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991.
992.
John P. Manos 《Biotechnic & histochemistry》1965,40(2):75-77
Removing cultures from roller tubes before staining eliminates the destaining which often occurs when the cells are first stained and then removed by embedding in collodion. The cells are fixed in situ, dehydrated, and covered with collodion (Merk's flexible) for 10 min. The collodion is poured off, the fluid residue lining the tube allowed to dry for 10 min, and the tube is filled with tap water. The collodion cast containing the cells is loosened and removed, cut into strips, placed on slides and blotted into firm contact. The collodion is then dehydrated and dissolved with absolute alcohol followed by a 1:1 mixture of alcohol and ether. The slides can then be rehydrated and stained by conventional methods. 相似文献
993.
994.
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998.
Yuhsi Matuq Pamela S. Adams Nozomu Nishi Hidetaro Yasumitsu John W. Crabb Robert J. Matusik Wallace L. McKeehan 《In vitro cellular & developmental biology. Plant》1989,25(6):581-584
Summary Rat prostate extracts contain an abundant 20–22 kilodalton heparin-binding protein with near identical chromatographic properties,
but only 0.2–1% of the mitogenic activity, of bovine brain heparin-binding growth factor-1 (acidic fibroblast growth factor).
Amino terminal amino acid sequence (met-met-thr-asp-lys-asn-leu-lys-lys-lys-ile-glu-gly-asn-trp-arg-thr-val-tyr-leu-ala-ala-ser-?-val-glu-lys-ile-asn-glu-gly-ser-pro)
and immunochemical analysis revealed that the protein is identical to the androgen-dependent protein “probasin”.
This work was supported in part by NCI grant CA37589 (W. L. M., J. W. C.) and the Medical Research Council of Canada (R. J.
M.). 相似文献
999.
Ilse P. Munyon John F. Hubstenberger Greory C. Phillips 《In vitro cellular & developmental biology. Plant》1989,25(3):293-296
Summary Androgenesis occurred from chile pepper (Capsicum annuum L.) anthers incubated in a continuous warm environment (29° C) with continuous light. Forty plantes and embryoids were retrieved
from anther cultures and anllyzed for isozyme markers. Of these, 35 exhibited a single allele for markers suggesting microspore
origin, while 5 were heterozygous indicating somatic tissue origin. Chromosome numbers were confirmed for 21 plantlets, of
which 16 were haploid and 5 were diploid. However, two plants exhibited a single allele for an isozyme marker but possessed
the diploid chromosome number, suggesting spontaneous doubling. Anther cultures also produced callus. Nearly 92% of the slow-growing
calli sampled were heterozygous for the isozyme marker, suggesting somatic tissue origin. More than 46% of the fast-growing
calli exhibited only one allele for the marker, indicating microspore origin. Callus did not regenerate plantlets. The occurrence
of both heterozygous and homozygous diploid plantlets from pepper anther cultures has important implications for applied breeding
programs. 相似文献
1000.
A simple,rapid protocol for adventitious shoot development from mature cotyledons of glycine max cv bragg 总被引:5,自引:0,他引:5
Seth Mante Ralph Scorza John Cordts 《In vitro cellular & developmental biology. Plant》1989,25(4):385-388
Mature soybean cotyledons (Maturity group VII) were cultured on modified MS containing 0–2.5 μM indole-butyric acid (IBA);
0–10 μM 6-benzylaminopurine (BAP) and 0.7% agar. Embryonic axes of explants were removed prior to culture initiation and cultures
were incubated at 24°C with 45–50 μE. s−1.M−2 of mixed irradiance with 16 h photoperiod. Shoot proliferation occurred at 0–2.5 μM IBA and 5–10 μM BAP, while in the presence
of 2.5 μM IBA alone, only roots developed. Abnormal shoots were produced with 2.5 μM IBA and 5–7.5 μM thidiazuron. Adventitious
shoot development started 7–14 d after culture initiation in the region where the embryonic axis was previously attached to
the cotyledon and shoots were visible within 28 days. The presence of the embryonic axis inhibited shoot morphogenesis. The
shoots were rooted on half strength MS inorganic salts plus vitamins, 2% sucrose, 0.5 μM NAA acid or 2.5–5 μM IBA, or 5–10
μM IAA, and 0.7% agar. Rooted plants were acclimatized under a mist in the greenhouse. This simple, rapid,in vitro adventitious shoot development protocol could be adapted for transformation/regeneration studies in soybean.
Trade and company names are used in the publication solely to provide specific information. Mention of a trade or company
name does not constitute a warranty or an endorsement by the U.S. Department of Agriculture to the exclusion of other products
or organizations not mentioned. 相似文献