Works matching Nondisjunction and aneuploidy
Results: 41
Cell biology: Nondisjunction, aneuploidy and tetraploidy.
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- Nature, 2006, v. 442, n. 7104, p. E9, doi. 10.1038/nature05139
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Cell biology: Nondisjunction, aneuploidy and tetraploidy (Reply).
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- Nature, 2006, v. 442, n. 7104, p. E10, doi. 10.1038/nature05140
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- Article
Aneuploidy in human oocytes: nondisjunction or predivision?
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- Cytogenetics & Cell Genetics, 2001, v. 94, n. 3/4, p. 241, doi. 10.1159/000048823
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Screening for parental mitotic nondisjunction as a cause of fetal aneuploidy.
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- Middle East Journal of Medical Genetics, 2018, v. 7, n. 1, p. 26, doi. 10.4103/MXE.MXE_1_18
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Aneuploidy in recurrent spontaneous aborters: the tendency to parental nondisjunction.
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- Clinical Genetics, 1984, v. 26, n. 1, p. 43, doi. 10.1111/j.1399-0004.1984.tb00786.x
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Does the Assessment of Nondisjunction Provide a More Sensitive Assay for the Detection of Aneugens?
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- Toxicological Sciences, 2017, v. 157, n. 1, p. 20, doi. 10.1093/toxsci/kfx014
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On the rate of aneuploidy reversion in a wild yeast model.
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- Genetics, 2025, v. 229, n. 2, p. 1, doi. 10.1093/genetics/iyae196
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Adaptation by Loss of Heterozygosity in Saccharomyces cerevisiae Clones Under Divergent Selection.
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- Genetics, 2019, v. 213, n. 2, p. 665, doi. 10.1534/genetics.119.302411
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Centromere-Proximal Meiotic Crossovers in Drosophila melanogaster Are Suppressed by Both HighlyRepetitive Heterochromatin and Proximity tothe Centromere.
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- Genetics, 2019, v. 213, n. 1, p. 113, doi. 10.1534/genetics.119.302509
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Nuclear envelope structural defect underlies the main cause of aneuploidy in ovarian carcinogenesis.
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- BMC Cell Biology, 2016, v. 17, p. 1, doi. 10.1186/s12860-016-0114-8
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Preimplantation lethality of monosomy for mouse chromosome 19.
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- Nature, 1979, v. 280, n. 5718, p. 144, doi. 10.1038/280144a0
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Cytogenetic mechanisms of aneuploidy in somatic cells of chemonuclear industry professionals with incorporated plutonium-239.
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- Russian Journal of Genetics, 2010, v. 46, n. 11, p. 1381, doi. 10.1134/S1022795410110141
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Folate Deficiency Triggers the Abnormal Segregation of a Region With Large Cluster of CG-Rich Trinucleotide Repeats on Human Chromosome 2.
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- Frontiers in Genetics, 2021, v. 11, p. 1, doi. 10.3389/fgene.2021.695124
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The decatenation checkpoint.
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- British Journal of Cancer, 2007, v. 96, n. 2, p. 201, doi. 10.1038/sj.bjc.6603537
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Chromosomal Damage Rate, Aging, and Diet<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 854, n. 1, p. 23, doi. 10.1111/j.1749-6632.1998.tb09889.x
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The effects of age and abnormal sperm count on the nondisjunction of spermatozoa.
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- Journal of Assisted Reproduction & Genetics, 2000, v. 17, n. 1, p. 51, doi. 10.1023/A:1009454114973
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Nondisjunction and transmission ratio distortion ofChromosome 2 in a (2.8) Robertsonian translocation mouse strain.
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- Mammalian Genome, 2006, v. 17, n. 3, p. 239, doi. 10.1007/s00335-005-0126-8
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Pentasomy 49,XXXXY Associated with a Chiari Type 1 Malformation and Cervical Syrinx.
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- Pediatric Neurosurgery, 2007, v. 43, n. 1, p. 47, doi. 10.1159/000097526
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Indication for thresholds of chromosome non-disjunction versus chromosome lagging induced by spindle inhibitors in vitro in human lymphocytes.
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- Mutagenesis, 1997, v. 12, n. 3, p. 133, doi. 10.1093/mutage/12.3.133
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Assessment of sex chromosome aneuploidy in sperm nuclei from 47,XXY and 46,XY/47,XXY males: comparison with fertile and infertile males with normal karyotype.
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- Molecular Human Reproduction, 2000, v. 6, n. 2, doi. 10.1093/molehr/6.2.107
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A case of double aneuploidy of Down and Klinefelter syndrome in an Indian infant: a detailed case report.
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- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00602-6
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Previous aneuploidic offspring in a young woman does not increase the risk for somatic random aneuploidy in subsequent pregnancies.
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- Acta Obstetricia et Gynecologica Scandinavica, 2006, v. 85, n. 8, p. 1003, doi. 10.1080/00016340600622577
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The origin of aneuploidy in humans: where we've been, where we're going.
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- Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2010, v. 20, p. S8, doi. 10.1016/S1472-6483(10)62283-3
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Cleavage versus blastocyst-stage embryo transfer.
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- 2008
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- Abstract
Chromosomal FISH analysis of unfertilized human oocytes and polar bodies.
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- Journal of Human Genetics, 2002, v. 47, n. 9, p. 488, doi. 10.1007/s100380200071
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Human Embryonic Stem Cells as Models for Aneuploid Chromosomal Syndromes.
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- Stem Cells, 2010, v. 28, n. 9, p. 1530, doi. 10.1002/stem.483
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Selfish centromeres and the wastefulness of human reproduction.
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- PLoS Biology, 2022, v. 20, n. 7, p. 1, doi. 10.1371/journal.pbio.3001671
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Study of the effects of 0.15 terahertz radiation on genome integrity of adult fibroblasts.
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- Environmental & Molecular Mutagenesis, 2018, v. 59, n. 6, p. 476, doi. 10.1002/em.22192
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Recurrent triploidy of maternal origin.
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- 2003
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- Report
Reconsideration of the safety and effectiveness of human oocyte cryopreservation.
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- Reproductive Biology & Endocrinology, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s12958-023-01071-z
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Effect of maternal age on the frequency of cytogenetic abnormalities in human oocytes.
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- Cytogenetic & Genome Research, 2005, v. 111, n. 3/4, p. 206, doi. 10.1159/000086891
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Mechanisms of aneuploidy induction in human oogenesis and early embryogenesis.
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- Cytogenetic & Genome Research, 2005, v. 111, n. 3/4, p. 237, doi. 10.1159/000086894
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Maternal aging and chromosomal abnormalities: new data drawn from in vitro unfertilized human oocytes.
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- Human Genetics, 2003, v. 112, n. 2, p. 195, doi. 10.1007/s00439-002-0852-x
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The incidence of aneuploidy in human oocytes assessed by conventional cytogenetic analysis.
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- Hereditas, 2004, v. 141, n. 2, p. 97, doi. 10.1111/j.1601-5223.2004.01803.x
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Fertility assessment in hybrids between monobrachially homologous Rb races of the house mouse from the island of Madeira: implications for modes of chromosomal evolution.
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- Heredity, 2011, v. 106, n. 2, p. 348, doi. 10.1038/hdy.2010.74
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Double Aneuploidy: 48,XXY,+18 in a Bedouin Boy.
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- Medical Principles & Practice, 1999, v. 8, n. 3, p. 241, doi. 10.1159/000026099
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The Histone Deacetylase Inhibitor Trichostatin A Has Genotoxic Effects in Human Lymphoblasts In Vitro.
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- Toxicological Sciences, 2006, v. 93, n. 2, p. 341, doi. 10.1093/toxsci/kfl068
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Population monitoring of trisomy 21: problems and approaches.
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- Molecular Cytogenetics (17558166), 2023, v. 16, n. 1, p. 1, doi. 10.1186/s13039-023-00637-1
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Premature separation of sister chromatids in human male meiosis.
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- Human Reproduction, 2008, v. 23, n. 4, p. 982, doi. 10.1093/humrep/dem427
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Loss of Drosophila Mei-41/ATR Alters Meiotic Crossover Patterning.
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- Genetics, 2018, v. 208, n. 2, p. 579, doi. 10.1534/genetics.117.300634
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Nondisjunction rates and abnormal embryonic development in a mouse cross between heterozygotes...
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- Genetics, 1995, v. 141, n. 2, p. 667, doi. 10.1093/genetics/141.2.667
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- Article