Pages that link to "Q30414714"
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The following pages link to Rate of spontaneous mutation at human loci encoding protein structure (Q30414714):
Displaying 27 items.
- ACP1GUA-1--a low-activity variant of human erythrocyte acid phosphatase: association with increased glutathione reductase activity (Q28367795) (← links)
- Characterization of triosephosphate isomerase mutants with reduced enzyme activity in Mus musculus (Q28586015) (← links)
- Failure to demonstrate mutations affecting protein structure or function in children with congenital defects or born prematurely (Q30413499) (← links)
- Mutation Rates for Enzyme and Morphological Loci in Barley ( HORDEUM VULGARE L.). (Q33950029) (← links)
- Biochemical and genetic identity of alpha-keto acid reductase and cytoplasmic malate dehydrogenase from human erythrocytes. (Q34164141) (← links)
- A "disproportion" between the frequency of rare electropmorphs and enzyme deficiency variants in Amerindians. (Q35199875) (← links)
- Origin of the triosephosphate isomerase isozymes in humans: genetic evidence for the expression of a single structural locus (Q35201703) (← links)
- Is there a difference among human populations in the rate with which mutation produces electrophoretic variants? (Q35364844) (← links)
- Electrophoretically detected germinal mutations induced in the mouse by ethylnitrosourea (Q35365564) (← links)
- Frequency of enzyme deficiency variants in erythrocytes of newborn infants (Q35464456) (← links)
- Frequency of thermostability variants: estimation of total "rare" variant frequency in human populations (Q36369419) (← links)
- Assigning a probability for paternity in apparent cases of mutation (Q40625840) (← links)
- Separation of allelic variants by two-dimensional electrophoresis (Q40632347) (← links)
- Mutation-rate determinations based on electrophoretic analysis of laboratory mice (Q41470117) (← links)
- Frequency and distribution of rare electrophoretic mobility variants in a population of human newborns in Ann Arbor, Michigan (Q44191884) (← links)
- Cell proliferation-associated expression of a recently evolved isozyme of triosephosphate isomerase (Q44196064) (← links)
- Deleterious mutations as an evolutionary factor: 1. The advantage of recombination (Q56341012) (← links)
- Characterization of a series of electrophoretic and enzyme activity variants of human glucose-phosphate isomerase (Q69723143) (← links)
- Characterization of three electrophoretic variants of human erythrocyte triosephosphate isomerase found in Japanese (Q70042492) (← links)
- Studies of the purine analog associated modulation of human erythrocyte acid phosphatase activity (Q70077133) (← links)
- Characterization of two new electrophoretic variants of human triosephosphate isomerase: stability, kinetic, and immunological properties (Q70393069) (← links)
- Electrophoretic variants of blood proteins in Japanese. III. Triosephosphate isomerase (Q70673811) (← links)
- Characteristics of enzymes of erythrocytes from newborn infants and adults: Activity, thermostability, and electrophoretic profile as a function of cell age (Q70992596) (← links)
- Incidence of inherited enzyme activity variants in feral mouse populations (Q71319659) (← links)
- Molecular features and immunological properties of lactate dehydrogenase C4 isozymes from mouse and rat testes (Q72698350) (← links)
- Dominant visible and electrophoretically expressed mutations induced in male mice exposed to ethylene oxide by inhalation (Q93557610) (← links)
- Hereditary triose phosphate isomerase deficiency: seven new homozygous cases (Q93648045) (← links)