Resultados de procura - Lavrov, Alexander

Genome scale analysis of pathogenic variants targetable for single base editing por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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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