|
Research Interests
The focus
of my research is to understand the contribution of synaptic morphological
plasticity to learning and memory. In the past few years, we have generated
transgenic mice in which catalytic activity of PAK, a critical regulator of
actin remodeling, is inhibited in the postnatal forebrain. Cortical neurons in
these mice exhibit abnormal synapse number and size, which correlates with
impaired cortical bidirectional plasticity and deficient long-term memory. Thus,
our results provide evidence for critical relationships between synaptic
morphology and bidirectional modifiability of synaptic strength in the cortex,
and consolidation of long-term memory.
Publications
| Title |
Journal |
Date |
Authors |
|
Altered
cortical synaptic morphology and impaired memory consolidation in
forebrain-specific dominant negative PAK transgenic mice |
Neuron
42:773-787 |
2004 |
Hayashi,
Mansuo Lu, Se-Young Choi, B. S.
Shankaranarayana Rao, Hae-Yoon Jung, Hey-Kyoung Lee, Dawei Zhang,
Sumantra Chattarji, Alfredo Kirkwood and Susumu Tonegawa |
|
Human
cytomegalovirus UL69 protein is required for efficient accumulation of
infected cells in the G1 phase of the cell cycle |
Proc. Natl. Acad. Sci. USA,
97:2692-2696 |
2000 |
Hayashi,
Mansuo Lu,
Catherine Blankenship and Thomas Shenk |
|
Human
cytomegalovirus UL69 protein induces cells to accumulate in the G1 phase
of the cell cycle |
J.
Virol.,73:676-683 |
1999 |
Lu,
Mansuo and Thomas
Shenk |
|
Human cytomegalovirus
infection inhibits cell cycle progression at multiple points, including
the transition from G1 to S. |
J.
Virol., 70:8850-8857 |
1996 |
Lu, Mansuo and Thomas Shenk |
Scholastic Achievements
| Dates |
School |
Degree |
Concentration |
2000-current |
Howard
Hughes Medical Institute |
postdoctoral
associate |
|
1998-current |
Massachusetts
Institute of Technology |
postdoctoral
fellow |
|
1993-1998 |
Princeton
University |
Ph.D |
Molecular
Biology |
| 1989-1993 |
Wuhan
University
|
B.S. |
Biochemistry |
|