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91.
Over a fifteen month period, beginning October, 1974, approximately 13 500 centrarchids were examined for evidence of infection with metacercaria of Clinostomum marginatum. Species checked included Lepomis macrochirus, L. gulosus, L. auritus, Pomoxis nigromaculatus and Micropterus salmoides. The study site was Par Pond (South Carolina, U.S.A.), an 1120 ha reservoir receiving thermal effluent from a nuclear production reactor. Except for the largemouth bass, M. salmoides , infection percentages among the five species were less than 1%. Among bass, infection varied seasonally, being highest from January to June. From the spring highs of approximately 25 %, the percentages dropped to lows of < 10% in July and August; there was a jump in September-October to another peak of 30% and then a steady decline through December when infection percentages were again less than 10%. Neither body condition nor length of the bass were related to infection percentage or metacercaria density. Infection percentage could not be related to the influence of thermal effluent. Infection percentages did vary from location to location within the Par Pond system. A significant rank correlation could be established between infection percentage and the amount of littoral zone present in the locality from which the bass were taken. It is suggested that the local 'bay effects' are the result of limited home and foraging ranges of the bass in relation to the amounts of littoral zone present in various locations of the reservoir. 相似文献
92.
Harald Esch Donald Wilson 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1967,54(2):256-267
Summary The sounds produced by the thoracic flight machinery of bees and flies appear to be composed of two main vibration modes. The lower frequency one corresponds to the wingbeat frequency. The higher frequency vibration, which is in the kcps. range, is reset in phase on every wingbeat half-cycle. Therefore Sonagraphic or Fourier analysis of the sounds gives only harmonics of the wingbeat frequency. However, oscillograms of the waveforms show that the higher frequency vibration is nearly independent of wingbeat frequency.The high frequency vibration is probably important in bee communication. We speculate that it is due to skeletal vibration which is relatively undamped by muscular and aerodynamic loading.
Supported by the Deutsche Forschungsgemeinschaft, and grant NB 03927 from the USPHS
Herrn Professor H. Autrum zum 60. Geburtstag gewidmet. 相似文献
Zusammenfassung Der Thorax von Insekten, deren Flugmuskeln einen myogenen Rhythmus zeigen, vibriert in Aktivitätsphasen meist mit zwei voneinander unabhängigen Frequenzen: Die erste wird durch die elastischen Eigenschaften des Skelets, die Kontraktionen der indirekten Flugmuskeln und die Belastung der Flügel bestimmt (Flügelschlagfrequenz). Sie kann über das Nervensystem mit Hilfe von Zusatzmuskeln geregelt werden. Die zweite Frequenz hängt vermutlich von den elastischen Eigenschaften der Thoraxkapsel ab und kann deshalb wahrscheinlich nur auftreten, wenn die indirekten Flugmuskeln momentan erschlaffen. Sie wird wahrscheinlich durch Muskeln verändert, die die Steifheit der Thoraxkapsel regulieren. Sie liegt meist im kHz-Bereich. Da ihre Phase in jedem halben Flügelschlag neu gesetzt wird, zeigt die Analyse im Sonagraph (Fourier Analyse) nur Harmonische der Flügelschlagfrequenz. Die Bedeutung der zweiten Frequenz für das Verhalten der Fliegen ist unbekannt. In der Kommunikation der Bienen könnte sie eine wichtige Rolle spielen, da die einzigen bisher bekannten Vibrationsrezeptoren, die Subgenualorgane, ihr Empfindlichkeitsmaximum bei 2,5 kHz haben.
Supported by the Deutsche Forschungsgemeinschaft, and grant NB 03927 from the USPHS
Herrn Professor H. Autrum zum 60. Geburtstag gewidmet. 相似文献
93.
94.
The major erythrotropin of bovine Cohn fraction V has the N-terminal sequence of insulin-like growth factor II with isoleucine at position 35 总被引:2,自引:0,他引:2
The major erythrotropin-like factor of bovine Cohn Fraction V has been isolated from commercial albumin preparations by reversed-phase HPLC. The N-terminal sequence of the major fraction with erythrotropin-like activity is practically identical to the sequence of bovine insulin-like growth factor II. Within the first 45 amino acids, the only difference was the presence of an isoleucine instead of a serine at amino acid 35. This substitution may affect the immunoreactivity of this peptide using antibodies against bovine or human insulin-like growth factor II. 相似文献
95.
Martin A. Mensah Matthew S. Hestand Maarten H. D. Larmuseau Mala Isrie Nancy Vanderheyden Matthias Declercq Erika L. Souche Jeroen Van Houdt Radka Stoeva Hilde Van Esch Koen Devriendt Thierry Voet Ronny Decorte Peter N. Robinson Joris R. Vermeesch 《PLoS genetics》2014,10(11)
The human sex chromosomes differ in sequence, except for the pseudoautosomal regions (PAR) at the terminus of the short and the long arms, denoted as PAR1 and PAR2. The boundary between PAR1 and the unique X and Y sequences was established during the divergence of the great apes. During a copy number variation screen, we noted a paternally inherited chromosome X duplication in 15 independent families. Subsequent genomic analysis demonstrated that an insertional translocation of X chromosomal sequence into theMa Y chromosome generates an extended PAR. The insertion is generated by non-allelic homologous recombination between a 548 bp LTR6B repeat within the Y chromosome PAR1 and a second LTR6B repeat located 105 kb from the PAR boundary on the X chromosome. The identification of the reciprocal deletion on the X chromosome in one family and the occurrence of the variant in different chromosome Y haplogroups demonstrate this is a recurrent genomic rearrangement in the human population. This finding represents a novel mechanism shaping sex chromosomal evolution. 相似文献
96.
Joke Vandewalle Marijke Bauters Hilde Van Esch Stefanie Belet Jelle Verbeeck Nathalie Fieremans Maureen Holvoet Jodie Vento Ana Spreiz Dieter Kotzot Edda Haberlandt Jill Rosenfeld Joris Andrieux Bruno Delobel Marie-Bertille Dehouck Koen Devriendt Jean-Pierre Fryns Peter Marynen Amy Goldstein Guy Froyen 《Human genetics》2013,132(10):1177-1185
Loss-of-function mutations in several different neuronal pathways have been related to intellectual disability (ID). Such mutations often are found on the X chromosome in males since they result in functional null alleles. So far, microdeletions at Xq24 reported in males always have been associated with a syndromic form of ID due to the loss of UBE2A. Here, we report on overlapping microdeletions at Xq24 that do not include UBE2A or affect its expression, in patients with non-syndromic ID plus some additional features from three unrelated families. The smallest region of overlap, confirmed by junction sequencing, harbors two members of the mitochondrial solute carrier family 25, SLC25A5 and SLC25A43. However, identification of an intragenic microdeletion including SLC25A43 but not SLC25A5 in a healthy boy excluded a role for SLC25A43 in cognition. Therefore, our findings point to SLC25A5 as a novel gene for non-syndromic ID. This highly conserved gene is expressed ubiquitously with high levels in cortex and hippocampus, and a presumed role in mitochondrial exchange of ADP/ATP. Our data indicate that SLC25A5 is involved in memory formation or establishment, which could add mitochondrial processes to the wide array of pathways that regulate normal cognitive functions. 相似文献
97.
Cellulomonas flavigena strain KU (ATCC 53703) is a cellulolytic, Gram-positive bacterium which produces large quantities of an insoluble exopolysaccharide (EPS) when grown in minimal media with a high carbon-to-nitrogen (C/N) ratio. Earlier studies proved the EPS is structurally identical to the linear β-1,3-glucan known as curdlan and provided evidence that the EPS functions as a carbon and energy reserve compound. We now report that C. flavigena KU also accumulates two intracellular, glucose-storage carbohydrates under conditions of carbon and energy excess. These carbohydrates were partially purified and identified as the disaccharide trehalose and a glycogen/amylopectin-type polysaccharide. A novel method is described for the sequential fractionation and quantitative determination of all three carbohydrates from culture samples. This fractionation protocol was used to examine the effects of C/N ratio and osmolarity on the accumulation of cellular carbohydrates in batch culture. Increasing the C/N of the growth medium caused a significant accumulation of curdlan and glycogen but had a relatively minor effect on accumulation of trehalose. In contrast, trehalose levels increased in response to increasing osmolarity, while curdlan levels declined and glycogen levels were generally unaffected. During starvation for an exogenous source of carbon and energy, only curdlan and glycogen showed substantial degradation within the first 24 h. These results support the conclusion that extracellular curdlan and intracellular glycogen can both serve as short-term reserve compounds for C. flavigena KU and that trehalose appears to accumulate as a compatible solute in response to osmotic stress. 相似文献
98.
99.
Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome 总被引:1,自引:0,他引:1 下载免费PDF全文
Kleefstra T Brunner HG Amiel J Oudakker AR Nillesen WM Magee A Geneviève D Cormier-Daire V van Esch H Fryns JP Hamel BC Sistermans EA de Vries BB van Bokhoven H 《American journal of human genetics》2006,79(2):370-377
A clinically recognizable 9q subtelomeric deletion syndrome has recently been established. Common features seen in these patients are severe mental retardation, hypotonia, brachycephaly, flat face with hypertelorism, synophrys, anteverted nares, cupid bow or tented upper lip, everted lower lip, prognathism, macroglossia, conotruncal heart defects, and behavioral problems. The minimal critical region responsible for this 9q subtelomeric deletion (9q-) syndrome has been estimated to be <1 Mb and comprises the euchromatin histone methyl transferase 1 gene (EHMT1). Previous studies suggested that haploinsufficiency for EHMT1 is causative for 9q subtelomeric deletion syndrome. We have performed a comprehensive mutation analysis of the EHMT1 gene in 23 patients with clinical presentations reminiscent of 9q subtelomeric deletion syndrome. This analysis revealed three additional microdeletions that comprise the EHMT1 gene, including one interstitial deletion that reduces the critical region for this syndrome. Most importantly, we identified two de novo mutations--a nonsense mutation and a frameshift mutation--in the EHMT1 gene in patients with a typical 9q- phenotype. These results establish that haploinsufficiency of EHMT1 is causative for 9q subtelomeric deletion syndrome. 相似文献
100.
Insectes Sociaux - Physiological constraints can limit thermal niche breadth in organisms, particularly for small-bodied ectotherms. Daily temperature fluctuations often surpass annual (seasonal)... 相似文献