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Ann Lin
Ann Lin
PhD Candidate, Stanford University
Verified email at stanford.edu
Title
Cited by
Cited by
Year
Off-target toxicity is a common mechanism of action of cancer drugs undergoing clinical trials
A Lin, CJ Giuliano, A Palladino, KM John, C Abramowicz, ML Yuan, ...
Science translational medicine 11 (509), eaaw8412, 2019
5322019
CRISPR/Cas9 mutagenesis invalidates a putative cancer dependency targeted in on-going clinical trials
A Lin, CJ Giuliano, NM Sayles, JM Sheltzer
Elife 6, e24179, 2017
1352017
Generating Single Cell–Derived Knockout Clones in Mammalian Cells with CRISPR/Cas9
CJ Giuliano, A Lin, V Girish, JM Sheltzer
Current Protocols in Molecular Biology 128, 2019
1192019
MELK expression correlates with tumor mitotic activity but is not required for cancer growth
CJ Giuliano, A Lin, JC Smith, AC Palladino, JM Sheltzer
Elife 7, e32838, 2018
852018
3D cell culture models and organ‐on‐a‐chip: Meet separation science and mass spectrometry
A Lin, F Sved Skottvoll, S Rayner, S Pedersen‐Bjergaard, G Sullivan, ...
Electrophoresis 41 (1-2), 56-64, 2020
602020
Discovering and validating cancer genetic dependencies: approaches and pitfalls
A Lin, JM Sheltzer
Nature Reviews Genetics 21 (11), 671-682, 2020
482020
Off-target toxicity is a common mechanism of action of cancer drugs undergoing clinical trials. Sci. Transl. Med. 11: eaaw8412
A Lin, CJ Giuliano, A Palladino, KM John, C Abramowicz, ML Yuan, ...
162019
Abstract 2149A: CRISPR/Cas9 mutagenesis invalidates a genetic target of clinical trials in cancer
A Lin, C Giuliano, N Sayles, J Smith, J Sheltzer
Cancer Research 77 (13 Supplement), 2149A-2149A, 2017
2017
Identification and characterization of survival-associated genomic features across tumor types
J Smith, A Lin, C Giuliano, JM Sheltzer
Cancer Research 77 (13 Supplement), 390-390, 2017
2017
Combining CRISPR/Cas9 mutagenesis and a small-molecule inhibitor to probe the function of MELK in cancer
CJ Giuliano, A Lin, JC Smith, AC Palladino, JM Sheltzer
bioRxiv, 203984, 2017
2017
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