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| Numéro |
Biologie Aujourd'hui
Volume 211, Numéro 3, 2017
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|---|---|---|
| Page(s) | 199 - 205 | |
| Section | Génétique et reproduction | |
| DOI | https://doi.org/10.1051/jbio/2017025 | |
| Publié en ligne | 7 février 2018 | |
- Aboura, A., Dupas, C., Tachdjian, G., Portnoï, M.-F., Bourcigaux, N., Dewailly, D., Frydman, R., Fauser, B., Ronci-Chaix, N., Donadille, B., Bouchard, P., Christin-Maitre, S. (2009). Array comparative genomic hybridization profiling analysis reveals deoxyribonucleic acid copy number variations associated with premature ovarian failure. J Clin Endocrinol Metab, 94, 11, 4540-4546. [CrossRef] [PubMed] [Google Scholar]
- Dudding, T.E., Lawrence, O., Winship, I., Froyen, G., Vandewalle, J., Scott, R., Shelling, A.N. (2010). Array comparative genomic hybridization for the detection of submicroscopic copy number variations of the X chromosome in women with premature ovarian failure. Hum Reprod, 25, 3159-3160. [CrossRef] [PubMed] [Google Scholar]
- Ford, C.E. (1961). The cytogenetic analysis of some disorder of sex development. Am J Obstet Gynecol, 82, 1154-1161. [CrossRef] [Google Scholar]
- Hyon, C., Mansour-Hendili, L., Chantot-Bastaraud, S., Donadille, B., Kerlan, V., Dodé, C., Jonard, S., Delemer, B., Gompel, A., Reznik, Y., Touraine, P., Siffroi, J.P., Christin-Maitre, S. (2016). Deletion of CPEB1 Gene: a rare but recurrent cause of premature ovarian insufficiency. J Clin Endocrinol Metab, 101, 2099-2104. [CrossRef] [PubMed] [Google Scholar]
- Jaillard, S., Akloul, L., Beaumont, M., Hamdi-Roze, H., Dubourg, C., Odent, S., Duros, S., Dejucq-Rainsford, N., Belaud-Rotureau, M.-A., Ravel, C. (2016). Array-CGH diagnosis in ovarian failure: identification of new molecular actors for ovarian physiology. J Ovarian Res, 9, 63-69. [CrossRef] [PubMed] [Google Scholar]
- Kallioniemi, A., Kallioniemi, O.P., Sudar, D., Rutovitz, D., Gray, J.W., Waldman, F., Pinkel, D. (1992). Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science, 258, 818-821. [CrossRef] [PubMed] [Google Scholar]
- Knauff, E.A.H., Blauw, H.M., Pearson, P.L., Kok, K., Wijmenga, C., Veldink, J.H., van den Berg, L.H., Bouchard, P., Fauser, B.C.J.M., Franke, L. (2011). Copy number variants on the X chromosome in women with primary ovarian insufficiency. Fertil Steril, 95, 1584-1588. [CrossRef] [PubMed] [Google Scholar]
- Lacombe, A., Lee, H., Zahed, L., Choucair, M., Muller, J.-M., Nelson, S.F., Salameh, W., Vilain, E. (2006). Disruption of POF1B binding to non-muscle actin filaments is associated with premature ovarian failure. Am J Hum Genet, 79, 113-119. [CrossRef] [Google Scholar]
- Ledig, S., Röpke, A., Wieacker, P. (2010). Copy number variants in premature ovarian failure and ovarian dysgenesis. Sex Dev, 4, 225-232. [CrossRef] [Google Scholar]
- Mansouri, M.R., Schuster, J., Badhai, J., Stattin, E.-L., Lösel, R., Wehling, M., Carlsson, B., Hovatta, O., Karlström, P.O., Golovleva, I., Toniolo, D., Bione, S., Peluso, J., Dahl, N. (2008). Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failure. Hum Mol Genet, 17, 3776-3783. [CrossRef] [PubMed] [Google Scholar]
- McGuire, M.M., Bowden, W., Engel, N.J., Ahn, H.W., Kovanci, E., Rajkovic, A. (2011). Genomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure. Fertil Steril, 95, 1595-1600. [CrossRef] [PubMed] [Google Scholar]
- Norling, A., Hirschberg, A.L., Rodriguez-Wallberg, K.A., Iwarsson, E., Wedell, A., Barbaro, M. (2014). Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform. Hum Reprod, 29, 1818-1827. [CrossRef] [PubMed] [Google Scholar]
- Quilter, C.R., Karcanias, A.C., Bagga, M.R., Duncan, S., Murray, A., Conway, G.S., Sargent, C.A., Affara, N.A. (2010). Analysis of X chromosome genomic DNA sequence copy number variation associated with premature ovarian failure (POF). Hum Reprod, 25, 2139-2150. [CrossRef] [PubMed] [Google Scholar]
- Simpson, J.L. (2008). Genetic and phenotypic heterogeneity in ovarian failure. Ann N Y Acad Sci, 1135, 146-154. [CrossRef] [PubMed] [Google Scholar]
- Simpson, J.L., Rajkovic, A. (1999). Ovarian differentiation and gonadal failure. Am J Med Genet, 89, 186-200. [CrossRef] [PubMed] [Google Scholar]
- Tay, J., Richter, J.D. (2001). Germ cell differentiation and synaptonemal complex formation are disrupted in CPEB knockout mice. Dev Cell, 1, 201-213. [CrossRef] [PubMed] [Google Scholar]
- Tšuiko, O., Nõukas, M., Žilina, O., Hensen, K., Tapanainen, J.S., Mägi, R., Kals, M., Kivistik, P.A., Haller-Kikkatalo, K., Salumets, A., Kurg, A. (2016). Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases. Hum Reprod, 31, 1913-1925. [CrossRef] [PubMed] [Google Scholar]
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