全文获取类型
收费全文 | 8876篇 |
免费 | 933篇 |
国内免费 | 14篇 |
专业分类
耳鼻咽喉 | 60篇 |
儿科学 | 341篇 |
妇产科学 | 280篇 |
基础医学 | 1393篇 |
口腔科学 | 146篇 |
临床医学 | 906篇 |
内科学 | 1815篇 |
皮肤病学 | 125篇 |
神经病学 | 717篇 |
特种医学 | 203篇 |
外科学 | 984篇 |
综合类 | 190篇 |
一般理论 | 7篇 |
预防医学 | 940篇 |
眼科学 | 112篇 |
药学 | 888篇 |
中国医学 | 10篇 |
肿瘤学 | 706篇 |
出版年
2021年 | 129篇 |
2020年 | 87篇 |
2019年 | 93篇 |
2018年 | 161篇 |
2017年 | 102篇 |
2016年 | 138篇 |
2015年 | 146篇 |
2014年 | 227篇 |
2013年 | 362篇 |
2012年 | 507篇 |
2011年 | 569篇 |
2010年 | 287篇 |
2009年 | 280篇 |
2008年 | 460篇 |
2007年 | 548篇 |
2006年 | 544篇 |
2005年 | 515篇 |
2004年 | 527篇 |
2003年 | 469篇 |
2002年 | 505篇 |
2001年 | 138篇 |
2000年 | 145篇 |
1999年 | 150篇 |
1998年 | 135篇 |
1997年 | 124篇 |
1996年 | 118篇 |
1995年 | 105篇 |
1994年 | 112篇 |
1993年 | 96篇 |
1992年 | 120篇 |
1991年 | 136篇 |
1990年 | 109篇 |
1989年 | 110篇 |
1988年 | 115篇 |
1987年 | 94篇 |
1986年 | 67篇 |
1985年 | 84篇 |
1984年 | 74篇 |
1983年 | 90篇 |
1982年 | 86篇 |
1981年 | 68篇 |
1980年 | 71篇 |
1979年 | 74篇 |
1978年 | 66篇 |
1977年 | 51篇 |
1976年 | 44篇 |
1975年 | 33篇 |
1974年 | 43篇 |
1973年 | 45篇 |
1972年 | 46篇 |
排序方式: 共有9823条查询结果,搜索用时 397 毫秒
71.
Kun?Guo Robert?G.?RobertsonEmail author Sasan?Mahmoodi Yoav?Tadmor Malcolm?P.?Young 《Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale》2003,150(3):363-374
Face perception plays a crucial role in primate social communication. We have investigated the pattern of eye movements produced
by rhesus monkeys (Macaca mulatta) as they viewed images of faces. Eye positions were recorded accurately using implanted eye coils, while neutral upright,
inverted and scrambled images of monkey and human faces were presented on a computer screen. The monkeys exhibited a similar
eye scan pattern while viewing familiar and unfamiliar monkey face images, or while viewing monkey and human face images.
No differences were observed in the distribution of viewing times, number of fixations, time into the trial of first saccade
to local facial features, and the temporal and spatial characteristics of viewing patterns across the facial images. However,
there was a greater probability of re-fixation of the eye region of unfamiliar faces during the first few seconds of the trial
suggesting that the eyes are important for the initial encoding of identity. Indeed, the highest fixation density was found
in the eye region of all the face images. The viewing duration and the number of fixations per image decreased when inverted
or scrambled faces were presented. The eye region in these modified images remained the primary area of fixation. However,
the number of fixations directed to the eyes decreased monotonically from the upright images through the inverted versions
to the scrambled face images. Nonetheless, the eyes remain the most salient facial substructure regardless of the arrangement
of other features, although the extent of salience which they attain may depend both on the low level properties of the eyes
and on the global arrangement of facial features.
Electronic Publication 相似文献
72.
McManamny P Chy HS Finkelstein DI Craythorn RG Crack PJ Kola I Cheema SS Horne MK Wreford NG O'Bryan MK De Kretser DM Morrison JR 《Human molecular genetics》2002,11(18):2103-2111
Spinal and bulbar muscular atrophy (SBMA) is an adult-onset motor neuron disease, caused by the expansion of a trinucleotide repeat (TNR) in exon 1 of the androgen receptor (AR) gene. This disorder is characterized by degeneration of motor and sensory neurons, proximal muscular atrophy, and endocrine abnormalities, such as gynecomastia and reduced fertility. We describe the development of a transgenic model of SBMA expressing a full-length human AR (hAR) cDNA carrying 65 (AR(65)) or 120 CAG repeats (AR(120)), with widespread expression driven by the cytomegalovirus promoter. Mice carrying the AR(120) transgene displayed behavioral and motor dysfunction, while mice carrying 65 CAG repeats showed a mild phenotype. Progressive muscle weakness and atrophy was observed in AR(120) mice and was associated with the loss of alpha-motor neurons in the spinal cord. There was no evidence of neurodegeneration in other brain structures. Motor dysfunction was observed in both male and female animals, showing that in SBMA the polyglutamine repeat expansion causes a dominant gain-of-function mutation in the AR. The male mice displayed a progressive reduction in sperm production consistent with testis defects reported in human patients. These mice represent the first model to reproduce the key features of SBMA, making them a useful resource for characterizing disease progression, and for testing therapeutic strategies for both polyglutamine and motor neuron diseases. 相似文献
73.
Salah E. M. El-Begawy Malcolm B. Huglin 《Macromolecular chemistry and physics.》1993,194(4):1105-1113
Significant drift in the compositions of copolymer and of unreacted monomer mixture is predicted to occur during the bulk copolymerization of N-vinyl-2-pyrrolidone (VP) with butyl acrylate (BA), when the inital feed mixture contains 75 wt.-% VP. The drift in copolymer composition has been confirmed by 1 the optical appearance and glass transition (Tg) behaviour of the products of the γ-ray initiated copolymerization at various fractional conversions (C) and 2 the Tg behaviour of low-conversion samples of poly(VP-co-BA) blended in propertions so as to simulate the overall composition of material that would be present cumulatively at selected values of C during an actual copolymerization. The compositions of unreacted monomer mixtures co-existing with copolymer at selected conversions have been calculated and intrinsic viscosities [η] of blends dissolved in these VP/BA mixtures have been measured. Theta conditions for the blends have been established turbidimetrically in chloroform/heptane and the corresponding values of [η]Θ measured. The chain expansion factors thereby derived from [η] and [η]Θ show a decreasing affinity of copolymer for residual monomer during the course of copolymerization. 相似文献
74.
Alexander S. Graphodatsky Polina L. Perelman Natalya V. Sokolovskaya Violetta R. Beklemisheva Natalya A. Serdukova Gauthier Dobigny Stephen J. O’Brien Malcolm A. Ferguson-Smith Fengtang Yang 《Chromosome research》2008,16(1):129-143
Canid species (dogs and foxes) have highly rearranged karyotypes and thus represent a challenge for conventional comparative
cytogenetic studies. Among them, the domestic dog is one of the best-mapped species in mammals, constituting an ideal reference
genome for comparative genomic study. Here we report the results of genome-wide comparative mapping of dog chromosome-specific
probes onto chromosomes of the dhole, fennec fox, and gray fox, as well as the mapping of red fox chromosome-specific probes
onto chromosomes of the corsac fox. We also present an integrated comparative chromosome map between the species studied here
and all canids studied previously. The integrated map demonstrates an extensive conservation of whole chromosome arms across
different canid species. In addition, we have generated a comprehensive genome phylogeny for the Canidae on the basis of the
chromosome rearrangements revealed by comparative painting. This genome phylogeny has provided new insights into the karyotypic
relationships among the canids. Our results, together with published data, allow the formulation of a likely Canidae ancestral
karyotype (CAK, 2n = 82), and reveal that at least 6–24 chromosomal fission/fusion events are needed to convert the CAK karyotype
to that of the modern canids.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
75.
As we age, our skeletal muscle becomes smaller and weaker. In addition, the remaining muscle is more susceptible to damage, particularly following exercise, recovery from damage is severely impaired and muscle is unable to adapt rapidly following sequential periods of exercise. The mechanisms by which skeletal muscle damage occurs are poorly understood and the role that an increased production of free radical species plays in this damage is controversial. However, evidence is emerging which suggests that an increased production of free radicals may act as an activator of the adaptive response in skeletal muscle, resulting in the increased production of antioxidant enzymes and heat shock proteins (HSPs). The increased content of these proteins facilitates rapid remodelling of muscle and provides considerable protection against subsequent periods of damaging exercise. There is considerable evidence that the production of free radicals is modified during the ageing process. The aim of this review is to examine the possible effects of this modification on the ability of muscle cells to respond to stress and the functional effect that this may have on our muscles as we age. 相似文献
76.
Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome families. 下载免费PDF全文
H L Gilbert J L Buxton C T Chan T McKay S Cottrell S Ramsden R M Winter M E Pembrey S Malcolm 《Journal of medical genetics》1997,34(8):651-655
We report the molecular characterisation of two families with Angelman syndrome referred for prenatal diagnosis, in which atypical molecular findings resulted in counselling dilemmas. The first is a familial case of Angelman syndrome in which the two affected children have mutations which affect the imprinting mechanism, as shown by the presence of paternal DNA methylation patterns at D15S63 and SNRPN and biparental inheritance of 15q11-q13 markers. DNA prepared from a 21 week fetal blood sample detected a fetus with normal maternal and paternal DNA methylation patterns at D15S63, but inheritance of the same maternal chromosome 15q11-q13 as the two affected sibs. This is probably a result of germline mosaicism in the mother. The second is a case of Angelman syndrome with an atypical deletion of 15q11-q13, which involves both unusual proximal and distal breakpoints. The deletion was characterised in order to assess the risk of Angelman syndrome in a second pregnancy in the mother of this child. 相似文献
77.
Taams LS Vukmanovic-Stejic M Smith J Dunne PJ Fletcher JM Plunkett FJ Ebeling SB Lombardi G Rustin MH Bijlsma JW Lafeber FP Salmon M Akbar AN 《European journal of immunology》2002,32(6):1621-1630
Anergic/suppressive CD4+CD25+ T cells have been proposed to play an important role in the maintenance of peripheral tolerance. Here we demonstrate that in humans these cells suppress proliferation to self antigens, but also to dietary and foreign antigens. The suppressive CD4+CD25+ T cells display a broad usage of the T cell receptor Vbeta repertoire,suggesting that they recognize a wide variety of antigens. They reside in the primed/memory CD4+CD45RO+CD45RB(low) subset and have short telomeres, indicating that these cells have the phenotype of highly differentiated CD4+ T cells that have experienced repeated episodes of antigen-specific stimulation in vivo. This suggests that anergic/suppressive CD4+CD25+ T cells may be generated in the periphery as a consequence of repeated antigenic encounter. This is supported by the observation that highly differentiated CD4+T cells can be induced to become anergic/suppressive when stimulated by antigen presented by non-professional antigen-presenting cells. We suggest that besides being generated in the thymus, CD4+CD25+ regulatory T cells may also be generated in the periphery. This would provide a mechanism for the generation of regulatory cells that induce tolerance to a wide array of antigens that may not be encountered in the thymus. 相似文献
78.
X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletions 总被引:5,自引:0,他引:5
Huber Irene; Bitner-Gllndzicz Maria; de Kok Yvette J.M.; van der Maarel Silvere M.; Ishikawa-Brush Yumiko; Monaco Anthony P.; Robinson David; Malcolm Susan; Pembrey Marcus E.; Brunner Han G.; Cremers Frans P.M.; Ropers Hans-Hilger 《Human molecular genetics》1994,3(7):1151-1154
We have found that the microsatellite marker AFM207zg5 (DXS995)maps to all previously described deletions which are associatedwith X-linked mixed deafness (DFN3) with or without choroideremiaand mental retardation. Employing this marker and pHU16 (DXS26)we have identified two partially overlapping yeast artificialchromosome clones which were used to construct a complete 850kb cosmid contig. Cosmids from this contig have been testedby Southern blot analysis on DNA from 16 unrelated males withX-linked deafness. Two novel microdeletions were detected inpatients which exhibit the characteristic DFN3 phenotype. Bothdeletions are completely contained within one of the known DFN3-deletions,but one of them does not overlap with two previously describeddeletions in patients with contiguous gene syndromes consistingof DFN3, chorolderemia, and mental retardation. Assuming thatonly a single gene is involved, this suggests that the DFN3gene spans a chromosomal region of at least 400 kb. 相似文献
79.
80.
Classification of anti-FcepsilonRI and anti-IgE autoantibodies in chronic idiopathic urticaria and correlation with disease severity 总被引:5,自引:0,他引:5
Sabroe RA Fiebiger E Francis DM Maurer D Seed PT Grattan CE Black AK Stingl G Greaves MW Barr RM 《The Journal of allergy and clinical immunology》2002,110(3):492-499
BACKGROUND: Circulating autoantibodies against FcepsilonRI, IgE, or both occur in approximately one third of patients with chronic idiopathic urticaria (CIU), but not all autoantibodies initiate histamine release. OBJECTIVE: We sought to classify patients with CIU into subsets on the basis of serum bioactivity and immunoreactivity and to examine the relationship between newly defined subtype and disease severity. METHODS: Sera from patients with CIU (n = 78), dermog-raphism (n = 15), and cholinergic urticaria (n = 10) and sera from healthy subjects (n = 39) were analyzed by means of Western blot analysis for anti-FcepsilonRI autoantibodies and for histamine release from basophils and dermal mast cells. In vivo reactivity of autologous serum was tested by means of intradermal injection, and CIU severity was determined on the basis of clinical interview. RESULTS: We classified sera from patients with CIU into 5 subsets: immunoreactive histamine-releasing anti-FcepsilonRI autoantibodies (n = 20 [26%]); immunoreactive anti-FcepsilonRI autoantibodies without histamine-releasing activity (n = 12 [15%]); anti-IgE-like autoantibodies (n = 7 [9%]); serum containing a mast cell-specific histamine-releasing factor (n = 7 [9%]); and sera with no identifiable factor (n = 32 [41%]). Patients with serum histamine-releasing activity had more severe urticaria than patients without such activity. Positive skin test responses to autologous sera were associated with histamine-releasing anti-FcepsilonRI autoantibodies but not with non-histamine-releasing anti-FcepsilonRI autoantibodies. Neither healthy subjects nor patients with dermographism or cholinergic urticaria had his-tamine-releasing anti-FcepsilonRI autoantibodies. CONCLUSION: These data support the specificity of functional anti-FcepsilonRI autoantibodies to CIU. The identification of distinctive subsets of patients suggests that other pathogenic mechanisms occur in CIU in addition to direct ligation of FcepsilonRI by autoantibodies causing dermal mast cell degranulation. Elucidating these mechanisms might lead to new treatments for CIU. 相似文献