact that occurrence of the Iowa mutant is correlated with early onset Alzheimer’s, suggests to use these peptides as candidates for computational studies of the structural determinants of the toxicity of Alzheimer’s disease. In order to compare the two observed Aβ structural motifs, we designed a computational study to probe the factors that affect the stability of parallel and antiparallel aggregates. Since the structural changes may occur on a timescale beyond that sampled in traditional molecular dynamics (MD), we employed a techniques of scaling the mass to reduce the solution ’s viscosity and compared the results to regular molecular dynamics. The knowledge gained from this study could provide insight into the mechanism of selection for antiparallel and parallel two fold structures.
Źródło:
TASK Quarterly. Scientific Bulletin of Academic Computer Centre in Gdansk; 2014, 18, 4; 365--371
1428-6394
Pojawia się w:
TASK Quarterly. Scientific Bulletin of Academic Computer Centre in Gdansk
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Bacterial community structure influenced by Coscinodiscus sp. in the Vistula river plume
Autorzy:
Ameryk, A.
Hahnke, R.L.
Gromisz, S.
Kownacka, J.
Zalewski, M.
Szymanek, L.
Calkiewicz, J.
Dunalska, J.
Harder, J.
Powiązania:
https://bibliotekanauki.pl/articles/47978.pdf
Data publikacji:
2014
Wydawca:
Polska Akademia Nauk. Instytut Oceanologii PAN
Tematy:
planktonic bacteria
Coscinodiscus
phytoplankton community
primary production
Vistula River
river plume
Baltic Sea
terminal restriction fragment length polymorphism
DNA extraction
16S rRNA gene
dissolved organic matter
Źródło:
Oceanologia; 2014, 56, 4
0078-3234
Pojawia się w:
Oceanologia
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Polimorficzność motywacji osób twórczych. Implikacje pedagogiczne
Autorzy:
Aneta, Bartnicka-Michalska,
Powiązania:
https://bibliotekanauki.pl/articles/892405.pdf
Data publikacji:
2015
Wydawca:
Uniwersytet Warszawski. Wydawnictwa Uniwersytetu Warszawskiego
Tematy:
interpreting artist
efficient personality
polymorphism of motivation
Opis:
In the article the hypothesis of motivational polymorphism in creativity is formulated and confirmed. The hypothesis assumes that activation of creative behaviour needs many different types of motivation, which are variations of one main motivation. The theoretical basis of this article rests on Józef Kozielecki’s concept of psychotransgressionism, which assumes that creative behaviour can be activated by three motivations: self-esteem motivation (hubristic), motivation of the meaning of life and motivation of self-efficiency. In this study on a sample of interpreting artists (N = 133), creative behaviour was measured using the STZ questionnaire (Strzałecki 2003). The motivational orientations were measured using the Polish adaptation of Power Motivation Scale (PMS) by Tokarz and Trzebińska (2011), the Polish adaptation of Life Attitude Profile questionnaire (LAP-R) by Klamut (2010) and the Polish adaptation of General Self- Efficacy Scale questionnaire (GSES) by Juczyński (2001). The results confirmed the hypothesis of a polymorphic nature of motivation in creative people. Educational implications of results are discussed.
Źródło:
Kwartalnik Pedagogiczny; 2015, 60(3 (237)); 34-52
0023-5938
Pojawia się w:
Kwartalnik Pedagogiczny
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Mutations in the COL1A1 and COL1A2 genes associated with osteogenesis imperfecta (OI) types I or III
Autorzy:
Augusciak-Duma, Aleksandra
Witecka, Joanna
Sieron, Aleksander
Janeczko, Magdalena
Pietrzyk, Jacek
Ochman, Karolina
Galicka, Anna
Borszewska-Kornacka, Maria
Pilch, Jacek
Jakubowska-Pietkiewicz, Elzbieta
Powiązania:
https://bibliotekanauki.pl/articles/1038526.pdf
Data publikacji:
2018
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
osteogenesis imperfecta
COL1A1
COL1A2
mutation
polymorphism
Opis:
Although over 85% of osteogenesis imperfecta (OI) cases are associated with mutations in the procollagen type I genes (COL1A1 or COL1A2), no hot spots for the mutations were associated with particular clinical phenotypes. Eight patients that were studied here, diagnosed with OI by clinical standards, are from the Polish population with no ethnic background indicated. Previously unpublished mutations were found in six out of those eight patients. Genotypes for polymorphisms (Sp1 - rs1800012 and PvuII - rs412777), linked to bone formation and metabolism were determined. Mutations were found in exons 2, 22, 50 and in introns 13 and 51 of the COL1A1 gene. In COL1A2, one mutation was identified in exon 22. Deletion type mutations in COL1A1 that resulted in OI type I had no effect on collagen type I secretion, nor on its intracellular accumulation. Also, a single base substitution in I13 (c.904-9 G>T) was associated with the OI type I. The OI type III was associated with a single base change in I51 of COL1A1, possibly causing an exon skipping. Also, a missense mutation in COL1A2 changing Gly→Cys in the central part of the triple helical domain of the collagen type I molecule caused OI type III. It affected secretion of the heterotrimeric form of procollagen type I. However, no intracellular accumulation of procollagen chains could be detected. Mutation in COL1A2 affected its incorporation into procollagen type I. The results obtained shall help in genetic counseling of OI patients and provide a rational support for making informed, life important decisions by them and their families.
Źródło:
Acta Biochimica Polonica; 2018, 65, 1; 79-86
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł

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