The origin of human aneuploidy: where we have been, where we are going.
about
Transmission distortion affecting human noncrossover but not crossover recombination: a hidden source of meiotic driveFrequent and efficient use of the sister chromatid for DNA double-strand break repair during budding yeast meiosisA review of trisomy X (47,XXX)Age-related decrease of meiotic cohesins in human oocytesConcise review: new paradigms for Down syndrome research using induced pluripotent stem cells: tackling complex human genetic diseaseAdvanced paternal age and reproductive outcome48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndromeShugoshin-2 is essential for the completion of meiosis but not for mitotic cell division in miceOocyte Maturation and DevelopmentPossible Role of Aurora-C in MeiosisThe spindle checkpoint and chromosome segregation in meiosisThe effect of sperm DNA fragmentation on miscarriage rates: a systematic review and meta-analysisProfiling of the mammalian mitotic spindle proteome reveals an ER protein, OSTD-1, as being necessary for cell division and ER morphologySelective disruption of aurora C kinase reveals distinct functions from aurora B kinase during meiosis in mouse oocytesBenzene exposure near the U.S. permissible limit is associated with sperm aneuploidyDynamics and ethics of comprehensive preimplantation genetic testing: a review of the challengesAll dosage compensation is local: gene-by-gene regulation of sex-biased expression on the chicken Z chromosomeSperm Aneuploidy in Faroese Men with Lifetime Exposure to Dichlorodiphenyldichloroethylene (p,p´-DDE) and Polychlorinated Biphenyl (PCB) PollutantsRNF212 is a dosage-sensitive regulator of crossing-over during mammalian meiosisMeiotic DNA double-strand breaks and chromosome asynapsis in mice are monitored by distinct HORMAD2-independent and -dependent mechanismsExpression of the novel maternal centrosome assembly factor Wdr8 is required for vertebrate embryonic mitosesA lack of coordination between sister-chromatids segregation and cytokinesis in the oocytes of B6.YTIR (XY) sex-reversed female miceUnusual trend in the prevalence of trisomy 13 in mothers aged 35 and older: A population based study of national congenital anomaly data.The maternal age-related first trimester risks for trisomy 21, 18 and 13 based on Danish first trimester data from 2005 to 2014.Molecular cartography: mapping the landscape of meiotic recombination.Phosphorylation-independent regulation of Atf1-promoted meiotic recombination by stress-activated, p38 kinase Spc1 of fission yeast.Molecular cytogenetics and cytogenomics of brain diseases.Pch2 links chromosome axis remodeling at future crossover sites and crossover distribution during yeast meiosisThe pch2Delta mutation in baker's yeast alters meiotic crossover levels and confers a defect in crossover interference.Genetic analysis of variation in human meiotic recombination.Meiotic recombination in human oocytes.Germ-line transmission of trisomy 21: Data from 80 families suggest an implication of grandmaternal age and a high frequency of female-specific trisomy rescue.Cytogenetic analysis of human embryos and embryonic stem cells derived from monopronuclear zygotesThe synaptonemal complex protein, Zip1, promotes the segregation of nonexchange chromosomes at meiosis I.A yeast's eye view of mammalian reproduction: cross-species gene co-expression in meiotic prophase.Maternal age-dependent APC/C-mediated decrease in securin causes premature sister chromatid separation in meiosis II.Discrete DNA sites regulate global distribution of meiotic recombination.Examining variation in recombination levels in the human female: a test of the production-line hypothesisSeparase phosphosite mutation leads to genome instability and primordial germ cell depletion during oogenesis.High-throughput knockout screen in Schizosaccharomyces pombe identifies a novel gene required for efficient homolog disjunction during meiosis I.
P2860
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P2860
The origin of human aneuploidy: where we have been, where we are going.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
The origin of human aneuploidy: where we have been, where we are going.
@en
type
label
The origin of human aneuploidy: where we have been, where we are going.
@en
prefLabel
The origin of human aneuploidy: where we have been, where we are going.
@en
P2093
P356
P1476
The origin of human aneuploidy: where we have been, where we are going.
@en
P2093
Heather Hall
Patricia Hunt
Terry Hassold
P304
P356
10.1093/HMG/DDM243
P478
16 Spec No. 2
P577
2007-10-01T00:00:00Z