We are testing a new system for linking grants to scientists.
The funding information displayed below comes from the
NIH Research Portfolio Online Reporting Tools and the
NSF Award Database.
The grant data on this page is limited to grants awarded in the United States and is thus partial. It can nonetheless be used to understand how funding patterns influence mentorship networks and vice-versa, which has deep implications on how research is done.
You can help! If you notice any innacuracies, please
sign in and mark grants as correct or incorrect matches.
Sign in to see low-probability grants and correct any errors in linkage between grants and researchers.
High-probability grants
According to our matching algorithm, Masaki Hayashi is the likely recipient of the following grants.
Years |
Recipients |
Code |
Title / Keywords |
Matching score |
1974 — 1987 |
Hayashi, Masaki |
N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
Template Activities of Intracellular Bacteriophage Dna @ University of California-San Diego |
1 |
1985 — 1992 |
Hayashi, Masaki |
R01Activity Code Description: To support a discrete, specified, circumscribed project to be performed by the named investigator(s) in an area representing his or her specific interest and competencies. |
Synthesis of Infectious Bacteriophage Particles @ University of California San Diego
The long-term objective of the proposed research is to elucidate the regulatory interactions of all the macromolecules involved in the virus assembly process. We have chosen the phi chi-174 system because physiology and genetics of the process of the phage assembly in vivo have been well characterized. We have set the following sequence as the most effective way to implement our research: (1) to establish a virus assembly pathway map that represents the processes occurring in the infected cells; (2) to develop an in vitro system that will mimic the in vivo situation and will synthesize biologically active viruses; (3) to identify all of the virus-coded proteins as well as the host-originated proteins that are needed for infectious virus synthesis and; (4) to elucidate the regulatory interactions of the macromolecules involved in the virus assembly processes. Based on a number of in vivo observations we are now able to propose a working hypothesis on the functions of most of the phage-coded genes. We have also developed an in vitro system which synthesizes infectious phage particles. The system is composed of purified phage coded proteins and uninfected host extract. These two systems will provide a complementary approach to each other in order to achieve the long-term objective. We hope that phi chi-174 system will provide a model system for the maturation processes of the other spherical viruses including animal and plant viruses.
|
1 |