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排序方式: 共有473条查询结果,搜索用时 15 毫秒
31.
Erickson RP Kiela M Devine PJ Hoyer PB Heidenreich RA 《Molecular reproduction and development》2002,62(2):167-173
Niemann-Pick type C disease is a progressive neurological disease with cholesterol storage in liver, and npc1-/- mice share these features and are sterile. We have searched for the cause of sterility and found normal folliculogenesis and progesterone levels but lack of implantation. Multiple drug resistance (MDR) P-glycoproteins are plasma membrane proteins implicated in the movement of drugs and lipids across membranes. Their functions are inhibited by progesterone, which has been shown to alter cellular cholesterol homeostasis and has implicated P-glycoproteins in the movement of cholesterol to the endoplasmic reticulum. We have introduced the mdr1a knockout into the npc1 mutant line. While the neurological disease continues at its usual rate, preventing the females from taking care of their litters, npc1-/-, mdr1a-/- females became fertile. Although the mdr1a P-glycoprotein co-localizes with caveolae, neither caveolin-1 nor npc1 levels were significantly altered in the livers of double homozygotes. The absence of mdr1a was confirmed by immunoblotting, but npc1 deficiency was not associated with consistent changes in cerebellar mdr1a in mdr1a+/+ mice. The results show that a mdr1a mutation is an in vivo suppressor of female sterility in npc1 deficient mice. 相似文献
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34.
Devine L Kieffer LJ Aitken V Kavathas PB 《Journal of immunology (Baltimore, Md. : 1950)》2000,164(2):833-838
The T cell coreceptor CD8 exists on mature T cells as disulfide-linked homodimers of CD8 alpha polypeptide chains and heterodimers of CD8 alpha- and CD8 beta-chains. The function of the CD8 alpha-chain for binding to MHC class I and associating with the tyrosine kinase p56lck was demonstrated with CD8 alpha alpha homodimers. CD8 alpha beta functions as a better coreceptor, but the actual function of CD8 beta is less clear. Addressing this issue has been hampered by the apparent inability of CD8 beta to be expressed without CD8 alpha. This study demonstrates that human, but not mouse, CD8 beta can be expressed on the cell surface without CD8 alpha in both transfected COS-7 cells and murine lymphocytes. By creating chimeric proteins, we show that the murine Ig domain of CD8 beta is responsible for the lack of expression of murine CD8 beta beta dimers. In contrast to CD8 alpha alpha, CD8 beta beta is unable to bind MHC class I in a cell-cell adhesion assay. Detection of this form of CD8 should facilitate studies on the function of the CD8 beta-chain and indicates that caution should be used when interpreting studies on CD8 function using chimeric protein with the murine CD8 beta beta Ig domain. In addition, we demonstrate that the Ig domains of CD8 alpha are also involved in controlling the ability of CD8 to be expressed. Mutation of B- and F-strand cysteine residues in CD8 alpha reduced the ability of the protein to fold properly and, therefore, to be expressed. 相似文献
35.
Because the H2O2 and O2
− generated during a pathogen-triggered oxidative burst could either protect or destroy a besieged plant cell, their synthesis
might be expected to be tightly regulated. We have examined the nature of this regulation as it is communicated between homologous
and heterologous oxidative-burst pathways, using both chemical (oligogalacturonic acid, harpin, fensulfothion) and mechanical
(osmotic stress) stimuli to induce the burst. We report here that the above three chemical elicitors attenuate a subsequent
oxidative burst induced in cultured soybean (Glycine max L.) cells by either the same (homologous desensitization) or a different chemical elicitor (heterologous desensitization).
Further, when the magnitude of the initial oxidative burst is maximal, the cells remain refractory to subsequent elicitation
for at least 10 min and then revive their sensitivities to re-stimulation with a half-time of >20 min. Mechanical stimulation
of the oxidative burst appears to be regulated by a different set of constraints. Although initiation of a mechanically induced
burst leads to attenuation of a subsequent mechanically induced burst, the same mechanical stimulus is peculiarly unable to
reduce a subsequent chemically induced burst. The converse is also true, suggesting that heterologous desensitization of the
oxidative burst does not extend to mixed chemical and mechanical/osmotic stimuli. However, communication between these disparate
forms of elicitation is still demonstrated to occur, since low-level chemical stimuli strongly synergize concurrent low-level
osmotic stimuli and vice versa. Furthermore, the pattern of synergy changes dramatically if one stimulus is administered immediately
prior to the other. Taken together, these data demonstrate that significant cross-talk occurs among the different signaling
pathways of the oxidative burst and that the overall process is tightly regulated.
Received: 10 January 2000 / Accepted: 22 February 2000 相似文献
36.
Mattevi VS Fiegenbaum M Salzano FM Weiss KM Moore J Monsalve MV Devine DV Hutz MH 《American journal of physical anthropology》2000,112(3):311-317
Haplotypes derived from five polymorphic restriction sites were determined in 50 Carrier-Sekani and 70 Mvskoke chromosomes, and the results were integrated with those previously obtained for 11 South American Indian populations. Eleven haplotypes were identified in the Mvskokes, while five were observed in the Carrier-Sekani. As in South American natives, haplotype 2 (+----) and 6 (-++ -+) were the most prevalent among the Mvskoke (46% and 30%, respectively). In the Carrier-Sekani, haplotype 2 was also the most common, but haplotype 5 (-+ -++) was somewhat more frequent (18%) than 6 (12%). High heterozygosities, as well as genetic differentiation, were observed among these two North American and two other South American groups (Mapuche and Xavante). They could be due to non-Indian admixture in the Mvskoke and Mapuche, but the findings in the other two populations require some other type of explanation. 相似文献
37.
Base Composition Skews, Replication Orientation, and Gene Orientation in 12 Prokaryote Genomes 总被引:21,自引:0,他引:21
Michael J. McLean Kenneth H. Wolfe Kevin M. Devine 《Journal of molecular evolution》1998,47(6):691-696
Variation in GC content, GC skew and AT skew along genomic regions was examined at third codon positions in completely sequenced
prokaryotes. Eight out of nine eubacteria studied show GC and AT skews that change sign at the origin of replication. The
leading strand in DNA replication is G-T rich at codon position 3 in six eubacteria, but C-T rich in two Mycoplasma species. In M. genitalium the AT and GC skews are symmetrical around the origin and terminus of replication, whereas its GC content variation has been
shown to have a centre of symmetry elsewhere in the genome. Borrelia burgdorferi and Treponema pallidum show extraordinary extents of base composition skew correlated with direction of DNA replication. Base composition skews
measured at third codon positions probably reflect mutational biases, whereas those measured over all bases in a sequence
(or at codon positions 1 and 2) can be strongly affected by protein considerations due to the tendency in some bacteria for
genes to be transcribed in the same direction that they are replicated. Consequently in some species the direction of skew
for total genomic DNA is opposite to that for codon position 3.
Received: 2 February 1998 / Accepted: 15 June 1998 相似文献
38.
CA Kalva-Filho EZ Campos VL Andrade ASR Silva AM Zagatto MCS Lima M Papoti 《Biology of sport / Institute of Sport》2015,32(4):333-337
The aims of the present study were to investigate the relationship of aerobic and anaerobic parameters with 400 m performance, and establish which variable better explains long distance performance in swimming. Twenty-two swimmers (19.1±1.5 years, height 173.9±10.0 cm, body mass 71.2±10.2 kg; 76.6±5.3% of 400 m world record) underwent a lactate minimum test to determine lactate minimum speed (LMS) (i.e., aerobic capacity index). Moreover, the swimmers performed a 400 m maximal effort to determine mean speed (S400m), peak oxygen uptake () and total anaerobic contribution (CANA). The CANA was assumed as the sum of alactic and lactic contributions. Physiological parameters of 400 m were determined using the backward extrapolation technique ( and alactic contributions of CANA) and blood lactate concentration analysis (lactic anaerobic contributions of CANA). The Pearson correlation test and backward multiple regression analysis were used to verify the possible correlations between the physiological indices (predictor factors) and S400m (independent variable) (p < 0.05). Values are presented as mean ± standard deviation. Significant correlations were observed between S400m (1.4±0.1 m·s-1) and LMS (1.3±0.1 m·s-1; r = 0.80), (4.5±3.9 L·min-1; r = 0.72) and CANA (4.7±1.5 L·O2; r= 0.44). The best model constructed using multiple regression analysis demonstrated that LMS and explained 85% of the 400 m performance variance. When backward multiple regression analysis was performed, CANA lost significance. Thus, the results demonstrated that both aerobic parameters (capacity and power) can be used to predict 400 m swimming performance. 相似文献
39.
Genetic control of bacterial suicide: regulation of the induction of PBSX in Bacillus subtilis. 总被引:1,自引:1,他引:1 下载免费PDF全文
PBSX is a phage-like bacteriocin (phibacin) of Bacillus subtilis 168. Bacteria carrying the PBSX genome are induced by DNA-damaging agents to lyse and produce PBSX particles. The particles cannot propagate the PBSX genome. The particles produced by this suicidal response kill strains nonlysogenic for PBSX. A 5.2-kb region which controls the induction of PBSX has been sequenced. The genes identified include the previously identified repressor gene xre and a positive control factor gene, pcf. Pcf is similar to known sigma factors and acts at the late promoter PL, which has been located distal to pcf. The first two genes expressed from the late promoter show homology to genes encoding the subunits of phage terminases. 相似文献
40.
Although a large proportion (44%) of the human genome is occupied by transposons and transposon-like repetitive elements, only a small proportion (<0.05%) of these elements remain active today. Recent evidence indicates that approximately 35-40 subfamilies of Alu, L1 and SVA elements (and possibly HERV-K elements) remain actively mobile in the human genome. These active transposons are of great interest because they continue to produce genetic diversity in human populations and also cause human diseases by integrating into genes. In this review, we examine these active human transposons and explore mechanistic factors that influence their mobilization. 相似文献