| Issue |
Title |
File |
| Vol 53, No 1 (2017) |
Results of molecular genetic testing in Russian patients with Pendred syndrome and allelic disorders |
(Eng)
|
|
Mironovich O.L., Bliznetz E.A., Markova T.G., Geptner E.N., Lalayants M.R., Zelikovich E.I., Tavartkiladze G.A., Polyakov A.V.
|
| Vol 53, No 1 (2017) |
Carriage of 2R allele at VNTR polymorphous site of XRCC5 gene increases risk of multiple sclerosis in an Iranian population |
(Eng)
|
|
Jahantigh D., Moghtaderi A., Narooie-Nejad M., Mousavi M., Moossavi M., Salimi S., Mohammadoo-Khorasani M.
|
| Vol 53, No 1 (2017) |
Association study of genetic markers of schizophrenia and its cognitive endophenotypes |
(Eng)
|
|
Bocharova A.V., Stepanov V.A., Marusin A.V., Kharkov V.N., Vagaitseva K.V., Fedorenko O.Y., Bokhan N.A., Semke A.V., Ivanova S.A.
|
| Vol 52, No 12 (2016) |
Mutation spectrum of the PAH gene in phenylketonuria patients in the Karachay-Cherkess Republic (Russia) |
(Eng)
|
|
Gundorova P., Stepanova A.A., Makaov A.K., Zinchenko R.A., Abaykhanova Z.M., Polyakov A.V.
|
| Vol 52, No 11 (2016) |
The analysis of association between type 2 diabetes and polymorphic markers in the CDKAL1 gene and in the HHEX/IDE locus |
(Eng)
|
|
Khodyrev D.S., Nikitin A.G., Brovkin A.N., Lavrikova E.Y., Lebedeva N.O., Vikulova O.K., Shamhalova M.S., Shestakova M.V., Mayorov M.Y., Potapov V.A., Nosikov V.V., Averyanov A.V.
|
| Vol 52, No 10 (2016) |
Alu insertion-deletion polymorphism of COL13A1 and LAMA2 genes: The analysis of association with longevity |
(Eng)
|
|
Erdman V.V., Nasibullin T.R., Tuktarova I.A., Somova R.S., Timasheva Y.R., Mustafina O.E., Karimov D.D.
|
| Vol 52, No 10 (2016) |
Population frequency and age of mutation G5741→A in gene NBAS which is a cause of SOPH syndrome in Sakha (Yakutia) Republic |
(Eng)
|
|
Maksimova N.R., Nogovicina A.N., Kurtanov K.A., Alekseeva E.I.
|
| Vol 52, No 8 (2016) |
The heteroplasmy level of some mutations in gene MT-CYB among women with asymptomatic atherosclerosis |
(Eng)
|
|
Sinyov V.V., Chicheva M.M., Barinova V.A., Ryzhkova A.I., Zilinyi R.I., Karagodin V.P., Postnov A.Y., Sobenin I.A., Orekhov A.N., Sazonova M.A.
|
| Vol 52, No 8 (2016) |
Association of gene polymorphisms of matrix metalloproteinases with reproductive losses in the first trimester of pregnancy |
(Eng)
|
|
Mashkina E.V., Kovalenko K.A., Marakhovskaya T.A., Saraev K.N., Belanova A.A., Shkurat T.P.
|
| Vol 52, No 8 (2016) |
Association of polymorphic markers of chemokine genes, their receptors, and CD14 gene with coronary atherosclerosis |
(Eng)
|
|
Nasibullin T.R., Yagafarova L.F., Yagafarov I.R., Timasheva Y.R., Erdman V.V., Tuktarova I.A., Mustafina O.E.
|
| Vol 52, No 6 (2016) |
Polymorphism of CD209 and TLR3 genes in populations of North Eurasia |
(Eng)
|
|
Barkhash A.V., Babenko V.N., Voevoda M.I., Romaschenko A.G.
|
| Vol 52, No 6 (2016) |
Aggression and empathy as genetic differentiation factors of urban population |
(Eng)
|
|
Atramentova L.A., Luchko E.N.
|
| Vol 52, No 6 (2016) |
Two novel mutations in gene SPG4 in patients with autosomal dominant spastic paraplegia |
(Eng)
|
|
Akhmetgaleyeva A.F., Khidiyatova I.M., Saifullina E.V., Idrisova R.F., Magzhanov R.V., Khusnutdinova E.K.
|
| Vol 52, No 5 (2016) |
The haplomatch program for comparing Y-chromosome STR-haplotypes and its application to the analysis of the origin of Don Cossacks |
(Eng)
|
|
Chukhryaeva M.I., Ivanov I.O., Frolova S.A., Koshel S.M., Utevska O.M., Skhalyakho R.A., Agdzhoyan A.T., Bogunov Y.V., Balanovska E.V., Balanovsky O.P.
|
| Vol 52, No 4 (2016) |
Mutational analysis of hemophilia B in Russia: Molecular-genetic study |
(Eng)
|
|
Surin V.L., Demidova E.Y., Selivanova D.S., Luchinina Y.A., Salomashkina V.V., Pshenichnikova O.S., Likhacheva E.A.
|
| Vol 52, No 4 (2016) |
Analysis of FOXO1A and FOXO3A gene allele association with human longevity |
(Eng)
|
|
Erdman V.V., Nasibullin T.R., Tuktarova I.A., Somova R.S., Mustafina O.E.
|
| Vol 52, No 3 (2016) |
Role of allelic genes of matrix metalloproteinases and their tissue inhibitors in the risk of peptic ulcer disease development |
(Eng)
|
|
Shaymardanova E.K., Nurgalieva A.K., Khidiyatova I.M., Gabbasova L.V., Kuramshina O.A., Kryukova A.Y., Sagitov R.B., Munasipov F.R., Khusnutdinova E.K.
|
| Vol 52, No 3 (2016) |
Haplotype analysis of oculopharyngeal muscular dystrophy (OPMD) locus in Yakutia |
(Eng)
|
|
Marusin A.V., Kurtanov H.A., Maksimova N.R., Swarovsakaja M.G., Stepanov V.A.
|
| Vol 52, No 2 (2016) |
Polymorphism (353)R>Q of gene of blood clotting factor VII and plasma hemostasis |
(Eng)
|
|
Bairova T.A., Gommellya M.V., Dolgich V.V., Philippov E.S., Kolesnikova L.I.
|
| Vol 52, No 2 (2016) |
Reliability of the search for 19 common mutations in the CFTR gene in Russian cystic fibrosis patients and the calculated frequency of the disease in Russian Federation |
(Eng)
|
|
Stepanova A.A., Krasovsky S.A., Polyakov A.V.
|
| Vol 52, No 2 (2016) |
The T-786C, G894T, and intron 4 VNTR (4a/b) polymorphisms of the endothelial nitric oxide synthase gene in prostate cancer cases |
(Eng)
|
|
Diler S.B., Öden A.
|
| Vol 52, No 2 (2016) |
A comparative analysis of methylation status of tumor suppressor genes in paired biopsy and serum samples from cervical cancer patients among north indian population |
(Eng)
|
|
Jha A.K., Sharma V., Nikbakht M., Jain V., Sehgal A., Capalash N., Kaur J.
|
| Vol 52, No 1 (2016) |
The dynamics of the composition of mtDNA haplotypes of the ancient population of the Altai Mountains from the early bronze age (3rd millennium BC) to the iron age (2nd–1st centuries BC) |
(Eng)
|
|
Gubina M.A., Kulikov I.V., Babenko V.N., Chikisheva T.A., Romashchenko A.G., Voevoda M.I., Molodin V.I.
|
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