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41.
Abstract Monoclonal antibodies have been developed and used as specific probe to locate and identify a 29-kDa molecule of axenic Entamoeba histolytica trophozoites. Monoclonal antibody produced by clone C8 (MoAb C8) strongly agglutinated the amoebic trophozoites. THe immunofluorescence of live E. histolytica trophozoites and surface fluorescence of acetone-fixed trophozoites by MoAb C8 indicated existence of a 29-kDa molecule on surface-associated plasma membrane of E. histolytica . The monoclonal antibody belonged to IgG1 isotype. The prior treatment of E. histolytica trophozoites with MoAb C8 resulted in significant ( P < 0.01) reduction in adherence of amoebic trophozoites to cultured Chinese Hamster Ovary cells and significant ( P < 0.01) reduction in cytotoxicity to cultured Baby Hamster Kidney cells. Pretreatment of amoebic trophozoites with MoAb C8 prior to cultivation in TPS-1 medium resulted in significant ( P < 0.01) reduction in growth of the parasite. Thus, the data suggested that the surface-exposed 29-kDa molecule may be one of the receptors involved in E. histolytica host cell interactions and may possibly modulate amoebic disease processes. 相似文献
42.
Chiara Pavanello Alice Ossoli Arianna Strazzella Patrizia Risè Fabrizio Veglia Marie Lhomme Paolo Parini Laura Calabresi 《Journal of lipid research》2022,63(7):100232
Mutations in the LCAT gene cause familial LCAT deficiency (Online Mendelian Inheritance in Man ID: #245900), a very rare metabolic disorder. LCAT is the only enzyme able to esterify cholesterol in plasma, whereas sterol O-acyltransferases 1 and 2 are the enzymes esterifying cellular cholesterol in cells. Despite the complete lack of LCAT activity, patients with familial LCAT deficiency exhibit circulating cholesteryl esters (CEs) in apoB-containing lipoproteins. To analyze the origin of these CEs, we investigated 24 carriers of LCAT deficiency in this observational study. We found that CE plasma levels were significantly reduced and highly variable among carriers of two mutant LCAT alleles (22.5 [4.0–37.8] mg/dl) and slightly reduced in heterozygotes (218 [153–234] mg/dl). FA distribution in CE (CEFA) was evaluated in whole plasma and VLDL in a subgroup of the enrolled subjects. We found enrichment of C16:0, C18:0, and C18:1 species and a depletion in C18:2 and C20:4 species in the plasma of carriers of two mutant LCAT alleles. No changes were observed in heterozygotes. Furthermore, plasma triglyceride-FA distribution was remarkably similar between carriers of LCAT deficiency and controls. CEFA distribution in VLDL essentially recapitulated that of plasma, being mainly enriched in C16:0 and C18:1, while depleted in C18:2 and C20:4. Finally, after fat loading, chylomicrons of carriers of two mutant LCAT alleles showed CEs containing mainly saturated FAs. This study of CEFA composition in a large cohort of carriers of LCAT deficiency shows that in the absence of LCAT-derived CEs, CEs present in apoB-containing lipoproteins are derived from hepatic and intestinal sterol O-acyltransferase 2. 相似文献
43.
44.
Myosin associated with the male germ cells of angiosperms interacts with actin, promoting transport of the non-motile generative
and later sperm cells in the pollen tube. Myosin localizing on the sperm cell plasma membrane seems negligible in Plumbago, as reflected by the absence of: (i) anti-myosin labeling using immunoelectron microscopy, (ii) sperm motility on actin matrices,
and (iii) electrophoretic movement changes after addition of antibody. Sperm cells injected directly into actively streaming
Nitella internodal cells, however, follow actin bundles and their movement is sensitive to ATP and Mg2+. This may be based on simple charge binding since negatively charged latex beads also migrate on actin, whereas neutral or
positively-charged latex beads do not. Sperm cells are negatively charged according to capillary microelectrophoresis, whereas
killed sperm cells, which are positively charged do not migrate. The sperm cell that normally fertilizes the egg has a higher
calculated charge (8.277 × 103 esu/cm2) compared with the sperm cell that fuses with the central cell (6.120 × 103 esu/cm2).
Received: 15 December 1998 / Accepted: 21 January 1999 相似文献
45.
Analyses of ITS sequences for 49 species of Olearia, including representatives from all currently recognised intergeneric sections, and 43 species from 23 other genera of Astereae,
rooted on eight sequences from Anthemideae, provide no support for the monophyly of this large and morphologically diverse
Australasian genus. Eighteen separate lineages of Olearia are recognised, including seven robust groups. Three of these groups and another eight species are placed within a primary
clade incorporating representatives of Achnophora, Aster, Brachyscome, Calotis, Camptacra, Erigeron, Felicia, Grangea, Kippistia, Lagenifera, Minuria, Oritrophium,
Peripleura, Podocoma, Remya, Solidago, Tetramolopium and Vittadinia. The remaining four groups and three individual species lie within a sister clade that also includes Celmisia, Chiliotrichum, Damnamenia, Pleurophyllum and Pachystegia. Relationships within each primary clade are poorly resolved. There is some congruence between this molecular estimate of
the phylogeny and the distribution of types of abaxial leaf-hair, which is the basis of the present sectional classification
of Olearia, but all states appear to have arisen more than once within the tribe. It is concluded that those species placed within the
second primary clade should be removed from the genus, but the extent to which species placed within the first primary clade
constitute a monophyletic group can only be resolved with further sequence data.
Received November 12, 2001; accepted April 29, 2002 Published online: November 22, 2002
Addresses of authors: Edward W. Cross, Centre for Plant Biodiversity Research, CSIRO, GPO Box 1600, Canberra, ACT 2601, Australia
(E-mail: ed.cross@csiro.au); Christopher J . Quinn, Royal Botanic Gardens, Mrs Macquaries Rd., Sydney, NSW 2000, Australia;
Steven J. Wagstaff, Landcare Research, PO Box 69, Lincoln 8152, New Zealand. 相似文献
46.
47.
Ablation of rat myenteric plexus with benzalkonium chloride has provided a model of intestinal aganglionosis, but the degenerative
responses are not well understood. We examined the effects of this detergent on neurons and glia, including expression of
c-Myc, c-Jun, JunB, and c-Fos, and on immunocytes in the guinea-pig ileum. Benzalkonium chloride (0.1%) or saline was applied
to the serosal surface of distal ileum. Tissues were analyzed 2, 3, or 7 days later and compared with cyclosporine-treated
and untreated animals. More than 90% of myenteric neurons were destroyed in ileal segments 3–7 days after benzalkonium-chloride
treatment. Glia withdrew processes from around neurons after 2 days and were mostly gone after 3 days. Neuronal c-Myc began
to disappear while c-Fos, c-Jun, and JunB were evident in some neuronal nuclei after 2 or 3 days. After 3 days, widespread
apoptosis was evident in the myenteric plexus. Populations of T cells, B cells, and macrophage-like cells in untreated and
saline-treated myenteric plexuses were substantially increased 3 and 7 days after benzalkonium-chloride treatment. Cyclosporine
delayed significant neuronal loss. We conclude that a variety of degenerative mechanisms may be active in this model, including
an immune response which may actively contribute to tissue destruction.
Received: 13 September 1996 / Accepted: 20 January 1997 相似文献
48.
49.
The concept of the blood-aqueous barrier is largely based on the use of horseradish peroxidase (HRP). The present investigation
was designed to check its reliability as a macromolecular tracer, especially with regard to the transport of plasma proteins.
Rabbits were killed 5 min to 24 h after being intravenously injected with HRP. The tracer diffused rapidly, reaching the aqueous
humor of the eye in 3 min or less and was detected at high concentration in the narrow space between the outer epithelial
layer of the ciliary epithelium and the wall of the pervious capillaries in the stroma of the processes. HRP appeared to migrate
from the blood to the posterior chamber, permeating the tight junctions, viz., the anatomical basis of the blood-aqueous barrier.
It was detected at higher concentration at the anterior surface of the iris, at short time intervals; this was interpreted
as penetration of the tracer from the aqueous humor of the anterior chamber. The choroid was also labeled in continuation
with the reaction in the stroma of the pars plana of the ciliary body which, in turn, sometimes reached the iris root. Therefore,
the pervious blood vessels of the choroid could be a source of macromolecules for the iris root. HRP also induced the formation
of lysosomes in the ciliary epithelium. This can hardly be accepted as the way in which plasma proteins are physiologically
transported to the aqueous humor. However, the pathway of HRP migration over short time intervals seems to be in agreement
with previous research indicating that the entrance of serum albumin into the posterior chamber is the first step of its incorporation
into the aqueous humor.
Received: 7 June 1996 / Accepted: 15 January 1997 相似文献
50.