Free Access
Issue
Med Sci (Paris)
Volume 31, Number 2, Février 2015
Page(s) 129 - 131
Section Nouvelles
DOI https://doi.org/10.1051/medsci/20153102005
Published online 04 March 2015
  1. Aittomaki K, Lucena JL, Pakarinen P, et al. Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure. Cell 1995 ; 82 : 959–968. [CrossRef] [PubMed] [Google Scholar]
  2. Caburet S, Zavadakova P, Ben-Neriah Z, et al. Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial premature ovarian failure. PLoS One 2012 ; 7 : e33412. [CrossRef] [PubMed] [Google Scholar]
  3. Caburet S, Arboleda VA, Llano E, et al. Mutant cohesin in premature ovarian failure. N Engl J Med 2014 ; 370 : 943–949. [CrossRef] [PubMed] [Google Scholar]
  4. Terret ME, Wassmann K. Le point faible méiotique : la première division. Med Sci (Paris) 2008 ; 24 : 197–204. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  5. Baudat F, Buard J, Grey C, de Massy B. Comment sont choisis les sites d’échanges entre chromosomes lors de la méiose ? Med Sci (Paris) 2011 ; 27 : 1053–1055. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  6. Llano E, Gomez HL, Garcia-Tunon I, et al. STAG3 is a strong candidate gene for male infertility. Hum Mol Genet 2014 ; 23 : 3421–3431. [CrossRef] [PubMed] [Google Scholar]
  7. Winters T, McNicoll F, Jessberger R. Meiotic cohesin STAG3 is required for chromosome axis formation and sister chromatid cohesion. EMBO J 2014 ; 33 : 1256–1270. [PubMed] [Google Scholar]
  8. Hopkins J, Hwang G, Jacob J, et al. Meiosis-specific cohesin component, Stag3 is essential for maintaining centromere chromatid cohesion, and required for DNA repair and synapsis between homologous chromosomes. PLoS Genet 2014 ; 10 : e1004413. [CrossRef] [PubMed] [Google Scholar]
  9. Fukuda T, Fukuda N, Agostinho A, et al. STAG3-mediated stabilization of REC8 cohesin complexes promotes chromosome synapsis during meiosis. EMBO J 2014 ; 33 : 1243–1255. [PubMed] [Google Scholar]
  10. Solomon DA, Kim T, Diaz-Martinez LA, et al. Mutational inactivation of STAG2 causes aneuploidy in human cancer. Science 2011 ; 333 : 1039–1043. [CrossRef] [PubMed] [Google Scholar]
  11. Kon A, Shih LY, Minamino M, et al. Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms. Nat Genet 2013 ; 45 : 1232–1237. [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.