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71.
Summary Chromatin fractions from Friend erythroleukemia cells after induction of differentiation by dimethylsulfoxide (DMSO) were compared in their biochemical characteristics to fractions from uninduced cells. Fractions were prepared by extracting chromatin from nuclei after mild micrococcal nuclease treatment with increasing concentrations of NaCl according to Sanders [1]. This procedure has been found to release chromatin containing hyperacetylated histones preferentially [2]. The fractions obtained by this procedure were analysed in respect to the amount of chromatin released, the amount of histone H1, the degree of acetylation of histone H4, the presence of non-histone proteins and the concentration of transcribed and non-transcribed sequences. It was found that the fractions differ in the amount of histone H1 present, in several non-histone proteins and in the acetylation of histonie H4, regardless whether induced or uninduced cells were analysed. The distribution of transcribed sequences versus non-transcribed sequences among the fractions was the same, demonstrating that this fractionation procedure, although leading to fractions with biochemical differences, is not able to discriminate functional states of chromatin and that the biochemical characteristics of the fractions may be common to both, active as well as inactive states of chromatin. 相似文献
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74.
Jan Heering Sebastian Kehrloesser Inga Maria Melzer Byung Il Lee Bernd Thiede Volker Dötsch Krishnaraj Rajalingam 《EMBO reports》2017,18(5):733-744
Caspases are key enzymes responsible for mediating apoptotic cell death. Across species, caspase‐2 is the most conserved caspase and stands out due to unique features. Apart from cell death, caspase‐2 also regulates autophagy, genomic stability and ageing. Caspase‐2 requires dimerization for its activation which is primarily accomplished by recruitment to high molecular weight protein complexes in cells. Here, we demonstrate that apoptosis inhibitor 5 (API5/AAC11) is an endogenous and direct inhibitor of caspase‐2. API5 protein directly binds to the caspase recruitment domain (CARD) of caspase‐2 and impedes dimerization and activation of caspase‐2. Interestingly, recombinant API5 directly inhibits full length but not processed caspase‐2. Depletion of endogenous API5 leads to an increase in caspase‐2 dimerization and activation. Consistently, loss of API5 sensitizes cells to caspase‐2‐dependent apoptotic cell death. These results establish API5/AAC‐11 as a direct inhibitor of caspase‐2 and shed further light onto mechanisms driving the activation of this poorly understood caspase. 相似文献
75.
Brigitte Jeschke Kerstin Uhl Bernd Weist Dirk Schröder Thomas Meitinger Christoph Döhlemann H.-P. Vosberg 《Human genetics》1998,102(3):299-304
Hypertrophic cardiomyopathy (HCM) is a genetically and clinically heterogeneous myocardial disease that is in most cases
familial and transmitted in a dominant fashion. The most frequently affected gene codes for the cardiac (ventricular) β-myosin
heavy chain. We have investigated the genetic cause of an isolated case of HCM, which was marked by an extremely severe phenotype
and a very early age of onset. HCM is normally not a disease of small children. The proband was a boy who had suffered cardiac
arrest at the age of 6.5years (resuscitation by cardioconversion). Upon screening of the β-myosin heavy chain gene as a candidate,
two missense mutations, one in exon19 (Arg719Trp) and a second in exon12 (Met349Thr), were identified. The Arg719Trp mutation
was de novo, as it was not found in the parents. In contrast, the Met349Thr mutation was inherited through the maternal grandmother.
Six family members were carriers of this mutation but only the proband was clinically affected. Segregation and molecular
analysis allowed us to assign the Met349Thr mutation to the maternal and the Arg719Trp de novo mutation to the paternal β-myosin
allele. Thus, the patient has no normal myosin. We interpret these findings in terms of compound heterozygosity of a dominant
(Arg719Trp) and a recessive (Met349Thr) mutation. Whereas a single mutated Arg719Trp allele would be sufficient to cause HCM,
the concurrent Met349Thr mutation alone does not apparently induce the disease. Nevertheless, it conceivably contributes to
the particularly severe phenotype.
Received: 15 September 1997 / Accepted: 26 November 1997 相似文献
76.
In clinical applications, colonization of metal implants by adhesive and biofilm-forming bacteria not only prolong healing
but create additional healthcare costs for implant revision and antimicrobial treatment. An in vitro assay was established
investigating the antimicrobial surface activity of external fixation pins intended for use in bone fractures and deformities.
Test articles made out of stainless steel and coated with a polymer-containing nanoparticulate silver were compared to non-coated
reference controls out of stainless steel, copper and titanium. Staphylococcus epidermidis, known as a predominant cause for implant-related infections was used as test organism. Test pins and bacteria were incubated
for a period of 20 h found to be sufficient for initiating biofilm formation. After removing non- and low-adherent bacteria
by rinsing, two methods were used to isolate high-adherent (sessile) bacteria from the implant surfaces. Besides shaking the
implants in a solution containing small glass beads, a cytobrush technique was used to mechanically harvest viable bacteria.
Finally, the amount of detached bacteria was determined by plate counts. Several parameters identified to be critical within
the different removal procedures such as the inoculum concentration and the shaking time in the presence of glass beads as
well as time of the cytobrush treatment were analysed. The final test scheme resulted in the use of an inoculum of 105 colony forming units (CFU) per millilitre, ten rinsing steps for the removal of low adherent bacteria and 5 min of shaking
in the presence of glass beads, detaching the high-adherent bacteria. Due to subjective variations impacting the outcome of
the procedure, the cytobrush technique was not favoured and finally rejected. Using the in vitro assay developed, it could
be demonstrated that fixation pins coated with silver show a 3 log step reduction in the number of biofilm-forming bacteria
compared to a non-coated stainless steel or titanium implant. Pins made out of copper showed the highest antimicrobial efficacy,
as the number of detached bacteria was found to be below the detection limit, they served as a positive control within this
test. 相似文献
77.
Stephanie Thoms Klaas E.A. Max Michael Wunderlich Tomas Jacso Bernd Reif Franz X. Schmid 《Journal of molecular biology》2009,391(5):918-2651
In previous work, a strongly stabilized variant of the β1 domain of streptococcal protein G (Gβ1) was obtained by an in vitro selection method. This variant, termed Gβ1-M2, contains the four substitutions E15V, T16L, T18I, and N37L. Here we elucidated the molecular basis of the observed strong stabilizations. The contributions of these four residues were analyzed individually and in various combinations, additional selections with focused Gβ1 gene libraries were performed, and the crystal structure of Gβ1-M2 was determined. All single substitutions (E15V, T16L, T18I, and N37L) stabilize wild-type Gβ1 by contributions of between 1.6 and 6.0 kJ mol− 1 (at 70 °C). Hydrophobic residues at positions 16 and 37 provide the major contribution to stabilization by enlarging the hydrophobic core of Gβ1. They also increase the tendency to form dimers, as shown by dependence on the concentration of apparent molecular mass in analytical ultracentrifugation, by concentration-dependent stability, and by a strongly increased van't Hoff enthalpy of unfolding. The 0.88-Å crystal structure of Gβ1-M2 and NMR measurements in solution provide the explanation for the observed dimer formation. It involves a head-to-head arrangement of two Gβ1-M2 molecules via six intermolecular hydrogen bonds between the two β strands 2 and 2′ and an adjacent self-complementary hydrophobic surface area, which is created by the T16L and N37L substitutions and a large 120° rotation of the Tyr33 side chain. This removal of hydrophilic groups and the malleability of the created hydrophobic surface provide the basis for the dimer formation of stabilized Gβ1 variants. 相似文献
78.
The transient receptor potential (TRP) multigene superfamily encodes integral membrane proteins that function as ion channels.
Members of this family are conserved in yeast, invertebrates and vertebrates. The TRP family is subdivided into seven subfamilies:
TRPC (canonical), TRPV (vanilloid), TRPM (melastatin), TRPP (polycystin), TRPML (mucolipin), TRPA (ankyrin) and TRPN (NOMPC-like);
the latter is found only in invertebrates and fish. TRP ion channels are widely expressed in many different tissues and cell
types, where they are involved in diverse physiological processes, such as sensation of different stimuli or ion homeostasis.
Most TRPs are non-selective cation channels, only few are highly Ca2+ selective, some are even permeable for highly hydrated Mg2+ ions. This channel family shows a variety of gating mechanisms, with modes of activation ranging from ligand binding, voltage
and changes in temperature to covalent modifications of nucleophilic residues. Activated TRP channels cause depolarization
of the cellular membrane, which in turn activates voltage-dependent ion channels, resulting in a change of intracellular Ca2+ concentration; they serve as gatekeeper for transcellular transport of several cations (such as Ca2+ and Mg2+), and are required for the function of intracellular organelles (such as endosomes and lysosomes). Because of their function
as intracellular Ca2+ release channels, they have an important regulatory role in cellular organelles. Mutations in several TRP genes have been
implicated in diverse pathological states, including neurodegenerative disorders, skeletal dysplasia, kidney disorders and
pain, and ongoing research may help find new therapies for treatments of related diseases. 相似文献
79.
Penski N Härtle S Rubbenstroth D Krohmann C Ruggli N Schusser B Pfann M Reuter A Gohrbandt S Hundt J Veits J Breithaupt A Kochs G Stech J Summerfield A Vahlenkamp T Kaspers B Staeheli P 《Journal of virology》2011,85(15):7730-7741
From infection studies with cultured chicken cells and experimental mammalian hosts, it is well known that influenza viruses use the nonstructural protein 1 (NS1) to suppress the synthesis of interferon (IFN). However, our current knowledge regarding the in vivo role of virus-encoded NS1 in chickens is much more limited. Here, we report that highly pathogenic avian influenza viruses of subtypes H5N1 and H7N7 lacking fully functional NS1 genes were attenuated in 5-week-old chickens. Surprisingly, in diseased birds infected with NS1 mutants, the IFN levels were not higher than in diseased birds infected with wild-type virus, suggesting that NS1 cannot suppress IFN gene expression in at least one cell population of infected chickens that produces large amounts of the cytokine in vivo. To address the question of why influenza viruses are highly pathogenic in chickens although they strongly activate the innate immune system, we determined whether recombinant chicken alpha interferon (IFN-α) can inhibit the growth of highly pathogenic avian influenza viruses in cultured chicken cells and whether it can ameliorate virus-induced disease in 5-week-old birds. We found that IFN treatment failed to confer substantial protection against challenge with highly pathogenic viruses, although it was effective against viruses with low pathogenic potential. Taken together, our data demonstrate that preventing the synthesis of IFN is not the primary role of the viral NS1 protein during infection of chickens. Our results further suggest that virus-induced IFN does not contribute substantially to resistance of chickens against highly pathogenic influenza viruses. 相似文献
80.
Eric O. Walliser Kazushige Tanabe Yoshinori Hikida Kotaro Shirai Bernd R. Schne 《Lethaia: An International Journal of Palaeontology and Stratigraphy》2019,52(3):410-428
Here, we present the first sclerochronological investigation of shells of the gigantic inoceramids Sphenoceramus schmidti and S. sachalinensis from the middle Campanian cold seep carbonate‐bearing strata of the Yezo Basin in Hokkaido (northern Japan). Stable carbon (δ13C) and oxygen (δ18O) isotope values were measured in the aragonitic and calcitic shell layers of both species and compared to those of other co‐occurring benthic (mainly bivalves and gastropods) and demersal molluscs (ammonites). Sedimentological and stable isotope data suggest that these bivalves lived near cold seeps and were exposed to high H2S level in the seawater. The inoceramid shells exhibited higher δ13C and lower δ18O values than the coeval non‐cold seep molluscs. We ascribed the anomalous isotopic pattern to a combination of vital and environmental effects determined by the hosting of chemosymbionts and the exposure to warm interstitial waters. Inoceramid δ13C minima coincided with growth lines and likely reflect changes in nutrient supply by the chemosymbionts. Absolute temperatures estimated from δ18O values of Sphenoceramus schmidti and S. sachalinensis were, on average, ca. 4–5°C warmer than those reconstructed for the non‐seepage environment (19.3 ± 0.7°C). Short‐term δ18O fluctuations of the inoceramid material indicate local temperature ranges of up to 5.2°C, that is four times larger than those reconstructed from the benthic and demersal fauna (1.3°C). In general, our data suggest that the stable carbon and oxygen isotope values of the studied Sphenoceramus spp. were strongly affected by short‐term fluctuations in seepage activity and do not reflect seasonal fluctuations. 相似文献