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From Split to Sibenik: the tortuous pathway in the cholinesterase field.

Taylor P.

Chem Biol Interact. 2010 Sep 6;187(1-3):3-9. doi: 10.1016/j.cbi.2010.05.005. Epub 2010 May 20.


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.

Am J Hum Genet. 1996 Jan;58(1):52-64.


A comprehensive list of cloned human DNA sequences.

Schmidtke J, Cooper DN.

Nucleic Acids Res. 1988;16 Suppl:r403-80.


Complex alternative splicing of acetylcholinesterase transcripts in Torpedo electric organ; primary structure of the precursor of the glycolipid-anchored dimeric form.

Sikorav JL, Duval N, Anselmet A, Bon S, Krejci E, Legay C, Osterlund M, Reimund B, Massoulié J.

EMBO J. 1988 Oct;7(10):2983-93.


Identification of the structural mutation responsible for the dibucaine-resistant (atypical) variant form of human serum cholinesterase.

McGuire MC, Nogueira CP, Bartels CF, Lightstone H, Hajra A, Van der Spek AF, Lockridge O, La Du BN.

Proc Natl Acad Sci U S A. 1989 Feb;86(3):953-7.


Comparison of butyrylcholinesterase and acetylcholinesterase.

Chatonnet A, Lockridge O.

Biochem J. 1989 Jun 15;260(3):625-34. Review. No abstract available.


Acetylcholinesterase and butyrylcholinesterase genes coamplify in primary ovarian carcinomas.

Zakut H, Ehrlich G, Ayalon A, Prody CA, Malinger G, Seidman S, Ginzberg D, Kehlenbach R, Soreq H.

J Clin Invest. 1990 Sep;86(3):900-8.


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.

Am J Hum Genet. 1990 May;46(5):934-42.


Membrane-enclosed crystals in Dictyostelium discoideum cells, consisting of developmentally regulated proteins with sequence similarities to known esterases.

Bomblies L, Biegelmann E, Döring V, Gerisch G, Krafft-Czepa H, Noegel AA, Schleicher M, Humbel BM.

J Cell Biol. 1990 Mar;110(3):669-79.


Molecular cloning and construction of the coding region for human acetylcholinesterase reveals a G + C-rich attenuating structure.

Soreq H, Ben-Aziz R, Prody CA, Seidman S, Gnatt A, Neville L, Lieman-Hurwitz J, Lev-Lehman E, Ginzberg D, Lipidot-Lifson Y, et al.

Proc Natl Acad Sci U S A. 1990 Dec;87(24):9688-92.


Primary structure of a collagenic tail peptide of Torpedo acetylcholinesterase: co-expression with catalytic subunit induces the production of collagen-tailed forms in transfected cells.

Krejci E, Coussen F, Duval N, Chatel JM, Legay C, Puype M, Vandekerckhove J, Cartaud J, Bon S, Massoulié J.

EMBO J. 1991 May;10(5):1285-93.


Low nucleotide diversity in man.

Li WH, Sadler LA.

Genetics. 1991 Oct;129(2):513-23.


Inactivation of the cholinesterase gene by Alu insertion: possible mechanism for human gene transposition.

Muratani K, Hada T, Yamamoto Y, Kaneko T, Shigeto Y, Ohue T, Furuyama J, Higashino K.

Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11315-9.


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.

Am J Hum Genet. 1992 May;50(5):1086-103.


Identification of two different point mutations associated with the fluoride-resistant phenotype for human butyrylcholinesterase.

Nogueira CP, Bartels CF, McGuire MC, Adkins S, Lubrano T, Rubinstein HM, Lightstone H, Van der Spek AF, Lockridge O, La Du BN.

Am J Hum Genet. 1992 Oct;51(4):821-8.


Substrate inhibition of acetylcholinesterase: residues affecting signal transduction from the surface to the catalytic center.

Shafferman A, Velan B, Ordentlich A, Kronman C, Grosfeld H, Leitner M, Flashner Y, Cohen S, Barak D, Ariel N.

EMBO J. 1992 Oct;11(10):3561-8.

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