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    Srinivasa Nalabolu

    TitleProgrammer Analyst 4
    SchoolUniversity of California, San Diego
    Address9500 Gilman Drive #0217
    CA La Jolla 92093
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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. Geisheker MR, Heymann G, Wang T, Coe BP, Turner TN, Stessman HAF, Hoekzema K, Kvarnung M, Shaw M, Friend K, Liebelt J, Barnett C, Thompson EM, Haan E, Guo H, Anderlid BM, Nordgren A, Lindstrand A, Vandeweyer G, Alberti A, Avola E, Vinci M, Giusto S, Pramparo T, Pierce K, Nalabolu S, Michaelson JJ, Sedlacek Z, Santen GWE, Peeters H, Hakonarson H, Courchesne E, Romano C, Kooy RF, Bernier RA, Nordenskjöld M, Gecz J, Xia K, Zweifel LS, Eichler EE. Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains. Nat Neurosci. 2017 Aug; 20(8):1043-1051. PMID: 28628100.
        View in: PubMed
      2. Stessman HA, Xiong B, Coe BP, Wang T, Hoekzema K, Fenckova M, Kvarnung M, Gerdts J, Trinh S, Cosemans N, Vives L, Lin J, Turner TN, Santen G, Ruivenkamp C, Kriek M, van Haeringen A, Aten E, Friend K, Liebelt J, Barnett C, Haan E, Shaw M, Gecz J, Anderlid BM, Nordgren A, Lindstrand A, Schwartz C, Kooy RF, Vandeweyer G, Helsmoortel C, Romano C, Alberti A, Vinci M, Avola E, Giusto S, Courchesne E, Pramparo T, Pierce K, Nalabolu S, Amaral DG, Scheffer IE, Delatycki MB, Lockhart PJ, Hormozdiari F, Harich B, Castells-Nobau A, Xia K, Peeters H, Nordenskjöld M, Schenck A, Bernier RA, Eichler EE. Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. Nat Genet. 2017 Feb 13. PMID: 28191889.
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      3. Tai CH, Yoon MY, Kim SK, Rege VD, Nalabolu S, Kredich NM, Schnackerz KD, Cook PF. Cysteine 42 is important for maintaining an integral active site for O-acetylserine sulfhydrylase resulting in the stabilization of the alpha-aminoacrylate intermediate. Biochemistry. 1998 Jul 28; 37(30):10597-604. PMID: 9692949.
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      4. Xiao S, Nalabolu S, Aster JC, Ma J, Abruzzo L, Jaffe ES, Stone R, Weissman SM, Hudson TJ, Fletcher JA. FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome. Nat Genet. 1998 Jan; 18(1):84-7. PMID: 9425908.
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      5. Chooback L, Karsten WE, Kulkarni G, Nalabolu S, Harris BG, Cook PF. Expression, purification, and characterization of the recombinant NAD-malic enzyme from Ascaris suum. Protein Expr Purif. 1997 Jun; 10(1):51-4. PMID: 9179290.
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      6. Gruen JR, Nalabolu S, Chu TW, Bowlus C, Fan WF, Goei VL, Wei H, Sivakamasundari R, Liu Y, Xu HX, Parimoo S, Nallur G, Ajioka R, Shukla H, Bray-Ward P, Pan J, Weissman SM. A transcription map of the major histocompatibility complex (MHC) class I region. Genomics. 1996 Aug 15; 36(1):70-85. PMID: 8812418.
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      7. Nalabolu S, Shukla H, Nallur G, Parimoo S, Weissman SM. Genes in a 220-kb region spanning the TNF cluster in human MHC. Genomics. 1996 Jan 15; 31(2):215-22. PMID: 8824804.
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      8. Tai CH, Nalabolu S, Simmons JW, Jacobson TM, Cook PF. Acid-base chemical mechanism of O-acetylserine sulfhydrylases-A and -B from pH studies. Biochemistry. 1995 Sep 26; 34(38):12311-22. PMID: 7547974.
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      9. Tai CH, Nalabolu S, Jacobson TM, Minter DE, Cook PF. Kinetic mechanisms of the A and B isozymes of O-acetylserine sulfhydrylase from Salmonella typhimurium LT-2 using the natural and alternative reactants. Biochemistry. 1993 Jun 29; 32(25):6433-42. PMID: 8518286.
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      10. Nalabolu S, Tai CH, Schnackerz KD, Cook PF. Mechanism of O-acetylserine sulfhydrylase fromSalmonella typhimurium LT-2. Amino Acids. 1992 Feb; 2(1-2):119-25. PMID: 24194279.
        View in: PubMed
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