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21.
Modifications of the cyclic AMP radioimmunoassay of Cailla et al. [in Hormones and Cell Regulation (J. Dumont and J. Nunez, eds.), Vol. 4, pp. 1-24, Elsevier/North-Holland, Amsterdam/New York (1980)] allowed its use in the determination of adenylate cyclase activity, which was otherwise precluded by high blank values. These high values originate mainly from chemically formed cyclic AMP and from ATP cross-reactivity. The simultaneous presence of ATP and magnesium ions generates cyclic AMP under the alkaline conditions used to succinylate the sample; this interference can be dealt with either by chelation of Mg2+ ions with EDTA during succinylation or by periodic acid oxidation of samples prior to succinylation. In addition, ATP itself contributes to blank values by its cross-reactivity, especially when working with high concentrations of this substrate. This interference can be decreased by a batch adsorption of ATP or oxidized ATP on alumina. Detailed procedures were discussed, with the choice of the additional steps to the standard method of Cailla et al. having to be made on the basis of the sensitivity requirements. When preventing ATP cyclization, the radioimmunoassay was as sensitive as methods using [alpha-32P]ATP as substrate. Elimination of ATP can improve the sensitivity by one order of magnitude. This method is especially interesting with high ATP concentrations and/or with low cyclic AMP production.  相似文献   
22.
Volker Lammert 《Zoomorphology》1985,105(5):308-316
Summary The fine structure of the protonephridia of Haplognathia rosea (Filospermoidea) and Gnathostomula paradoxa (Bursovaginoidea) is described. Each protonephridium consists of three different cells: (1) a monociliated terminal cell which constitutes the filtration area, (2) a nonciliated canal cell showing a special protonephridial outlet system, and (3) an intraepidermal cell — the nephroporus cell — constituting the nephroporus. The protonephridia are arranged serially. There is no canal system connecting the protonephridial units.Protonephridial characters in other Bilateria are considered. The pattern of characters in the protonephridia in the last common gnathostomulid stem species and presumed apomorphies in the protonephridia of the Gnathostomulida investigated are discussed.Abbreviations used in figures ac acessory centriole - AC additional epidermal cell - bb basal body - bl basal lamina - bm bundle of microvilli - c cilium - cc cilium duct cell - cd cilium duct - cr ciliary rootlet - crs structures resembling ciliary rootlets - di diplosome - ds desmosome - dy dictyosome - f filtration area - g granules - m mitochondrium - mv microvillus - n nucleus - NC nephroporus cell - np nephroporus - oc outlet canal - TC terminal cell - tl tubules of lacunar system  相似文献   
23.
The extraction, purification and structural characterization of two lipid A precursors (Ia and Ib) differing only in one hexadecanoic acid are described. Both precursors were synthesized at elevated temperatures by a new mutant of Salmonella typhimurium (mutant Ts5) which is conditionally defective in synthesis of the 3-deoxy-d-manno-octulosonic acid region of lipopolysaccharides.Both precursors were purified by repeated phenol/chloroform/petroleum ether (PCP) extractions followed by thin layer chromatography. Teh precursor preparation was free of lipopolysaccharides and phospholipids and contained less than 0.1% protein. Structural analysis which included chemical degradation procedures as well as positive ion laser desorption (LDMS) mass spectroscopy of dephosphorylated lipid A precursors showed together that precursor Ia represents a diphosphorylated glucosamine disaccharide containing two ester, two amide-linked residues of 3-hydroxytetradecanoic acid and lacks the ester-linked dodecanoic, tetradecanoic and hexadecanoic acid as well as 3-deoxy-d-manno-octulosonic acid. Precursor Ib has the same basic structure as precursor Ia, but contains in addition one mol of hexadecanoic acid per mol disaccharide which is linked to the 3-hydroxy group of the amide-bound 3-hydroxy-tetradecanoic acid of the reducing, terminal glucosamine residue.The structure of precursor Ib supports the conclusion that hexadecanoic acid incorporation occurs at an early stage in lipid A biosynthesis prior to the attachment of 3-deoxy-d-manno-octulosonic acid and/or other polar substituents.Abbreviations LDMS laser desorption mass spectrometry - KDO 3-Deoxy-d-manno-octulosonic acid - Ts5 Salmonella typhimurium mutant Ts5 - PCP phenol/chloroform/petroleum ether - H2F2 hydrogen fluoride This work is dedicated to Prof. Dr. Drews, Freiburg, on the occasion of his 60th birthday  相似文献   
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Alberti  Gerd  Storch  Volker 《Zoomorphology》1974,79(2):133-153
Zoomorphology - Die licht- und elektronenmikroskopische Untersuchung der Prosomadrüsen der Spinnmilben Bryobia praetiosa, Bryobia rubrioculus und Tetranychus urticae (Tetranychidae,...  相似文献   
26.
Zusammenfassung Das Epithel der Kopfanhänge von elf marinen und Süßwasserprosobranchiern besteht aus prismatischen bis kubischen Stützzellen mit meist dichtem Mikrovillussaum und z.T. Pigmentgranula sowie Sinneszellen, die fast immer in Form sekundärer Sinneszellen vorliegen; nur bei Patella coerulea kommen vermutlich auch primäre Sinneszellen vor. Ihr Zytoplasma ist apikal durch glattwandige E. R.-Zisternen, helle Bläschen und Mikrotubuli gekennzeichnet. Außerdem tragen diese Zellen Zilien und stehen basal mit Nervenendigungen in Kontakt, die sich in drei Gruppen einteilen lassen: 1. Vermutlich cholinerge Endigungen mit optisch leeren Bläschen (Ø 600–800 Å). 2. Endigungen mit dense core vesicles (Ø 1000–1100 Å). Die Annahme, daß diese Endigungen biogene Amine enthalten, wird durch fluoreszenzmikroskopische Befunde gestützt. 3. Endigungen mit großen (Ø 3000–4000 Å) neurosekretorischen Elementargranula.
Structure and innervation of the cephalic tentacles of Prosobranch molluscs
Summary The epithelium of the cephalic tentacles of eleven marine and freshwater prosobranch snails consists of villus bearing supporting cells, which partly contain pigment granules, and sensory cells, which occur in form of secondary sensory cells with the exception of Patella coerulea which presumably possesses primary sensory cells. These receptor cells are characterized as chemoreceptors by apical cilia, smooth surfaced E.R., microtubulues and empty vesicles. At their bases they are in close contact with nerve endings which can be classified in three groups: 1. presumably cholinergic endings with clear vesicles (Ø 600–800 Å). 2. endings with dense core vesicles (Ø 1000–1100 Å). The assumption that these endings contain biogenic amines is supported by positive fluorescence microscopical tests. 3. Endings with big (Ø 3000–4000 Å) neurosecretory elementary granules.
Herrn Prof. Dr. W. Bargmann danke ich für die Überlassung eines Arbeitsplatzes im Anatomischen Institut Kiel.  相似文献   
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Summary In the species studied song appears to have two functions; an epigamic function = Display Song, and a contact function = Solitary Song. Solitary Song appears to be common to all the species studied. Its utterance indicates that the bird is unpaired or separated from another individual with which it has formed a bond. InUraeginthus bengalus, U. angolensis, andAmandava amandava Solitary Song is also uttered by the hen in similar circumstances. InLonchura punctulata, A. amandava, andEuodice malabarica song is usually but not completely inhibited by the presence of a mate, in whose absence Solitary Song will be uttered even when other individuals of the same species are present. In the species studied of the generaEstrilda, Lagonosticta, andUraeginthus Solitary Song is inhibited by the continued close proximity of another bird even though this may be of the same sex or of a different species and may elicit aggressive or fleeing reactions; but conditions of close association with a bird other than a suitable mate would presumably only occur under captive conditions. There appears to be a distance factor controlling such inhibition. There is evidence of the inhibition of song due to the presence of a mate in other passerine species.  相似文献   
29.
Cultured Burkitt cells were examined by immunofluorescence, autoradiography, and electron microscopy in an effort to identify the stainable cells with those harboring herpes-type virus particles. Immediately after a 2-hr pulse of (3)H-thymidine, from 30 to 60% of the cells revealed heavy nuclear labeling. In most cases the grains were evenly dispersed, but in about 3 to 5% the grains showed a focal distribution and occasionally they extended into the cytoplasm. Such nuclear foci were rarely seen at 8 hr after the pulse. When the analysis was restricted to preselected immunofluorescent cells, up to 80% showed label at 8 hr and cytoplasmic grains were prominent. To reduce cellular deoxyribonucleic acid (DNA) synthesis, cells were X-irradiated with 3,000 to 6,000 R, and the isotope pulse was applied 1, 4, or 7 days later. Whereas the total number of labeled cells decreased in roughly twofold steps at the respective intervals (from 40 to 10%), the incorporation of (3)H-thymidine into fluorescent cells was not affected by X irradiation. In each series, about 70% of the fluorescent cells contained label when they were examined at 24 and 48 hr after the pulse, whereas at 8 and 72 hr fewer were positive. At the earlier intervals, unlabeled fluorescent cells most likely represented cells which had completed viral DNA synthesis prior to the pulse; at the later intervals, unlabeled fluorescent cells were probably cells which commenced viral replication after the pulse. These data support the conclusion that the immunofluorescent cells are the ones which harbor virus, and also confirm the expectation that the virus is a DNA virus from a member of the herpes group. This conclusion was firmly established by sectioning and electron microscopic examination of individual fluorescent cells, all of which contained numerous virus particles, whereas the nonstained cells prepared in a similar manner were free of them.  相似文献   
30.
Zusammenfassung Der heranwachsende Junggimpel empfängt während seiner Nestlingszeit und den sich anschließenden Wochen bis zum Erlangen der Selbständigkeit von den Eltern Eindrücke, die sein späteres Geschlechtsverhalten und seine stimmliche Entwicklung entscheidend beeinflussen. Ein normales Geschlechtsverhalten entwickelt sich nur dann, wenn der Jungvogel von den eigenen Eltern oder Artgenossen aufgezogen wird. Erfolgt die Aufzucht durch andere Lebewesen (Kanarienvogel, Mensch), so tritt eine mehr oder weniger deutliche Prägung der sozialen und sexuellen Reaktion auf diese Arten ein. Mit dieser Prägung geht eine Fixation der Lautäußerungen (Lockruf, Gesang) an die der Eltern — vor allem des Vaters — Hand in Hand. Trägt der Vater normale Lockrufe und den arttypischen Gesang vor, so erfährt auch der Junggimpel eine ormale stimmliche Entwicklung. Sind aber Lockrufe und Gesang in Klangfarbe und Komposition abweichend, so lernt der Jungvogel selektiv alle diese Abweichungen und behält sie zeitlebens bei. Ein Jungmännchen, das von Kanarien aufgezogen wurde, erlernte unter einer Schar anderer Junggimpel den Gesang des einzigen anwesenden Kanarienmännchens und gab ihn an seine Söhne weiter. Vier Jahre später sangen die Urenkel dieses Vogels noch die Kanarienstrophen in unveränderter Form. — Von Menschen aufgezogene Gimpel konzentrieren ihren Lerneifer auf die Lautäußerungen des Pflegers; sie erlernen vorgepfiffene Melodien: bis zu drei kurze Volkslieder. Während die jungen Männchen ausschließlich dem Gesang des Vaters ihre Aufmerksamkeit zuwenden, nehmen die Weibchen nach ihrer Verpaarung neben den vom Vater erlernten Motiven auch solche aus dem Gesang des Gatten auf. Nur der erste Partner hat auf ihre Gesanganusbildung Einfluß.Die sensible Periode der stimmlichen Entwicklung fällt mit der Zeit zusammen, in der frühsexuelle Stimmungen den Junggimpel beherrschen. Sein Lerneifer ist auf dasjenige Lebewesen konzentriert, das ihn aufzog und dem er — aus dem daraus erwachsenen hohen Grade persönlicher Bindung heraus — seine ersten sexuellen Anträge machte.  相似文献   
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