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151.
Summary In vertebrae of genetically selected sucrose-fed diabetic rats a statistically significant bone deficit was found after diabetes had been present for about 8 months. No osteopenia was observed in diabetic rats following treatment with estrogenic hormone for 5–7 months. The development of osseous centers in the end plates of the vertebrae was retarded in diabetic rats, but was about normal in diabetic rats given estrogen.—No differences were noted in the growth zones or in the tendency to develop articular lesions in rats of the various groups. Possible differences in the amount of GAG in intervertebral discs of diabetic and non-diabetic rats respectively await further confirmation.These investigations were aided by grant No. 2 RO1 EYO 1837-03, of the Institute of Arthritis and Metabolic Disease, National Institutes of Health, Bethesda, Maryland, USA.We are indebted to Professor Dr J. Rüttner, Institute of Pathology, University of Zürich, for his permission to use the calculator. 相似文献
152.
In vivo generation of hydrogen peroxide from 6-hydroxydopamine 总被引:1,自引:0,他引:1
153.
Antigenic determinants in amyloid deposits 总被引:4,自引:0,他引:4
154.
155.
PITC derivatives in amino acid analysis 总被引:10,自引:0,他引:10
Refined methods for separating PTC-amino acids on reverse phase columns may pose a challenge to traditional ion exchange techniques. 相似文献
156.
Meiotic arrest and aneuploidy in MLH3-deficient mice 总被引:22,自引:0,他引:22
Lipkin SM Moens PB Wang V Lenzi M Shanmugarajah D Gilgeous A Thomas J Cheng J Touchman JW Green ED Schwartzberg P Collins FS Cohen PE 《Nature genetics》2002,31(4):385-390
MutL homolog 3 (Mlh3) is a member of a family of proteins conserved during evolution and having dual roles in DNA mismatch repair and meiosis. The pathway in eukaryotes consists of the DNA-binding components, which are the homologs of the bacterial MutS protein (MSH 2 6), and the MutL homologs, which bind to the MutS homologs and are essential for the repair process. Three of the six homologs of MutS that function in these processes, Msh2, Msh3 and Msh6, are involved in the mismatch repair of mutations, frameshifts and replication errors, and two others, Msh4 and Msh5, have specific roles in meiosis. Of the four MutL homologs, Mlh1, Mlh3, Pms1 and Pms2, three are involved in mismatch repair and at least two, Pms2 and Mlh1, are essential for meiotic progression in both yeast and mice. To assess the role of Mlh3 in mammalian meiosis, we have generated and characterized Mlh3(-/-) mice. Here we show that Mlh3(-/-) mice are viable but sterile. Mlh3 is required for Mlh1 binding to meiotic chromosomes and localizes to meiotic chromosomes from the mid pachynema stage of prophase I. Mlh3(-/-) spermatocytes reach metaphase before succumbing to apoptosis, but oocytes fail to complete meiosis I after fertilization. Our results show that Mlh3 has an essential and distinct role in mammalian meiosis. 相似文献
157.
A rapidly moving crack in a brittle material is often idealized as a one-dimensional object with a singular tip, moving through a two-dimensional material. However, in real three-dimensional materials, tensile cracks form a planar surface whose edge is a rapidly moving one-dimensional singular front. The dynamics of these fronts under repetitive interaction with material inhomogeneities (asperities) and the morphology of the fracture surface that they create are not yet understood. Here we show that perturbations to a crack front in a brittle material result in long-lived and highly localized waves, which we call 'front waves' These waves exhibit a unique characteristic shape and propagate along the crack front at approximately the Rayleigh wave speed (the speed of sound along a free surface). Following interaction, counter-propagating front waves retain both their shape and amplitude. They create characteristic traces along the fracture surface, providing cracks with both inertia and a new mode of dissipation. Front waves are intrinsically three-dimensional, and cannot exist in conventional two-dimensional theories of fracture. Because front waves can transport and distribute asperity-induced energy fluctuations throughout the crack front, they may help to explain how cracks remain a single coherent entity, despite repeated interactions with randomly dispersed asperities. 相似文献
158.
J P Steiner T M Dawson M Fotuhi C E Glatt A M Snowman N Cohen S H Snyder 《Nature》1992,358(6387):584-587
The immunophilins cyclophilin and FK506 binding protein (FKBP) are small, predominantly soluble proteins that bind the immunosuppressant drugs cyclosporin A and FK506, respectively, with high affinity, and which seem to mediate their pharmacological actions. The Ca(2+)-dependent protein phosphatase, calcineurin, binds the cyclophilin-cyclosporin A and FKBP-FK506 complexes, indicating that calcineurin might mediate the actions of these drugs. A physiological role for the immunophilins in the nervous system is implied by a close homology between the structure of NINA A, a protein in the neural retina of Drosophila, and cyclophilin, as well as by the high density of FKBP messenger RNA in brain tissue. Here we report that the levels of FKBP and mRNA in rat brain are extraordinarily high and that their regional localization is virtually identical to that of calcineurin, indicating that there may be a physiological link between calcineurin and the immunophilins. We also show that at low concentrations FK506 and cyclosporin A enhance the phosphorylation of endogenous protein substrates in brain tissue and in intact PC12 cells, indicating that these drugs may inhibit phosphatase activity by interacting with the immunophilin-calcineurin complexes. 相似文献
159.
Dissection of the protein kinase cascade by which nerve growth factor activates MAP kinases. 总被引:42,自引:0,他引:42
Mitogen activated protein (MAP) kinases (MAPKs) are a family of protein-serine/threonine kinases activated as an early intracellular response to a variety of hormones and growth factors. They are unique in requiring both serine/threonine and tyrosine phosphorylation to become active and are the only examples of protein-serine/threonine kinases activated by tyrosine phosphorylation. Nerve growth factor (NGF) promotes differentiation of phaeochromocytoma (PC12) cells, which respond by conversion within hours from a chromaffin-like to a sympathetic neuron-like phenotype. NGF stimulation of PC12 cells increases the activity of two protein kinases by greater than 20-fold within minutes, both strikingly similar to MAPKs. They are inactivated by either protein-tyrosine phosphatases or the protein-serine/threonine phosphatase termed protein phosphatase 2A (ref. 8), they activate protein S6 kinase-II (refs 9, 10), and they phosphorylate identical threonine residues on myelin basic protein (our unpublished results) to those phosphorylated by other MAPKs. Immunological data indicate that these protein kinases, termed peak-I and peak-II (Fig. 1a) are probably ERK2 and ERK1, respectively, two widely expressed MAPK isoforms. Here we identify the 'MAP kinase kinases' (MAPKKs) in PC12 cells which are activated by NGF and report that MAPKKs are dependent on serine/threonine phosphorylation for activity and promote phosphorylation of serine/threonine and tyrosine residues on MAPKs. 相似文献
160.
M. M. Cohen Claudia Hastings C. F. Nadler D. M. Lay 《Cellular and molecular life sciences : CMLS》1971,27(9):1084-1086
Résumé Des cultures obtenues à partir d'hybrides femelles entre deux espèces deMeriones à 44 chromosomes et différant par l'acrocentrie (M. shawi) ou la métacentrie (M. libycus) de l'X ont permis l'étude de clones cellulaires. C'est alors tantôt l'X métacentrique, tantôt l'X acrocentrique qui se révèle inactivé («latereplicating»). Bien que la proportion 1/1, significative d'une inactivation due uniquement au hasard, n'ait pas été rigoureusement observée, ces résultats sont nettement en faveur de l'hypothèse deLyon.
Supported by Project No. 417 from the U.S. Children's Bureau and National Science Foundation (Grant No. GB 5676X). 相似文献
Supported by Project No. 417 from the U.S. Children's Bureau and National Science Foundation (Grant No. GB 5676X). 相似文献