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41.
Morphological and ecological complexity in early eukaryotic ecosystems. 总被引:18,自引:0,他引:18
Molecular phylogeny and biogeochemistry indicate that eukaryotes differentiated early in Earth history. Sequence comparisons of small-subunit ribosomal RNA genes suggest a deep evolutionary divergence of Eukarya and Archaea; C27-C29 steranes (derived from sterols synthesized by eukaryotes) and strong depletion of 13C (a biogeochemical signature of methanogenic Archaea) in 2,700 Myr old kerogens independently place a minimum age on this split. Steranes, large spheroidal microfossils, and rare macrofossils of possible eukaryotic origin occur in Palaeoproterozoic rocks. Until now, however, evidence for morphological and taxonomic diversification within the domain has generally been restricted to very late Mesoproterozoic and Neoproterozoic successions. Here we show that the cytoskeletal and ecological prerequisites for eukaryotic diversification were already established in eukaryotic microorganisms fossilized nearly 1,500 Myr ago in shales of the early Mesoproterozoic Roper Group in northern Australia. 相似文献
42.
J. K. Walter V. Castro M. Voss K. Gast C. Rueckert J. Piontek Ingolf E. Blasig 《Cellular and molecular life sciences : CMLS》2009,66(22):3655-3662
Occludin is a self-associating transmembrane tight junction protein affected in oxidative stress. However, its function is
unknown. The cytosolic C-terminal tail contains a coiled coil-domain forming dimers contributing to the self-association.
Studying the hypothesis that the self-association is redox-sensitive, we found that the dimerization of the domain depended
on the sulfhydryl concentration of the environment in low-millimolar range. Under physiological conditions, monomers and dimers
were detected. Masking the sulfhydryl residues in the domain prevented the dimerization but affected neither its helical structure
nor cylindric shape. Incubation of cell extracts containing full-length occludin with sulfhydryl reagents prevented the dimerization;
a cysteine/alanine exchange mutant also did not show dimer formation. This demonstrates, for the first time, that disulfide
bridge formation of the domain is involved in the occludin dimerization. It is concluded that the redox-dependent dimerization
of occludin may play a regulatory role in the tight junction assembly under physiological and pathological conditions. 相似文献
43.
We record eight species of exotic fishes as established, reproducing populations in certain springs in Clark, Lincoln, and Nye counties. Nevada. These include an unidentified species of Hypostomus, Cyprinus carpio, Poecilia mexicana, Poecilia reticulata, a Xiphophorus hybrid, and Cichlasoma nigrofasciatum. Tilapia mariae, established in a spring near the Overton Arm of Lake Mead, and Tilapia zilli, established in a golf course pond in Pahrump Valley, are recorded for the first time from Nevada waters. Though populations of transplanted Gambusia affinis persist, other populations of Poecilia latipinna are apparently no longer extant. Cichlasoma severum, Notemigonus crysoleucas, Poecilia latipinna, and Carassius auratus were apparently eradicated from Rogers Spring in 1963. 相似文献
44.
Here, we give a historical overview of the search for genetic variants that influence the susceptibility of an individual to a chronic disease, from RA Fisher's seminal work to the current excitement of whole-genome association studies (WGAS). We then discuss the concepts behind the identification of common variants as disease causal factors and contrast them to the basic ideas that underlie the rare variant hypothesis. The identification of rare variants involves the careful selection of candidate genes to examine, the availability of highly efficient resequencing techniques and the appropriate assessment of the functional consequences of the implicated variant. We believe that this strategy can be successfully applied at present in order to unravel the contribution of rare variants to the multifactorial inheritance of common diseases, which could lead to the implementation of much needed preventative screening schemes. 相似文献
45.
Höglinger GU Melhem NM Dickson DW Sleiman PM Wang LS Klei L Rademakers R de Silva R Litvan I Riley DE van Swieten JC Heutink P Wszolek ZK Uitti RJ Vandrovcova J Hurtig HI Gross RG Maetzler W Goldwurm S Tolosa E Borroni B Pastor P;PSP Genetics Study Group Cantwell LB Han MR Dillman A van der Brug MP Gibbs JR Cookson MR Hernandez DG Singleton AB Farrer MJ Yu CE Golbe LI Revesz T Hardy J Lees AJ Devlin B Hakonarson H Müller U Schellenberg GD 《Nature genetics》2011,43(7):699-705
Progressive supranuclear palsy (PSP) is a movement disorder with prominent tau neuropathology. Brain diseases with abnormal tau deposits are called tauopathies, the most common of which is Alzheimer's disease. Environmental causes of tauopathies include repetitive head trauma associated with some sports. To identify common genetic variation contributing to risk for tauopathies, we carried out a genome-wide association study of 1,114 individuals with PSP (cases) and 3,247 controls (stage 1) followed by a second stage in which we genotyped 1,051 cases and 3,560 controls for the stage 1 SNPs that yielded P ≤ 10(-3). We found significant previously unidentified signals (P < 5 × 10(-8)) associated with PSP risk at STX6, EIF2AK3 and MOBP. We confirmed two independent variants in MAPT affecting risk for PSP, one of which influences MAPT brain expression. The genes implicated encode proteins for vesicle-membrane fusion at the Golgi-endosomal interface, for the endoplasmic reticulum unfolded protein response and for a myelin structural component. 相似文献
46.
Danielle Kamato Partha Mitra Felicity Davis Narin Osman Rebecca Chaplin Peter J. Cabot Rizwana Afroz Walter Thomas Wenhua Zheng Harveen Kaur Margaret Brimble Peter J. Little 《Cellular and molecular life sciences : CMLS》2017,74(8):1379-1390
Seven transmembrane G protein-coupled receptors (GPCRs) have gained much interest in recent years as it is the largest class among cell surface receptors. G proteins lie in the heart of GPCRs signalling and therefore can be therapeutically targeted to overcome complexities in GPCR responses and signalling. G proteins are classified into four families (Gi, Gs, G12/13 and Gq); Gq is further subdivided into four classes. Among them Gαq and Gαq/11 isoforms are most crucial and ubiquitously expressed; these isoforms are almost 88% similar at their amino acid sequence but may exhibit functional divergences. However, uncertainties often arise about Gαq and Gαq/11 inhibitors, these G proteins might also have suitability to the invention of novel-specific inhibitors for each isoforms. YM-254890 and UBO-QIC are discovered as potent inhibitors of Gαq functions and also investigated in thrombin protease-activated receptor (PAR)-1 inhibitors and platelet aggregation inhibition. The most likely G protein involved in PAR-1 stimulates responses is one of the Gαq family isoforms. In this review, we highlight the molecular structures and pharmacological responses of Gαq family which may reflect the biochemical and molecular role of Gαq and Gαq/11. The advanced understanding of Gαq and Gαq/11 role in GPCR signalling may shed light on our understanding on cell biology, cellular physiology and pathophysiology and also lead to the development of novel therapeutic agents for a number of diseases. 相似文献
47.
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy 总被引:20,自引:0,他引:20
Gerull B Heuser A Wichter T Paul M Basson CT McDermott DA Lerman BB Markowitz SM Ellinor PT MacRae CA Peters S Grossmann KS Drenckhahn J Michely B Sasse-Klaassen S Birchmeier W Dietz R Breithardt G Schulze-Bahr E Thierfelder L 《Nature genetics》2004,36(11):1162-1164
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is associated with fibrofatty replacement of cardiac myocytes, ventricular tachyarrhythmias and sudden cardiac death. In 32 of 120 unrelated individuals with ARVC, we identified heterozygous mutations in PKP2, which encodes plakophilin-2, an essential armadillo-repeat protein of the cardiac desmosome. In two kindreds with ARVC, disease was incompletely penetrant in most carriers of PKP2 mutations. 相似文献
48.
Lebrun F Terrier R Bazzano A Bélanger G Bird A Bouchet L Dean A Del Santo M Goldwurm A Lund N Morand H Parmar A Paul J Roques JP Schönfelder V Strong AW Ubertini P Walter R Winkler C 《Nature》2004,428(6980):293-296
The Milky Way is known to be an abundant source of gamma-ray photons, now determined to be mainly diffuse in nature and resulting from interstellar processes. In the soft gamma-ray domain, point sources are expected to dominate, but the lack of sensitive high-resolution observations did not allow for a clear estimate of the contribution from such sources. Even the best imaging experiment revealed only a few point sources, accounting for about 50% of the total Galactic flux. Theoretical studies were unable to explain the remaining intense diffuse emission. Investigating the origin of the soft gamma-rays is therefore necessary to determine the dominant particle acceleration processes and to gain insights into the physical and chemical equilibrium of the interstellar medium. Here we report observations in the soft gamma-ray domain that reveal numerous compact sources. We show that these sources account for the entirety of the Milky Way's emission in soft gamma-rays, leaving at most a minor role for diffuse processes. 相似文献
49.
Walter F Bertoldi F Carilli C Cox P Lo KY Neri R Fan X Omont A Strauss MA Menten KM 《Nature》2003,424(6947):406-408
Observations of molecular hydrogen in quasar host galaxies at high redshifts provide fundamental constraints on galaxy evolution, because it is out of this molecular gas that stars form. Molecular hydrogen is traced by emission from the carbon monoxide molecule, CO; cold H2 itself is generally not observable. Carbon monoxide has been detected in about ten quasar host galaxies with redshifts z > 2; the record-holder is at z = 4.69 (refs 1-3). Here we report CO emission from the quasar SDSS J114816.64 + 525150.3 (refs 5, 6) at z = 6.42. At that redshift, the Universe was only 1/16 of its present age, and the era of cosmic reionization was just ending. The presence of about 2 x 1010 M\circ of H2 in an object at this time demonstrates that molecular gas enriched with heavy elements can be generated rapidly in the youngest galaxies. 相似文献
50.
Varon R Gooding R Steglich C Marns L Tang H Angelicheva D Yong KK Ambrugger P Reinhold A Morar B Baas F Kwa M Tournev I Guerguelcheva V Kremensky I Lochmüller H Müllner-Eidenböck A Merlini L Neumann L Bürger J Walter M Swoboda K Thomas PK von Moers A Risch N Kalaydjieva L 《Nature genetics》2003,35(2):185-189