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31.
Molecular phylogenetics at the population/species interface in cave spiders of the southern Appalachians (Araneae:Nesticidae:Nesticus) 总被引:5,自引:0,他引:5
This paper focuses on the relationship between population genetic structure
and speciation mechanisms in a monophyletic species group of Appalachian
cave spiders (Nesticus). Using mtDNA sequence data gathered from 256
individuals, I analyzed patterns of genetic variation within and between
populations for three pairs of closely related sister species. Each
sister-pair comparison involves taxa with differing distributional and
ecological attributes; if these ecological attributes are reflected in
basic demographic differences, then speciation might proceed differently
across these sister taxa comparisons. Both frequency-based and gene tree
analyses reveal that the genetic structure of the Nesticus species studied
is characterized by similar and essentially complete population
subdivision, regardless of differences in general ecology. These findings
contrast with results of prior genetic studies of cave-dwelling arthropods
that have typically revealed variation in population structure
corresponding to differences in general ecology. Species fragmentation
through both extrinsic and intrinsic evolutionary forces has resulted in
discrete, perhaps independent, populations within morphologically defined
species. Large sequence divergence values observed between populations
suggest that this independence may extend well into the past. These
patterns of mtDNA genealogical structure and divergence imply that species
as morphological lineages are currently more inclusive than basal
evolutionary or phylogenetic units, a suggestion that has important
implications for the study of speciation mechanisms.
相似文献
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34.
Sperm-chromatin maturation in the mouse 总被引:1,自引:0,他引:1
M. G. Manfredi Romanini M. Biggiogera D. Formenti A. Fraschini S. Garagna C. Pellicciari C. A. Redi 《Histochemistry and cell biology》1986,84(4-6):484-491
Summary Cytochemical techniques were used to study chromatin during spermiogenesis and sperm maturation in the mouse, starting from the stages at which the substitution of somatic histones by testis-specific proteins occurs. It was possible to distinguish and analyze the different temporal incidence of two processes involved in sperm maturation, i.e. chromatin condensation (a tridimensional highly compacted arrangement) and chromatin stabilization (a tough structure, which protects the genome DNA). The first process, involving a reduction in the nuclear size and a decrease in the amount of sperm DNA accessible to specific cytochemical reactions and stainings, was found to reach its maximum in caput-epididymidis spermatozoa, in which electron microscopy revealed that the sheared chromatin was mainly organized into 120--thick knobby fibers. No further changes were found in sperm up to their appearance in the fallopian tubes. On the contrary, chromatin stabilization, the onset of which occurs in the testis (at the late spermatid stage) via the formation of -S–S- cross-links, is completed in the vas deferens, where chromatin has a superstructure consisting of thicker fibers, with diameters of 210 and 350 . The reductive cleavage of disulfides in vas-deferens spermatozoa does not completely destroy the superstructure of sperm chromatin, which could indicate coiling of the basic knobby fiber. In fact, when the ion concentration was increased, the chromatin of vas-deferens spermatozoa appeared to be organized into fibers with diameters similar to those of the caput epididymidis. This unique organization of mature sperm chromatin should have an essential role in the fast swelling of spermatozoa during fertilization.In honour of Prof. P. van Duijn 相似文献
35.
C. Pellicciari M. Danova M. Giordano A. M. Fuhrman Conti† G. Mazzini E. Wang‡ E. Ronchetti A. Riccardi M. G. Manfredi Romanini 《Cell proliferation》1991,24(5):469-479
EUE cells adapted to grow for long times in a hypertonic medium have a longer cell cycle than those growing in isotonic medium. To elucidate whether this lengthening involves specific cycle phases to differing extents, the expression of two cycle-related protein, PCNA and statin, was studied by dual parameter flow cytometry of indirect immunofluorescence protein labelling and DNA content. In isotonic medium, most cells, in all the cycle phases, were PCNA positive; in contrast, PCNA negative cells and statin positive cells were very few in number and only fell in the G0/1 range of DNA contents. In hypertonic medium, the frequency of PCNA positive cells was lower, and that of statin positive cells higher, than in isotonic medium, particularly in the G0/1 range of DNA contents: this suggests that a G0 block occurs under long-term hypertonic stress. Consistently, dual parameter flow cytometric measurement of BrdUrd immunofluorescence labelling and DNA content showed that fewer cells entered S phase in hypertonic medium and their progression through the S phase was slower; evidence was also found for the occurrence of a G2 block. These kinetics changes were fully reversible in isotonic medium, thus indicating the adaptive nature of the EUE response to hypertonicity. 相似文献
36.
C Pellicciari G Marchese M G Bottone M G Manfredi Romanini 《Basic and applied histochemistry》1987,31(4):501-509
The process of DNA digestion with DNase I was monitored in interphase chromatin of differentiated cells by flow cytometry after DNA staining with either the intercalating dye propidium iodide (PI) or the AT specific dye Hoechst 33258 (HO). Nuclei from the liver, kidney and spleen of the mouse were studied after different digestion times (0 to 120 min). During the first 30 min of treatment, a tissue specific digestion pattern was found after PI staining; from 60 min onward, the digestion curves ran parallel, with minor quantitative differences among the cell types. After HO staining, the digestion kinetics appeared to be similar for all the cell types; this is likely due to the peculiar base composition of the mouse genome, where inactive c-heterochromatin is exceptionally AT-rich. No quantitative correlation was found between interphase "heterochromatin" and chromatin DNA which is resistant to DNase I cleavage, while the amount of DNase-I-sensitive DNA does not correspond to the interphase "euchromatic" component. It was confirmed that the flow cytometric approach is a tool for quantifying relative changes in the functional state of chromatin in differentiated cell systems. 相似文献
37.
C Pellicciari D Formenti M Zuccotti R Stanyon M G Manfredi Romanini 《Cytogenetics and cell genetics》1988,47(1-2):1-4
Genome size was measured as the amount of Feulgen-stained DNA in six species of the family Hylobatidae and in a hybrid of the gibbon (Hylobates muelleri) and siamang (Symphalangus syndactylus). The family, on the whole, exhibits a wider range of genome sizes than pongids; in particular, the siamang has about 15% more DNA than the 44-chromosome Hylobates species of the "lar" group. Quantitative analysis of C-heterochromatin in hybrid metaphases showed that the difference in genome size of the parental species correlates with the amount of C-band-positive material. Hylobatids are the only group of primates in which karyotype diversification has taken place with a massive quantitative change in constitutive heterochromatin. 相似文献
38.
Communication Studies currently undergoes a crisis of paradigms that requires an ontological review that must begin with a
debate about the conditions of possibility of every communicational phenomena. In this article we argue that semiosis offers
a conceptual framework that allows for the study of communication as qualitative action. Semiosis, or the action of the sign,
is here defined as a fundamental process based on perception that models the world of species, creating cognition and culture.
At the core of semiosis are dynamic structures that the authors have defined as ‘ontological diagrams’. The first purpose
of Semiotics of Communication is to understand how these modeling systems evolve ontologically and phylogenically, producing,
in the case of human culture, means of communication ever more varied and technologically advanced. 相似文献
39.
C. Pellicciari C. Filippini L. De Grada A. M. Fuhrman Conti M. G. Manfredi Romanini 《Cell biochemistry and function》1995,13(1):1-8
Long-term exposure to hypertonic (HT) culture media has been found to perturb the cell cycle and change gene expression in various animal cell types. A lower growth rate, with exit of cells from the cycling compartment has been observed previously in human transformed EUE. cells. The aim of this study was to investigate if the kinetic changes after long-term HT stress, were typical of transformed cells or could be also found in primary cultures of normal cells. Human transformed cells from normal and neoplastic tissues, and normal human cells of epithelial and connective origin have been studied. After the incorporation of bromodeoxyuridine (BrdUrd), the frequency of S-phase cells was estimated by dual-parameter flow cytometry of DNA content versus BrdUrd immuno-labelling; the total growth fraction was also estimated, after immunolabelling with an anti-PCNA antibody. We also investigated, by polyacrylamide gel electrophoresis, changes in the amount of a 35 kDa protien band, which increased in EUE cells grown in an HT medium, and which may be directly involved in cell resistance to hypertonicity. Lower BrdUrd labelling indices and higher frequencies of cells in the G0/1 range of DNA content were common features of all the cells in HT media, irrespective of their tissue of origin; other cycle phases may also be involved, depending on the cell type considered. The mechanisms by which cells cope with the HT environment could however, differ, since only some cell types showed an increase of the 35 kDa stress protein found originally in HT EUE cells. 相似文献
40.