Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Yulia A. Maksimova"'
Autor:
Lyudmila G. Ananyeva, Alexandr A. Doroshenko, Sergey S. Ilenok, Yana O. Karymova, Michail V. Korovkin, Yulia A. Maksimova, Alexey V. Pesterev, Oleg N. Protsky, Olesya V. Savinova, Maria O. Khrushcheva
Publikováno v:
Известия Томского политехнического университета: Инжиниринг георесурсов, Vol 332, Iss 12, Pp 114-123 (2021)
The relevance of the study is caused by the need to develop the oil and gas industry in Western Siberia by identifying unconventional (including low-permeability) reservoirs and assessing their prospects for development. The aim: to increase the effi
Externí odkaz:
https://doaj.org/article/d6ba52521b0e42a28d25a76bcd7ca681
Publikováno v:
Известия Томского политехнического университета: Инжиниринг георесурсов, Vol 331, Iss 10, Pp 91-98 (2020)
The relevance of the study is caused by the need to summarize the accumulated experience and information on application of generally accepted methods for analyzing the effectiveness of the pressure maintenance system, identifying the advantages and d
Externí odkaz:
https://doaj.org/article/9624632f303d45498e9d2dee98d4238a
Autor:
Yulia A. Maksimova, Alexander S. Dubenskiy, Lyudmila A. Pavlova, Ilya V. Shigapov, Dmitry M. Korshunov, Irina F. Seregina, Vadim A. Davankov, Mikhail A. Bolshov
Publikováno v:
Molecules, Vol 27, Iss 19, p 6746 (2022)
In this paper, we propose the combined procedure of noble metal (NM) determination, including fire assay, acid digestion, and reversible dynamic sorptive preconcentration, followed by flow-injection ICP-MS. Reversible preconcentration of all NMs was
Externí odkaz:
https://doaj.org/article/ef7da94a976247568b93a264a9a4d638
Autor:
Yury P. Pokholkov, Igor O. Muravlev, Valery A. Zhadan, Olga Yu. Korneva, Maria Yu. Chervach, Galina N. Klimova, Liliya A. Leonova, Yulia A. Maksimova, Anna A. Pershina, Olesya V. Savinova, Sergei A. Stepanov
Publikováno v:
Inzhenernoe obrazovanie. :46-57
Autor:
Asia R. Shorina, Dmitry V. Yudkin, Yulia V. Maksimova, Svetlana A. Romanenko, Natalya A. Lemskaya
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-4 (2021)
Background The presence of small supernumerary marker chromosomes (sSMCs) in a karyotype leads to diagnostic questions because the resulting extra material may cause abnormal development depending on the origin of the duplication/triplication. Becaus
Autor:
Vadim A. Davankov, I. F. Seregina, Mikhail A. Bolshov, A.S. Dubenskiy, Ilya V. Shigapov, L. A. Pavlova, Yulia A. Maksimova
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 151:1291-1303
Natural sources of noble metals (Ru, Rh, Pd, Os, Ir, Pt, Au) are exhaustible, thus the extraction of metal from anthropogenic sources seems very promising. This work presents an investigation of new N-heterocyclic sorbents based on polyvinylpyridine
Autor:
Alexander A. Dolskiy, Polina L. Perelman, Yulia V. Maksimova, Svetlana A. Romanenko, Dmitry V. Yudkin, Elena A Filimonova, Dmitry Yu Prokopov, Mariia A Rezakova, Natalya A. Lemskaya, Asia R. Shorina
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-13 (2021)
Molecular Cytogenetics
Molecular Cytogenetics
Background There are many reports on rearrangements occurring separately in the regions of chromosomes 9p and 15q affected in the case under study. 15q duplication syndrome is caused by the presence of at least one extra maternally derived copy of th
Autor:
Petrus J. de Vries, Elena Belousova, Mirjana P. Benedik, Tom Carter, Vincent Cottin, Paolo Curatolo, Maria Dahlin, Lisa D'Amato, Guillaume Beaure d'Augères, José C. Ferreira, Martha Feucht, Carla Fladrowski, Christoph Hertzberg, Sergiusz Jozwiak, John A. Lawson, Alfons Macaya, Ruben Marques, Rima Nabbout, Finbar O'Callaghan, Jiong Qin, Valentin Sander, Matthias Sauter, Seema Shah, Yukitoshi Takahashi, Renaud Touraine, Sotiris Youroukos, Bernard Zonnenberg, John C. Kingswood, Anna C. Jansen, Nobuo Shinohara, Shigeo Horie, Masaya Kubota, Jun Tohyama, Katsumi Imai, Mari Kaneda, Hideo Kaneko, Yasushi Uchida, Tomoko Kirino, Shoichi Endo, Yoshikazu Inoue, Katsuhisa Uruno, Ayse Serdaroglu, Zuhal Yapici, Banu Anlar, Sakir Altunbasak, Olga Lvova, Oleg Valeryevich Belyaev, Oleg Agranovich, Elena Vladislavovna Levitina, Yulia Vladimirovna Maksimova, Antonina Karas, Yuwu Jiang, Liping Zou, Kaifeng Xu, Yushi Zhang, Guoming Luan, Yuqin Zhang, Yi Wang, Meiling Jin, Dingwei Ye, Weiping Liao, Liemin Zhou, Jie Liu, Jianxiang Liao, Bo Yan, Yanchun Deng, Li Jiang, Zhisheng Liu, Shaoping Huang, Hua Li, Kijoong Kim, Pei-Lung Chen, Hsiu-Fen Lee, Jeng-Dau Tsai, Ching-Shiang Chi, Chao-Ching Huang, Kate Riney, Deborah Yates, Patrick Kwan, Surachai Likasitwattanakul, Charcrin Nabangchang, Lunliya Thampratankul Krisnachai Chomtho, Kamornwan Katanyuwong, Somjit Sriudomkajorn, Jo Wilmshurst, Reeval Segel, Tal Gilboa, Michal Tzadok, Aviva Fattal-Valevski, Panagiotis Papathanasopoulos, Antigone Syrigou Papavasiliou, Stylianos Giannakodimos, Stylianos Gatzonis, Evangelos Pavlou, Meropi Tzoufi, A. M. H. Vergeer, Marc Dhooghe, Hélène Verhelst, Filip Roelens, Marie Cecile Nassogne, Pierre Defresne, Liesbeth De Waele, Patricia Leroy, Nathalie Demonceau, Benjamin Legros, Patrick Van Bogaert, Berten Ceulemans, Lina Dom, Pierre Castelnau, Anne De Saint Martin, Audrey Riquet, Mathieu Milh, Claude Cances, Jean-Michel Pedespan, Dorothee Ville, Agathe Roubertie, Stéphane Auvin, Patrick Berquin, Christian Richelme, Catherine Allaire, Sophie Gueden, Sylvie Nguyen The Tich, Bertrand Godet, Maria Luz Ruiz Falco Rojas, Jaume Campistol Planas, Antonio Martinez Bermejo, Patricia Smeyers Dura, Susana Roldan Aparicio, Maria Jesus Martinez Gonzalez, Javier Lopez Pison, Manuel Oscar Blanco Barca, Eduardo Lopez Laso, Olga Alonso Luengo, Francisco Javier Aguirre Rodriguez, Ignacio Malaga Dieguez, Ana Camacho Salas, Itxaso Marti Carrera, Eduardo Martinez Salcedo, Maria Eugenia Yoldi Petri, Ramon Cancho Candela, Ines da Conceicao Carrilho, Jose Pedro Vieira, José Paulo da Silva Oliveira Monteiro, Miguel Jorge Santos de Oliveira Ferreira Leao, Catarina Sofia Marceano Ribeiro Luis, Carla Pires Mendonca, Milda Endziniene, Jurgis Strautmanis, Inga Talvik, Maria Paola Canevini, Antonio Gambardella, Dario Pruna, Salvatore Buono, Elena Fontana, Bernardo Dalla Bernardina, Carmen Burloiu, Iuliu Stefan Bacos Cosma, Mihaela Adela Vintan, Laura Popescu, Karel Zitterbart, Jaroslava Payerova, Ladislav Bratsky, Zuzana Zilinska, Ursula Gruber-Sedlmayr, Matthias Baumann, Edda Haberlandt, Kevin Rostasy, Ekaterina Pataraia, Frances Elmslie, Clare Ann Johnston, Pamela Crawford, Peter Uldall, Paul Uvebrant, Olof Rask, Marit Bjoernvold, Eylert Brodtkorb, Andreas Sloerdahl, Ragnar Solhoff, Martine Sofie Gilje Jaatun, Marek Mandera, Elzbieta Janina Radzikowska, Mariusz Wysocki, Michael Fischereder, Gerhard Kurlemann, Bernd Wilken, Adelheid Wiemer-Kruel, Klemens Budde, Klaus Marquard, Markus Knuf, Andreas Hahn, Hans Hartmann, Andreas Merkenschlager, Regina Trollmann
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Background: Knowledge is increasing about TSC-Associated Neuropsychiatric Disorders (TAND), but little is known about the potentially confounding effects of intellectual ability (IA) on the rates of TAND across age, sex, and genotype. We evaluated TA
Autor:
Natalya A. Lemskaya, Ekaterina M. Galanina, Irina S. Kolesnikova, Yulia V. Maksimova, Dmitry V. Yudkin, Asia R. Shorina, Alexander S. Graphodatsky, Alexander A. Dolskiy
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 19, Iss 2, Pp 129-134 (2018)
Egyptian Journal of Medical Human Genetics; Vol 19, No 2 (2018); 129-134
Egyptian Journal of Medical Human Genetics; Vol 19, No 2 (2018); 129-134
Background: Intellectual disability (ID) is an important medical and social problem that can be caused by different genetic and environmental factors. One such factor could be rDNA amplification and changes in rRNA expression and maturation. Aim of t
Autor:
Yulia V. Maksimova, Alexander A. Dolskiy, Natalya A. Lemskaya, Asia R. Shorina, Dmitry V. Yudkin, Irina S. Kolesnikova
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 19, No 2 (2018); 141-145
Egyptian Journal of Medical Human Genetics, Vol 19, Iss 2, Pp 141-145 (2018)
Egyptian Journal of Medical Human Genetics, Vol 19, Iss 2, Pp 141-145 (2018)
Background: The Robertsonian translocations inherited from parents with a normal phenotype are often discovered through children with pathogenesis. The exact causes of pathologies in children with clinical manifestations are often unknown and vary gr