Microarray analysis reveals abnormal chromosomal complements in over 70% of 14 normally developing human embryos.
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Detecting mosaicism in trophectoderm biopsies: current challenges and future possibilitiesPre-implantation genetic testing in ART: who will benefit and what is the evidence?Uterine selection of human embryos at implantationIdentification of mosaic and segmental aneuploidies by next-generation sequencing in preimplantation genetic screening can improve clinical outcomes compared to array-comparative genomic hybridization.Current status of comprehensive chromosome screening for elective single-embryo transfer.Genetics. Genome mosaicism--one human, multiple genomes.The origin, mechanisms, incidence and clinical consequences of chromosomal mosaicism in humans.Oligonucleotide arrays vs. metaphase-comparative genomic hybridisation and BAC arrays for single-cell analysis: first applications to preimplantation genetic diagnosis for Robertsonian translocation carriers.Array comparative genomic hybridization analyses of all blastomeres of a cohort of embryos from young IVF patients revealed significant contribution of mitotic errors to embryo mosaicism at the cleavage stageA healthy delivery of twins by assisted reproduction followed by preimplantation genetic screening in a woman with X-linked dominant incontinentia pigmenti.The chromosomal constitution of embryos arising from monopronuclear oocytes in programmes of assisted reproductionEvaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study.The parental origin correlates with the karyotype of human embryos developing from tripronuclear zygotesPositional changes of a pluripotency marker gene during structural reorganization of fibroblast nuclei in cloned early bovine embryos.Evidence of Selection against Complex Mitotic-Origin Aneuploidy during Preimplantation DevelopmentHuman embryos commonly form abnormal nuclei during development: a mechanism of DNA damage, embryonic aneuploidy, and developmental arrest.Irregular cleavage of early preimplantation human embryos: characteristics of patients and pregnancy outcomes.Genomic analysis of hESC pedigrees identifies de novo mutations and enables determination of the timing and origin of mutational events.A simple and rapid flow cytometry-based assay to identify a competent embryo prior to embryo transferThe accuracy of chromosomal microarray testing for identification of embryonic mosaicism in human blastocysts.Totipotency and lineage segregation in the human embryo.Assisted reproductive technology results: why are live-birth percentages so low?Advances in preimplantation genetic diagnosis/screening.The human endometrium as a sensor of embryo quality.Mosaicism and clinical genetics.Successful Implantation from the Embryonic Aspect.The adverse outcome pathway (AOP) for chemical binding to tubulin in oocytes leading to aneuploid offspring.Whole-Exome Sequencing and Whole-Genome Sequencing in Critically Ill Neonates Suspected to Have Single-Gene Disorders.Mosaicism in Preimplantation Human Embryos: When Chromosomal Abnormalities Are the Norm.Mouse is the new woman? Translational research in reproductive immunology.Applying Multivariate Adaptive Splines to Identify Genes With Expressions Varying After Diagnosis in Microarray Experiments.Can IVF influence human evolution?The why, the how and the when of PGS 2.0: current practices and expert opinions of fertility specialists, molecular biologists, and embryologistsMitotic spindle disruption in human preimplantation embryos activates the spindle assembly checkpoint but not apoptosis until Day 5 of development.Zygotes segregate entire parental genomes in distinct blastomere lineages causing cleavage-stage chimerism and mixoploidy.Tripolar mitosis and partitioning of the genome arrests human preimplantation development in vitro.Dedifferentiation into blastomere-like cancer stem cells via formation of polyploid giant cancer cellsChromosome constitution of human embryos generated after in vitro maturation including 3-isobutyl-1-methylxanthine in the oocyte collection medium.Mosaic variegated aneuploidy in mouse BubR1 deficient embryos and pregnancy loss in human.Preimplantation genetic diagnosis/screening by comprehensive molecular testing.
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P2860
Microarray analysis reveals abnormal chromosomal complements in over 70% of 14 normally developing human embryos.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
Microarray analysis reveals ab ...... ally developing human embryos.
@en
Microarray analysis reveals ab ...... ally developing human embryos.
@nl
type
label
Microarray analysis reveals ab ...... ally developing human embryos.
@en
Microarray analysis reveals ab ...... ally developing human embryos.
@nl
prefLabel
Microarray analysis reveals ab ...... ally developing human embryos.
@en
Microarray analysis reveals ab ...... ally developing human embryos.
@nl
P2093
P2860
P356
P1433
P1476
Microarray analysis reveals ab ...... mally developing human embryos
@en
P2093
A Mertzanidou
E Vanneste
J R Vermeesch
P2860
P304
P356
10.1093/HUMREP/DES362
P407
P50
P577
2012-10-09T00:00:00Z