C F Bartels - JoVE Visualize

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Clinical Biochemistry|October 1, 1990

Phenotypic and molecular biological analysis of human butyrylcholinesterase variantsB N La Du, C F Bartels, C P Nogueira, et al.

American Journal of Human Genetics|January 1, 1996

Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) geneS L Primo-Parmo, C F Bartels, B Wiersema, et al.

American Journal of Human Genetics|May 1, 1992

DNA mutation associated with the human butyrylcholinesterase K-variant and its linkage to the atypical variant mutation and other polymorphic sitesC F Bartels, F S Jensen, O Lockridge, et al.

Proceedings of the National Academy of Sciences of the United States of America|October 1, 1987

Brain cDNA clone for human cholinesteraseC McTiernan, S Adkins, A Chatonnet, et al.

The Journal of Biological Chemistry|April 15, 1991

Use of the polymerase chain reaction for homology probing of butyrylcholinesterase from several vertebratesM Arpagaus, A Chatonnet, P Masson, et al.

Proceedings of the National Academy of Sciences of the United States of America|February 1, 1989

Identification of the structural mutation responsible for the dibucaine-resistant (atypical) variant form of human serum cholinesteraseM C McGuire, C P Nogueira, C F Bartels, et al.

American Journal of Human Genetics|May 1, 1990

Identification of a frameshift mutation responsible for the silent phenotype of human serum cholinesterase, Gly 117 (GGT----GGAG)C P Nogueira, M C McGuire, C Graeser, et al.

American Journal of Human Genetics|October 1, 1992

Identification of two different point mutations associated with the fluoride-resistant phenotype for human butyrylcholinesteraseC P Nogueira, C F Bartels, M C McGuire, et al.

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Showing results (21-30 of 28) with videos related to

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You have reached the last page of results.This site can display upto 28 results.

Clinical Biochemistry|October 1, 1990

Phenotypic and molecular biological analysis of human butyrylcholinesterase variantsB N La Du, C F Bartels, C P Nogueira, et al.

American Journal of Human Genetics|January 1, 1996

Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) geneS L Primo-Parmo, C F Bartels, B Wiersema, et al.

American Journal of Human Genetics|May 1, 1992

DNA mutation associated with the human butyrylcholinesterase K-variant and its linkage to the atypical variant mutation and other polymorphic sitesC F Bartels, F S Jensen, O Lockridge, et al.

Proceedings of the National Academy of Sciences of the United States of America|October 1, 1987

Brain cDNA clone for human cholinesteraseC McTiernan, S Adkins, A Chatonnet, et al.

The Journal of Biological Chemistry|April 15, 1991

Use of the polymerase chain reaction for homology probing of butyrylcholinesterase from several vertebratesM Arpagaus, A Chatonnet, P Masson, et al.

Proceedings of the National Academy of Sciences of the United States of America|February 1, 1989

Identification of the structural mutation responsible for the dibucaine-resistant (atypical) variant form of human serum cholinesteraseM C McGuire, C P Nogueira, C F Bartels, et al.

American Journal of Human Genetics|May 1, 1990

Identification of a frameshift mutation responsible for the silent phenotype of human serum cholinesterase, Gly 117 (GGT----GGAG)C P Nogueira, M C McGuire, C Graeser, et al.

American Journal of Human Genetics|October 1, 1992

Identification of two different point mutations associated with the fluoride-resistant phenotype for human butyrylcholinesteraseC P Nogueira, C F Bartels, M C McGuire, et al.

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