Výsledky vyhledávání - "B V, Skriabin"

[Simple methods of enzymatic amplification of DNA for clinical practice]

Autor: A I, Kuz'min, S E, Khal'chitskiĭ, B V, Skriabin, O K, Kaboev, E I, Shvarts

Publikováno v: Molekuliarnaia genetika, mikrobiologiia i virusologiia. (8)

The methods for enzymatic DNA amplification in vitro that allow to avoid the step of preliminary DNA extraction and purification are proposed. Lysates of blood cells in the solution or immobilized on the nylon membrane filters and dried blood spots o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c03928e32400b80d1ed0f6385c0d045f
https://pubmed.ncbi.nlm.nih.gov/1784305

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[Study of polymorphism in human rRNA gene clusters]

Autor: B V, Skriabin, V M, Gindilis, N S, Kupriianova, M Ia, Timofeeva

Publikováno v: Genetika. 25(7)

Human ribosomal DNA (rDNA) probe specific for the 3' end of the 28S rRNA gene was used for detecting standard restriction fragments' length polymorphism (RFLPs) in the non-transcribed spacer. The conditions for hybridization of rDNA probe which elimi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4cc8fb733d44eeda1060cebf37dd8f22
https://pubmed.ncbi.nlm.nih.gov/2572510

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[Identification of a nature of mutation in the 12th exon of phenylalanine hydroxylase gene in patients with phenylketonuria]

Autor: B V, Skriabin, L A, Koval'chuk, S E, Khal'chitskiĭ, A A, Gol'tsov, O K, Kaboev, O V, Plutalov, Iu A, Berlin, E I, Shvarts

Publikováno v: Bioorganicheskaia khimiia. 15(12)

Upon amplification in vitro of the 12th exon area of the human phenylalanine hydroxylase gene followed by allele-specific hybridisation of the amplification product with synthetic probes and its sequencing by the Maxam-Gilbert method, a C----T transi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::32048640f470957cc6b82e1385725d38
https://pubmed.ncbi.nlm.nih.gov/2634967

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[Study of polymorphism in human rRNA gene clusters. Population and familial analysis of basic types of RFLP]

Autor: B V, Skriabin, N I, Voskoboĭnik, A Ia, Ose, V M, Gindilis

Publikováno v: Genetika. 25(8)

The frequency and average amount of copy number per genome were defined for standard and a number of new variants of BamHI 5'-NTS RFLP from populations of Moscow, Riga and individuals with Down syndrome. It was demonstrated that the populations studi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3dd65b37635861ea87528441117a6817
https://pubmed.ncbi.nlm.nih.gov/2573559

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