Search Results - "Demidova, I. A."

Identification of Chimeric NTRK3 Genes in Papillary Thyroid Cancer Cells by Analyzing the Imbalance of the Expression of 5’ and 3’ mRNA Fragments by Oskorbin, I. P., Ivanov, A. A., Smertina, M. A., Demidova, I. A., Boyarskikh, U. A., Kechin, A. A., Bakharev, S. Yu, Samuilenkova, O. V., Vihlyanov, I. V., Kushlinskii, N. E., Filipenko, M. L.

“…The standard for detecting chimeric genes of neurotrophic receptor tyrosine kinases ( NTRK ) is next generation sequencing (NGS). However, this analysis is…”
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Legality and Legal Order as Social Criteria of Legal Culture of Society: Theoretical Aspect by Demidova, I. A.

“…The Author proceeds from the fact that in modern political and legal realities, the most important social indicator of the legal culture of society is the…”
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Unexplained autism is frequently associated with low-level mosaic aneuploidy by Yurov, Y B, Vorsanova, S G, Iourov, I Y, Demidova, I A, Beresheva, A K, Kravetz, V S, Monakhov, V V, Kolotii, A D, Voinova-Ulas, V Y, Gorbachevskaya, N L

“…Background: Autism is a common childhood neurodevelopmental disorder with a possible genetic background. About 5–10% of autism cases are associated with…”
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Chromosomal mosaicism in spontaneous abortions: Analysis of 650 cases by Vorsanova, S. G, Iourov, I. Yu, Kolotii, A. D, Beresheva, A. K, Demidova, I. A, Kurinnaya, O. S, Kravets, V. S, Monakhov, V. V, Soloviev, I. V, Yurov, Yu. B

“…It is known that up to 50% spontaneous abortions (SA) in the first trimester of pregnancy are associated with chromosomal abnormalities. We studied mosaic…”
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Variability in the heterochromatin regions of the chromosomes and chromosomal anomalies in children with autism: identification of genetic markers of autistic spectrum disorders by Vorsanova, S G, Yurov, I Yu, Demidova, I A, Voinova-Ulas, V Yu, Kravets, V S, Solov'ev, I V, Gorbachevskaya, N L, Yurov, Yu B

“…Cytogenetic and molecular cytogenetic analysis of children with autism (90 subjects) and their mothers (18 subjects) is presented. Anomalies and fragility were…”
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Resolution on the results of Advisory Board “Searching the effective methods of testing and treating patients with NSCLC caused by NTRK gene fusions by Artamonova, E. V., Breder, V. V., Vladimirova, L. Yu, Demidova, I. A., Imyanitov, E. N., Laktionov, К. К., Matrosova, M. P., Orlov, S. V., Rodionov, E. О., Sakaeva, D. D., Sekacheva, M. I., Smolin, A. V., Fadeeva, N. V., Filipenko, M. L.

“…The Advisory Board was held on December 24, 2021. The molecular genetic research lead specialists and national lead oncologists discussed issues of diagnosis…”
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Cytogenetic and molecular-cytogenetic investigation of Rett syndrome: analysis of 31 cases by Vorsanova, S G, Demidova, I A, Ulas, V Yu, Soloviev, I V, Kazantzeva, L Z, Yurov, Yu B

“…RETT syndrome (RS) is a progressive encephalopathy restricted to the female sex. In the present study we investigated 30 females and one male with RS by…”
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Use of the new 2013 ASCO/CAP guidelines to study HERS status by fluorescence in situ hybridization in patients with breast cancer by Demidova, I A, Tsepenshchikova, E O, Gikalo, M B

“…Despite the long-term history of HER2 testing in breast cancer (BC), the results of its study are frequently interpreted ambiguously. The introduction of the…”
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New possibilities in the treatment of EGFR mutation-positive non-small-cell lung cancer patients after the progression on a 1st and 2nd generation EGFR tyrosine kinase inhibitors by Laktionov, K K, Reutova, E V, Nelyubina, L A, Pitkevich, M Yu, Okruzhnova, M A, Ardzinba, M S, Yudin, D I, Demidova, I A, Zaretsky, A R

“…Targeted therapy has opened a new era in treatment of patients with non-small-cell lung cancer associated with mutations of the epidermal growth factor…”
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Genomic instability in the brain: chromosomal mosaicism in schizophrenia by Yurov, Y B, Vorsanova, S G, Demidova, I A, Kravets, V S, Vostrikov, V M, Soloviev, I V, Uranova, N A, Iourov, I Y

“…Experimental verification of the hypothesis about the possible involvement of the mosaic genome variations (mosaic aneuploidy) in the pathogenesis of a number…”
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Clinical and genetic characteristics of the X chromosome distal long arm microduplications encompassing the MECP2 gene by Voinova, V Yu, Vorsanova, S G, Yurov, Yu B, Kolotiy, A D, Davidova, Yu I, Demidova, I A, Novikov, P V, Iourov, I Yu

“…Microduplications of the long arm of the X chromosome including the MECP2 gene are relatively common causes of neurodevelopmental disorders in males. Authors…”
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Cytogenetic, Molecular-Cytogenetic, and Clinical-Genealogical Studies of the Mothers of Children with Autism: A Search for Familial Genetic Markers for Autistic Disorders by Vorsanova, S. G., Voinova, V. Yu, Yurov, I. Yu, Kurinnaya, O. S., Demidova, I. A., Yurov, Yu. B.

“…State-of-the-art cytogenetic and molecular-cytogenetic methods for studying human chromosomes were used to analyze chromosomal anomalies and variants in…”
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Methods of molecular biology for detection of genetic aberrations and monitoring of residual disease in acute myeloid leukemia by I. A. Demidova

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Subchromosomal microdeletion identified by molecular karyotyping using DNA microarrays (array CGH) in Rett syndrome girls negative for MECP2 gene mutations by Vorsanova, S G, Iurov, I Iu, Voinova, V Iu, Kurinnaia, O S, Zelenova, M A, Demidova, I A, Ulas, E V, Iurov, Iu B

“…Molecular karyotyping using DNA microarrays (array CGH) was applied for identification of subchromosomal microdeletions in a cohort of 12 girls with clinical…”
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Cytogenetic, molecular cytogenetic, clinical and genealogical study of mothers of children with autism: a search for family genetic markers of autistic disorders by Vorsanova, S G, Voinova, V Iu, Iurov, I Iu, Kurinnaia, O S, Demidova, I A, Iurov, Iu B

“…Using modern cytogenetic and molecular cytogenetic techniques towards the study of human chromosomes, an analysis of chromosomal abnormalities/chromosomal…”
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Legal Culture of the State Law Enforcement Service in the Republic of Belarus: Activity and Value-Normative Aspects by Demidova, Irina A.

“…The importance of law enforcement in all spheres of public life, as well as public administration is conditioned by the objective need to ensure law and order…”
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Non-disjunction of chromosome 21, alphoid DNA variation, and sociogenetic features of Down syndrome by Vorsanova, S G, Iourov, I Y, Beresheva, A K, Demidova, I A, Monakhov, V V, Kravets, V S, Bartseva, O B, Goyko, E A, Soloviev, I V, Yurov, Y B

“…The analysis of non-disjunction of chromosome 21 and alphoid DNA variation by using cytogenetic and molecular cytogenetic techniques (quantitative fluorescence…”
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18p- Syndrome: an unusual case and diagnosis by in situ hybridization with chromosome 18-specific alphoid DNA sequence by VORSANOVA, S. G, YUROV, Y. B, ALEXANDROV, I. A, DEMIDOVA, I. A, MITKEVICH, S. P, TIRSKAIA, A. F

“…A patient with an atypical clinical picture of 18p- syndrome is described. By the in situ hybridization technique we localized the chromosome 18-specific…”
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Transplantations of allogenic and autologous hemopoietic stem cells in acute leukemia (results of 20-year experience) by Savchenko, V G, Liubimova, L S, Parovichnikova, E N, Mendeleeva, L P, Mamotiuk, K S, Demidova, I A, Gribanova, E O, Gal'tseva, I V, Pokrovskaia, O S, Kuz'mina, L A, Zhelnova, E I, Kliasova, G A, Glasko, E N, Kaplanskaia, I B, Poreshina, L P, Kut'ina, R M, Shpakova, A P, Shtareva, E M, Varlamova, S V, Kalinin, N N

“…To analyse results of transplantation of allogenic and autologous hemopoietic stem cells (allo-THSC and auto-THSC) with myeloablation preconditioning in…”
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Hereditary ovarian cancer by I A Demidova

“…Epithelial carcinoma or ovarian cancer (OC) is the fifth most common cause of cancer mortality in women, and hereditary/familial OC occurs in 15-20% of all…”
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