Chromosome instability is common in human cleavage-stage embryos. (Q53398239)

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scientific article published on 26 April 2009

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English	Chromosome instability is common in human cleavage-stage embryos.	scientific article published on 26 April 2009

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Chromosome instability is common in human cleavage-stage embryos. (English)

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Miikka Vikkula

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Peter Konings

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Peter Konings

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Geert Verbeke

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Geert Verbeke

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Thomas D'Hooghe

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Thomas D'Hooghe

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Thierry Voet

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Thierry Voet

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Joris R Vermeesch

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Joris R Vermeesch

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Yves Moreau

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Yves Moreau

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Evelyne Vanneste

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Cédric Le Caignec

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Michèle Ampe

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Cindy Melotte

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Sophie Debrock

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Mustapha Amyere

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Frans Schuit

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Jean-Pierre Fryns

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11

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19396175

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English

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publication date

26 April 2009

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19396175

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published in

Nature Medicine

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19396175

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13 May 2018

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volume

15

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19396175

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http://europepmc.org/abstract/MED/19396175

issue

5

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19396175

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13 May 2018

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http://europepmc.org/abstract/MED/19396175

page(s)

577-583

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Chromosome instability, chromosome transcriptome, and clonal evolution of tumor cell populations

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Defining 'chromosomal instability'.

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https://pubmed.ncbi.nlm.nih.gov/19396175

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Self-correction of chromosomally abnormal embryos in culture and implications for stem cell production.

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Mechanisms of aneuploidy induction in human oogenesis and early embryogenesis

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Single-cell chromosomal imbalances detection by array CGH

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Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions

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Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro.

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Increased rate of aneuploid embryos in young women with previous aneuploid conceptions

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Detection of chromosomal structural alterations in single cells by SNP arrays: a systematic survey of amplification bias and optimized workflow

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Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH)-Re-evaluation of chromosome aberration rates in early spontaneous abortions

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Chromosomal abnormalities and embryo development in recurrent miscarriage couples

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Aneuploidy and confined chromosomal mosaicism in the developing human brain.

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Preimplantation genetic screening reveals a high incidence of aneuploidy and mosaicism in embryos from young women undergoing IVF

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Abnormal phenotypes in uniparental disomy (UPD): fundamental aspects and a critical review with bibliography of UPD other than 15.

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12 December 2020

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Chromosome analysis of blastomeres from human embryos by using comparative genomic hybridization

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19396175

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12 December 2020

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The impact of LH-containing gonadotropins on diploidy rates in preimplantation embryos: long protocol stimulation

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Centric fission--simple and complex mechanisms.

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https://pubmed.ncbi.nlm.nih.gov/19396175

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12 December 2020

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Human gene expression first occurs between the four- and eight-cell stages of preimplantation development

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Telomere dysfunction promotes non-reciprocal translocations and epithelial cancers in mice

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Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements

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Analysis of the evolution of chromosome abnormalities in human embryos from Day 3 to 5 using CGH and FISH.

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Comparison of blastocyst transfer with or without preimplantation genetic diagnosis for aneuploidy screening in couples with advanced maternal age: a prospective randomized controlled trial.

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What next for preimplantation genetic screening?

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12 December 2020

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Neocentromeres: new insights into centromere structure, disease development, and karyotype evolution

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ESHRE PGD consortium data collection VII: cycles from January to December 2004 with pregnancy follow-up to October 2005.

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PubMed

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12 December 2020

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Comprehensive chromosomal analysis of human preimplantation embryos using whole genome amplification and single cell comparative genomic hybridization

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12 December 2020

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Interstitial deletions and intrachromosomal amplification initiated from a double-strand break targeted to a mammalian chromosome

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12 December 2020

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Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19396175

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12 December 2020

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inferred from PubMed ID database lookup

High resolution array-CGH analysis of single cells

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19396175

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12 December 2020

based on heuristic

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Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridization

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19396175

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12 December 2020

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Fluorescence in situ hybridization reanalysis of day-6 human blastocysts diagnosed with aneuploidy on day 3.

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12 December 2020

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Identifiers

DOI

10.1038/NM.1924

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Europe PubMed Central

PubMed publication ID

19396175

retrieved

13 May 2018

reference URL

http://europepmc.org/abstract/MED/19396175

PubMed publication ID

19396175

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19396175

retrieved

13 May 2018

reference URL

http://europepmc.org/abstract/MED/19396175

ResearchGate publication ID

24361815

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