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Association of COL1A1, ESR1, and VDR gene polymorphisms with the risk of pelvic floor dysfunction in postpartum women
Mikhelson A., Lukianova K., Lazukina M., Varlamova A., Tretyakova T., Varaksin A., Konstantinova E., Maslakova T.
Analysis of HLA class I gene (G) polymorphic alleles in pregnant women in the North-West Region of the Russian Federation
Shengelia M., Bespalova O., Ivashchenko T., Frank N., Sultanov I., Nasykhova Y., Glotov A.
Chronic cervicitis associated with human papillomavirus and markers of inflammation in women of reproductive age
Amirkhanyan A., Bairamova G., Kiselev V., Prilepskaya V., Poloznikov A., Burmenskaya O., Babkina I., Asaturova A.
ROLE OF GENETIC AND AUTOIMMUNE DISORDERS IN THE DEVELOPMENT OF PREMATURE OVARIAN FAILURE
SHAMILOVA N., MARCHENKO L., DOLGUSHINA N., KUZNETSOVA E., ZALETAYEV D.
Somatic mutations in MED 12 gene exon 2 in women with a single uterine fibroid or multiple ones
Sogoyan N., Kuznetsova M., Asaturova A., Adamyan L., Trofimov D.
THE FMR1 GENE: NEW POSSIBILITIES OF ASSESSING THE OVARIAN RESERVE
SHAMILOVA N., MARCHENKO L.
A change in the concentration of extracellular DNA during pregnancy
Karapetyan A., Krasnyi A., Sadekova A., Khlestova G., Balashov I., Baev O.
CAN THE FMR1 GENE BE CONSIDERED AS A PREDICTOR OF EARLY OVARIAN AGING?
SHAMILOVA N., MARCHENKO L.
Molecular genetic and endocrine predictors of menstrual cycle regulation in patients with polycystic ovary syndrome undergoing metformin treatment
Chernukha G., Naidukova A., Kaprina E., Miroshina E., Donnikov A.
The role of the FMR1 gene in the development of reproductive and neurological disorders
Marchenko L., Rshtuni S., Zaretskaya N., Pikhut P., Mashaeva R.
Congenital adrenal hypoplasia caused by 21-hydroxylase deficiency in patients undergoing an assisted reproductive technology programs
Glinkina Z., Kuzmichev L., Bakharev V., Dzenis I., Azizova G., Mikayelyan V., Ikonnikov M.
Molecular genetic predictors of polycystic ovary syndrome and its androgenic phenotypes
Chernukha G., Naidukova A., Kaprina E., Donnikov A.
WIF-1 gene methylation in cervical squamous intraepithelial lesions
Sukhikh G., Ashrafyan L., Bairamova G., Babkina I., Chernova V., Osipyants A., Korolkova A., Poloznikov A., Asfarova G., Mullabaeva S., Kogan E., Muizhnek E., Drukh V., Kiselev V.
The role of interleukin-8 (IL-8) and polymorphism of IL-8 gene in formation of external genital endometriosis in patients of reproductive age
Avanesova T., Levkovich M., Ermolova N., Palieva N., Petrov Y.
Genetic factors in the development of recurrent miscarriage: An overview of the data of meta-analyses
Trifonova E., Ganzha O., Gabidulina T., Devyatyarova L., Sotnikova L., Stepanov V.
A study of polymorphisms rs3020434, rs11742635, rs124577644, rs12637801, rs2861221, and rs17677069 in women with uterine leiomyomas and a family history of the disease
Sogoyan N., Kuznetsova M., Lolomadze E., Mikhailovskaya G., Mishina N., Trofimov D., Adamyan L.
FMR1 GENE POLYMORPHISM IN POLYCYSTIC OVARY SYNDROME
Tabeeva G., Nemova Y., Naidukova A., Kuznetsova E., Zaletaev D., Chernukha G.
Interleukin-10 production and secretion in blood in relation to interleukin-10 A-1082G polymorphism in pregnant women with fetal growth restriction
Malyshkina A., Boiko Y., Sotnikova N., Panova I., Fetisova I., Voronin D., Mileeva P.
PRESENTATION OF NONRANDOM X CHROMOSOME INACTIVATION AND ANDROGEN RECEPTOR GENE POLYMORPHISM IN DIFFERENT PHENOTYPES OF POLYCYSTIC OVARY SYNDROME
CHERNUKHA G., NEMOVA Y., BLINOVA I., RUDENKO V.
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