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101.
102.
Expression of N-linked sialyl Le(x) determinants and O-glycans in the carbohydrate moiety of human amniotic fluid transferrin during pregnancy 总被引:3,自引:0,他引:3
Transferrin, a glycoprotein involved in iron transport in body fluids, was
isolated from amniotic fluid of a hydramniospatient by sequential
anion-exchange chromatography and gel filtration. The N-glycans of human
amniotic fluid transferrin (hAFT) were enzymatically liberated by PNGase-F
digestion, isolated by gel filtration and fractionated by (high-pH)
anion-exchange chromatography. After alkaline borohydride treatment of
native hAFT, the released O-glycans were isolated by gel filtration and
fractionated by anion-exchange chroma-tography. Structure elucidation of 14
N- and 2 O-glycans was performed by 500 or 600 MHz1H-NMR spectroscopy.
Besides conventional N-glycans established earlier for human serum
transferrin (hST), new (alpha1-3)-fucosylated N- glycans were found,
representing sialyl Le(x) elements. Furthermore, as compared to hST, a
higher degree of (alpha1-6)-fucosylation and an increase in branching from
di- to triantennary compounds has been detected. The presence of O-glycans
is demonstrated for the first time in transferrin.
相似文献
103.
104.
JP Reyes A Huanosta-Gutiérrez A López-Rodríguez A Martínez-Torres 《Channels (Austin, Tex.)》2015,9(2):88-95
We studied the effects of mutations of positively charged amino acid residues in the pore of X. tropicalis TMEM16A calcium-activated chloride channels: K613E, K628E, K630E; R646E and R761E. The activation and deactivation kinetics were not affected, and only K613E showed a lower current density. K628E and R761E affect anion selectivity without affecting Na+ permeation, whereas K613E, R646E and the double mutant K613E + R646E affect anion selectivity and permeability to Na+. Furthermore, altered blockade by the chloride channel blockers anthracene-9-carboxylic acid (A-9-C), 4, 4''-Diisothiocyano-2,2''-stilbenedisulfonic acid (DIDS) and T16inh-A01 was observed. These results suggest the existence of 2 binding sites for anions within the pore at electrical distances of 0.3 and 0.5. These sites are also relevant for anion permeation and blockade. 相似文献
105.
Corbin LJ Blott SC Swinburne JE Sibbons C Fox-Clipsham LY Helwegen M Parkin TD Newton JR Bramlage LR McIlwraith CW Bishop SC Woolliams JA Vaudin M 《Mammalian genome》2012,23(3-4):294-303
Osteochondrosis is a developmental orthopaedic disease that occurs in horses, other livestock species, companion animal species, and humans. The principal aim of this study was to identify quantitative trait loci (QTL) associated with osteochondritis dissecans (OCD) in the Thoroughbred using a genome-wide association study. A secondary objective was to test the effect of previously identified QTL in the current population. Over 300 horses, classified as cases or controls according to clinical findings, were genotyped for the Illumina Equine SNP50 BeadChip. An animal model was first implemented in order to adjust each horse's phenotypic status for average relatedness among horses and other potentially confounding factors which were present in the data. The genome-wide association test was then conducted on the residuals from the animal model. A single SNP on chromosome 3 was found to be associated with OCD at a genome-wide level of significance, as determined by permutation. According to the current sequence annotation, the SNP is located in an intergenic region of the genome. The effects of 24 SNPs, representing QTL previously identified in a sample of Hanoverian Warmblood horses, were tested directly in the animal model. When fitted alongside the significant SNP on ECA3, two of these SNPs were found to be associated with OCD. Confirmation of the putative QTL identified on ECA3 requires validation in an independent sample. The results of this study suggest that a significant challenge faced by equine researchers is the generation of sufficiently large data sets to effectively study complex diseases such as osteochondrosis. 相似文献
106.
The robustness of two phylogenetic methods: four-taxon simulations reveal a slight superiority of maximum likelihood over neighbor joining 总被引:3,自引:3,他引:3
The robustness (sensitivity to violation of assumptions) of the maximum-
likelihood and neighbor-joining methods was examined using simulation.
Maximum likelihood and neighbor joining were implemented with Jukes-
Cantor, Kimura, and gamma models of DNA substitution. Simulations were
performed in which the assumptions of the methods were violated to varying
degrees on three model four-taxon trees. The performance of the methods was
evaluated with respect to ability to correctly estimate the unrooted
four-taxon tree. Maximum likelihood outperformed neighbor joining in 29 of
the 36 cases in which the assumptions of both methods were satisfied. In
133 of 180 of the simulations in which the assumptions of the
maximum-likelihood and neighbor-joining methods were violated, maximum
likelihood outperformed neighbor joining. These results are consistent with
a general superiority of maximum likelihood over neighbor joining under
comparable conditions. They extend and clarify an earlier study that found
an advantage for neighbor joining over maximum likelihood for
gamma-distributed mutation rates.
相似文献
107.
108.
Alistair JP Brown 《Genome biology》2010,11(5):302
A report of the symposium on Signaling and Systems Biology held during the Society for General Microbiology Spring Meeting,
29-30 March 2010, Edinburgh, UK. 相似文献
109.
110.