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101.
We compared some processes characteristic for both apoptosis and terminal differentiation of epidermal keratinocytes. It can be proposed that nonapoptotic programmed cell death takes place during differentiation of keratinocytes. Apoptosis and terminal differentiation of keratinocytes appear to be different events but some similar molecular mechanisms are involved in both processes.__________Translated from Ontogenez, Vol. 36, No. 2, 2005, pp. 85–89.Original Russian Text Copyright © 2005 by Terskikh, Vasilev. 相似文献
102.
A. V. Vasiliev P. V. Makarov O. S. Rogovaya R. A. Gundorova V. V. Terskikh 《Biology Bulletin》2005,32(1):1-3
We propose to treat deep corneal burns by grafting a living stromal equivalent, since keratocyte death and stromal destruction are the main factors of ulceration and destruction of the eye. A technique was developed for isolation and grafting a living stroma equivalent. Twenty one patients with deep corneal defects were treated. A stable therapeutic effect was observed in 95% cases. The advantage of the developed method is a partial recovery of affected corneal transparency.Translated from Izvestiya Akademii Nauk, Seriya Biologicheskaya, No. 1, 2005, pp. 5–8.Original Russian Text Copyright © 2005 by Vasiliev, Makarov, Rogovaya, Gundorova, Terskikh 相似文献
103.
We compared some processes characteristic for both apoptosis and terminal differentiation of epidermal keratinocytes. It can be proposed that nonapoptotic programmed cell death takes place during differentiation of keratinocytes. Apoptosis and terminal differentiation of keratinocytes appear to be different processes but some similar molecular mechanisms are involved in these processes. 相似文献
104.
Balakirev ES Chechetkin VR Lobzin VV Ayala FJ 《Molecular biology and evolution》2005,22(10):2063-2072
We perform spectral entropy and GC content analyses in the beta-esterase gene cluster, including the Est-6 gene and the psiEst-6 putative pseudogene, in seven species of the Drosophila melanogaster species subgroup. psiEst-6 combines features of functional and nonfunctional genes. The spectral entropies show distinctly lower structural ordering for psiEst-6 than for Est-6 in all species studied. Our observations agree with previous results for D. melanogaster and provide additional support to our hypothesis that after the duplication event Est-6 retained the esterase-coding function and its role during copulation, while psiEst-6 lost that function but now operates in conjunction with Est-6 as an intergene. Entropy accumulation is not a completely random process for either gene. Structural entropy is nucleotide dependent. The relative normalized deviations for structural entropy are higher for G than for C nucleotides. The entropy values are similar for Est-6 and psiEst-6 in the case of A and T but are lower for Est-6 in the case of G and C. The GC content in synonymous positions is uniformly higher in Est-6 than in psiEst-6, which agrees with the reduced GC content generally observed in pseudogenes and nonfunctional sequences. The observed differences in entropy and GC content reflect an evolutionary shift associated with the process of pseudogenization and subsequent functional divergence of psiEst-6 and Est-6 after the duplication event. 相似文献
105.
We studied formation of epithelial cysts during cultivation of the primary keratinocytes in a collagen gel. Two stages--epithelial spheroid and cysts--can be recognized in the histogenesis process. Keratinocyte migration prevails at the initial stages of morphogenesis. The stage of spheroid can be described by active cell proliferation. Stratification of spheroid epithelium takes place at the stage of epithelial cysts, while the rate of keratinocytes proliferation decreases. Formation of epithelial cysts is induced by morphogene(s) of mesenchymal origin. The obtained data indicate partial dissociation of keratinocyte proliferation and migration during cytogenesis. 相似文献
106.
Deirdre M Murphy Vasily V Ivanenkov Terence L Kirley 《The Journal of biological chemistry》2002,277(8):6162-6169
Cysteine-to-serine mutations were constructed to test the functional and structural significance of the three non-extracellular cysteine residues in ecto-nucleoside-triphosphate diphosphohydrolase 3 (eNTPDase3). None of these cysteines were found to be essential for enzyme activity. However, Cys(10), located on the short N-terminal cytoplasmic tail, was found to be responsible for dimer formation occurring via oxidation during membrane preparation as well as for dimer cross-linking resulting from exogenously added sulfhydryl-specific cross-linking agents. The resistance to further cross-linking of these dimers into higher order oligomers by lysine-specific cross-linkers suggests that this enzyme may form its native tetrameric structure as a "dimer of dimers" with nonequivalent interactions between subunits. Cys(501), located in the hydrophobic C-terminal membrane-spanning domain of eNTPDase3, was found to be the site of chemical modification by a sulfhydryl-specific reagent, p-chloromercuriphenylsulfonic acid (pCMPS), leading to inhibition of enzyme activity. The effect of pCMPS was negligible after dissociation of the enzyme into monomers by Triton X-100, suggesting that the mechanism of inhibition is dependent on the oligomeric structure. Because Cys(501) is accessible for modification by the membrane-impermeant reagent pCMPS, we hypothesize that eNTPDase3 (and possibly other eNTPDases) contains a water-filled crevice allowing access of water and hydrophilic compounds to at least part of the protein's C-terminal membrane-spanning helix. 相似文献
107.
108.
Hepatic and pancreatic effects of polyenoylphosphatidylcholine in rats with alloxan-induced diabetes
Vyacheslav Buko Oxana Lukivskaya Vasily Nikitin Yury Tarasov Lev Zavodnik Alexandr Borodinsky Bronislava Gorenshtein Barbara Janz Karl-Josef Gundermann Rainer Schumacher 《Cell biochemistry and function》1996,14(2):131-137
Polyenoylphosphatidylcholine (PPC: 100 or 300 mg kg?1 b.w., by gastric intubation for 30 days) produced a clearcut protection of the liver of rats treated with alloxan (150 mg kg?1 b.w., i.p.). The liver of rats treated with alloxan was characterized by hydropic dystrophy and lymphocytic infiltrations. Treatment with alloxan increased serum γ-GT and ALAT activities. The liver structure of rats treated with PPC did not differ from the liver of control animals. PPC normalized the biochemical abnormalities caused by the diabetes. The number of pancreatic islets and β/α; cell ratio decreased in the diabetic rats. A number of β-cells in this group did not contain granules. PPC prevented the decrease in the number of islets and the β/α; cell ratio in the pancreas of the diabetic rats. The intensity of staining of β-cell granules in the pancreas of PPC-treated rats had a position intermediate between the control and diabetic groups. Alloxan increased the blood glucose content where treatment with PPC decreased this. The results suggest that PPC acts as a cytoprotector in the liver and pancreas of rats with experimental diabetes induced by alloxan. 相似文献
109.