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101.
C. A. Johnson R. A. Løvstad E. Walaas O. Walaas 《Cellular and molecular life sciences : CMLS》1970,26(2):134-135
Résumé On sait que la plasmine céruléenne crystalline rétroplacentaire humaine ainsi qua la plasmine apocérulécnne empêchent l'hémaglutination virale. Cet effet pourrait être attribué aux résidus d'acide sialique, car l'action préventive disparaît après traitement de la plasmine céruléenne par la neuraminidase. 相似文献
102.
Å. Thureson-Klein R. L. Klein H. Lagercrantz L. Stjärne 《Cellular and molecular life sciences : CMLS》1970,26(9):994-995
Résumé Les vésicules de la NA du nerf splénique de Buf ont été obtenues par gradient de centrifugation («sucrose-heavy water»), Le rapport NA/protéine observé est de 4 à 7 fois plus élevé que celui qui a été mentionné précédemment. L'examen préliminaire de cette fraction, par microscopie électronique, révèle une couche importante et pratiquement pure de vésicules à la surface du sédiment.
Supported by Research Career Program Award No. 5-K03-HE-0592 from the Nat. Heart and Lung Inst. and Research Grant No. 5-R01-GM15490 from the Nat. Inst. Gen. Med. Sci., U.S.P.H.S.
Supported by the Swedish Medical Research Council No. K70-14X-2479-03A and Knut and Alice Wallenbergs Foundation. 相似文献
Supported by Research Career Program Award No. 5-K03-HE-0592 from the Nat. Heart and Lung Inst. and Research Grant No. 5-R01-GM15490 from the Nat. Inst. Gen. Med. Sci., U.S.P.H.S.
Supported by the Swedish Medical Research Council No. K70-14X-2479-03A and Knut and Alice Wallenbergs Foundation. 相似文献
103.
R. J. Morin 《Cellular and molecular life sciences : CMLS》1970,26(8):829-831
Zusammenfassung Bei Bebrütung von Arterien in Gegenwart von Östradiol wurde der Einbau von14C-Azetat und14C-Cholin in Phosphatidylcholin deutlich vermehrt. 相似文献
104.
G. Prota S. Crescenzi G. Misuraca R. A. Nicolaus 《Cellular and molecular life sciences : CMLS》1970,26(10):1058-1059
Riassunto Mediante esperimenti in vitro, è stato accertato che i primi stadi della biosintesi delle feomelanine conducono alla formazione di derivati diidrobenzotiazinici, ai quali sono state assegnate le strutture III e IV.
This investigation was supported by a grant from the Laboratorio di Chimica e Fisica per lo Studio delle Molecole di Interesse Biologico del C.N.R., Napoli. 相似文献
This investigation was supported by a grant from the Laboratorio di Chimica e Fisica per lo Studio delle Molecole di Interesse Biologico del C.N.R., Napoli. 相似文献
105.
R. Tenconi C. Baccichetti Dr. F. Zacchello E. Sartori 《Cellular and molecular life sciences : CMLS》1970,26(11):1238-1239
Riassunto Frammenti di cute di due soggetti affetti da glicogenosi tipo II e dei loro genitori e fratelli sono stati coltivati in vitro. Sia nelle culture dei pazienti che dei loro familiari si è osservata la presenza di materiale metacromatico dopo colorazione con blu di toluidina 0. Nei leucociti di tutti i familiari esaminati l'attività della -1,4-glucosidasi è risultata ridotta. 相似文献
106.
R. G. Knodell P. P. Toskes H. A. Reber F. P. Brooks 《Cellular and molecular life sciences : CMLS》1970,26(5):515-517
Zusammenfassung Nachweis, dass die Zufuhr von dibutyryl-zyklischem AMP (DcAMP) in vitro die Enzymproduktion erhöht und zwar mit nur geringer Gewichtsveränderung des Kaninchenpankreas. Die Enzymproduktion wird ebenso durch Theophyllin vermehrt und es wird vermutet, das DcAMP der Vermittler der pankreozymen Wirkung im Kaninchen ist. 相似文献
107.
Galectins in cell growth and apoptosis 总被引:23,自引:0,他引:23
Fourteen members of the galectin family, proteins with conserved carbohydrate-recognition domains that bind β-galactoside,
have been cloned and more are expected to be discovered in the near future. Many aspects of galectin biology have been thoroughly
explored, and functional studies have implicated these proteins in cell growth, differentiation and apoptosis, in addition
to cell adhesion, chemoattraction and cell migration. In some cases a galectin can either promote or suppress cell growth,
depending on the cell types and doses used. Galectin-3 is the only member known so far to inhibit apoptosis, while galectin-1,
-7 and -9 promote this cellular process. Galectins can act either extracellularly or intracellularly to exert effects on cell
growth and apoptosis.
RID="*"
ID="*"Corresponding author. 相似文献
108.
Averna M De Tullio R Capini P Salamino F Pontremoli S Melloni E 《Cellular and molecular life sciences : CMLS》2003,60(12):2669-2678
The amount of calpastatin directly available in cytosol is under the control of [Ca2+] and [cyclic AMP]. Prolonged calpain activation also promotes degradation of calpastatin. The fluctuation of calpastatin concentration in cell soluble fraction is accompanied by an initial decrease in calpastatin gene expression, followed by a fivefold increase in its expression when the inhibitor protein is degraded. This process can be conceptualized as a mechanism to regulate calpastatin availability in the cell. This conclusion is supported by the fact that calpain, the other component of this proteolytic system, undergoes changes in its levels of expression in a much more limited manner. Furthermore, this process can be observed both in cells exposed to different natural stimuli, or in other cell lines. Modification of calpastatin gene expression might represent a new tool for the in vivo control of the regulatory machinery required for the modulation of Ca2+-dependent proteolysis.Received 18 July 2003; received after revision 3 September 2003; accepted 23 September 2003 相似文献
109.
110.
Lymphatic reprogramming of blood vascular endothelium by Kaposi sarcoma-associated herpesvirus 总被引:22,自引:0,他引:22
Hong YK Foreman K Shin JW Hirakawa S Curry CL Sage DR Libermann T Dezube BJ Fingeroth JD Detmar M 《Nature genetics》2004,36(7):683-685
Kaposi sarcoma is considered a neoplasm of lymphatic endothelium infected with Kaposi sarcoma-associated herpesvirus. It is characterized by the expression of lymphatic lineage-specific genes by Kaposi sarcoma tumor cells. Here we show that infection of differentiated blood vascular endothelial cells with Kaposi sarcoma-associated herpesvirus leads to their lymphatic reprogramming; induction of approximately 70% of the main lymphatic lineage-specific genes, including PROX1, a master regulator of lymphatic development; and downregulation of blood vascular genes. 相似文献