全文获取类型
收费全文 | 747篇 |
免费 | 80篇 |
出版年
2023年 | 5篇 |
2022年 | 4篇 |
2021年 | 11篇 |
2020年 | 13篇 |
2019年 | 19篇 |
2018年 | 17篇 |
2017年 | 19篇 |
2016年 | 28篇 |
2015年 | 29篇 |
2014年 | 32篇 |
2013年 | 51篇 |
2012年 | 64篇 |
2011年 | 51篇 |
2010年 | 28篇 |
2009年 | 18篇 |
2008年 | 44篇 |
2007年 | 47篇 |
2006年 | 41篇 |
2005年 | 49篇 |
2004年 | 48篇 |
2003年 | 43篇 |
2002年 | 36篇 |
2001年 | 2篇 |
2000年 | 4篇 |
1999年 | 9篇 |
1998年 | 9篇 |
1997年 | 6篇 |
1996年 | 10篇 |
1995年 | 3篇 |
1994年 | 10篇 |
1993年 | 4篇 |
1992年 | 4篇 |
1991年 | 10篇 |
1990年 | 8篇 |
1989年 | 2篇 |
1988年 | 5篇 |
1987年 | 2篇 |
1986年 | 3篇 |
1985年 | 4篇 |
1984年 | 3篇 |
1983年 | 3篇 |
1981年 | 3篇 |
1980年 | 5篇 |
1972年 | 4篇 |
1970年 | 2篇 |
1969年 | 3篇 |
1968年 | 4篇 |
1952年 | 1篇 |
1949年 | 1篇 |
1948年 | 1篇 |
排序方式: 共有827条查询结果,搜索用时 15 毫秒
1.
A specific β-adrenergic-stimulated cyclic AMP generating system has been evidenced in rat posterior pituitary. This is clearly demonstrated by: 1) the adenylate cyclase (AC) affinity for stimulants was in the order ISO > NA > DA, and 2) propranolol, a specific β-adrenergic receptor blocker, was the only antagonist of the system. Clonidine and apomorphine were completely inactive, thus excluding an α-adrenergic and/or dopaminergic component in this AC system. Our data also indicate that dopaminergic receptors present in both pituitary lobes are not coupled to an AC. 相似文献
2.
3.
L. Kádasi J. Gécz J. Matúšek T. Krivušová V. Ferák M. Devoto J. Hruškovič G. Romeo 《Human genetics》1992,89(3):305-306
Summary Analysis of a sample of 50 unrelated cystic fibrosis (CF) patients and 46 nuclear families from Slovakia (Czechoslovakia) by the polymerase chain reaction and Southern hybridization revealed that the proportion of the F508 mutation was 58% in this population, and that the frequency of the B (i.e., KM19/XV2c [1–2]) haplotype was increased in both F508 and nonF508 CF chromosomes (98% and 46%, respectively). These results support the view that the trans-European gradient of the F508 frequency is of a geographical rather than of an ethnic origin, and that in Slavonic populations, there exists an as yet unidentified but frequent CF mutation other than F508, associated with the B haplotype. 相似文献
4.
Cell cycle regulation of the E2F transcription factor involves an interaction with cyclin A. 总被引:84,自引:0,他引:84
We have examined E2F binding activity in extracts of synchronized NIH 3T3 cells. During the G0 to G1 transition, there is a marked increase in the level of active E2F. Subsequently, there are changes in the nature of E2F-containing complexes. A G1-specific complex increases in abundance, disappears, and is then replaced by another complex as S phase begins. Analysis of extracts of thymidine-blocked cells confirms that the complexes are cell cycle regulated. We also show that the cyclin A protein is a component of the S phase complex. Each complex can be dissociated by the adenovirus E1A 12S product, releasing free E2F. The release of E2F from the cyclin A complex coincides with the stimulation of an E2F-dependent promoter. We suggest that these interactions control the activity of E2F and that disruption of the complexes by E1A contributes to a loss of cellular proliferation control. 相似文献
5.
Katrin Kausch Clemens R. Müller Tiemo Grimm Kenneth Ricker Marcella Rietschel Sabine Rudnik-Schöneborn Klaus Zerres 《Human genetics》1991,86(3):317-318
Summary Two recent articles have reported the linkage of a gene for recessive spinal muscular atrophy (SMA) on the chromosome region 5q11.2–13.3. Our data show no linkage of the dominantly inherited forms of SMA to this chromosome region. 相似文献
6.
7.
A new iridoid glucoside has been isolated from Stachytarpheta mutabilis and assigned the structure and configuration of 6β-hydroxyipolamiide on the basis of 1H NMR and 13C NMR evidence. The conversion of this compound into penta- acetyllamiol proved the above assignment. 相似文献
8.
Giovanna P. Marziani Longo Marcella Bracale Gianfranca Rossi Claudio P. Longo 《Plant molecular biology》1990,14(4):569-573
Cotyledons were excised from imbibed watermelon seeds, grown for 4 days in darkness on water or 10 M benzyladenine (BA) and then tested for the presence of the light-harvesting chlorophyll a/b protein (LHCP) and its mRNA. LHCP was assayed immunologically by western blotting of SDS gels: the protein was present in plastids, but it was not recovered with the thylakoid fraction. Antibodies directed against LHCP precipitated a 32 kDa polypeptide from translation products of poly(A) RNA of cotyledons only if these had been grown on BA. Taken together the data suggest that in absence of light cytokinins are necessary for the maintenance of a detectable level of LHCP-mRNA as well as for synthesis of the protein. 相似文献
9.
Marcella Carcupino Anna Maria Fausto Maria Luisa Bernardino Ortega Marzio Zapparoli Massimo Mazzini 《Zoomorphology》1996,116(3):103-110
Spermatophore development and ultrastructure of the mature sperm of Craterostigmus tasmanianus were studied using light and electron microscopy. In C. tasmanianus, as in the Scolopendromorpha, the spermatophore develops within the vas deferens. The latter consists of three parts, each
with a different morphology. The first may be involved in guiding the sperm to roll up into typical ring-like structures,
while the other two, which show an evident secretory activity, secrete the acellular wall of the spermatophores. The ultrastructure
of mature spermatozoa showed that a very close similarity exists between Craterostigmomorpha and Lithobiomorpha, especially
regarding the organization of the connecting piece. Based on this similarity, we consider the Craterostigmomorpha together
with the Scolopendromorpha, Geophilomorpha and Lithobiomorpha (=Pleurostigmophora) to be the sister group of the Scutigeromorpha.
Accepted: 2 June 1996 相似文献
10.
A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3. 总被引:1,自引:1,他引:0 下载免费PDF全文
R. Fujita E. Bingham P. Forsythe C. McHenry V. Aita B. A. Navia K. Dry M. Segal M. Devoto G. Bruns A. F. Wright J. Ott P. A. Sieving A. Swaroop 《American journal of human genetics》1996,59(1):152-158
Genetic loci for X-linked retinitis pigmentosa (XLRP) have been mapped between Xp11.22 and Xp22.13 (RP2, RP3, RP6, and RP15). The RP3 gene, which is responsible for the predominant form of XLRP in most Caucasian populations, has been localized to Xp21.1 by linkage analysis and the map positions of chromosomal deletions associated with the disease. Previous linkage studies have suggested that RP3 is flanked by the markers DXS1110 (distal) and OTC (proximal). Patient BB was thought to have RP because of a lesion at the RP3 locus, in addition to chronic granulomatous disease, Duchenne muscular dystrophy (DMD), mild mental retardation, and the McLeod phenotype. This patient carried a deletion extending approximately 3 Mb from DMD in Xp21.3 to Xp21.1, with the proximal breakpoint located approximately 40 kb centromeric to DXS1110. The RP3 gene, therefore, is believed to reside between DXS1110 and the proximal breakpoint of the BB deletion. In order to refine the location of RP3 and to ascertain patients with RP3, we have been analyzing several XLRP families for linkage to Xp markers. Linkage analysis in an American family of 27 individuals demonstrates segregation of XLRP with markers in Xp21.1, consistent with the RP3 subtype. One affected mate shows a recombination event proximal to DXS1110. Additional markers within the DXS1110-OTC interval show that the crossover is between two novel polymorphic markers, DXS8349 and M6, both of which are present in BB DNA and lie centromeric to the proximal breakpoint. This recombination places the XLRP mutation in this family outside the BB deletion and redefines the location of RP3. 相似文献