Joomyeong Kim
Appearance
Joomyeong Kim | |
---|---|
Born | Joomyeong Kim |
Nationality | South Korean |
Education | LSU Medical Center at New Orleans, LA (Ph. D.) Seoul National University (M.S., B.S.) |
Alma mater | LSU Medical Center at New Orleans, LA (Ph. D., 1995) |
Scientific career | |
Fields | Epigenetics |
Institutions | Oak Ridge National Laboratory Lawrence Livermore National Laboratory Louisiana State University |
Joomyeong Kim is a Russell Thompson, Jr. Family Professor of Biology at Louisiana State University and the principal investigator of his own lab. His research interests include genomic imprinting and epigenetics.
Dr. Kim's laboratory has recently investigated imprinting regulatory mechanism and the functions of imprinted genes,[1] including researching the function of the AEBP2 and PEG3 genes,[2][3] the latter of which Kim's research has suggested plays a role in mammalian reproduction.[4]
Education
- Ph.D. Biochemistry and Molecular Biology, LSU Medical Center at New Orleans, LA (Advisor, Dr. Prescott L. Deininger)
- M.S. Microbiology, Seoul National University, Seoul, South Korea (Advisor, Dr. John Jeongbin Yim) (1988)
- B.S. Microbiology, Seoul National University, Seoul, South Korea (1986)
Personal life
Kim is married and has two children.[citation needed]
Selected publications
- J.D. Kim, H. Kim, E.B. Ekram, S.Y. Yu, C. Faulk, and J. Kim (2011). Rex1/Zfp42 as an epigenetic regulator for genomic imprinting. Hum. Mol. Genet. 20, 1353-1362.
- K. Kang, J. Kim, J.H. Chung and D. Lee (2011). Decoding the genome with an integrative analysis tool: Combinatorial CRM Decoder. Nucleic Acids Research (in press).
- H. Kim, K. Kang, M.B. Ekram, T.-Y. Roh, and J. Kim (2011). Aebp2 as an epigenetic regulator for neural crest cells. PLoS ONE.
- J. Kim, W.D. Frey, H. Hongzhi, H. Kim, M.B. Ekram, A. Bakshi, M. Faisal, B.P.U. Perera, A. Ye, R. Teruyama (2013). Peg3 Mutational Effects on Reproduction and Placenta-Specific Gene Families
References
- ^ "Joomyeong Kim".
- ^ Kim J, Ashworth L, Branscomb E, Stubbs L (August 1997). "The human homolog of a mouse-imprinted gene, PEG3, maps to a zinc finger gene-rich region of human chromosome 19q13.4". Genome Res. 7 (5): 532–40. doi:10.1101/gr.7.5.532. PMC 310658. PMID 9149948.
- ^ "Entrez Gene: PEG3 paternally expressed 3".
- ^ Kim J; Frey Wesley D.; He Hongzhi; Ekram Muhammed B.; Bakshi Arundhati; Faisal Mohammed; Perera Bambarendage P. U.; Ye An; Teruyama Ryoichi (December 31, 2013). "Peg3 Mutational Effects on Reproduction and Placenta-Specific Gene Families". Retrieved May 22, 2014.
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External links