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1.
Histochemical characteristics of chemoreceptor organs (Glomera) 总被引:1,自引:1,他引:0
Summary Some important histochemical characteristics of the carotid, aortic and coronary glomera have been studied in man and the rabbit.All glomera present a similar histochemical pattern. Type I glomus cells contain acetylcholinesterase, monoamine oxidase and norepinephrine. Type II glomus cells are highly positive for cholinesterase, carbonic anhydrase and nucleoside phosphatases hut they do not contain acetylcholinesterase nor catecholamines. It is postulated that the type I glomus cell is the true chemoreceptor cell. Together with the type II glomus cell, which is considered to be a special type of glial cell, a functional metabolic unit is established. Efferent nerve fibres could be adrenergic; by way of cholinergic transmission action potentials could be initiated in the afferent nerve fibres.The following Abbreviations will be used AChE
acetylcholinesterase
- ChE
cholinesterase
- iso-OMPA
tetraisopropylpyrophosphoramide
- DFP
di-isopropylfluorophosphate
- 62C47
15-bis-(4-trimethylammonium-phenyl) pentan-3-one-diiodide
- CAH
carbonic anhydrase
- ATP-ase
adenosine triphosphatase
- NP-ases
nucleoside phosphatases
- UDP
uridine diphosphate
- UTP
uridine triphosphate
- IDP
inosine diphosphate
- CTP
cytidine triphosphate
- CaFoMa
calcium-formol-macrodex
- Glut
glutaraldehyde
- TPP-ase
thiamine pyrophosphatase
- MAO
monoamine oxidase
- CA
catecholamines
- NE
norepinephrine 相似文献
2.
The relationship between the amount of exercise-induced muscle damage and the release of creatine kinase (CK), aspartate aminotransferase (AST), and lactate dehydrogenase (LD) was studied. Gender differences in enzyme release and histological damage were also studied. Serial pre- and postexercise blood samples were drawn from untrained male and female catheterized Wistar rats that ran 1.5 or 2.5 h on a treadmill (incline 10 degrees). Three days postexercise, muscle damage was quantified morphometrically in five different hindlimb and forearm muscles. The 1.5 and 2.5 h of exercise elicited histological damage only in the soleus muscle. Significant plasma CK, AST, and LD elevations were found immediately postexercise both in male and female rats. However, the enzyme release was significantly greater in males than in females. Part of this could be explained by differences in clearance rates between males and females. No gender difference in amount of histological damage was found. The actual volume of histological muscle damage was significantly less than the calculated muscle damage based on enzyme release. An increase in the exercise duration from 1.5 to 2.5 h resulted in a disproportional increase in both histological muscle damage and muscle enzyme release. From the present study it is concluded that muscle enzyme release is not clearly reflected in histological muscle damage. 相似文献
3.
Do anthocorid predators respond to synomones from Psylla-infested pear trees under field conditions?
Because Y-tube olfactometer experiments in the laboratory showed a response of anthocorid bugs to odour fromPsylla-infested leaves, it was of interest to assess its relevance under field circumstances. This was done by measuring the density
of predatory bugs on pear trees adjacent toPsylla-infested or control trees that were covered with fine mesh gauze-screens. In this way odours from these caged trees could
spread through the screen, while contact with thePsylla prey in the cage was prevented. The density of anthocorid predators around cages with heavily infested trees was significantly
higher than around uncaged control trees and around cages containing uninfested or little infested trees. Covering a cage
withPsylla-infested trees by an airtight plastic sheet led to an immediate drop in the density of anthocorid predators, whereas removal
of the sheet led to predator aggregation again. The results of these field experiments strongly support the hypothesis that
anthocorid predators respond to volatile chemicals emanating fromPsylla-infested pear trees. 相似文献
4.
Functional topography and ultrastructure of periarticular mechanoreceptors in the lateral elbow region of the rat 总被引:1,自引:0,他引:1
The distribution and ultrastructure of sensory nerve endings were investigated in the deep lateral elbow region of the rat. Three zones of distribution of mechanoreceptors were distinguished, each in relation to the functional architecture of the connective and muscular tissue in that area: (1) a zone with muscle spindles, Golgi tendon organs, free nerve endings and single small lamellated corpuscles ('muscle-tendon spectrum'), situated in the middle third of the supinator muscle and its superficial aponeurosis; (2) a zone with small lamellated corpuscles and free nerve endings, situated pericapsularly to the humeroradial joint capsule ('shearing spectrum'): this moderately dense, irregular connective tissue is covered by the proximal continuation of the supinator's aponeurosis, and muscle fibers insert from beneath this aponeurosis, which displays, as a part of the joint capsule, a strong collagenous tissue plate; (3) a zone with only free nerve endings within the tendon-like, most proximal part of the supinator's aponeurosis, inserting into the periosteal layer of the lateral humeral epicondyle ('endotenonial spectrum'): it is part of the joint capsule. The ultrastructure of these sensory endings is described and the distribution pattern of the mechanoreceptors observed is discussed in relation to the classification into 'muscle receptors' and 'joint receptors'. 相似文献
5.
An antibody against SSEA-5 glycan on human pluripotent stem cells enables removal of teratoma-forming cells 总被引:1,自引:0,他引:1
Tang C Lee AS Volkmer JP Sahoo D Nag D Mosley AR Inlay MA Ardehali R Chavez SL Pera RR Behr B Wu JC Weissman IL Drukker M 《Nature biotechnology》2011,29(9):829-834
An important risk in the clinical application of human pluripotent stem cells (hPSCs), including human embryonic and induced pluripotent stem cells (hESCs and hiPSCs), is teratoma formation by residual undifferentiated cells. We raised a monoclonal antibody against hESCs, designated anti-stage-specific embryonic antigen (SSEA)-5, which binds a previously unidentified antigen highly and specifically expressed on hPSCs--the H type-1 glycan. Separation based on SSEA-5 expression through fluorescence-activated cell sorting (FACS) greatly reduced teratoma-formation potential of heterogeneously differentiated cultures. To ensure complete removal of teratoma-forming cells, we identified additional pluripotency surface markers (PSMs) exhibiting a large dynamic expression range during differentiation: CD9, CD30, CD50, CD90 and CD200. Immunohistochemistry studies of human fetal tissues and bioinformatics analysis of a microarray database revealed that concurrent expression of these markers is both common and specific to hPSCs. Immunodepletion with antibodies against SSEA-5 and two additional PSMs completely removed teratoma-formation potential from incompletely differentiated hESC cultures. 相似文献
6.
7.
8.
Establishment of human embryonic stem cell-transfected clones carrying a marker for undifferentiated cells. 总被引:20,自引:0,他引:20
R Eiges M Schuldiner M Drukker O Yanuka J Itskovitz-Eldor N Benvenisty 《Current biology : CB》2001,11(7):514-518
Human embryonic stem (ES) cells are pluripotent cell lines that have been derived from the inner cell mass (ICM) of blastocyst stage embryos [1--3]. They are characterized by their ability to be propagated indefinitely in culture as undifferentiated cells with a normal karyotype and can be induced to differentiate in vitro into various cell types [1, 2, 4-- 6]. Thus, human ES cells promise to serve as an unlimited cell source for transplantation. However, these unique cell lines tend to spontaneously differentiate in culture and therefore are difficult to maintain. Furthermore, colonies may contain several cell types and may be composed of cells other than pluripotent cells [1, 2, 6]. In order to overcome these difficulties and establish lines of cells with an undifferentiated phenotype, we have introduced a reporter gene that is regulated by a promoter of an ES cell-enriched gene into the cells. For the introduction of DNA into human ES cells, we have established a specific transfection protocol that is different from the one used for murine ES cells. Human ES cells were transfected with enhanced green fluorescence protein (EGFP), under the control of murine Rex1 promoter. The transfected cells show high levels of GFP expression when in an undifferentiated state. As the cells differentiate, this expression is dramatically reduced in monolayer cultures as well as in the primitive endoderm of early stage (simple) embryoid bodies (EBs) and in mature EBs. The undifferentiated cells expressing GFP can be analyzed and sorted by using a Fluorescence Activated Cell Sorter (FACS). Thus, we have established lines of human ES cells in which only undifferentiated cells are fluorescent, and these cells can be followed and selected for in culture. We also propose that the pluripotent nature of the culture is made evident by the ability of the homogeneous cell population to form EBs. The ability to efficiently transfect human ES cells will provide the means to study and manipulate these cells for the purpose of basic and applied research. 相似文献
9.
10.
Eline Lindeman Frank Spaans Jos Reulen Pieter Leffers Jan Drukker 《Journal of electromyography and kinesiology》1999,9(6):427-384
In a randomized clinical trial the efficacy of strength training was studied in patients with myotonic dystrophy (n=33) and in patients with Charcot-Marie-Tooth disease (n=29). Measurements were performed at the start and after 8, 16 and 24 weeks of progressive resistance training. Surface electromyography (SEMG) of proximal leg muscles was recorded during isometric knee extension at maximum voluntary contraction (MVC) and at 20, 40, 60 and 80% of MVC. Changes in MVC, maximum electrical activity and torque–EMG ratios (TER) were calculated. Fatigue was studied by determining the changes in endurance and in the decline of the median frequency (Fmed) of the SEMG during a sustained contraction at 80% MVC. These parameters showed no significant changes after the training in either of the diagnostic groups. Only the Charcot-Marie-Tooth training group showed a gradual significant increase in mean MVC over the whole training period (21%). After 24 weeks, the increase in mean RMS was similar (25%), but this was mainly due to a sharp rise during the first 8 weeks of training (20%). The findings indicate that the initial strength increase was due to a neural factor, while the subsequent increase was mainly due to muscle hypertrophy. 相似文献