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K-Ras4B lipoprotein synthesis: Biochemical characterization, functional properties, and dimer formation

Protein expression and purification, 2012-07, Vol.84 (1), p.86-93

Dementiev, Alexey

2012

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Biochemical and structural basis for the pharmacological inhibition of nuclear hormone receptor PPARγ by inverse agonists

The Journal of biological chemistry, 2022-11, Vol.298 (11), p.102539, Article 102539

2022

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Structures of human plasma β–factor XIIa cocrystallized with potent inhibitors

Blood advances, 2018-03, Vol.2 (5), p.549-558

2018

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Tendencies and prospects in the digital economy development in Russia

SHS web of conferences, 2018, Vol.55, p.1011

2018

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Shape-Based Virtual Screening of a Billion-Compound Library Identifies Mycobacterial Lipoamide Dehydrogenase Inhibitors

ACS bio & med chem au, 2023-12, Vol.3 (6), p.507-515

2023

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High resolution crystal structure of the FAK FERM domain reveals new insights on the Druggability of tyrosine 397 and the Src SH3 binding site

BMC molecular and cell biology, 2019-05, Vol.20 (1), p.10-9, Article 10

2019

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Basis for the Specificity and Activation of the Serpin Protein Z-dependent Proteinase Inhibitor (ZPI) as an Inhibitor of Membrane-associated Factor Xa

The Journal of biological chemistry, 2010-06, Vol.285 (26), p.20399-20409

2010

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The Allosteric Mechanism of Activation of Antithrombin as an Inhibitor of Factor IXa and Factor Xa

The Journal of biological chemistry, 2013-11, Vol.288 (47), p.33611-33619

2013

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Spain vs Portugal: the turbulent past and the complicated present

Iberoamerikanskie tetradi, 2018-06 (2), p.14-21

Dementiev, Alexey

2018

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Portugal of Salazar, an Indispensable Ally of Spain of Franco during the Civil War in 1936—1939

ISTORIYA, 2019, Vol.10 (2)

Dementiev, Alexey

2019

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Molecular Mechanism of Inhibition of Acid Ceramidase by Carmofur

Journal of medicinal chemistry, 2019-01, Vol.62 (2), p.987-992

2019

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Structure and enzymatic characterization of CelD endoglucanase from the anaerobic fungus Piromyces finnis

Applied microbiology and biotechnology, 2023-10, Vol.107 (19), p.5999-6011

2023

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Active Site Distortion Is Sufficient for Proteinase Inhibition by Serpins

The Journal of biological chemistry, 2006-02, Vol.281 (6), p.3452-3457

2006

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The ternary complex of antithrombin-anhydrothrombin-heparin reveals the basis of inhibitor specificity

Nature structural & molecular biology, 2004-09, Vol.11 (9), p.863-867

2004

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The pesticidal Cry6Aa toxin from Bacillus thuringiensis is structurally similar to HlyE-family alpha pore-forming toxins

BMC biology, 2016-08, Vol.14 (1), p.71-71, Article 71

2016

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The allosteric mechanism of activation of antithrombin as an inhibitor of factor IXa and factor Xa: heparin-independent full activation through mutations adjacent to helix D

The Journal of biological chemistry, 2013-11, Vol.288 (47), p.33611-33619

2013

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Rv0100, a proposed acyl carrier protein in Mycobacterium tuberculosis: expression, purification and crystallization. Corrigendum

Acta crystallographica. Section F, Structural biology communications, 2020-04, Vol.76 (4), p.192-193

2020

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Visual-Motor Reaction Parameters as Indicators of Fatigue in Emergency Medical Personnel

ЗДОРОВЬЕ НАСЕЛЕНИЯ И СРЕДА ОБИТАНИЯ - ЗНиСО / PUBLIC HEALTH AND LIFE ENVIRONMENT, 2023-02, p.32-37

2023

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WAYS TO OPTIMIZE THE LEARNING PROCESS AT A MEDICAL UNIVERSITY

PERSONALITY IN A CHANGING WORLD: HEALTH, ADAPTATION, DEVELOPMENT, 2024-06, Vol.12 (2 (45)), p.94-106

2024

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Active site distortion is sufficient for proteinase inhibition by serpins: structure of the covalent complex of alpha1-proteinase inhibitor with porcine pancreatic elastase

The Journal of biological chemistry, 2006-02, Vol.281 (6), p.3452-3457

2006

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Canonical Inhibitor-like Interactions Explain Reactivity of α1-Proteinase Inhibitor Pittsburgh and Antithrombin with Proteinases

The Journal of biological chemistry, 2003-09, Vol.278 (39), p.37881-37887

2003

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Canonical Inhibitor-like Interactions Explain Reactivity of Î±1-Proteinase Inhibitor Pittsburgh and Antithrombin with Proteinases

The Journal of biological chemistry, 2003-09, Vol.278 (39), p.37881

2003

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Canonical inhibitor-like interactions explain reactivity of alpha1-proteinase inhibitor Pittsburgh and antithrombin with proteinases

The Journal of biological chemistry, 2003-09, Vol.278 (39), p.37881-37887

2003

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XPS study of U, Cs and Sr ionic forms in the "hot" particles formed due to the nuclear power plant accident simulation

Journal of nuclear science and technology, 2002-11, Vol.39 (sup3), p.477-480

2002

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Prospects of low-modulus alloys of the TI-(15-20)NB-(5-10)TA system for engineering implants used in traumatology and orthopedics. A preclinical study

Geniĭ ortopedii = Genij ortopedii, 2022-12, Vol.28 (6), p.830-836

2022

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K-Ras4B lipoprotein synthesis: Biochemical characterization, functional properties, and dimer formation

Biochemical and structural basis for the pharmacological inhibition of nuclear hormone receptor PPARγ by inverse agonists

Structures of human plasma β–factor XIIa cocrystallized with potent inhibitors

Tendencies and prospects in the digital economy development in Russia

Shape-Based Virtual Screening of a Billion-Compound Library Identifies Mycobacterial Lipoamide Dehydrogenase Inhibitors

High resolution crystal structure of the FAK FERM domain reveals new insights on the Druggability of tyrosine 397 and the Src SH3 binding site

Basis for the Specificity and Activation of the Serpin Protein Z-dependent Proteinase Inhibitor (ZPI) as an Inhibitor of Membrane-associated Factor Xa

The Allosteric Mechanism of Activation of Antithrombin as an Inhibitor of Factor IXa and Factor Xa

Spain vs Portugal: the turbulent past and the complicated present

Portugal of Salazar, an Indispensable Ally of Spain of Franco during the Civil War in 1936—1939

Molecular Mechanism of Inhibition of Acid Ceramidase by Carmofur

Structure and enzymatic characterization of CelD endoglucanase from the anaerobic fungus Piromyces finnis

Active Site Distortion Is Sufficient for Proteinase Inhibition by Serpins

The ternary complex of antithrombin-anhydrothrombin-heparin reveals the basis of inhibitor specificity

The pesticidal Cry6Aa toxin from Bacillus thuringiensis is structurally similar to HlyE-family alpha pore-forming toxins

The allosteric mechanism of activation of antithrombin as an inhibitor of factor IXa and factor Xa: heparin-independent full activation through mutations adjacent to helix D

Rv0100, a proposed acyl carrier protein in Mycobacterium tuberculosis: expression, purification and crystallization. Corrigendum

Visual-Motor Reaction Parameters as Indicators of Fatigue in Emergency Medical Personnel

WAYS TO OPTIMIZE THE LEARNING PROCESS AT A MEDICAL UNIVERSITY

Active site distortion is sufficient for proteinase inhibition by serpins: structure of the covalent complex of alpha1-proteinase inhibitor with porcine pancreatic elastase

Canonical Inhibitor-like Interactions Explain Reactivity of α1-Proteinase Inhibitor Pittsburgh and Antithrombin with Proteinases

Canonical Inhibitor-like Interactions Explain Reactivity of Î±1-Proteinase Inhibitor Pittsburgh and Antithrombin with Proteinases

Canonical inhibitor-like interactions explain reactivity of alpha1-proteinase inhibitor Pittsburgh and antithrombin with proteinases

XPS study of U, Cs and Sr ionic forms in the "hot" particles formed due to the nuclear power plant accident simulation

Prospects of low-modulus alloys of the TI-(15-20)NB-(5-10)TA system for engineering implants used in traumatology and orthopedics. A preclinical study

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