A Molecular Genetic Analysis of RPE65-Associated Forms of Inherited Retinal Degenerations in the Russian Federation

por Stepanova, Anna, Ogorodova, Natalya, Kadyshev, Vitaly, Shchagina, Olga, Kutsev, Sergei, Polyakov, Aleksandr
Publicado 2023

Ontogenetic and Pathogenetic Views on Somatic Chromosomal Mosaicism

por Iourov, Ivan Y., Vorsanova, Svetlana G., Yurov, Yuri B., Kutsev, Sergei I.
Publicado 2019

Chromosome Instability, Aging and Brain Diseases

por Iourov, Ivan Y., Yurov, Yuri B., Vorsanova, Svetlana G., Kutsev, Sergei I.
Publicado 2021

Somatic mosaicism in the diseased brain

por Iourov, Ivan Y., Vorsanova, Svetlana G., Kurinnaia, Oxana S., Kutsev, Sergei I., Yurov, Yuri B.
Publicado 2022

Pilot Program of Newborn Screening for 5q Spinal Muscular Atrophy in the Russian Federation

por Mikhalchuk, Kristina, Shchagina, Olga, Chukhrova, Alena, Zabnenkova, Viktoria, Chausova, Polina, Ryadninskaya, Nina, Vlodavets, Dmitry, Kutsev, Sergei I., Polyakov, Alexander
Publicado 2023

The Cytogenomic “Theory of Everything”: Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and Aging

por Iourov, Ivan Y., Vorsanova, Svetlana G., Yurov, Yuri B., Zelenova, Maria A., Kurinnaia, Oxana S., Vasin, Kirill S., Kutsev, Sergei I.
Publicado 2020

New Regions With Molecular Alterations in a Rare Case of Insulinomatosis: Case Report With Literature Review

por Anoshkin, Kirill, Vasilyev, Ivan, Karandasheva, Kristina, Shugay, Mikhail, Kudryavtseva, Valeriya, Egorov, Alexey, Gurevich, Larisa, Mironova, Anna, Serikov, Alexey, Kutsev, Sergei, Strelnikov, Vladimir
Publicado 2021

Pediatric chordoma associated with tuberous sclerosis complex: A rare case report with a thorough analysis of potential therapeutic molecular targets

por Anoshkin, Kirill, Zosen, Denis, Karandasheva, Kristina, Untesco, Maxim, Volodin, Ilya, Alekseeva, Ekaterina, Parfenenkova, Anna, Snegova, Eugenia, Kim, Aleksandr, Dorofeeva, Marina, Kutsev, Sergei, Strelnikov, Vladimir
Publicado 2022

Antioxidant Properties of Fullerene Derivatives Depend on Their Chemical Structure: A Study of Two Fullerene Derivatives on HELFs

por Sergeeva, Vasilina, Kraevaya, Olga, Ershova, Elizaveta, Kameneva, Larisa, Malinovskaya, Elena, Dolgikh, Olga, Konkova, Marina, Voronov, Iliya, Zhilenkov, Alexander, Veiko, Natalia, Troshin, Pavel, Kutsev, Sergei, Kostyuk, Svetlana
Publicado 2019

Evaluation of the Complex p.[Leu467Phe;Phe508del] CFTR Allele in the Intestinal Organoids Model: Implications for Therapy

por Kondratyeva, Elena, Efremova, Anna, Melyanovskaya, Yuliya, Voronkova, Anna, Polyakov, Alexander, Bulatenko, Nataliya, Adyan, Tagui, Sherman, Viktoriya, Kovalskaia, Valeriia, Petrova, Nika, Starinova, Marina, Bukharova, Tatiana, Kutsev, Sergei, Goldshtein, Dmitry
Publicado 2022

Aneuploidy and Confined Chromosomal Mosaicism in the Developing Human Brain

por Yurov, Yuri B., Iourov, Ivan Y., Vorsanova, Svetlana G., Liehr, Thomas, Kolotii, Alexei D., Kutsev, Sergei I., Pellestor, Franck, Beresheva, Alfia K., Demidova, Irina A., Kravets, Viktor S., Monakhov, Viktor V., Soloviev, Ilia V.
Publicado 2007

Abnormal Hypermethylation of CpG Dinucleotides in Promoter Regions of Matrix Metalloproteinases Genes in Breast Cancer and its Relation to Epigenomic Subtypes and HER2 Overexpressi...

por Simonova, Olga A., Kuznetsova, Ekaterina B., Tanas, Alexander S., Rudenko, Viktoria V., Poddubskaya, Elena V., Kekeeva, Tatiana V., Trotsenko, Ivan D., Larin, Sergey S., Kutsev, Sergei I., Zaletaev, Dmitry V., Nemtsova, Marina V., Strelnikov, Vladimir V.
Publicado 2020

Health Characteristics of Patients with Cystic Fibrosis whose Genotype Includes a Variant of the Nucleotide Sequence c.3140-16T>A and Functional Analysis of this Variant

por Kondratyeva, Elena, Bukharova, Tatyana, Efremova, Anna, Melyanovskaya, Yuliya, Bulatenko, Natalia, Davydenko, Ksenia, Filatova, Alexandra, Skoblov, Mikhail, Krasovsky, Stanislav, Petrova, Nika, Polyakov, Alexander, Adyan, Tagui, Amelina, Elena, Shadrina, Vera, Zhekaite, Elena, Zodbinova, Aysa, Chernyak, Alexander, Zinchenko, Rena, Kutsev, Sergei, Goldshtein, Dmitry
Publicado 2021

Multiple Chromoanasynthesis in a Rare Case of Sporadic Renal Leiomyosarcoma: A Case Report

por Anoshkin, Kirill Igorevich, Karandasheva, Kristina Olegovna, Goryacheva, Kristina Mikhaylovna, Pyankov, Denis Valer’yevich, Koshkin, Philipp Aleksandrovich, Pavlova, Tatiana Vladimirovna, Bobin, Alexandr Nikolaevich, Shpot, Evgeniy Valer’yevich, Chernov, Yaroslav Nikolayevich, Vinarov, Andrei Zinov’yevich, Zaletaev, Dmitry Vladimirovich, Kutsev, Sergei Ivanovich, Strelnikov, Vladimir Viktorovich
Publicado 2020

Vitamin D Status Among Children With Juvenile Idiopathic Arthritis: A Multicenter Prospective, Non-randomized, Comparative Study

por Kondratyeva, Elena I., Odinaeva, Nuriniso D., Klimov, Leonid Ya, Podchernyaeva, Nadeshda S., Ilenkova, Natalya I., Dolbnya, Svetlana V., Zhekaite, Elena K., Kuryaninova, Victoria A., Kotova, Yuliya V., Tikhaya, Margarita I., Shitkovskaya, Elena P., Bychina, Liubov V., Drepa, Tamara G., Zodbinova, Aisa E., Melyanovskaya, Yuliya L., Petrova, Nika V., Loshkova, Elena V., Kutsev, Sergei I.
Publicado 2022