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Author Report for: Primo-Parmo SL

Contact information:

Primo-Parmo Sergio L
Departments of Genetics and Biochemistry., UFPR, Calxa Postal 19071, Curitiba-Parana 81504 (Deceased)
Phone : (55) 41266 3633/255
Fax :

    Title: Characterization of a soluble mouse liver enzyme capable of hydrolyzing diisopropyl phosphorofluoridate
    Billecke SS, Primo-Parmo SL, Dunlop CS, Doorn JA, La Du BN, Broomfield CA
    Ref: Chemico-Biological Interactions, 119-120:251, 1999 : PubMed


    Title: Paraoxonase inhibits high-density lipoprotein oxidation and preserves its functions. A possible peroxidative role for paraoxonase
    Aviram M, Rosenblat M, Bisgaier CL, Newton RS, Primo-Parmo SL, La Du BN
    Ref: J Clinical Investigation, 101:1581, 1998 : PubMed


    Title: Characterization of an unstable variant (BChE115D) of human butyrylcholinesterase
    Primo-Parmo SL, Lightstone H, La Du BN
    Ref: Pharmacogenetics, 7:27, 1997 : PubMed


    Title: Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene
    Primo-Parmo SL, Bartels CF, Wiersema B, van der Spek AF, Innis JW, La Du BN
    Ref: American Journal of Human Genetics, 58:52, 1996 : PubMed


    Title: The human serum paraoxonase/arylesterase gene (PON1) is one member of a multigene family
    Primo-Parmo SL, Sorenson RC, Teiber JF, La Du BN
    Ref: Genomics, 33:498, 1996 : PubMed


    Title: Prolonged response to succinylcholine: a new variant of plasma cholinesterase that is identified as normal by traditional phenotyping methods
    Greenberg CP, Primo-Parmo SL, Pantuck EJ, La Du BN
    Ref: Anesthesia & Analgesia, 81:419, 1995 : PubMed


    Title: Reconsideration of the catalytic center and mechanism of mammalian paraoxonase/arylesterase
    Sorenson RC, Primo-Parmo SL, Kuo CL, Adkins S, Lockridge O, La Du BN
    Ref: Proc Natl Acad Sci U S A, 92:7187, 1995 : PubMed


    Title: An improved method for butyrylcholinesterase phenotyping [published erratum appears in Biochem Genet 1994 Oct;32(9-10):379]
    Picheth G, Fadel-Picheth C, Primo-Parmo SL, Chautard-Freire-Maia EA, Vieira MM
    Ref: Biochemical Genetics, 32:83, 1994 : PubMed


    Title: [Identification of two different genetic mutation associated with silent phenotypes for human serum cholinesterase in Japanese]
    Hidaka K, Iuchi I, Yamasaki T, Ohhara M, Shoda T, Primo-Parmo SL, La Du BN
    Ref: Rinsho Byori, 40:535, 1992 : PubMed


    Title: Heterogeneity of the Silent Phenotype of Human Butyrylcholinesterase - Identification of Eight New Mutations
    Primo-Parmo SL, Bartels CF
    Ref: In Multidisciplinary approaches to cholinesterase functions - Proceedings of Fourth International Meeting on Cholinesterases, (Shafferman, A. and Velan, B., Eds) Plenum Press, New York:61, 1992 : PubMed


    Title: The C5 isozyme of serum cholinesterase and adult weight
    Chautard-Freire-Maia EA, Primo-Parmo SL, Picheth G, Lourenco MA, Vieira MM
    Ref: Hum Hered, 41:330, 1991 : PubMed


    Title: Frequencies of atypical serum cholinesterase among Caucasians and Negroes from southern Brazil
    Chautard-Freire-Maia EA, Primo-Parmo SL, Canever de Lourenco MA, Culpi L
    Ref: Hum Hered, 34:388, 1984 : PubMed


    Title: Absence of linkage between the serum cholinesterase (CHE1) and rhesus (RH) loci
    Primo-Parmo SL, Chautard-Freire-Maia EA
    Ref: Hum Genet, 60:284, 1982 : PubMed


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Mail to: Nicolas Lenfant, Thierry Hotelier, Yves Bourne, Pascale Marchot and Arnaud Chatonnet.
Please cite: Lenfant 2013 Nucleic.Acids.Res. or Marchot Chatonnet 2012 Prot.Pept Lett.
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