全文获取类型
收费全文 | 7437篇 |
免费 | 860篇 |
国内免费 | 3篇 |
出版年
2021年 | 149篇 |
2020年 | 88篇 |
2019年 | 120篇 |
2018年 | 131篇 |
2017年 | 119篇 |
2016年 | 184篇 |
2015年 | 300篇 |
2014年 | 319篇 |
2013年 | 397篇 |
2012年 | 502篇 |
2011年 | 481篇 |
2010年 | 291篇 |
2009年 | 260篇 |
2008年 | 403篇 |
2007年 | 417篇 |
2006年 | 380篇 |
2005年 | 328篇 |
2004年 | 311篇 |
2003年 | 318篇 |
2002年 | 328篇 |
2001年 | 121篇 |
2000年 | 120篇 |
1999年 | 130篇 |
1998年 | 101篇 |
1997年 | 60篇 |
1996年 | 62篇 |
1995年 | 72篇 |
1994年 | 66篇 |
1993年 | 51篇 |
1992年 | 77篇 |
1991年 | 83篇 |
1990年 | 89篇 |
1989年 | 71篇 |
1988年 | 85篇 |
1987年 | 72篇 |
1986年 | 66篇 |
1985年 | 72篇 |
1984年 | 66篇 |
1983年 | 70篇 |
1982年 | 51篇 |
1981年 | 41篇 |
1980年 | 59篇 |
1979年 | 59篇 |
1978年 | 51篇 |
1977年 | 50篇 |
1974年 | 41篇 |
1973年 | 53篇 |
1972年 | 49篇 |
1971年 | 46篇 |
1969年 | 47篇 |
排序方式: 共有8300条查询结果,搜索用时 343 毫秒
61.
Camilynn I. Brannan Debra J. Gilbert Jeffrey D. Ceci Yoichi Matsuda Verne M. Chapman John A. Mercer Harvey Eisen Laura A. Johnston Neal G. Copeland Nancy A. Jenkins 《Genomics》1992,13(4):1075-1081
We have used an interspecific backcross between C57BL/6J and Mus spretus to derive a molecular genetic linkage map of chromosome 15 that includes 25 molecular markers and spans 93% of the estimated length of chromosome 15. Using a second interspecific backcross that was analyzed with a centromere-specific marker, we were also able to position our map with respect to the chromosome 15 centromere. This map provides molecular access to many discrete regions on chromosome 15, thus providing a framework for establishing relationships between cloned DNA markers and known mouse mutations and for identifying homologous genes in mice and humans that may be involved in disease. 相似文献
62.
Monica J. Justice Bebra J. Gilbert Kenneth W. Kinzler Bert Vogelstein Authur M. Buchberg Jeffrey D. Ceci Yoichi Matsuda Verne M. Chapman Christos Patriotis Antonios Makris Philip N. Tsichlis Nancy A. Jenkins Neal G. Copeland 《Genomics》1992,13(4):1281-1288
An interspecific backcross between C57BL/6J and Mus spretus was used to generate a molecular genetic linkage map of mouse chromosome 18 that includes 23 molecular markers and spans approximately 86% of the estimated length of the chromosome. The Apc, Camk2a, D18Fcr1, D18Fcr2, D18Leh1, D18Leh2, Dcc, Emb-rs3, Fgfa, Fim-2/Csfmr, Gnal, Grl-1, Grp, Hk-1rs1, Ii, Kns, Lmnb, Mbp, Mcc, Mtv-38, Palb, Pdgfrb, and Tpl-2 genes were mapped relative to each other in one interspecific backcross. A second interspecific backcross and a centromere-specific DNA satellite probe were used to determine the distance of the most proximal chromosome 18 marker to the centromere. The interspecific map extends the known regions of linkage homology between mouse chromosome 18 and human chromosomes 5 and 18 and identifies a new homology segment with human chromosome 10p. It also provides molecular access to many regions of mouse chromosome 18 for the first time. 相似文献
63.
Donna Robbins Colin A. Chapman Richard W. Wrangham 《Primates; journal of primatology》1991,32(3):301-305
Gibbons and spider monkeys have similar diets, body size, and locomotor patterns. They are therefore expected to be subject
to similar socioecological rules. However their grouping patterns differ. Gibbons live in small stable groups, whereas spider
monkey form unstable sub-groups that vary from small to large during different seasons. If similar principles apply to the
two species, food abundance should vary more for spider monkeys than for gibbons; food density should be similar for the two
species when spider monkey sub-groups are the same size as gibbon groups; and the highest level of food abundance should be
higher for spider monkeys than for gibbons. These predictions are upheld for a comparison of particular populations ofHylobates muelleri andAteles geoffroyi. 相似文献
64.
D D Wagner S Saffaripour R Bonfanti J E Sadler E M Cramer B Chapman T N Mayadas 《Cell》1991,64(2):403-413
Endothelial cells store the multimeric adhesive glycoprotein von Willebrand factor (vWf), which promotes the formation of a platelet plug at the site of vessel injury. To investigate the packaging of vWf into the granules called Weibel-Palade bodies, we expressed pro-vWf cDNA and cDNA lacking the prosequence in a variety of cell lines. Storage granules formed only in cells that contain a regulated pathway of secretion. Furthermore, packaging required the prosequence. Pro-vWf, lacking the C-terminal region involved in interchain disulfide bonding, formed granules. We conclude that the signal for storage is universal in that an adhesive glycoprotein can be stored by a hormone-secreting cell; the storage of vWf is independent of its covalent multimeric structure; the unusual rod shape of Weibel-Palade bodies is due to vWf; and the vWf propolypeptide is necessary for the formation of vWf storage granules. 相似文献
65.
Mauricio M. Bustos Fatma A. Kalkan Kathryn A. VandenBosch Timothy C. Hall 《Plant molecular biology》1991,16(3):381-395
An intron-less phaseolin gene [15] was used to express phaseolin polypeptides in transgenic tobacco plants. The corresponding amounts of phaseolin immunoreactive polypeptides and mRNA were similar to those found in plants transformed with a bean genomic DNA sequence that encodes an identical -phaseolin subunit. These results justified the use of the intron-less gene for engineering of the phaseolin protein by oligonucleotide-directed mutagenesis. Each and both of the two Asn residues that serve as glycan acceptors in wild-type phaseolin were modified to prevent N-linked glycosylation. Wild-type (wti–) and mutant phaseolin glycoforms (dgly
1, dgly
2 and dgly
1,2) were localized to the protein body matrix by immunogold microscopy. Although quantitative slot-blot hybridization analysis showed similar levels of phaseolin mRNA in transgenic seed derived from all constructs, seed from the dgly
1 and dgly
2 mutations contained only 41% and 73% of that expressed from the wild-type control; even less (23%) was present in seed of plants transformed with the phaseolin dgly
1,2 gene. Additionally, the profile of 25–29 kDa processed peptides was different for each of the glycoforms, indicating that processing of the full-length phaseolin polypeptides was modified. Thus, although targeting of phaseolin to the protein body was not eliminated by removal of the glycan side-chains, decreased accumulation and stability of the full-length phaseolin protein in transgenic tobacco seed were evident.Abbreviations bp
base pair(s)
- DAF
days after flowering
- GUS
-glucuronidase
- kb
kilobase
- kDa
kilodalton 相似文献
66.
Eugene M. Rinchik Terry Magnuson Bernadette Holdener-Kenny Gavin Kelsey Albert Bianchi Claudio J. Conti Fran?ois Chartier Kathryn A. Brown Stephen D. M. Brown Josephine Peters 《Mammalian genome》1992,3(Z1):S104-S120
Chair of Committee for Mouse Chromosome 7 相似文献
67.
L C Teh C J Ormandy A S Surus R L Sutherland G E Chapman 《Hormones et métabolisme》1988,20(5):278-281
The distribution of 125I radioactivity in the liver, kidneys, adrenals and serum of male rats was measured 10 minutes after an intravenous bolus of 125I-labelled human growth hormone (hGH) was administered in the presence or absence of a large excess of ovine growth hormone or ovine prolactin. The hGH binding sites in the adrenals had displacement properties characteristic of lactogenic receptors, whereas those in the liver had displacement properties characteristic of somatogenic receptors. Bovine and ovine adrenal microsomal membrane fractions contained high affinity (Ka = 1.4-3.3 nM-1) binding sites for hGH which showed ligand specificity typical of lactogenic receptors. It is concluded that the hGH binding site in the adrenal gland is a classical lactogenic receptor and that this tissue is a convenient and rich (42.6 +/- 6.4 fmol hGH specifically bound/mg protein) source of receptor suitable for further characterization. 相似文献
68.
69.
Platelet activating factor is a potent stimulant of the production of active oxygen species by human monocyte-derived macrophages 总被引:6,自引:0,他引:6
M Rouis F Nigon M J Chapman 《Biochemical and biophysical research communications》1988,156(3):1293-1301
Platelet activating factor (PAF; C16), 1-O-Hexadecyl-2-acetyl-sn-glycero-3-phosphorylcholine) stimulated the production of active oxygen species by human monocyte-derived macrophages in culture. An optimal response was observed at a concentration of 13 microM PAF with half-maximal stimulation at 5 microM. The generation of superoxide ion (O2-) and hydrogen peroxide (H2O2) in response to PAF was inhibited specifically by a PAF-antagonist (1-O-Hexadecyl-2-acetyl-sn-glycero-3-phospho (N,N,N,-trimethyl) hexanolamine; such generation varied with the degree of maturation of cultured monocytes into macrophages. Production of active oxygen species increased progressively to reach a maximal level between days 4 to 6 of culture and remained maximal to day 12, after which it decreased progressively. Phorbol 12-myristate-13-acetate (PMA) and opsonized zymosan also stimulated generation of O2- and H2O2. PAF was however distinguished by its potent capacity to stimulate O2- and H2O2 production even at late stages of macrophage maturation (18 days), at which time both PMA and zymosan lacked significant effect. These findings suggest that PAF is a factor of potential relevance to the inflammatory role of the macrophage in atherogenesis. 相似文献
70.
Activation by reduction of the resting form of cytochrome c oxidase: tests of different models and evidence for the involvement of CuB 总被引:4,自引:0,他引:4
J M Wrigglesworth J Elsden A Chapman N Van der Water M F Grahn 《Biochimica et biophysica acta》1988,936(3):452-464
(1) The reaction of the resting form of oxidised cytochrome c oxidase from ox heart with dithionite has been studied in the presence and absence of cyanide. In both cases, cytochrome a reduction in 0.1 M phosphate (pH 7) occurs at a rate of 8.2.10(4) M-1.s-1. In the absence of cyanide, ferrocytochrome a3 appears at a rate (kobs) of 0.016 s-1. Ferricytochrome a3 maintains its 418 nm Soret maximum until reduced. The rate of a3 reduction is independent of dithionite concentration over a range 0.9 mM-131 mM. In the presence or cyanide, visible and EPR spectral changes indicate the formation of a ferric a3/cyanide complex occurs at the same rate as a3 reduction in the absence of cyanide. A g = 3.6 signal appears at the same time as the decay of a g = 6 signal. No EPR signals which could be attributed to copper in any significant amounts could be detected after dithionite addition, either in the presence or absence of cyanide. (2) Addition of dithionite to cytochrome oxidase at various times following induction of turnover with ascorbate/TMPD, results in a biphasic reduction of cytochrome a3 with an increasing proportion of the fast phase of reduction occurring after longer turnover times. At the same time, the predominant steady state species of ferri-cytochrome a3 shifts from high to low spin and the steady-state level of reduction of cytochrome a drops indicating a shift in population of the enzyme molecules to a species with fast turnover. In the final activated form, oxygen is not required for fast internal electron transfer to cytochrome a3. In addition, oxygen does not induce further electron uptake in samples of resting cytochrome oxidase reduced under anaerobic conditions in the presence of cyanide. Both findings are contrary to predictions of certain O-loop types of mechanism for proton translocation. (3) A measurement of electron entry into the resting form of cytochrome oxidase in the presence of cyanide, using TMPD or cytochrome c under anaerobic conditions, shows that three electrons per oxidase enter below a redox potential of around +200 mV. An initial fast entry of two electrons is followed by a slow (kobs approximately 0.02 s) entry of a third electron.(ABSTRACT TRUNCATED AT 400 WORDS) 相似文献