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181.
182.
The ratio of loculus volume to the volume of the entire anther began to increase from the microspore mother cell stage and
reached 32.3% at anthesis. The content of the loculus was examined in Lilium during pollen development and two waves could be distinguished. From the premeiotic stage until the vacuolated microspore
stage, the loculus consisted of neutral polysaccharides, pectins and proteins. These substances originated from tapetal activity
from the premeiotic stage until the young microspore stage. Dictyosomes and rough endoplasmic reticulum seemed to be involved
in tapetal secretion, although, in some mitochondria, vesicles progressively developed as early as premeiosis and increased
until the young microspore stage, which could reveal their involvement in the secretion process. At this stage, numerous cytoplasmic
vesticles containing material similar to the locular material fused with the plasma membrane of the tapetum so that vesicle
content was in contact with the loculus. It seems that tapetal and callose wall degradation at the late tetrad stage may also
have contributed to the production of material in the loculus. From pollen mitosis to anthesis, the anther loculus contained
mainly the pollenkitt which was synthesized in the tapetum between the young microspore stage and the vacuolated microspore
stage. At the young microspore stage, proplastids divided and developed into elaioplasts and smooth endoplasmic reticulum
(SER) increased dramatically. Pollenkitt had a double origin: some droplets were extruded directly from the plastid stroma
through the plastid envelopes; the others were unsaturated lipid globules, which presumably derived from the interaction between
SER saccules and plastids.
Received: 2 September 1997 / Revision accepted: 12 March 1998 相似文献
183.
PCR-based assays of mendelian polymorphisms from anonymous single-copy nuclear DNA: techniques and applications for population genetics 总被引:5,自引:0,他引:5
This paper outlines a PCR-based approach for population genetics that
offers several advantages over conventional Southern blotting methods for
revealing restriction-fragment-length polymorphisms (RFLPs) in nuclear DNA.
Primers are constructed from clones isolated from a nuclear DNA library,
and these primers subsequently are employed in in vitro syntheses of
homologous regions. Amplified products are then screened directly for RFLPs
by using gel-staining procedures. Population applications for this
PCR-based approach, including potential strengths and weaknesses, are
exemplified by two RFLP data sets generated to estimate (a) male-mediated
gene flow in the green turtle (Chelonia mydas) and (b) geographic
population genetic structure in the American oyster (Crassostrea
virginica). Restriction assays of amplified products from 14 or 15
independent primer pairs in each species revealed polymorphisms at several
loci that proved highly informative in the population genetic analyses. In
general, the Mendelian polymorphisms produced by this PCR-based approach
will provide useful genetic markers for population studies, particularly in
situations where simpler and less expensive allozyme methods have failed,
for whatever reason, to provide adequate information.
相似文献
184.
A nuclear gene for higher level phylogenetics: phosphoenolpyruvate carboxykinase tracks mesozoic-age divergences within Lepidoptera (Insecta) 总被引:3,自引:0,他引:3
The sequence of phosphoenolpyruvate carboxykinase (PEPCK) has been
previously identified as a promising candidate for reconstructing
Mesozoic-age divergences (Friedlander, Regier, and Mitter 1992, 1994). To
test this hypothesis more rigorously, 597 nucleotides of aligned PEPCK
coding sequence (approximately 30% of the coding region) were generated
from 18 species representing Mesozoic-age lineages of moths (Insecta:
Lepidoptera) and outgroup taxa. Relationships among basal Lepidoptera are
well established by morphological analysis, providing a strong test for the
utility of a gene which has not previously been used in systematics.
Parsimony and other phylogenetic analyses were conducted on nucleotides by
codon positions (nt1, nt2, nt3) separately and in combination, and on amino
acids, for comparison to the test phylogeny. The highest concordance was
achieved with nt1 + nt2, for which one of two most-parsimonious trees was
identical to the test phylogeny, and with all nucleotides when nt3 was
down-weighted sevenfold or higher, for which a single most-parsimonious
tree identical to the test phylogeny resulted. Substitutions in nt3
approached saturation in many, but not all, pairwise comparisons and their
exclusion or severe downweighting greatly increased the degree of
concordance with the test phylogeny. Neighbor-joining analysis confirms
this finding. The utility of PEPCK for phylogenetics is demonstrated over a
time span for which few other suitable genes are currently available.
相似文献
185.
The purpose of this paper is to assess the extent of gene identity and
differentiation at 33 dinucleotide repeat loci (377 total alleles) within
and among three European and three Native American populations. In order to
do this, we show that a maximum-likelihood method proposed for phylogenetic
trees (Cavalli-Sforza and Piazza 1975) can be used to estimate gene
identity (Nei 1987) with respect to any hierarchical structure. This method
allows gene differentiation to be evaluated with respect to any internal
node of a hierarchy. It also allows a generalization of F- and G-statistics
to situations with unequal expected levels of differentiation. Our
principal finding is that levels of genetic differentiation are unique to
specific populations and levels of nesting. The populations of European
origin show very little internal differentiation; moreover, their
continental average is close to the total population defined by the
aggregate of Europeans and Native Americans. By contrast, the Native
American populations show moderate levels of internal differentiation, and
a great distance between their continental average and the total. The
results of analyses of subsets of loci that were selected to have high gene
diversities in either Europeans or Native Americans closely parallel those
from the total set of loci. This suggests that the principal results are
unlikely to be caused by a European ascertainment bias in locus selection.
In summary, our findings demonstrate that partitions of gene diversity into
within- and between-populations components are heavily biased by the
populations analyzed and the models fitted. Optimistically, however, more
information is available to analyze population history and evolution by
quantifying, as we have done, the uniqueness of patterns of
differentiation.
相似文献
186.
Daniel JC Kronauer Caspar Schöning Lars B Vilhelmsen Jacobus J Boomsma 《BMC evolutionary biology》2007,7(1):56
Background
Army ants are the prime arthropod predators in tropical forests, with huge colonies and an evolutionary derived nomadic life style. Five of the six recognized subgenera of Old World Dorylus army ants forage in the soil, whereas some species of the sixth subgenus (Anomma) forage in the leaf-litter and some as conspicuous swarm raiders on the forest floor and in the lower vegetation (the infamous driver ants). Here we use a combination of nuclear and mitochondrial DNA sequences to reconstruct the phylogeny of the Dorylus s.l. army ants and to infer the evolutionary transitions in foraging niche and associated morphological adaptations. 相似文献187.
Lopez JV; Culver M; Stephens JC; Johnson WE; O'Brien SJ 《Molecular biology and evolution》1997,14(3):277-286
Differential rates of nucleotide substitution among different gene segments
and between distinct evolutionary lineages is well documented among
mitochondrial genes and is likely a consequence of locus-specific selective
constraints that delimit mutational divergence over evolutionary time. We
compared sequence variation of 18 homologous loci (15 coding genes and 3
parts of the control region) among 10 mammalian mitochondrial DNA genomes
which allowed us to describe different mitochondrial evolutionary patterns
and to produce an estimation of the relative order of gene divergence. The
relative rates of divergence of mitochondrial DNA genes in the family
Felidae were estimated by comparing their divergence from homologous
counterpart genes included in nuclear mitochondrial DNA (Numt, pronounced
"new might"), a genomic fossil that represents an ancient transfer of 7.9
kb of mitochondrial DNA to the nuclear genome of an ancestral species of
the domestic cat (Felis catus). Phylogenetic analyses of mitochondrial
(mtDNA) sequences with multiple outgroup species were conducted to date the
ancestral node common to the Numt and the cytoplasmic (Cymt) mtDNA genes
and to calibrate the rate of sequence divergence of mitochondrial genes
relative to nuclear homologous counterparts. By setting the fastest
substitution rate as strictly mutational, an empirical "selective
retardation index" is computed to quantify the sum of all constraints,
selective and otherwise, that limit sequence divergence of mitochondrial
gene sequences over time.
相似文献
188.
Analysis of the nucleotide tightly associated with isolated erythrocyte cytoskeletons show it to be ADP, rather then ATP. This confirms that at least a major part of the erythrocyte actin is in the F-form. A re-evaluation of the stoichiometry of spectrin and actin in the erythrocyte (taking account of a gross difference between the color responses of the two proteins on staining of electrophoretic gels) leads to values of 1x10(5) and 5x10(5) for the number of molecules of spectrin tetramer and actin respectively per cell. It has been found possible to perform spectrophotometric DNAase I assays fro actin on lysed whole cells. The concentration of monomeric actin at 0 degrees C is approximately 16 μg/ml packed cells. After washing the lysed cells the monomer pool is not re-established, indicating that only a small proportion of the actin subunits are free to dissociate. The actin monomer concentration in the cytosol remains unchanged after equilibration of the cells with cytochalasin E. The ability of actin-containing complexes in the membrane to nucleate the polymerization of added G-actin was measured fluorimetrically; it was found that membranes incubated with cytochalasin E were completely inert with respect to nucleating activity under conditions that favor appreciable growth at the slowly-growing (“pointed”) ends of free actin filaments. This suggests that these ends of the actin “protofilaments” in the red cell are blocked or sterically obstructed. After treatment of the membranes with guanidine hydrochloride under conditions that dissociate F-actin, the measured concentration of actin monomer rises to approximately 180 μg/ml of packed cells, which is nearly 70 percent of the total actin content. On treatment with trypsin in the presence of DNAase, the spectrin and 4.1 are extensively degraded, but the actin remains undamaged. This treatment, followed by exposure to guanidine hydrochloride, causes a further rise in the concentration of actin responsive to the DNAase assay to 250 μg/ml of cells, compared with 270 μg/ml estimated by densitometry of stained gels. The oligomeric complex, consisting of actin, spectrin, and 4.1, that is extracted from the membrane at low ionic strength, generates no detectable actin monomer after the same treatment. From literature data on the number of cytochalasin binding sites per cell and our value for the total actin content, we obtain a number-average degree of polymerization for actin in the membrane of 12-17. The results lead to a model for the structure of the cytoskeletal network and suggest some consequences of metabolic depletion. 相似文献
189.
Xue Bao Martijn C Koorengevel Marian J A Groot Koerkamp Amir Homavar Amrah Weijn Stefan Crielaard Mike F Renne Joseph H Lorent Willie JC Geerts Michal A Surma Muriel Mari Frank C P Holstege Christian Klose Anton I P M de Kroon 《The EMBO journal》2021,40(20)
Phosphatidylcholine (PC) is an abundant membrane lipid component in most eukaryotes, including yeast, and has been assigned multiple functions in addition to acting as building block of the lipid bilayer. Here, by isolating S. cerevisiae suppressor mutants that exhibit robust growth in the absence of PC, we show that PC essentiality is subject to cellular evolvability in yeast. The requirement for PC is suppressed by monosomy of chromosome XV or by a point mutation in the ACC1 gene encoding acetyl‐CoA carboxylase. Although these two genetic adaptations rewire lipid biosynthesis in different ways, both decrease Acc1 activity, thereby reducing average acyl chain length. Consistently, soraphen A, a specific inhibitor of Acc1, rescues a yeast mutant with deficient PC synthesis. In the aneuploid suppressor, feedback inhibition of Acc1 through acyl‐CoA produced by fatty acid synthase (FAS) results from upregulation of lipid synthesis. The results show that budding yeast regulates acyl chain length by fine‐tuning the activities of Acc1 and FAS and indicate that PC evolved by benefitting the maintenance of membrane fluidity. 相似文献
190.
Moreau MF Libouban H Legrand E Baslé MF Audran M Chappard D 《Journal of musculoskeletal & neuronal interactions》2001,1(3):209-213
In man, hypogonadism is a risk factor for osteoporosis. Orchidectomy (ORX) in the rat leads to an imbalance between resorption and formation resulting in bone loss. We have measured whole body weight, lean and fat mass, whole bone mass (BMC) in the ORX rat model by dual X-ray densitometry (DXA). Forty-eight male Wistar rats (18-19 weeks old) were studied at 2, 4, 8 and 16 weeks. In each group, 6 rats were ORX and 6 sham-operated were used as control. DXA was performed on the whole body and isolated tibia. The whole body weight of the ORX animals became significantly decreased only at 16 weeks. Whole body BMC was reduced from 8 weeks in the ORX group. The most striking result was a net decrease in lean mass that reached -15.7% at 16 weeks. On the other hand, fat mass remained unchanged during the time series in the ORX animals. 相似文献