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31.
R. A. E. Tilney-Bassett Dr. O. A. L. Abdel-Wahab 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1982,62(2):185-191
Summary Two distinct segregation patterns are recognized after G X W plastid crosses in Pelargonium. Type I parents produce offspring in which maternal zygotes are frequent, biparental intermediate, and paternal zygotes rare (MZ>BPZ>PZ), as defined by the presence or absence of green or white plastids in the young embryos into which the zygotes develop. Type II parents produce offspring in which maternal and paternal zygotes are frequent with biparental zygotes the least frequent class (MZ>BPZPr1Pr1. Type II plants, which do not breed true, are regarded as heterozygotes — Pr1Pr2. The nuclear gene is symbolized as Pr as it is presumed to control alternative patterns of plastid segregation through an effect on plastid replication.Selfs and intercrosses of heterozygous plants segregate in an unexpected 1:1 ratio and not the expected 3:1 (1:2:1). The alternative homozygote — Pr2Pr2 — could not be detected. Reciprocal crosses between heterozygotes (Pr1Pr2) and homozygotes (Pr1Pr1) give the expected 1:1 ratio when the Pr2 allele is derived from the male, whereas there is often, but not always, a highly significant deviation from 1:1 when the Pr2 allele is derived from the female.A simple explanation, which is not wholly satisfactory, is to assume that Pr2 is a gametophytic lethal on the female side. An alternative, or additional, explanation is that an incompatibility mechanism is involved in which Pr1 is a self-compatible allele, Pr2 a self-incompatible allele, and Pr1-Pr2 cross-compatible alleles. Successful fertilization is then determined by sporophytic control on the male side and gametophytic control on the female side. 相似文献
32.
Sokolova VA Kustova ME Arbuzova NI Sorokin AV Moskaliova OS Bass MG Vasilyev VB 《Molecular reproduction and development》2004,68(3):299-307
To study human diseases associated with mutations in mitochondrial DNA one needs an animal model in which the distribution of abnormal mtDNA and its impact on the phenotype might be followed. We isolated human mitochondria from HepG2 cell culture and microinjected them into murine zygotes, upon which those were transplanted to the pseudopregnant mice. PCR with species-specific primers allowed detecting human mtDNA in the tissues of 7-13-day embryos. No serious alterations in the development of transmitochondrial embryos were noticed. Among various organs/tissues of the 13-day embryos, human mtDNA was detected only in the heart, skeletal muscles, and stomach, which is in line with its uneven distribution among the blastomeres of an early mouse embryo that we described previously. In four recipient females, the microinjected zygotes were allowed to develop to term, the four neonate males of their joint litter were sacrificed, and in three of them human mtDNA was detected in the heart, skeletal muscles, stomach, brain, testes, and bladder. Six females of that joint litter were grown and mated to intact males. In the progeny (F1) of one of the females two mice were carrying human mtDNA in the heart, skeletal muscles, stomach, brain, lungs, uterus, ovaries, and kidneys. The study confirms the possibility to obtain transmitochondrial mice carrying human mtDNA that is transmitted to the animals of the next generation. Our results also indicate that among the organs to which human mtDNA is distributed some are more likely to receive it than others. 相似文献
33.
Nicola L. Barclay Desi Kocevska Wichor M. Bramer Eus J. W. Van Someren Philip Gehrman 《Genes, Brain & Behavior》2021,20(4):e12717
Twin studies of insomnia exhibit heterogeneity in estimates of heritability. This heterogeneity is likely because of sex differences, age of the sample, the reporter and the definition of insomnia. The aim of the present study was to systematically search the literature for twin studies investigating insomnia disorder and insomnia symptoms and to meta-analyse the estimates of heritability derived from these studies to generate an overall estimate of heritability. We further examined whether heritability was moderated by sex, age, reporter and insomnia symptom. A systematic literature search of five online databases was completed on 24 January 2020. Two authors independently screened 5644 abstracts, and 160 complete papers for the inclusion criteria of twin studies from the general population reporting heritability statistics on insomnia or insomnia symptoms, written in English, reporting data from independent studies. We ultimately included 12 papers in the meta-analysis. The meta-analysis focussed on twin intra-class correlations for monozygotic and dizygotic twins. Based on these intra-class correlations, the meta-analytic estimate of heritability was estimated at 40%. Moderator analyses showed stronger heritability in females than males; and for parent-reported insomnia symptoms compared with self-reported insomnia symptoms. There were no other significant moderator effects, although this is likely because of the small number of studies that were comparable across levels of the moderators. Our meta-analysis provides a robust estimate of the heritability of insomnia, which can inform future research aiming to uncover molecular genetic factors involved in insomnia vulnerability. 相似文献
34.
James Griesemer Matthew H. Haber Grant Yamashita Lisa Gannett 《Biology & philosophy》2005,20(2-3):517-544
The themes, problems and challenges of developmental systems theory as described in Cycles of Contingency are discussed. We argue in favor of a robust approach to philosophical and scientific problems of extended heredity and the integration of behavior, development, inheritance, and evolution. Problems with Sterelny's proposal to evaluate inheritance systems using his `Hoyle criteria' are discussed and critically evaluated. Additional support for a developmental systems perspective is sought in evolutionary studies of performance and behavior modulation of fitness. 相似文献
35.
G. A. Galau T. A. Wilkins 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1989,78(1):23-30
Summary Alloplasmic male sterile (cms) and restoration-of-fertility (Rf) lines of the AD allotetraploid Gossypium hirsutum were earlier derived from the presumed introgression of the cytoplasm of the D species G. harknessii. To confirm that this happened and address its significance, cytoplasms of the maternal progenitor, backcross intermediates, derived breeding lines, related A, D, and F species, and a synthetic AD tetraploid were examined by agarose and polyacrylamide gel electrophoresis of 140 restriction enzyme fragments of chloroplast DNA. Length mutations of 10–50 nucleotides predominate over site loss/gain mutations. Chloroplast DNA is maternally inherited and that of G. harknessii has been maintained in the cms lines for at least 13 successive generations without detectable alteration. Chloroplast DNA divergence is consistent with current nuclear genome classification and shows that the A progenitor was the maternal parent of the AD tetraploids. As predicted from incompatability models of cms, the degree of male sterility in alloplasmic Gossypium tetraploids is correlated with the extent of evolutionary divergence of their cytoplasms. It is suggested that the A genome in the AD tetraploids dominates those nuclear-cytoplasm interactions reflected by male fertility. 相似文献
36.
Interdigital pattern distribution in 101 nuclear families is analyzed, and the genes of this phenotype controlling either Ⅲ or Ⅳ area, right or left hand are all on the same locus. Genes controlling Ⅲ or Ⅳ area is mosaic dominant. One gene controls a couple of corresponding areas on both right and left hands. Different genes' phenotypes have different asymmetric degrees. There are 6 kinds of perfectible dominant genes and one inperfectible dominant gene. This is interdigital pattern' s major gene locus. There also finds a Ⅲ pattern' s recessive gene very occasionally. These genes' frequen- cies in random population are calculated. This heredity mode can be applied to parentage identification etc. 相似文献
37.
38.
Plastid development in the primary leaf of Echinochloa crus-galli (L.) Beauv. var. oryzicola (Vasing.) Ohwi was followed during 5 d of anoxic germination and growth. Plastids develop slowly from simple spheroidal proplastids into larger pleomorphic plastids with several stromal membranes and many peripheral membrane vesicles. A small prolamellar body is present at 96 h with perforated (pro)thylakoids extending into the stroma. Changes in starch grains and plastoglobuli are evidence of carbohydrate and lipid metabolism. Plastid division is indicated by dumbbell plastid profiles after 4 d of anoxia. These results demonstrate that plastids not only maintain their integrity during anaerobic germination but also show developmental changes involving an increase in internal membrane complexity, although to a lesser extent than in etiolated shoots.Abbreviation PLB
prolamellar body
Scientific paper No. 6167. College of Agriculture, Washington State University, Pullman 相似文献
39.
The behavior of centrioles in zygotes and female gametes developing parthenogenetically in the anisogamous brown alga Cutieria cyiindrica Okamura was studied using electron and immunofluorescence microscopy. Two pairs of centrioles, detected using anti-centrin antibody, were observed in the vicinity of the male and female nuclei, respectively, just after plasmogamy. The fluorescence intensity of one of the two centrin foci became weak 6 h after plasmogamy and finally disappeared. It was impossible to determine whether the male- or female-derived centrioles disappeared in zygotes, because there was nothing to detect morphological differences between the two centrioles. However, a prominent anti-centrin staining focus was located at the condensed male nucleus in zygotes in which karyogamy had not occurred yet. As a result, it was considered that the maternally inherited centrioles had selectively disappeared during development in C. cylindrica. The paternal inheritance of centrioles in zygotes was also confirmed by electron microscopy. Considering previous observations from oogamous and isogamous species of brown algae, we concluded that the paternal inheriance of centrioles could be universal in the brown algae. 相似文献
40.
Over ten years, the individuals of an orthoclone of Notommata copeus gradually lost their sensitivity to photoperiod. This loss is transmissible but reversible in three generations. It is endogenous but not chromosomal. The hypothesis is forwarded that it is induced by external factors, and quite possibly crowding. 相似文献