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V C Bode

Showing results (21-30 of 27) with videos related to

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Journal of Molecular Biology|September 25, 1973
The lambda head-tail joining reaction: purification, properties and structure of biologically active heads and tailsD P Harrison, D T Brown, V C Bode
Genetics|October 1, 1973
The lambda F mutants belong to two cistronsC E Boklage, E C Wong, V C Bode
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1990
Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylaseJ D McDonald, V C Bode, W F Dove, et al.
Progress in Clinical and Biological Research|January 1, 1990
The use of N-ethyl-N-nitrosourea to produce mouse models for human phenylketonuria and hyperphenylalaninemiaJ D McDonald, V C Bode, W F Dove, et al.
Genetics|February 1, 1988
hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesisV C Bode, J D McDonald, J L Guenet, et al.
Journal of Neurochemistry|February 1, 1988
Biochemical defect of the hph-1 mouse mutant is a deficiency in GTP-cyclohydrolase activityJ D McDonald, R G Cotton, I Jennings, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 25, 2000
Effects of ENU dosage on mouse strainsM J Justice, D A Carpenter, J Favor, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Journal of Molecular Biology|September 25, 1973
The lambda head-tail joining reaction: purification, properties and structure of biologically active heads and tailsD P Harrison, D T Brown, V C Bode
Genetics|October 1, 1973
The lambda F mutants belong to two cistronsC E Boklage, E C Wong, V C Bode
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1990
Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylaseJ D McDonald, V C Bode, W F Dove, et al.
Progress in Clinical and Biological Research|January 1, 1990
The use of N-ethyl-N-nitrosourea to produce mouse models for human phenylketonuria and hyperphenylalaninemiaJ D McDonald, V C Bode, W F Dove, et al.
Genetics|February 1, 1988
hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesisV C Bode, J D McDonald, J L Guenet, et al.
Journal of Neurochemistry|February 1, 1988
Biochemical defect of the hph-1 mouse mutant is a deficiency in GTP-cyclohydrolase activityJ D McDonald, R G Cotton, I Jennings, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 25, 2000
Effects of ENU dosage on mouse strainsM J Justice, D A Carpenter, J Favor, et al.
Pageof 3