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71.
72.
A comparative Golgi study of Cajal foetal cells 总被引:1,自引:0,他引:1
73.
We describe in detail an automated and highly sensitive functional assay for calcium-coupled receptors (those receptors whose activation results in an increase in intracellular calcium levels) utilizing coelenterazine-charged aequorin as a probe for intracellular calcium levels ([Ca(2+)](i)). The assay was originally established to investigate Galpha(q)-coupled prostanoid receptors, which are members of the G-protein-coupled receptor (GPCR) superfamily, signaling through elevation of [Ca(2+)](i), initially focusing on the human EP(1) prostanoid receptor (hEP(1)). The parental human embryonic kidney cell line 293-AEQ17, developed by Button and Brownstein (Cell Calcium 14, 663-671, 1993), constitutively expresses apoaequorin and was used to develop a clonal cell line which stably coexpresses hEP(1). This cell line was used to optimize assay parameters in order to maximize accuracy and throughput in an automated 96-well format with the result that each 96-well plate can be completed in 70 min. Use of this flexible system will greatly simplify the functional analysis of GPCRs and other receptors which when activated result in increases in [Ca(2+)](i). 相似文献
74.
Prostaglandin (PG) synthesis and metabolism was studied in human fetal kidney, lung, small intestine, heart, brain and liver (gestational ages: 10, 12, 14, 18 and 23 weeks) and pregnant uterus (4-40 weeks of pregnancy). PG synthesis was increased in the myometrium during pregnancy while the capacity of metabolism did not change. PG synthesis increased in lung and kidney (4-fold), brain (20-fold) and small intestine (2-fold) but not in heart or liver. Metabolic activity increased only in fetal kidney and lung. 相似文献
75.
It was previously shown that porcine PHI is 30 times less potent than VIP in relaxing the rat gastric fundus; the relaxant potency of rat PHI and its 2 C-terminally extended forms PHI-Gly and PHV(1-42) in the rat gastric fundus was compared here with that of VIP, porcine PHI and PHM. The rank order of potency in relaxing the precontracted fundus tissues was VIP greater than rat PHI greater than PHM greater than PHV greater than PHI-Gly greater than porcine PHI, rat PHI being only 2 times less potent than VIP. In the presence of antioxidants, the potency and efficacy of porcine PHI increased, but the peptide was still the least potent of the series tested. The results illustrate the importance of using species-related peptides and are compatible with a cotransmitter role of rat PHI in nonadrenergic noncholinergic neurotransmission of the rat gastric fundus. 相似文献
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Razvan Nitu Alexandru Florin Rogobete Fuat Gundogdu Sonia Tanasescu Ovidiu Boruga Adriana Sas Sonia Elena Popovici Delia Hutanu Ciprian Pilut Cristian Andrei Sarau Adrian Constantin Candea Adrian Tudor Stan Liviu Marius Moise 《Biochemical genetics》2017,55(4):281-290
One of the main causes of death in the world is lung cancer. According to the World Health Organization, the annual incidence of lung cancer increases significantly. Moreover, lung cancer accounts for one of the highest mortality rates, mainly due to late detection. Numerous studies have been conducted in order to identify new biomarkers for early diagnosis and for monitoring and evaluation of lung cancer stages. An ideal biomarker candidate is represented by the analysis of microRNAs expression. In this paper, we want to summarize microRNAs expressions in lung cancer. We also want to present the expression of microRNAs depending on the evolution of lung cancer. For this study, we analyzed the studies available in scientific databases, such as PubMed and Scopus. The studies were selected using the search keywords “microRNAs expression,” “lung cancer,” and “genetic biomarkers.” The most significant articles were selected for the study, following rigorous analysis. To evaluate and monitor lung cancer, the expression of microRNAs may be used successfully due to increased specificity and selectivity. However, further studies are needed on the assignment and validation of microRNAs for each type of lung cancer, respectively, for each stage of evolution. 相似文献
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79.
Daryl F. Sas Judy K. Lundy Laurence J. Miller 《In vitro cellular & developmental biology. Plant》1989,25(8):730-736
Summary Due to limited growth potential of primary cultures and the absence of continuous lines of healthy enteric smooth muscle,
we have studied the culture behavior of neoplastic gastrointestinal smooth muscle cells. Forty-six human enteric smooth muscle
neoplasms (leiomyomas and leiomyosarcomas) were studied while fresh and/or after culture in vitro and growth in vivo in athymic
nude mice, with assessments made of morphology, growth characteristics, and biochemical markers of differentiation. The state
of differentiation of the tumors varied, with well-differentiated tumors tending to express binding sites for the gastrointestinal
hormone cholecystokinin, whereas less well-differentiated tumors did not. Poorly differentiated tumors were the easiest to
establish in culture in vitro and to grow in vivo in nude mice. When the cells placed directly into culture proliferated to
confluent density, they underwent morphologic differentiation from a spread, fibroblastlike shape to a slender spindle morphology,
with these cells possessing fewer biosynthetic organelles and arranging themselves in characteristic “hill and valley” arrays.
However, the highly differentiated characteristics of expression of desmin or cholecystokinin-binding sites were not observed
in cultured cells. In contrast, cells that had been passaged in nude mice before culture displayed a proliferative phenotype
and failed to undergo morphologic differentiation on reaching confluent density. Four human enteric smooth muscle cell lines
(documented by chromosomal analysis) originating in stomach, jejunum, ileum, and rectum were established using this strategy.
This work was supported by grants DK32878 and DK34988 from the National Institutes of Health, Bethesda, MD. 相似文献
80.
A study was made of the microsomal lipid peroxidation of the pregnant human uterus and placenta. It was found that the lipid peroxidation of the microsomal fraction of the uterus is specific for prostaglandin formation: the lipid peroxidation was enhanced by arachidonic acid, and inhibited by anti-prostaglandins. Accordingly, it is suitable as a screening test for the pharmacological examination of anti-prostaglandin effects. The lipid peroxidation in the placenta is not specific. In both tissues examined the lipid peroxidation is linked to ascorbic acid. 相似文献