Loading...
Sign in to edit your profile (add interests, mentoring, photo, etc.)

    Khue Nguyen

    TitleProject Scientist
    SchoolUniversity of California, San Diego
    DepartmentPediatrics
    Address200 W. Arbor Drive #8467
    CA San Diego 92103
    vCardDownload vCard

      Collapse Bibliographic 
      Collapse Publications
      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.
      List All   |   Timeline
      1. Nguyen K, 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
      2. Nguyen K, Nyhan WL. Quantification of various APP-mRNA isoforms and epistasis in Lesch-Nyhan disease. Neurosci Lett. 2017 Feb 10; 643:52-58. PMID: 28192196.
        View in: PubMed
      3. Nguyen K, 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 Jan 19; 1-11. PMID: 28102781.
        View in: PubMed
      4. Nguyen K, 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 Jan 03; 1-7. PMID: 28045594.
        View in: PubMed
      5. Nguyen K, Nyhan WL. Mutation in the Human HPRT1 Gene and the Lesch-Nyhan Syndrome. Nucleosides Nucleotides Nucleic Acids. 2016 Aug 2; 35(8):426-33. PMID: 27379977.
        View in: PubMed
      6. Nguyen K. Epigenetic Regulation in Amyloid Precursor Protein with Genomic Rearrangements and the Lesch-Nyhan Syndrome. Nucleosides Nucleotides Nucleic Acids. 2015 Oct 3; 34(10):674-90. PMID: 26398526.
        View in: PubMed
      7. Nguyen K, Nyhan WL. Lesch-Nyhan Syndrome in a Family with a Deletion Followed by an Insertion within the HPRT1 Gene. Nucleosides Nucleotides Nucleic Acids. 2015 Jun 3; 34(6):442-7. PMID: 25965333.
        View in: PubMed
      8. Nguyen K. The human ß-amyloid precursor protein: biomolecular and epigenetic aspects. Biomol Concepts. 2015 Mar 1; 6(1):11-32. PMID: 25719338.
        View in: PubMed
      9. Nguyen K. 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
      10. Fu R, Ceballos-Picot I, Torres RJ, Larovere LE, Yamada Y, Nguyen K, 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.
        View in: PubMed
      11. Nguyen K, 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
      12. Nguyen K, 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
      13. Nguyen K, 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
      14. Nguyen K, 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
      15. Nguyen K, 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
      16. Nguyen K, 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
      17. Naviaux RK, Nguyen K. POLG mutations associated with Alpers syndrome and mitochondrial DNA depletion. Ann Neurol. 2005 Sep; 58(3):491. PMID: 16130100.
        View in: PubMed
      18. Naviaux RK, Nguyen K. POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion. Ann Neurol. 2004 May; 55(5):706-12. PMID: 15122711.
        View in: PubMed
      19. Nguyen K, Gendrault JL, Wolff CM. Poly-L-lysine dissolves fibrillar aggregation of the Alzheimer beta-amyloid peptide in vitro. Biochem Biophys Res Commun. 2002 Mar 8; 291(4):764-8. PMID: 11866430.
        View in: PubMed