- 2022 - 2026 Establishment of on-site rapid diagnosis and risk analysis of cutaneous leishmaniasis
- 2020 - 2023 Why do certain regions and populations differ in transmission of the same species of human and non-human primate malaria parasites?
- 2017 - 2022 Toward an elucidation of transmission mechanisms and pathological conditions of leishmaniasis and Chagas disease
- 2017 - 2020 Why polymorphism and spread of resistance genes in drug-resistant Plasmodium falciparum occur in specific regions
- 2016 - 2019 Systematics and transmission ecology of novel liver flukes causing human illness in Ecuador
- 2015 - 2018 Confirmation of eradication and early detection of relapse of lymphatic filariasis by labor saving spatial distribution grasp system
- 2014 - 2018 Why malaria infections including non-human primate malaria infection occurred in specific group
- 2012 - 2015 Confirmation of the elimination of filariasis and early finding of its recurrence by habitant friendly urine diagnosis and vector mosquito investigation
- 2009 - 2011 Post-C. elegans nematode model~Large intestinal parasitism of Strongyloides ratti~
- 2008 - 2011 Problems and their solution in the final stage of the Global Program to Eliminate Lymphatic Filariasis
- 2006 - 2008 Infection of Strongyloides ratti in the large intestine as a survival strategy, and the role of autophagy
- 2005 - 2007 Research to Facilitate Elimination of Lymphatic Filariasis in Asia and Africa, and the Application of the Results
- 2007 - 糞線虫の生活史における遺伝子発現の変化と制御
- 2003 - 2005 Worm expulsion and large intestine parasitism of Strongyloides ratti as the survival strategy
- 2002 - 2005 Basic and Operational Researches for The Global Elimination of Lymphatic Filariasis
- 2003 - 寄生虫診断法の開発
- 1998 - 1999 プロテオグリカン、PG-Mが示す抗-細胞接着活性のシグナル伝達機構
Show all