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排序方式: 共有113条查询结果,搜索用时 281 毫秒
1.
The Streptomyces plasmid SCP2*: its functional analysis and development into useful cloning vectors 总被引:43,自引:0,他引:43
Detailed restriction maps of the plasmid SCP2* and its deletion derivative pSCP103 were constructed. DNA fragments carrying hygromycin (Hyg), thiostrepton (Thio) or viomycin-resistance (VioR) determinants were inserted into pSCP103, and various segments were deleted from the resulting plasmids. Changes in plasmid phenotypes associated with these insertions and deletions allowed the localisation and characterisation of plasmid replication, stability, transfer and fertility functions. Several useful cloning vectors were constructed. They are able to maintain large (greater than 30 kb) DNA inserts, with stable inheritance at a low copy number (1-2 per chromosome) and without structural rearrangements, in Streptomyces hosts. The vectors have a broad host range in the genus Streptomyces. One of them (pIJ903) is a shuttle vector for Streptomyces and Escherichia coli. 相似文献
2.
A Brassica nigra genetic linkage map was developed from a highly polymorphic cross analyzed with a set of low copy number Brassica RFLP probes. The Brassica genome is extensively duplicated with eight distinct sets of chromosomal segments, each present in three copies, covering virtually the whole genome. Thus, B. nigra could be descended from a hexaploid ancestor. A comparative analysis of B. nigra, B. oleracea and B. rapa genomes, based on maps developed using a common set of RFLP probes, was also performed. The three genomes have distinct chromosomal structures differentiated by a large number of rearrangements, but collinear regions involving virtually the whole of each the three genomes were identified. The genic contents of B. nigra, B. oleracea and B. rapa were basically equivalent and differences in chromosome number (8, 9 and 10, respectively) are probably the result of chromsome fusions and/or fissions. The strong conservation of overall genic content across the three Brassica genomes mirrors the conservation of genic content observed over a much longer evolutionary span in cereals. However, the rate of chromosomal rearrangement in crucifers is much higher than that observed in cereal genomes. 相似文献
3.
Molecular phylogenies in angiosperm evolution 总被引:8,自引:0,他引:8
Martin W; Lydiate D; Brinkmann H; Forkmann G; Saedler H; Cerff R 《Molecular biology and evolution》1993,10(1):140-162
We have cloned and sequenced cDNAs for the glyceraldehyde-3-phosphate
dehydrogenase of glycolysis, gapC, from a bryophyte, a gymnosperm, and
three angiosperms. Phylogenetic analyses are presented for these data in
the context of other gapC sequences and in parallel with published
nucleotide sequences for the chloroplast encoded gene for the large subunit
of ribulose-1,5-bisphosphate carboxylase/oxygenase (rbcL). Relative-rate
tests were performed for these genes in order to assess variation in
substitution rate for coding regions, along individual plant lineages
studied. The results of both gene analyses suggest that the deepest
dichotomy within the angiosperms separates not magnoliids from remaining
angiosperms, but monocotyledons from dicotyledons, in sharp contrast to
prediction from the Euanthial theory for angiosperm evolution. Furthermore,
these chloroplast and nuclear sequence data taken together suggest that the
separation of monocotyledonous and dicotyledonous lineages took place in
late Carboniferous times [approximately 300 Myr before the present (Mybp)].
This date would exceed but be compatible with the late-Triassic
(approximately 220 Mybp) occurrence of fossil reproductive structures of
the primitive angiosperm Sanmiguelia lewisii.
相似文献
4.
mtDNA diversity in rhesus monkeys reveals overestimates of divergence time and paraphyly with neighboring species 总被引:4,自引:0,他引:4
Reconstructions of the human-African great ape phylogeny by using
mitochondrial DNA (mtDNA) have been subject to considerable debate. One
confounding factor may be the lack of data on intraspecific variation. To
test this hypothesis, we examined the effect of intraspecific mtDNA
diversity on the phylogenetic reconstruction of another Plio- Pleistocene
radiation of higher primates, the fascicularis group of macaque (Macaca)
monkey species. Fifteen endonucleases were used to identify 10 haplotypes
of 40-47 restriction sites in M. mulatta, which were compared with similar
data for the other members of this species group. Interpopulational,
intraspecific mtDNA diversity was large (0.5%- 4.5%), and estimates of
divergence time and branching order incorporating this variation were
substantially different from those based on single representatives of each
species. We conclude that intraspecific mtDNA diversity is substantial in
at least some primate species. Consequently, without prior information on
the extent of genetic diversity within a particular species, intraspecific
variation must be assessed and accounted for when reconstructing primate
phylogenies. Further, we question the reliability of hominoid mtDNA
phylogenies, based as they are on one or a few representatives of each
species, in an already depauperate superfamily of primates.
相似文献
5.
Comparative mapping in Arabidopsis and Brassica, fine scale genome collinearity and congruence of genes controlling flowering time 总被引:6,自引:0,他引:6
Ulf Lagercrantz Joanna Putterill George Coupland Derek Lydiate 《The Plant journal : for cell and molecular biology》1996,9(1):13-20
The model dicotyledonous plant, Arabidopsis thaliana , is closely related to Brassica crop species. It is intended that information concerning the genetic control of basic biological processes in Arabidopsis will be transferable to other species. Genome collinearity and its potential to facilitate the identification of candidate genes in Arabidopsis homologous to genes controlling important agronomic traits in Brassica was investigated. Genetic mapping in B. nigra identified two loci influencing flowering time (FT), with loci on linkage groups 2 and 8 explaining 53% and 12% of the total variation in FT, respectively. The CO gene exerts an important control over FT in A. thaliana , and B. nigra homologues of CO probably also play an important role in regulating FT. B. nigra homologues of CO were identified on linkage groups 2 and 8, the homologue on group 2 was coincident with the major locus controlling FT while the homologue on group 8 was within the 90% confidence interval of the weaker FT gene. The CO homologue on group 2 exhibits abundant allelic variation suggesting that it naturally controls a wide range of flowering times. Fine-scale A. thaliana/B. nigra comparative mapping demonstrated short-range collinearity between the genomes of Arabidopsis and Brassica . Eleven DNA fragments spaced over a 1.5 Mb contig in A. thaliana were used as RFLP probes in B. nigra . Three collinear representations of the A. thaliana contig were identified in B. nigra , with one interrupted by a large chromosomal inversion. Collinearity over this range will allow the resources generated by the Arabidopsis genome project to facilitate map-based cloning in Brassica crops. 相似文献
6.
Comparison of Flowering Time Genes in Brassica Rapa, B. Napus and Arabidopsis Thaliana 总被引:15,自引:0,他引:15
T. C. Osborn C. Kole IAP. Parkin A. G. Sharpe M. Kuiper D. J. Lydiate M. Trick 《Genetics》1997,146(3):1123-1129
The major difference between annual and biennial cultivars of oilseed Brassica napus and B. rapa is conferred by genes controlling vernalization-responsive flowering time. These genes were compared between the species by aligning the map positions of flowering time quantitative trait loci (QTLs) detected in a segregating population of each species. The results suggest that two major QTLs identified in B. rapa correspond to two major QTLs identified in B. napus. Since B. rapa is one of the hypothesized diploid parents of the amphidiploid B. napus, the vernalization requirement of B. napus probably originated from B. rapa. Brassica genes also were compared to flowering time genes in Arabidopsis thaliana by mapping RFLP loci with the same probes in both B. napus and Arabidopsis. The region containing one pair of Brassica QTLs was collinear with the top of chromosome 5 in A. thaliana where flowering time genes FLC, FY and CO are located. The region containing the second pair of QTLs showed fractured collinearity with several regions of the Arabidopsis genome, including the top of chromosome 4 where FRI is located. Thus, these Brassica genes may correspond to two genes (FLC and FRI) that regulate flowering time in the latest flowering ecotypes of Arabidopsis. 相似文献
7.
RFLP mapping in Brassica nigra indicates differing recombination rates in male and female meioses. 总被引:3,自引:0,他引:3
A genetic linkage map of Brassica nigra, comprised of 288 loci in eight linkage groups, was constructed. The linkage groups varied in size from 72 to 159 cM and the total map length was 855 cM. The recurrent parent used in the backcross was extremely heterozygous. This allowed recombination to be estimated separately for female (recurrent parent) meiosis and male (F1) meiosis over a large proportion of the genome. Significant differences between male and female recombination frequencies were observed on all six linkage groups where data was available for both sexes. Enhanced male recombination frequencies were observed that were associated with proterminal regions, while enhanced female recombination frequencies were adjacent to putative centromeres. It is possible that the distinct genotypes of the F1 (male) and recurrent (female) parents contributed to the observed differences in recombination. However, this study emphasizes the need to consider potential sex differences, in both the rate and the position of recombination, when planning genetic experiments and breeding programmes. 相似文献
8.
Blackleg disease of crucifers, caused by the fungus Leptosphaeria maculans, is a major concern to oilseed rape producers worldwide. Brassica species containing the B genome have high levels of resistance to blackleg. Brassica juncea F2 and first-backcross (B1) populations segregating for resistance to a PG2 isolate of L. maculans were created. Segregation for resistance to L. maculans in these populations suggested that resistance was controlled by two independent genes, one dominant and one recessive in nature. A map of the B. juncea genome was constructed using segregation in the F2 population of a combination of restriction fragment length polymorphism (RFLP) and microsatel lite markers. The B. juncea map consisted of 325 loci and was aligned with previous maps of the Brassica A and B genomes. The gene controlling dominant resistance to L. maculans was positioned on linkage group J13 based on segregation for resistance in the F2 population. This position was confirmed in the B1 population in which the resistance gene was definitively mapped in the interval flanked by pN199RV and sB31143F. The provisional location of the recessive gene controlling resistance to L. maculans on linkage group J18 was identified using a subset of informative F2 individuals. 相似文献
9.
10.
Hegedus D Baldwin D O'Grady M Braun L Gleddie S Sharpe A Lydiate D Erlandson M 《Archives of insect biochemistry and physiology》2003,53(1):30-47
The activities of digestive protease within the midgut of Mamestra configurata (bertha armyworm) larvae were examined using specific substrates and protease inhibitors. The bulk of the activity was associated with serine proteases comprising trypsin-, chymotrypsin-, and elastase-like enzymes. At least 10-15 serine protease isozymes were detected using one-dimension gelatin gel electrophoresis. Cysteine or aspartic protease activities were not present; however, amino- and carboxypeptidase activities were associated with the midgut extract. Midgut proteases were active in the pH range of 5.0-12.0 with peaks at pH 7.5 and 11.0. In general, the middle region of the midgut exhibited a higher pH (approximately 8.0) than either the posterior or anterior regions (approximately 7.3-7.7). Moulting larvae possessed a neutral gut pH that was 0.5-1.5 units below that of feeding larvae. Degenerate PCR and expressed sequence tag (EST)-based approaches were used to isolate 30 distinct serine protease encoding cDNAs from a midgut-specific cDNA library including 8 putative trypsins, 9 chymotrypsins, 1 elastase, and 12 whose potential activities could not be determined. cDNAs encoding three amino- and two carboxypeptidases were also identified. Larvae feeding upon artificial diet containing 0.2% soybean trypsin inhibitor experienced a significant delay in development. 相似文献