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931.
932.
Antonios N. Gargalionis Lina S. Malakou Christos Adamopoulos Christina Piperi Irene Theohari Marjan Nokhbehsaim James Deschner Georgios Kokkalis Penelope Korkolopoulou Evangelia Papadavid Athanasios G. Papavassiliou Efthimia K. Basdra 《生物化学与生物物理学报:疾病的分子基础》2018,1864(10):3468-3476
Psoriatic plaques tend to localize to the knees and elbows, areas that are particularly subject to mechanical stress resulting from bending and friction. Moreover, plaques often develop at sites of mechanical trauma or injury (Koebner phenomenon). Nevertheless, mechanotransduction has never been linked to psoriasis. Polycystins (polycystin-1, PC1; polycystin-2, PC2) are mechanosensitive molecules that function as key regulators of cellular mechanosensitivity and mechanotransduction. The aim of this in vitro study was to investigate the role of polycystins in the development of psoriasis. We showed that PC1 knockdown in HaCaT cells led to an elevated mRNA expression of psoriasis-related biomarkers Ki-67, IL-6, TNF-α, VEGF and Bcl-2, while PC1 functional inhibition was accompanied by increased cell proliferation and migration of HaCaT cells. In addition, PC1 knockdown via siRNA in HaCaT cells was followed by activation of critical molecules of the mTOR and MAPK pathways and this mTOR pathway activation was ERK-dependent. Furthermore, loss of PC1 protein expression and elevated levels of activated mTOR substrates were also observed in human samples of psoriatic plaques. Overall, our study suggests that the PC1/ERK/mTOR signaling axis represents a novel potential mechanism in psoriasis pathogenesis. 相似文献
933.
Lower Fasted‐State but Greater Increase in Muscle Protein Synthesis in Response to Elevated Plasma Amino Acids in Obesity
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934.
935.
Christos Spanos Elaina M. Maldonado Ciarán P. Fisher Petchpailin Leenutaphong Ernesto Oviedo-Orta David Windridge Francisco J. Salguero Alexandra Bermúdez-Fajardo Mark E. Weeks Caroline Evans Bernard M. Corfe Naila Rabbani Paul J. Thornalley Michael H. Miller Huan Wang John F. Dillon Alberto Quaglia Anil Dhawan Emer Fitzpatrick J. Bernadette Moore 《Proteome science》2018,16(1):4
Background
Non-alcoholic fatty liver disease (NAFLD) is the most common liver disease worldwide. However, its molecular pathogenesis is incompletely characterized and clinical biomarkers remain scarce. The aims of these experiments were to identify and characterize liver protein alterations in an animal model of early, diet-related, liver injury and to assess novel candidate biomarkers in NAFLD patients.Methods
Liver membrane and cytosolic protein fractions from high fat fed apolipoprotein E knockout (ApoE?/?) animals were analyzed by quantitative proteomics, utilizing isobaric tags for relative and absolute quantitation (iTRAQ) combined with nano-liquid chromatography and tandem mass spectrometry (nLC-MS/MS). Differential protein expression was confirmed independently by immunoblotting and immunohistochemistry in both murine tissue and biopsies from paediatric NAFLD patients. Candidate biomarkers were analyzed by enzyme-linked immunosorbent assay in serum from adult NAFLD patients.Results
Through proteomic profiling, we identified decreased expression of hepatic glyoxalase 1 (GLO1) in a murine model. GLO1 protein expression was also found altered in tissue biopsies from paediatric NAFLD patients. In vitro experiments demonstrated that, in response to lipid loading in hepatocytes, GLO1 is first hyperacetylated then ubiquitinated and degraded, leading to an increase in reactive methylglyoxal. In a cohort of 59 biopsy-confirmed adult NAFLD patients, increased serum levels of the primary methylglyoxal-derived advanced glycation endproduct, hydroimidazolone (MG-H1) were significantly correlated with body mass index (r?=?0.520, p <?0.0001).Conclusion
Collectively these results demonstrate the dysregulation of GLO1 in NAFLD and implicate the acetylation-ubquitination degradation pathway as the functional mechanism. Further investigation of the role of GLO1 in the molecular pathogenesis of NAFLD is warranted.936.
Christos Spanos Elaina M. Maldonado Ciarán P. Fisher Petchpailin Leenutaphong Ernesto Oviedo-Orta David Windridge Francisco J. Salguero Alexandra Bermúdez-Fajardo Mark E. Weeks Caroline Evans Bernard M. Corfe Naila Rabbani Paul J. Thornalley Michael H. Miller Huan Wang John F. Dillon Alberto Quaglia Anil Dhawan Emer Fitzpatrick J. Bernadette Moore 《Proteome science》2018,16(1):13
937.
938.
Christos P. Carvounis Sherman D. Levine Nicholas Franki Richard M. Hays 《The Journal of membrane biology》1979,49(3):269-281
Summary Urea and water transport across the toad bladder can be separately activated by low concentrations of vasopressin or 8 Br-cAMP. Employing this method of selective activation, we have determined the reflection coefficient () of urea and other small molecules under circumstances in which the bladder was transporting urea or water. An osmotic method for the determination of was used, in which the ability of a given solute to retard water efflux from the bladder was compared to that of raffinose (=1.0) or water (=0). When urea transport was activated (low concentration of vasopressin), for urea and other solutes was low, (urea,0.08–0.39;acetamide, 0.55; ethylene glycol, 0.60). When water transport was activated (0.1mm 8 Br-cAMP) urea approached 1.0 urea also approached 1.0 at high vasopressin concentrations. In a separate series of studies, urea was determined in the presence of 2×10–5
m KMnO4 in the luminal bathing medium. Under these conditions, when urea transport is selectively blocked, urea rose from a value of 0.12 to 0.89. Thus, permanganate appears to close the urea transport channel. These findings indicate that the luminal membrane channels for water and solutes differ significantly in their dimensions. The solute channels, limited in number, have relatively large radii. They carry a small fraction (approximately 10%) of total water flow. The water transport channels, on the other hand, have small radii, approximately the size of a water molecule, and exclude solutes as small as urea. 相似文献
939.
Sirlei Daffre Per Kylsten Christos Samakovlis Dan Hultmark 《Molecular & general genetics : MGG》1994,242(2):152-162
Lysozyme has been studied in insects as part of the system of inducible antibacterial defence in the haemolymph. We recently found two Drosophila lysozyme genes that are constitutively expressed in the digestive tract, and are probably involved in the digestion of bacteria in the food. To obtain an overview of the lysozyme genes in this species and their possible roles in immunity and digestion, we have now characterized all six lysozyme genes in the cloned part of the lysozyme locus at 61F, and a seventh gene that maps to the same chromosomal location. The expression of the genes follows four different patterns: firstly, four closely related genes, LysB, C, D and E, are all strongly expressed in the midgut of larvae and adults; secondly, LysP is expressed in the adult salivary gland; thirdly, LysS is expressed mainly in the gastric caecae of larvae; and finally, LysX is primarily expressed in the metamorphosing midgut of late larvae and early pupae. The LysD-like genes and LysS are strongly repressed in artificially infected animals, possibly reflecting a malaise reaction in the digestive tract. None of the genes is expressed in the fat body or haemocytes. Thus rather than being a component of the haemolymph, the Drosophila lysozymes are found mainly in the digestive tract where they are expressed at a high level. Furthermore all genes, except LysP, encode acidic proteins, in contrast to the strongly basic typical lysozymes. This is highly reminiscent of the situation in ruminants, where the lysozymes have been recruited for the digestion of symbiotic bacteria in the stomach. 相似文献
940.
The cobalt(II) addition compounds [Co(X-salo)2(Y)], where X-salo is the anion of substituted salicylaldehydes (X = 3-OCH3, 5-CH3, 5-Cl, 5-NO2 and Y = the neutral 1,10 phenanthroline or neocuproine), were synthesized and characterized by physicochemical and spectral (IR, UV-Vis) data. Theoretical calculations (DFT, ZINDO, TD DFT) with gaussian 03 for the prediction of the electronic spectrum for the compounds, gave good correlation with the experimental one in the solid state and in solution. The cyclic voltammetry study in CH3CN gave all the expected waves for the redox processes of the metal Co(II) and the ligands phen or neoc and salicylaldehydes. The X-ray diffraction study of three compounds [Co(5-NO2-salo)2(phen)], [Co(5-CH3-salo)2(neoc)] and [Co(5-Cl-salo)2(neoc)] verified their analogous proposed octahedral arrangement of the ligands around the cobalt(II) atom. 相似文献