Li Q, Li Z, Luo T, Shi H
Mol Biomed. 2022; 3(1):47.
PMID: 36539659
PMC: 9768098.
DOI: 10.1186/s43556-022-00110-2.
Gao X, Yang Z, Xu C, Yu Q, Wang M, Song J
Ann Transl Med. 2022; 10(6):274.
PMID: 35433966
PMC: 9011253.
DOI: 10.21037/atm-22-757.
Kotelevets L, Chastre E
Cancers (Basel). 2021; 13(17).
PMID: 34503076
PMC: 8428372.
DOI: 10.3390/cancers13174264.
Dameri M, Ferrando L, Cirmena G, Vernieri C, Pruneri G, Ballestrero A
Int J Mol Sci. 2021; 22(13).
PMID: 34281208
PMC: 8268401.
DOI: 10.3390/ijms22137154.
Buikhuisen J, Gomez Barila P, Torang A, Dekker D, de Jong J, Cameron K
Cancers (Basel). 2021; 13(4).
PMID: 33673003
PMC: 7918753.
DOI: 10.3390/cancers13040801.
Effect of Capivasertib in Patients With an AKT1 E17K-Mutated Tumor: NCI-MATCH Subprotocol EAY131-Y Nonrandomized Trial.
Kalinsky K, Hong F, McCourt C, Sachdev J, Mitchell E, Zwiebel J
JAMA Oncol. 2020; 7(2):271-278.
PMID: 33377972
PMC: 7774047.
DOI: 10.1001/jamaoncol.2020.6741.
Landscape analysis of adjacent gene rearrangements reveals BCL2L14-ETV6 gene fusions in more aggressive triple-negative breast cancer.
Lee S, Hu Y, Loo S, Tan Y, Bhargava R, Lewis M
Proc Natl Acad Sci U S A. 2020; 117(18):9912-9921.
PMID: 32321829
PMC: 7211963.
DOI: 10.1073/pnas.1921333117.
Distinct functions of AKT isoforms in breast cancer: a comprehensive review.
Hinz N, Jucker M
Cell Commun Signal. 2019; 17(1):154.
PMID: 31752925
PMC: 6873690.
DOI: 10.1186/s12964-019-0450-3.
Patient-Driven Discovery, Therapeutic Targeting, and Post-Clinical Validation of a Novel Fusion-Driven Cancer.
Slotkin E, Diolaiti D, Shukla N, Dela Cruz F, Clark J, Gundem G
Cancer Discov. 2019; 9(5):605-616.
PMID: 30877085
PMC: 6497560.
DOI: 10.1158/2159-8290.CD-18-0953.
MicroRNA-433 targets AKT3 and inhibits cell proliferation and viability in breast cancer.
Hu X, Wang J, He W, Zhao P, Ye C
Oncol Lett. 2018; 15(3):3998-4004.
PMID: 29556282
PMC: 5844142.
DOI: 10.3892/ol.2018.7803.
Triple-negative breast cancer: the importance of molecular and histologic subtyping, and recognition of low-grade variants.
Pareja F, Geyer F, Marchio C, Burke K, Weigelt B, Reis-Filho J
NPJ Breast Cancer. 2017; 2:16036.
PMID: 28721389
PMC: 5515338.
DOI: 10.1038/npjbcancer.2016.36.
Recurrent and pathological gene fusions in breast cancer: current advances in genomic discovery and clinical implications.
Veeraraghavan J, Ma J, Hu Y, Wang X
Breast Cancer Res Treat. 2016; 158(2):219-32.
PMID: 27372070
PMC: 4979600.
DOI: 10.1007/s10549-016-3876-y.
Cancer: hunting rare somatic mutations.
Marx V
Nat Methods. 2016; 13(4):295-9.
PMID: 27027586
DOI: 10.1038/nmeth.3803.
Emerging Role of Genomic Rearrangements in Breast Cancer: Applying Knowledge from Other Cancers.
Paratala B, Dolfi S, Khiabanian H, Rodriguez-Rodriguez L, Ganesan S, Hirshfield K
Biomark Cancer. 2016; 8(Supple 1):1-14.
PMID: 26917980
PMC: 4756769.
DOI: 10.4137/BIC.S34417.
Pugh et al. reply.
Pugh T, Banerji S, Meyerson M
Nature. 2015; 520(7547):E12-4.
PMID: 25877207
DOI: 10.1038/nature14266.