Search Results - "Salomashkina, V V"

Literature review and clinical observation of acquired idiopathic hemophilia with a new missense mutation in the factor VIII gene (His2026Arg) by Ershov, V I, Gadaev, I Yu, Perina, F G, Surin, V L, Salomashkina, V V, Pshenichnikova, O S, Zozulya, N I

“…The article provides review of possible mechanisms of inhibitor coagulopathies, in particular of acquired hemophilia A. This pathology is an extremely rare…”
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Molecular serological characteristics of weak D antigen types of the Rhesus system by L L Golovkina, A G Stremoukhova, T D Pushkina, R S Kalandarov, G V Atroshchenko, M N Vasilyeva, V L Surin, V V Salomashkina, O S Pshenichnikova, G Yu Miterev, E N Parovichnikova, V G Savchenko

“…Aim. To estimate the spread of weak D antigen types of the Rhesus system in the citizens of the Russian Federation and a possibility of serologically…”
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New data on the phylogeography and genetic diversity of the brown bear Ursus arctos Linnaeus, 1758 of Northeastern Eurasia (mtDNA control region polymorphism analysis) by Salomashkina, V. V, Kholodova, M. V, Tuten’kov, O. Yu, Moskvitina, N. S, Erokhin, N. G

“…An analysis of polymorphism of the fragment of the control region of mitochondrial DNA of 53 tissue samples of the brown bear Ursus arctos from several regions…”
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Active spread of β-thalassemia beyond the thalassemia belt: A study on a Russian population by Shchemeleva, Ekaterina, Salomashkina, Valentina V, Selivanova, Daria, Tsvetaeva, Nina, Melikyan, Anait, Doronina, Liliya, Surin, Vadim L

“…β-Thalassemia is a disease traditionally associated with thalassemia belt countries. Nonetheless, as global migration intensifies, β-thalassemia-causing…”
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Mutational analysis of hemophilia B in Russia: Molecular-genetic study by Surin, V. L., Demidova, E. Yu, Selivanova, D. S., Luchinina, Yu. A., Salomashkina, V. V., Pshenichnikova, O. S., Likhacheva, E. A.

“…Hemophilia B is a hereditary X-linked coagulation disorder. This pathology is caused by various defects in the factor IX gene, which is, being about 34 kb long…”
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A founder effect in hemophilia A patients from Russian Ural region with a new p.(His634Arg) variant in F8 gene by Salomashkina, Valentina V., Pshenichnikova, Olesya S., Perina, Farida G., Surin, Vadim L.

“…Hemophilia A is a clotting disease caused by defects in the F8 gene. A lot of them are described and most are unique or have polyphyletic origin. We here study…”
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New data on the phylogeography and genetic diversity of the brown bear Ursus arctos Linnaeus, 1758 of northeastern Eurasia (mtDNA control region polymorphism analysis) by Salomashkina, V V, Kholodova, M V, Tiuten'kov, O Iu, Moskvitina, N S, Erokhin, N G

“…An analysis of polymorphism of the fragment of the control region of mitochondrial DNA of 53 tissue samples of the brown bear Ursus arctos from several regions…”
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Phylogeography of ancient and modern brown bears from eastern Eurasia by Molodtseva, Anna S, Makunin, Alexey I, Salomashkina, Valentina V, Kichigin, Ilya G, Vorobieva, Nadezhda V, Vasiliev, Sergey K, Shunkov, Mikhail V, Tishkin, Alexey A, Grushin, Sergey P, Anijalg, Peeter, Tammeleht, Egle, Keis, Marju, Boeskorov, Gennady G, Mamaev, Nikolai, Okhlopkov, Innokenty M, Kryukov, Alexey P, Lyapunova, Elena A, Kholodova, Marina V, Seryodkin, Ivan V, Saarma, Urmas, Trifonov, Vladimir A, Graphodatsky, Alexander S

“…Abstract The brown bear (Ursus arctos) is an iconic carnivoran species of the Northern Hemisphere. Its population history has been studied extensively using…”
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Molecular serological characteristics of weak D antigen types of the Rhesus system by Golovkina, L L, Stremoukhova, A G, Pushkina, T D, Kalandarov, R S, Atroshchenko, G V, Vasilyeva, M N, Surin, V L, Salomashkina, V V, Pshenichnikova, O S, Miterev, G Yu, Parovichnikova, E N, Savchenko, V G

“…to estimate the spread of weak D antigen types of the Rhesus system in the citizens of the Russian Federation and a possibility of serologically identifying…”
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PF335 MUTATION SPECTRUM OF F8 GENE IN HEMOPHILIA A PATIENTS FROM RUSSIA by Pshenichnikova, O., Salomashkina, V., Surin, V., Likhacheva, E., Zozulya, N., Perina, F.

“…Background: Congenital hemophilia A (HA) is an inherited recessive X‐linked bleeding disorder caused by a wide spectrum of mutations in the F8 gene and…”
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Genetic variability of brown bear (Ursus arctos L., 1758) by Salomashkina, V. V., Kholodova, M. V., Semenov, U. A., Muradov, A. S., Malkhasyan, A.

“…We perform an analysis of the diversity of the control region fragment (570 bp) and ten nuclear microsatellite loci for 36 specimens of the brown bear ( Ursus…”
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New Missense Mutation His2026Arg in the Factor VIII Gene Was Revealed in Two Female Patients with Clinical Manifestation of Hemophilia A by Surin, V. L., Salomashkina, V. V., Pshenichnikova, O. S., Perina, F. G., Bobrova, O. N., Ershov, V. I., Budanova, D. A., Gadaev, I. Yu, Konyashina, N. I., Zozulya, N. I.

“…Hemophilia A is a recessive X-linked hereditary disease, so its manifestation in women is extremely rare and can be a result of an asymmetric X-chromosome…”
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Mutational Analysis of Hemophilia B in Russia: Molecular-Genetic Study by Surin, V L, Demidova, E Yu, Selivanova, D S, Luchinina, Yu A, Salomashkina, V V, Pshenichnikova, O S, Likhacheva, E A

“…Hemophilia B is a hereditary X-linked coagulation disorder. This pathology is caused by various defects in the factor IX gene, which is, being about 34 kb long…”
Get more information

A founder effect in hemophilia A patients from Russian Ural region with a new p.(His634Arg) variant in F8 gene by Salomashkina, Valentina V., Pshenichnikova, Olesya S., Perina, Farida G., Surin, Vadim L.

“…Hemophilia A is a clotting disease caused by defects in the F8 gene. A lot of them are described and most are unique or have polyphyletic origin. We here study…”
Get full text