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Zusammenfassung Die an Innenepidermiszellen der Zwiebelschuppe vonAllium cepa zu beobachtenden schlauchförmigen intraplasmatischen Vakuolen, in der vorliegenden Arbeit kurz als Schläuche bezeichnet, werden näher untersucht. Sie heben sich im Protoplasma im Phasenkontrast als nichtkontrastierte, massearme Zonen ab. Diese Gebilde werden als Elemente des endoplasmatischen Retikulums (ER) angesprochen. Vergleichende Literaturstudien bekräftigen diese Ansicht.An tierischen Zellen wurden mehrfach im positiven Phasenkontrast dunkle, längliche oder netzförmige Gebilde als Elemente des ER erkannt. Die bei Pflanzenzellen auftretenden, äußerlich sehr ähnlichen Gebilde sind dagegen Plasmaleisten. Sie entstehen zwischen vergrößerten vakuolenartigen Elementen des ER.In jedem Fall ist es notwendig, streng zwischen dem ER sensu strictu, welches aus den Membranen und der von diesen umschlossenen intrazisternalen Phase (IZP) besteht, und dem Grundplasma, der extrazisternalen Phase (EZP), in der die Organellen liegen, zu unterscheiden. Im Lichtmikroskop (Phasenkontrast) werden an erwachsenen Pflanzenzellen die Membranen des ER nicht aufgelöst. Wenn die Membranen aber auseinanderweichen und die IZP durch Wasseraufnahme ein größeres Volumen einnimmt, kann man den Kontrastunterschied zwischen IZP und EZP sehen.Wir danken den optischen Werken C. Reichert A. G., Wien, für die leihweise Überlassung einer phasenoptischen Ausrüstung und der Firma Werfft-Chemie, Wien, für das Tetracyclin-Präparat Achromycin- Lederle. 相似文献
54.
Jürgen Beckmann Armin Mehlich Werner Schröder Herbert R. Wenzel Harald Tschesche 《The protein journal》1989,8(1):101-113
The semisynthesis of homologues of aprotinin, the bovine pancreatic trypsin inhibitor, is described. The P1 lysine15 residue was replaced by two methods. The first procedure, which consisted of two enzymatic steps for the incorporation of other amino acids has previously been described. The second approach consisted of six steps of both enzymatic and chemical nature. The modified inhibitor, in which the lysine15-alanine16 peptide bond is hydrolyzed, was used as the starting material. All carboxyl groups of the modified inhibitor were esterified with methanol; the lysine15 methylester group was then selectively hydrolyzed. Afterward, lysine15 itself was split off. Arginine, glutamic acid, methionine, andl-2-aminohexanoic acid (norleucine, Nle) were incorporated using water-soluble carbodiimide combined with an acylation catalyst. The methylester group was used to prevent polymerization. The reactive-site peptide bonds were resynthesized using either chymotrypsin or trypsin. 相似文献
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Carl Harald Janson Mahmood Jeddi Tehrani H»kan Mellstedt Hans Wigzell 《Cancer immunology, immunotherapy : CII》1989,28(3):225-232
Summary A murine anti-idiotypic monoclonal antibody (mAb), F1, (IgG2a) was produced against the variable part of the T-cell receptor for antigen (Ti, /) on the tumor cells of a patient with T-cell chronic lymphatic leukemia (CD3+, 8+, 4–). The molecular weight of the protein reactive with mAb F1, comodulation and coprecipitation with anti-CD3 antibody, and the restricted tumor-cell reactivity strongly support the anti-idiotypic nature of mAb F1. MAb F1 also stained 4% of peripheral blood lymphocytes of healthy donors. MAb F1 did not stimulate the tumor cells to DNA synthesis, but stimulated a fraction of the normal peripheral blood lymphocytes, mAb F1 did not mediate antibody-dependent cellular cytotoxicity or complement lysis to any significant degree in vitro. Three infusions of 1–10 mg anti-idiotypic mAb were given over a period of 4 weeks. The plasma half-life for mAb F1 was 3 h in the first 2 h after infusion and 44 h from 2 h to 120 h after infusion. After each treatment a rapid decrease of circulating tumor cells was seen. During the observation period an 80% reduction of the total circulating tumor cells was noted. After the second infusion, IgM and IgG antimouse antibodies were detected. Side-effects from therapy were fever, chills, nausea, vomiting, diarrhea, tachycardia, increase in systolic blood pressure and shortness of breath. Thus, in T-cell malignancies a major reduction of circulating tumor cells can be accomplished by low doses of anti-idiotypic mAb. Anti-idiotypic mAb might be a therapeutic agent of significant importance. 相似文献
57.
T S Elton C C Stephan G R Taylor M G Kimball M M Martin J N Durand S Oparil 《Biochemical and biophysical research communications》1992,184(2):1067-1073
A rat genomic Southern blot, probed with a type I angiotensin II receptor probe, demonstrated that two highly homologous type I angiotensin II receptors were present. A rat genomic library was subsequently screened and four clones were isolated. From restriction mapping, differential hybridization, polymerase chain reaction amplification and sequence analyses we have determined that there are two unique type I angiotensin II receptor genes. The first of these genes corresponds to the published rat vascular complementary DNA sequence; the second, corresponds to a novel receptor not previously described. 相似文献
58.
Jan Aaseth Harald Frey Eystein Glattre Gunnar Norheim Jetmund Ringstad Yngvar Thomassen 《Biological trace element research》1990,24(2-3):147-152
Recently, we found that prediagnostic serum selenium concentration was significantly lower for cases developing thyroid cancer (n=43) than for controls. We assumed that redistribution of serum selenium into the affected tissue took place in the prediagnostic period. The present study was carried out to determine the physiological concentration of selenium in the thyroid, since very few data are available in the literature. The concentrations of selenium in the thyroid (n=45) and liver samples from Norwegians who had died because of acute illness or accidents were determined by hydride generation atomic absorption spectrometry. The mean selenium concentration was found to be 0.72±0.44 μg/g in the thyroid and 0.45±0.11 μg/g in the liver tissue. The surprisingly high concentration of selenium in apparently normal thyroids indicates that selenium has important functions in this organ. The remarkably broad range, together with the observation that no significant correlation exists between thyroid and liver concentrations, suggest that factors other than the selenium status are important determinants for the selenium concentration in the thyroid gland. This observation is consistent with our hypothesis that in carcinogenesis, prediagnostic processes influence the serum-/thyroid-ratio of selenium. 相似文献
59.
60.
Roelof-Jan Oostra Stephan Kemp Pieter A. Bolhuis Elisabeth M. Sleeker-Wagemakers 《Human genetics》1996,97(4):500-505
Leber’s hereditary optic neuropathy (LHON) is a maternally inherited disorder of the optic nerves. It has been proposed that
the specific mutations in the mitochondrial DNA (mtDNA) that are associated with LHON require and X-chromosomally encoded
permissive factor in order to become expressed. This would explain both the preponderance of male patients and the fact that
most carriers of specific mtDNA mutations remain unaffected. Although linkage studies have been negative so far, the existence
of such a factor has not been ruled out. We investigated the genealogical data of 24 large LHON pedigrees and concluded that
the presumed X-linked factor would be recessively inherited and that at least 57% of the affected females would be heterozygous.
Therefore, these females must be the victim of nonrandom X-chromosomal inactivation (skewed lyonization). However, analysis
of X-chromosomal methylation patterns in 16 LHON-affected females revealed substantial skewing in only 15%–20% of cases, which
is not significantly different from the patterns in 49 controls. Moreover, we found the frequency of LHON in daughters of
affected heterozygous females to be twice to three times as high as in daughters of unaffected heterozygous females, which
cannot be explained by an X-chromosomally inherited factor. We conclude that the results of our investigations do not support
the hypothesis that LHON is a digenic disease with an X-linked factor being the main cause of loss of vision in the presence
of relevant mtDNA mutations.
Received: 1 June 1995 / Revised: 20 September 1995 相似文献