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11.
A novel gene that encodes a protein with a putative src homology 3 domain is a candidate gene for familial juvenile nephronophthisis 总被引:3,自引:0,他引:3
12.
Peter Sandner Bernhard Gess Konrad Wolf Armin Kurtz 《Pflügers Archiv : European journal of physiology》1996,431(6):905-912
There is accumulating evidence from in vitro experiments that the gene expression of the vascular endothelial growth factor
(VEGF) is, like that of the erythropoietin (EPO) gene, regulated by the oxygen tension and by divalent cations such as cobalt.
Since the information about the regulation of VEGF gene expression in vivo is rather scarce, this study aimed to examine the
influence of hypoxia and of cobalt on VEGF gene expression in different rat organs and to compare it with that on EPO gene
expression. To this end male Sprague-Dawley rats were exposed to carbon monoxide (0.1% CO), hypoxia (8% O2 ) or to cobalt chloride (12 and 60 mg/kg s.c.) for 6 h. mRNA levels for VEGF- 188, -164, and -120 amino acid isoforms in
lungs, hearts, kidneys and livers were semiquantitated by RNase protection. For these organs we found a rank order of VEGF
mRNA abundance of lung >> heart > kidney = liver. EPO mRNA levels were semiquantitated in kidneys and livers. Hypoxia, CO
and cobalt increased EPO mRNA levels 60-fold, 140-fold and 5-fold, respectively, in the kidneys, and 11-fold, 11-fold and
3-fold, respectively, in the livers. None of these manoeuvres caused significant changes of VEGF mRNA in lung, heart or kidneys.
Only in the livers did hypoxia lead to a significant (50%) increase of VEGF mRNA. These findings suggest that, in contrast
to the in vitro situation, the expression of the VEGF gene in normal rat tissues is rather insensitive to hypoxia. In consequence,
the in vivo regulation of the VEGF and the EPO genes appear to differ substantially, suggesting that the regulation of the
VEGF and EPO genes may not follow the same essential mechanisms in vivo.
Received: 31 July 1995/Received after revision: 20 November 1995/Accepted: 27 November 1995 相似文献
13.
Hebenstreit H Papadi H Konrad G Seitinger G Reisenberger FJ Kratochvil A Berger A 《Acta medica Austriaca》2000,27(2):45-48
Since the beginning of 1994 standardized primary radical resection was performed in benign thyroid diseases at the surgical department, Barmherzige Brueder Hospital, Graz. In multinodular euthyroid goiter bilateral lobectomy or near total lobectomy respectively was done. In case of Graves' disease unilateral lobectomy and contralateral near total resection or "en bloc" thyroidectomy was performed. In accordance with literature a significant reduction of recurrent laryngeal nerve paralysis from approximately 9% to 1.2% occurred in our patients if this surgical procedure was performed consequently. Hypocalcemia rate after surgery needing treatment was approximately 1% at the time of demission. 相似文献
14.
Various salient histological features were rated from + to +++ in a semiquantitative evaluation of a series of 155 cases of fibrous histiocytoma. Relations between individual histological features, as well as between histological findings, localisation and size of lesions, and age or sex of the patient were tested statistically. Most impressive was an inverse proportional relationship between cellular and fibrillar densities: highly cellular fibrous histiocytomas chiefly showed little fiber formation. Accordingly, cases with marked fiber formation were distinguished by low cellularity. Based on this statistically significant relation, 3 subtypes could be classified on a scale of increasing fiber formation and decreasing cellular density. The majority of cases showed medium cellularity and fibrillar density, with distinct storiform (spokewheel or "whirlygig") pattern which is compatible with typical storiform histocytoma, including clincally progressive, recurrant FH and/or "dermatofibrosarcoma protuberans". The typical patient was more frequently female than male, 40 years of age with a 0.5 to 1.0 cm size tumor node in the lower extremities located in the corium, often with beginning infiltration of the subcutaneous fat tissue. 相似文献
15.
H. Bechtold J. Lorenz L. S. Weilemann T. Meinertz D. Trenk K. Andrassy E. Jähnchen 《Journal of molecular medicine (Berlin, Germany)》1984,62(18):885-886
Summary In three patients treated with cephalosporins (one patient with latamoxef, two patients with cefazedone) vitamin K1 was injected to investigate whether this was followed by an increase in vitamin K1 2,3-epoxide plasma concentrations as compared to controls. Such a rise in K1-epoxide concentrations in the plasma can be demonstrated following treatment with coumarins. This reflects an inhibition of the vitamin K1-epoxide reductase in the liver. Coumarins are thought to induce hypoprothrombinaemia by such a mechanism. In all three patients we found a considerable increase in the vitamin K1-epoxide plasma concentrations following injection of 10 mg vitamin K1, whereas in normal subjects only traces of K1-epoxide could be detected (<0.030 µg/ml). The K1-epoxide concentrations found in our three patients treated with cephalosporins were 0.12, 0.16 and 0.19 µg/ml, respectively. This indicates that latamoxef or cefazedone might reduce clotting factor synthesis by a coumarin-like mechanism of action in these patients. Although the effect of cephalosporins in enhancing vitamin K1-epoxide plasma concentrations is less than that of coumarins, it might cause severe hypoprothrombinaemia in the presence of latent vitamin K deficiency.Abbreviation PT
prothrombin time
- TT
thrombin time
- PTT
partial thromboplastin time
- PC
platelet count
- ICU
intensive care unit
- EEG
electroencephalogram
- K1-epoxide
vitamin K1 2,3-epoxide 相似文献
16.
Jonathan T. Sims Venkatesh Krishnan Ching-Yun Chang Sarah M. Engle Giacomo Casalini George H. Rodgers Nicoletta Bivi Brian J. Nickoloff Robert J. Konrad Stephanie de Bono Richard E. Higgs Robert J. Benschop Silvia Ottaviani Anabela Cardoso Ajay Nirula Mario Corbellino Justin Stebbing 《The Journal of allergy and clinical immunology》2021,147(1):107-111
17.
G. Aumüller Paul-Martin Holterhus Lutz Konrad Burkhard von Rahden Olaf Hiort Murielle Esquenet Guido Verhoeven 《Anatomy and embryology》1998,197(3):199-208
As it is suggested that the androgen receptor mechanism is required for prostatic development, we attempted to determine
the appearance, expression and distribution of the androgen receptor in embryonic, infantile and pubertal human prostate.
Using mono- and polyclonal antibodies and a digoxigenin-labeled 713 bp riboprobe, the androgen receptor expression in paraffin
sections of fetal, infantile, and pubertal prostates was studied at the protein and RNA level. Under highly standardized conditions,
application of the polyclonal antibodies resulted in a weak cytoplasmic and nuclear labeling of the epithelium of fetal glands.
No immunoreaction was obtained with monoclonal antibodies. Applying the polyclonal antibody to pubertal and adult specimens,
immunoreactivity of the androgen receptor was positive in nuclei of adluminal and basal epithelial cells, in interstitial
and vascular smooth muscle cells and vascular endothelium, whereas ganglionic cells and enteroendocrine cells were negative.
In situ hybridization with the digoxigenin-labeled riboprobe gave clear positive results already in epithelium of very young
fetal specimens. A semiquantitative visual evaluation of in situ hybridizations showed that intermediate intensity of expression
was increased in pubertal and adult specimens, whereas strong expression was reduced in prostatic epithelium. Conclusions:
The essential findings are: (1) an early expression of androgen receptor mRNA in the fetal prostate; (2) no immunoreaction
of monoclonal antibodies against the androgen receptor in the same specimens, (3) a decrease of androgen receptor mRNA expression,
but increase in immunoreactivity of the androgen receptor protein with the onset of glandular maturation during puberty.
Accepted: 29 September 1997 相似文献
18.
Connections between transsexualism and delinquency have been considered in only a few publications to date. The authors report on a forensic psychiatric case with a transsexual development after committing an offence based on sexual deviations. Transsexualism in this context seems to represent an attempt for the symbolic solution of a conflict of identity. This should be interpreted in the context of psychotherapy and not be misunderstood as a symptom proving the diagnosis of manifest transsexualism by orientation on pure phenomenological criteria. 相似文献
19.
20.
Hänsch GM Radsak M Wagner C Reis B Koch A Breitbart A Andrassy K 《Kidney international》1999,55(5):1811-1818
BACKGROUND: Wegener's granulomatosis is a systemic inflammatory disease of unknown etiology. Many studies suggest that autoimmune reactions are involved, and there is good evidence for the participation of immunocompetent cells. In that context, we examined the activation of polymorphonuclear neutrophils (PMNs) of patients with Wegener's granulomatosis. METHODS: In a prospective study, the expression on the surface of PMNs of CD64 and of the major histocompatibility class II (MHC II) antigen was measured by cytofluorometry in whole blood. The expression of those antigens was correlated to disease activity. RESULTS: Up to 15% of the peripheral PMNs of patients with active disease expressed MHC II. Follow-up studies showed that expression correlated closely with disease activity and that it decreased rapidly under immunosuppressive therapy. Expression of CD64 was seen in approximately 50% of the patients, regardless of disease activity. CONCLUSION: MHC II expression on PMNs might serve as a novel diagnostic marker for active disease and appears to be suitable for monitoring immunotherapy. Moreover, our data provide evidence that PMNs, which are normally MHC II negative, acquire MHC II antigens in the course of disease and may be an unrecognized function within the afferent limb of the immune response. 相似文献