Chromosome abnormalities identified by comparative genomic hybridization in embryos from women with repeated implantation failure.
about
Polar body diagnosis - a step in the right direction?Identification of mosaic and segmental aneuploidies by next-generation sequencing in preimplantation genetic screening can improve clinical outcomes compared to array-comparative genomic hybridization.Uterine receptivity to human embryonic implantation: histology, biomarkers, and transcriptomics.Selection of competent blastocysts for transfer by combining time-lapse monitoring and array CGH testing for patients undergoing preimplantation genetic screening: a prospective study with sibling oocytesTwo different microarray technologies for preimplantation genetic diagnosis and screening, due to reciprocal translocation imbalances, demonstrate equivalent euploidy and clinical pregnancy rates.Comprehensive analysis of karyotypic mosaicism between trophectoderm and inner cell massChromosomal mosaicism in human preimplantation embryos: a systematic review.Preimplantation genetic diagnosis and chromosome analysis of blastomeres using comparative genomic hybridization.Whole genome amplification in preimplantation genetic diagnosisIdentification of chromosomal errors in human preimplantation embryos with oligonucleotide DNA microarray.Randomized comparison of next-generation sequencing and array comparative genomic hybridization for preimplantation genetic screening: a pilot studyCan Comprehensive Chromosome Screening Technology Improve IVF/ICSI Outcomes? A Meta-AnalysisNew array approaches to explore single cells genomesMechanisms of aneuploidy induction in human oogenesis and early embryogenesis.Assisted reproduction technology and defects of genomic imprinting.Investigation and treatment of repeated implantation failure following IVF-ET.Studying meiosis: a review of FISH and M-FISH techniques used in the analysis of meiotic processes in humans.Predictive value of preimplantation genetic diagnosis for aneuploidy screening in repeated IVF-ET cycles among women with recurrent implantation failure.Use of comprehensive chromosomal screening for embryo assessment: microarrays and CGH.Preimplantation genetic screening (PGS) with Comparative genomic hybridization (CGH) following day 3 single cell blastomere biopsy markedly improves IVF outcomes while lowering multiple pregnancies and miscarriages.Aneuploidy in the human cleavage stage embryo.The human cleavage stage embryo is a cradle of chromosomal rearrangements.Whole-chromosome aneuploidy analysis in human oocytes: focus on comparative genomic hybridization.Chromosomal instability in mammalian pre-implantation embryos: potential causes, detection methods, and clinical consequences.Pituitary suppression before frozen embryo transfer is beneficial for patients suffering from idiopathic repeated implantation failure.Increased susceptibility to maternal aneuploidy demonstrated by comparative genomic hybridization analysis of human MII oocytes and first polar bodies.DNA microarray reveals that high proportions of human blastocysts from women of advanced maternal age are aneuploid and mosaic.Comparative genomic hybridization selection of blastocysts for repeated implantation failure treatment: a pilot study.The cytogenetics of polar bodies: insights into female meiosis and the diagnosis of aneuploidy.Transcriptomic profiling of human oocytes: association of meiotic aneuploidy and altered oocyte gene expression.Microarray analysis reveals abnormal chromosomal complements in over 70% of 14 normally developing human embryos.Preimplantation genetic diagnosis/screening by comprehensive molecular testing.ESHRE PGD Consortium 'Best practice guidelines for clinical preimplantation genetic diagnosis (PGD) and preimplantation genetic screening (PGS)'.The origins of genetic variation between individual human oocytes and embryos: implications for infertility.A retrospective study of preimplantation embryos diagnosed with monosomy by fluorescence in situ hybridization (FISH).Detailed FISH analysis of day 5 human embryos reveals the mechanisms leading to mosaic aneuploidy.Breakage-fusion-bridge cycles leading to inv dup del occur in human cleavage stage embryos.PGD for a complex chromosomal rearrangement by array comparative genomic hybridization.
P2860
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P2860
Chromosome abnormalities identified by comparative genomic hybridization in embryos from women with repeated implantation failure.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Chromosome abnormalities ident ...... repeated implantation failure.
@en
Chromosome abnormalities ident ...... repeated implantation failure.
@nl
type
label
Chromosome abnormalities ident ...... repeated implantation failure.
@en
Chromosome abnormalities ident ...... repeated implantation failure.
@nl
prefLabel
Chromosome abnormalities ident ...... repeated implantation failure.
@en
Chromosome abnormalities ident ...... repeated implantation failure.
@nl
P2093
P356
P1476
Chromosome abnormalities ident ...... repeated implantation failure.
@en
P2093
Callaghan T
Voullaire L
Williamson R
P304
P356
10.1093/MOLEHR/8.11.1035
P577
2002-11-01T00:00:00Z