Search Results - "LUNGA, I. N"

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  1. 1

    Retro- and prospective evaluation of dynamics of some mutational events by BOCHKOV, N. P, GRIGORIAN, S. D, LUNGA, I. N, NIKOLAEVA, I. V, PRUSSAKOV, V. M, TIKHOPOY, M. V

    Published in Human genetics (1986)
    “…The dynamics of some mutational events were studied in a Siberian town with a chemical industry. Retro- and prospective evaluations of the frequency of…”
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  2. 2

    Polymorphism of exon 4 in the CANP-3 gene in patients with primary myopathies by Lipatova, N A, Krakhmaleva, I N, Shishkin, S S, Shakhovskaia, N I, Podnikova, N I, Lunga, I N, Tarksh, M A, Gerasimova, N L

    Published in Genetika (01-12-1999)
    “…The structures of the gene for calpain (CANP-3) and of the DMD gene were analyzed in patients with primary myopathies [limb-girdle muscular distrophy (LGMD)…”
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  3. 3

    Influence of low doses of ionizing radiation on tenascin expression in hybridoma cell systems by Lunga, I N

    “…One of the achievements of the modern radiation ecology is the preparation and application of stable eukariotic cell lines to solve various problems occurring…”
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  4. 4

    Assortative mating in the population of a modern city by Bochkov, N P, Nikolaeva, I V, Tikhopoĭ, M V, Lunga, I N, Prusakov, V M

    Published in Genetika (01-07-1984)
    “…An investigation of the population of modern Siberian city Angarsk was carried out. The sample consisted of 13746 individuals in the age interval from 21 to 60…”
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  5. 5

    Cytogenetic damage and the degree of reparative synthesis in the lymphocytes of chemical industry workers by Stukalov, S V, Lunga, I N

    Published in Gigiena i sanitarija (01-12-1991)
    “…A thiophosphamide-induced increase of repair DNA-synthesis in lymphocytes in shown. To include cytogenetic studies in a genetic- and epidemiologic programme of…”
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  6. 6

    A databank on Russian families with hereditary neuromuscular diseases by Lunga, I N, Shishkin, S S, Shakhovskaia, N I, Gerasimova, N L, Zelinskaia, D I, Khodunova, A A, Shakhovskiĭ, V A, Tarksh, M A, Krakhmaleva, I N

    “…The information about 5 thousands Russian families with hereditary neuromuscular disorders (HNMD) was collected by means of both different genetic…”
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  7. 7

    The use of low doses of prednisolone for the treatment of patients with Duchenne-Becker myodystrophy by Shakhovskaia, N I, Shishkin, S S, Skozobtseva, L F, Shakhovskiĭ, V A, Rodnikova, N I, Lunga, I N, Tarksh, M A, Gerasimova, N L, Krakhmaleva, I N

    “…A special program for long-term application of low-dose prednisolone treatment in Duchenne-Becker muscular dystrophy with complex control of the patients'…”
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  8. 8

    Genotoxic effects of the complex interaction of industrial factors by Lunga, I N, Trubnikov, V I, Smirnova, G V

    Published in Gigiena i sanitarija (01-06-1993)
    “…Results of genoepidemiological study of reproduction function of workers in plastic goods production are presented. Incidence of spontaneous abortions (SA) in…”
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  9. 9

    The association of ovarian cancer with various genetic markers by Akulenko, L V, Lunga, I N, Chudina, A P

    Published in Genetika (01-06-1989)
    “…The distribution of blood groups AB0, Rh, P1, MN and Haptoglobins among ovarian cancer patients was studied. Significant associations between ovarian cancer…”
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  10. 10
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    Evaluation of the incidence of congenital developmental defects in newborn infants based on an analysis of archival documentation by Nikolaeva, I V, Lunga, I N, Viktorov, V V

    Published in Gigiena i sanitarija (01-03-1989)
    “…Incidence of congenital malformations in the newborn was analyzed on the basis of the medical archives, thus the possibility of using the obtained data for…”
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  12. 12
  13. 13

    Analysis of genotoxic effects of individual factors on chemical industry workers by Lunga, I N, Trubnikov, V I

    “…The article provides data on the study of occupational and non-occupational factors relating to the prevalence of early spontaneous abortions in couples…”
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  14. 14

    Expression of tenascin in lymphoid cells and changes in it upon exposure to low doses of x-rays by Safronova, E E, Lunga, I N, Shishkin, S S

    Published in Voprosy meditsinskoi khimii (01-07-1995)
    “…The oncofetal protein tenascin was detected in some strains of lymphoid cells: murine myeloma X-63, murine hybridoma MLC-1 and K-48 and T-cell plasmacytoma…”
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  15. 15

    Discriminant functions for the diagnosis of twin zygosity from questionnaire data by Lunga, I N, Trubnikov, V I, Sergeev, A S

    Published in Genetika (01-11-1982)
    “…Discriminant and successive analyses of formalized data obtained on the basis of questionnaire response were carried out in 232 twin samples of the same sex to…”
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    Use of two-dimensional O'Farrell electrophoresis for studying polymorphism of blood proteins by Golubeva, M V, Lunga, I N, Shishkin, S S

    Published in Voprosy meditsinskoi khimii (01-05-1991)
    “…Blood plasma of 50 healthy volunteers was analyzed using two-dimensional electrophoresis by O'Farrell. After staining with Coomassie R-250 and subsequent…”
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  18. 18

    Structural analysis of the correlations of genetic markers with physiological indices by Lunga, I N, Trubnikov, V I, Koshechkin, V A, Medvedeva, M I

    Published in Genetika (01-02-1984)
    “…The structure of phenotypic and genetic correlations between ABO blood groups, MN, Rh(D), haptoglobins and concentration indications of the total cholesterol,…”
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  19. 19

    Frequencies of ABO system blood groups and haptoglobins in Uzbekistan. The problems of sampling studies by Revazov, A A, Asanov, A Iu, Lunga, I N, Bakhramov, S M

    Published in Genetika (01-07-1983)
    “…The results of the analysis of the distribution of blood group gene frequencies of ABO and haptoglobins (Hp) systems for four regions of Uzbek SSR are…”
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  20. 20

    Dynamic evaluation of the incidence of hereditary pathology by an accounting of spontaneous abortions and congenital developmental defects by Bochkov, N P, Prusakov, V M, Nikolaeva, I V, Tikhopoĭ, M V, Lunga, I N

    Published in TSitologiia i genetika (01-11-1982)
    “…A new method is suggested to control the mutation process in man by the dynamics of hereditary pathology frequency. The paper presents data on registration of…”
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