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101.
de Beer VJ Bender SB Taverne YJ Gao F Duncker DJ Laughlin MH Merkus D 《American journal of physiology. Heart and circulatory physiology》2011,300(5):H1950-H1959
We previously demonstrated that endothelin (ET)-mediated coronary vasoconstriction wanes with increasing exercise intensity via a nitric oxide- and prostacyclin-dependent mechanism (Ref. 23). Therefore, we hypothesized that the waning of ET coronary vasoconstriction during exercise is the result of decreased production of ET and/or decreased ET receptor sensitivity. We investigated coronary ET receptor sensitivity using intravenous infusion of ET and coronary ET production using intravenous infusion of the ET precursor Big ET, at rest and during continuous treadmill exercise at 3 km/h in 16 chronically instrumented swine. In the systemic vasculature, Big ET and ET induced similar changes in hemodynamic parameters at rest and during continuous exercise at 3 km/h, indicating that exercise does not alter ET production or receptor sensitivity in the systemic vasculature. In the coronary vasculature, infusion of ET resulted in similar dose-dependent decreases in coronary blood flow and coronary venous oxygen tension and saturation at rest and during exercise. In contrast, administration of Big ET resulted in dose-dependent decreases in coronary blood flow, as well as coronary venous oxygen tension and saturation at rest. These effects of Big ET were significantly reduced during exercise. Altogether, our data indicate that continuous exercise at 3 km/h attenuates ET-mediated coronary vasoconstriction through reduced production of ET from Big ET rather than through reduced ET sensitivity of the coronary vasculature. The decreased ET production during exercise likely contributes to metabolic coronary vasodilation. 相似文献
102.
Coronary blood flow is tightly coupled to myocardial oxygen consumption to maintain a consistently high level of myocardial
oxygen extraction. This tight coupling has been proposed to depend on periarteriolar, oxygen tension, signals released from
cardiomyocytes (adenosine acting on K
ATP
+
channels), and/or the endothelium (prostanoids, nitric oxide, endothelin [ET]) and autonomic influences (catecholamines),
but the contribution of each of these regulatory pathways and their interactions are still incompletely understood. Until
recently, experimental studies into the regulation of coronary blood flow during exercise were principally performed in the
dog. We have performed several studies on the regulation of vasomotor tone in coronary resistance vessels in chronically instrumented
exercising swine. These studies have shown that the coronary resistance vessels in swine lack significant α-adrenergic control,
but that these vessels are subject to β-adrenergic feed-forward control during exercise, which is aided by a parasympathetic
withdrawal. In addition, withdrawal of an ET-mediated vasoconstrictor influence also contributes to exercise-induced coronary
vasodilation. Coronary blood flow regulation by endothelial and metabolic vasodilator pathways contributes to resting vasomotor
tone regulation but does not appear to contribute to the exercise-induced coronary vasodilation. Furthermore, blockade of
one vasodilator pathway is not compensated by an increased contribution of the other vasodilator mechanisms, suggesting that
porcine coronary vasomotor control by endothelial and metabolic factors occurs in a linear additive rather than a nonlinear
synergistic fashion. 相似文献
103.
Masatoshi Togami Daphne Blazka Jun Hayashi 《In vitro cellular & developmental biology. Plant》1988,24(7):699-704
Summary A serum-free, hormone and attachment factor supplemented culture for rat H4 hepatoma cells was established. In the defined
medium (Dulbecco's Modified Eagle's +Ham's F12+insulin, transferrin, fibronectin liver cell growth factor, and sodium selenite),
H4 cells grew equally well as in 10% fetal bovine serum supplemented medium. H4 cells in either defined or serum-containing
culture conditions produce transferrin but not albumin or alpha-fetoprotein. In this paper we have studied the effect of various
hormones and pressor peptides on the production of angiotensinogen by H4 cells cultured in defined conditions. Only glucocorticoid
hormone had a significant effect on the production of angiotensinogen, whereas other hormones previously reported to exert
their effect on angiotensinogen production had little or no effect.
This work was supported by grant P01 CA37589 from the National Institutes of Health, Bethesda, MD. 相似文献
104.
Xiuqing Wang Daphne Moutsoglou 《In vitro cellular & developmental biology. Animal》2009,45(10):584-591
Primary fibroblast-like cells isolated from the peripheral blood of a healthy pig were immortalized by transduction of cells
with a replication-defective retrovirus vector expressing the E6/E7 proteins of human papillomavirus type 16 (pLXSN-16E6E7).
The immortalized cells grow rapidly in cell culture and exhibit a distinct cell surface phenotype that was positive for CD90,
CD44, collagen I, and vimentin and negative for CD14 and MHC II. Additionally, these immortalized blood derived-fibroblast-like
cells had the potential to differentiate into osteoblasts and adipocytes in vitro as evidenced by the deposition of calcium,
increased alkaline phosphatase activity, upregulated osteogenic and adipogenic marker gene expression, and accumulation of
fat droplets in cells when osteogenic (dexamethasone, ascorbic acid, and β-glycerophosphate) or adipogenic supplements (dexamethasone,
3-isobutyl-1-methylxanthine, indomethacin, and insulin) were added to the culture. Overall, the results suggest that the immortalized
blood-derived fibroblast-like cells exhibit some of the features of mesenchymal precursor cells, which may have implications
in tissue repair and remodeling process. 相似文献
105.
Jiao Chen Daphne Weihs Fred J. Vermolen 《Biomechanics and modeling in mechanobiology》2018,17(2):367-386
Cell migration, known as an orchestrated movement of cells, is crucially important for wound healing, tumor growth, immune response as well as other biomedical processes. This paper presents a cell-based model to describe cell migration in non-isotropic fibrin networks around pancreatic tumor islets. This migration is determined by the mechanical strain energy density as well as cytokines-driven chemotaxis. Cell displacement is modeled by solving a large system of ordinary stochastic differential equations where the stochastic parts result from random walk. The stochastic differential equations are solved by the use of the classical Euler–Maruyama method. In this paper, the influence of anisotropic stromal extracellular matrix in pancreatic tumor islets on T-lymphocytes migration in different immune systems is investigated. As a result, tumor peripheral stromal extracellular matrix impedes the immune response of T-lymphocytes through changing direction of their migration. 相似文献
106.
In this paper, we explore modeling overlapping biological processes. We discuss a probabilistic model of overlapping biological processes, gene membership in those processes, and an addition to that model that identifies regulatory mechanisms controlling process activation. A key feature of our approach is that we allow genes to participate in multiple processes, thus providing a more biologically plausible model for the process of gene regulation. We present algorithms to learn each model automatically from data, using only genomewide measurements of gene expression as input. We compare our results to those obtained by other approaches and show that significant benefits can be gained by modeling both the organization of genes into overlapping cellular processes and the regulatory programs of these processes. Moreover, our method successfully grouped genes known to function together, recovered many regulatory relationships that are known in the literature, and suggested novel hypotheses regarding the regulatory role of previously uncharacterized proteins. 相似文献
107.
108.
Summary The substitution of far-red for the first six hours of a prolonged irradiation with red light resulted in a large increase in anthocyanin yield, which was greater than the combined yields from far-red and red when the two treatments were given separately. When intermittent far-red irradiation was followed by a single short exposure to red, a considerable amount of anthocyanin was formed, although each treatment given separately had little effect. Four hours continuous far-red alone yielded some anthocyanin and also resulted in a further large increase in the effect of a short red treatment; this terminal red effect was fully reversible by a subsequent brief exposure to far-red. It is concluded that at least two photochemical reactions are involved in the responses to red and far-red, the first leading to the formation of substrate(s) used in the second reaction.When red light preceded exposure to the far-red/red irradiation sequence, the far-red enhancement effect was almost entirely lost and the anthocyanin yield approached that in red light. The effect of the red pre-irradiation treatment is attributed to destruction of phytochrome and it is suggested that phytochrome is the only pigment mediating anthocyanin synthesis in red and far-red. A possible interpretation is that the high-energy reaction in far-red and the low energy red/far-red reversible reaction are mediated by different forms of phytochrome.The substitution of blue for the first six hours of a prolonged irradiation with red light also resulted in a synergistic increase in anthocyanin yield; the enhancement effect of blue light was, however, not prevented by prior exposure to red. It is concluded that phytochrome is not the only pigment mediating the reactions occurring in blue light. The synergism between blue and red suggests that the high-energy reaction in blue light may lead to the production of substrates for phytochrome action.
Zusammenfassung Die Substitution der ersten 6 Std einer Hellrot-Dauerbestrahlung durch Dunkelrot führte zu einem starken Anstieg im Anthocyangehalt, der höher war als die Summe aus Dunkelrot und Hellrot, wenn beide Bestrahlungen getrennt gegeben wurden. Folgte auf intermittierende Dunkelrot-Bestrahlung eine einmalige Dosis Hellrot, bildete sich eine beträchtliche Menge Anthocyan, obwohl jede Bestrahlung für sich kaum wirksam war. 4 Std Dauerdunkelrot induzierten bereits meßbare Anthocyanbildung, die durch kurze Hellrot-Bestrahlung weiter gesteigert werden konnte; der Effekt dieser terminalen Dosis Hellrot konnte durch nachfolgende kurze Dunkelrot-Bestrahlung wieder rückgängig gemacht werden. Daraus wird geschlossen, daß wenigstens zwei photochemische Reaktionen bei Bestrahlung mit Hellrot und Dunkelrot ablaufen, wobei die erste Substrat(e) für die zweite produziert.Wurde vor einer Dunkelrot-Hellrot-Sequenz mit Hellrot bestrahlt, ging die fördernde Wirkung von Dunkelrot fast vollständig verloren und der Anthocyangehalt entsprach annähernd dem in Hellrot. Der Effekt der Hellrot-Vorbestrahlung wird auf die Destruktion von Phytochrom zurückgeführt und es wird vermutet, daß Phytochrom das einzige Pigment ist, das bei der Anthocyansynthese in Hellrot und Dunkelrot beteiligt ist. Eine mögliche Interpretation wäre, daß die Hochenergiereaktion in Dunkelrot und die Hellrot-Dunkelrot reversible Niederenergiereaktion durch verschiedene Formen von Phytochrom vermittelt werden.Die Substitution der ersten 6 Std einer Dauerbelichtung mit Hellrot durch Blau ergab ebenfalls eine synergistische Zunahme im Anthocyangehalt. Der fördernde Effekt von Blaulicht konnte jedoch durch Vorbestrahlung mit Hellrot nicht verhindert werden. Daraus wird geschlossen, daß Phytochrom nicht das einzige Pigment sein kann, das die Reaktionen in Blaulicht vermittelt. Der Synergismus zwischen Blau und Hellrot läßt vermuten, daß die Hochenergiereaktion in Blau zur Produktion von Substrat führt, mit dem Phytochrom reagieren kann.相似文献
109.
Horse liver alcohol dehydrogenase (HLADH) has been non‐covalently immobilized on an immobilized artificial membrane (IAM) high‐performance liquid chromatography (HPLC) stationary phase. The resulting IAM‐HLADH retained the reductive activity of native HLADH as well as the enzyme's enantioselectivity and enantiospecificity. HLADH was also immobilized in an IAM HPLC stationary phase prepacked in a 13 × 4.1 mm ID column to create an immobilized enzyme reactor (HLADH‐IMER). The reactor was connected through a switching valve to a column containing a chiral stationary phase (CSP) based upon p‐methylphenylcarbamate derivatized cellulose (Chiralcel OJR‐CSP). The results from the combined HLADH‐IMER/CSP and chromatographic system demonstrate that the enzyme retained its activity and stereoselectivity after immobilization in the column and that the substrate and products from the enzymatic reduction could be transferred to a second column for analytical or preparative separation. The combined HLADH‐IMER/CSP system is a prototype for the preparative on‐line use of cofactor‐dependent enzymes in large‐scale chiral syntheses. Chirality 11:39–45, 1999. © 1999 Wiley‐Liss, Inc. 相似文献
110.
Human glutaredoxin 3 (Glrx3) is an essential [2Fe-2S]-binding protein with ill-defined roles in immune cell response, embryogenesis, cancer cell growth, and regulation of cardiac hypertrophy. Similar to other members of the CGFS monothiol glutaredoxin (Grx) family, human Glrx3 forms homodimers bridged by two [2Fe-2S] clusters that are ligated by the conserved CGFS motifs and glutathione (GSH). We recently demonstrated that the yeast homologues of human Glrx3 and the yeast BolA-like protein Fra2 form [2Fe-2S]-bridged heterodimers that play a key role in signaling intracellular iron availability. Herein, we provide biophysical and biochemical evidence that the two tandem Grx-like domains in human Glrx3 form similar [2Fe-2S]-bridged complexes with human BolA2. UV-visible absorption and circular dichroism, resonance Raman, and electron paramagnetic resonance spectroscopic analyses of recombinant [2Fe-2S] Glrx3 homodimers and [2Fe-2S] Glrx3-BolA2 complexes indicate that the Fe-S coordination environments in these complexes are virtually identical to those of the analogous complexes in yeast. Furthermore, we demonstrate that apo BolA2 binds to each Grx domain in the [2Fe-2S] Glrx3 homodimer forming a [2Fe-2S] BolA2-Glrx3 heterotrimer. Taken together, these results suggest that the unusual [2Fe-2S]-bridging Grx-BolA interaction is conserved in higher eukaryotes and may play a role in signaling cellular iron status in humans. 相似文献