全文获取类型
收费全文 | 197篇 |
免费 | 22篇 |
出版年
2021年 | 2篇 |
2019年 | 2篇 |
2018年 | 4篇 |
2017年 | 2篇 |
2016年 | 3篇 |
2015年 | 7篇 |
2014年 | 6篇 |
2013年 | 13篇 |
2012年 | 6篇 |
2011年 | 11篇 |
2010年 | 7篇 |
2009年 | 6篇 |
2008年 | 7篇 |
2007年 | 2篇 |
2006年 | 8篇 |
2005年 | 3篇 |
2004年 | 4篇 |
2003年 | 9篇 |
2002年 | 10篇 |
2001年 | 4篇 |
2000年 | 6篇 |
1999年 | 5篇 |
1998年 | 6篇 |
1995年 | 5篇 |
1994年 | 2篇 |
1992年 | 4篇 |
1991年 | 4篇 |
1990年 | 2篇 |
1989年 | 7篇 |
1988年 | 3篇 |
1987年 | 4篇 |
1982年 | 2篇 |
1981年 | 2篇 |
1977年 | 2篇 |
1976年 | 3篇 |
1974年 | 3篇 |
1968年 | 5篇 |
1962年 | 2篇 |
1961年 | 1篇 |
1959年 | 1篇 |
1957年 | 10篇 |
1947年 | 1篇 |
1934年 | 1篇 |
1931年 | 1篇 |
1929年 | 1篇 |
1928年 | 1篇 |
1926年 | 2篇 |
1925年 | 1篇 |
1924年 | 1篇 |
1923年 | 1篇 |
排序方式: 共有219条查询结果,搜索用时 109 毫秒
1.
2.
3.
Yaffa Mizrachi Peter I. Lelkes Richard L. Ornberg Gertrude Goping Harvey B. Pollard 《Cell and tissue research》1989,256(2):365-372
Summary Chromaffin cells in the adrenal medulla are found in close proximity to capillary endothelial cells, thereby forming the classical endocrine complex. To examine the possible chemical basis of their interaction in more detail, we have grown bovine adrenal medullary endothelial (BAME) cells in monolayer cultures and added to them pheochromocytoma (PC12) cells, a chromaffin tumor cell line of rats. The PC12 cells were chosen because of the similarities they share with adrenal medullary chromaffin cells. PC12 cells rapidly attached to BAME cells cultures, their rate of adhesion being significantly enhanced over binding of PC12 cells to either uncoated plates or to monolayers of unrelated cell cultures. Consistent with this observation, we noted that the extracellular matrix (ECM) derived from the BAME cells did not enhance PC12 cell adhesion and did not promote neurite sprouting as previously described for ECM derived from corneal endothelial cells. The specific adhesion between PC12 and BAME cells could be abolished by cell surface extracts derived from these two cells but not by extracts derived from unrelated cell types. This activity was heat-labile, sensitive to trypsin and, to a lesser extent, to neuraminidase. We therefore conclude that PC12 cells may interact with BAME cells by specific proteinaceous adhesive factors associated with their plasma membranes. These interactions might represent the formative role of cell-cell contacts in the organization of the developing adrenal gland.Abbreviations
BAME
bovine adrenal medullary endothelial cells
-
DMEM
Dulbecco's modified essential medium
-
ECM
extracellular matrix
-
EMEM
Eagle's modified essential medium
-
FCS
fetal calf serum
-
PBS
phosphate-buffered saline
-
PC12
rat pheochromocytoma cells 相似文献
4.
Ko Fujita Dr. Gordon Guroff Ephraim Yavin Gerthrud Goping Richard Orenberg Philip Lazarovici 《Neurochemical research》1990,15(4):373-383
Biotinylated derivatives of tetanus toxin were prepared and isolated by chromatofocusing and ganglioside-affinity chromatography. Biotinylation was monitored by the appearance of a 210,00 dalton complex upon SDS-polyacrylamide gel electrophoresis in the presence of avidin, and by selective binding to an avidin-Sepharose gel. At molar biotin:toxin ratios from 11 to 201 only biotinylated derivatives with low toxicity were obtained; these derivatives, however, retained 60–80% of their specific binding affinity for brain synaptosomes. A biotinylated tetanus toxin derivative purified by ganglioside-affinity chromatography was used to identify and localize tetanus toxin binding sites on PC12 cells. Electron microscopic analysis with streptavidin-gold revealed very low levels of tetanus toxin binding sites on the surface of untreated cells, and the appearance of such binding sites during the second week of nerve growth factor-induced differentiation. Examination of micrographs of the differentiated cells indicated that the tetanus toxin binding sites sites are concentrated on the neurites, with relatively few appearing on the cell bodies. Cognate studies using125I-labeled, affinity-purified tetanus toxin revealed an increase in PC12 binding capacity from about 0.07 nmol/mg protein in untreated cells to 0.8 nmoles/mg protein in cells treated for 14 days with nerve growth factor. Cells treated in suspension for 2–3 weeks with nerve growth factor do not express tetanus toxin binding sites; upon plating, these cells required one week for the appearance of binding sites, although neurites grew much more rapidly from these primed cells. The high binding capacity of these tetanus toxin sites, as well as their sensitivity to neuraminidase, is indicative of a polysialoganglioside structure. The advantages of biotinylated tetanus toxin derivatives are discussed and the significance of nerve growth factor-differentiated PC12 cells grown as monolayers as a model for the study of the development, localization, and function of neuraminidase-sensitive tetanus toxin binding sites is presented.Abbreviations PBS
phosphate-buffered saline
- STS
sucrose-Tris-serum solution
- NGF
nerve growth factor
- C
collagen
- PL
polylysine
- BBG
bovine brain ganglioside mixture
- GM1
gafactosyl-N-acetylgalactosaminyl-[N-acetylneuraminyl]-galactosylglucosyl ceramide
- GD1a
[N-acetylneuraminyl]-galactosyl-N-acetylgalactosaminyl-[N-acetylneuraminyl]-galactosylglucosyl ceramide
- GT1a
[N-aceylneuraminyl]-galactosyl-N-acetylgalactosaminyl-[N-acetylneuraminyl]-galactosylglucosyl ceramide
- GD1b
galactosyl-N-acetylgalactosaminyl-[N-acetylneuraminyl-N-acetylneuraminyl]-galactosylglucosyl ceramide
- GT1b
[N-acetylneuraminyl]-galactosyl-N-acetylgalactosaminyl-[N-acetylneuraminyl-N-acetylneuraminyl] galactosylglucosyl ceramide
- NANA
N-acetylneuraminic acid 相似文献
5.
6.
Mitogen- and isoproterenol-induced changes of [Ca2+]i in T cells attached to a glass substrate were examined. Murine (C57BL/6) splenic T cells were attached to coverslips or 35-mm dishes (MatTek) precoated with Cell Tak® (3.5 µg/cm2). The cells were then loaded with fluorescent dye (2 µg/ml of fura2-AM or fluo3-AM) and changes in [Ca2+]i in a population of cells (using a spectrofluorometer) or in single cells (using a confocal microscope) were measured during continuous superfusion. Population measurements of [Ca2+]i demonstrated that concanavalin A (Con A, 2 or 5 µg/ml) caused an increase in [Ca2+]i that rose to a peak and then declined to a steady state. The concentration-response relationship (0.05–5 µg/ml) had an EC50 of 0.3 µg/ml. Isoproterenol decreased the Con A-induced elevation of steady state [Ca2+]i. In single cell studies, the increase in [Ca2+]i in response to Con A typically occurred in about 50% of the cells in a microscope field, and the delay before activation varied among cells. Taken together, these data demonstrate that Cell Tak® can be used to attach T cells to glass coverslips and will be useful for the study of signaling mechanisms in T cells. 相似文献
7.
Zhi Jian Yu Changbae Jin Robin William Rockhold Beth Hoskins Ing Kang Ho 《Neurochemical research》1993,18(11):1203-1209
Wistar-Kyoto and spontaneously hypertensive rats received i.v. infusions of cocaine hydrochloride (60 mg/kg per day) for 3, 7, and 14 days, or saline for 7 days. Acute cocaine challenge (40 mg/kg, s.c.) was given to treated and control rats 24 hr after the termination of each infusion period. There were no strain differences in brain levels of cocaine during cocaine infusion, nor after cocaine challenges. There were no strain differences in resting levels of [3H]dopamine release. Release of [3H]dopamine decreased in nuclei accumbens of 7- and 14-day cocaine-infused animals. Release of [3H]dopamine was maximal in both brain regions 2 hr after acute cocaine challenge. After 14 days of cocaine infusion, cocaine challenge in both strains reduced [3H]dopamine release in the nucleus accumbens, but not in the striatum; the reduction being greater in Wistar-Kyoto rats. The behavioral tolerance which accompanies similar cocaine infusion regimens may be related to striatal tolerance to cocaine-induced dopamine release. 相似文献
8.
9.
10.
Prof. Dr. Habil. Karl Schumann Dipl. Agr. Ing. Klaus-Stefan Kühne 《Archives Of Phytopathology And Plant Protection》2013,46(5):465-472
Schwantes, H.O.: Biologie der Pilze. Eine Einführung in die angewandte Mykologie. 478 S., 60 Abb., 29 Tab. Verlag Eugen Ulmer, Stuttgart, 1996, UNI‐Taschenbücher 1871, 42,80 DM. ISBN 3–8252–1871–6 Westhoff, P.; Jeske, H.; Jürgens, G.; Kloppstock, K.; Link, G.: Molekulare Entwicklungsbiologie. Vom Gen zur Pflanze. Georg Thieme Verlag Stuttgart, New York; 1996; 112 Abb., 19 Tab. ISBN 3–13–102021–0 McNamara, K.J. (Herausgeber): Evolutionary Change and Heterochrony. John Wiley &; Sons; Chichester, New York, Brisbane, Toronto, Singapur (1995), ISBN 0–471–95837–9 Sobral, B.W.S. (Herausgeber): The Impact of Plant Molecular Genetics. Birkhäuser Verlag AG Basel (1996), ISBN 3–7643–3802–4 McIntosh, R.A.; Wellings, C.R.; Park, R.F.: Wheat rusts ‐ An atlas of resistance genes. 200 S., 119 Bildseiten, Kluwer Academic Publishers, Dordrecht, Boston, London, 1995, 125,00 Dfl., ISBN 0–7923–3430–2 Friedrich, G.; Rode, H. (Hsg.): Pflanzenschutz im integrierten Obstbau. Verlag Eugen Ulmer Stuttgart. 1996. 494 S., 128 Farbfotos, 94 Zeichnungen, 41 Tab., 3. völlig neubearbeitete Auflage. Preis 88,‐DM; ISBN 3–8001–5541–9 Nultsch, W.: Allgemeine Botanik. 10. neubearbeitete erweiterte Auflage. Georg Thieme Verlag Stuttgart New York. 1996, 602 Seiten, 234 Abb. in 525 Einzeldarstellungen, 19 Boxen. Glossarium mit 752 Stichworten. Preis 44,‐DM; ISBN 3–13–383310–3 Berndt, J.: Umweltbiochemie. Uni‐Taschenbücher 1838. Gustav Fischer Verlag Stuttgart Jena. 1995; 278 S., 101 Abb., 33 Tab., Preis 34.80 DM. UTB‐ISBN 3–8252–1838–4 Kalusche, D.: Ökologie in Zahlen. Eine Datensammlung in Tabellen mit über 10.000 Einzelwerten. Gustav Fischer Verlag. Stuttgart, Jena, New York. 1996. 415 S. Preis 54, ‐DM; ISBN 3–437–20521–8 相似文献