The human cleavage stage embryo is a cradle of chromosomal rearrangements.
about
Single cell genomics: advances and future perspectivesNew insights into the generation and role of de novo mutations in health and diseaseSingle-cell paired-end genome sequencing reveals structural variation per cell cycle.Concurrent whole-genome haplotyping and copy-number profiling of single cells.Human embryos commonly form abnormal nuclei during development: a mechanism of DNA damage, embryonic aneuploidy, and developmental arrest.Timing, rates and spectra of human germline mutation.Gain of FAM123B and ARHGEF9 in an Obese Man with Intellectual Disability, Congenital Heart Defects and Multiple Supernumerary Ring Chromosomes.Chromothripsis and beyond: rapid genome evolution from complex chromosomal rearrangementsNon-meiotic chromosome instability in human immature oocytesGenomic instability: Crossing pathways at the origin of structural and numerical chromosome changes.Physiological Aspects of Female Fertility: Role of the Environment, Modern Lifestyle, and Genetics.Prenatal and pre-implantation genetic diagnosis.Mitotic 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.Microarray analysis reveals abnormal chromosomal complements in over 70% of 14 normally developing human embryos.Genome stability of bovine in vivo-conceived cleavage-stage embryos is higher compared to in vitro-produced embryos.Chromosome segregation regulation in human zygotes: altered mitotic histone phosphorylation dynamics underlying centromeric targeting of the chromosomal passenger complex.Validation of copy number variation sequencing for detecting chromosome imbalances in human preimplantation embryos.Partial deletion of DEPDC5 in a child with focal epilepsy.Structural chromosomal abnormalities detected during CVS analysis and their role in the prenatal ascertainment of cryptic subtelomeric rearrangements
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P2860
The human cleavage stage embryo is a cradle of chromosomal rearrangements.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 09 February 2011
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vedecký článok
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vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
@cs
name
The human cleavage stage embryo is a cradle of chromosomal rearrangements.
@en
The human cleavage stage embryo is a cradle of chromosomal rearrangements.
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type
label
The human cleavage stage embryo is a cradle of chromosomal rearrangements.
@en
The human cleavage stage embryo is a cradle of chromosomal rearrangements.
@nl
prefLabel
The human cleavage stage embryo is a cradle of chromosomal rearrangements.
@en
The human cleavage stage embryo is a cradle of chromosomal rearrangements.
@nl
P2093
P2860
P356
P1476
The human cleavage stage embryo is a cradle of chromosomal rearrangements.
@en
P2093
P2860
P304
P356
10.1159/000324235
P577
2011-02-09T00:00:00Z