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141.
The initial steps in taste and olfaction result from the activation by
chemical stimuli of taste receptor cells (TRCs) and olfactory receptor
neurons (ORNs). In parallel with these two pathways is the chemosensitive
trigeminal pathway whose neurons terminate in the oral and nasal cavities
and which are activated by many of the same chemical stimuli that activate
TRCs and ORNs. In a recent single unit study we investigated the responses
of rat chorda tympani and glossopharnygeal neurons to a variety of
bitter-tasting alkaloids, including nicotine, yohimbine, quinine,
strychnine and caffeine, as well as capsaicin, the pungent ingredient in
hot pepper. Here we apply many of these same compounds to cultured rat
trigeminal ganglion (TG) neurons and measure changes in intracellular
calcium [Ca2+]i to determine whether TG neurons will respond to these same
compounds. Of the 89 neurons tested, 34% responded to 1 mM nicotine, 7% to
1 mM caffeine, 5% to 1 mM denatonium benzoate, 22% to 1 mM quinine
hydrochloride, 18% to 1 mM strychnine and 55% to 1 microM capsaicin. These
data suggest that neurons from the TG respond to the same bitter-tasting
chemical stimuli as do TRCs and are likely to contribute information sent
to the higher CNS regarding the perception of bitter/irritating chemical
stimuli.
相似文献
142.
143.
Dissociation of MIF production and cell proliferation 总被引:19,自引:0,他引:19
144.
Pablo Jimenez Brundelet 《Biotechnic & histochemistry》1973,48(4):173-175
To provide a routine check for the presence of ferric iron in sections, Perls' method was combined with hematoxylin and eosin as follows. Deparaffinized sections of formalin-fixed tissues are stained in Perls' reagent (1:1 2%, w/v, of potassium ferrocyanide in distilled water and 2%, v/v, concentrated HCl in distilled water) for 20 min. After brief rinsing in distilled water stain sections in Mayer's hemalum, wash in tap water for 5 min, counterstain in 0.5% (w/v) eosin B in 50% ethyl alcohol for 15 sec. Rinse in tap water, dehydrate and mount as usual. 相似文献
145.
146.
J O McGee M H Jimenez A M Felix G J Cardinale S Udenfriend 《Archives of biochemistry and biophysics》1973,154(1):483-487
A number of substituted bradykinin analogs were prepared in which the proline in position 3 was replaced by analogs of proline. All of the bradykinin analogs, with the exception of l-azetidine-2-carboxyl3-bradykinin showed significant ability to inhibit prolyl hydroxylase activity. Addition of an l-glutamyl residue to the amino terminus of 3,4-dehydro-l-prolyl3-bradykinin and trans-4-hydroxy-l-prolyl3-bradykinin resulted in competitive inhibitors of increased effectiveness with Ki, values approximately 10?4m. One of the peptides, l-3,4-dehydro-l-prolyl3-bradykinin, appeared to serve as a substrate for prolyl hydroxylase. 相似文献
147.
Analysis of ethylene‐induced gene regulation during carposporogenesis in the red seaweed Grateloupia imbricata (Rhodophyta)
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Pilar Garcia‐Jimenez Montserrat Montero‐Fernández Rafael R. Robaina 《Journal of phycology》2018,54(5):681-689
Ethylene favors carposporogenesis in the red seaweed Grateloupia imbricata. Analyses of cystocarp development in vitro in thalli treated with ethylene suggest an interconnection between polyamine and ethylene biosynthesis pathways. Yet, little is known about molecular mechanisms underlying carposporogenesis. Here, we used droplet digital PCR to analyze genes encoding enzymes related to polyamine (Spermidine [Spd] synthase) and ethylene (ACC synthase) synthesis; a pivotal compound of both pathways (S‐adenosyl methionine synthase, SAMS); the gene that encodes amine oxidase, which is involved in polyamine degradation, and a candidate gene involved in seaweed reproduction (ornithine decarboxylase, ODC). In addition, we analyzed genes encoding proteins related to stress and reactive oxygen species, ascorbate peroxidase (APX), cytochrome P450 and WD 40. We characterized gene expression in fertilized and fertile thalli from G. imbricata that were exposed to ethylene for 15 min at two time points after treatment (1 and 7 d). The differential gene expression of SAMS, Spd synthase, ACC synthase, and cytochrome P450 was related to disclosure and development of cystocarps in fertilized thalli that transitioned from having no visible cystocarps at 1 d to developing cystocarps at 7 d. Likewise, cytochrome P450 was associated with cystocarp disclosure and maturation. In addition, amine oxidase and APX were involved in fine‐tuning polyamine and reactive oxygen species during carposporogenesis, respectively, whereas WD 40 did so in relation to ethylene signaling. Expression of the candidate gene ODC was increased when cystocarps were not visible (fertilized thalli, 1d), as previously described. This analysis suggests developmental stage‐specific roles for these genes during carposporogenesis. 相似文献
148.
149.
Contryphan-R is a disulfide-constrained octapeptide containing a D-tryptophan that was isolated recently from venom of the cone shell Conus radiatus. The polypeptide is present in two forms in solution due to cis-trans isomerization at hydroxyproline 3. The solution structure of the major form of this unusual polypeptide, determined from NMR data, consists of a well-defined fold containing a non-hydrogen-bonded chain reversal from Gly1 to Glu5, which includes a cis-hydroxyproline and a D-Trp, and a type I beta-turn from Glu5 to Cys8. The presence of a putative salt bridge between the Glu5 carboxyl group and the N-terminal ammonium group is investigated by using various solvation models during energy minimization and is compared with the results of a pH titration. A comparison of the structure of contryphan-R with other cyclic peptide structures highlights some of the key structural determinants of these peptides and suggests that the contryphan-R fold could be exploited as a scaffold onto which unrelated protein binding surfaces could be grafted. Comparison with small disulfide-bridged loops in larger proteins shows that contryphan-R is similar to a commonly occurring loop structure found in proteins. 相似文献
150.
L Jimenez R Ignar S Smalls P Grech J Hamilton Y Bosko D English 《Journal of industrial microbiology & biotechnology》1999,22(2):93-95
PCR assays were compared with standard microbiological methods for rapid detection of the United States Pharmacopoeia (USP)
bacterial indicators in artificially contaminated samples of raw materials and cosmetic/pharmaceutical products. DNA primers
containing the specific sequences of the uidA gene of the β-glucuronidase enzyme for Escherichia coli, the membrane lipoprotein gene oprL for Pseudomonas aeruginosa, and the 16S ribosomal gene for Staphylococcus aureus were used for detection in the PCR reaction. Contaminated samples were incubated for 24 h at 35°C. After incubation in broth
media with and without 4% Tween 20, samples were streaked on selective growth media. After 5–6 days, all microbial indicators
were morphologically and biochemically identified using standard methods while detection and identification by the PCR-based
assays was completed within 27–30 h. Rapid PCR detection of E. coli, S. aureus, and P. aeruginosa will allow a faster quality evaluation and release of raw materials and cosmetic/pharmaceutical products sensitive to microbial
contamination.
Received 21 June 1998/ Accepted in revised form 11 January 1999 相似文献