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Khue Nguyen

TitleProject Scientist
InstitutionUniversity of California San Diego
DepartmentPediatrics
Address200 W. Arbor Drive #8467
San Diego CA 92103
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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    1. Nguyen KV, Naviaux RK, Nyhan WL. Novel mutation in the human HPRT1 gene and the Lesch-Nyhan disease. Nucleosides Nucleotides Nucleic Acids. 2017 Nov 02; 36(11):704-711. PMID: 29185864.
      View in: PubMed
    2. Nguyen KV, Silva S, Troncoso M, Naviaux RK, Nyhan WL. Lesch-Nyhan disease in two families from Chiloé Island with mutations in the HPRT1 gene. Nucleosides Nucleotides Nucleic Acids. 2017 Jul 03; 36(7):452-462. PMID: 28524722.
      View in: PubMed
    3. Nguyen KV, Nyhan WL. Quantification of various APP-mRNA isoforms and epistasis in Lesch-Nyhan disease. Neurosci Lett. 2017 Mar 16; 643:52-58. PMID: 28192196.
      View in: PubMed
    4. Nguyen KV, Leydiker K, Wang R, Abdenur J, Nyhan WL. A neurodevelopmental disorder with a nonsense mutation in the Ox-2 antigen domain of the amyloid precursor protein (APP) gene. Nucleosides Nucleotides Nucleic Acids. 2017 May 04; 36(5):317-327. PMID: 28102781.
      View in: PubMed
    5. Nguyen KV, Naviaux RK, Nyhan WL. Human HPRT1 gene and the Lesch-Nyhan disease: Substitution of alanine for glycine and inversely in the HGprt enzyme protein. Nucleosides Nucleotides Nucleic Acids. 2017 Feb; 36(2):151-157. PMID: 28045594.
      View in: PubMed
    6. Nguyen KV, Nyhan WL. Mutation in the Human HPRT1 Gene and the Lesch-Nyhan Syndrome. Nucleosides Nucleotides Nucleic Acids. 2016 Aug 02; 35(8):426-33. PMID: 27379977.
      View in: PubMed
    7. Nguyen KV. Epigenetic Regulation in Amyloid Precursor Protein with Genomic Rearrangements and the Lesch-Nyhan Syndrome. Nucleosides Nucleotides Nucleic Acids. 2015; 34(10):674-90. PMID: 26398526.
      View in: PubMed
    8. Nguyen KV. The human ß-amyloid precursor protein: biomolecular and epigenetic aspects. Biomol Concepts. 2015 Mar; 6(1):11-32. PMID: 25719338.
      View in: PubMed
    9. Nguyen KV, Nyhan WL. Lesch-Nyhan Syndrome in a Family with a Deletion Followed by an Insertion within the HPRT1 Gene. Nucleosides Nucleotides Nucleic Acids. 2015; 34(6):442-7. PMID: 25965333.
      View in: PubMed
    10. Nguyen KV. Epigenetic regulation in amyloid precursor protein and the Lesch-Nyhan syndrome. Biochem Biophys Res Commun. 2014 Apr 18; 446(4):1091-5. PMID: 24680827.
      View in: PubMed
    11. Fu R, Ceballos-Picot I, Torres RJ, Larovere LE, Yamada Y, Nguyen KV, Hegde M, Visser JE, Schretlen DJ, Nyhan WL, Puig JG, O'Neill PJ, Jinnah HA. Genotype-phenotype correlations in neurogenetics: Lesch-Nyhan disease as a model disorder. Brain. 2014 May; 137(Pt 5):1282-303. PMID: 23975452; PMCID: PMC3999711.
    12. Nguyen KV, Nyhan WL. Identification of novel mutations in the human HPRT gene. Nucleosides Nucleotides Nucleic Acids. 2013; 32(3):155-60. PMID: 23473102.
      View in: PubMed
    13. Nguyen KV, Naviaux RK, Paik KK, Nyhan WL. Lesch-Nyhan syndrome: mRNA expression of HPRT in patients with enzyme proven deficiency of HPRT and normal HPRT coding region of the DNA. Mol Genet Metab. 2012 Aug; 106(4):498-501. PMID: 22766437.
      View in: PubMed
    14. Nguyen KV, Naviaux RK, Paik KK, Nakayama T, Nyhan WL. Lesch-Nyhan variant syndrome: real-time rt-PCR for mRNA quantification in variable presentation in three affected family members. Nucleosides Nucleotides Nucleic Acids. 2012; 31(8):616-29. PMID: 22908952.
      View in: PubMed
    15. Nguyen KV, Naviaux RK, Paik KK, Nyhan WL. Novel mutations in the human HPRT gene. Nucleosides Nucleotides Nucleic Acids. 2011 Jun; 30(6):440-5. PMID: 21780909.
      View in: PubMed
    16. Nguyen KV, Naviaux RK, Patra S, Barshop BA, Nyhan WL. Novel mutations in the human MCCA and MCCB gene causing methylcrotonylglycinuria. Mol Genet Metab. 2011 Feb; 102(2):218-21. PMID: 21071250.
      View in: PubMed
    17. Nguyen KV, Sharief FS, Chan SS, Copeland WC, Naviaux RK. Molecular diagnosis of Alpers syndrome. J Hepatol. 2006 Jul; 45(1):108-16. PMID: 16545482.
      View in: PubMed
    18. Naviaux RK, Nguyen KV. POLG mutations associated with Alpers syndrome and mitochondrial DNA depletion. Ann Neurol. 2005 Sep; 58(3):491. PMID: 16130100.
      View in: PubMed
    19. Naviaux RK, Nguyen KV. POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion. Ann Neurol. 2004 May; 55(5):706-12. PMID: 15122711.
      View in: PubMed
    20. Nguyen KV, Gendrault JL, Wolff CM. Poly-L-lysine dissolves fibrillar aggregation of the Alzheimer beta-amyloid peptide in vitro. Biochem Biophys Res Commun. 2002 Mar 08; 291(4):764-8. PMID: 11866430.
      View in: PubMed