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Poliakov

Showing results (561-570 of 704) with videos related to

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Klinicheskaia Laboratornaia Diagnostika|December 18, 2013
[The first experience of application of standardized genotype technique of identification of HIV-tropism]A É Lopatukhin, D E Kireev, A N Poliakov, et al.
Molecular Vision|March 31, 2017
Appropriately differentiated ARPE-19 cells regain phenotype and gene expression profiles similar to those of native RPE cellsWilliam Samuel, Cynthia Jaworski, Olga A Postnikova, et al.
Aviakosmicheskaia I Ekologicheskaia Meditsina = Aerospace and Environmental Medicine|January 1, 1992
[Water-salt metabolism and its hormonal regulation studied in the 2nd joint Soviet-French space flight]A I Grigor'ev, V B Noskov, V V Poliakov, et al.
Molecular Vision|March 20, 2014
Multiple A2E treatments lead to melanization of rod outer segment-challenged ARPE-19 cellsEugenia Poliakov, Natalya V Strunnikova, Jian-kang Jiang, et al.
Pediatric Neurology|November 9, 2015
Corpus Callosum Diffusion and Connectivity Features in High Functioning Subjects With Pyridoxine-Dependent EpilepsySandra L Poliachik, Seth D Friedman, Andrew V Poliakov, et al.
Science (New York, N.Y.)|May 20, 2006
The structure of an infectious P22 virion shows the signal for headful DNA packagingGabriel C Lander, Liang Tang, Sherwood R Casjens, et al.
Molecular Biology of the Cell|December 26, 2014
Emergence and subsequent functional specialization of kindlins during evolution of cell adhesivenessJulia Meller, Igor B Rogozin, Eugenia Poliakov, et al.
Journal of Neurosurgery. Pediatrics|June 12, 2012
Multimodality localization of the sensorimotor cortex in pediatric patients undergoing epilepsy surgeryCarter D Wray, Tim M Blakely, Sandra L Poliachik, et al.
Khirurgiia|March 19, 2013
[Clinic and genetic polymorphism of Brugada syndrome in Russian patients, caused by mutation in SCN5A gene]E V Zakliaz'minskaia, A G Shestak, A Sh Revishvili, et al.
Vestnik Oftalmologii|July 2, 2013
[Clinical and molecular genetic analysis of hereditary optic neuropathies]S É Avetisov, N L Sheremet, O K Vorob'eva, et al.
Pageof 71

Showing results (561-570 of 704) with videos related to

Sort By:
Pageof 71
Klinicheskaia Laboratornaia Diagnostika|December 18, 2013
[The first experience of application of standardized genotype technique of identification of HIV-tropism]A É Lopatukhin, D E Kireev, A N Poliakov, et al.
Molecular Vision|March 31, 2017
Appropriately differentiated ARPE-19 cells regain phenotype and gene expression profiles similar to those of native RPE cellsWilliam Samuel, Cynthia Jaworski, Olga A Postnikova, et al.
Aviakosmicheskaia I Ekologicheskaia Meditsina = Aerospace and Environmental Medicine|January 1, 1992
[Water-salt metabolism and its hormonal regulation studied in the 2nd joint Soviet-French space flight]A I Grigor'ev, V B Noskov, V V Poliakov, et al.
Molecular Vision|March 20, 2014
Multiple A2E treatments lead to melanization of rod outer segment-challenged ARPE-19 cellsEugenia Poliakov, Natalya V Strunnikova, Jian-kang Jiang, et al.
Pediatric Neurology|November 9, 2015
Corpus Callosum Diffusion and Connectivity Features in High Functioning Subjects With Pyridoxine-Dependent EpilepsySandra L Poliachik, Seth D Friedman, Andrew V Poliakov, et al.
Science (New York, N.Y.)|May 20, 2006
The structure of an infectious P22 virion shows the signal for headful DNA packagingGabriel C Lander, Liang Tang, Sherwood R Casjens, et al.
Molecular Biology of the Cell|December 26, 2014
Emergence and subsequent functional specialization of kindlins during evolution of cell adhesivenessJulia Meller, Igor B Rogozin, Eugenia Poliakov, et al.
Journal of Neurosurgery. Pediatrics|June 12, 2012
Multimodality localization of the sensorimotor cortex in pediatric patients undergoing epilepsy surgeryCarter D Wray, Tim M Blakely, Sandra L Poliachik, et al.
Khirurgiia|March 19, 2013
[Clinic and genetic polymorphism of Brugada syndrome in Russian patients, caused by mutation in SCN5A gene]E V Zakliaz'minskaia, A G Shestak, A Sh Revishvili, et al.
Vestnik Oftalmologii|July 2, 2013
[Clinical and molecular genetic analysis of hereditary optic neuropathies]S É Avetisov, N L Sheremet, O K Vorob'eva, et al.
Pageof 71