Výsledky vyhledávání - Lavrov, Alexander

Genome scale analysis of pathogenic variants targetable for single base editing Autor Lavrov, Alexander V., Varenikov, Georgi G., Skoblov, Mikhail Yu

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Detection of Fusarium infected seeds of cereal plants by the fluorescence method Autor Dorokhov, Alexey, Moskovskiy, Maksim, Belyakov, Mikhail, Lavrov, Alexander, Khamuev, Victor

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Long noncoding RNA landscapes specific to benign and malignant thyroid neoplasms of distinct histological subtypes Autor Yakushina, Valentina D., Strelnikov, Vladimir V., Tanas, Alexander S., Lavrov, Alexander V.

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Cultivation and Differentiation Change Nuclear Localization of Chromosome Centromeres in Human Mesenchymal Stem Cells Autor Voldgorn, Yana I., Adilgereeva, Elmira P., Nekrasov, Evgeny D., Lavrov, Alexander V.

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Improving Homology-Directed Repair in Genome Editing Experiments by Influencing the Cell Cycle Autor Smirnikhina, Svetlana A., Zaynitdinova, Milyausha I., Sergeeva, Vasilina A., Lavrov, Alexander V.

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Frequent variations in cancer-related genes may play prognostic role in treatment of patients with chronic myeloid leukemia Autor Lavrov, Alexander V., Chelysheva, Ekaterina Y., Smirnikhina, Svetlana A., Shukhov, Oleg A., Turkina, Anna G., Adilgereeva, Elmira P., Kutsev, Sergey I.

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3D Metal–Organic Frameworks Based on Co(II) and Bithiophendicarboxylate: Synthesis, Crystal Structures, Gas Adsorption, and Magnetic Properties Autor Dubskikh, Vadim A., Lysova, Anna A., Samsonenko, Denis G., Lavrov, Alexander N., Kovalenko, Konstantin A., Dybtsev, Danil N., Fedin, Vladimir P.

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Copy number variation analysis in cytochromes and glutathione S-transferases may predict efficacy of tyrosine kinase inhibitors in chronic myeloid leukemia Autor Lavrov, Alexander V., Ustaeva, Oksana A., Adilgereeva, Elmira P., Smirnikhina, Svetlana A., Chelysheva, Ekaterina Y., Shukhov, Oleg A., Shatokhin, Yuriy V., Mordanov, Sergey V., Turkina, Anna G., Kutsev, Sergey I.

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Complex Diagnostics of Non-Specific Intellectual Developmental Disorder Autor Levchenko, Olga, Dadali, Elena, Bessonova, Ludmila, Demina, Nina, Rudenskaya, Galina, Matyushchenko, Galina, Markova, Tatiana, Anisimova, Inga, Semenova, Natalia, Shchagina, Olga, Ryzhkova, Oxana, Zinchenko, Rena, Galkina, Varvara, Voinova, Victoria, Nagieva, Sabina, Lavrov, Alexander

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Exome, transcriptome and miRNA analysis don’t reveal any molecular markers of TKI efficacy in primary CML patients Autor Lavrov, Alexander V., Chelysheva, Ekaterina Yu., Adilgereeva, Elmira P., Shukhov, Oleg A., Smirnikhina, Svetlana A., Kochergin-Nikitsky, Konstantin S., Yakushina, Valentina D., Tsaur, Grigory A., Mordanov, Sergey V., Turkina, Anna G., Kutsev, Sergey I.

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Novel Copper(II) Complexes with Dipinodiazafluorene Ligands: Synthesis, Structure, Magnetic and Catalytic Properties Autor Fomenko, Iakov S., Afewerki, Medhanie, Gongola, Marko I., Vasilyev, Eugene S., Shul’pina, Lidia S., Ikonnikov, Nikolay S., Shul’pin, Georgiy B., Samsonenko, Denis G., Yanshole, Vadim V., Nadolinny, Vladimir A., Lavrov, Alexander N., Tkachev, Alexey V., Gushchin, Artem L.

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P.F508del editing in cells from cystic fibrosis patients Autor Smirnikhina, Svetlana A., Kondrateva, Ekaterina V., Adilgereeva, Elmira P., Anuchina, Arina A., Zaynitdinova, Milyausha I., Slesarenko, Yana S., Ershova, Angelina S., Ustinov, Kirill D., Yasinovsky, Matvei I., Amelina, Elena L., Voronina, Ekaterina S., Yakushina, Valentina D., Tabakov, Vyacheslav Yu., Lavrov, Alexander V.

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Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder Autor Polla, Daniel L., Fard, Mohammad Ali Farazi, Tabatabaei, Zahra, Habibzadeh, Parham, Levchenko, Olga A., Nikuei, Pooneh, Makrythanasis, Periklis, Hussain, Mureed, von Hardenberg, Sandra, Zeinali, Sirous, Fallah, Mohammad-Sadegh, Schuurs-Hoeijmakers, Janneke H. M., Shahzad, Mohsin, Fatima, Fareeha, Fatima, Neelam, Kaat, Laura Donker, Bruggenwirth, Hennie T., Fleming, Leah R., Condie, John, Ploski, Rafal, Pollak, Agnieszka, Pilch, Jacek, Demina, Nina A., Chukhrova, Alena L., Sergeeva, Vasilina S., Venselaar, Hanka, Masri, Amira T., Hamamy, Hanan, Santoni, Federico A., Linda, Katrin, Ahmed, Zubair M., Kasri, Nael Nadif, de Brouwer, Arjan P. M., Bergmann, Anke K., Hethey, Sven, Yavarian, Majid, Ansar, Muhammad, Riazuddin, Saima, Riazuddin, Sheikh, Silawi, Mohammad, Ruggeri, Gaia, Pirozzi, Filomena, Eftekhar, Ebrahim, Sheshdeh, Afsaneh Taghipour, Bahramjahan, Shima, Mirzaa, Ghayda M., Lavrov, Alexander V., Antonarakis, Stylianos E., Faghihi, Mohammad Ali, van Bokhoven, Hans

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Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy Autor Voisin, Norine, Schnur, Rhonda E., Douzgou, Sofia, Hiatt, Susan M., Rustad, Cecilie F., Brown, Natasha J., Earl, Dawn L., Keren, Boris, Levchenko, Olga, Geuer, Sinje, Verheyen, Sarah, Johnson, Diana, Zarate, Yuri A., Hančárová, Miroslava, Amor, David J., Bebin, E. Martina, Blatterer, Jasmin, Brusco, Alfredo, Cappuccio, Gerarda, Charrow, Joel, Chatron, Nicolas, Cooper, Gregory M., Courtin, Thomas, Dadali, Elena, Delafontaine, Julien, Del Giudice, Ennio, Doco, Martine, Douglas, Ganka, Eisenkölbl, Astrid, Funari, Tara, Giannuzzi, Giuliana, Gruber-Sedlmayr, Ursula, Guex, Nicolas, Heron, Delphine, Holla, Øystein L., Hurst, Anna C.E., Juusola, Jane, Kronn, David, Lavrov, Alexander, Lee, Crystle, Lorrain, Séverine, Merckoll, Else, Mikhaleva, Anna, Norman, Jennifer, Pradervand, Sylvain, Prchalová, Darina, Rhodes, Lindsay, Sanders, Victoria R., Sedláček, Zdeněk, Seebacher, Heidelis A., Sellars, Elizabeth A., Sirchia, Fabio, Takenouchi, Toshiki, Tanaka, Akemi J., Taska-Tench, Heidi, Tønne, Elin, Tveten, Kristian, Vitiello, Giuseppina, Vlčková, Markéta, Uehara, Tomoko, Nava, Caroline, Yalcin, Binnaz, Kosaki, Kenjiro, Donnai, Dian, Mundlos, Stefan, Brunetti-Pierri, Nicola, Chung, Wendy K., Reymond, Alexandre

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PEDIA: prioritization of exome data by image analysis Autor Hsieh, Tzung-Chien, Mensah, Martin A., Pantel, Jean T., Aguilar, Dione, Bar, Omri, Bayat, Allan, Becerra-Solano, Luis, Bentzen, Heidi B., Biskup, Saskia, Borisov, Oleg, Braaten, Oivind, Ciaccio, Claudia, Coutelier, Marie, Cremer, Kirsten, Danyel, Magdalena, Daschkey, Svenja, Eden, Hilda David, Devriendt, Koenraad, Wilson, Sandra, Douzgou, Sofia, Đukić, Dejan, Ehmke, Nadja, Fauth, Christine, Fischer-Zirnsak, Björn, Fleischer, Nicole, Gabriel, Heinz, Graul-Neumann, Luitgard, Gripp, Karen W., Gurovich, Yaron, Gusina, Asya, Haddad, Nechama, Hajjir, Nurulhuda, Hanani, Yair, Hertzberg, Jakob, Hoertnagel, Konstanze, Howell, Janelle, Ivanovski, Ivan, Kaindl, Angela, Kamphans, Tom, Kamphausen, Susanne, Karimov, Catherine, Kathom, Hadil, Keryan, Anna, Knaus, Alexej, Köhler, Sebastian, Kornak, Uwe, Lavrov, Alexander, Leitheiser, Maximilian, Lyon, Gholson J., Mangold, Elisabeth, Reina, Purificación Marín, Carrascal, Antonio Martinez, Mitter, Diana, Herrador, Laura Morlan, Nadav, Guy, Nöthen, Markus, Orrico, Alfredo, Ott, Claus-Eric, Park, Kristen, Peterlin, Borut, Pölsler, Laura, Raas-Rothschild, Annick, Randolph, Linda, Revencu, Nicole, Fagerberg, Christina Ringmann, Robinson, Peter Nick, Rosnev, Stanislav, Rudnik, Sabine, Rudolf, Gorazd, Schatz, Ulrich, Schossig, Anna, Schubach, Max, Shanoon, Or, Sheridan, Eamonn, Smirin-Yosef, Pola, Spielmann, Malte, Suk, Eun-Kyung, Sznajer, Yves, Thiel, Christian T., Thiel, Gundula, Verloes, Alain, Vrecar, Irena, Wahl, Dagmar, Weber, Ingrid, Winter, Korina, Wiśniewska, Marzena, Wollnik, Bernd, Yeung, Ming W., Zhao, Max, Zhu, Na, Zschocke, Johannes, Mundlos, Stefan, Horn, Denise, Krawitz, Peter M.

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