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Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
July 25, 2000
Enzyme-activity mutants in Mus musculus. I. Phenotypic description and genetic characterization of ethylnitrosourea-induced mutations
W Pretsch
Genetical Research
|
April 28, 1999
Glutathione reductase activity deficiency in homozygous Gr1a1Neu mice does not cause haemolytic anaemia
W Pretsch
Genetical Research
|
April 1, 1989
Eight independent Ldh-1 mutations of the mouse recovered in mutagenicity experiments: biochemical characteristics and chromosomal localization
W Pretsch
Biochemical Genetics
|
February 1, 1992
Characterization of two electrophoretic lactate dehydrogenase-A mutants in Mus musculus
S Merkle, W Pretsch
Comparative Biochemistry and Physiology. B, Comparative Biochemistry
|
March 1, 1992
A glucosephosphate isomerase (GPI) null mutation in Mus musculus: evidence that anaerobic glycolysis is the predominant energy delivering pathway in early post-implantation embryos
S Merkle, W Pretsch
Genetics
|
December 1, 1989
Characterization of triosephosphate isomerase mutants with reduced enzyme activity in Mus musculus
S Merkle, W Pretsch
Blood
|
January 1, 1993
Glucose-6-phosphate isomerase deficiency associated with nonspherocytic hemolytic anemia in the mouse: an animal model for the human disease
S Merkle, W Pretsch
Genetical Research
|
October 1, 1990
Genetic localization and phenotypic expression of X-linked cataract (Xcat) in Mus musculus
J Favor, W Pretsch
Biochemical Genetics
|
February 1, 1990
Glucose phosphate isomerase enzyme-activity mutants in Mus musculus: genetical and biochemical characterization
W Pretsch, S Merkle
Biochemical Genetics
|
June 1, 1984
An inherited variant of mouse sn-glycerol-3-phosphate dehydrogenase detected by isoelectric focusing: genetical and biochemical analyses
W Pretsch, D J Charles
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of 4
Search research articles
Search
Showing results (1-10 of 38) with videos related to
Sort By:
Page
of 4
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
July 25, 2000
Enzyme-activity mutants in Mus musculus. I. Phenotypic description and genetic characterization of ethylnitrosourea-induced mutations
W Pretsch
Genetical Research
|
April 28, 1999
Glutathione reductase activity deficiency in homozygous Gr1a1Neu mice does not cause haemolytic anaemia
W Pretsch
Genetical Research
|
April 1, 1989
Eight independent Ldh-1 mutations of the mouse recovered in mutagenicity experiments: biochemical characteristics and chromosomal localization
W Pretsch
Biochemical Genetics
|
February 1, 1992
Characterization of two electrophoretic lactate dehydrogenase-A mutants in Mus musculus
S Merkle, W Pretsch
Comparative Biochemistry and Physiology. B, Comparative Biochemistry
|
March 1, 1992
A glucosephosphate isomerase (GPI) null mutation in Mus musculus: evidence that anaerobic glycolysis is the predominant energy delivering pathway in early post-implantation embryos
S Merkle, W Pretsch
Genetics
|
December 1, 1989
Characterization of triosephosphate isomerase mutants with reduced enzyme activity in Mus musculus
S Merkle, W Pretsch
Blood
|
January 1, 1993
Glucose-6-phosphate isomerase deficiency associated with nonspherocytic hemolytic anemia in the mouse: an animal model for the human disease
S Merkle, W Pretsch
Genetical Research
|
October 1, 1990
Genetic localization and phenotypic expression of X-linked cataract (Xcat) in Mus musculus
J Favor, W Pretsch
Biochemical Genetics
|
February 1, 1990
Glucose phosphate isomerase enzyme-activity mutants in Mus musculus: genetical and biochemical characterization
W Pretsch, S Merkle
Biochemical Genetics
|
June 1, 1984
An inherited variant of mouse sn-glycerol-3-phosphate dehydrogenase detected by isoelectric focusing: genetical and biochemical analyses
W Pretsch, D J Charles
Page
of 4