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Latest Documents Most Cited Documents Contributed Authors Related Sources Related Keywords

FDG uptake in PET is associated with the tumor microenvironment in metastatic lymph nodes and prognosis in N2 lung adenocarcinoma

2022 ◽  
Author(s):  
Kotaro Nomura ◽  
Tokiko Nakai ◽  
Yukino Nishina ◽  
Naoya Sakamoto ◽  
Tomohiro Miyoshi ◽  
...  
Keyword(s):  
Tumor Microenvironment ◽  
Lymph Nodes ◽  
Lung Adenocarcinoma ◽  
Metastatic Lymph Nodes ◽  
Fdg Uptake ◽  
Metastatic Lymph

scholarly journals Surgical volume threshold to improve 3‐year survival in designated cancer care hospitals in 2004–2012 in Japan

2022 ◽  
Author(s):  
Sumiyo Okawa ◽  
Takahiro Tabuchi ◽  
Kayo Nakata ◽  
Toshitaka Morishima ◽  
Shihoko Koyama ◽  
...  
Keyword(s):  
Cancer Care ◽  
Surgical Volume

scholarly journals Treatment patterns and survival in advanced unresectable esophageal squamous cell cancer: a population‐based study

2022 ◽  
Author(s):  
Marieke Pape ◽  
Pauline A.J. Vissers ◽  
Judith de Vos‐Geelen ◽  
Maarten C.C.M. Hulshof ◽  
Suzanne S. Gisbertz ◽  
...  
Keyword(s):  
Squamous Cell ◽  
Squamous Cell Cancer ◽  
Cell Cancer ◽  
Population Based ◽  
Treatment Patterns ◽  
Esophageal Squamous Cell Cancer ◽  
Population Based Study

scholarly journals C1QBP regulates T cells mitochondrial fitness to affect their survival, proliferation and anti‐tumor immune function

2022 ◽  
Author(s):  
Hui Tian ◽  
Gang Wang ◽  
Qiping Wang ◽  
Baofu Zhang ◽  
Guan Jiang ◽  
...  
Keyword(s):  
T Cells ◽  
Immune Function

scholarly journals In this Issue

2022 ◽  
Vol 113 (1) ◽  
pp. 5-6

scholarly journals CORRECTION

2022 ◽  
Vol 113 (1) ◽  
pp. 365-365

scholarly journals Issue Information

2022 ◽  
Vol 113 (1) ◽  
pp. 1-4

scholarly journals Oncogenic FGFR1 mutation and amplification in common cellular origin in a composite tumor with neuroblastoma and pheochromocytoma

2021 ◽  
Author(s):  
Keiji Tasaka ◽  
Hiroo Ueno ◽  
Kai Yamasaki ◽  
Takahiro Okuno ◽  
Tomoya Isobe ◽  
...  
Keyword(s):  
Cellular Origin ◽  
Composite Tumor ◽  
Fgfr1 Mutation
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