Nickolai A Barlev

Nickolai A Barlev

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Nickolai A Barlev

Nickolai A Barlev

Publications by authors named "Nickolai A Barlev"

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Lysine-specific post-translational modifications of proteins in the life cycle of viruses.

Cell Cycle 2019 Sep 10;18(17):1995-2005. Epub 2019 Jul 10.

a Laboratory of Intracellular Signaling, Moscow Institute of Physics and Technology , Dolgoprudny, Moscow Region , Russian Federation.

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http://dx.doi.org/10.1080/15384101.2019.1639305DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6681785PMC
September 2019

EMT: A mechanism for escape from EGFR-targeted therapy in lung cancer.

Biochim Biophys Acta Rev Cancer 2019 01 10;1871(1):29-39. Epub 2018 Nov 10.

Petrov Institute of Oncology, Saint-Petersburg, Russia. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S0304419X183014
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http://dx.doi.org/10.1016/j.bbcan.2018.10.003DOI Listing
January 2019

Ca -depended signaling pathways regulate self-renewal and pluripotency of stem cells.

Cell Biol Int 2018 Sep 19;42(9):1086-1096. Epub 2018 Jun 19.

Institute of Cytology RAS, Saint-Petersburg 194064, Russia.

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http://dx.doi.org/10.1002/cbin.10998DOI Listing
September 2018

Specific Drug Delivery to Cancer Cells with Double-Imprinted Nanoparticles against Epidermal Growth Factor Receptor.

Nano Lett 2018 08 9;18(8):4641-4646. Epub 2018 Jul 9.

Laboratory of Gene Expression and Regulation , Institute of Cytology , 194064 Saint Petersburg , Russia.

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http://dx.doi.org/10.1021/acs.nanolett.7b03206DOI Listing
August 2018

Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018.

Authors:
Lorenzo Galluzzi Ilio Vitale Stuart A Aaronson John M Abrams Dieter Adam Patrizia Agostinis Emad S Alnemri Lucia Altucci Ivano Amelio David W Andrews Margherita Annicchiarico-Petruzzelli Alexey V Antonov Eli Arama Eric H Baehrecke Nickolai A Barlev Nicolas G Bazan Francesca Bernassola Mathieu J M Bertrand Katiuscia Bianchi Mikhail V Blagosklonny Klas Blomgren Christoph Borner Patricia Boya Catherine Brenner Michelangelo Campanella Eleonora Candi Didac Carmona-Gutierrez Francesco Cecconi Francis K-M Chan Navdeep S Chandel Emily H Cheng Jerry E Chipuk John A Cidlowski Aaron Ciechanover Gerald M Cohen Marcus Conrad Juan R Cubillos-Ruiz Peter E Czabotar Vincenzo D'Angiolella Ted M Dawson Valina L Dawson Vincenzo De Laurenzi Ruggero De Maria Klaus-Michael Debatin Ralph J DeBerardinis Mohanish Deshmukh Nicola Di Daniele Francesco Di Virgilio Vishva M Dixit Scott J Dixon Colin S Duckett Brian D Dynlacht Wafik S El-Deiry John W Elrod Gian Maria Fimia Simone Fulda Ana J García-Sáez Abhishek D Garg Carmen Garrido Evripidis Gavathiotis Pierre Golstein Eyal Gottlieb Douglas R Green Lloyd A Greene Hinrich Gronemeyer Atan Gross Gyorgy Hajnoczky J Marie Hardwick Isaac S Harris Michael O Hengartner Claudio Hetz Hidenori Ichijo Marja Jäättelä Bertrand Joseph Philipp J Jost Philippe P Juin William J Kaiser Michael Karin Thomas Kaufmann Oliver Kepp Adi Kimchi Richard N Kitsis Daniel J Klionsky Richard A Knight Sharad Kumar Sam W Lee John J Lemasters Beth Levine Andreas Linkermann Stuart A Lipton Richard A Lockshin Carlos López-Otín Scott W Lowe Tom Luedde Enrico Lugli Marion MacFarlane Frank Madeo Michal Malewicz Walter Malorni Gwenola Manic Jean-Christophe Marine Seamus J Martin Jean-Claude Martinou Jan Paul Medema Patrick Mehlen Pascal Meier Sonia Melino Edward A Miao Jeffery D Molkentin Ute M Moll Cristina Muñoz-Pinedo Shigekazu Nagata Gabriel Nuñez Andrew Oberst Moshe Oren Michael Overholtzer Michele Pagano Theocharis Panaretakis Manolis Pasparakis Josef M Penninger David M Pereira Shazib Pervaiz Marcus E Peter Mauro Piacentini Paolo Pinton Jochen H M Prehn Hamsa Puthalakath Gabriel A Rabinovich Markus Rehm Rosario Rizzuto Cecilia M P Rodrigues David C Rubinsztein Thomas Rudel Kevin M Ryan Emre Sayan Luca Scorrano Feng Shao Yufang Shi John Silke Hans-Uwe Simon Antonella Sistigu Brent R Stockwell Andreas Strasser Gyorgy Szabadkai Stephen W G Tait Daolin Tang Nektarios Tavernarakis Andrew Thorburn Yoshihide Tsujimoto Boris Turk Tom Vanden Berghe Peter Vandenabeele Matthew G Vander Heiden Andreas Villunger Herbert W Virgin Karen H Vousden Domagoj Vucic Erwin F Wagner Henning Walczak David Wallach Ying Wang James A Wells Will Wood Junying Yuan Zahra Zakeri Boris Zhivotovsky Laurence Zitvogel Gerry Melino Guido Kroemer

Cell Death Differ 2018 03 23;25(3):486-541. Epub 2018 Jan 23.

Paris Descartes/Paris V University, Paris, France.

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http://dx.doi.org/10.1038/s41418-017-0012-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864239PMC
March 2018

Non-alcoholic fatty liver disease severity is modulated by transglutaminase type 2.

Cell Death Dis 2018 02 15;9(3):257. Epub 2018 Feb 15.

National Institute for Infectious Diseases, IRCCS "Lazzaro Spallanzani", Rome, Italy.

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http://dx.doi.org/10.1038/s41419-018-0292-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833377PMC
February 2018

Effects of mycoplasma infection on the host organism response via p53/NF-κB signaling.

J Cell Physiol 2018 01 26;234(1):171-180. Epub 2018 Aug 26.

Institute of Cytology RAS, Laboratory of Gene Expression Regulation, Saint-Petersburg, Russia.

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http://dx.doi.org/10.1002/jcp.26781DOI Listing
January 2018

Proapoptotic modification of substituted isoindolinones as MDM2-p53 inhibitors.

Bioorg Med Chem Lett 2017 12 20;27(23):5197-5202. Epub 2017 Oct 20.

St. Petersburg State Institute of Technology (Technical University), St. Petersburg 190013, Russia.

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http://dx.doi.org/10.1016/j.bmcl.2017.10.049DOI Listing
December 2017

BTK blocks the inhibitory effects of MDM2 on p53 activity.

Oncotarget 2017 Dec 20;8(63):106639-106647. Epub 2017 Nov 20.

Department of Molecular and Cell Biology, Mechanisms of Cancer and Aging Laboratory, University of Leicester, Leicester, UK.

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http://www.oncotarget.com/fulltext/22543
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http://dx.doi.org/10.18632/oncotarget.22543DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739762PMC
December 2017

BTK Modulates p53 Activity to Enhance Apoptotic and Senescent Responses.

Cancer Res 2016 09 26;76(18):5405-14. Epub 2016 Jul 26.

Mechanisms of Cancer and Aging Laboratory, Department of Molecular and Cell Biology, University of Leicester, Leicester, United Kingdom. Cancer Research UK Leicester Centre, Leicester, United Kingdom.

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http://cancerres.aacrjournals.org/content/early/2016/07/26/0
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http://cancerres.aacrjournals.org/content/canres/early/2016/
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http://cancerres.aacrjournals.org/cgi/doi/10.1158/0008-5472.
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http://dx.doi.org/10.1158/0008-5472.CAN-16-0690DOI Listing
September 2016

Current genome editing tools in gene therapy: new approaches to treat cancer.

Curr Gene Ther 2015 ;15(5):511-29

Head of the Laboratory of Gene Expression Regulation, Institute of Cytology RAS, Saint-Petersburg, Tihkoretsky ave, 4, 194064, Russia.

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May 2016

Regulation of Endoribonuclease Activity of Alpha-Type Proteasome Subunits in Proerythroleukemia K562 Upon Hemin-Induced Differentiation.

Protein J 2016 Feb;35(1):17-23

Institute of Cytology of the Russian Academy of Sciences, St. Petersburg, Russia, 194064.

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http://dx.doi.org/10.1007/s10930-015-9642-xDOI Listing
February 2016

Immunoaffinity purification of the functional 20S proteasome from human cells via transient overexpression of specific proteasome subunits.

Protein Expr Purif 2014 May 28;97:37-43. Epub 2014 Feb 28.

Institute of Cytology, Russian Academy of Science, Tikhoretsky ave. 4, 194064 Saint Petersburg, Russia; Institute of Nanobiotechnologies, Saint Petersburg State Polytechnical University, Polytechnicheskaya 29, 195251 Saint Petersburg, Russia. Electronic address:

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http://dx.doi.org/10.1016/j.pep.2014.02.011DOI Listing
May 2014

DNA damage-induced ubiquitylation of proteasome controls its proteolytic activity.

Oncotarget 2013 Sep;4(9):1338-48

Institute of Cytology, Russian Academy of Sciences, St-Petersburg, Russia.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3824523PMC
http://dx.doi.org/10.18632/oncotarget.1060DOI Listing
September 2013

Hot and toxic: hyperthermia and anti-mitotic drugs in cancer therapy.

Cell Cycle 2013 Aug 30;12(16):2533. Epub 2013 Jul 30.

Institute of Cytology, Russian Academy of Sciences, St Petersburg, Russia.

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http://dx.doi.org/10.4161/cc.25841DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3865038PMC
August 2013

Role of proteasomes in transcription and their regulation by covalent modifications.

Front Biosci 2008 May 1;13:7184-92. Epub 2008 May 1.

Institute of Cytology, Russian Academy of Sciences, 4, Tikhoretsky ave., Saint-Petersburg, 194064, Russia.

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http://dx.doi.org/10.2741/3220DOI Listing
May 2008

Regulation of p53 activity through lysine methylation.

Nature 2004 Nov 3;432(7015):353-60. Epub 2004 Nov 3.

Howard Hughes Medical Institute, Division of Nucleic Acids Enzymology, Department of Biochemistry, Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.

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http://www.nature.com/articles/nature03117
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http://dx.doi.org/10.1038/nature03117DOI Listing
November 2004