Search Results - "Matsko, Dmitry E"

Detection of EGFR mutations and EML4‐ALK rearrangements in lung adenocarcinomas using archived cytological slides by Mitiushkina, Natalia V., Iyevleva, Aglaya G., Poltoratskiy, Artiom N., Ivantsov, Alexandr O., Togo, Alexandr V., Polyakov, Igor S., Orlov, Sergey V., Matsko, Dmitry E., Novik, Viktor I., Imyanitov, Evgeny N.

“…BACKGROUND Although the molecular analysis of epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) in archived lung cancer tissues is…”
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Mixed epithelial/mesenchymal metaplastic carcinoma (carcinosarcoma) of the breast in BRCA1 carrier by Suspitsin, Evgeny N., Sokolenko, Anna P., Voskresenskiy, Dmitry A., Ivantsov, Alexandr O., Shelehova, Kseniya V., Klimashevskiy, Valery F., Matsko, Dmitry E., Semiglazov, Vladimir F., Imyanitov, Evgeny N.

“…This case report describes a 35-year-old woman who was diagnosed with mixed epithelial/mesenchymal metaplastic carcinoma (carcinosarcoma) of the breast…”
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Nonrandom distribution of oncogene amplifications in bilateral breast carcinomas: Possible role of host factors and survival bias by Suspitsin, Evgeny N., Sokolenko, Anna P., Togo, Alexandr V., Lazareva, Yulia R., Turkevich, Elena A., Matsko, Dmitry E., Henrich, Kai‐Oliver, Borresen‐Dale, Anne‐Lise, Schwab, Manfred, Cornelisse, Cees J., Imyanitov, Evgeny N.

“…Amplification of HER2, C‐MYC and CCND1 oncogenes is a hallmark of breast cancer (BC); however, its involvement in the bilateral form of this disease has not…”
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High prevalence and breast cancer predisposing role of the BLM c.1642 C>T (Q548X) mutation in Russia by Sokolenko, Anna P., Iyevleva, Aglaya G., Preobrazhenskaya, Elena V., Mitiushkina, Nathalia V., Abysheva, Svetlana N., Suspitsin, Evgeny N., Kuligina, Ekatherina Sh, Gorodnova, Tatiana V., Pfeifer, Werner, Togo, Alexandr V., Turkevich, Elena A., Ivantsov, Alexandr O., Voskresenskiy, Dmitry V., Dolmatov, Georgy D., Bit-Sava, Elena M., Matsko, Dmitry E., Semiglazov, Vladimir F., Fichtner, Iduna, Larionov, Alexey A., Kuznetsov, Sergey G., Antoniou, Antonis C., Imyanitov, Evgeny N.

“…The BLM gene belongs to the RecQ helicase family and has been implicated in the maintenance of genomic stability. Its homozygous germline inactivation causes…”
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What Tactics Should a Surgeon Choose to Treat a Black Extracerebral Tumor? A Case Report of Psammomatous Melanotic Schwannoma of the Meckel Cave and Literature Review by Moisak, Galina I., Matsko, Dmitry E., Chernov, Sergey V., Dmitriev, Aleksandr B., Amelin, Mikhail E., Zhelbunova, Elena A., Chernov, Mikhail F., Rzaev, Jamil A.

“…Neoplasms located in the Meckel cave account for 0.2%–0.5% of all intracranial tumors. This area is the site of many types of pathologic lesions, most often…”
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Breast cancer sensitivity to neoadjuvant therapy in BRCA1 and CHEK2 mutation carriers and non-carriers by Pfeifer, Werner, Sokolenko, Anna P., Potapova, Olga N., Bessonov, Alexandr A., Ivantsov, Alexandr O., Laptiev, Sergey A., Zaitseva, Olga A., Yatsuk, Olga S., Matsko, Dmitry E., Semiglazova, Tatiana Yu, Togo, Alexandr V., Imyanitov, Evgeny N.

“…Breast carcinomas caused by inheritance of cancer-predisposing germ-line mutations have specific bioclinical features. This study aimed to analyze the efficacy…”
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Myxopapillary Ependymoma of Lumbar Soft Tissue: A Case Report With Gene Expression Evaluation by Shelekhova, Ksenya V., Egorenkov, Vitaly V., Kheinstein, Valery A., Konstantinova, Anastasia M., Iyevleva, Aglaya, Imyanitov, Evgeny N., Matsko, Marina V., Matsko, Dmitry E.

“…Primary extraspinal myxopapillary ependymoma (MPE) is an exceptionally rare lesion that is mainly located in the subcutaneous sacrococcygeal region. We…”
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High frequency of BRCA1 5382insC mutation in Russian breast cancer patients by Sokolenko, Anna P., Mitiushkina, Natalia V., Buslov, Konstantin G., Bit-Sava, Elena M., Iyevleva, Aglaya G., Chekmariova, Elena V., Kuligina, Ekatherina Sh, Ulibina, Yulia M., Rozanov, Maxim E., Suspitsin, Evgeny N., Matsko, Dmitry E., Chagunava, Oleg L., Trofimov, Dmitry Yu, Devilee, Peter, Cornelisse, Cees, Togo, Alexandr V., Semiglazov, Vladimir F., Imyanitov, Evgeny N.

“…BRCA1 5382insC variant was repeatedly detected in Jewish breast cancer (BC) families residing in USA and Israel as well as in non-Jewish familial BC patients…”
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KIT mutations in Russian patients with mucosal melanoma by Abysheva, Svetlana N, Iyevleva, Aglaya G, Efimova, Nina V, Mokhina, Yulia B, Sabirova, Feruza A, Ivantsov, Alexandr O, Artemieva, Anna S, Togo, Alexandr V, Moiseyenko, Vladimir M, Matsko, Dmitry E, Imyanitov, Evgeny N

“…A single institution series of 48 mucosal melanomas (MMs) has been analyzed for the presence of KIT mutations using high-resolution melting and sequencing of…”
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High efficacy of first-line gefitinib in non-Asian patients with EGFR-mutated lung adenocarcinoma by Moiseyenko, Vladimir M, Procenko, Svetlana A, Levchenko, Evgeny V, Barchuk, Alexey S, Moiseyenko, Fedor V, Iyevleva, Aglaya G, Mitiushkina, Nathalia V, Togo, Alexandr V, Semionov, Igor I, Ivantsov, Alexandr O, Matsko, Dmitry E, Imyanitov, Evgeny N

“…Several Asian studies demonstrated feasibility of front-line administration of gefitinib for the treatment of non-small cell lung carcinomas (NSCLCs) harboring…”
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NBS1 657del5 mutation may contribute only to a limited fraction of breast cancer cases in Russia by Buslov, Konstantin G., Iyevleva, Aglaya G., Chekmariova, Elena V., Suspitsin, Evgeny N., Togo, Alexandr V., Kuligina, Ekatherina Sh, Sokolenko, Anna P., Matsko, Dmitry E., Turkevich, Elena A., Lazareva, Yulia R., Chagunava, Oleg L., Bit‐Sava, Elena M., Semiglazov, Vladimir F., Devilee, Peter, Cornelisse, Cees, Hanson, Kaido P., Imyanitov, Evgeny N.

“…The gene for Nijmegen chromosomal breakage syndrome (NBS1) plays a role in a variety of processes protecting chromosomal stability. Recently, it was suggested…”
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CHEK2 1100delC mutation is frequent among Russian breast cancer patients by Chekmariova, Elena V, Sokolenko, Anna P, Buslov, Konstantin G, Iyevleva, Aglaya G, Ulibina, Yulia M, Rozanov, Maxim E, Mitiushkina, Natalia V, Togo, Alexandr V, Matsko, Dmitry E, Voskresenskiy, Dmitry A, Chagunava, Oleg L, Devilee, Peter, Cornelisse, Cees, Semiglazov, Vladimir F, Imyanitov, Evgeny N

“…This study was aimed to assess the role of CHEK2 1100delC mutation in breast cancer (BC) predisposition in Russia. The 1100delC allele was detected in 14/660…”
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Rapid symptomatic improvement in gefitinib-treated patients with EGFR-mutated lung cancer: possible role of downregulation of inflammatory molecules? by Suspitsin, Evgeny N, Levchenko, Evgeny V, Moiseyenko, Fedor V, Ivantsov, Alexandr O, Radzhabova, Samira A, Matsko, Dmitry E, Moiseyenko, Vladimir M, Imyanitov, Evgeny N

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Down-staging of EGFR mutation-positive advanced lung carcinoma with gefitinib followed by surgical intervention: follow-up of two cases by Levchenko, Evgeny V, Moiseyenko, Vladimir M, Matsko, Dmitry E, Iyevleva, Aglaya G, Ivantsov, Alexandr O, Yargnian, Stepan M, Anisimov, Valentin V, Semionov, Igor I, Imyanitov, Evgeny N

“…Non-small cell lung carcinomas (NSCLC) carrying a mutation in the epidermal growth factor receptor (EGFR) gene show unprecedented sensitivity to gefitinib or…”
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Benign Schwannoma With Perineurioma-Like Areas: A Clinicopathologic Study of 11 Cases by Kazakov, Dmitry V., Magro, Gaetano, Yu Orlov, Andrey, Shelekhova, Ksenya V., Matsko, Dmitry E., Spagnolo, Dominic V., Michal, Michal

“…Eleven schwannomas are described. All tumors were well demarcated and surrounded by a true capsule or pseudocapsule and manifested Antoni A and Antoni B areas,…”
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Measurement of DPD and TS transcripts aimed to predict clinical benefit from fluoropyrimidines: confirmation of the trend in Russian colorectal cancer series and caution regarding the gene referees by Iyevleva, Aglaya G, Buslov, Konstantin G, Togo, Alexandr V, Matsko, Dmitry E, Filimonenko, Vasily P, Moiseyenko, Vladimir M, Imyanitov, Evgeny N

“…Measurement of intratumoral expression of dihydropyrimidine dehydrogenase (DPD) and thymidylate synthase (TS) may have some value in predicting the response to…”
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High sensitivity of BRCA1 -associated tumors to cisplatin monotherapy: report of two cases by Moiseyenko, Vladimir M, Protsenko, Svetlana A, Brezhnev, Nikita V, Maximov, Sergey Ya, Gershveld, Eduard D, Hudyakova, Marina A, Lobeiko, Oksana S, Gergova, Madina M, Krzhivitskiy, Pavel I, Semionov, Igor I, Matsko, Dmitry E, Iyevleva, Aglaya G, Sokolenko, Anna P, Sherina, Nathalia Yu, Kuligina, Ekatherina Sh, Suspitsin, Evgeny N, Togo, Alexandr V, Imyanitov, Evgeny N

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Breast cancer sensitivity to neo-adjuvant therapy in BRCA1 and CHEK2 mutation carriers and non-carriers by Pfeifer, Werner, Sokolenko, Anna P, Potapova, Olga N, Bessonov, Alexandr A, Ivantsov, Alexandr O, Laptiev, Sergey A, Zaitseva, Olga A, Yatsuk, Olga S, Matsko, Dmitry E, Semiglazova, Tatiana Yu, Togo, Alexandr V, Imyanitov, Evgeny N

“…Breast carcinomas caused by inheritance of cancer-predisposing germ-line mutations have specific bioclinical features. This study aimed to analyze the efficacy…”
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Ovarian cancer patient with germline mutations in both BRCA1 and NBN genes by Porhanova, Nathalia V, Sokolenko, Anna P, Sherina, Nathalia Yu, Ponomariova, Daria N, Tkachenko, Nathalia N, Matsko, Dmitry E, Imyanitov, Evgeny N

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High frequency of BRCA1, but not CHEK2 or NBS1 (NBN), founder mutations in Russian ovarian cancer patients by Suspitsin, Evgeny N, Sherina, Nathalia Yu, Ponomariova, Daria N, Sokolenko, Anna P, Iyevleva, Aglaya G, Gorodnova, Tatyana V, Zaitseva, Olga A, Yatsuk, Olga S, Togo, Alexandr V, Tkachenko, Nathalia N, Shiyanov, Grigory A, Lobeiko, Oksana S, Krylova, Nadezhda Yu, Matsko, Dmitry E, Maximov, Sergey Ya, Urmancheyeva, Adel F, Porhanova, Nathalia V, Imyanitov, Evgeny N

“…A significant portion of ovarian cancer (OC) cases is caused by germ-line mutations in BRCA1 or BRCA2 genes. BRCA testing is cheap in populations with founder…”
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