Discovery of epigenetic biomarkers for the noninvasive diagnosis of fetal disease
Identifieur interne : 002817 ( Istex/Curation ); précédent : 002816; suivant : 002818Discovery of epigenetic biomarkers for the noninvasive diagnosis of fetal disease
Auteurs : Kimberly Bunce [États-Unis] ; Tianjiao Chu [États-Unis] ; Urvashi Surti [États-Unis] ; William Allen Hogge [États-Unis] ; David G. Peters [États-Unis]Source :
- Prenatal Diagnosis [ 0197-3851 ] ; 2012-06.
English descriptors
- KwdEn :
- Aneuploidy, Biomarkers, Chem, Chiu, Chorionic villus sampling, Chromosome, Clin, Clin chem, Cpgs, Differentially, Differentially methylated, Dmrs, Epigenetic, Epigenetic biomarker discovery, Epityper, Fetal, Fetal alleles, Fetal aneuploidy, Fetal trisomy, Genome, Gestational, Gestational weeks, Hypermethylated, Hypothetical protein, Isoform, John wiley sons, Leung, Locus, Mass spectrometry, Maternal, Maternal leukocytes, Maternal plasma, Methylated, Methylation, Microarray, Microarray analysis, Noninvasive, Noninvasive detection, Noninvasive diagnosis, Placental, Potential biomarkers, Prenatal, Prenatal diagnosis, Primer, Proteinase inhibitor, Selective recovery, Trisomy.
- Teeft :
- Aneuploidy, Biomarkers, Chem, Chiu, Chorionic villus sampling, Chromosome, Clin, Clin chem, Cpgs, Differentially, Differentially methylated, Dmrs, Epigenetic, Epigenetic biomarker discovery, Epityper, Fetal, Fetal alleles, Fetal aneuploidy, Fetal trisomy, Genome, Gestational, Gestational weeks, Hypermethylated, Hypothetical protein, Isoform, John wiley sons, Leung, Locus, Mass spectrometry, Maternal, Maternal leukocytes, Maternal plasma, Methylated, Methylation, Microarray, Microarray analysis, Noninvasive, Noninvasive detection, Noninvasive diagnosis, Placental, Potential biomarkers, Prenatal, Prenatal diagnosis, Primer, Proteinase inhibitor, Selective recovery, Trisomy.
Abstract
The primary goal of this study was to identify CpG sites in the human genome that are differentially methylated in DNA obtained from chorionic villus sampling (CVS) samples and gestational age‐matched maternal blood cell (MBC) samples.
Url:
DOI: 10.1002/pd.3853
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when="2012-06">2012-06</date></imprint><idno type="ISSN">0197-3851</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0197-3851</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aneuploidy</term><term>Biomarkers</term><term>Chem</term><term>Chiu</term><term>Chorionic villus sampling</term><term>Chromosome</term><term>Clin</term><term>Clin chem</term><term>Cpgs</term><term>Differentially</term><term>Differentially methylated</term><term>Dmrs</term><term>Epigenetic</term><term>Epigenetic biomarker discovery</term><term>Epityper</term><term>Fetal</term><term>Fetal alleles</term><term>Fetal aneuploidy</term><term>Fetal trisomy</term><term>Genome</term><term>Gestational</term><term>Gestational weeks</term><term>Hypermethylated</term><term>Hypothetical protein</term><term>Isoform</term><term>John wiley sons</term><term>Leung</term><term>Locus</term><term>Mass spectrometry</term><term>Maternal</term><term>Maternal leukocytes</term><term>Maternal plasma</term><term>Methylated</term><term>Methylation</term><term>Microarray</term><term>Microarray analysis</term><term>Noninvasive</term><term>Noninvasive detection</term><term>Noninvasive diagnosis</term><term>Placental</term><term>Potential biomarkers</term><term>Prenatal</term><term>Prenatal diagnosis</term><term>Primer</term><term>Proteinase inhibitor</term><term>Selective recovery</term><term>Trisomy</term></keywords><keywords scheme="Teeft" xml:lang="en"><term>Aneuploidy</term><term>Biomarkers</term><term>Chem</term><term>Chiu</term><term>Chorionic villus sampling</term><term>Chromosome</term><term>Clin</term><term>Clin chem</term><term>Cpgs</term><term>Differentially</term><term>Differentially methylated</term><term>Dmrs</term><term>Epigenetic</term><term>Epigenetic biomarker discovery</term><term>Epityper</term><term>Fetal</term><term>Fetal alleles</term><term>Fetal aneuploidy</term><term>Fetal trisomy</term><term>Genome</term><term>Gestational</term><term>Gestational weeks</term><term>Hypermethylated</term><term>Hypothetical protein</term><term>Isoform</term><term>John wiley sons</term><term>Leung</term><term>Locus</term><term>Mass spectrometry</term><term>Maternal</term><term>Maternal leukocytes</term><term>Maternal plasma</term><term>Methylated</term><term>Methylation</term><term>Microarray</term><term>Microarray analysis</term><term>Noninvasive</term><term>Noninvasive detection</term><term>Noninvasive diagnosis</term><term>Placental</term><term>Potential biomarkers</term><term>Prenatal</term><term>Prenatal diagnosis</term><term>Primer</term><term>Proteinase inhibitor</term><term>Selective recovery</term><term>Trisomy</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract">The primary goal of this study was to identify CpG sites in the human genome that are differentially methylated in DNA obtained from chorionic villus sampling (CVS) samples and gestational age‐matched maternal blood cell (MBC) samples.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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