Khue Vu Nguyen
Eco Science Journals
Editor Name: Khue Vu Nguyen
Dsigneation: Full Project Scientist
Country: USA
University: University of California
Email: khuenguyen52@yahoo.com
BIOGRAPHY
Khue
Vu Nguyen (born in Ha Noi, Viet Nam) is currently Full Project Scientist in the
Departments of Medicine and Pediatrics, University of California, San Diego,
School of Medicine, San Diego, California, U.S.A. He has studied at University
Louis Pasteur, Strasbourg, France: B.S. in Biochemistry, M.S. in Molecular
Biology, Ph.D. in Macromolecular Physical Chemistry, Ph.D. in Physical Sciences
(Doctorat d’Etat es Sciences Physiques). He has worked as Scientist in
different French and U.S. Research Institutions and Companies. He
is
author and co-author of numerous publications and holder of many patents. He is
listed in Who’s Who in the World, Who’s Who in America, etc. He is member of
different academic organizations such as American Society for Microbiology,
American Chemical Society. He is invited reviewer of different scientific
journals such as Molecular Genetics and Metabolism, AGE: Journal of the
American Aging Association. He is also editorial board member of different
scientific journals such as International Journal of Medicine and Molecular
Medicine, Open Journal of Endocrine and Metabolic Diseases. He is Scientist
Reviewer for grant proposals of the Metabolic Disease Two (MB-2) of the Peer
Review Medical Research Program (PRMRP) for the U.S. Department of Defense
Congressionally Directed Medical Research Programs (CDMRP).
RESEARCH INTEREST: Genetic diseases,
Neurodevelopmental and Neurodegenerative disorders, and cancer
PUBLICATION:
1. K.V. NGUYEN, R.K.
NAVIAUX and W.L. NYHAN Human HPRT1 gene and the Lesch-Nyhan disease:
substitution of alanine for glycine and inversely in the HGprt enzyme protein.
Nucleosides, Nucleotides and Nucleic Acids, 36, 151-157 (2017).
2. K.V. NGUYEN and W.L.
NYHAN Quantification of various APP-mRNA isoforms and epistasis in Lesch-Nyhan
disease. Neuroscience Letters, 643, 52-58 (2017).
3. K.V. NGUYEN, K.
LEYDIKER, R. WANG, J. ABDENUR and W.L. NYHAN A neurodevelopmental disorder with
a nonsense mutation in the Ox-2 antigen domain of the amyloid precursor protein
(APP) gene. Nucleosides, Nucleotides and Nucleic Acids, 36, 317-327 (2017).
4. K.V. NGUYEN, S. SILVA,
M. TRONCOSO, R.K. NAVIAUX and W.L. NYHAN Lesch-Nyhan disease in two families
from Chiloe Island with mutations in the HPRT1 gene. Nucleosides, Nucleotides
and Nucleic Acids, 36, 452-462 (2017).
5. K.V. NGUYEN Epigenetics
in rare diseases. Journal of Rare Disorders: Diagnosis & Therapy, 3:1
(2017).
6. K.V. NGUYEN, R.K.
NAVIAUX and W.L. NYHAN Novel mutation in the human HPRT1 gene and the
Lesch-Nyhan disease. Nucleosides, Nucleotides and Nucleic Acids, 36, 704-711
(2017).
7. K.V. NGUYEN Alzheimer’s
disease. AIMS Neuroscience, 5, 74-80 (2018).
8. K.V. NGUYEN Treatment of
genetic disease. OBM Genetics, 2, 1-15 (2018).
9. K.V. NGUYEN Lesch-Nyhan
Disease. Enliven: Pediatrics and Neonatal Biology, 5, 001 (2018).
10. K.V. NGUYEN, K. LI and
R.K. NAVIAUX Immobilization of firefly luciferase on the cell plasma membrane
as a quantitative biosensor for measurement of ATP in the pericellular space in
live mammalian cells. Journal of Biochemistry and Biotechnology, 2, 1-10
(2019).
11. K.V. NGUYEN Potential
epigenomic co-management in rare diseases and epigenetic therapy. Nucleodises,
Nucleotides and Nucleic Acids, 38, 752-780 (2019).
12. K.V. NGUYEN β-Amyloid
precursor protein (APP) and the human diseases. AIMS Neuroscience, 6, 273-281
(2019).
13. K.V. NGUYEN, R.K.
NAVIAUX and W.L. NYHAN Lesch-Nyhan Disease: I. Construction of expression
vectors for hypoxanthine-guanine phosphoribosyltransferase (HGprt) enzyme and
amyloid precursor protein (APP). Nucleosides, Nucleotides and Nucleic Acids,
39, 905-922 (2020).