The use of FNA samples for whole-exome sequencing and detection of somatic mutations in breast cancer surgical specimens-Reference-Cited by-同舟云学术

The use of FNA samples for whole-exome sequencing and detection of somatic mutations in breast cancer surgical specimens

Published:2015-08-11 Issue:11 Volume:123 Page:669-677
ISSN:1934-662X
Container-title:Cancer Cytopathology
language:en
Short-container-title:Cancer Cytopathology

Author:

Lee Han-Byoel¹,Joung Je-Gun²,Kim Jisun³,Lee Kyung-Min⁴,Ryu Han Suk⁵,Lee Hae-Ock²,Moon Hyeong-Gon¹⁴,Park Woong-Yang²⁶,Noh Dong-Young¹⁴,Han Wonshik¹⁴

Affiliation:

1. Department of Surgery; Seoul National University College of Medicine; Seoul Republic of Korea

2. Samsung Genome Institute, Samsung Medical Center; Seoul Republic of Korea

3. Department of Surgery; Asan Medical Center; Seoul Republic of Korea

4. Cancer Research Institute, Seoul National University College of Medicine; Seoul Republic of Korea

5. Department of Pathology; Seoul National University College of Medicine; Seoul Republic of Korea

6. Department of Molecular Cell Biology; Sungkyunkwan University School of Medicine; Seoul Republic of Korea

Funder

National Research Foundation of Korea (NRF) grant funded by the Korean government (Ministry of Science, Information/Communication Technology, and Future Planning)

Publisher

Wiley

Subject

Cancer Research,Oncology

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4. Gene expression profiles obtained from fine-needle aspirations of breast cancer reliably identify routine prognostic markers and reveal large-scale molecular differences between estrogen-negative and estrogen-positive tumors;Pusztai;Clin Cancer Res,2003

5. Total RNA yield and microarray gene expression profiles from fine-needle aspiration biopsy and core-needle biopsy samples of breast carcinoma;Symmans;Cancer,2003

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