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Multiplex Gene Expression Profiling of In Vivo Isolated Circulating Tumor Cells in High-Risk Prostate Cancer Patients

Clinical chemistry (Baltimore, Md.), 2018-02, Vol.64 (2), p.297-306

2018

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Global preamplification simplifies targeted mRNA quantification

Scientific reports, 2017-03, Vol.7 (1), p.45219-45219, Article 45219

2017

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Bias in Whole Genome Amplification: Causes and Considerations

Methods in molecular biology (Clifton, N.J.), 2015-01, Vol.1347, p.15

2015

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Identification of Breast Cancer Stem Cell Related Genes Using Functional Cellular Assays Combined With Single-Cell RNA Sequencing in MDA-MB-231 Cells

Frontiers in genetics, 2019, Vol.10, p.500-500

2019

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Spatial tumour gene signature discriminates neoplastic from non-neoplastic compartments in colon cancer: unravelling predictive biomarkers for relapse

Journal of translational medicine, 2023-08, Vol.21 (1), p.528-528, Article 528

2023

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A Multi-Analyte Approach for Improved Sensitivity of Liquid Biopsies in Prostate Cancer

Cancers, 2020-08, Vol.12 (8), p.2247

2020

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Detection and Characterization of Circulating Tumor Cells by the CellSearch Approach

Methods in molecular biology (Clifton, N.J.), 2015-01, Vol.1347, p.263

2015

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In Vivo Detection of Circulating Tumor Cells in High-Risk Non-Metastatic Prostate Cancer Patients Undergoing Radiotherapy

Cancers, 2019-07, Vol.11 (7), p.933

2019

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Are morphological criteria sufficient for the identification of circulating tumor cells in renal cancer?

Journal of translational medicine, 2013-09, Vol.11 (1), p.214-214, Article 214

2013

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Resolving tumor heterogeneity: genes involved in chordoma cell development identified by low-template analysis of morphologically distinct cells

PloS one, 2014-02, Vol.9 (2), p.e87663

2014

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Extended ultrastructural characterization of chordoma cells: the link to new therapeutic options

PloS one, 2014-12, Vol.9 (12), p.e114251-e114251

2014

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Whole Genome Amplification in Genomic Analysis of Single Circulating Tumor Cells

Methods in molecular biology (Clifton, N.J.), 2015-01, Vol.1347, p.221

2015

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Whole Genome Amplification by Isothermal Multiple Strand Displacement Using Phi29 DNA Polymerase

Methods in molecular biology (Clifton, N.J.), 2015-01, Vol.1347, p.111

2015

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Using Multiplex PCR for Assessing the Quality of Whole Genome Amplified DNA

Methods in molecular biology (Clifton, N.J.), 2015-01, Vol.1347, p.119

2015

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Whole Genome Amplification of Labeled Viable Single Cells Suited for Array-Comparative Genomic Hybridization

Methods in molecular biology (Clifton, N.J.), 2015-01, Vol.1347, p.233

2015

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Construction of a DNA Library on Microbeads Using Whole Genome Amplification

Methods in molecular biology (Clifton, N.J.), 2015-01, Vol.1347, p.87

2015

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Using In Situ Padlock Probe Technology to Detect mRNA Splice Variants in Tumor Cells

Methods in molecular biology (Clifton, N.J.), 2020, Vol.2148, p.361

2020

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We All Are Multitudes: Microchimerism, Evolution and Health

Journal of reproductive immunology, 2023-09, Vol.159, p.104010, Article 104010

2023

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Verification of the genomic identity of candidate microchimeric cells

Chimerism, 2011-07, Vol.2 (3), p.63-64

2011

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Sample Preparation Methods Following CellSearch Approach Compatible of Single-Cell Whole-Genome Amplification: An Overview

Methods in molecular biology (Clifton, N.J.), 2015, Vol.1347, p.57

2015

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Principles of Whole-Genome Amplification

Methods in molecular biology (Clifton, N.J.), 2015, Vol.1347, p.1

2015

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Copy Number Variation Analysis by Array Analysis of Single Cells Following Whole Genome Amplification

Methods in molecular biology (Clifton, N.J.), 2015, Vol.1347, p.197

2015

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Laser Microdissection of FFPE Tissue Areas and Subsequent Whole Genome Amplification by Ampli1

Methods in molecular biology (Clifton, N.J.), 2015, Vol.1347, p.141

2015

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Transcriptomic Characterization of the Human Cell Cycle in Individual Unsynchronized Cells

Journal of molecular biology, 2017-12, Vol.429 (24), p.3909-3924

2017

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In Situ Detection and Quantification of AR-V7, AR-FL, PSA, and KRAS Point Mutations in Circulating Tumor Cells

Clinical chemistry (Baltimore, Md.), 2018-03, Vol.64 (3), p.536-546

2018

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Multiplex Gene Expression Profiling of In Vivo Isolated Circulating Tumor Cells in High-Risk Prostate Cancer Patients

Global preamplification simplifies targeted mRNA quantification

Bias in Whole Genome Amplification: Causes and Considerations

Identification of Breast Cancer Stem Cell Related Genes Using Functional Cellular Assays Combined With Single-Cell RNA Sequencing in MDA-MB-231 Cells

Spatial tumour gene signature discriminates neoplastic from non-neoplastic compartments in colon cancer: unravelling predictive biomarkers for relapse

A Multi-Analyte Approach for Improved Sensitivity of Liquid Biopsies in Prostate Cancer

Detection and Characterization of Circulating Tumor Cells by the CellSearch Approach

In Vivo Detection of Circulating Tumor Cells in High-Risk Non-Metastatic Prostate Cancer Patients Undergoing Radiotherapy

Are morphological criteria sufficient for the identification of circulating tumor cells in renal cancer?

Resolving tumor heterogeneity: genes involved in chordoma cell development identified by low-template analysis of morphologically distinct cells

Extended ultrastructural characterization of chordoma cells: the link to new therapeutic options

Whole Genome Amplification in Genomic Analysis of Single Circulating Tumor Cells

Whole Genome Amplification by Isothermal Multiple Strand Displacement Using Phi29 DNA Polymerase

Using Multiplex PCR for Assessing the Quality of Whole Genome Amplified DNA

Whole Genome Amplification of Labeled Viable Single Cells Suited for Array-Comparative Genomic Hybridization

Construction of a DNA Library on Microbeads Using Whole Genome Amplification

Using In Situ Padlock Probe Technology to Detect mRNA Splice Variants in Tumor Cells

We All Are Multitudes: Microchimerism, Evolution and Health

Verification of the genomic identity of candidate microchimeric cells

Sample Preparation Methods Following CellSearch Approach Compatible of Single-Cell Whole-Genome Amplification: An Overview

Principles of Whole-Genome Amplification

Copy Number Variation Analysis by Array Analysis of Single Cells Following Whole Genome Amplification

Laser Microdissection of FFPE Tissue Areas and Subsequent Whole Genome Amplification by Ampli1

Transcriptomic Characterization of the Human Cell Cycle in Individual Unsynchronized Cells

In Situ Detection and Quantification of AR-V7, AR-FL, PSA, and KRAS Point Mutations in Circulating Tumor Cells

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