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991.
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993.
Okiyoneda T Niibori A Harada K Kohno T Michalak M Duszyk M Wada I Ikawa M Shuto T Suico MA Kai H 《Biochimica et biophysica acta》2008,1783(9):1585-1594
Cystic fibrosis (CF) is caused by the mutation in CF transmembrane conductance regulator (CFTR), a cAMP-dependent Cl(-) channel at the plasma membrane of epithelium. The most common mutant, DeltaF508 CFTR, has competent Cl(-) channel function, but fails to express at the plasma membrane since it is retained in the endoplasmic reticulum (ER) by the ER quality control system. Here, we show that calnexin (CNX) is not necessary for the ER retention of DeltaF508 CFTR. Our data show that CNX knockout (KO) does not affect the biosynthetic processing, cellular localization or the Cl(-) channel function of DeltaF508 CFTR. Importantly, cAMP-induced Cl(-) current in colonic epithelium from CNX KO/DeltaF508 CFTR mice was comparable with that of DeltaF508 CFTR mice, indicating that CNX KO failed to rescue the ER retention of DeltaF508 CFTR in vivo. Moreover, we show that CNX assures the efficient expression of WT CFTR, but not DeltaF508 CFTR, by inhibiting the proteasomal degradation, indicating that CNX might stimulate the productive folding of WT CFTR, but not DeltaF508 CFTR, which has folding defects. 相似文献
994.
The cryptic plasmid (pAT) of Agrobacterium tumefaciens was not required for virulence or attachment to plant surfaces. However, mutations in the attC and attG genes located on pAT caused the bacteria to become avirulent and non-attaching on tomato, carrot, and Bryophyllum daigremontiana. This was the case whether the mutation was in the copy of the genes located on pAT or whether it was carried in a second copy of the attA-G operon located on a plasmid in cells that contained a wild-type copy of pAT. Thus attC and attG mutations are dominant negative mutations. The mechanism by which these mutations block attachment and virulence is unknown. 相似文献
995.
Wecht JM Weir JP Goldstein DS Krothe-Petroff A Spungen AM Holmes C Bauman WA 《American journal of physiology. Heart and circulatory physiology》2008,294(1):H190-H197
Direct effects of vasoactive substances on blood pressure can be examined in individuals with tetraplegia due to disruption of descending spinal pathways to sympathetic preganglionic neurons, as cervical lesions interfere with baroreceptor reflex buffering of sympathetic outflow. In this study, we assessed effects of the nitric oxide synthase inhibitor nitro-L-arginine methyl ester (L-NAME) on mean arterial pressure, heart rate, and plasma norepinephrine concentrations in individuals with tetraplegia vs. effects shown in a neurologically intact control group. Seven individuals with tetraplegia and seven age-matched controls received, on separate visits and in the following order, placebo (30 ml normal saline) and 0.5, 1, 2, and 4 mg/kg L-NAME intravenously over 60 min. Supine hemodynamic data were collected, and blood was sampled at the end of each infusion and at 120, 180, and 240 min thereafter. L-NAME increased mean arterial pressure, and the relative increase was greater in the tetraplegia group than in the control group. Heart rate was reduced after L-NAME administration in both groups. L-NAME decreased plasma norepinephrine in the control group but not in the group with tetraplegia. These findings suggest that reflexive sympathoinhibition normally buffers the pressor response to nitric oxide synthase inhibition, an effect that is not evident in individuals with tetraplegia as a result of decentralized sympathetic vasomotor control. 相似文献
996.
Frederique Ponchel Robert J Verburg Sarah J Bingham Andrew K Brown John Moore Andrew Protheroe Kath Short Catherine A Lawson Ann W Morgan Mark Quinn Maya Buch Sarah L Field Sarah L Maltby Aurelie Masurel Susan H Douglas Liz Straszynski Ursula Fearon Douglas J Veale Poulam Patel Dennis McGonagle John Snowden Alexander F Markham David Ma Jacob M van Laar Helen A Papadaki Paul Emery John D Isaacs 《Arthritis research & therapy》2004,7(1):1-13
We previously demonstrated prolonged, profound CD4+ T-lymphopenia in rheumatoid arthritis (RA) patients following lymphocyte-depleting therapy. Poor reconstitution could result either from reduced de novo T-cell production through the thymus or from poor peripheral expansion of residual T-cells. Interleukin-7 (IL-7) is known to stimulate the thymus to produce new T-cells and to allow circulating mature T-cells to expand, thereby playing a critical role in T-cell homeostasis. In the present study we demonstrated reduced levels of circulating IL-7 in a cross-section of RA patients. IL-7 production by bone marrow stromal cell cultures was also compromised in RA. To investigate whether such an IL-7 deficiency could account for the prolonged lymphopenia observed in RA following therapeutic lymphodepletion, we compared RA patients and patients with solid cancers treated with high-dose chemotherapy and autologous progenitor cell rescue. Chemotherapy rendered all patients similarly lymphopenic, but this was sustained in RA patients at 12 months, as compared with the reconstitution that occurred in cancer patients by 3–4 months. Both cohorts produced naïve T-cells containing T-cell receptor excision circles. The main distinguishing feature between the groups was a failure to expand peripheral T-cells in RA, particularly memory cells during the first 3 months after treatment. Most importantly, there was no increase in serum IL-7 levels in RA, as compared with a fourfold rise in non-RA control individuals at the time of lymphopenia. Our data therefore suggest that RA patients are relatively IL-7 deficient and that this deficiency is likely to be an important contributing factor to poor early T-cell reconstitution in RA following therapeutic lymphodepletion. Furthermore, in RA patients with stable, well controlled disease, IL-7 levels were positively correlated with the T-cell receptor excision circle content of CD4+ T-cells, demonstrating a direct effect of IL-7 on thymic activity in this cohort. 相似文献
997.
Christopher M. Richards Ann Reilley Darren Touchell Michael F. Antolin Christina Walters 《Conservation Genetics》2004,5(6):853-859
Seed collections in gene banks are useful for the preservation of wild germplasm, providing inexpensive insurance for species that survive in conventional cold storage (–18 °C). Seeds that cannot survive these conditions must be pretreated with cryoprotectants and stored at liquid nitrogen temperatures, which presents unique technical and methodological challenges. Implicit in this approach is the assumption that these added manipulations do not change the genetic diversity of the preserved collections. We used polymorphic microsatellite markers for an endangered aquatic grass, Texas wild rice (Zizania texana), to conduct a preliminary evaluation of the effects of cryogenic preservation of mature embryos on genetic diversity. Using several statistical approaches, we show that allele frequencies did not change in collections of seeds that underwent cryopreservation (cryoprotected) compared to those samples that was not exposed to cryopreservation (control). The retention of the allelic diversity at the five loci examined suggests that there were no significant changes in genetic diversity due to treatments and that these protocols may be appropriate for ex situ conservation of genetically diverse wild germplasm. 相似文献
998.
Coastal estuaries are useful model systems to study the ecological and evolutionary responses of organisms to highly variable, discontinuous habitats. For this study, the molecular population genetic diversity of the planktonic calanoid copepod Acartia tonsa (Dana, 1849) was described based on DNA sequence variation for a 183 base-pair region of the mitochondrial 16S rRNA gene. Samples of A. tonsa were collected from four estuaries on the Atlantic coast of the USA during 1993 and 1994, one estuary on the Gulf of Mexico coast in 1994, and one site on the Pacific coast of the USA in 1994. Dispersal of A. tonsa was shown to be restricted, with significant population genetic structuring between different estuaries. For all but the closely-adjacent MA and RI samples, frequencies of haplotypes and/or length polymorphisms within one haplotype (caused by insertion/deletion mutations) revealed highly significant genetic differentiation and geographic isolation. Mt16S haplotypes of A. tonsa from Atlantic and Gulf of Mexico estuaries were assorted among four deeply-diverged clades. Haplotypes within each clade differed by <2%, while differences among clades of 10% to 14% approached those between described Acartia species (e.g., 19% to 28% among A. clausi, A. hudsonica, and A. longiremis). Atlantic and Pacific coast samples identified as A. tonsa had no haplotypes in common and genetic differences between haplotypes ranged from 18% to 29%; phylogenetic analysis supported the separation of Pacific coast A. tonsa as a distinct species. We hypothesize that the observed patterns of molecular genetic diversity and structure of A. tonsa resulted from responses to historical climatic variation, including episodic range compression and displacement, and alteration of NW Atlantic coastal and estuarine environments. 相似文献
999.
Mohamed Mohideen Quwailid Alison Hugill Neil Dear Lucie Vizor Sara Wells Emma Horner Shelly Fuller Jessica Weedon Hamish McMath Paul Woodman David Edwards David Campbell Susan Rodger Joanne Carey Ann Roberts Pete Glenister Zuzanna Lalanne Nick Parkinson Emma L. Coghill Richard McKeone Sam Cox John Willan Andy Greenfield David Keays Saffron Brady Nigel Spurr Ian Gray Jackie Hunter Steve D.M. Brown Roger D. Cox 《Mammalian genome》2004,15(8):585-591
N-ethyl-N-nitrosourea (ENU) introduces mutations throughout the mouse genome at relatively high efficiency. Successful high-throughput phenotype screens have been reported and alternative screens using sequence-based approaches have been proposed. For the purpose of generating an allelic series in selected genes by a sequence-based approach, we have constructed an archive of over 4000 DNA samples from individual F1 ENU-mutagenized mice paralleled by frozen sperm samples. Together with our previously reported archive, the total size now exceeds 6000 individuals. A gene-based screen of 27.4 Mbp of DNA, carried out using denaturing high-performance liquid chromatography (DHPLC), found a mutation rate of 1 in 1.01 Mbp of which 1 in 1.82 Mbp were potentially functional. Screening of whole or selected regions of genes on subsets of the archive has allowed us to identify 15 new alleles from 9 genes out of 15 tested. This is a powerful adjunct to conventional mutagenesis strategies and has the advantage of generating a variety of alleles with potentially different phenotypic outcomes that facilitate the investigation of gene function. It is now available to academic collaborators as a community resource. 相似文献
1000.