ResearcherKyoto UniversityActive in the last 2 years
Kazuto Nishio
Matched on ORCID iD 0000-0002-8275-0846; OpenAlex author ID A5004282323, A5112565205. Sources: OpenAlex.
Their work
- Papers
- 9 (first author 0, last author 4)
- Trials
- 0
- Grants
- 0
- Labs led
- 1
- Collaborators
- 36
2012: 1 paper · 2013: none · 2014: 1 paper · 2015: 2 papers · 2016: none · 2017: 1 paper · 2018: none · 2019: none · 2020: 1 paper · 2021: none · 2022: 1 paper · 2023: 1 paper · 2024: 1 paper
Papers 9
- ACA-28, an ERK MAPK Signaling Modulator, Exerts Anticancer Activity through ROS Induction in Melanoma and Pancreatic Cancer Cells. Co-author DOI 10.1155/2024/7683793↗
- Impact of Smad4 and p53 mutations on the prognosis of patients with pancreatic ductal adenocarcinoma undergoing chemotherapy. Co-author DOI 10.1007/s10147-023-02396-w↗
- ACAGT-007a, an ERK MAPK Signaling Modulator, in Combination with AKT Signaling Inhibition Induces Apoptosis in KRAS Mutant Pancreatic Cancer T3M4 and MIA-Pa-Ca… Co-author DOI 10.3390/cells11040702↗
- BRCA2 Reversion Mutation Identified by Liquid Biopsy After Durable Response to FOLFIRINOX in BRCA2-Associated Pancreatic Cancer. Co-author DOI 10.1097/mpa.0000000000001672↗
- Clinical significance of Akt2 in advanced pancreatic cancer treated with erlotinib. Last author DOI 10.3892/ijo.2017.3961↗
- Activin signal promotes cancer progression and is involved in cachexia in a subset of pancreatic cancer. Last author DOI 10.1016/j.canlet.2014.10.037↗
- Randomized phase II/III clinical trial of elpamotide for patients with advanced pancreatic cancer: PEGASUS-PC Study. Co-author DOI 10.1111/cas.12674↗
- Homozygous deletion of the activin A receptor, type IB gene is associated with an aggressive cancer phenotype in pancreatic cancer. Last author DOI 10.1186/1476-4598-13-126↗
- Plasma concentrations of angiogenesis-related molecules in patients with pancreatic cancer. Last author DOI 10.1093/jjco/hyr178↗
Closest collaborators
The 25 strongest of 36 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.
- Golam Iftakhar Khandakar · 2 shared papers, 2022–2024 · strength 0.37
- Paper ACA-28, an ERK MAPK Signaling Modulator, Exerts Anticancer Activity through ROS Induction in Melanoma and Pancreatic Ca… DOI 10.1155/2024/7683793↗
- Paper ACAGT-007a, an ERK MAPK Signaling Modulator, in Combination with AKT Signaling Inhibition Induces Apoptosis in KRAS Mut… DOI 10.3390/cells11040702↗
- Teruaki Takasaki · 2 shared papers, 2022–2024 · strength 0.37
- Paper ACA-28, an ERK MAPK Signaling Modulator, Exerts Anticancer Activity through ROS Induction in Melanoma and Pancreatic Ca… DOI 10.1155/2024/7683793↗
- Paper ACAGT-007a, an ERK MAPK Signaling Modulator, in Combination with AKT Signaling Inhibition Induces Apoptosis in KRAS Mut… DOI 10.3390/cells11040702↗
- Reiko Sugiura · 2 shared papers, 2022–2024 · strength 0.37
- Paper ACA-28, an ERK MAPK Signaling Modulator, Exerts Anticancer Activity through ROS Induction in Melanoma and Pancreatic Ca… DOI 10.1155/2024/7683793↗
- Paper ACAGT-007a, an ERK MAPK Signaling Modulator, in Combination with AKT Signaling Inhibition Induces Apoptosis in KRAS Mut… DOI 10.3390/cells11040702↗
- Masatoshi Kudo · 5 shared papers, 2012–2023 · strength 0.33
- Paper Impact of Smad4 and p53 mutations on the prognosis of patients with pancreatic ductal adenocarcinoma undergoing chemoth… DOI 10.1007/s10147-023-02396-w↗
- Paper Clinical significance of Akt2 in advanced pancreatic cancer treated with erlotinib. DOI 10.3892/ijo.2017.3961↗
- Paper Activin signal promotes cancer progression and is involved in cachexia in a subset of pancreatic cancer. DOI 10.1016/j.canlet.2014.10.037↗
- Ken Kamata · 2 shared papers, 2017–2023 · strength 0.22
- Hitoshi Okada · 1 shared paper, 2024 · strength 0.21
- Yosuke Togashi · 4 shared papers, 2014–2017 · strength 0.18
- Paper Clinical significance of Akt2 in advanced pancreatic cancer treated with erlotinib. DOI 10.3892/ijo.2017.3961↗
- Paper Activin signal promotes cancer progression and is involved in cachexia in a subset of pancreatic cancer. DOI 10.1016/j.canlet.2014.10.037↗
- Paper Randomized phase II/III clinical trial of elpamotide for patients with advanced pancreatic cancer: PEGASUS-PC Study. DOI 10.1111/cas.12674↗
- Masayuki Kitano · 4 shared papers, 2012–2017 · strength 0.17
- Paper Clinical significance of Akt2 in advanced pancreatic cancer treated with erlotinib. DOI 10.3892/ijo.2017.3961↗
- Paper Activin signal promotes cancer progression and is involved in cachexia in a subset of pancreatic cancer. DOI 10.1016/j.canlet.2014.10.037↗
- Paper Homozygous deletion of the activin A receptor, type IB gene is associated with an aggressive cancer phenotype in pancre… DOI 10.1186/1476-4598-13-126↗
- Kosuke Minaga · 1 shared paper, 2023 · strength 0.16
- Yasuo Otsuka · 1 shared paper, 2023 · strength 0.16
- Mamoru Takenaka · 1 shared paper, 2023 · strength 0.16
- Hidekazu Tanaka · 1 shared paper, 2023 · strength 0.16
- Kentaro Yamao · 1 shared paper, 2023 · strength 0.16
- Tomohiro Kondo · 1 shared paper, 2020 · strength 0.10
- Manabu Muto · 1 shared paper, 2020 · strength 0.10
- Masashi Kanai · 1 shared paper, 2020 · strength 0.10
- Junichi Matsubara · 1 shared paper, 2020 · strength 0.10
- Hiroki Sakamoto · 2 shared papers, 2014–2015 · strength 0.08
- Paper Activin signal promotes cancer progression and is involved in cachexia in a subset of pancreatic cancer. DOI 10.1016/j.canlet.2014.10.037↗
- Paper Homozygous deletion of the activin A receptor, type IB gene is associated with an aggressive cancer phenotype in pancre… DOI 10.1186/1476-4598-13-126↗
- Eri Banno · 1 shared paper, 2017 · strength 0.06
- Akira Fukutomi · 1 shared paper, 2015 · strength 0.04
- Shinichi Ohkawa · 1 shared paper, 2015 · strength 0.04
- Nobumasa Mizuno · 1 shared paper, 2015 · strength 0.04
- Masayuki Furukawa · 1 shared paper, 2015 · strength 0.04
- Narikazu Boku · 1 shared paper, 2015 · strength 0.04
- Hiroshi Ishii · 1 shared paper, 2015 · strength 0.04
How to reach this person
A chain of introductions through people who have published, run trials or held grants together (warm_path@1: fewest links first, then the strongest). Built from public records only; no contact details are kept.