Free Access
| Issue |
Biologie Aujourd'hui
Volume 211, Number 3, 2017
|
|
|---|---|---|
| Page(s) | 199 - 205 | |
| Section | Génétique et reproduction | |
| DOI | https://doi.org/10.1051/jbio/2017025 | |
| Published online | 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]
Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.
Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.
Initial download of the metrics may take a while.