Zobrazeno 1 - 10
of 40
pro vyhledávání: '"V M, Kozlova"'
Autor:
T. S. Belysheva, T. V. Nasedkina, V. V. Semenova, V. M. Kozlova, E. V. Sharapova, S. N. Mikhailova, T. T. Valiev, S. R. Varfolomeeva
Publikováno v:
Russian Journal of Pediatric Hematology and Oncology. 9:60-74
Genodermatoses are a heterogeneous group of hereditary diseases that are characterized by predominantly skin lesions. To date, there are more than 200 genetically determined skin diseases, representing about 35 % of all hereditary syndromes. In some
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1107e2b008691c8da041009302e596d3
https://doi.org/10.21682/2311-1267-2022-9-2-60-74
https://doi.org/10.21682/2311-1267-2022-9-2-60-74
Autor:
T. S. Belysheva, T. V. Nasedkina, T. T. Valiev, N. V. Matinyan, O. A. Malikhova, V. V. Semenova, V. M. Kozlova, T. P. Kazubskaya, Y. V. Vishnevskaya, S. N. Mikhailova, S. R. Varfolomeeva
Publikováno v:
Russian Journal of Pediatric Hematology and Oncology. 8:95-102
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e2a32cb1a676212354f98daf3db995d
https://doi.org/10.21682/2311-1267-2021-8-4-95-102
https://doi.org/10.21682/2311-1267-2021-8-4-95-102
Autor:
М. А. Bolokhonova, V. Yu. Panarina, E. V. Sharapova, S. N. Mikhailova, Т. Т. Valiev, V. M. Kozlova
Publikováno v:
Medical alphabet. :16-19
Gorlin-Golts syndrome is a genetic determined disease, characterized by multisystem features and associated with different malignancies, which are more aggressive with very unfavorable prognosis. By literature data this syndrome is a rare pathology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed5cfc65228fa217decf27774a2a1fec
https://doi.org/10.33667/2078-5631-2021-37-16-19
https://doi.org/10.33667/2078-5631-2021-37-16-19
Publikováno v:
Современная онкология, Vol 3, Iss 4, Pp 173-179 (2001)
Нефробластома - одна из наиболее часто встречающихся злокачественных эмбриональных опухолей у детей.Сторонники морфологического подт
Externí odkaz:
https://doaj.org/article/5b40009ad8d344298618c505439db74d
Autor:
Yu.O. Redin, V. M. Kozlova
Publikováno v:
Russian Journal of Pacific Geology. 8:187-199
The Au-Bi-Te mineralization is found and studied at the Serebryanoe deposit in Eastern Transbaikalia. The microprobe analyses of the native gold and sulfides and the sulfur isotopic composition of the sulfides are presented. The early gold-pyrite-ars
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bbe1dd601470fcd1ec6e8c7f2b0e2da
https://doi.org/10.1134/s1819714014030087
https://doi.org/10.1134/s1819714014030087
Autor:
R. F. Garkavtseva, V. M. Kozlova, M. A. Shabanov, Tatiana P. Kazubskaya, V. K. Musatov, V. Yu. Sel'chuk, A. V. Mikhailovskii, E. I. Trofimov
Publikováno v:
Scopus-Elsevier
The identification of hereditary variants of cutaneous melanoma and analysis of the role of hereditary factors and syndromes predisposing to cutaneous melanoma were carried out. The involvement of individual nevus phenotypes in the development of thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::206d9c1cf2231a3559df567140489b4c
https://doi.org/10.1023/b:ruge.0000013451.88898.38
https://doi.org/10.1023/b:ruge.0000013451.88898.38
Autor:
T P, Kazubskaia, V M, Kozlova, T T, Kondrat'eva, A I, Pavlovskaia, A V, Marakhonov, A V, Baranova, N I, Ivanova, A A, Stepanova, A V, Poliakov, N F, Belev, V Zh, Brzhezovskiĭ
Publikováno v:
Arkhiv patologii. 76(5)
To determine the genetic forms of follicular cell thyroid carcinoma (FCTC) (papillary and follicular thyroid carcinoma (PTC and FTC)), to identify criteria to individually predict the development of the same disease for relatives, and to assess the r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::308b65dfbe16178c92d26c3c4cb63cb3
https://pubmed.ncbi.nlm.nih.gov/25543402
https://pubmed.ncbi.nlm.nih.gov/25543402
Autor:
T P, Kazubskaia, V M, Kozlova, V K, Musatov, A V, Mikhaĭlovskiĭ, M A, Shabanov, E I, Trofimov, V Iu, Sel'chuk, R F, Gar'kavtseva
Publikováno v:
Genetika. 40(1)
The identification of hereditary variants of cutaneous melanoma and analysis of the role of hereditary factors and syndromes predisposing to cutaneous melanoma were carried out. The involvement of individual nevus phenotypes in the development of thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7ca831a796f404be4e54c128f62e881c
https://pubmed.ncbi.nlm.nih.gov/15027204
https://pubmed.ncbi.nlm.nih.gov/15027204
Autor:
O V, Babenko, S V, Saakian, A F, Brovkina, V M, Kozlova, V V, Strel'nikov, D V, Zaletaev, M V, Nemtsova
Publikováno v:
Molekuliarnaia biologiia. 36(4)
The spectrum and frequencies of RB1 structural defects were studied in tumors and peripheral blood lymphocytes of patients with various forms of retinoblastoma. Single strand conformation polymorphism (SSCP) and heteroduplex (HA) analyses, along with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::704b9b408445f3b9510e428bc064b743
https://pubmed.ncbi.nlm.nih.gov/12173465
https://pubmed.ncbi.nlm.nih.gov/12173465
Publikováno v:
Vestnik oftalmologii. 118(1)
The first experience with molecular diagnosis of retinoblastoma (RB) in Russia is presented. A protocol based on the use of up-to-date molecular diagnostic methods helps detect structural and functional abnormalities in RB1 gene, diagnose RB in dispu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::817506de8aa204e486f22ab8661b05fd
https://pubmed.ncbi.nlm.nih.gov/11898356
https://pubmed.ncbi.nlm.nih.gov/11898356