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101.
H. Ueda Takeshi Baba Nobuo Terada Yasuko Kato Shigeo Tsukahara Shinichi Ohno 《Histochemistry and cell biology》1997,108(3):243-248
It is known that the retina contains the protein dystrophin in the ribbon synapse, but the ultrastructural analysis is not
yet fully elucidated. Our previous study reported that dystrophin is localized under the rod cell membranes in rat retinas.
In the present study, we have investigated the relationship between dystrophin-rich regions of rod cell membranes and other
neuronal processes in mouse retinas with a monoclonal antibody raised against the human dystrophin C-terminus. Immunoblotting,
immunofluorescence stainings, and immunoelectron microscopy were employed. Immunoblotting analysis indicated that mouse retinas
possessed some of the dystrophin isoforms of approximately 260 kDa, 140 kDa, and 70 kDa molecular weight. Confocal images
showed a punctate appearance in the outer plexiform layer, as previously described. Immunoelectron microscopy showed that
dystrophin immunoreactive products were always observed at submembranous dense regions of the rod spherule abutting bipolar
processes. These results suggest that retinal dystrophin may be closely involved in signal transmission from rods to bipolar
cells.
Accepted: 7 May 1997 相似文献
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Matsumoto Yuuki Kaneita Yoshitaka Jike Maki Osaki Yoneatsu Kanda Hideyuki Higuchi Susumu Itani Osamu Otsuka Yuichiro 《Sleep and biological rhythms》2021,19(3):325-336
Sleep and Biological Rhythms - This study aimed to assess the success of the Japanese government’s “Early to bed, early to rise, and don’t forget your breakfast” (EB, ER,... 相似文献
107.
Siriporn Pota Sinchai Chatasiri Yoshitaka Ono Yuichi Yamaoka Makoto Kakishima 《Mycoscience》2013,54(1):19-28
Phakopsora meliosmae, a macrocyclic autoecious rust fungus, is reported to occur on several Meliosma species widely distributed in Asia. Despite the apparent broad host range, a recent molecular phylogenetic study indicated that two rust populations on Meliosma myriantha and Meliosma tenuis respectively in Japan were biologically distinct. To clarify the biological and taxonomic relationships of these populations, cross inoculations and comparative morphological examinations were carried out. Cross inoculations using basidiospores and aeciospores confirmed the macrocyclic, autoecious nature of the life cycle in both rust populations and showed that the two populations were distinct in their host specificity. Furthermore, they were found to be distinct in the structure of the aecial peridium surface, the size and wall thickness of uredinial paraphyses, and the urediniospore size and shape. Consequently, the fungal population on M. tenuis is taxonomically separated from P. meliosmae originally proposed for the fungus on M. myriantha. A new name, Phakopsora orientalis, is proposed for the fungus on M. tenuis. 相似文献
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Takuya Kitamura Tatsuro NaganumaKensuke Abe Kanae NakaharaYusuke Ohno Akio Kihara 《Biochimica et Biophysica Acta (BBA)/Molecular and Cell Biology of Lipids》2013,1831(8):1395-1401
The accumulation of reactive aldehydes is implicated in the development of several disorders. Aldehyde dehydrogenases (ALDHs) detoxify aldehydes by oxidizing them to the corresponding carboxylic acids. Among the 19 human ALDHs, ALDH3A2 is the only known ALDH that catalyzes the oxidation of long-chain fatty aldehydes including C16 aldehydes (hexadecanal and trans-2-hexadecenal) generated through sphingolipid metabolism. In the present study, we have identified that ALDH3B1 is also active in vitro toward C16 aldehydes and demonstrated that overexpression of ALDH3B1 restores the sphingolipid metabolism in the ALDH3A2-deficient cells. In addition, we have determined that ALDH3B1 is localized in the plasma membrane through its C-terminal dual lipidation (palmitoylation and prenylation) and shown that the prenylation is required particularly for the activity toward hexadecanal. Since knockdown of ALDH3B1 does not cause further impairment of the sphingolipid metabolism in the ALDH3A2-deficient cells, the likely physiological function of ALDH3B1 is to oxidize lipid-derived aldehydes generated in the plasma membrane and not to be involved in the sphingolipid metabolism in the endoplasmic reticulum. 相似文献
110.
Yoshiro Naito Hisashi Sawada Makiko Oboshi Aya Fujii Shinichi Hirotani Toshihiro Iwasaku Yoshitaka Okuhara Akiyo Eguchi Daisuke Morisawa Mitsumasa Ohyanagi Takeshi Tsujino Tohru Masuyama 《PloS one》2013,8(10)
Although iron is reported to be associated with the pathogenesis of chronic kidney disease, it is unknown whether iron participates in the pathophysiology of nephrosclerosis. Here, we investigate whether iron is involved in the development of hypertensive nephropathy and the effects of iron restriction on nephrosclerosis in salt- loaded stroke-prone spontaneously hypertensive rats (SHRSP). SHRSP were given either a normal or high-salt diet for 8 weeks. Another subset of SHRSP were fed a high-salt with iron-restricted diet. SHRSP given a high-salt diet developed severe hypertension and nephrosclerosis. As a result, survival rate was decreased after 8 weeks diet. Importantly, massive iron accumulation and increased iron content were observed in the kidneys of salt-loaded SHRSP, along with increased superoxide production, urinary 8-Hydroxy-2′-deoxyguanosine excretion, and urinary iron excretion; however, these changes were markedly attenuated by iron restriction. Of interest, expression of cellular iron transport proteins, transferrin receptor 1 and divalent metal transporter 1, was increased in the tubules of salt-loaded SHRSP. Notably, iron restriction attenuated the development of severe hypertension and nephrosclerosis, thereby improving survival rate in salt-loaded SHRSP. Taken together, these results suggest a novel mechanism by which iron plays a role in the development of hypertensive nephropathy and establish the effects of iron restriction on salt-induced nephrosclerosis. 相似文献