首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   304篇
  免费   36篇
  2018年   4篇
  2017年   5篇
  2016年   8篇
  2015年   10篇
  2014年   7篇
  2013年   8篇
  2012年   10篇
  2011年   11篇
  2010年   17篇
  2009年   8篇
  2008年   12篇
  2007年   17篇
  2006年   20篇
  2005年   12篇
  2004年   8篇
  2003年   4篇
  2002年   11篇
  2001年   3篇
  2000年   9篇
  1999年   7篇
  1997年   5篇
  1995年   3篇
  1993年   5篇
  1992年   2篇
  1991年   5篇
  1990年   2篇
  1989年   3篇
  1987年   3篇
  1986年   4篇
  1985年   6篇
  1984年   4篇
  1983年   2篇
  1982年   2篇
  1981年   4篇
  1980年   5篇
  1979年   5篇
  1978年   4篇
  1977年   5篇
  1976年   2篇
  1975年   9篇
  1974年   6篇
  1973年   3篇
  1972年   9篇
  1971年   5篇
  1970年   12篇
  1969年   4篇
  1968年   2篇
  1967年   5篇
  1965年   4篇
  1964年   2篇
排序方式: 共有340条查询结果,搜索用时 15 毫秒
271.
The geographical distribution, ecological characteristics, flowering and fruiting times, and pollinating agents of Passiflora alata are considered and related to molecular genetic data gathered simultaneously. The first report on this species in Rio Grande do Sul was made in 1934, only in cultivated gardens. Approximately 20 years later, however, the species was already classified as efferata (wild) in Porto Alegre's suburbs. The data presented here, together with the DNA investigations, indicate that P. alata is actively colonizing previously unoccupied areas of this region.  相似文献   
272.
The authors have studied the interaction between the abnormal oocyte mutation and an inversion of the X chromosome, In( 1)sc4, which has a proximal breakpoint in or near the heterochromatic region (ABO) that maternally interacts with the abo product. It has been demonstrated that the presence of X chromosomes carrying this inversion, besides a marked increase in the severity of the maternal effect of the abo mutation, produces a zygotic effect resulting in the lethality of the progeny of stocks homozygous for abo and sc4. These results indicate that the sc4 inversion carries an abnormal region indispensable for the development of abo zygotes from sc4;abo mothers.  相似文献   
273.
The electrophoretic patterns of esterase D (ESD; E.C.3.1.1.1) and carbonic anhydrase 2 (CA 2, E.C.4.2.1.1) were studied in 147 specimens ofCebus apella. Three phenotypes were detected at the esterase D system,ESD 1 allele showing a frequency of 44%, markedly different from those observed in Old World monkeys. CA2 also proved to be polymorphic, with three alleles being detected at the following frequencies:CA2 1, 98%;CA2 2 andCA2 3, both 1%. The CA2 activity was absent in newborn animals and in fetuses.  相似文献   
274.
A wild population situated in the border of the distributions ofSaimiri sciureus macrodon andS. boliviensis peruviensis, in the Peruvian Amazonia, was studied in relation to 22 protein loci. These genetic markers provided indications of secondary intergradation between these two taxa, reinforcing previous morphological and cytogenetic evidences. Continued studies in this region on the hybrids' viability and fertility may be important for decisions related to the taxonomy of this genus.  相似文献   
275.
One hundred and forty-three sakis (Pithecia), 107 bearded sakis (Chiropotes), and 7 red uakaris (Cacajao) were studied in relation to 18 genetic loci expressed on blood through electrophoretic techniques. Eight of the 18 loci showed intrapopulational variation. The low level of genetic diversity found inPithecia could be a consequence of a decrease in populational size due to intense habitat destruction. The genetic distances between the species investigated were:Pithecia ×Chiropotes: 0.49;Pithecia ×Cacajao: 0.57;Cacajao ×Chiropotes: 0.18–0.20. These results suggest, in accordance with other data, thatChiropotes andCacajao constitute a sister group within the pithecines.  相似文献   
276.
Summary Thirty-two pairs of Caucasoid twins, 16 monozygotic (MZ) and 16 dizygotic (DZ) of the same sex, were studied in relation to the C-bands of chromosomes 1, 9, and 16. Concordance was not absolute among MZ, the best evaluation of the degree of genetic determination for these traits being 0.40 for chromosome 16, 0.64 for chromosome 1, and 0.73 for chromosome 9. Possible explanations for the failure to obtain 100% concordance are methodologic shortcomings, intercell variations in chromosome contraction, and unequal mitotic crossing over.  相似文献   
277.
A total of 302 White and 904 Black children six, nine and 12 years of age were studied for the eruption of their permanent teeth. Differences between the two ethnic groups were not large, but the Black subjects were generally more precocious at the beginning of the process (especially the girls, both in the upper and lower incisors). At nine and 12 years of age, however, these dissimilarities disappear. The latter do not seem to be related to distinct rates of extraction or agenesis of deciduous teeth. No significant differences were observed in the degree of asymmetry present in the permanent dentition of the White and Black individuals studied.  相似文献   
278.
Senescence and human chromosome changes.   总被引:2,自引:0,他引:2  
Chromosome counts and a search for structural abnormalities were performed in cultured leukocytes from 60 elderly subjects (ages 62-96) and 60 controls (ages 10-13). A total of 3900 cells were examined, 3600 in 3-day cultured and 300 in cultivations maintained for 2 days. Our results and those obtained by other investigators indicate clearly that there is an increase in the level of aneuploidy and of structural abnormalities in the blood of aged persons. There is an excess of missing C-group chromosomes in elderly females, but no consistent preferential loss was observed among the males. In contrast with two previous studies, we found a significant decrease of aneuploid cells in 3-day cultures, as compared to those cultivated for 2 days only.  相似文献   
279.
A total of 2, 490 South American Indians affiliated with 10 tribes were studied for esterases A1, A2, A3, B, D, and carbonic anhydrases 1 and 2. Wide variation was observed in the prevalence of ESD1, the extreme values being 0. 44, encountered among the Xikrin, and 0. 95, found among the Cashinawa. Seven of the 10 frequencies fell within the interval of 0. 66–0. 87. These results were integrated with those of earlier surveys. In a general way we observe lower values in the eastern and Atlantic Coast groups, but this is mainly due to the low frequencies found among the Gê tribes and the Caingang, who speak a language which has many affinities with Gê. High prevalences were observed among the tropical forest tribes. A fair amount of intervillage, intratribal variation was found among the Ticuna and Caingang. No variability was detected in the A1, A2, A3, B esterases. In the carbonic anhydrases we confirmed the presence of a “private polymorphism” among the Baniwa.  相似文献   
280.
Data are presented on electrophoretic variants of 25 polypeptides found in the blood serum and erythrocytes, in 812 individuals from three Amerindian tribes, the Pano, the Baniwa, and the Kanamari. Two "private polymorphisms" were encountered, of PEPB in the Pano and CAII in the Baniwa. A single example of a different PEPB variant was encountered in the Baniwa, and two possible examples of an unstable variant of HGB A2 in the Kanamari. In addition, the well-known A variant of ACP1, the Duarte variant of GALT, the 2 variant of Hp and the 2 variant of PGM1 occurred in polymorphic proportions in all three tribes, and the TFDChi variant was present as a polymorphism in the Baniwa. These data have recently been incorporated into a treatment which concludes that the eight electrophoretically-defined "private polymorphisms" thus far encountered in Amerindian tribes can be explained by a mutation pressure of 0.7 x 10(-5)/locus/generation on the assumption of neutrality of the phenotypes in question (Neel and Thompson, '78).  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号