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91.
92.
Mohammed Hadi Latifi Kunalan Ganthel Shanmugam Rukmanikanthan Azura Mansor Tunku Kamarul Mehmet Bilgen 《Biomedical engineering online》2012,11(1):1-1
The first publication of the work [1] did not present one of the authors' names. Kunalan Ganthel has now been added to the author list. In addition, Habib Sherkat has been added to the Acknowledgements, with thanks for providing help with the use of hyperelastic module of Abaqus Software. 相似文献
93.
Alihossein Saberi Elahe Salari Sayyed Mahmood Latifi 《Mutation Research - Genetic Toxicology and Environmental Mutagenesis》2013,750(1-2):92-95
Ionizing radiation is known as a classical mutagen capable of inducing various kinds of stable and unstable chromosomal aberrations. The percentage of cells with chromosomal aberrations was analyzed in peripheral blood lymphocytes of occupationally exposed workers in radiotherapy, CT-scan, angiography and healthy controls. The incidence of all types of aberrations (gap, acentric fragment, dicentric and ring) in exposed subjects were higher than those observed in healthy controls (P = 0.0001). However, the frequency of aberrant cells with dicentric and ring chromosome in exposed subjects were not significantly different from those in controls. To see whether there is a significant difference in the incidence of chromosomal aberrations among three groups, they were compared for all types of observed aberrations. No significant difference was found between radiotherapy and CT-scan groups (P = 0.838). The percentage of aberrant cells observed, for angiography groups were significantly higher than radiotherapy (P = 0.0001) and CT-scan (P = 0.0001) group. Taken together these data suggest that the cumulative effects of low level chronic exposure to ionizing radiation is higher for those who occupationally exposed in angiography. 相似文献
94.
Azarmehr Zahra Ranji Najmeh Khazaei Koohpar Zeinab Habibollahi Hadi 《Molecular biology reports》2021,48(3):2533-2542
Molecular Biology Reports - The aim of this study was to consider the expression of farnesoid X receptor (Fxr), liver X receptor (LXRα) and sirtuin 1 (Sirt1), oxidative stress, inflammation,... 相似文献
95.
96.
Abedien Zabardasti Ali Kakanejadi Fatemeh Ghenaatian Zeinab Bigleri 《Molecular simulation》2013,39(12):960-968
Ab initio and density functional calculations are used to analyse the interaction between a molecule of the cyanuric acid and one, two and three molecules of water at B3LYP/6-311++ G(d,p) and MP2/6-311++ G(d,p) computational levels. Also, the cooperative effect (CE) in terms of the stabilisation energy of clusters is calculated and discussed. Depending on the geometry of clusters under study, the cooperative, non- or anti-CE was found with an increasing cluster size. Red shifts of N–H and C = O stretching frequencies illustrate a good dependence on the CE. The atoms in molecules theory is used to analyse the CE on topological parameters. 相似文献
97.
Latifi R Tahsini L Karamzadeh B Safari N Nam W de Visser SP 《Archives of biochemistry and biophysics》2011,507(1):4-13
Manganese-oxo porphyrins have been well studied as biomimetic models of cytochromes P450 and are known to be able to catalyze substrate hydroxylation reactions. Recent experimental studies [J.Y. Lee, Y.-M. Lee, H. Kotani, W. Nam, S. Fukuzumi, Chem. Commun. (2009) 704] showed that Mn(V)-oxo porphyrins react rapidly with 10-methyl-9,10-dihydroacridine (AcrH(2)) via a proton-coupled-electron-transfer followed by an electron transfer. In this work, we present a computational study on the reactivity patterns of Mn(V)-oxo and Mn(IV)-oxo with respect to AcrH(2). This study shows that although both oxidants are capable of hydroxylating AcrH(2), the Mn(V)-oxo species is the more active oxidant. We have generalized these observations with thermodynamic cycles that explain the reaction mechanisms and electron transfer processes. For the Mn(V)-oxo mechanism the reactions proceed with a fast spin state crossing from the ground state singlet to the triplet spin state prior to a hydrogen atom transfer followed by another electron transfer. The present results are fully consistent with previous studies on iron-oxo porphyrins and manganese-oxo porphyrins and shows that the interplay of low lying singlet and triplet spin state surfaces influences the reaction mechanisms and kinetics. 相似文献
98.
Shams Nemat Shakarami Gandabeh Zeinab Nazifi Narges Forouharmehr Ali Jaydari Amin Rashidian Ehsan 《International journal of peptide research and therapeutics》2020,26(3):1527-1539
International Journal of Peptide Research and Therapeutics - Salmonella is a gram-negative bacterium belonging to the Enterobacteriaceae family. One of the major known serotypes of this bacterium... 相似文献
99.
Lova Satyanarayana Matsa Advithi Rangaraju Viswamitra Vengaldas Mona Latifi Hossein Mehraban Jahromi Venkateshwari Ananthapur Pratibha Nallari 《PloS one》2013,8(7)
Dilated Cardiomyopathy (DCM) is characterized by systolic dysfunction, followed by heart failure necessitating cardiac transplantation. The genetic basis is well established by the identification of mutations in sarcomere and cytoskeleton gene/s. Modifier genes and environmental factors are also considered to play a significant role in the variable expression of the disease, hence various mechanisms are implicated and one such mechanism is oxidative stress. Nitric Oxide (NO), a primary physiological transmitter derived from endothelium seems to play a composite role with diverse anti-atherogenic effects as vasodilator. Three functional polymorphisms of endothelial nitric oxide synthase (NOS3) gene viz., T-786C of the 5′ flanking region, 27bp VNTR in intron4 and G894T of exon 7 were genotyped to identify their role in DCM. A total of 115 DCM samples and 454 controls were included. Genotyping was carried out by PCR -RFLP method. Allelic and genotypic frequencies were computed in both control & patient groups and appropriate statistical tests were employed. A significant association of TC genotype (T-786C) with an odds ratio of 1.74, (95% CI 1.14 - 2.67, p = 0.01) was observed in DCM. Likewise the GT genotypic frequency of G894T polymorphism was found to be statistically significant (OR 2.10, 95% CI 1.34–3.27, p = 0.0011), with the recessive allele T being significantly associated with DCM (OR 1.64, 95% CI 1.18 - 2.30, p = 0.003). The haplotype carrying the recessive alleles of G894T and T-786C, C4bT was found to exhibit 7 folds increased risk for DCM compared to the controls. Hence C4bT haplotype could be the risk haplotype for DCM. Our findings suggest the possible implication of NOS3 gene in the disease phenotype, wherein NOS3 may be synergistically functioning in DCM associated heart failure via the excessive production of NO in cardiomyocytes resulting in decreased myocardial contractility and systolic dysfunction, a common feature of DCM phenotype. 相似文献
100.
Kujtim Latifi Vladimir Feygelman Eduardo G. Moros Thomas J. Dilling Craig W. Stevens Geoffrey G. Zhang 《PloS one》2013,8(12)