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Ming Qi, Ph.D.

Ming Qi, Ph.D.

About Me

Faculty Appointments

Adjunct Professor - Department of Pathology and Laboratory Medicine (SMD)

Credentials

Education

PhD | Univ of Pittsburgh. Molecular Biology. 1991

MS | China - Free-Standing Inst. Genetics. 1985

BS | China - Free-Standing Inst. Biology. 1982

Research

Molecular pathology of genetic diseases seeks to explain why a given genetic change should result in a particular clinical phenotype. With its rapid progress, the knowledge in the field not only forms the cutting edge of biomedical research, but at the same time it has immediate application to the d...
Molecular pathology of genetic diseases seeks to explain why a given genetic change should result in a particular clinical phenotype. With its rapid progress, the knowledge in the field not only forms the cutting edge of biomedical research, but at the same time it has immediate application to the diagnosis of more and more diseases, and has great potential for the management of those diseases. Clinical symptoms are often the end result of a long chain of causation and complicate genetic interaction. The goals of the research in this laboratory, collaborated with multiple laboratories inside and outside the University, are to developing new tests for molecular diagnosis, and identify new genes responsible for bone and cardiovascular genetic diseases. Approaches of gene functional cloning, positional candidate gene cloning, and gene knock-out/in have been used in these studies.

Publications

Journal Articles

Defective motor behavior and neural gene expression in RIIbeta-protein kinase A mutant mice.

Brandon EP, Logue SF, Adams MR, Qi M, Sullivan SP, Matsumoto AM, Dorsa DM, Wehner JM, McKnight GS, Idzerda RL

The Journal of neuroscience : the official journal of the Society for Neuroscience.. 1998 May 1518 (10):3639-49. Epub 1900 01 01.

Disruption of the m1 receptor gene ablates muscarinic receptor-dependent M current regulation and seizure activity in mice.

Hamilton SE, Loose MD, Qi M, Levey AI, Hille B, McKnight GS, Idzerda RL, Nathanson NM

Proceedings of the National Academy of Sciences of the United States of America.. 1997 November 2594 (24):13311-6. Epub 1900 01 01.

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1.

Li L, Krantz ID, Deng Y, Genin A, Banta AB, Collins CC, Qi M, Trask BJ, Kuo WL, Cochran J, Costa T, Pierpont ME, Rand EB, Piccoli DA, Hood L, Spinner NB

Nature genetics.. 1997 July 16 (3):243-51. Epub 1900 01 01.

Impaired hippocampal plasticity in mice lacking the Cbeta1 catalytic subunit of cAMP-dependent protein kinase.

Qi M, Zhuo M, Skålhegg BS, Brandon EP, Kandel ER, McKnight GS, Idzerda RL

Proceedings of the National Academy of Sciences of the United States of America.. 1996 February 2093 (4):1571-6. Epub 1900 01 01.