Â鶹AV

¡¾Academic Papers¡¿
?TALEN-mediated single-base-pair editing identification of an intergenic mutation upstream of BUB1B as causative of PCS ( MVA) syndrome, PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 111(4), 1461-1466, 20140128
?Xist expression from an Xist YAC transgene carried on the Mouse Y chromosome, Human molecular genetics, 5(4), 451-459, 19960401
?Genetic Mapping using Microcell-mediated chromosome transfer suggests a Locus for Nijmegen Breakage syndrome at Chromosome 8q21-24, American Journal of Human Genetics, 60(6), 1487, 19970401

¡¾·¡»å³Ü³¦²¹³Ù¾±´Ç²Ô¡¿
We give a lecture on human genetics to medical students, a lecture on integrated radiation medical science to postgraduate students, and a lecture to phoenix leading program students.

¡¾¸é±ð²õ±ð²¹°ù³¦³ó¡¿
The purpose of our research group is to identify underlying genes for rare genetic disorders and to elucidate their functions. Following research projects are being carried out.
£±£®Molecular mechanism of carcinogenesis due to chromosome instability.
£²£®Molecular and cellular basis of primary microcephaly.
£³£®Molecular and cellular basis of human ciliopathy.
£´£®Identification of genetic factors responsible for individual differences in radiosensitivity.