Free Access
Med Sci (Paris)
Volume 31, Number 2, Février 2015
Page(s) 129 - 131
Section Nouvelles
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]

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