TY - JOUR
T1 - Pheochromocytomas and Paragangliomas, Genetically Diverse and Minimalist, All at Once!
AU - Dahia, Patricia L.M.
N1 - Publisher Copyright:
© 2017 Elsevier Inc.
PY - 2017/2/13
Y1 - 2017/2/13
N2 - Pheochromocytomas and paragangliomas are infrequent, genetically heterogeneous neuroendocrine tumors. In this issue of Cancer Cell, Fishbein et al. report novel driver genes, pathogenic mechanisms, and markers of malignancy. Notably, the new findings support the long-held view that these tumors distinctively arise from a single driver event, either inherited or acquired.
AB - Pheochromocytomas and paragangliomas are infrequent, genetically heterogeneous neuroendocrine tumors. In this issue of Cancer Cell, Fishbein et al. report novel driver genes, pathogenic mechanisms, and markers of malignancy. Notably, the new findings support the long-held view that these tumors distinctively arise from a single driver event, either inherited or acquired.
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U2 - 10.1016/j.ccell.2017.01.009
DO - 10.1016/j.ccell.2017.01.009
M3 - Short survey
C2 - 28196587
AN - SCOPUS:85012905288
SN - 1535-6108
VL - 31
SP - 159
EP - 161
JO - Cancer Cell
JF - Cancer Cell
IS - 2
ER -