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Dorothea Bedigian Sebsebe Demissew Paul Gepts Daniel F. Austin Neil A. Harriman John Klock Sarah Walshaw John Richard Stepp Beverly J. Brown Julie Polley David Winston Barbara Pickersgill Patrick Van Damme Nina L. Etkin Beronda L. Montgomery Linda Perry Stephen E Siebert Robert J. Krueger Kathleen McConnell Wendy Applequist Mary Theresa Bonhage-Freund Karol Chandler-Ezell 《Economic botany》2005,59(4):395-412
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Daniel F. Austin Richard Felger Karol Chandler-Ezell Michael J. Balick Kurt Allerslev Reynertson Alfredo Gomez-Beloz My Lien T. Nguyen Rob Dean Neil A. Harriman Dorothea Bedigian Mary Theresa Bonhage-Freund Wendy Applequist Linda M. Lyon John Klock My Lien T. Nguyen 《Economic botany》2005,59(2):197-209
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Mitochondrial protein import motor: differential role of Tim44 in the recruitment of Pam17 and J-complex to the presequence translocase 总被引:1,自引:0,他引:1 下载免费PDF全文
Hutu DP Guiard B Chacinska A Becker D Pfanner N Rehling P van der Laan M 《Molecular biology of the cell》2008,19(6):2642-2649
The presequence translocase of the mitochondrial inner membrane (TIM23 complex) mediates the import of preproteins with amino-terminal presequences. To drive matrix translocation the TIM23 complex recruits the presequence translocase-associated motor (PAM) with the matrix heat shock protein 70 (mtHsp70) as central subunit. Activity and localization of mtHsp70 are regulated by four membrane-associated cochaperones: the adaptor protein Tim44, the stimulatory J-complex Pam18/Pam16, and Pam17. It has been proposed that Tim44 serves as molecular platform to localize mtHsp70 and the J-complex at the TIM23 complex, but it is unknown how Pam17 interacts with the translocase. We generated conditional tim44 yeast mutants and selected a mutant allele, which differentially affects the association of PAM modules with TIM23. In tim44-804 mitochondria, the interaction of the J-complex with the TIM23 complex is impaired, whereas unexpectedly the binding of Pam17 is increased. Pam17 interacts with the channel protein Tim23, revealing a new interaction site between TIM23 and PAM. Thus, the motor PAM is composed of functional modules that bind to different sites of the translocase. We suggest that Tim44 is not simply a scaffold for binding of motor subunits but plays a differential role in the recruitment of PAM modules to the inner membrane translocase. 相似文献
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Polysialic acid in the plasticity of the developing and adult vertebrate nervous system 总被引:1,自引:0,他引:1
Rutishauser U 《Nature reviews. Neuroscience》2008,9(1):26-35
Polysialic acid (PSA) is a cell-surface glycan with an enormous hydrated volume that serves to modulate the distance between cells. This regulation has direct effects on several cellular mechanisms that underlie the formation of the vertebrate nervous system, most conspicuously in the migration and differentiation of progenitor cells and the growth and targeting of axons. PSA is also involved in a number of plasticity-related responses in the adult CNS, including changes in circadian and hormonal patterns, adaptations to pain and stress, and aspects of learning and memory. The ability of PSA to increase the plasticity of neural cells is being exploited to improve the repair of adult CNS tissue. 相似文献
129.
Choudhury K Zander D Kube M Reinhardt R Clos J 《International journal for parasitology》2008,38(12):1411-1423
Resistance to treatment is a growing problem in efforts to control Old World leishmaniasis. Parasites resistant to new therapeutics such as miltefosine have not been reported from the field yet but based on experimental evidence, may appear soon. Therefore, we attempted to identify genetic markers that may correlate with miltefosine resistance. Using a functional cloning approach, we have isolated a gene from Leishmania infantum that, upon over-expression, confers protection not only against miltefosine, but also against Sb(III), the active principle of anti-leishmanial antimonials. The gene encodes a very large putative polypeptide of 299 kDa that shows no similarities to known proteins or functional motifs. Database mining and karyotyping experiments suggest that in L. infantum this gene is part of a 44-kbp duplicated region that is found on two separate chromosomes, CHR08 and CHR29. 相似文献
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Stephen D. Dertinger Yuhchyau Chen Richard K. Miller Kelly J. Brewer Therese Smudzin Dorothea K. Torous Nikki E. Hall Kristine A. Olvany Francis G. Murante Carol R. Tometsko 《Mutation Research - Genetic Toxicology and Environmental Mutagenesis》2003,542(1-2):77-87
The frequency of micronuclei (also known as Howell–Jolly bodies) in peripheral blood erythrocytes of humans is extremely low due to the efficiency with which the spleen sequesters and destroys these aberrant cells. In the past, this has precluded erythrocyte-based analyses from effectively measuring chromosome damage. In this report, we describe a high-throughput, single-laser flow cytometric system for scoring the incidence of micronucleated reticulocytes (MN-RET) in human blood. Differential staining of these cells was accomplished by combining the immunochemical reagent anti-CD71-FITC with a nucleic acid dye (propidium iodide plus RNase). The immunochemical reagent anti-CD42b-PE was also incorporated into the procedure in order to exclude platelets which can interfere with analysis. This analytical system was evaluated with blood samples from ten healthy volunteers, one splenectomized subject, as well as samples collected from nine cancer patients before and over the course of radio- or chemotherapy. The mean frequency of MN-RET observed for the healthy subjects was 0.09%. This value is nearly two orders of magnitude higher than frequencies observed in mature erythrocytes, and is approximately half the MN-RET frequency observed for the splenectomized subject (0.20%). This suggests that the spleen’s effect on micronucleated cell incidence can be minimized by restricting analyses to the youngest (CD71-positive) fraction of reticulocytes. Furthermore, MN-RET frequencies were significantly elevated in patients undergoing cancer therapy. Collectively, these data establish that micronuclei can be quantified in human peripheral blood reticulocytes with a single-laser flow cytometer, and that these measurements reflect the level of chromosome damage which has occurred in red marrow space. 相似文献