Accès gratuit
Numéro
Med Sci (Paris)
Volume 20, Numéro 6-7, Juin-Juillet 2004
Page(s) 691 - 696
Section M/S revues
DOI https://doi.org/10.1051/medsci/2004206-7691
Publié en ligne 15 juin 2004
  1. Hassold T, Hunt PA. To err (meiotically) is human : The genesis of human aneuploidy. Nat Rev Genet 2001; 2 : 280–91.
  2. Sherman SL, Takaesu N, Freeman SB, et al. Trisomy 21 : Association between reduced recombination and nondisjunction. Am J Hum Genet 1991; 49 : 608–20.
  3. Hassold T, Merrill M, Adkins K, et al. Recombinaison and maternal age-dependent non-disjunction : Molecular studies of trisomy 16. Am J Hum Genet 1995; 57 : 867–74.
  4. Lamb NE, Feingold E, Savage A, et al. Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21. Hum Mol Genet 1997; 6 : 1391–9.
  5. Hawley RS, Frazier JA, Rasooly R. Separation anxiety : The etiology of nondisjunction in flies and people. Hum Mol Genet 1994; 3 : 1521–8.
  6. Koehler KE, Hawley RS, Sherman S, Hassold T. Recombination and nondisjunction in humans and flies. Hum Mol Genet 1996; 5 : 1495–504.
  7. Ross LO, Maxfield R, Dawson D. Exchanges are not equally able to enhance meiotic chromosome segregation in yeast. Proc Natl Acad Sci USA 1996; 93 : 4979–83.
  8. Jacobs PA. The chromosome complement of human gametes. Oxf Rev Reprod Biol 1992; 14 : 47–72.
  9. Angell RR. Predivision in human oocytes at meiosis I : A mechanism for trisomy formation in man. Hum Genet 1991; 86 : 383–7.
  10. Angell R. First-meiotic-division nondisjunction in human oocytes. Am J Hum Genet 1997; 61 : 23–32.
  11. Mahmood R, Brierley CH, Faed MJ, et al. Mechanisms of maternal aneuploidy : FISH analysis of oocytes and polar bodies in patients undergoing assisted conception. Hum Genet 2000; 106 : 620–6.
  12. Sandalinas M, Marquez C, Munne S. Spectral karyotyping of fresh, non-inseminated oocytes. Mol Hum Reprod 2002; 8 : 580–5.
  13. Martini E, Flaherty SP, Swann NJ, et al. FISH analysis of six chromosomes in unfertilized human oocytes after polar body removal. J Assist Reprod Genet 2000; 17 : 276–83.
  14. Wall MB, Marks K, Smith TA, et al. Cytogenetic and fluorescent in situ hybridization chromosomal studies on in vitro fertilized and intracytoplasmic sperm injected failed-fertilized’ human oocytes. Hum Reprod 1996; 11 : 2230–8.
  15. Pellestor F, Andréo B, Arnal F, et al. Maternal aging and chromosomal abnormalities : New data drawn from in vitro unfertilized human oocytes. Hum Genet 2003; 112 : 195–203.
  16. Dailey T, Dale B, Cohen J, Munne S. Association between nondisjunction and maternal age in meiosis-II human oocytes. Am J Hum Genet 1996; 59 : 176–84.
  17. Nasmyth K, Peters JM, Uhlmann F. Splitting the chromosome : cutting the ties that bind sister chromatids. Science 2000; 288 : 1379–85.
  18. Parisi S, McKay MJ, Molnar M, et al. Rec8p, a meiotic recombination and sister chromatid cohesion phosphoprotein of the Rad21p family conserved from fission yeast to humans. Mol Cell Biol 1999; 19 : 3515–28.
  19. Bickel S, Orr-Weaver TL, Balicky E. The sister-chromatid cohesion protein ORD is required for chiasma maintenance in Drosophila oocytes. Current Biology 2002; 12 : 925–9.
  20. Wolstenholme J, Angell RR. Maternal age and trisomy - a unifying mechanism of formation. Chromosoma 2000; 109 : 435–8.
  21. Steuerwald N, Cohen J, Herrera RJ, et al. Association between spindle assembly checkpoint expression and maternal age in human oocytes. Mol Hum Reprod 2001; 7 : 49–55.
  22. Pellestor F, Andréo B, Arnal F, et al. Mechanisms of non-disjunction in human female meiosis : the co-existence of two modes of malsegregation evidenced by the karyotyping of 1397 in vitro unfertilized oocytes. Hum Reprod 2002; 17 : 2134–45.
  23. Lo AW, Liao GC, Rocchi M, Choo KH. Extreme reduction of chromosome-specific alpha-satellite array is unusually common in human chromosome 21. Genome Res 1999; 9 : 895–908.
  24. Maratou K, Siddique Y, Kessling AM, Davies GE. Variation in alphoid DNA size and trisomy 21 : a possible cause of nondisjunction. Hum Genet 2000; 106 : 525–30.
  25. LeMaire-Adkins R, Radke K, Hunt PA. Lack of checkpoint control at the metaphase/anaphase transition : a mechanism of meiotic nondisjunction in mammalian females. J Cell Biol 1997; 139 : 1611–9.
  26. Hodges CA, Hunt PA. Simultaneous analysis of chromosomes and chromosome-associated pro teins in mammalian oocytes and embryons. Chromosoma 2002; 11 : 165–9.

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