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81.
The specification of a germ cell as sperm or oocyte and determination of cell number remain unsolved questions in developmental biology. This paper examines Caenorhabditis elegans FOG-1, a CPEB-related RNA-binding protein that controls the sperm fate. We find that abundant FOG-1 protein is observed transiently in germ cells just prior to their expression of an early sperm-differentiation marker. As the germline tissue elongates, abundant FOG-1 appears more and more distally as sperm become specified, but disappears when the germ line switches to oogenesis. This dynamic pattern is controlled by both globally acting and germline-specific sex-determining regulators. Importantly, the extent of FOG-1 expression corresponds roughly to sperm number in wild-type and mutants, altering sperm number. By contrast, three other key regulators of the sperm/oocyte decision do not similarly correspond to sperm number. We suggest that FOG-1 is precisely modulated in both time and space to specify sperm fate and control sperm number. 相似文献
82.
41名肢残者十六项人格特质测验 总被引:1,自引:1,他引:1
张丹 《中国心理卫生杂志》1989,3(6):248-249,271
应用“卡特尔十六项人格特质测验问卷”,对41名肢残者和40名健全人进行对照研究。结果表明,肢残人较健全人在孤独性上具有明显的差异,偏于缄默,固执,关注外界信息,具有一定的防卫倾向。肢残人富于实验性,较健全人更自由、激进、好学,具有较强的独立工作能力,希望生活更充实多彩。在各项能力水平上,肢残上与健全人没有显著差别。不同性别肢残人人格特质在敏感性上差异明显,女性较理智和着重现实,而男性则偏于敏感,易感情用事。 相似文献
83.
G. S. Yakobson S. G. Dobrovol'skaya G. M. Vakulin 《Bulletin of experimental biology and medicine》1978,85(4):502-506
The pattern of injury and repair in the liver of Wistar rats depending on sex, the phase of the estrous cycle, and also under the conditions of deficiency of female sex hormones and after injection of -estradiol into ovariectomized rats was studied by morphometric, histo chemical, and electron-microscopic methods. Structural disturbances caused by CCl4 were found to be increased and reparative reactions inhibited in the liver of females both during the period of a natural increase in the blood estrogen concentration and under the influence of exogenous estradiol, and ovariectomy also had a protective effect. In males, structural changes in the liver were more marked than in females with a low blood estrogen level and differend only a little from those in females during the period of increased secretion of sex steroids.Central Research Laboratory, Novosibirsk Medical Institute. (Presented by Academician of the Academy of Medical Sciences of the USSR V. P. Kaznacheev.) Translated from Byulleten' Éksperimental'noi Biologii i Meditsiny, Vol. 85, No. 4, pp. 460–464, April, 1978. 相似文献
84.
José M. González-García Carmen Antonio José A. Suja Julio S. Rufas 《Chromosome research》1996,4(2):124-132
We have determined the number and location of the nucleolar organizing regions in spermatocytes ofGraphosoma italicum (2n=12A+ XY/XX) by means of silver impregnation, chromomycin A3/distamycin A staining and fluorescencein situ hybridization. The identification of only one nucleolar organizing region located at one of the X chromosome ends has provided a suitable cytological marker to analyse the segregation of this univalent and that of the XY pseudobivalent during the first and second meiotic divisions respectively. Our results clearly show that at first meiotic metaphase the chromatids of the X chromosome are orientated with their long axes perpendicular to the polar axis. Although the kinetic activity is restricted to only one end in both X chromatids during the first meiotic division, both ends of the same chromatid have the same probability of showing such kinetic activity. In this sense, we also report that the chromatid segregation maybe initiated either at the same sister chromatid ends or at opposite ends in each chromatid. Thus, this indicates a sex chromatid independence as regards to the chromatid segregation during the first meiotic division. Throughout the second meiotic division both ends of the X chromatid are involved with the same probability in the end-to-end association to conform the XY pseudobivalent. This also implies a random localization of the kinetic activity at the ends opposite to those involved in the end-to-end association.accepted for publication by J. S. (Pat) Heslop-Harrison 相似文献
85.
The maternal dominance hypothesis has been derived from workwith humans which shows that women who are more dominant thanother women are more likely to conceive sons. In both animalsand humans dominance is a characteristic or personality trait,underpinned by testosterone and responsive to a range of environmentalchanges: physical, social and psychological. Studies of thesex ratio in the social sciences and animal behaviour eithersupport or are compatible with the idea that the sex-determiningrole of X- and Y-chromosome bearing spermatozoa may be precededby factors under maternal control which provide for differentialaccess of spermatozoa. Findings in reproductive physiology andphysiological psychology suggest that folh'cular testosteroneor a related hormone may play a critical role. Reproductivephysiologists have already identified maternal mechanisms whichcould provide the context for such a model. 相似文献
86.
Morel F Gallon F Amice V Le Bris MJ Le Martelot MT Roche S Valéri A Derrien V Herry A Amice J De Braekeleer M 《Human reproduction (Oxford, England)》2002,17(10):2552-2555
BACKGROUND: Several studies have shown an increased frequency of constitutional chromosome aberrations in male and female partners of couples examined prior to ICSI. We conducted a cohort study to determine whether there was an increase in numerical sex chromosome mosaicism among couples undergoing ICSI compared with fertile couples. METHODS: Cytogenetic investigations were performed in 228 females and 208 males seen for ICSI between January 1997 and March 2001. They were matched to control females and males. RESULTS: Sex chromosome loss or gain was observed in at least one cell from 24.1% of ICSI women in comparison with 22% of controls (not significant). A significant difference between these two groups was found when X chromosome loss in at least two cells was considered, 9.6% for ICSI females versus 4.8% for controls (P = 0.01). No significant difference was observed between male groups concerning loss or gain of the X or Y chromosome. CONCLUSION: Our results support previously published studies indicating that the loss of an X chromosome in a single cell in females undergoing ICSI is probably an artefact. However, they suggest that a woman could have true sex chromosome mosaicism when two 45,X0 cells are found. 相似文献
87.
A naive, sexually matureD. melanogaster male tested with a young, sexually immature male will perform vigorous courtship, but the mature male will perform much less courtship if he is subsequently tested with a second young male. This phenomenon is called experience-dependent courtship modification (EDCM). We have shown that exposure to either or both of the two courtship-stimulating pheromones that immature males synthesize is sufficient to induce EDCM. 相似文献
88.
Central precocious puberty and abnormal chromosomal patterns 总被引:1,自引:0,他引:1
Central precocious puberty (PP) can be caused by chromosomal aberrations. We report three patients presenting with central
PP in whom karyotype analysis demonstrated abnormal chromosomal patterns. The first patient was affected by the triple-X syndrome,
commonly characterized by premature ovarian failure. The second patient, a girl with inv dup(15)(pter→q12::q12→pter), had
a chromosomal aberration involving an imprinted region of the human genome, whose deletion is commonly associated with Prader-Willi
syndrome (PWS) and hypogonadotrophic hypogonadism. The third patient was a boy carrying a rare chromosome abnormality, the
duplication of chromosome 9 (q22→qter). All patients had mental retardation, which was mild in patient 1, moderate in patient
2, and severe in case 3. They underwent treatment with luteinizing hormone releasing hormone (LHRH) analogs, which were able
to stop the progression of the sexual development. We confirm that chromosomal aberrations are an important cause of central
PP, and that karyotype analysis in patients with PP and mental retardation, even if mild, is necessary because chromosomal
abnormalities can be present. 相似文献
89.
Treiber FA Turner JR Davis H Strong WB 《International journal of behavioral medicine》1997,4(4):278-291
Two hundred forty-six children (96 Whites, of whom 51 were mates; 150 African- Americans, of whom 69 were males) with a familial
history of essential hypertension (EH) were re-evaluated 5 years after an initial evaluation. During the initial visit, anthropometric,
demographic, and resting cardiovascular (CV) parameters (designated initial baseline levels) were assessed. These CV parameters
(systolic and diastolic blood pressure [BP], heart rate, cardiac output index [CI], and total peripheral resistance index
[TPRI]) were also measured during postural challenge, a video game challenge, and a cold pressor task. At follow-up, resting
CV parameters were again evaluated, and designated as follow-up resting levels. Moderate temporal stability (r range = .43-.56) was observed for all resting CV parameters. Mean stress responses for each CV parameter for all 3 stressors
during the initial visit were positively related to the respective CV follow-up resting level. BP stress responses to postural
change and video game challenge were found to be significant independent predictors of future resting BP after controlling
for standard EH risk factors. Follow-up resting CI was not predicted by any stress responses, whereas follow-up resting TPRI
was predicted by TPRI responses to the video game after controlling for standard EH risk Factors. These results contrast with
those from an earlier 1-year follow-up. where stress responses for neither CI nor TPRI predicted follow-up resting levels.
It appears that, as children get older. TPRI stress responses play a stronger role in vasoconstrictive function.
This research was supported by National Institutes of Health Grant HL41781. 相似文献
90.
Autosome and Sex Chromosome Diversity Among the African Pygmy Mice, Subgenus Nannomys (Murinae; Mus)
Frédéric Veyrunes Josette Catalan Bruno Sicard Terence J. Robinson Jean-Marc Duplantier Laurent Granjon Gauthier Dobigny Janice Britton-Davidian 《Chromosome research》2004,12(4):369-382
The African pygmy mice, subgenus Nannomys, constitute the most speciose lineage of the genus Mus with 19 recognized species. Although morphologically very similar, they exhibit considerable chromosomal diversity which is here confirmed and extended by the G-banding analysis of 65 mice from West and South Africa. On the basis of their karyotype and distribution area, the specimens were assigned to at least five species. Extensive differentiation both within and between species was observed that involved almost exclusively Robertsonian translocations, 23 of which are newly described. Two of the rearrangements were sex chromosome-autosome translocations, associated in some cases with partial deletions of the X or Y chromosomes. Several authors have predicted that the highly deleterious effect of this rearrangement would be reduced if the sex and autosomal segments were insulated by a block of centromeric heterochromatin. The C-banding analyses performed showed that among the species carrying X-autosome translocations, one followed the expected pattern, while the other did not. In this case, functional isolation of the sex and autosome compartments must involve other repetitive sequences or genomic traits that require further molecular characterization. Such studies will provide insight into the causes and consequences of the high diversity of sex chromosome rearrangements in this subgenus. 相似文献