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排序方式: 共有433条查询结果,搜索用时 9 毫秒
221.
Alderman Sarah L. Crossley Dane A. Elsey Ruth M. Gillis Todd E. 《Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology》2020,190(2):243-252
Journal of Comparative Physiology B - We recently described lasting changes in the cardiac proteome of American alligators (Alligator mississippiensis) reared under hypoxic conditions, that... 相似文献
222.
Sander G. Basten Erica E. Davis Ad J. M. Gillis Ellen van Rooijen Hans Stoop Nikolina Babala Ive Logister Zachary G. Heath Trudy N. Jonges Nicholas Katsanis Emile E. Voest Freek J. van Eeden Rene H. Medema René F. Ketting Stefan Schulte-Merker Leendert H. J. Looijenga Rachel H. Giles 《PLoS genetics》2013,9(4)
Seminoma is a subclass of human testicular germ cell tumors (TGCT), the most frequently observed cancer in young men with a rising incidence. Here we describe the identification of a novel gene predisposing specifically to seminoma formation in a vertebrate model organism. Zebrafish carrying a heterozygous nonsense mutation in Leucine-Rich Repeat Containing protein 50 (lrrc50 also called dnaaf1), associated previously with ciliary function, are found to be highly susceptible to the formation of seminomas. Genotyping of these zebrafish tumors shows loss of heterozygosity (LOH) of the wild-type lrrc50 allele in 44.4% of tumor samples, correlating with tumor progression. In humans we identified heterozygous germline LRRC50 mutations in two different pedigrees with a family history of seminomas, resulting in a nonsense Arg488* change and a missense Thr590Met change, which show reduced expression of the wild-type allele in seminomas. Zebrafish in vivo complementation studies indicate the Thr590Met to be a loss-of-function mutation. Moreover, we show that a pathogenic Gln307Glu change is significantly enriched in individuals with seminoma tumors (13% of our cohort). Together, our study introduces an animal model for seminoma and suggests LRRC50 to be a novel tumor suppressor implicated in human seminoma pathogenesis. 相似文献
223.
A Willems E Falsen B Pot E Jantzen B Hoste P Vandamme M Gillis K Kersters J De Ley 《International journal of systematic bacteriology》1990,40(4):384-398
Pseudomonas facilis and Pseudomonas delafieldii are inappropriately assigned to the genus Pseudomonas. They belong to the acidovorans rRNA complex in rRNA superfamily III (i.e., the beta subclass of the Proteobacteria). The taxonomic relationships of both of these species, two groups of clinical isolates (E. Falsen [EF] group 13 and EF group 16), and several unidentified or presently misnamed strains were examined by using DNA:rRNA hybridization, numerical analyses of biochemical and auxanographic features and of fatty acid patterns, polyacrylamide gel electrophoresis of cellular proteins, and DNA:DNA hybridization. These organisms form a separate group within the acidovorans rRNA complex, and we propose to transfer them to a new genus, Acidovorax. We describe the following three species in this genus: the type species, Acidovorax facilis (formerly Pseudomonas facilis), with type strain LMG 2193 (= CCUG 2113 = ATCC 11228); Acidovorax delafieldii (for the former Pseudomonas delafieldii and most of the EF group 13 strains), with type strain LMG 5943 (= CCUG 1779 = ATCC 17505); and Acidovorax temperans (for several former Pseudomonas and Alcaligenes strains and most of the EF group 16 strains), with type strain CCUG 11779 (= LMG 7169). 相似文献
224.
D. J. Hole G. C. Watt G. Davey-Smith C. L. Hart C. R. Gillis V. M. Hawthorne 《BMJ (Clinical research ed.)》1996,313(7059):711-716
OBJECTIVE: To assess the relation between forced expiratory volume in one second (FEV1) and subsequent mortality. DESIGN: Prospective general population study. SETTING: Renfrew and Paisley, Scotland. SUBJECTS: 7058 men and 8353 women aged 45-64 years at baseline screening in 1972-6. MAIN OUTCOME MEASURE: Mortality from all causes, ischaemic heart disease, cancer, hung and other cancers, stroke, respiratory disease, and other causes of death after 15 years of follow up. RESULTS: 2545 men and 1894 women died during the follow up period. Significant trends of increasing risk with diminishing FEV1 are apparent for both sexes for all the causes of death examined after adjustment for age, cigarette smoking, diastolic blood pressure, cholesterol concentration, body mass index, and social class. The relative hazard ratios for all cause mortality for subjects in the lowest fifth of the FEV1 distribution were 1.92 (95% confidence interval 1.68 to 2.20) for men and 1.89 (1.63 to 2.20) for women. Corresponding relative hazard ratios were 1.56 (1.26 to 1.92) and 1.88 (1.44 to 2.47) for ischaemic heart disease, 2.53 (1.69 to 3.79) and 4.37 (1.84 to 10.42) for lung cancer, and 1.66 (1.07 to 2.59) and 1.65 (1.09 to 2.49) for stroke. Reduced FEV1 was also associated with an increased risk for each cause of death examined except cancer for lifelong nonsmokers. CONCLUSIONS: Impaired lung function is a major clinical indicator of mortality risk in men and women for a wide range of diseases. The use of FEV1 as part of any health assessment of middle aged patients should be considered. Smokers with reduced FEV1 should form a priority group for targeted advice to stop smoking. 相似文献
225.
226.
Two life-history variants of Arctic charr (Salvelinus alpinus), anadromous and lake-resident, have been previously identified in lakes of Southern Baffin Island, Nunavut, Canada. In accordance
with classical life-history theory, it is hypothesised that anadromous charr will delay maturation in both size and age, and
have increased fecundity (per spawning event) in comparison with lake-resident charr. Sagittal otoliths and biological data
were collected for both life-history variants within the three studied lakes: Iqalugaarjuit, Qasigiat and Qinngu. Sagittal
otoliths were embedded in epoxy resin, cross-sectioned for age determination, and imaged for back-calculation (size and age).
Back-calculated data in each lake were fit to von Bertalanffy growth models for each life-history variant and compared via
analysis of residual sums of squares. Anadromous charr had greater mean size at maturity and experienced a delay in mean age
at maturity in comparison with lake-residents. The relationship between size and fecundity or egg diameter did not differ
between the two life-history variants. Growth models indicate that the overall growth coefficients of lake-resident and anadromous
charr were different in all three studied lakes. The Brody growth coefficient for all lake-resident charr populations was
greater than anadromous individuals indicating that maximum length was reached at a rapid rate, resulting in a smaller asymptotic
length. Indirect evidence suggests that anadromous and lake-resident charr belong to one reproductive population. Future genetic
analysis is necessary to further determine the degree of divergence between the life-history variants. 相似文献
227.
228.
Jamie H. Rosenblum Lichtenstein Yi-Hsiang Hsu Igor M. Gavin Thomas C. Donaghey Ramon M. Molina Khristy J. Thompson Chih-Lin Chi Bruce S. Gillis Joseph D. Brain 《PloS one》2015,10(5)
BackgroundMolds can cause respiratory symptoms and asthma. We sought to use isolated peripheral blood mononuclear cells (PBMCs) to understand changes in cytokine and chemokine levels in response to mold and mycotoxin exposures and to link these levels with respiratory symptoms in humans. We did this by utilizing an ex vivo assay approach to differentiate mold-exposed patients and unexposed controls. While circulating plasma chemokine and cytokine levels from these two groups might be similar, we hypothesized that by challenging their isolated white blood cells with mold or mold extracts, we would see a differential chemokine and cytokine release.ConclusionsThese findings demonstrate that chronic mold exposures induced changes in inflammatory and immune system responses to specific mold and mycotoxin challenges. These responses can differentiate mold-exposed patients from unexposed controls. This strategy may be a powerful approach to document immune system responsiveness to molds and other inflammation-inducing environmental agents. 相似文献
229.
230.
Caitrin W. McDonough Nancy K. Gillis Abdullah Alsultan Shin-Wen Chang Marina Kawaguchi-Suzuki Jason E. Lang Mohamed Hossam A. Shahin Thomas W. Buford Nihal M. El Rouby Ana C.C. Sá Taimour Y. Langaee John G. Gums Arlene B. Chapman Rhonda M. Cooper-DeHoff Stephen T. Turner Yan Gong Julie A. Johnson 《PloS one》2013,8(10)
We sought to identify novel pharmacogenomic markers for HDL-C response to atenolol in participants with mild to moderate hypertension. We genotyped 768 hypertensive participants from the Pharmacogenomic Evaluation of Antihypertensive Responses (PEAR) study on the Illumina HumanCVD Beadchip. During PEAR, participants were randomized to receive atenolol or hydrochlorothiazide. Blood pressure and cholesterol levels were evaluated at baseline and after treatment. This study focused on participants treated with atenolol monotherapy. Association with atenolol induced HDL-C change was evaluated in 232 whites and 152 African Americans using linear regression. No SNPs achieved a Bonferroni corrected P-value. However, we identified 13 regions with consistent association across whites and African Americans. The most interesting of these regions were seven with prior associations with HDL-C, other metabolic traits, or functional implications in the lipid pathway: GALNT2, FTO, ABCB1, LRP5, STARD3NL, ESR1, and LIPC. Examples are rs2144300 in GALNT2 in whites (P=2.29x10-4, β=-1.85 mg/dL) and rs12595985 in FTO in African Americans (P=2.90x10-4, β=4.52 mg/dL), both with consistent regional association (P<0.05) in the other race group. Additionally, baseline GALNT2 expression differed by rs2144300 genotype in whites (P=0.0279). In conclusion, we identified multiple gene regions associated with atenolol induced HDL-C change that were consistent across race groups, several with functional implications or prior associations with HDL-C. 相似文献