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151.
ER-phagosome fusion defines an MHC class I cross-presentation compartment in dendritic cells 总被引:1,自引:0,他引:1
Guermonprez P Saveanu L Kleijmeer M Davoust J Van Endert P Amigorena S 《Nature》2003,425(6956):397-402
Induction of cytotoxic T-cell immunity requires the phagocytosis of pathogens, virus-infected or dead tumour cells by dendritic cells. Peptides derived from phagocytosed antigens are then presented to CD8+ T lymphocytes on major histocompatibility complex (MHC) class I molecules, a process called "cross-presentation". After phagocytosis, antigens are exported into the cytosol and degraded by the proteasome. The resulting peptides are thought to be translocated into the lumen of the endoplasmic reticulum (ER) by specific transporters associated with antigen presentation (TAP), and loaded onto MHC class I molecules by a complex "loading machinery" (which includes tapasin, calreticulin and Erp57). Here we show that soon after or during formation, phagosomes fuse with the ER. After antigen export to the cytosol and degradation by the proteasome, peptides are translocated by TAP into the lumen of the same phagosomes, before loading on phagosomal MHC class I molecules. Therefore, cross-presentation in dendritic cells occurs in a specialized, self-sufficient, ER-phagosome mix compartment. 相似文献
152.
Jean Eisenstaedt 《Archive for History of Exact Sciences》1986,35(2):115-185
Sans résumé 相似文献
153.
G. Jean 《Cellular and molecular life sciences : CMLS》1961,17(9):428-429
Summary Preliminary results of a statistical survey of electron micrographs of thrombocytes from 15 patients with haemorrhagic diathesis are reported. The possible significance of ultrastructural changes in relation to factor 3 activity and metabolism deficiency are discussed. 相似文献
154.
155.
WEN HanJie Jean CARIGNAN HU RuiZhong FAN HaiFeng CHANG Bin YANG GuangShu 《科学通报(英文版)》2007,52(17):2443-2447
The selenium isotopic ratios have been measured in the Yutangba Se deposit, Hubei Province, China. The results show that the δ 82/76SeNIST values vary from -12.77‰ to 4.93‰, which is the largest Se iso- topic variation found so far in natural terrestrial samples. The sample Ytb-5 of high-selenium carbona-ceous shale has the lightest Se isotopic composition with a δ 82/76SeNIST value of -12.77‰. On the basis of variations of Se isotope in the deposit along with other geological and geochemical evidence, the "redox model" is suggested to favor the explanation of the occurrence of native Se in the deposit. The application to the Yutangba Se deposit with the discovery of large Se isotopic fractionation for natural samples indicates the potential of Se isotope as a new geochemical tracer. 相似文献
156.
Crow YJ Leitch A Hayward BE Garner A Parmar R Griffith E Ali M Semple C Aicardi J Babul-Hirji R Baumann C Baxter P Bertini E Chandler KE Chitayat D Cau D Déry C Fazzi E Goizet C King MD Klepper J Lacombe D Lanzi G Lyall H Martínez-Frías ML Mathieu M McKeown C Monier A Oade Y Quarrell OW Rittey CD Rogers RC Sanchis A Stephenson JB Tacke U Till M Tolmie JL Tomlin P Voit T Weschke B Woods CG Lebon P Bonthron DT Ponting CP Jackson AP 《Nature genetics》2006,38(8):910-916
Aicardi-Goutières syndrome (AGS) is an autosomal recessive neurological disorder, the clinical and immunological features of which parallel those of congenital viral infection. Here we define the composition of the human ribonuclease H2 enzyme complex and show that AGS can result from mutations in the genes encoding any one of its three subunits. Our findings demonstrate a role for ribonuclease H in human neurological disease and suggest an unanticipated relationship between ribonuclease H2 and the antiviral immune response that warrants further investigation. 相似文献
157.
Delous M Baala L Salomon R Laclef C Vierkotten J Tory K Golzio C Lacoste T Besse L Ozilou C Moutkine I Hellman NE Anselme I Silbermann F Vesque C Gerhardt C Rattenberry E Wolf MT Gubler MC Martinovic J Encha-Razavi F Boddaert N Gonzales M Macher MA Nivet H Champion G Berthélémé JP Niaudet P McDonald F Hildebrandt F Johnson CA Vekemans M Antignac C Rüther U Schneider-Maunoury S Attié-Bitach T Saunier S 《Nature genetics》2007,39(7):875-881
Cerebello-oculo-renal syndrome (CORS), also called Joubert syndrome type B, and Meckel (MKS) syndrome belong to the group of developmental autosomal recessive disorders that are associated with primary cilium dysfunction. Using SNP mapping, we identified missense and truncating mutations in RPGRIP1L (KIAA1005) in both CORS and MKS, and we show that inactivation of the mouse ortholog Rpgrip1l (Ftm) recapitulates the cerebral, renal and hepatic defects of CORS and MKS. In addition, we show that RPGRIP1L colocalizes at the basal body and centrosomes with the protein products of both NPHP6 and NPHP4, known genes associated with MKS, CORS and nephronophthisis (a related renal disorder and ciliopathy). In addition, the RPGRIP1L missense mutations found in CORS individuals diminishes the interaction between RPGRIP1L and nephrocystin-4. Our findings show that mutations in RPGRIP1L can cause the multiorgan phenotypic abnormalities found in CORS or MKS, which therefore represent a continuum of the same underlying disorder. 相似文献