A method of high-throughput functional evaluation of EGFR gene variants of unknown significance in cancer.
about
Implementation of "Clinical Sequencing" in Cancer Genome Medicine in Japan.Current and Future Molecular Testing in NSCLC, What Can We Expect from New Sequencing Technologies?Hemorrhage of a pancreatic metastasis from lung adenocarcinoma after osimertinib therapyThe effectiveness of afatinib and osimertinib in a Chinese patient with advanced lung adenocarcinoma harboring a rare triple EGFR mutation (R670W/H835L/L833V): a case report and literature reviewMultiplexed assays of variant effects contribute to a growing genotype-phenotype atlas
P2860
A method of high-throughput functional evaluation of EGFR gene variants of unknown significance in cancer.
description
2017 nî lūn-bûn
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2017年の論文
@ja
2017年学术文章
@wuu
2017年学术文章
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2017年学术文章
@zh-cn
2017年学术文章
@zh-hans
2017年学术文章
@zh-my
2017年学术文章
@zh-sg
2017年學術文章
@yue
2017年學術文章
@zh-hant
name
A method of high-throughput fu ...... nknown significance in cancer.
@en
A method of high-throughput fu ...... nknown significance in cancer.
@nl
type
label
A method of high-throughput fu ...... nknown significance in cancer.
@en
A method of high-throughput fu ...... nknown significance in cancer.
@nl
prefLabel
A method of high-throughput fu ...... nknown significance in cancer.
@en
A method of high-throughput fu ...... nknown significance in cancer.
@nl
P2093
P2860
P50
P1476
A method of high-throughput fu ...... unknown significance in cancer
@en
P2093
Fumiyuki Takahashi
Kazuhisa Takahashi
Kazuya Takamochi
Kenji Suzuki
Masaaki Nagano
Naoko Shimada
Takuo Hayashi
Yoshiyuki Suehara
P2860
P356
10.1126/SCITRANSLMED.AAN6566
P407
P577
2017-11-01T00:00:00Z