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Clinical features of the microRNA genes methylation in borderline ovarian tumors and depending on the histological structure in ovarian malignancies
Lukina S.S., Burdennyy A.M., Filippova E.A., Pronina I.V., Kazubskaya T.P., Kushlinsky D.N., Utkin D.O., Braga E.A., Loginov V.I., Kushlinskii N.E.
A clinical case of familial enteropathic acrodermatitis caused by a new genetic mutation in exon 10 of the SLC39A4 gene
Stadnikova A.S., Tamrazova O.B., Zakharova I.N., Dmitrieva Y.A., Taganov A.V., Yudina A.E., Bagramova G.E.
Association of VEGFA gene rs2010963 polymorphism with cervical cancer and its progression
Rogalev A.V., Kishenya M.S., Pishchulina S.V., Khomutov E.V.
CYP2C19 gene polymorphism and its impact on the long-term prognosis after myocardial infarction
Solodun M.V., Yakushin S.S., Moseichuk K.A., Filippov E.V.
The case of paroxysmal kinesigenic dyskinesia: a long way from a symptom to the diagnosis
Kim N.L., Yamin M.A.
A clinical case of partial androgen resistance syndrome (Reifenstein syndrome)
Dzeranova L.K., Pigarova E.A., Ivannikova E.V., Kurilo L.F., Chernykh V.B., Polyakov A.V.
POLYMORPHISM OF CHRONIC GLOMERULONEPHRITIS ASSOCIATION WITH ADPRT1 GENE VAL762ALA
Kamyshova E.S., Shvetsov M.Y., Shestakov A.E., Kutyrina I.M., Nosikov V.V.
A case of late manifestation of primary adrenal insufficiency in the autoimmune polyglandular syndrome type 1
Troshina V.V., Grebennikova T.A., Belaya Z.E.
THE MOLECULAR PATHOGENESIS OF BLADDER CANCER
Nemtsova M.V., Kushlinskii N.E.
Challenges of the differential diagnosis between the subtypes of the junctional epidermolysis bullosa: presentation of two clinical cases
Kotalevskaya Y.Y., Marycheva N.M.
DEVELOPMENT OF A MULTIPLEX ALLELE-SPECIFIC REAL-TIME PCR METHOD FOR DETECTION OF PIK3CA GENE SOMATIC MUTATIONS AND ITS VALIDATION IN THE TUMORS OF BREAST CANCER PATIENTS
Filipenko M.L., Shamovskaya D.V., Oskina N.A., Oscorbin I.P., Khrapov E.A., Ovchinnikova L.K., Gershteyn E.S., Kushlinskii N.E.
Reproductive system status and the algorithm to solve fertility issues in men with cystic fibrosis
Repina S.A., Krasovskiy S.A., Shmarina G.V., Shtaut M.I., Zhekayte E.K., Voronkova A.Y., Sherman V.D., Kondratyeva E.I., Chernykh V.B.
Characteristics of the mutation spectrum identified by comprehensive investigation of the CFTR gene in the Russian patients
Petrova N.V., Marakhonov A.Y., Vasilyeva T.A., Kashirskaya N.Y., Kondratyeva E.I., Zhekayte E.K., Voronkova A.Y., Sherman V.D., Galkina V.A., Ginter E.K., Kutsev S.I., Zinchenko R.A.
Polymorphism of the adiponutrin gene (PNPLA3) in the indigenous inhabitants of the Republic of Sakha (Yakutia) with type 2 diabetes mellitus
Kurtanov K.A., Sydykova L.A., Pavlova N.I., Filippova N.P., Dodokhov V.V., Apsolikhova G.A., Solov'eva N.A., D'yakonova A.T., Neustroeva L.M., Varlamova M.A., Borisova N.V.
Evaluation of an association of the rs1801133 MTHFR gene polymorphism with folic acid deficiency in obese patients
Pogozheva A.V., Sorokina E.Y., Aristarkhova T.V.
Molecular and genetic diagnostics of inflammatory bowel diseases
Kuznetsova D.A., Razumov A.S., Merzlyakov M.V., Vavin G.V., Repnikova R.V.
1 - 16 of 16 Items

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