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51.
The objective of the study was to examine salivary biomarker response to fluid consumption in exercising athletes. Exercise induces stress on the body and salivary alpha amylase (sAA) and salivary cortisol are useful biomarkers for activity in the sympathoadrenal medullary system and the hypothalamic pituitary adrenal axis which are involved in the stress response. Fifteen college students were given 150 ml and 500 ml of water on different days and blinded to fluid condition. The exercise protocol was identical for both fluid conditions using absolute exercise intensities ranging from moderate to high. Saliva was collected prior to exercise, post moderate and post high intensities and analyzed by Salimetrics assays. Exercise was significant for sAA with values different between pre-exercise (85 ± 10 U · ml−1) and high intensity (284 ± 30 U · ml−1) as well as between moderate intensity (204 ± 32 U · ml−1) and high intensity. There was no difference in sAA values between fluid conditions at either intensity. Exercise intensity and fluid condition were each significant for cortisol. Cortisol values were different between pre-exercise (0.30 ± 0.03 ug · dL−1) and high intensity (0.45 ± 0.05 ug · dL−1) as well as between moderate intensity (0.33 ± 0.04 ug · dL−1) and high intensity. Moderate exercise intensity cortisol was lower in the 500 ml condition (0.33 ± 0.03 ug · dL−1) compared with the 150 ml condition (0.38 ± 0.03 ug · dL−1). This altered physiological response due to fluid consumption could influence sport performance and should be considered. In addition, future sport and exercise studies should control for fluid consumption. 相似文献
52.
53.
不同退化阶段高寒草甸土壤化学计量特征 总被引:14,自引:1,他引:13
为了阐明不同退化阶段高寒草甸土壤的化学计量特征,沿着高寒草甸退化的梯度选取了原生嵩草草甸、轻度退化草甸和严重沙化草甸,测定了高寒草甸退化过程中不同深度土壤的有机碳、全氮、全磷和全钾含量。结果表明:随着高寒草甸的退化,0~100cm土壤的有机碳、全氮、全磷和全钾含量以及碳氮比、碳磷比、碳钾比、氮磷比、氮钾比和磷钾比均呈降低趋势,且土壤有机碳对高寒草甸退化的敏感性最高,全氮、全磷和全钾的敏感性依次降低,表层20cm的土壤有机碳和全氮可作为表征高寒草甸退化程度最敏感的土壤养分指标。另外,随着草甸的退化,土壤的有机碳、全氮、全磷和全钾含量及其化学计量比的垂直分布明显不同:随着土壤深度的增加,原生嵩草草甸和轻度退化草甸的土壤有机碳、全氮和全磷含量以及碳氮比、碳磷比、碳钾比、氮磷比、氮钾比和磷钾比在0~40cm范围内锐减,在40cm以下缓慢降低并趋于稳定;而沙化草甸土壤的有机碳、全氮、全磷和全钾及其化学计量比随着土壤深度的增加保持不变。 相似文献
54.
BACKGROUND: Altered cholesterol metabolism and defects in cholesterol biosynthesis may influence abnormal central nervous system (CNS) development. During early stages of embryonic development, high levels of cholesterol are needed by rapidly proliferating cells that utilize cholesterol as a key cell membrane component. Alterations in cholesterol levels are influenced by variations in the apolipoprotein E (apoE) and apolipoprotein B (apoB) genes. The purpose of our study was to explore the possible association between infant genetic variations in the apoE and apoB genes and spina bifida (SB) risk. METHODS: Genomic DNA was extracted from newborn screening blood spots obtained from 26 infants with SB and 73 non-malformed control infants. ApoE and apoB genotypes were determined by restriction enzyme digestion of PCR amplification products. RESULTS: Genotype frequencies for the apoE and apoB polymorphisms were not statistically different between case and control infants. For each apoB polymorphism, however, the frequency of the wild-type allele was higher in SB infants as compared to controls. Additionally, the apoE genotype E2/E3 was observed more frequently in the controls than in SB infants [15% in controls compared to 4% in cases; OR = 0.2 (0-1.6)]. CONCLUSIONS: Results from this study suggest that genetic variations in the apoE and apoB genes, known to regulate cholesterol metabolism, do not substantially contribute to the risk of SB in infants. 相似文献
55.
56.
Despite the fact that neural tube defects (NTDs) are the most common congenital malformations of the central nervous system, investigators have yet to identify responsible gene(s). Research efforts have been productive in the identification of environmental factors, such as periconceptional folic acid supplementation, that modulate risk for the development of NTDs. Studies of the folic acid biosynthetic pathway led to the discovery of an association between elevated levels of homocysteine and NTD risk. Researchers subsequently identified single nucleotide polymorphisms in the gene coding for the enzyme 5,10-methylenetetrahydrofolate reductase (MTHFR). Association studies suggested it was a potential risk factor for NTDs, because the thermolabile form of the enzyme led to elevated homocysteine concentrations when folic acid intake is low. Numerous studies analyzing MTHFR variants have resulted in positive associations with increased NTD risk only in certain populations, suggesting that these variants are not large contributors to the etiology of NTDs. With our limited understanding of the genes involved in regulating NTD susceptibility, the paucity of data on how folic acid protects the developing embryo, as well as the observed decrease in birth prevalence of NTDs following folic acid supplementation and food fortification, it makes little sense for prospective parents to be tested for MTHFR variants, or for variants of other known folate pathway genes. 相似文献
57.
Walter RB; Rolig RL; Kozak KA; McEntire B; Morizot DC; Nairn RS 《Molecular biology and evolution》1993,10(6):1227-1238
Fishes represent the stem vertebrate condition and have maintained several
gene arrangements common to mammalian genomes throughout the 450 Myr of
divergence from a common ancestor. One such syntenic arrangement includes
the GPI-PEPD enzyme association on Xiphophorus linkage group IV and human
chromosome 19. Previously we assigned the Xiphophorus homologue of the
human ERCC2 gene to linkage group U5 in tight association with the CKM
locus. CKM is also tightly linked to the ERCC2 locus on human chromosome
19, leading to speculation that human chromosome 19 may have arisen by
fusion of two ancestral linkage groups which have been maintained in
fishes. To investigate this hypothesis further, we isolated and sequenced
Xiphophorus fish genomic regions exhibiting considerable sequence
similarity to the human DNA ligase 1 amino acid sequence. Comparison of the
fish DNA ligase sequence with those of other species suggests several modes
of amino acid conservation in this gene. A 2.2-kb restriction fragment
containing part of an X. maculatus DNA ligase 1 exon was used in backcross
hybrid mapping with 12 enzyme or RFLP loci. Significant linkage was
observed between the nucleoside phosphorylase (NP2) and the DNA ligase
(LIG1) loci on Xiphophorus linkage group VI. This assignment suggests that
the association of four DNA repair-related genes on human chromosome 19 may
be the result of chance chromosomal rearrangements.
相似文献
58.
Angstrom J; Teneberg S; Milh MA; Larsson T; Leonardsson I; Olsson BM; Halvarsson MO; Danielsson D; N aslund I; Ljungh A; Wadstrom T; Karlsson KA 《Glycobiology》1998,8(4):297-309
The possible role of glycosphingolipids as adhesion receptors for the human
gastric pathogen Helicobacter pylori was examined by use of radiolabeled
bacteria, or protein extracts from the bacterial cell surface, in the
thin-layer chromatogram binding assay. Of several binding specificities
found, the binding to lactosylceramide is described in detail here, the
others being reported elsewhere. By autoradiography a preferential binding
to lactosylceramide having sphingosine/phytosphingosine and 2-D hydroxy
fatty acids was detected, whereas lactosylceramide having sphingosine and
nonhydroxy fatty acids was consistently nonbinding. A selective binding of
H. pylori to lactosylceramide with phytosphingosine and 2-D hydroxy fatty
acid was obtained when the different lactosylceramide species were
incorporated into liposomes, but only in the presence of cholesterol,
suggesting that this selectivity may be present also in vivo . Importantly,
lactosylceramide with sphingosine and hydroxy fatty acids does not bind in
this assay. Furthermore, a lactosylceramide-based binding pattern obtained
for different trisaccharide glycosphingolipids is consistent with the
assumption that this selectivity is due to binding of a conformation of
lactosylceramide in which the oxygen of the 2-D fatty acid hydroxyl group
forms a hydrogen bond with the Glc hydroxy methyl group, yielding an
epitope presentation different from other possible conformers. An
alternative conformation that may come into consideration corresponds to
the crystal structure found for cerebroside, in which the fatty acid
hydroxyl group is free to interact directly with the adhesin. By isolating
glycosphingolipids from epithelial cells of human stomach from seven
individuals, a binding of H.pylori to the diglycosylceramide region of the
non-acid fraction could be demonstrated in one of these cases. Mass
spectrometry showed that the binding-active sample contained
diglycosylceramides with phytosphingosine and 2-D hydroxy fatty acids with
16-24 carbon atoms in agreement with the results related above.
相似文献
59.
Moreno E; Lanne B; Vazquez AM; Kawashima I; Tai T; Fernandez LE; Karlsson KA; Angstrom J; Perez R 《Glycobiology》1998,8(7):695-705
P3 is a mouse monoclonal antibody (mAb) that binds to several NeuGc-
containing gangliosides. It also reacts with antigens expressed in human
breast tumors (Vazquez et al. (1995) Hybridoma , 14, 551-556). In this
work, the binding specificity of P3 has been characterized in more detail
using a panel of glycolipids that included several disialylated
gangliosides and several chemical derivatives of NeuGc-GM3. The carboxyl
group and the nitrogen function of sialic acid were found to play important
roles in the antibody binding, whereas the glycerol tail appears to be
nonrelevant. Molecular modeling was used to analyze the binding data,
including the finding that P3 selectively recognizes the internal NeuGc in
GD3. For this purpose, conformational studies of GD3 were performed using
molecular dynamics. It was concluded that sialic acid binds the P3 antibody
through its upper face (the one on which the carboxyl group is exposed) and
the C4-C5 side of the sugar ring, whereas none or very little contact
between the galactose residue and the protein is evident. Conformational
analysis of GD3 revealed that, despite the large flexibility of the
NeuGcalpha8NeuGc linkage, the P3 binding epitope on the external sialic
acid is not well exposed for any of the possible conformations this linkage
can adopt, whereas the internal sialic acid presents the epitope in a
proper way for several of these conformations. As a final result, a
coherent picture of the epitope that fits the wide binding data was
obtained.
相似文献
60.
Restriction mapping is used to estimate nucleotide sequence polymorphism
when the regions to be studied are too long or too numerous to be
sequenced. Restriction mapping is less costly than DNA sequencing, but it
does not allow direct measurement of underlying nucleotide polymorphism. It
is therefore useful to be able to estimate underlying nucleotide
polymorphism from observations of polymorphism in restriction maps, as this
offers some of the resolution afforded by DNA sequencing at a reduced cost.
Previous estimators of underlying nucleotide polymorphism have assumed that
each restriction-enzyme- binding site contains, at most, a single
polymorphic nucleotide position (the low-polymorphism-frequency
assumption), and this assumption has placed an upper limit on the level of
polymorphism that can be resolved by these estimators. The present study
documents an estimator which allows relaxation of this assumption. The new
estimator more accurately estimates underlying nucleotide polymorphism when
the polymorphism level is high enough to falsify the low-polymorphism-
frequency assumption. The new estimator therefore yields good results for
data sets that are too divergent for analysis by present methods.
相似文献