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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
51

Neural tube defects : pathogenesis and gene-teratogen interaction in the mouse

Dempsey, Ellen E. January 1981 (has links)
No description available.
52

Characterization of the renal and the bone phenotypes of the Npt2 knock out mouse

Hoag, Hannah M. January 1999 (has links)
No description available.
53

Effect of gamete of origin and gene dose in X-linked hypophosphatemic mice

Qiu, Zheng-qing January 1993 (has links)
No description available.
54

Functional characterization of the renal brush-border membrane Na+-Pi cotransporter in normal and X-linked HYP mice

Harvey, Natalie January 1991 (has links)
No description available.
55

Cell interactions in abnormal neural tube and neural crest cell development of splotch mice

Moase, Connie E. (Connie Evelyn) January 1991 (has links)
No description available.
56

Genetics and epigenetics of cortisone-induced cleft palate in the mouse

Vekemans, Michael John Jacques. January 1981 (has links)
No description available.
57

Expression of stem-loop binding protein during murine oogenesis and pre-implantation development

Champigny, Marc. January 1998 (has links)
No description available.
58

Isolation and characterization of a mouse renal sodium phosphate cotransporter gene and construction of a gene targeting knock-out vector

Hewson, A. Stacy (Allison Stacy) January 1996 (has links)
No description available.
59

Characterization of the neural cell adhesion molecule N-CAM in splotch mutant mouse embryos

Neale, Sondra-Ann January 1993 (has links)
No description available.
60

Genetic architecture of reproductive and growth traits in laboratory mice

Jamison, Margaret Godwin January 1976 (has links)
This investigation was undertaken to determine the relative importance of additive, dominance, epistatic, maternal and sex-linkage effects for reproduction and growth traits in mice. Two selected lines of mice, extremes in phenotype for gain from 21 to 42 days of age, were used in a triple test cross design. The high line had completed 24 generations of selection for increased postweaning gain while the low line was three generations behind. Generations 1 and 2 generated F₁ and F₂ lines, generations 3 and 4, replicates, were the backcross of F₂ males to high, low and F₁ females. Reproductive traits measured on each dam were number born per litter, mortality of young from birth to 5 days, number of days from exposure of male to littering and 12-day litter weight. Height traits measured on each offspring were 12-, 21-, 42- and 56-day body weights. Three gain traits were computed for each individual: 12-21, 21-42 and 42-56 day gain. Analyses of the data were of two levels. The first-order tests used components of means to determine adequacy of various genetic models and obtain estimates of their parameters. Four genetic models tested were: (1) containing additive-dominance effects only, (2) adding non-allelic interactions, (3) containing additive and dominance autosomal and sex-linked effects and (4) containing additive and dominance autosomal and maternal effects. Second-order tests using components of variation were used to detect epistasis and estimate additive, dominance and environmental sources of variation. Results showed that additive effects were important for reproductive traits except littering time and mortality of young from birth to 5 days. Body weights at 12, 42 and 56 days of age in both sexes had significant additive variance components. Percent contributions of additive variation to the phenotypic expression for body weight were 17.4 and 9.5% of 12-day weights, 33.8 and 5.4% of the 42-day weights, and 32.9 and 29.5% of 56-day weights for males and females, respectively. Gain from 21-42 days of age showed significant additive genetic variation, 20.9 and 12.0% in males and females, respectively. Estimates of dominance components for littering traits were all zero. A few weight traits showed dominance to be a significant source of genetic variation but percent contribution to phenotypic variation was quite small. Traits for which epistatic interaction were important genetic influences were littering time, mortality from birth to 5 days and 12-day individual weight for males and females. Weaker epistatic interactions were found for body weights at 21 and 56 days of age. Maternal effects, both additive and dominance, were large genetic contributors to the phenotypic variation for littering and weight traits. For all reproductive traits and 12-day individual body weight, estimates of maternal components were as large as the additive component, but for 21-, 42- and 56-day weights and 12-21, 21-42 and 42-56 gain, additive effects are much larger. Sex-linkage is not an important genetic force in growth traits of mice. / Doctor of Philosophy

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