Search Results - "Amosenko, F A"

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  1. 1

    K-ras, BRCA1/2, and CHEK2 mutations and loss of heterozygosity at 9p, 17p, and 18q in sporadic adenocarcinoma of the pancreas by Amosenko, F. A., Kazubskaya, T. P., Gromyko, O. E., Matveeva, T. I., Korchagina, E. L., Nasedkina, T. V., Garkavtseva, R. F., Kalinin, V. N.

    Published in Molecular biology (New York) (01-06-2009)
    “…The diagnostic significance of molecular markers was assessed for the most common somatic aberrations at the K-ras, TP53, CDKN2A , and MADH4 loci, as well as…”
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  2. 2

    Mutation analysis of K-ras protooncogene in colorectal adenocarcinomas and polyps in Russian patients by Amosenko, F. A, Korchagina, E. L, Matveeva, T. I, Vaganov, Yu. E, Vlasov, S. B, Poltavets, N. V, Veselov, V. V, Garkavtseva, R. F, Polyakov, A. V

    Published in Russian journal of genetics (01-05-2010)
    “…To estimate diagnostic value of K-ras mutations during cancer risk group formation, they were studied in the samples of sporadic carcinomas (n = 58), benign (n…”
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  3. 3

    Comparison of different methods of molecular-genetic analysis of somatic mutations in K-ras gene in patients with colorectal cancer by Amosenko, F A, Karpov, I V, Poliakov, A V, Kovalenko, S P, Shamanin, V A, Liubchenko, L N

    “…Two approaches to somatic point mutations in 12 and 13 codones of K-ras gene were analyzed: PCR/SSCP/ACRS/sequencing and allele-specific PCR in the real-life…”
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  4. 4

    Analysis of K-ras, BRCA1/2, CHEK2 mutations and microsatellite markers (loss of heterozygosity at 9p, 17p and 18q) in sporadic pancreas adenocarcinomas by Amosenko, F A, Kazubskaia, T P, Gromyko, O E, Matveeva, T I, Korchagina, E L, Nasedkina, T V, Gar'kavtseva, R F, Kalinin, V N

    Published in Molekuliarnaia biologiia (01-05-2009)
    “…The purpose of this study was to investigate informativety and clinical significance of most frequent somatic alterations in K-ras, TP53, CDKN2A, MADH4 and…”
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  5. 5

    Biochip analysis of BRCA1/2 and CHEK2 common mutations in ovarian cancer and primary multiple tumors involving the ovaries (Russian population) by Fedorova, O. E., Lyubchenko, L. N., Payanidi, Yu. G., Kazubskaya, T. P., Amosenko, F. A., Garkavtseva, R. F., Zasedatelev, A. S., Nasedkina, T. V.

    Published in Molecular biology (New York) (01-02-2007)
    “…Ovarian cancer (OC) is among the leading causes of cancer-related mortality in women. A high risk of OC (lifetime estimates ranging 10-60%) is determined by…”
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  6. 6

    Use of protamine sulphate for elimination of substrate DNA in poliovaccines produced on continuous cell lines by Amosenko, F A, Svitkin, Y V, Popova, V D, Terletskaya, E N, Timofeev, A V, Elbert, L B, Lashkevich, V A, Drozdov, S G

    Published in Vaccine (01-03-1991)
    “…Cell substrate DNA was shown to be an abundant contaminant in the clarified preparations of the Sabin type 1, 2 and 3 poliovaccines produced on a continuous…”
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  7. 7

    Analysis of BRCA1/2 and CHEK2 mutations in ovarian cancer and primary multiple tumors involving the ovaries. Patients of Russian population using biochips by Fedorova, O E, Liubchenko, L N, Paiadini, Iu G, Kazubskaia, T P, Amosenko, F A, Gar'kavtseva, R F, Zasedatelev, A S, Nasedkina, T V

    Published in Molekuliarnaia biologiia (01-01-2007)
    “…Ovarian cancer (OC) is one of the leading cause of cancer death in women. Inherited BRCA1 and BRCA2 mutations strikingly increase OC risk (with lifetime risk…”
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  8. 8

    Three novel mutations in the RET proto-oncogene by Kalinin, V N, Amosenko, F A, Shabanov, M A, Lubchenko, L N, Hosch, S B, Garkavtseva, R F, Izbicki, J R

    “…Medullary thyroid carcinoma (MTC) occurs as a sporadic tumor or in connection with inherited cancer syndromes of multiple endocrine neoplasia type 2 and…”
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  10. 10

    MEDULLARY THYROID CANCER AS PART OF MEN 2B SYNDROME. CASE REPORT by L. N. Lyubchenko, F. A. Amosenko, M. G. Filippova, V. Z. Dobrokhotova, E. G. Matyakin

    Published in Opukholi golovy i shei (01-04-2015)
    “…MEN 2B syndrome is a subtype of the multiple endocrine neoplasia type 2. It is characterized by the development of aggressive forms of medullary thyroid cancer…”
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  11. 11

    Detection of KRAS mutations in tumor cells using biochips by Emel'ianova, M A, Amosenko, F A, Chudinov, A V, Surzhikov, S A, Kazubskaia, T P, Liubchenko, L N, Nasedkina, T V

    Published in Molekuliarnaia biologiia (01-09-2011)
    “…Somatic mutations in the KRAS gene are important markers of some types of tumors, for example, pancreatic cancer, and may be useful in early diagnostics. A…”
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  12. 12

    TUB9 polymorphism in the CFTR gene of cystic fibrosis patients, carriers, and healthy donors from the Moscow region. SSCP and restriction analyses by Amosenko, F A, Trubnikova, I S, Zakhar'ev, V M, Bannikov, V M, Sazonova, M A, Petrova, N V, Kapranov, N I, Kaplinin, V N

    Published in Genetika (01-02-1997)
    “…Data on the screening of 266 non-delta F508 chromosomes (42 cystic fibrosis patients, 43 carriers, and 48 healthy donors from the Moscow region) for the…”
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  13. 13

    Mutation analysis of K-ras protooncogene in colorectal adenocarcinomas and polyps in Russian patients by Amosenko, F A, Korchagina, E L, Matveeva, T I, Vaganov, Iu E, Vlasov, S B, Poltavets, N V, Veselov, V V, Gar'kavtseva, R F, Poliakov, A V

    Published in Genetika (01-05-2010)
    “…To estimate diagnostic value of K-ras mutations during cancer risk group formation, they were studied in the samples of sporadic carcinomas (n = 33) and…”
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  14. 14

    Analysis of mutations in the RET proto-oncogene in patients with medullary thyroid tumor by Amosenko, F A, Brzhezovskiĭ, V Zh, Liubchenko, L N, Shabanov, M A, Kozlova, V M, Vanushko, V E, Kazubskaia, T P, Gar'kavtseva, R F, Kalinin, V N

    Published in Genetika (01-06-2003)
    “…The spectrum of mutations of the RET protooncogene was analyzed in Russian patients with inherited or sporadic medullary thyroid carcinoma (MTC). Four RET…”
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  15. 15

    Molecular diagnosis of multiple type 2 endocrine neoplasia by Amosenko, F A, Pushkash, K, Frilling, A, Kozlova, V N, Liubchenko, L N, Kazubskaia, T P, Brelysh, K E, Gar'kavtseva, R F, Kalinin, V N

    “…The paper reviews the data on the molecular structure of the protooncogene RET encoding for receptor-type protein kinase, on the mechanism of transformation of…”
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  16. 16

    Molecular genetic analysis of TUB18 and TUB20 intragenic polymorphism and various mutations of the CFTR gene in the Moscow region by Sazonova, M A, Amosenko, F A, Kapranov, N I, Kalinin, V N

    Published in Genetika (01-09-1997)
    “…Allelic frequencies of two intron polymorphisms in the cystic fibrosis transmembrane regulator (CFTR) gene, TUB18 and TUB20, were estimated on chromosomes of…”
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  17. 17
  18. 18

    A new inherited RET proto-oncogene mutation associated with familial medullary thyroid carcinoma and polymorphisms in adjacent regions by Kalinin, V N, Amosenko, F A, Puskas, C, Frilling, A, Broelsch, C E, Pushkash, K, Brel'sh, K E

    Published in Genetika (01-08-1998)
    “…A new point mutation, TCG(Ser)-->GCG(Ala) in codon 891, exon 15 of the RET protooncogene was revealed in two patients from a pedigree with familial medullary…”
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  19. 19

    Analysis of various polymorphic markers of the CFTR gene in cystic fibrosis patients and healthy donors from the Moscow region by Amosenko, F A, Sazonova, M A, Kapranov, N I, Trubnikova, I S, Kalinin, V N

    Published in Genetika (01-04-1995)
    “…Allelic frequencies at three polymorphic markers in the CFTR gene were detected on chromosomes derived from cystic fibrosis (CF) patients and healthy donors…”
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  20. 20

    The purification of tick-borne encephalitis virus preparations of cellular DNA by El'bert, L B, Terletskaia, E N, Timofeev, A V, Amosenko, F A, Khapchaev, Iu Kh, Mironova, L L, Svitkin, Iu V, Vorovich, M F, Lisitsyna, E A

    Published in Voprosy virusologiĭ (01-05-1990)
    “…According to the WHO requirements, the concentration of cellular DNA in vaccine preparations produced by pooling virus from continuous cell lines is limited to…”
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