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Wyszukujesz frazę "Gayathri Upeksha Amarakoon, A. A. D." wg kryterium: Autor

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    Wyświetlanie 1-4 z 4
    Tytuł:
    Hypothesis of Selected Mendelian Traits Among Random Asian Population
    Autorzy:
    Gayathri Upeksha Amarakoon, A. A. D.
    Powiązania:
    https://bibliotekanauki.pl/articles/1179198.pdf
    Data publikacji:
    2017
    Wydawca:
    Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
    Tematy:
    Hitchhiker’s thumb
    Mid digital hair
    Toung rolling
    Widow’s peak
    Opis:
    This discusses the prospects for understanding the genetic basis of few selected traits in humans. Phylogenetic analysis provides a path to identify genes and biological processes underlying any trait influenced by inheritance. We suggest that different experimental approaches should be undertaken for traits caused by common genetic variants versus those arising from rare genetic variants. We discuss the intellectual foundations of genetic of Mendelian traits in humans by examining the degree of freedom of four particular factors , namely toung rolling (1.307), hitchhiker’s tumb (3.22), widow’s peak (44.825) and mid digital hair (92.825).
    Źródło:
    World Scientific News; 2017, 83; 216-223
    2392-2192
    Pojawia się w:
    World Scientific News
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Emerging and detection of Dengue viral infection in Sri Lanka
    Autorzy:
    Amarakoon, A. A. D. Gayathri Upeksha
    Powiązania:
    https://bibliotekanauki.pl/articles/1188088.pdf
    Data publikacji:
    2016
    Wydawca:
    Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
    Tematy:
    IgG
    RT-PCR
    IgM
    acute infection
    Aedes mosquitos
    Opis:
    Emerging of dengue infection has increased dramatically in Sri Lanka in recent years. Initial infection with a particular serotype is known as primary infection which is usually asymptomatic or mild disease manifestations. Although cross reactive T cells and cross reactive antibodies have been shown to contribute to disease pathogenesis, these mechanisms alone do not explain the immune - pathological mechanisms leading to severe infection. However, this study has suggested that antigen antibody detection and viral RNA detection in host blood contribute to the occurrence of disease. Therefore, it is important to further investigate the quality of dengue specific immune responses and confirmation of dengue RNA content in patients with acute severe dengue and asymptomatic dengue infection.
    Źródło:
    World Scientific News; 2016, 56; 97-109
    2392-2192
    Pojawia się w:
    World Scientific News
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Detection of C677T & A1298C mutations within the MTHFR gene by PCR and RFLP assays and assessment of risk factor of Hyperhomocysteinemia
    Autorzy:
    Amarakoon, A. A. D. Gayathri Upeksha
    Fernandopulle, Neil
    Powiązania:
    https://bibliotekanauki.pl/articles/1182887.pdf
    Data publikacji:
    2016
    Wydawca:
    Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
    Tematy:
    mthfr gene
    dna methylation
    hyperhomocysteinemia
    Opis:
    The MTHFR gene within the human genome, codes for the synthesis of Methylenetetrahydrofolate Reductase enzyme, which reduces 5,10-Methylenetetrahydrofolate to 5-Methyltetrahydrofolate, which in turn, is the major circulatory form of folate in the blood. Folate, in this form, among it’s other functions, is involved in reducing the homocysteine levels in the blood, whose elevated levels lead to Hyperhomocysteinemia, causing various major disorders. Mutations within the gene lead to impairment of gene function, in turn causing the homocysteine levels to rise. The C677T and A1298C mutations are the main causative agents for MTHFR gene disruption. During the course of the project, a total of 79 samples were analyzed for the presence of these mutations. The blood samples were first subjected to PCR, giving two separate DNA fragments each responsible for either of the conditions. The fragments were then subjected to RFLP analysis to detect the mutations. The results were finally given with respect to the risk factor faced by each individual based on a molecular diagnostic point of view.
    Źródło:
    World Scientific News; 2016, 53, 3; 253-274
    2392-2192
    Pojawia się w:
    World Scientific News
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    An overview of Human Papilloma Virus
    Autorzy:
    Amarakoon, A. A. D. Gayathri Upeksha
    Daulagala, S. W. P. L.
    Fathima, Fara
    Powiązania:
    https://bibliotekanauki.pl/articles/1182889.pdf
    Data publikacji:
    2016
    Wydawca:
    Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
    Tematy:
    Papilloma virus; cervical cancer; RNA genome; control region
    Opis:
    Cervical cancer is the second commonest cause of cancer among women. According to the World Health Organization (WHO) data, in 2006 there were 1.4 million women who were suffering from cervical cancer and 80% of deaths among them were of women from developing countries. Genital infection with Human Papilloma Virus (HPV) is one of the major etiological factors for developing cervical cancers in almost all countries (World Health Organization, 2005). Papilloma viruses were first identified, cloned and sequenced from cervical tumor specimens and were subsequently established as important causative agents for the development of cervical cancer. Differences in prevalence rates are observed worldwide. Infection is more common in sexually active young women of 18-30 years and a reduction in acquisition of infection is observed after 30 years. The situation of Cervical cancer in Sri Lanka is identified as the second most common cancer among women in Sri Lanka and approximately 7.74 million women are included in the risk category. It is reported that nearly 850 die from cervical cancer each year.
    Źródło:
    World Scientific News; 2016, 53, 3; 275-308
    2392-2192
    Pojawia się w:
    World Scientific News
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
      Wyświetlanie 1-4 z 4

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