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831.
Louis Faso Richard S. Trowbridge Wei Quan Xiu-Lan Yao Edmund C. Jenkins Alma Maciulis Thomas D. Bunch Henry M. Wisniewski 《In vitro cellular & developmental biology. Animal》1994,30(4):226-235
Summary A strain of cerebral endothelial cells was established from isolated cortical microvessels of caprine brain. These cells,
which are referred to as ECl cells, can be routinely subcultured to 32 passages without the loss of differentiated morphologic
and immunologic traits. The ability to routinely subculture ECl cells is an important asset, given that isolated cerebral
endothelial cells in mammals generally lose their differentiated traits after only 2 to 3 passages.
ECl cells were shown to contain Factor VIII-related antigen, which is a specific marker for cells of endothelial origin. ECl
cells morphologically demonstrated a scarcity of pinocytotic vesicles on their apical surfaces, a lack of trans-cytoplasmic
vesicles, and the ability to form in culture confluent monolayers with tight junctional complexes. Therefore, ECl cells possess
specific antigenic and ultrastructural features which classify them as being small vessel endothelial cells of the blood-brain
barrier type. Cytogenetic evaluation of ECl cells demonstrated a normal female goat 60,XX karyotype and confirmed the apparent
non-transformed nature of ECl cells due to the lack of chromosome abnormalities or rearrangements. Using scanning electron
microscopy, ECl cells were also shown to form confluent monolayers on mixed nitrocellulose filters, a feature that will enable
the development of an in vitro system to study trans-endothelial transport. Given that ECl cells are readily subcultured and
grow well on nitrocellulose filters, and that they resemble cerebral endothelium in vivo, it seems evident that ECl cells
can be used as a versatile model for the study of blood-brain barrier function, regulation, and pathology. 相似文献
832.
Neil C. Talbot Vernon G. Pursel Caird E. Rexroad Jr. Thomas J. Caperna Anne M. Powell Roger T. Stone 《In vitro cellular & developmental biology. Animal》1994,30(12):851-858
Summary The secondary culture of non-transformed parenchymal hepatocytes has not been possible. STO feeder cell-dependent secondary
cultures of fetal pig hepatocytes were established by colony isolation from primary cultures of 26-d fetal livers. The liver
cells had the typical polygonal morphology of parenchymal hepatocytes. They also spontaneously differentiated to form small
biliary canaliculi between individual cells or progressed further to large multicellular duct-like structures or cells undergoing
gross lipid accumulation and secretion. The secondary hepatocyte cultures expressed alpha-fetoprotein (AFP), albumin, and
β-fibrinogen mRNA, and conditioned medium from the cells contained elevated levels of transferrin and albumin. STO feeder
cell co-culture may be useful for the sustainable culture of hepatocytes from other species. 相似文献
833.
By the use of EPR spectroscopy, it has been shown that acyl nitroso compounds can act as spin traps for short-lived radicals with the formation of acyl aminoxyl radicals. The reaction was studied for the system benzohydroxamicacid[Ph-C (= O)N(H)] - dimethyl sulfoxide - hydrogen peroxide. The acyl aminoxyl radicals appeared almost immediately when the reaction mixture was irradiated in situ in the EPR cavity with UV light. The trapping reaction involved two photochemical reactions, i.e. the oxidation of the hydroxamic acid to the acyl nitroso compound Ph-C (= O)NO, and the formation of methyl radicals from dimethyl sulfoxide. The EPR spectra are superpositions of the spectra of two species of acyl aminoxyl radicals, i.e. the radicals Ph-C (= O)N(O·)H formed by oxidation of the parent benzohydrox-amic acid, and the radical Ph-C (= O)N(O·)CH3, formed by trapping of methyl radicals. 相似文献
834.
Thomas Bartels und Wilfried Meyer 《Journal of Ornithology》1993,134(3):301-307
Zusammenfassung Unter Einsatz einer neuartigen, direkt vergrößernden Röntgentechnologie wurde die Konstruktion des Schnabelskeletts von schlupfreifen Jungvögeln untersucht. Wie die bei Verwendung sog. Mikrofokus-Röntgengeräte erzielten Röntgenaufnahmen erkennen lassen, weist das Schnabelskelett der Schlüpflinge — unabhängig vom Entwicklungsmodus — bei allen untersuchten Formen einen recht einheitlichen Bau auf. Sowohl der Ossifikationsgrad der Kiefer als auch die spezifische Osteoarchitektur der Knochenelemente des Schnabelapparates, insbesondere im Bereich der Substantia spongiosa des Os praemaxillare können als anatomische Anpassungen an die beim Sprengen der Eischale auftretenden mechanischen Belastungen des Kieferskeletts gewertet werden.
Construction principles of the beak skeleton in the hatchling
Summary The structure of the beak skeleton of hatchlings was analysed using a new direct magnifying X-ray technique. The application of these microfocus X-ray systems reveals a quite uniform construction of the beak skeleton in the hatchlings, independent from the mode of development of the bird species groups studied (precocial, altricial etc.). The amount of ossification as well as the specific osteoarchitecture of the jaw bones of the beak apparatus — especially in the region of Substantia spongiosa of the Os praemaxillare — may be considered as an anatomical adaptation to mechanical stress of the jaw bones during picking of the eggshell.相似文献
835.
Thomas Krüppel Volker Furchbrich Wolfgang Lueken 《The Journal of membrane biology》1993,135(3):253-260
Electrical responses upon mechanostimulation at the posterior cell end were investigated in the marine hypotrichous ciliate Euplotes vannus. A new mechanostimulator was developed to mimic stimuli that are identical with those involved in cell-cell collisions. The receptor potential hyperpolarized by 18–35 mV within 12–25 msec, reached a peak value of -62 mV with a delay of 4–9 msec after membrane deformation, and was deactivated after 50–70 msec. Cirri were stimulated to beat accelerated backward. The corresponding receptor current exerted a similar time course with a peak of 2.4 nA. The shift of the reversal potential by 57.6 mV at a tenfold increase of [K+]
0
identifies potassium ions as current carriers within the development of the receptor potential. An intracellular K concentration of 355 mmol/liter was calculated for cells in a medium that was composed similar to sea-water. The mechanically activated potassium current was totally inhibited by extracellular TEA and intracellular Cs+, and partially inhibited by extracellular 4-AP. The total inhibition of the current by injected EGTA points to a Ca dependence of the posterior mechanosensitivity. It was confirmed by the increase of the peak current amplitude with rising [Ca2+]
0
. Sodium presumably repolarizes the receptor potential because the repolarization was delayed and after-depolarizations were eliminated in media without sodium. Since deciliation did not affect mechano-sensitivity, the corresponding ion channels reside within the soma membrane.The authors wish to thank Mr. Norbert Spreckelmeier from the electronics workshop and Mr. Herbert Lutter from the fine-mechanical workshop of the department for their excellent work, Mrs. G. Key and Mr. H. Mikoleit for skillful technical assistance and for preparing the figures. This work was supported by Deutsche Forschungsgemeinschaft, SFB 171, C7. 相似文献
836.
837.
Abstract: The L1- and F11-like axonal glycoproteins, implicated in neurite outgrowth and fasciculation, are members of the Ig superfamily comprising multiple fibronectin type III-like domains. Their Ig-like and fibronectin type III-related domains are likely to be composed of seven β-strands arranged in two opposing β-sheets of highly similar topology. Whereas the F11-like molecules lack a transmembrane sequence and are anchored in the plasma membrane by a glycosylphosphatidylinositol, the L1 -like molecules comprise cytoplasmic domains with highly conserved sequence motifs. Most of the latter proteins occur in different isoforms generated by alternative pre-mRNA splicing, which has not been documented for molecules of the F11 subgroup. L1 -like proteins undergo heterophils as well as homophilic interactions, whereas only the former mode of binding was observed for F11 -like proteins. Evidence is accumulating that these Ig superfamily molecules with fibronectin type III-like domains are interacting in a complex manner with each other and molecules of the extracellular matrix. Investigations assigning structure to function reveal that their individual extracellular domains serve distinct binding activities. Recent studies also suggest that L1 and NCAM are implicated in the transduction of transmembrane signals. 相似文献
838.
Cell Cycle Arrest of Proliferating Neuronal Cells by Serum Deprivation Can Result in Either Apoptosis or Differentiation 总被引:4,自引:1,他引:3
M. Keith Howard Lindsey C. Burke Carolina Mailhos Arnold Pizzey Christopher S. Gilbert† W. Durward Lawson‡ Mary K. L. Collins§ N. Shaun B. Thomas David S. Latchman 《Journal of neurochemistry》1993,60(5):1783-1791
Abstract: Apoptotic cell death plays a critical role in the development of the nervous system. The death of mature nondividing neurons that fail to receive appropriate input from the target field has been extensively studied. However, the mechanisms mediating the extensive cell death occurring in areas of the developing brain where proliferating neuroblasts differentiate into mature nondividing neurons have not been analyzed. We show here that the cell cycle arrest of a proliferating cell of neuronal origin by removal of serum results in either apoptotic cell death or differentiation to a mature nondividing neuronal cell. The proportion of cells undergoing death or differentiation is influenced in opposite directions by treatment of the cells with cyclic AMP and retinoic acid. This suggests that following the withdrawal of signals stimulating neuroblast cell division, neuronal cells either can cease to suppress a constitutive suicide pathway and hence die by apoptosis or, alternatively, can differentiate into a mature neuronal cell. Regulation of the balance between apoptosis and neuronal differentiation could therefore play a critical role in controlling the numbers of mature neurons that form. 相似文献
839.
Synaptic Vesicle Traffic: Rush Hour in the Nerve Terminal 总被引:6,自引:0,他引:6
840.
Involvement of Calcium Channels in Depolarization-Evoked Release of Adenosine from Spinal Cord Synaptosomes 总被引:3,自引:1,他引:2
Abstract: The potential involvement of L- and N-type voltage-sensitive calcium (Ca2+ ) channels and a voltage-independent receptor-operated Ca2+ channel in the release of adenosine from dorsal spinal cord synaptosomes induced by depolarization with K+ and capsaicin was examined. Bay K 8644 (10 n M ) augmented release of adenosine in the presence of a partial depolarization with K+ (addition of 6 m M ) but not capsaicin (1 and 10 μ M ). This augmentation was dose dependent from 1 to 10 n M and was followed by inhibition of release from 30 to 100 n M . Nifedipine and nitrendipine inhibited the augmenting effect of Bay K 8644 in a dose-dependent manner, but neither antagonist had any effect on release of adenosine produced by K+ (24 m M ) or capsaicin (1 and 10 μ M ) ω-Conotoxin inhibited K+ -evoked release of adenosine in a dose-dependent manner but had no effect on capsaicin-evoked release. Ruthenium red blocked capsaicin-induced release of adenosine but had no effect on K+ -evoked release. Although L-type voltage-sensitive Ca2+ channels can modulate release of adenosine when synaptosomes are partially depolarized with K+ , N-type voltage-sensitive Ca2+ channels are primarily involved in K+ -evoked release of adenosine. Capsaicin-evoked release of adenosine does not involve either L- or N-type Ca2+ channels, but is dependent on a mechanism that is sensitive to ruthenium red. 相似文献