The cytogenetics of polar bodies: insights into female meiosis and the diagnosis of aneuploidy.

The cytogenetics of polar bodies: insights into female meiosis and the diagnosis of aneuploidy.

Εμφάνιση άλλων εκδόσεων (1)

Female meiosis is comprised by two cell divisions, meiosis I (MI) and II (MII) and two different stages at which the development of the oocyte is temporarily halted. In the case of MI, this pause can potentially last for four to five decades. This added layer of complexity distinguishes female gamet...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	Fragouli, E, Alfarawati, S, Goodall, N, Sánchez-García, J, Colls, P, Wells, D
Μορφή:	Journal article
Γλώσσα:	English
Έκδοση:	2011

Παρόμοια τεκμήρια

The cytogenetics of polar bodies: Insights into female meiosis and the diagnosis of aneuploidy
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Έκδοση: (2011)

Simultaneous assessment of aneuploidy, polymorphisms, and mitochondrial DNA content in human polar bodies and embryos with the use of a novel microarray platform.
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THE PROGRESS OF CHROMOSOME ABNORMALITIES FROM MEIOSIS TO THE BLASTOCYST STAGE
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First births after preimplantation genetic diagnosis of structural chromosome abnormalities using comparative genomic hybridization and microarray analysis.
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The origin and impact of embryonic aneuploidy
ανά: Fragouli, E, κ.ά.
Έκδοση: (2013)

The origin and impact of embryonic aneuploidy.
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The incidence and origin of segmental aneuploidy in human oocytes and preimplantation embryos
ανά: Babariya, D, κ.ά.
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Morphological and cytogenetic assessment of cleavage and blastocyst stage embryos.
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Cytogenetic analysis of human blastocysts with the use of FISH, CGH and aCGH: scientific data and technical evaluation
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Έκδοση: (2010)

ARE PATIENTS UNDERGOING PGD FOR CHROMOSOME REARRANGEMENTS AT INCREASED RISK OF ANEUPLOIDY AFFECTING CHROMOSOMES UNRELATED TO THEIR REARRANGEMENT (INTERCHROMOSOMAL EFFECT)?
ανά: Alfarawati, S, κ.ά.
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Comprehensive chromosome screening of polar bodies and blastocysts from couples experiencing repeated implantation failure.
ανά: Fragouli, E, κ.ά.
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Cytogenetic analysis of human blastocysts with the use of FISH, CGH and aCGH: scientific data and technical evaluation.
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Embryos of robertsonian translocation carriers exhibit a mitotic interchromosomal effect that enhances genetic instability during early development
ανά: Alfarawati, S, κ.ά.
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Aneuploidy in the human blastocyst.
ανά: Fragouli, E, κ.ά.
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Aneuploidy screening for embryo selection.
ανά: Fragouli, E, κ.ά.
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Segmental chromosome imbalance in human oocytes and preimplantation embryos: incidence, origin and clinical relevance
ανά: Wells, D, κ.ά.
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Embryos of robertsonian translocation carriers exhibit a mitotic interchromosomal effect that enhances genetic instability during early development.
ανά: Samer Alfarawati, κ.ά.
Έκδοση: (2012-01-01)

Correction: Embryos of Robertsonian Translocation Carriers Exhibit a Mitotic Interchromosomal Effect That Enhances Genetic Instability during Early Development.
ανά: Samer Alfarawati, κ.ά.
Έκδοση: (2022-08-01)

Correction: Embryos of Robertsonian Translocation Carriers Exhibit a Mitotic Interchromosomal Effect That Enhances Genetic Instability during Early Development
ανά: Samer Alfarawati, κ.ά.
Έκδοση: (2022-08-01)

Altered levels of mitochondrial DNA are associated with female age, aneuploidy, and provide an independent measure of embryonic implantation potential.
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Έκδοση: (2015-06-01)

A NOVEL TOOL ALLOWS SIMULTANEOUS GENOMIC AND CYTOGENETIC ASSESSMENT OF OOCYTES AND EMBRYOS AND YIELDS UNIQUE DATA OF SCIENTIFIC AND CLINICAL IMPORTANCE
ανά: Wells, D, κ.ά.
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Microarray-CGH for the assessment of aneuploidy in human polar bodies and oocytes.
ανά: Jaroudi, S, κ.ά.
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Current status and future prospects of noninvasive preimplantation genetic testing for aneuploidy
ανά: Fragouli, E, κ.ά.
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Comparative genomic hybridization of oocytes and first polar bodies from young donors.
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Application of Molecular Cytogenetic Technique for Rapid Prenatal Diagnosis of Aneuploidies in Iranian Population
ανά: Habib Nasiri, κ.ά.
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Causes and estimated incidences of sex-chromosome misdiagnosis in preimplantation genetic diagnosis of aneuploidy
ανά: Ravichandran, K, κ.ά.
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TRANCRIPTOMIC PROFILING OF CUMULUS CELLS FROM NORMAL AND ANEUPLOID OOCYTES: TOWARDS A NON-INVASIVE DIAGNOSIS OF MEIOTIC ANEUPLOIDY
ανά: Fragouli, E, κ.ά.
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Questions about the accuracy of polar body analysis for preimplantation genetic screening.
ανά: Fragouli, E, κ.ά.
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A skewed sex ratio following blastocyst culture is a consequence of embryo grading systems that prioritise male embryos for transfer.
ανά: Wells, D, κ.ά.
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Use of comprehensive chromosomal screening for embryo assessment: microarrays and CGH.
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Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation.
ανά: Wells, D, κ.ά.
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Alteration of gene expression in human cumulus cells as a potential indicator of oocyte aneuploidy.
ανά: Fragouli, E, κ.ά.
Έκδοση: (2012)

Polymorphisms in the MTHFR gene influence embryo viability and the incidence of aneuploidy
ανά: Enciso, M, κ.ά.
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Chromosome architecture and low cohesion bias acrocentric chromosomes towards aneuploidy during mammalian meiosis
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CHROMOSOME BREAKAGE IN OOCYTES AND EMBRYOS: ASSESSMENT OF FREQUENCY, ORIGIN AND CLINICAL RELEVANCE OF GENETIC INSTABILITY DURING PREIMPLANTATION DEVELOPMENT
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Follicle-specific predisposition to aneuploidy as revealed by transcriptomic analysis of cumulus cells
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The role of preimplantation genetic diagnosis in diagnosing embryo aneuploidy.
ανά: Munné, S, κ.ά.
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The relationship between blastocyst morphology, chromosomal abnormality, and embryo gender.
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Telomere length and aneuploidy: clinical and biological insights into human preimplantation embryos
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