Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Valentina M, Kozlova"'
Autor:
Tatiana S. Belysheva, Tatiana V. Nasedkina, Timur T. Valiev, Elena V. Sharapova, Vera V. Semenova, Valentina M. Kozlova, Svetlana N. Mikhaylova, Irina S. Kletskaya, Alexey V. Butuzov, Yana V. Vishnevskaja, Valeria V. Lozovaya, Olga A. Gusarova, Armen O. Tumanyan, Olga A. Malichova, Svetlana R. Varfolomeeva
Publikováno v:
Вопросы современной педиатрии, Vol 22, Iss 4, Pp 331-342 (2023)
Background. Hereditary polyposis syndromes (HPS) are a group of rare genetic diseases characterized by multiple epithelial lesions in the gastrointestinal tract (GIT) with high risk of malignancy and neoplasia development in other localizations. The
Externí odkaz:
https://doaj.org/article/011e6e7a0dea4c1fbb5c37943a6d301f
Autor:
Valentina M. Kozlova, Ekaterina E. Zelenova, Timur T. Valiev, Vera V. Semenova, Tatiana N. Nasedkina, Svetlana N. Mikhailova
Publikováno v:
Педиатрическая фармакология, Vol 20, Iss 6 (2023)
Hematooncological diseases head the list in the structure of malignant neoplasms of childhood. Somatic mutations in tumor clone cells have been well studied, included in modern classifications, and are used to stratify patients into prognostic risk g
Externí odkaz:
https://doaj.org/article/126b010ce10247869ad7c3b24284a231
Autor:
Vladimir G. Polyakov, Ruslan V. Shishkov, Aleksei A. Ilyin, Severskaya N. Viktorovna, Natalia V. Ivanova, Roman I. Pimenov, Valentina M. Kozlova, Faina A. Amosenko, Ludmila N. Lubchenko, Tatyiana P. Kazubskaya, Alentina I. Pavlovskaya, Oleg P. Bleznukov, Natalia A. Koshechkina, Elena V. Mikhaylova, Tamara R. Panferova, Irina I. Matveeva, Irina N. Serebryakova, Svetlana N. Mikhaylova, Victor S. Medvedev, Pavel A. Isaev, Pavel O. Rumyantsev, Alexandr U. Abrosimov, Natalia U. Kalinchenko
Publikováno v:
Клиническая и экспериментальная тиреоидология, Vol 12, Iss 1, Pp 22-33 (2016)
Genetically caused medullary thyroid cancer (MTC) is associated with unfavorable survival prognosis, so it makes necessary to develop new diagnostic techniques to reveal pre-clinical stage of disease as well as to introduce into clinical practice the
Externí odkaz:
https://doaj.org/article/90e86b64155241c3acf2c2b1131c150e
Autor:
Irina V. Bure, Ekaterina A. Alekseeva, Dmitry S. Mikhaylenko, Vladimir V Strelnikov, Marina V. Nemtsova, A.I. Kalinkin, Tatiana L Ushakova, Dmitry V. Zaletaev, Ekaterina B. Kuznetsova, Sergey I. Kutsev, Tatiana P. Kazubskaya, O. V. Babenko, Galina G. Chesnokova, Alexander S Tanas, Valentina M. Kozlova
Publikováno v:
Cancers, Vol 13, Iss 5068, p 5068 (2021)
Cancers
Volume 13
Issue 20
Cancers
Volume 13
Issue 20
Our aim was to identify RB1 alterations causing hereditary low penetrance retinoblastoma and to evaluate how the parental origin of an RB1 mutation affects its phenotypic expression. By NGS and MLPA, RB1 mutations were found in 191 from 332 unrelated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4c97c700def6768c140e782e667b2cc
https://www.mdpi.com/2072-6694/13/20/5068
https://www.mdpi.com/2072-6694/13/20/5068
Autor:
Ekaterina A, Alekseeva, Olga V, Babenko, Valentina M, Kozlova, Tatiana L, Ushakova, Tatiana P, Kazubskaya, Marina V, Nemtsova, Galina G, Chesnokova, Dmitry S, Mikhaylenko, Irina V, Bure, Alexey I, Kalinkin, Ekaterina B, Kuznetsova, Alexander S, Tanas, Sergey I, Kutsev, Dmitry V, Zaletaev, Vladimir V, Strelnikov
Publikováno v:
Cancers
Simple Summary Some families with hereditary retinoblastoma exhibit mild phenotype with low penetrance and variable expressivity, including complete absence of clinical signs of the disease in some carriers of the germline RB1 mutation. The identific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a67607cd9704d8aa22277248e4ec56d2
https://pubmed.ncbi.nlm.nih.gov/34680218
https://pubmed.ncbi.nlm.nih.gov/34680218