about
CRISPR/Cas9-mediated gene editing in human tripronuclear zygotesARTs in action in nonhuman primates: symposium summary--advances and remaining issuesGermline energetics, aging, and female infertilityHuman oocyte developmental potential is predicted by mechanical properties within hours after fertilizationDiagnosis of abnormal human fertilization status based on pronuclear origin and/or centrosome numberIdentification of differentially expressed markers in human follicular cells associated with competent oocytes.Cytogenetic analysis of human embryos and embryonic stem cells derived from monopronuclear zygotesNew tools for embryo selection: comprehensive chromosome screening by array comparative genomic hybridization.The origin, mechanisms, incidence and clinical consequences of chromosomal mosaicism in humans.Chromosome segregation analysis in human embryos obtained from couples involving male carriers of reciprocal or Robertsonian translocation.The moral imperative to continue gene editing research on human embryos.Molecular cytogenetics of human single pronucleated zygotesDevelopmental ability of chromosomally abnormal human embryos to develop to the blastocyst stage.Human chorionic gonadotropin (hCG) in the secretome of cultured embryos: hyperglycosylated hCG and hCG-free beta subunit are potential markers for infertility management and treatment.A healthy delivery of twins by assisted reproduction followed by preimplantation genetic screening in a woman with X-linked dominant incontinentia pigmenti.Embryological strategies for overcoming recurrent assisted reproductive technology treatment failure.Chromosome microduplication in somatic cells decreases the genetic stability of human reprogrammed somatic cells and results in pluripotent stem cells.Developmental stage on day-5 and fragmentation rate on day-3 can influence the implantation potential of top-quality blastocysts in IVF cycles with single embryo transferPreimplantation genetic diagnosis for couples with a Robertsonian translocation: practical information for genetic counseling.Direct Unequal Cleavages: Embryo Developmental Competence, Genetic Constitution and Clinical Outcome.The relationship of pronuclear stage morphology and chromosome status at cleavage stageSpermatogenic patterns and early embryo development after intracytoplasmic sperm injection in severe oligoasthenozoospermiaDifferent probe combinations for assessment of postzygotic chromosomal imbalances in human embryos.Chromosomal Aneuploidies and Early Embryonic Developmental ArrestLive births resulting from 0PN-derived embryos in conventional IVF cycles.Oogonial stem cells as a model to study age-associated infertility in women.Targeted disruption of Nrg1 in granulosa cells alters the temporal progression of oocyte maturationDiagnosis of human preimplantation embryo viability.An Overview on Prenatal Screening for Chromosomal Aberrations.Establishment, characterization, and differentiation of a karyotypically normal human embryonic stem cell line from a trisomy-affected embryo.Karyomapping and how is it improving preimplantation genetics?Challenges of Genetic Screening of In Vitro Fertilized Human Embryos Using Current Technologies.Maintenance of the inner cell mass in human blastocysts from fragmented embryos.Impact of sperm genome decay on Day-3 embryo chromosomal abnormalities from advanced-maternal-age patients.Potential of zygotes to produce live births can be identified by the size of the male and female pronuclei just before their membranes break down.High percentages of embryos with 21, 18 or 13 trisomy are related to advanced paternal age in donor egg cycles.Zygote score and status 1 or 2 days after cleavage and assisted reproduction outcome.Analysis of donor heterogeneity as a factor affecting the clinical outcome of oocyte donation.Good quality blastocyst from non-/mono-pronuclear zygote may be used for transfer during IVF.Abnormalities in centrosome number in human embryos and embryonic stem cells.
P2860
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P2860
description
1998 nî lūn-bûn
@nan
1998 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Chromosome abnormalities in human embryos.
@ast
Chromosome abnormalities in human embryos.
@en
Chromosome abnormalities in human embryos.
@nl
type
label
Chromosome abnormalities in human embryos.
@ast
Chromosome abnormalities in human embryos.
@en
Chromosome abnormalities in human embryos.
@nl
prefLabel
Chromosome abnormalities in human embryos.
@ast
Chromosome abnormalities in human embryos.
@en
Chromosome abnormalities in human embryos.
@nl
P356
P1476
Chromosome abnormalities in human embryos.
@en
P304
P356
10.1093/HUMUPD/4.6.842
P577
1998-11-01T00:00:00Z