USE OF PREIMPLANTATION DIAGNOSIS WITHIN THE FRAMEWORK OF AN ASSISTED REPRODUCTIVE TECHNOLOGY PROGRAM FOR MARRIED COUPLES WITH A COMBINATION OF MUTATIONS AT THE AZF LOCUS OF THE Y CHROMOSOME AND CFTR GENE POLYMORPHISM IN HUSBANDS
- 作者: BELYAEVA N.A1, GLINKINA Z.I1, SOKUR S.A1, GUBAYEVA Z.M1, DOLGUSHINA N.V1, KALININIA E.A1
-
隶属关系:
- Academician V. I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development of Russia
- 期: 编号 4-1 (2012)
- 页面: 54-58
- 栏目: Articles
- URL: https://journals.eco-vector.com/0300-9092/article/view/246713
- ID: 246713
如何引用文章
详细
全文:
![受限制的访问](https://journals.eco-vector.com/lib/pkp/templates/images/icons/text_lock.png)
作者简介
N. BELYAEVA
Academician V. I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development of Russia
Email: n_belyaeva@oparina4.ru
Moscow
Zh. GLINKINA
Academician V. I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development of RussiaMoscow
S. SOKUR
Academician V. I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development of RussiaMoscow
Z. GUBAYEVA
Academician V. I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development of RussiaMoscow
N. DOLGUSHINA
Academician V. I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development of RussiaMoscow
E. KALININIA
Academician V. I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development of RussiaMoscow
参考
- Черных В.Б. Генетические факторы мужского бесплодия. Всероссийская научно-практическая конференция «Молекулярные методы диагностики моногенных заболеваний: возможности и перспективы»: Материалы // Мед. генетика. — 2006. — № 2, прил. — С. 8—14.
- Черных В.Б., Чухрова А.Л., Бескоровайная Т.С. и др. Типы делеций Y-хромосомы и их частота у мужчин с бесплодием // Генетика. — 2006. — Т. 42, № 8. — С. 1130—1136.
- Черных В.Б. AZF делеции — частая генетическая причина бесплодия у мужчин: современное состояние исследований // Пробл. репрод. — 2009. — № 1. — С. 10—15.
- Черных В.Б., Степанова А.А., Бескоровайная Т.С. Частота и спектр мутаций и 1VS8-Т-полипорфизма гена CFTR среди российских мужчин с бесплодием // Генетика. - 2010. - № 46, № 6. - С. 844-852.
- Ceylan G.G., Ceylan С., Elyas Н. Genetic anomalies in patients with severe oligozoospermia and azoospermia in eastern Turkey: a prospective study // Genet. Mol. Res. - 2009. - Vol. 8, № 3. - P. 915-922.
- Ferlin A., Arredi B., Speltra E. et al. Molecular and clinical characterization of Y-chromosome microdeletions in infertile men: a 10-year experience in Italy // J. Clin. Endocrinol. Metab. - 2007. - Vol. 92. - P. 762-770.
- Huleyuk N., Zastavna D., Tyrkus M. et al. Complex cytogenetic and molecular-genetic analysis of males with spermatogenesis failure // Tsitol. Genet. - 2010. - Vol. 44, № 6. - P. 51-56.
- Lee S.H., Ahn S.Y., Lee K.W. et al. Intracytoplasmic sperm injection may lead to vertical transmission, expansion, and de novo occurrence of Y-chromosome microdeletions in male fetuses // Fertil. and Steril. - 2006. - Vol. 85. -P. 1512-1515.
- Mateu E., Rodrigo L., Martinez M.C. et al. Aneuploidies in embryos and spermatozoa from patients with Y-chromosome microdeletions // Fertil. Steril. - 2010. - Vol. 94. - Р. 28742877.
- Patrat С., Bienvenu Т., Janny L. et al. Clinical data and parenthood of 63 infertile and Y-microdeleted men // Fertil. and Steril. - 2010. - Vol. 93. - P. 822-832.
- Poongothai J., Gopenath T.S., Manonayaki S. Genetics of human male infertility // Singapore Med. J. - 2009. -Vol. 50. - P. 336-347.
- Sachdeva K., Saxena R., Majumdar A. et al. Mutation studies in the CFTR gene in Asian Indian subjects with congenital bilateral absence of vas deferens: report of two novel mutations and four novel variants // Genet. Test. Mol. Biomarkers. - 2011. - Vol. 15. - Р. 307-312.
- Tomaiuolo R., Fausto M., Elce A. et al. Enhanced frequency of CFTR gene variants in couples who are candidates for assisted reproductive technology treatment // Clin. Chem. Lab. Med. - 2011. - Vol. 49. - P. 1289-1293.
补充文件
![](/img/style/loading.gif)