Multiple mutation analyses in single tumor cells with improved whole genome amplification.
about
Laser capture microscopy.Genome-wide detection of single-nucleotide and copy-number variations of a single human cellAssessment of whole genome amplification-induced bias through high-throughput, massively parallel whole genome sequencingLaser capture microdissection: Big data from small samplesLarge fragment Bst DNA polymerase for whole genome amplification of DNA from formalin-fixed paraffin-embedded tissuesNon-invasive prenatal detection of trisomy 21 using tandem single nucleotide polymorphismsLaser-assisted microdissection: applications in molecular pathology.Technical advance: single pollen typing combined with laser-mediated manipulation.Whole genome amplification of DNA from laser capture-microdissected tissue for high-throughput single nucleotide polymorphism and short tandem repeat genotypingSCOMP is superior to degenerated oligonucleotide primed-polymerase chain reaction for global amplification of minute amounts of DNA from microdissected archival tissue samples.New developments in the analysis of gene expression.Laser-assisted microdissection applied to frozen surgical pathologic specimens - methodological aspects on RT-PCR.Laser microdissection in translational and clinical research.18q loss of heterozygosity in microsatellite stable colorectal cancer is correlated with CpG island methylator phenotype-negative (CIMP-0) and inversely with CIMP-low and CIMP-high.Sample selection algorithm to improve quality of genotyping from plasma-derived DNA: to separate the wheat from the chaff.Detection of chromosomal structural alterations in single cells by SNP arrays: a systematic survey of amplification bias and optimized workflow.Automatic retrieval of single microchimeric cells and verification of identity by on-chip multiplex PCRDetection and clinical importance of micrometastatic disease.Latent membrane protein 1 deletion mutants accumulate in reed-sternberg cells of human immunodeficiency virus-related Hodgkin's lymphoma.Detection of SYT-SSX fusion transcripts in both epithelial and spindle cell areas of biphasic synovial sarcoma using laser capture microdissectionAlterations in p53 predict response to preoperative high dose chemotherapy in patients with gastric cancerComparison of multiple displacement amplification (MDA) and multiple annealing and looping-based amplification cycles (MALBAC) in single-cell sequencingNRAS mutations are rare in colorectal cancer.Characterization of whole genome amplified (WGA) DNA for use in genotyping assay development.The future is now: single-cell genomics of bacteria and archaeaCytokeratins and other sensitive markers for esophageal cancer and metastases.Whole genome amplification in preimplantation genetic diagnosisPhylogenetic fate mapping.Sequencing genomes from single cells by polymerase cloning.Variants in the HEPSIN gene are associated with prostate cancer in men of European origin.Most multifocal papillary thyroid carcinomas acquire genetic and morphotype diversity through subclonal evolution following the intra-glandular spread of the initial neoplastic clone.Methods of molecular analysis: mutation detection in solid tumours.Digital MDA for enumeration of total nucleic acid contamination.Plasmodium falciparum strains harboring dihydrofolate reductase with the I164L mutation are absent in Malawi and Zambia even under antifolate drug pressureWRN promoter methylation possibly connects mucinous differentiation, microsatellite instability and CpG island methylator phenotype in colorectal cancer.Bone marrow micrometastasis in breast cancer.Novel Degenerate PCR Method for Whole-Genome Amplification Applied to Peru Margin (ODP Leg 201) Subsurface SamplesMolecular analysis of microdissected tumors and preneoplastic intraductal lesions in pancreatic carcinomaCpG island methylator phenotype (CIMP) of colorectal cancer is best characterised by quantitative DNA methylation analysis and prospective cohort studiesFrequent genetic alterations in simple urothelial hyperplasias of the bladder in patients with papillary urothelial carcinoma.
P2860
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P2860
Multiple mutation analyses in single tumor cells with improved whole genome amplification.
description
1999 nî lūn-bûn
@nan
1999 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Multiple mutation analyses in ...... ed whole genome amplification.
@ast
Multiple mutation analyses in ...... ed whole genome amplification.
@en
type
label
Multiple mutation analyses in ...... ed whole genome amplification.
@ast
Multiple mutation analyses in ...... ed whole genome amplification.
@en
prefLabel
Multiple mutation analyses in ...... ed whole genome amplification.
@ast
Multiple mutation analyses in ...... ed whole genome amplification.
@en
P2093
P2860
P1476
Multiple mutation analyses in ...... ed whole genome amplification.
@en
P2093
A Hartmann
E Heinmöller
F Hofstädter
J Rüschoff
S Wallinger
W Dietmaier
P2860
P356
10.1016/S0002-9440(10)65254-6
P407
P577
1999-01-01T00:00:00Z