全文获取类型
收费全文 | 14771篇 |
免费 | 1141篇 |
国内免费 | 10篇 |
专业分类
15922篇 |
出版年
2021年 | 158篇 |
2020年 | 113篇 |
2019年 | 146篇 |
2018年 | 197篇 |
2017年 | 197篇 |
2016年 | 262篇 |
2015年 | 448篇 |
2014年 | 468篇 |
2013年 | 688篇 |
2012年 | 869篇 |
2011年 | 747篇 |
2010年 | 557篇 |
2009年 | 459篇 |
2008年 | 680篇 |
2007年 | 669篇 |
2006年 | 665篇 |
2005年 | 642篇 |
2004年 | 629篇 |
2003年 | 660篇 |
2002年 | 634篇 |
2001年 | 185篇 |
2000年 | 141篇 |
1999年 | 172篇 |
1998年 | 208篇 |
1997年 | 185篇 |
1996年 | 183篇 |
1995年 | 180篇 |
1994年 | 150篇 |
1993年 | 181篇 |
1992年 | 150篇 |
1991年 | 163篇 |
1990年 | 145篇 |
1989年 | 130篇 |
1988年 | 148篇 |
1987年 | 140篇 |
1986年 | 118篇 |
1985年 | 161篇 |
1984年 | 191篇 |
1983年 | 168篇 |
1982年 | 164篇 |
1981年 | 176篇 |
1980年 | 139篇 |
1979年 | 126篇 |
1978年 | 146篇 |
1977年 | 123篇 |
1976年 | 102篇 |
1975年 | 120篇 |
1974年 | 99篇 |
1973年 | 96篇 |
1970年 | 79篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
61.
62.
Qu Zhengxing; Sharkey Robert M.; Hansen Hans J.; Goldenberg David M.; Leung Shui-on 《Glycobiology》1997,7(6):803-809
Two humanized antibody mutants, hLL2HCN1 and hLL2HCN5, engineeredwith CH1 domain-appended carbohydrates (CHOs) were generatedto facilitate site-specific conjugation of radionudides andanti-cancer drugs to antibodies. Such site-specific conjugationmay minimize the incidence of immunoreactlvity perturbationas is often observed with random conjugation. Since the compositionsand structures of CHOs are important in determining the chemistry,efficiency, and extent of conjugation, the sequences of theCH1-appended CHOs were determined by exoglycosidase digestionsand fluorophore-assisted CHO electrophoresis (FACE). The CHOspecies attached at HCN1 and HCN5 sites in hLL2HCN1 and IJLL2HCN5,respectively, were distinct from each other, heterogeneous,and extensively processed. All of these CHOs were corefucosylatedcomplex-type oligosaccharides and contained Gal (galactose)and GlcNAc (N-acetylglucosamine) residues in the outer branches.Some of the outer branches were composed of Gal 相似文献
63.
64.
Frieder Schauer Kirsten Henning Helmut Pscheidl Rolf M. Wittich Peter Fortnagel Heinz Wilkes Volker Sinnwell Wittko Francke 《Biodegradation》1995,6(2):173-180
Trichosporon beigelii SBUG 752 was able to transform diphenyl ether. By TLC, HPLC, GC, GC-MS, NMR- and UV-spectroscopy, several oxidation products were identified. The primary attack was initiated by a monooxygenation step, resulting in the formation of 4-hydroxydiphenyl ether, 2-hydroxydiphenyl ether and 3-hydroxydiphenyl ether (48:47:5). Further oxidation led to 3,4-dihydroxydiphenyl ether. As a characteristic product resulting from the cleavage of an aromatic ring, the lactone of 2-hydroxy-4-phenoxymuconic acid was identified. The possible mechanism of ring cleavage to yield this metabolite is discussed. 相似文献
65.
In nerve tissue the histochemical nicotinamide adenine dinucleotide phosphate-diaphorase (NADPH-d) reaction is considered a suitable marker for nitric oxide synthase (NOS) activity. We have previously shown that the NOS-specific inhibitorl-nitroarginine (l-NNA) can block NADPH-d staining in intermediolateral (IML) neurons of the rat spinal cord; such a reaction might serve as a control for the presence of a NOS-related catalytic activity, i.e.,l-NNA-dependent NO synthesis in these neurons. However,l-NNA inhibition of neuronal NADPH-d is inconsistent and is therefore disputed by others. This prompted us to reinvestigate the reaction conditions to provide a standardized protocol for inhibition experiments. In IML neurons of formaldehyde-fixed spinal cord tissue, inhibition of NADPH-d reaction was tested by preincubation of frozen sections with the flavin-binder diphenylene iodonium chloride (DPI, 10 M-1 mM) which blocked the NADPH-d reaction in a concentration-dependent way, suggesting an inverse relationship of inhibitor concentration and final reaction product generated. Preincubation with the NOS-specific inhibitorl-NNA in glycine-NaOH buffer (pH 8.5–9.5) but notl-nitroarginine methyl ester (l-NAME) revealed a concentration-dependent blocking effect on neuronal NADPH-d comparable to the effects seen with DPI, suggesting the existence of al-NNA sensitive NADPH-d activity. Blocking withl-NNA (100 M-10 mM) was prevented by excessl-arginine (10–100 mM), suggesting competitive binding sites. NADPH-d staining was not inhibited by 7-nitro indazole, another NOS inhibitor. Thus, in formaldehyde-fixed nervous tissue both DPI andl-NNA inhibit the NOS-associated catalytic NADPH-d activity, thereby preventing NADPH-dependent conversion of nitroblue tetrazolium to formazan.Presented in the Workshop Detection of NO-synthases at the XXXVI Symposium of the Society for Histochemistry on Oxy Radicals, 20–23 September 1994, Heidelberg, Germany 相似文献
66.
Altered flower/fruit clusters of the kitul palm used as roosts by the short-nosed fruit bat, Cynopterus sphinx (Chiroptera: Pteropodidae) 总被引:1,自引:0,他引:1
The short-nosed fruit bat (Cynopterus sphinx) creates bell-shaped cavities in flower/fruit clusters of the kitul palm (Caryota urens) by chewing and severing flower and fruit strings. These cavities (stem tents) in which the bats roost are usually about one metre deep and 30 cm in diameter. We observed groups of bats roosting in fully-formed stem tents during the daytime, and the construction and subsequent occupancy of newly formed tent cavities. Stem tents are similar in principle to leaf tents except, instead of being formed when bats chew veins and the surrounding tissues of leaves, stem tents are formed in C. urens when bats completely cut several of the central flower/fruit strings. Flower/fruit strings are mostly severed when they are in an immature stage, at times when they are thin and widely spaced. Once these strings thicken and become heavily-laden with mature fruits, bats cannot penetrate the cluster to sever them. Our observations suggest that a single male enters an immature flower or fruit cluster either from below or the sides and severs the central strings along the peduncle. In early phases of stem-tent construction, C. sphinx severs flower/fruit strings at a rate of about one or two per day, and cluster alteration may continue upwards to two months. Only one immature flower/fruit cluster on a C. urens tree is available for alteration by bats at any given time. That this bat does not roost in the fruit/flower cluster during the day, when a tent is under construction, and the accumulation of chewed flower and fruit strings beneath such a cluster in the morning, suggests that tent construction by C. sphinx is a night-time activity. 相似文献
67.
Ruben G. G. Leenders Hans W. ScheerenPieter H. J. Houba Epie Boven Hidde J. Haisma 《Bioorganic & medicinal chemistry letters》1995,5(24):2975-2980
The synthesis, antiproliferative effect and enzymatic hydrolysis of daunomycin-3′-N- and -4′-O-phosphate and -sulfate derivatives and of daunomycin-3′-N-CO-β-glucuronide and -β-glucoside, designed to be prodrugs in ADEPT are described. The phosphate derivatives were almost as toxic as the parent drug whereas the sulfates were not hydrolyzed by aryl sulfatases. Glucuronyl and glucosyl prodrugs were found to be useful for application in ADEPT. 相似文献
68.
Hans Bohn 《Molecular and cellular biochemistry》1978,20(2):67-75
Summary A review of the present knowledge of human fibrin-stabilizing factors (FSFs) is given. Thus far three human FSFs have been isolated and characterized, namely the FSFs from plasma, platelets and placentae.Placental and platelet FSF are identical; their molecules are composed of two identical polypeptide chains (subunits A) having a molecular weight of 80.000 daltons which are held together by non-covalent bonds. The subunit structure of these FSFs can be written A2.The molecules of plasma FSF (factor XIII) also contain 2 subunits A but in addition another component (subunit S, molecular weight 180.000 daltons) which are held together by non-covalent bonds, too. The subunit structure of plasma factor XIII can be written A2S.The physical and immunochemical properties as well as the amino acid and carbohydrate composition of the FSFs, respectively of the subunits A and S are reported.The biological active part in the FSFs resides in subunit A. The biological role of subunit S is unknown. Protein S occurs in normal plasma in a free state, too; it combines with placental or platelet FSF to form a complex A2S which is indistinguishable from plasma factor XIII. It has been suggested to designate protein S as FSF-binding globulin.The human FSFs are proenzymes which have to be activated by thrombin. The activation step is a limited proteolysis resulting in the release of a peptide (36 amino acid residues) from subunit A. The enzymes formed are transglutaminases; they crosslink the fibrin molecules by the formation of -glutamyl-s-lysine bonds, a process which is designated as fibrin-stabilization.The different methods which exist for assessment of the FSFs are reported. Deficiencies in FSFs which occur can be either hereditary or acquired. The possibilities of substituting FSFs in cases of deficiency and for accelerating wound healing after major surgeries are described. 相似文献
69.
70.
The fat body of developing mid- and late fourth instar larvae of a midge, Chironomus thummi, has been investigated by means of the benzidine reaction for the localization of haemoglobin within cells. In the subepidermal fat body the reaction deposits of the haemoglobin pseudo-peroxidase activity appear predominantly in the intracisternal cavities of ER and the Golgi, and later, in the pharate pupal stage, in small dense granules (0.5–1 μm in. diameter).All the major protein bands of fat body extracts, which are resolved in electrophoresis, give the benzidine reaction and show incorporation of 14C-amino levulinic acids, in this case a specific marker for haemoglobin synthesis. In addition, labelled proteins show identical electrophoretic mobility as the haemoglobins of the haemolymph, suggesting that haemoglobins are synthesized in the fat body. Two types of fat body cells seem to differ with respect to their rôle in haemoglobin metabolism. 相似文献