Публикации отдела молекулярной генетики

   









 

    

  1. Mandelshtam M.Ju., Lipovetskyi B.M., Schwartzman A.L., Gaitskhoki V.S. (1993) A novel deletion in the low density lipoprotein receptor gene in a patient with familial hypercholesterolemia from Petersburg// Human Mutation - 2(4), 256- 260.

  2. Patkin E.L., Kustova M.E., Noniaschvili E.M. (1994): DNA breaks in nuclei of preimplantation mouse embryo as revealed in situ. Cytobios 79, 235-240. 

  3. Shavlovski M.M., Chebotar N.A., Konopistseva L.A., Zakharova E.T., Kachourin A.M., Vassiliev V.B., Gaitskhoki V.S. (1995) Embryotoxicity of silver ions is diminished by ceruloplasmin - further evidence for its role in the transport of copper. BioMetals, , 8, 122-128.

  4. De Filippis V., Vassiliev V.B., Beltramini M., Fontana A., Salvato B., Gaitskhoki V.S. (1996) Evidence for the molten globule state of human apo-ceruloplasmin. Biochim. Biophys. Acta, 1297, 119-123.

  5. Vassiliev V.B., Kachurin A.M., Rocco G.-P., Beltramini M., Salvato B., Gaitskhoki V.S. (1997) Copper depletion/repletion of human ceruloplasmin is followed by the changes in its spectral features and functional properties. J. Inorg. Biochem., 65, 167-174.

  6. Vasilyev V.B., Sokolova V.A., Sorokin A.V., Bass M.G., Arbuzova N.I., Patkin E.L., Golubkov V.I., Dyban A.P., Gaitskhoki V.S. (1999) Persistence of human mitochondrial DNA throughout the development to the blastocyst of mouse zygotes microinjected with human mitochondria. Zygote, 7, 279-283.

  7. Zakharova E.T., Shavlovski M.M., Bass M.G., Gridasova A.A., Pulina M.O., De Filippis V., Beltramini M., Di Muro P., Salvato B., Fontana A., Vasilyev V.B., Gaitskhoki V.S. (2000) Interaction of lactoferrin with ceruloplasmin. Arch. Biochim. Biophys., 374, 222-228.

  8. Patkin E.L., Kustova M.E., Dyban A.P. (1994): Spontaneous sister-chromatids differentiation (SCD) and sister-chromatid exchanges (SCEs) in chromosomes of mouse blastocyst. Cytogen. Cell Genet. 66, 31-32.

  9. Patkin E.L., Kustova M.E., Noniaschvili E.M. (1995): DNA single-strand breaks in chromosomes of early mouse embryos as detected by in situ nick translation. Genome 38, 381-384.

  10. Молекулярная гетерогенность семейной гиперхолестеринемии в Санкт-Петербургской популяции - Генетика, 1995, т.31 , сс.521-527

  11. Patkin E.L. (1997): Asymmetry of sister chromatids methylation of preimplantation mouse embryo chromosomes as revealed by nick translation in situ. Cytogenet. Cell Genet. 77, 82-83.

  12. Рунова О.Л., Мандельштам М.Ю., Голубков В.И., Суконина В.Е., Денисенко А.Д., Гайцхоки В.С Экспрессия фрагмента кДНК рецептора липопротеинов низкой плотности человека, кодирующего лиганд-связывающий домен рецептора, в клетках Escherichia coli - Биохимия, 1997,т.62, сс.1037-1045

  13. Mandelshtam M.Ju., Chakir Kh., Shevtsov S.P., Golubkov V.I., Skobeleva N.A., Lipovetsky B.M., Konstantinov V.O., Denisenko A.D., Gaitskhoki V.S., Schwartz E.I. (1998) Prevalence of Lithuanian mutation among St.Petersburg Jews with familial hypercholesterolemia// Human Mutation, 12 (4), 255-258.

  14. Chakir Kh., Mandelshtam M.Ju., Shevtsov S.P., Golubkov V.I., Skobeleva N.A., Schur Yu.A., Zakharova F.M., Lipovetskyi B.M., Konstantinov V.O., Denisenko A.D., Gaitskhoki V.S., Schwartz E.I. (1998) Two novel low density lipoprotein receptor gene mutations (E397X and 347delGCC) in St.Petersburg familial hypercholesterolemia// Molecular Genetics and Metabolism 65 (4), 311-314.

  15. Patkin E.L., Kustova M.E., Perticone P.(1998) The influence of demethylation agents on the preimplanataion mouse development. Zygote, 6,351-358.

  16. Popov A., Baranova T.V., Suchkova I., Smirnov A., Golubkov V., Sorokin A., Patkin E. (1999) The modelling of heterochromatic regions in transgenic mice. Cytogenet. Cell Genet. 85, 95.

  17. Suchkova I, Strunnikova M., Sorokin A., Golubkov V., Gaitskhoki V., Patkin E. (1999) The effect of foreign satDNA integration on F2 transgenic embryo development. Cytogenet. Cell Genet. 85, 108.

  18. Попов А. В., Смирнов А.Ф., Сучкова И.О., Баранова Т.В., Сорокин А.В., Гайцхоки В.С., Паткин Е.Л. Моделирование гетерохроматиновых районов у трансгенных мышей при переносе фрагмента сатДНК-IV Bos taurus L. // Генетика -2000.-т.36.-№8.-стр.930-935. 

  19. Гайцхоки В.С.,Паткин Е.Л. Cателлитные ДНК и болезни - возможные механизмы. .Тринуклеотидные повторы. Генетика. 2000, 713-728.

  20. Паткин Е.Л., Гайцхоки В.С. Cателлитные ДНК и болезни - возможные механизмы: Нестабильность минисателлитов. Генетика.

  21. Tomashevski A.Yu., Melnik T.N., Narizhneva N.V., Shavlovski M.M., Vasiliev V.B., and Uversky V.N. (1999) The Alpha-fetoprotein molecule has one or two rigid domains depending on the protein purification and procedure. Prot. Pept. Lett. 6 (4), 237-244.

  22. Molon A.-M., Di Muro P., Bubacco L., Vasilyev V., Salvato B., Beltramini M., Conze W., Hellmann N. and Decker H. (2000) Molecular heterogeneity of the hemocyanin isolated from the king crab Paralithodes camtschaticae. Eur. J. Biochem. 267, 7046-7057.

  23. Vasilyev V., Sokolova V., Arbuzova N., Sorokin A., Bass M. (2001) Human mtDNA persists in some organs of mouse embryos and of neonate mice originated from zygotes microinjected with human mitochondria. Mitochondrion 1 (Suppl.1), S94-S95. 

  24. Pulina M.O., Zakharova E.T., Sokolov A.V., Shavlovski M.M., Bass M.G., Solovyov K.V., Kokryakov V.N. and Vasilyev V.B. (2002) Studies of the ceruloplasmin-lactoferrin complex. Biochem. Cell. Biol. 80 (1), 35-39.