Search Results - "Luk'ianenko, A. V"

Molecular genetic study of acute intermittent porphyria in Russia: Mutation analysis and functional polymorphism search in porphobilinogen deaminase gene by Surin, V. L, Luchinina, Yu. A, Selivanova, D. S, Pustovoit, Ya. S, Karpova, I. V, Pivnik, A. V, Luk'ianenko, A. V, Kravchenko, S. K

“…Acute intermittent porphyria (AIP) is an autosomal dominant hereditary disease, caused by partial deficiency of porphobilinogen deaminase (PBGD), one of the…”
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Stability of Structures and Asymptotics of Nonlinear Parabolic Type Equations Solutions with Transformation of Arguments by Kornuta, A. A., Lukianenko, V. A.

“…The paper considers a parabolic-type functional differential equation with rotation and radial compression transformations on a ring, a circle and a…”
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Stable Structures of Nonlinear Parabolic Equations with Transformation of Spatial Variables by Kornuta, A. A., Lukianenko, V. A.

“…Problem review of existence and stability nonlinear parabolic functionally differential equations structures with transformation of spatial variables. Such…”
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Dynamics of solutions of nonlinear functional differential equation of parabolic type by Kornuta, Anshelika, Lukianenko, Vladimir

“…Purpose of this work is to study the initial-boundary value problem for a parabolic functional-differential equation in an annular region, which describes the…”
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Metaheuristic Algorithms for Multiagent Routing Problems by Germanchuk, M. S., Lemtyuzhnikova, D. V., Lukianenko, V. A.

“…The problems of constructing routes in complex networks by many sales agents are considered. Formalization leads to pseudo-Boolean discrete optimization…”
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Pseudo-Boolean Conditional Optimization Models for a Class of Multiple Traveling Salesmen Problems by Germanchuk, M. S., Kozlova, M. G., Lukianenko, V. A.

“…We consider knowledge-oriented models, problems, and algorithms for routing traveling salesmen in complex networks. The formalization leads to models of…”
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Molecular genetic study of acute intermittent porphyria in Russia: mutation analysis and functional polymorphism search in porphobilinogen deaminase gene by Surin, V L, Luchinina, Iu A, Selivanova, D S, Pustovoĭt, Ia S, Karpova, I S, Pivnik, A V, Luk'ianenko, A V, Kravchenko, S K

“…Acute intermittent porphyria (AIP) is an autosomal dominant hereditary disease, caused by partial deficiency of porphobilinogen deaminase (PBGD), one of the…”
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Analysis of the AluI polymorphism in intron 1 of the human coagulation factor VIII gene: a new marker for the hemophilia A carrier detection by Surin, V L, Luk'ianenko, A V, Luchinina, Iu A

“…Frequencies of the CIT SNP alleles at position 2403 of the human coagulation factor VIII gene intron 1, containing the AluI restriction endonuclease…”
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Nonlinear Optics Problem with Transformation of a Spatial Variable and an Oblique Derivative by Kornuta, A. A., Lukianenko, V. A.

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Analysis of the AluI polymorphism in intron 1 of the human coagulation factor VIII gene: A new marker for the hemophilia a carrier detection by Surin, V. L., Lukianenko, A. V., Luchinina, Yu. A.

“…Frequencies of the C/T SNP alleles at position 2403 of the human coagulation factor VIII gene intron 1, containing the AluI restriction endonuclease…”
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The spectrum of beta-thalassemia mutations in Azerbaijan by Tagiev, A F, Surin, V L, Gol'tsov, A A, Lukianenko, A V, Solovyev GYa, Gulieva, E A, Plutalov, O V, Kaboev, O K, Mamedova, T A, Dadasheva, T S

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New efficient extragenic microsatellite markers for hemophilia A carrier state diagnostics by Surin, V L, Luk'ianenko, A V, Luchinina, Iu A

“…In search of new efficient markers for genetic diagnostics of hemophilia A, two tri-nucleotide microsatellite repeats (STR) at chromosome X loci, which flank…”
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Acute porphyrias: problem of primary diagnosis in Russia and CIS countries by Karpova, I V, Pustovoĭt, Ia S, Luchinina, Iu A, Surin, V L, Luk'ianenko, A V, Kravshenko, S K, Kremenetskaia, A M

“…To analyse manifestations and experience in primary screening diagnosis of acute porphyrias which are rarely encountered and little known by general…”
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General principles of treatment of mine-explosive wounds of ENT-organs by Beliakin, S A, Egorov, V I, Luk'ianenko, A V

“…The relevance of diagnosis and treatment of mine-explosive wounds ENT high. Treatment of explosives, Russian Academy of Sciences-the challenge and consists of…”
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A novel frameshift mutation causing beta-thalassaemia in Azerbaijan by Schwartz, E I, Gol'tsov, A A, Kaboev, O K, Alexeev, A A, Solovyev GYa, Surin, V L, Lukianenko, A V, Vinogradov, S V, Berlin YuA

“…The human hereditary syndrome of beta -thalassaemia is caused by a number of mutations located in beta -globin gene mostly between its TATA-box and second…”
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Study of hybridization in four species of ground squirrels (spermophilus: Rodentia, Sciuridae) by molecular genetic methods by Ermakov, O A, Surin, V L, Titov, S V, Tagiev, A F, Luk'ianenko, A V, Formozov, N A

“…Four species of ground squirrel--yellow (Spermophilus fulvus), russet (S. major), small (S. pygmaeus), and spotted (S. suslicus)--occur in the Volga region…”
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Three new mutations in the porphobilinogen deaminase gene, detected in acute intermittent porphyria patients from Russia by Surin, V L, Luk'ianenko, A V, Karpova, I V, Misiurin, A V, Pustovot, Ia S, Pivnik, A V

“…Porphobilinogen deaminase (PBGD) is a key enzyme of the heme biosynthetic pathway. Defects in the PBGD gene lead to an autosomal dominant disease, acute…”
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The initial results of detecting mutations in the gene of the porphobilinogen deaminase enzyme in patients with acute intermittent porphyria in Russia by Pivnik, A V, Pustovoĭt, Ia S, Karpova, I V, Surin, V L, Luk'ianenko, A V

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Clinical manifestations of porphyrin metabolism disorders by Pustovoĭt, Ia S, Karpova, I V, Pivnik, A V, Surin, V L, Luk'ianenko, A V, Luchinina, Iu A

“…To characterize patients with various nosological unities [symbol: see text] of porphyria in accordance with their age, clinical symptoms, provoking factors,…”
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Molecular nature of mutations causing beta zero-thalassaemia in Azerbaijan by Solovyev, G Y, Gol'tsov, A A, Surin, V L, Lebedenko, E N, Kaboev, O K, Lukianenko, A V, Alekseev, A A, Plutalov, O V, Dadasheva, T S, Rustamov, R Sh

“…Beta zero-thalassaemia comprises a series of closely related haemoglobinopathies which are widely spread in some areas (the Mediterranean, Caucasus, Central…”
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