Search Results - "Gervas, P"

DNA methylome analysis reveals potential alterations contributing to the progression of bronchial hyperplasia by Ponomaryova, A. A., Schegoleva, A. A., Gervas, P. A., Pancova, O. V., Gerashchenko, T. S., Zarubin, A. A., Perelmuter, V. M., Cherdyntseva, N. V., Denisov, E. V.

“…Background Squamous cell lung cancer (SCLC) arises from bronchial changes: basal cell hyperplasia (BCH), squamous metaplasia (SM), and dysplasia. However, the…”
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Analysis of Methylome of Different Forms of Basal Cell Hyperplasia and Squamous Cell Metaplasia of Bronchial Epithelium by Ponomaroyva, A. A., Schegoleva, A. A., Gervas, P. A., Gerashchenko, T. S., Pankova, O. V., Ershov, N. I., Perelmuter, V. M., Cherdyntseva, N. V., Denisov, E. V.

“…Squamous cell lung cancer (SCLC) occurs as a result of dysregenerative changes in the bronchial epithelium: basal cell hyperplasia (BCH), squamous cell…”
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Exome Sequencing: the Search for Mutations Associated with Hereditary Breast and Ovarian Cancers in the Tuvan Ethnic Group (A Pilot Study) by Gervas, P., Molokov, A., Zarubin, A., Shivit-Ool, A. A., Babyshkina, N., Shefer, N., Topolnitsky, E., Pisareva, L., Choinzonov, E., Cherdyntseva, N.

“…Whole exome sequencing of peripheral blood samples from Tuvan females diagnosed with breast and ovarian cancers (BC/OC) was performed to search for new genes…”
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NGS for detection of mutations of the EGFR gene in plasma DNA of patients with the lung cancer by Pisareva, E., Gornostaeva, E., Gervas, P., Gutkina, N., Kudryavtsev, A., Cherdyntseva, N., Karpov, I., Shamanin, V., Kovalenko, S.

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Circulating tumor cells in breast cancer: functional heterogeneity, pathogenetic and clinical aspects by Cherdyntseva, N V, Litviakov, N V, Denisov, E V, Gervas, P A, Cherdyntsev, E S

“…Each patient has a unique history of cancer ecosystem development, resulting in intratumor heterogeneity. In order to effectively kill the tumor cells by…”
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P114 by Gervas, P, Perelmuter, V

“…Background Lung cancers are characterized by the genetic alterations that often affect a common group of oncogenic signaling pathways. Identification of…”
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MONITORING OF EGFR MUTATIONS IN THE CIRCULATING TUMOR DNA FROM BLOOD PLASMA OF PATIENTS WITH NON-SMALL CELL LUNG CANCER by Shamanin, V. A., Karpov, I. V., Gervas, P. А., Cherdyntseva, N. V., Simolina, E. I., Kozlov, V. V., Kovalenko, S. P.

“…Activating mutations of EGFR are associated with sensitivity of non-small cell lung cancer (NSCLC ) to tyrosine kinase inhibitors (TKI). Liquid biopsy using…”
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Endogenous and exogenous risk factors affecting the incidence of breast cancer in the population of Yakutia by Tikhonov, D. G., Molokov, A. Yu, Belyavskaya, V. A., Ananina, O. A., Gervas, P. A.

“…The purpose of the study : to analyze the breast cancer incidence and breast cancer risk factors for the population of the Republic of Sakha (Yakutia) in…”
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Variability of the mitochondrial genome in young Yakut patients with breast cancer by Tikhonov, D. G., Egorov, A. N., Golubenko, M. V., Molokov, A. Yu, Belyavskaya, V. A., Gervas, P. A., Skryabin, N. A.

“…Background . The Sakha (Yakutia) population, the indigenous population of Siberia living in Yakutia, has one of the lowest rates of breast cancer (BC)…”
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34P New pathogenic germline mutation in ATM gene in Khakass breast cancer patients by Gervas, P., Cherdyntseva, N.

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Nivolumab monotherapy in metastatic colorectal cancer: current approaches to response evaluation by Babyshkina, N. N., Dronova, T. A., Gervas, P. A., Popova, N. O., Dobrodeev, A. Yu, Kostromitsky, D. N., Afanasyev, S. G., Goldberg, V. E., Cherdyntseva, N. V.

“…Aim of the study: a systematic analysis of the modern literature data on the nivolumab monotherapy efficacy in patients with metastatic colorectal cancer…”
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New mutation of the TP53 gene associated with the hereditary breast cancer in a young Tuvinian woman by Gervas, P. A., Molokov, A. Yu, Zarubin, A. A., Ponomareva, A. A., Babyshkina, N. N., Belyavskaya, V. A., Pisareva, L. F., Choynzonov, E. L., Cherdyntseva, N. V.

“…Background. The identification of the ethnospecific mutations associated with hereditary breast cancer remains challenging. Next generation sequencing (Ngs)…”
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Ethnic aspects of hereditary breast cancer by Gervas, P. A., Molokov, A. Yu, Panpherova, E. V., Pisareva, L. Ph, Cherdyntseva, N. V.

“…This study aimed to reveal the spectrum of BRca1 and BRca2 genes mutation in various ethnic groups of the Russian Federation. asystematic literature search…”
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177P Pathogenicity reclassification of unknown significance variants related to early-onset breast cancer women of mongoloid origin by Gervas, P., Molokov, A., Cherdyntseva, N.

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New germline RAD51D gene variant in the Mongol breast cancer patients by Molokov, A., Gervas, P., Cherdyntseva, N.

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Age-related function of tumor suppressor gene TP53:contribution to cancer risk and progression by Cherdyntseva, N V, Gervas, P A, Litvyakov, N V, Stakcheeva, M N, Ponomaryeva, A A, Dobrodeev, A Yu, Denisov, E V, Belyavskaya, V A, Choinzonov, E L

“…To examine the influence of combined genotypes of TP53 (exon 4, intron 3, intron 6) and XRCC1 (codon 10) on lung cancer age of onset. TP53 polymorphisms in…”
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Non-BRCA hereditary gene mutations in the Mongol breast cancer patients of Russia by Gervas, P., Denisov, E., Kiselev, A., Molokov, A., Ivanova, A., Choynzonov, E., Cherdyntseva, N.

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Genetic status of p53 in stomach cancer: somatic mutations and polymorphism of codon 72 by Belyavskaya, V A, Vardosanidze, V K, Smirnova, O Yu, Karakin, E I, Savkin, I V, Gervas, P A, Cherdyntseva, N V, Voevoda, M I

“…The incidence of somatic mutagenesis of p53 oncosuppressor protein in malignant tumors of the stomach and genetic polymorphism of p53 were studied in patients…”
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An expert system for the composition of formal Spanish poetry by Gervás, Pablo

“…The present paper presents an application that composes formal poetry in Spanish in a semiautomatic interactive fashion. Automatic Spanish Poetry Expert and…”
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P114: Intratumor heterogeneity of driver mutations in lung adenocarcinoma by Gervas, P., Perelmuter, V.

“…Lung cancers are characterized by the genetic alterations that often affect a common group of oncogenic signaling pathways. Identification of biologically…”
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