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Cynthia Bartels

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Chemicals & Drugs

Genes & Molecular Sequences

Amino Acid Sequence

Concepts & Ideas

Physiology

Procedures

Polymerase Chain Reaction

Anatomy

CHO Cells

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Co-Publications
Name
28
Lockridge, Oksana
13
La Du, Bert
11
Masson, Patrick
8
Froment, Marie-Thérèse
7
Van Der Spek, Abraham
5
Schopfer, Lawrence
4
Arpagaus, Martine
3
Chatonnet, Arnaud
3
Xie, W
2
Ribes, Fabien
2
Ruddon, RW
2
Hajra, Amiya
2
Bedows, Elliott
2
Altamirano, CV
2
Miller-Lindholm, Amanda

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Publications

TOP 3
Schnetz Michael P; Bartels Cynthia F; Shastri Kuntal; Balasubramanian Dheepa; Zentner Gabriel E; Balaji Ravishankar; Zhang Xiaodong; Song Lingyun; Wang Zhenghe; Laframboise Thomas; Crawford Gregory E; Scacheri Peter C
Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns.
Schopfer Lawrence M; Voelker Troy; Bartels Cynthia F; Thompson Charles M; Lockridge Oksana
Reaction kinetics of biotinylated organophosphorus toxicant, FP-biotin, with human acetylcholinesterase and human butyrylcholinesterase.
Masson Patrick; Nachon Florian; Bartels Cynthia F; Froment Marie-Therese; Ribes Fabien; Matthews Cedric; Lockridge Oksana
High activity of human butyrylcholinesterase at low pH in the presence of excess butyrylthiocholine.

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Geonetwork of Cynthia Bartels (preview)

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All Publications

2009: Schnetz Michael P; Bartels Cynthia F; Shastri Kuntal; Balasubramanian Dheepa; Zentner Gabriel E; Balaji Ravishankar; Zhang Xiaodong; Song Lingyun; Wang Zhenghe; Laframboise Thomas; Crawford Gregory E; Scacheri Peter C
Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns.
Genome research 2009;19(4):590-601.
2005: Schopfer Lawrence M; Voelker Troy; Bartels Cynthia F; Thompson Charles M; Lockridge Oksana
Reaction kinetics of biotinylated organophosphorus toxicant, FP-biotin, with human acetylcholinesterase and human butyrylcholinesterase.
Chemical research in toxicology 2005;18(4):747-54.
2003: Masson Patrick; Nachon Florian; Bartels Cynthia F; Froment Marie-Therese; Ribes Fabien; Matthews Cedric; Lockridge Oksana
High activity of human butyrylcholinesterase at low pH in the presence of excess butyrylthiocholine.
European journal of biochemistry / FEBS 2003;270(2):315-24.
2002: Duysen Ellen G; Bartels Cynthia F; Lockridge Oksana
Wild-type and A328W mutant human butyrylcholinesterase tetramers expressed in Chinese hamster ovary cells have a 16-hour half-life in the circulation and protect mice from cocaine toxicity.
The Journal of pharmacology and experimental therapeutics 2002;302(2):751-8.
2002: Masson Patrick; Schopfer Lawrence M; Bartels Cynthia F; Froment Marie-Thérèse; Ribes Fabien; Nachon Florian; Lockridge Oksana
Substrate activation in acetylcholinesterase induced by low pH or mutation in the pi-cation subsite.
Biochimica et biophysica acta 2002;1594(2):313-24.
2001: Josse D; Lockridge O; Xie W; Bartels C F; Schopfer L M; Masson P
The active site of human paraoxonase (PON1).
Journal of applied toxicology : JAT 2001;21 Suppl 1():S7-11.
2000: Bartels C F; Xie W; Miller-Lindholm A K; Schopfer L M; Lockridge O
Determination of the DNA sequences of acetylcholinesterase and butyrylcholinesterase from cat and demonstration of the existence of both in cat plasma.
Biochemical pharmacology 2000;60(4):479-87.
2000: Altamirano C V; Bartels C F; Lockridge O
The butyrylcholinesterase K-variant shows similar cellular protein turnover and quaternary interaction to the wild-type enzyme.
Journal of neurochemistry 2000;74(2):869-77.
1999: Miller-Lindholm A K; Bedows E; Bartels C F; Ramey J; Maclin V; Ruddon R W
A naturally occurring genetic variant in the human chorionic gonadotropin-beta gene 5 is assembly inefficient.
Endocrinology 1999;140(8):3496-506.
1999: Xie W; Altamirano C V; Bartels C F; Speirs R J; Cashman J R; Lockridge O
An improved cocaine hydrolase: the A328Y mutant of human butyrylcholinesterase is 4-fold more efficient.
Molecular pharmacology 1999;55(1):83-91.
1998: Vanlinthout L E; Bartels C F; Lockridge O; Callens K; Booij L H
Prolonged paralysis after a test dose of mivacurium in a patient with atypical serum cholinesterase.
Anesthesia and analgesia 1998;87(5):1199-202.
1998: Masson P; Froment M T; Fortier P L; Visicchio J E; Bartels C F; Lockridge O
Butyrylcholinesterase-catalysed hydrolysis of aspirin, a negatively charged ester, and aspirin-related neutral esters.
Biochimica et biophysica acta 1998;1387(1-2):41-52.
1997: Masson P; Fortier P L; Albaret C; Froment M T; Bartels C F; Lockridge O
Aging of di-isopropyl-phosphorylated human butyrylcholinesterase.
The Biochemical journal 1997;327 ( Pt 2)():601-7.
1997: Masson P; Froment M T; Bartels C F; Lockridge O
Importance of aspartate-70 in organophosphate inhibition, oxime re-activation and aging of human butyrylcholinesterase.
The Biochemical journal 1997;325 ( Pt 1)():53-61.
1997: Masson P; Legrand P; Bartels C F; Froment M T; Schopfer L M; Lockridge O
Role of aspartate 70 and tryptophan 82 in binding of succinyldithiocholine to human butyrylcholinesterase.
Biochemistry 1997;36(8):2266-77.
1996: Masson P; Froment M T; Bartels C F; Lockridge O
Asp7O in the peripheral anionic site of human butyrylcholinesterase.
European journal of biochemistry / FEBS 1996;235(1-2):36-48.
1996: Primo-Parmo S L; Bartels C F; Wiersema B; van der Spek A F; Innis J W; La Du B N
Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene.
American journal of human genetics 1996;58(1):52-64.
1994: Jbilo O; Bartels C F; Chatonnet A; Toutant J P; Lockridge O
Tissue distribution of human acetylcholinesterase and butyrylcholinesterase messenger RNA.
Toxicon : official journal of the International Society on Toxinology 1994;32(11):1445-57.
1994: Kris M; Jbilo O; Bartels C F; Masson P; Rhode S; Lockridge O
Endogenous butyrylcholinesterase in SV40 transformed cell lines: COS-1, COS-7, MRC-5 SV40, and WI-38 VA13.
In vitro cellular & developmental biology. Animal 1994;30A(10):680-9.
1994: Masson P; Froment M T; Sorenson R C; Bartels C F; Lockridge O
Mutation His322Asn in human acetylcholinesterase does not alter electrophoretic and catalytic properties of the erythrocyte enzyme.
Blood 1994;83(10):3003-5.
1993: Bedows E; Huth J R; Suganuma N; Bartels C F; Boime I; Ruddon R W
Disulfide bond mutations affect the folding of the human chorionic gonadotropin-beta subunit in transfected Chinese hamster ovary cells.
The Journal of biological chemistry 1993;268(16):11655-62.
1993: Bartels C F; Zelinski T; Lockridge O
Mutation at codon 322 in the human acetylcholinesterase (ACHE) gene accounts for YT blood group polymorphism.
American journal of human genetics 1993;52(5):928-36.
1992: Nogueira C P; Bartels C F; McGuire M C; Adkins S; Lubrano T; Rubinstein H M; Lightstone H; Van der Spek A F; Lockridge O; La Du B N
Identification of two different point mutations associated with the fluoride-resistant phenotype for human butyrylcholinesterase.
American journal of human genetics 1992;51(4):821-8.
1992: Jensen F S; Bartels C F; La Du B N
Structural basis of the butyrylcholinesterase H-variant segregating in two Danish families.
Pharmacogenetics 1992;2(5):234-40.
1992: Bartels C F; Jensen F S; Lockridge O; van der Spek A F; Rubinstein H M; Lubrano T; La Du B N
DNA mutation associated with the human butyrylcholinesterase K-variant and its linkage to the atypical variant mutation and other polymorphic sites.
American journal of human genetics 1992;50(5):1086-103.
1992: Bartels C F; James K; La Du B N
DNA mutations associated with the human butyrylcholinesterase J-variant.
American journal of human genetics 1992;50(5):1104-14.
1991: Arpagaus M; Chatonnet A; Masson P; Newton M; Vaughan T A; Bartels C F; Nogueira C P; La Du B N; Lockridge O
Use of the polymerase chain reaction for homology probing of butyrylcholinesterase from several vertebrates.
The Journal of biological chemistry 1991;266(11):6966-74.
1991: La Du B N; Bartels C F; Nogueira C P; Arpagaus M; Lockridge O
Proposed nomenclature for human butyrylcholinesterase genetic variants identified by DNA sequencing.
Cellular and molecular neurobiology 1991;11(1):79-89.
1990: La Du B N; Bartels C F; Nogueira C P; Hajra A; Lightstone H; Van der Spek A; Lockridge O
Phenotypic and molecular biological analysis of human butyrylcholinesterase variants.
Clinical biochemistry 1990;23(5):423-31.
1990: Bartels C F; van der Spek A F; La Du B N
Two polymorphisms in the non-coding regions of the BCHE gene.
Nucleic acids research 1990;18(20):6171.
1990: Nogueira C P; McGuire M C; Graeser C; Bartels C F; Arpagaus M; Van der Spek A F; Lightstone H; Lockridge O; La Du B N
Identification of a frameshift mutation responsible for the silent phenotype of human serum cholinesterase, Gly 117 (GGT----GGAG).
American journal of human genetics 1990;46(5):934-42.
1990: Arpagaus M; Kott M; Vatsis K P; Bartels C F; La Du B N; Lockridge O
Structure of the gene for human butyrylcholinesterase. Evidence for a single copy.
Biochemistry 1990;29(1):124-31.
1989: McGuire M C; Nogueira C P; Bartels C F; Lightstone H; Hajra A; Van der Spek A F; Lockridge O; La Du B N
Identification of the structural mutation responsible for the dibucaine-resistant (atypical) variant form of human serum cholinesterase.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(3):953-7.
1987: McTiernan C; Adkins S; Chatonnet A; Vaughan T A; Bartels C F; Kott M; Rosenberry T L; La Du B N; Lockridge O
Brain cDNA clone for human cholinesterase.
Proceedings of the National Academy of Sciences of the United States of America 1987;84(19):6682-6.
1987: Lockridge O; Bartels C F; Vaughan T A; Wong C K; Norton S E; Johnson L L
Complete amino acid sequence of human serum cholinesterase.
The Journal of biological chemistry 1987;262(2):549-57.

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