A method for accurate detection of genomic microdeletions using real-time quantitative PCR.
about
Prevalence and prognostic impact of allelic imbalances associated with leukemic transformation of Philadelphia chromosome-negative myeloproliferative neoplasmsEctopic KIT copy number variation underlies impaired migration of primordial germ cells associated with gonadal hypoplasia in cattle (Bos taurus)A novel technique for measuring variations in DNA copy-number: competitive genomic polymerase chain reaction.Large-scale copy number variants (CNVs): distribution in normal subjects and FISH/real-time qPCR analysis.Partial duplication of the PRLR and SPEF2 genes at the late feathering locus in chicken.Unambiguous molecular detections with multiple genetic approach for the complicated chromosome 22q11 deletion syndrome.Molecular allelokaryotyping of T-cell prolymphocytic leukemia cells with high density single nucleotide polymorphism arrays identifies novel common genomic lesions and acquired uniparental disomyAccurate, fast and cost-effective diagnostic test for monosomy 1p36 using real-time quantitative PCR.A teratocarcinoma-like human embryonic stem cell (hESC) line and four hESC lines reveal potentially oncogenic genomic changesReal-time relative qPCR without reference to control samples and estimation of run-specific PCR parameters from run-internal mini-standard curves.Analysis of protocadherin alpha gene enhancer polymorphism in bipolar disorder and schizophrenia.SNPs and real-time quantitative PCR method for constitutional allelic copy number determination, the VPREB1 marker case.Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome.Multiplexed quantitative real-time PCR to detect 22q11.2 deletion in patients with congenital heart disease.A case of 3q29 microdeletion syndrome involving oral cleft inherited from a nonaffected mosaic parent: molecular analysis and ethical implications.Integration of SNP and mRNA arrays with microRNA profiling reveals that MiR-370 is upregulated and targets NF1 in acute myeloid leukemia.Genotype-phenotype correlation in 22q11.2 deletion syndrome.Mapping the deletion endpoints in individuals with 22q11.2 deletion syndrome by droplet digital PCRSimple, rapid and inexpensive quantitative fluorescent PCR method for detection of microdeletion and microduplication syndromes.Large scale variation in DNA copy number in chicken breeds.Constitutive function of the Ikaros transcription factor in primary leukemia cells from pediatric newly diagnosed high-risk and relapsed B-precursor ALL patients.Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndromeComparison of Gene Expression in Human Embryonic Stem Cells, hESC-Derived Mesenchymal Stem Cells and Human Mesenchymal Stem Cells.Molecular characterization of the tumor-suppressive function of nischarin in breast cancer.Identification and Characterization of a Differentially Expressed Gene (07E12) in the Infective Larvae of the Parasitic Nematode Ascaris suum.A comprehensive analysis of common copy-number variations in the human genome.Real-time PCR machine system modeling and a systematic approach for the robust design of a real-time PCR-on-a-chip system.Older patients with normal karyotype acute myeloid leukemia have a higher rate of genomic changes compared to young patients as determined by SNP array analysisMALDI-TOF-MS Assay to Detect the Hemizygous 22q11.2 Deletion in DNA from Dried Blood Spots.A pyrosequencing-based assay for the rapid detection of the 22q11.2 deletion in DNA from buccal and dried blood spot samples.Histone methylation-mediated silencing of miR-139 enhances invasion of non-small-cell lung cancer.High-Resolution Genomic Profiling of Disseminated Tumor Cells in Prostate CancerCopy-number analysis of topoisomerase and thymidylate synthase genes in frozen and FFPE DNAs of colorectal cancers.Phenotypic and molecular evaluation of a chromosome 1q region with linkage and association to type 2 diabetes in humans.Evaluation of real-time quantitative PCR as a standard cytogenetic diagnostic tool for confirmation of microarray (aCGH) results and determination of inheritance.The DNMT1/PCNA/UHRF1 disruption induces tumorigenesis characterized by similar genetic and epigenetic signatures.Genome structural variation discovery and genotypingDisruption of the non-canonical WNT pathway in lung squamous cell carcinoma.Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations.Accurate quantification of chromosomal lesions via short tandem repeat analysis using minimal amounts of DNA
P2860
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P2860
A method for accurate detection of genomic microdeletions using real-time quantitative PCR.
description
2005 nî lūn-bûn
@nan
2005 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
A method for accurate detectio ...... ing real-time quantitative PCR
@nl
A method for accurate detectio ...... ng real-time quantitative PCR.
@ast
A method for accurate detectio ...... ng real-time quantitative PCR.
@en
type
label
A method for accurate detectio ...... ing real-time quantitative PCR
@nl
A method for accurate detectio ...... ng real-time quantitative PCR.
@ast
A method for accurate detectio ...... ng real-time quantitative PCR.
@en
prefLabel
A method for accurate detectio ...... ing real-time quantitative PCR
@nl
A method for accurate detectio ...... ng real-time quantitative PCR.
@ast
A method for accurate detectio ...... ng real-time quantitative PCR.
@en
P2093
P2860
P356
P1433
P1476
A method for accurate detectio ...... ng real-time quantitative PCR.
@en
P2093
Anne S Bassett
Eva W C Chow
Laura Moldovan
Rosanna Weksberg
Simon Hughes
P2860
P2888
P356
10.1186/1471-2164-6-180
P407
P577
2005-12-13T00:00:00Z
P5875
P6179
1027536776