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1.
SUMMARY: Effects of PMSG and genotype on various measures of reproductive efficiency were investigated. Prenatal data were obtained at 40 d of gestation from 96 gilts representing four genotypes. Data on Duroc (D), Yorkshire (Y), Synthetic (Large White × Landrace) (SYN), and Crossbred Duroc × Yorkshire (XB) gilts were collected from January, 1990 through May, 1991. Litter size (LS) data were collected from 482 farrowings of siblings. Treatment with exogenous hormones significantly increased number of corpora lutea (CL), number of embryos (EN), ovum wastage, (OVWS) and embryo length (ELG). Breed group differences (P < .05) were detected for natural ovulation rate, hormone-induced ovulation rate, CL, OVWS, ELG, embryo weight, ovum success, uterine length, ovary weight, range and variance of within-litter embryo weight (RWT and VWT), and litter size born alive. Natural ovulation rates for D, Y, SYN and XB were 10.46 ± 1.61, 12.64 ± 1.41, 14.10 ± .99 and 10.90 ± 1.47, and hormone-induced ovulation rates were 15.00 ± 1.53, 17.69 ± 1.40, 19.43 ± 1.17 and 12.19 ± 1.43, respectively. Range and variance of within-litter embryo length were not affected by either treatment or genotype. Increases in RWT and VWT observed in D and XB gilts after PMSG treatment did not adversely affect embryo survival to 40 d gestation. Significant genetic differences existed for litter size at birth. The PMSG treatment and interactions with PMSG were not significant for litter size born alive. Breed groups seem to differ for CL and EN in response to PMSG but only Yorkshire showed any response in LS (P < .10). Although PMSG increased ovulation rate in siblings by 4.06 ova and number of embryos at 40 d gestation by 1.87 compared with control gilts, there were no differences in litter size born alive due to PMSG treatment. The increase in ovulation rate and number of embryos generated by PMSG seems to be negated by fetal losses occurring both before and after 40 d of gestation. ZUSAMMENFASSUNG: Einflüsse von Stutenserum-Gonadotropin (PMSG) auf Reproduktionsmerkmale von vier Genotypen bei Jungsauen Einflüsse von PMSG und Genotyp auf verschiedene Merkmale der Reproduktion wurden untersucht. Daten wurden am 40. Tr?chtigkeitstag von 96 Jungsauen von vier Genotypen-Duroc (D), Yorkshire (Y), Synthetik (Edelschwein × Landrasse (SYN)) und Kreuzungen-Duroc × Yorkshire (XB) zwischen Januar 1990 und Mai 1991 erhoben. Wurfgr??e (LS) wurden von 492 Würfen von Geschwistertieren erhoben. Behandlung mit exogenem Hormon steigert signifikant die Zahl der Gelbk?rper (CL), Zahl der Embryonen (EN), Ovarverlust (OVWS) und Embryol?nge (ELG). Differenzen zwischen Genotypen wurden für natürliche und hormoninduzierte Ovulationsrate, CL, OVWS, ELG, Embryogewicht, Embryoerfolg, Geb?rmutterl?nge, Ovargewicht, Streuungsbereich und Varianz des Embryogewichtes von Wurfgeschwistern (RWT und VWT) und Zahl lebendgeborener Ferkel erhoben. Die natürlichen Ovulationsraten für D, Y, SYN und XB waren 10,46 ± 1,61, 12,64 ± 1,41, 14,10 ± 0,99 und 10,90 ± 1,47, und die hormoninduzierten 15,00 ± 1,53, 17,69 ± 1,40, 19,43 ± 1,17 und 12,19 ± 1,43. Streuungsbereich und Varianz zwischen Embryonenl?nge eines Wurfes wurden weder durch Behandlung noch Genotyp tangiert. Steigerungen in RWT und VWT in D und XB Jungsauen nach Hormonbehandlung hat Embryoüberleben bis 40 Tage nicht beeintr?chtigt. Signifikante genetische Unterschiede existieren zwischen Wurfgr??e bei Geburt. Hormonbehandlungen und Interaktionen mit Genotypen waren für die Wurfgr??e nicht signifikant. Rassengruppen scheinen für CL und EN im Hinblick auf Hormonbehandlung sich zu unterscheiden, aber nur Yorkshire zeigten Reaktion bei LS (P < .1). Obwohl das Hormon die Ovulationsrate um 4,06 Eier und Zahl der Embryonen bei 40 Tagen um 1,87 gegenüber Kontrollsauen vergr??erte, verblieben keine Unterschiede in Wurf gr??e. Die Steigerung der Ovulationsrate und Zahl der Embryonen nach Hormonbehandlung scheint durch F?talverluste vor und nach 40 Tagen Tr?chtigkeit eliminiert zu werden.  相似文献   
2.
Objectives were to determine whether the oMt1a-oGH transgene shows normal Mendelian segregation and whether oMt1a-oGH mice exhibit normal growth without the zinc supplementation required to increase plasma oGH levels and stimulate growth. Transgenic mice were reciprocally backcrossed for four generations to high growth and control lines to form lines GM and GR, respectively. In the fifth generation, hemizygous transgenic mice (T/-) were crossed within each line. Pooled across backcross generations, there was a deficit (P < 0.001) of T/- progeny in lines GM (31.6%) and GR (22.2%) compared with expected (50%). In the T/- x T/- cross, the combined percentage of homozygous (T/T) and hemizygous transgenic mice was less (P < 0.001) than expected (75%) in both GM (44.2%) and GR (38.5%). Backcross T/- mice had lower (P < 0.05) 3-wk BW and lower (P < 0.001) 6-wk BW and 3- to 6-wk postweaning gains than nontransgenic mice. Similar genotypic differences were found in the T/- x T/- cross. No significant growth differences were found between T/T and T/- progeny. Using segregation ratios from the T/- x T/- mating, the relative fitness estimates of T/T, T/-, and -/- (nontransgenic) mice were 0.345, 0.223, and 1.0, respectively, in line GM and 0.218, 0.205, and 1.0 in line GR. Fitness estimates in the back-cross for T/- and -/- were 0.463 and 1.0 in line GM and 0.285 and 1.0 in line GR. Abnormal segregation ratios may be due to germline mosaicism or reduced fitness due to differential embryo survival. Reduced growth of oMt1a-oGH transgenic mice when the transgene is switched off suggests a subtle developmental abnormality, which may contribute to a reduction in fitness.  相似文献   
3.
Genetic factors affecting female reproductive performance in lines of mice with a known history of selection were estimated from a 5 X 5 diallel cross. Lines were selected as follows: large litter size at birth (L+); large 6-wk body weight (W+); an index for large litter size and small 6-wk body weight (L+W-); the complementary index (L-W+) and randomly (K). Partitioning of direct and correlated responses for litter size, 6-wk body weight and related traits into average direct genetic (li) and average maternal genetic (mi) effects indicated that the magnitude of differences in li exceeded those in mi. Lines having positive responses in li were W+ greater than L+ greater than L-W+ for dam body weight, L+ greater than L+W- greater than W+ for litter size and L+ greater than (W+, L+W-) for litter birth weight, whereas L-W+ responded negatively for litter size. A positive association was found between mi for litter size and dam body weight, W+ and L-W+ being high and L+ and L+W- low for both traits. Female infertility and time from male exposure to parturition had relatively small correlated responses. Line rankings in general combining ability (gi) and net line effects were similar for the respective traits. Depending upon the line and trait involved, the relative contribution of average direct genetic and line direct heterotic (hi) effects to general combining ability [gi = (1/2) li + hi] varied. Line heterosis refers to average heterosis in crosses involving that line. Direct heterosis ( hij ) for each trait differed considerably among crosses. The three crosses showing the highest hij for litter size at birth, W+ X L-W+ (1.78), L+ X W+ (1.28) and L-W+ X L+W- (1.22), possibly had loci contributing directional dominance to litter size with frequencies of parental lines deviating in opposite directions relative to mean gene frequency. The correlation between absolute difference in parental line means and hij for litter size was not significant, suggesting that the magnitudes of absolute differences in parental means were not reliable predictors of divergence in gene frequency. Crossbred performance increased linearly with midparent values for litter size at birth (b = .88 +/- .09, R2 = .92) and dam parturition body weight (b = 1.13 +/- .04, R2 = .99), the latter trait showing an increase (P less than .01) in heterosis as midparent values increased.  相似文献   
4.
The purpose of this study was to evaluate selection in lines of transgenic mice. Two replicates of lines that either carried or did not carry the sheep metallothionein-1a sheep growth hormone transgene (oMt1a-oGH) were established. The host lines had been previously selected for rapid growth or selected randomly. Within-litter selection for increased 8-wk body weight was carried out for 13 generations. The frequency of oMt1a-oGH was monitored in all generations in the transgenic lines, but no genotypic information regarding the transgene was used as an aid to selection. The oMt1a-oGH was activated from weaning, at 3 wk, until 8 wk of age by adding ZnSO4 to the drinking water. Zinc stimulation of the transgene was not done during mating, gestation, or lactation. Data on body weights and weight gains were analyzed with a conventional mixed model and with an animal model. Genetic progress was achieved in all lines subjected to directional selection. In the control background, response to selection for 8-wk body weight was larger in the nontransgenic lines than in the transgenic lines, whereas no difference was found in the selected background. The frequency of the transgene was increased from the initial .5 to .62 in the randomly selected background but decreased to .04 in lines from a selected background. The REML estimates of variance components and genetic gain estimates varied greatly between the two methods. In general, there was better agreement between the realized heritability estimates and the heritability estimates obtained from the conventional mixed model analysis than between realized heritability estimates and results obtained using the animal model. Favorable correlated responses were obtained for 3- and 6-wk body weights and on 3- to 6- and 6- to 8-wk weight gains. Correlated responses to selection were larger in the selected than in the nonselected background but were not affected by the presence of the transgene. Results suggest that constructs similar to the oMt1a-oGH, which allow tight regulation, may be successfully incorporated into commercial livestock and should have larger effects in populations that have not been subject to selection.  相似文献   
5.
The objective of this study was to determine if selection response for increased litter size in pigs could be partially attributed to three type 1 marker loci coding for genes known to affect litter size: oestrogen receptor (ESR), retinol‐binding protein 4 (RBP4) and follistatin (FS). In the high litter size line (LS), pigs from the largest litters, based on number of pigs born alive (NBA), were retained to parent the next generation. A randomly selected control line (LC) was maintained. Gilts were reared in litters of 10 pigs or less to minimize maternal effects. Pigs were measured at generations 10–12. Additional traits scored were number of fully formed pigs (NFF) and number of mummified fetuses (MUM). Breeding values for NFF and NBA were greater (p < 0.05) in LS than LC in generations 11 and 12, but no significant line differences were found for MUM. The A allele of the ESR locus was fixed in both lines. After adjustment for effects of genetic drift, frequency of the two alleles segregating for the FS and RBP4 loci did not differ significantly between lines. No significant additive or dominance effects of the FS markers were detected for NFF, NBA and MUM in either LS or LC. Response to selection for increased litter size could not be attributed to effects at the ESR, RBP4 or FS loci.  相似文献   
6.
Black-tailed prairie dogs (Cynomys ludovicianus) currently live in metapopulations in the parts of their range where plague, caused by the bacterium Yesinia pestis, has invaded. Prairie dogs are highly susceptible to the pathogen, with most animals within towns dying during Y. pestis outbreaks. A review of population genetic studies of prairie dogs demonstrates considerable differentiation between prairie dog towns. Despite declines and fluctuations in size of prairie dog populations, they continue to harbor considerable genetic variation. This results from continual dispersal and gene flow, likely along low-lying drainages that connect towns. When combined with estimates of population size, the landscape genetic approach described here will provide precise estimates of dispersal and gene flow, in addition to evaluation of long-term stability of prairie dog metapopulations.  相似文献   
7.
Genetic differences in natural vs hormone-induced ovulation rates were compared in immature female mice from five lines that had undergone long-term single-trait and antagonistic index selection for litter size and(or) 6-wk BW. Lines used were control (K); high litter size (L+); high BW (W+); low litter size and high BW (L-W+); and high litter size and low BW (L+W-). Natural ovulation rate at a mean age of 34.3 d and hormone-induced (5 IU of pregnant mare's serum gonadotropin followed 2 d later by 5 IU of human chorionic gonadotropin) superovulation rate at a fixed age of 31 d were obtained. Total number of eggs ovulated was affected by line (P less than .001), treatment (P less than .001), and line x treatment interaction (P less than .001). Line differences were subsequently tested within treatment because of the significant line x treatment interaction. Line differences were important (P less than .001) for natural ovulation, hormone-induced ovulation, and response to hormones. Mean natural ovulation rates for K, L+, W+, L-W+, and L+W- were 14.1, 19.8, 15.1, 13.6, and 16.4, respectively. Selection changed ovulation rate by 40, 16, 7, and -4% in the L+, L+W-, W+ and L-W+ lines, respectively (P less than .01). Hormone-induced ovulation rates in K, L+, W+, L-W+, and L+W- were 32.3, 24.6, 19.6, 20.9, and 22.1, respectively. Exogenous hormones increased ovulation by 18.2, 4.8, 4.6, 7.3, and 5.7 ova for K, L+, W+, L-W+, and L+W-, respectively (P less than .001). Lines with lower natural ovulation rates had higher responses to superovulation. Increased ovulation rate due to treatment ranged from 24.3% in L+ to 129% in K. These results indicate significant differences among lines in ovarian response to exogenous hormones.  相似文献   
8.
Two independent methods were used to identify the mouse chromosomes on which are located two families of immunoglobulin (Ig)-like genes that are rearranged and expressed in T lymphocytes. The genes coding for the alpha subunit of T-cell receptors are on chromosome 14 and the gamma genes, whose function is yet to be determined, are on chromosome 13. Since genes for the T-cell receptor beta chain were previously shown to be on mouse chromosome 6, all three of the Ig-like multigene families expressed and rearranged in T cells are located on different chromosomes, just as are the B-cell multigene families for the Ig heavy chain, and the Ig kappa and lambda light chains. The findings do not support earlier contentions that genes for T-cell receptors are linked to the Ig heavy chain locus (mouse chromosome 12) or to the major histocompatibility complex (mouse chromosome 17).  相似文献   
9.
Much has been gained from genomic and evolutionary studies of species. Combining the perspectives of these different approaches suggests that an integrated phylogenomic approach will be beneficial.  相似文献   
10.
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