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Pseudogenes as Functionally Significant Elements of the Genome

Biochemistry (Moscow), 2018-11, Vol.83 (11), p.1332-1349

2018

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Functions of noncoding sequences in mammalian genomes

Biochemistry (Moscow), 2014-12, Vol.79 (13), p.1442-1469

2014

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The PTENP1 Pseudogene, Unlike the PTEN Gene, Is Methylated in Normal Endometrium, As Well As in Endometrial Hyperplasias and Carcinomas in Middle-Aged and Elderly Females

Actanaturae, 2018-01, Vol.10 (1), p.43-50

2018

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problem of the eukaryotic genome size

Biochemistry (Moscow), 2008-12, Vol.73 (13), p.1519-1552

2008

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Special features of assessing the strength of nuclear reactor equipment under dynamic loads

Vestnik Samarskogo universiteta. Aèrokosmičeskaâ tehnika, tehnologii i mašinostroenie (Online), 2023-06, Vol.22 (2), p.57-66

2023

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C0598: Thrombophilia Influence on the Intensity of the Intravascular Microcoagulation at the Patients with Atherothrombosis and Chronic Obstructive Pulmonary Disease

Thrombosis research, 2014-05, Vol.133, p.S55-S55

2014

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C0070: Treatment of DVT: Evaluation of Safety and Efficacy

Thrombosis research, 2014-05, Vol.133, p.S65-S65

2014

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Ensuring vibration characteristics of reactor plant centrifugal pumping equipment

Vestnik Samarskogo universiteta. Aèrokosmičeskaâ tehnika, tehnologii i mašinostroenie (Online), 2023-05, Vol.22 (1), p.112-120

2023

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Intracardiac Thrombosis in a Child With Hereditary Thrombophilia

Kardiologiia, 2016-01, Vol.56 (1), p.101

2016

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Model for calculating the risk of venous thrombosis

Rossiĭskiĭ kardiologicheskiĭ zhurnal, 2019-06 (5), p.37-43

2019

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Plasminogen activator inhibitor type 1 gene polymorphism and thromboses in patients with antiphospholipid syndrome

Terapevtic̆eskii arhiv, 2013, Vol.85 (1), p.76

2013

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Polymorphism of the plasminogen activator inhibitor type 1 gene, plasminogen level and thromboses in patients with the antiphospholipid syndrome

Biochemistry (Moscow). Supplement. Series B, Biomedical chemistry, 2013-03, Vol.7 (1), p.1-15

2013

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Polymorphism of the plasminogen activator inhibitor type 1 gene, plasminogen level and thrombosis in patients with antiphospholipid syndrome

Biomeditsinskaia khimiia, 2014-01, Vol.60 (1), p.72-93

2014

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Methylation of the pseudogene PTENP1 5′-terminal region in endometrial cancer and hyperplasia

Russian journal of bioorganic chemistry, 2013-07, Vol.39 (4), p.397-405

2013

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Unique polymorphism of the CYP21A2 gene encoding 21-hydroxylase in female patients with the signs of hyperandrogenism

Russian journal of bioorganic chemistry, 2012-09, Vol.38 (5), p.500-506

2012

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new DNA diagnostic system for the detection of human CYP21 gene mutations associated with adrenal cortex hyperplasia

Russian journal of bioorganic chemistry, 2010-05, Vol.36 (3), p.325-335

2010

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Another model for risk assessment of venous thrombosis

AIP Conference Proceedings, 2022, Vol.2425 (1)

2022

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Morphological signs of mitochondrial cytopathy in skeletal muscles and micro-vessel walls in a patient with cerebral artery dissection associated with MELAS syndrome

Arkhiv patologii, 2012-03, Vol.74 (2), p.51

2012

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Polymorphism of 5,10-methylenetetrahydropholate reductase, prothrombin, and coagulation factor V genes in young patients with ischemic stroke

Klinicheskaia meditsina, 2012, Vol.90 (3), p.37

2012

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The A3243G mitochondrial DNA mutation in cerebral artery dissections

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova, 2012, Vol.112 (1), p.84

2012

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Genetic mechanisms of hereditary hemostasis disorders

Biochemistry (Moscow), 2002-01, Vol.67 (1), p.33-46

Patrushev, L I

2002

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Eukaryotic noncoding DNA sequences provide genes with an additional protection against chemical mutagens

Russian journal of bioorganic chemistry, 2006-07, Vol.32 (4), p.368-372

2006

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THROMBOPHILIA AND INTENSITY OF THE INTRAVASCULAR MICROCOAGULATION IN PATIENTS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE, ATHEROTHROMBOSIS

Rat͡s︡ionalʹnai͡a︡ farmakoterapii͡a︡ v kardiologii, 2014-01, Vol.10 (3), p.293-298

2014

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Genomic noncoding sequences and the size of eukaryotic cell nucleus as important factors of gene protection from chemical mutagens

Bioorganicheskaia khimiia, 2007-07, Vol.33 (4), p.474

2007

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A new DNA diagnostic system for the detection of human CYP21 gene mutations associated with adrenal cortex hyperplasia

Bioorganicheskaia khimiia, 2010-05, Vol.36 (3), p.354

2010

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Pseudogenes as Functionally Significant Elements of the Genome

Functions of noncoding sequences in mammalian genomes

The PTENP1 Pseudogene, Unlike the PTEN Gene, Is Methylated in Normal Endometrium, As Well As in Endometrial Hyperplasias and Carcinomas in Middle-Aged and Elderly Females

problem of the eukaryotic genome size

Special features of assessing the strength of nuclear reactor equipment under dynamic loads

C0598: Thrombophilia Influence on the Intensity of the Intravascular Microcoagulation at the Patients with Atherothrombosis and Chronic Obstructive Pulmonary Disease

C0070: Treatment of DVT: Evaluation of Safety and Efficacy

Ensuring vibration characteristics of reactor plant centrifugal pumping equipment

Intracardiac Thrombosis in a Child With Hereditary Thrombophilia

Model for calculating the risk of venous thrombosis

Plasminogen activator inhibitor type 1 gene polymorphism and thromboses in patients with antiphospholipid syndrome

Polymorphism of the plasminogen activator inhibitor type 1 gene, plasminogen level and thromboses in patients with the antiphospholipid syndrome

Polymorphism of the plasminogen activator inhibitor type 1 gene, plasminogen level and thrombosis in patients with antiphospholipid syndrome

Methylation of the pseudogene PTENP1 5′-terminal region in endometrial cancer and hyperplasia

Unique polymorphism of the CYP21A2 gene encoding 21-hydroxylase in female patients with the signs of hyperandrogenism

new DNA diagnostic system for the detection of human CYP21 gene mutations associated with adrenal cortex hyperplasia

Another model for risk assessment of venous thrombosis

Morphological signs of mitochondrial cytopathy in skeletal muscles and micro-vessel walls in a patient with cerebral artery dissection associated with MELAS syndrome

Polymorphism of 5,10-methylenetetrahydropholate reductase, prothrombin, and coagulation factor V genes in young patients with ischemic stroke

The A3243G mitochondrial DNA mutation in cerebral artery dissections

Genetic mechanisms of hereditary hemostasis disorders

Eukaryotic noncoding DNA sequences provide genes with an additional protection against chemical mutagens

THROMBOPHILIA AND INTENSITY OF THE INTRAVASCULAR MICROCOAGULATION IN PATIENTS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE, ATHEROTHROMBOSIS

Genomic noncoding sequences and the size of eukaryotic cell nucleus as important factors of gene protection from chemical mutagens

A new DNA diagnostic system for the detection of human CYP21 gene mutations associated with adrenal cortex hyperplasia

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