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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1983 1
1985 1
1987 1
1990 4
1991 4
1992 3
1993 2
2020 0
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16 results
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Page 1
The human serum paraoxonase/arylesterase polymorphism.
Eckerson HW, Wyte CM, La Du BN. Eckerson HW, et al. Am J Hum Genet. 1983 Nov;35(6):1126-38. Am J Hum Genet. 1983. PMID: 6316781 Free PMC article.
Inhibition of human red blood cell N-acetyltransferase.
Voice RA, Manis M, Weber WW. Voice RA, et al. Drug Metab Dispos. 1993 Jan-Feb;21(1):181-3. Drug Metab Dispos. 1993. PMID: 8095216
DNA mutations associated with the human butyrylcholinesterase J-variant.
Bartels CF, James K, La Du BN. Bartels CF, et al. Am J Hum Genet. 1992 May;50(5):1104-14. Am J Hum Genet. 1992. PMID: 1349196 Free PMC article.
DNA mutation associated with the human butyrylcholinesterase K-variant and its linkage to the atypical variant mutation and other polymorphic sites.
Bartels CF, Jensen FS, Lockridge O, van der Spek AF, Rubinstein HM, Lubrano T, La Du BN. Bartels CF, et al. Am J Hum Genet. 1992 May;50(5):1086-103. Am J Hum Genet. 1992. PMID: 1570838 Free PMC article.
Identification of a frameshift mutation responsible for the silent phenotype of human serum cholinesterase, Gly 117 (GGT----GGAG).
Nogueira CP, McGuire MC, Graeser C, Bartels CF, Arpagaus M, Van der Spek AF, Lightstone H, Lockridge O, La Du BN. Nogueira CP, et al. Am J Hum Genet. 1990 May;46(5):934-42. Am J Hum Genet. 1990. PMID: 2339692 Free PMC article.
The cloned butyrylcholinesterase (BCHE) gene maps to a single chromosome site, 3q26.
Allderdice PW, Gardner HA, Galutira D, Lockridge O, LaDu BN, McAlpine PJ. Allderdice PW, et al. Genomics. 1991 Oct;11(2):452-4. doi: 10.1016/0888-7543(91)90154-7. Genomics. 1991. PMID: 1769657 Free article.
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