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Abstract 3115: A single institution experience with droplet digital polymerase chain reaction (dd-PCR) liquid biopsy (LB) for therapeutic decision in advanced solid tumors
Abstract 3115: A single institution experience with droplet digital polymerase chain reaction (dd-PCR) liquid biopsy (LB) for therapeutic decision in advanced solid tumors
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Abstract 3115: A single institution experience with droplet digital polymerase chain reaction (dd-PCR) liquid biopsy (LB) for therapeutic decision in advanced solid tumors

Murad, Andre Marcio ; Casali-da-Rocha, José Claudio ; Carneiro, Juliana Garcia

Cancer research (Chicago, Ill.), 2020-08, Vol.80 (16_Supplement), p.3115-3115 [Periódico revisado por pares]

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Microfluidic-Based Multiplex qRT-PCR Identifies Diagnostic and Prognostic microRNA Signatures in the Sera of Prostate Cancer Patients
Microfluidic-Based Multiplex qRT-PCR Identifies Diagnostic and Prognostic microRNA Signatures in the Sera of Prostate Cancer Patients
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Microfluidic-Based Multiplex qRT-PCR Identifies Diagnostic and Prognostic microRNA Signatures in the Sera of Prostate Cancer Patients

MOLTZAHN, Felix ; OLSHEN, AdamB ; BAEHNER, Lauren ; PEEK, Andrew ; FONG, Lawrence ; STÖPPLER, Hubert ; SIMKO, Jeffry ; HILTON, Joan F ; CARROLL, Peter ; BLELLOCH, Robert

Cancer research (Chicago, Ill.), 2011-01, Vol.71 (2), p.550-560 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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Genetic heterogeneity of the epidermal growth factor receptor in non-small cell lung cancer cell lines revealed by a rapid and sensitive detection system, the peptide nucleic acid-locked nucleic acid PCR clamp
Genetic heterogeneity of the epidermal growth factor receptor in non-small cell lung cancer cell lines revealed by a rapid and sensitive detection system, the peptide nucleic acid-locked nucleic acid PCR clamp
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Genetic heterogeneity of the epidermal growth factor receptor in non-small cell lung cancer cell lines revealed by a rapid and sensitive detection system, the peptide nucleic acid-locked nucleic acid PCR clamp

NAGAI, Yoshiaki ; MIYAZAWA, Hitoshi ; HAGIWARA, Koichi ; HU QUN ; TANAKA, Tomoaki ; UDAGAWA, Kiyoshi ; KATO, Motoyasu ; FUKUYAMA, Shunichiro ; YOKOTE, Akemi ; KOBAYASHI, Kunihiko ; KANAZAWA, Minoru

Cancer research (Chicago, Ill.), 2005-08, Vol.65 (16), p.7276-7282 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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4
Normalization of real-time quantitative reverse transcription-PCR data: A model-based variance estimation approach to identify genes suited for normalization, applied to bladder and colon cancer data sets
Normalization of real-time quantitative reverse transcription-PCR data: A model-based variance estimation approach to identify genes suited for normalization, applied to bladder and colon cancer data sets
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Normalization of real-time quantitative reverse transcription-PCR data: A model-based variance estimation approach to identify genes suited for normalization, applied to bladder and colon cancer data sets

ANDERSEN, Claus Lindbjerg ; JENSEN, Jens Ledet ; ØRNTOFT, Torben Falck

Cancer research (Chicago, Ill.), 2004-08, Vol.64 (15), p.5245-5250 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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Quantitative multiplex methylation-specific PCR assay for the detection of promoter hypermethylation in multiple genes in breast cancer
Quantitative multiplex methylation-specific PCR assay for the detection of promoter hypermethylation in multiple genes in breast cancer
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Quantitative multiplex methylation-specific PCR assay for the detection of promoter hypermethylation in multiple genes in breast cancer

FACKLER, Mary Jo ; MCVEIGH, Megan ; MEHROTRA, Jyoti ; BLUM, Marissa A ; LANGE, Julie ; LAPIDES, Amanda ; GARRETT, Elizabeth ; ARGANI, Pedram ; SUKUMAR, Saraswati

Cancer research (Chicago, Ill.), 2004-07, Vol.64 (13), p.4442-4452 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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6
Abstract 49: Agreement of immunohistochemistry, fluorescence in situ hybridization, real-time quantitative polymerase-chain reaction, and quantitative reverse transcriptase PCR for Her-2/Neu status assessment in breast cancer patients: a single center, retrospective m
Abstract 49: Agreement of immunohistochemistry, fluorescence in situ hybridization, real-time quantitative polymerase-chain reaction, and quantitative reverse transcriptase PCR for Her-2/Neu status assessment in breast cancer patients: a single center, retrospective m
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Abstract 49: Agreement of immunohistochemistry, fluorescence in situ hybridization, real-time quantitative polymerase-chain reaction, and quantitative reverse transcriptase PCR for Her-2/Neu status assessment in breast cancer patients: a single center, retrospective m

Zoppoli, Gabriele ; Garuti, Anna ; Rocco, Ilaria ; Palermo, Claudia ; Cirmena, Gabriella ; Carminati, Enrico ; Friedman, Daniele ; Verdun di Cantogno, Ludovica ; Sapino, Anna ; Patrone, Franco ; Ballestrero, Alberto

Cancer research (Chicago, Ill.), 2013-04, Vol.73 (8_Supplement), p.49-49 [Periódico revisado por pares]

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7
P1-07-22: A Venezuelan Study of Breast Cancer Estrogen Receptor, Progesterone Receptor and HER2 Receptor Expression by the Standard Method, Immunohistochemistry (IHC), Compared to a New Method, Quantitative Reverse Transcription Polymerase Chain Reaction (RT-PCR)
P1-07-22: A Venezuelan Study of Breast Cancer Estrogen Receptor, Progesterone Receptor and HER2 Receptor Expression by the Standard Method, Immunohistochemistry (IHC), Compared to a New Method, Quantitative Reverse Transcription Polymerase Chain Reaction (RT-PCR)
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P1-07-22: A Venezuelan Study of Breast Cancer Estrogen Receptor, Progesterone Receptor and HER2 Receptor Expression by the Standard Method, Immunohistochemistry (IHC), Compared to a New Method, Quantitative Reverse Transcription Polymerase Chain Reaction (RT-PCR)

Marin, C-EM ; Ramirez, AC ; Baehner, FL ; Yoshizawa, C ; Acosta, MM

Cancer research (Chicago, Ill.), 2011-12, Vol.71 (24_Supplement), p.P1-P1-07-22 [Periódico revisado por pares]

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8
Development of a Multiplex Quantitative PCR Signature to Predict Progression in Non―Muscle-Invasive Bladder Cancer
Development of a Multiplex Quantitative PCR Signature to Predict Progression in Non―Muscle-Invasive Bladder Cancer
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Development of a Multiplex Quantitative PCR Signature to Predict Progression in Non―Muscle-Invasive Bladder Cancer

ROU WANG ; MORRIS, David S ; CHINNAIYAN, Arul M ; TOMLINS, Scott A ; LONIGRO, Robert J ; TSODIKOV, Alexander ; MEHRA, Rohit ; GIORDANO, Thomas J ; PRIYA KUNJU, L ; LEE, Cheryl T ; WEIZER, Alon Z

Cancer research (Chicago, Ill.), 2009-05, Vol.69 (9), p.3810-3818 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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9
Immunobead-PCR : a technique for the detection of circulating tumor cells using immunomagnetic beads and the polymerase chain reaction
Immunobead-PCR : a technique for the detection of circulating tumor cells using immunomagnetic beads and the polymerase chain reaction
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Immunobead-PCR : a technique for the detection of circulating tumor cells using immunomagnetic beads and the polymerase chain reaction

HARDINGHAM, J. E ; KOTASEK, D ; FARMER, B ; BUTLER, R. N ; JING-XIAN MI ; SAGE, R. E ; DOBROVIC, A

Cancer research (Chicago, Ill.), 1993-08, Vol.53 (15), p.3455-3458 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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10
Transcription profile of Kaposi's sarcoma-associated herpesvirus in primary kaposi's sarcoma lesions as determined by real-time PCR arrays
Transcription profile of Kaposi's sarcoma-associated herpesvirus in primary kaposi's sarcoma lesions as determined by real-time PCR arrays
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Transcription profile of Kaposi's sarcoma-associated herpesvirus in primary kaposi's sarcoma lesions as determined by real-time PCR arrays

DITTMER, Dirk P

Cancer research (Chicago, Ill.), 2003-05, Vol.63 (9), p.2010-2015 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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