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1.
H. Christopher Wilson Nadine C. Milos 《In vitro cellular & developmental biology. Plant》1987,23(5):323-331
Summary This study investigates the nutritional requirements ofXenopus laevis neural crest cells and melanophores developing in vitro. A comparison is made between the growth and differentiation of cells
in serum-containing medium and a chemically defined, serum-free medium that we have designed. Our chemically defined medium
is more efficient than serum-supplemented medium in promoting proliferation of these cells. Several supplements are required
to enhance culture development. These include insulin, α-melanocyte stimulating hormone, somatotropin, luteotrophic hormone,
linoleic acid, uridine, and putrescine. In addition, collagen and fibronectin provide the most conductive environment tested
for cell migration and adhesion.
This work was supported by establishment and major equipment grants from the Alberta Heritage Foundation for Medical Research
to N. C. M. Nadine C. Milos is a Heritage Medical Research Scholar of the Alberta Heritage Foundation for Medical Research. 相似文献
2.
Djordje Boskov Mirjana Jocic Ksenija Jovanovic Milos Ljubisavljevic Radmila Anastasijevic 《Biological cybernetics》1994,71(4):341-348
Spike discharges of skeletomotor neurons innervating triceps surae muscles elicited by white noise modulated transmembrane
current stimulation and muscle stretch were studied in decerebrated cats. The white noise modulated current intensity ranged
from 4.3 to 63.2 nA peak-to-peak, while muscle stretches ranged from 100 μm to 4.26 mm peak-to-peak. The neuronal responses
were studied by averaging the muscle length records centered at the skeletomotor action potentials (peri-spike average, PSA)
and by Wiener analysis. Skeletomotor spikes appeared after a sharp peak in PSA of the injected current, preceded by a longer-lasting
smaller wavelet of either depolarizing or hyperpolarizing direction. The PSA amplitude was not related to the injected current
amplitude nor showed any differences related to the motor unit type. The PSA amplitudes were virtually independent of the
stretching amplitude σ, after an initial increase with stretching amplitudes in the range of 15–40 μm (S.D.), or 100–270 μm
peak-to-peak.Analyses of cross-spectra indicated a small or absent increase in gain with frequency in response to injected
current, but about 20 dB/decade in the range 10–100 Hz in response to muscle stretch. The peaks of both Wiener kernels in
response to current injection appear to decrease with the amplitude of injected current, but this decrease was not statistically
significant. The narrow first-order kernels suggest that the transfer function between the current input and spike discharge
is lowpass with a wide passband, i.e. there is very little change in dynamics. The values of the second-order kernels appear
to be nonzero only along the main diagonal. This is characteristic of a simple Hammerstein type cascade, i.e. a zero memory
nonlinearity followed by a linear system. Small values of second-order kernels away from the origin and narrow first-order
kernels suggest that the linear cascade contributes very little to the overall dynamic response.In contrast to Wiener kernels
found in response to current injection, the Wiener kernels in response to stretch showed a decreasing trend with stretch amplitude.
The size of the second-order kernels decreased to a somewhat larger extent with input amplitude than that of the first-order
kernels, indicating an amplitude-dependent nonlinearity. Overall, the transformation between length and spike output was described
as an LNNL cascade with second-order nonlinearities.
Received: 1 April 1993/Accepted in revised form: 24 March 1994 相似文献
3.
Milos Legner W. Gary Sprules 《Journal of Aquatic Ecosystem Stress and Recovery (Formerly Journal of Aquatic Ecosystem Health)》1993,2(3):221-227
Samples of microplankton and larger nanoplankton (5 to 200 m) are preserved with a combination of Lugol's solution and DaFano's fixative. Organisms are then settled on a gelatin-coated slide, dried and embedded in 40 percent glycerin. Counting and sizing is performed under a microscope using a drawing tube, which facilitates measuring the organisms with a microcomputer-interfaced caliper. An interactive computer program, written in BASIC, allows for estimating the volumes of cells in up to 40 shape/species categories. The program then saves data on a disk, retrieves them, and calculates the results either for individual species (abundance, biomass, and mean cell volume) or as a pooled size spectrum of all organisms measured. 相似文献
4.
G N Martha Y N Frunchak S K Frost D G Thibaudeau N C Milos 《Biochemical and biophysical research communications》1990,166(2):695-700
The white mutant of the Mexican axolotl, A. mexicanum, involves an ectodermal defect which prevents melanophore colonization. Endogenous lectins have been suggested to function in neural crest-derived melanophore adhesion in other animals. To determine if differences in endogenous lectins exist in dark and white axolotls during melanophore colonization, white and dark ectoderm and carcass tissues have been assayed for lectin activity at premigratory, early migratory, and late migratory neural crest stages. Lectin content (specific for D-glucosamine, N-acetyl-D-glucosamine and D-mannose) increases significantly during early migration only in dark ectoderm and white carcass tissues, whereas white ectoderm and dark carcass lectin activities remain close to premigration levels. Neural crest cells in these embryos are associated with regions of high lectin activity suggesting that the differences in endogenous lectins may be involved in establishment of the dark/white phenotype. 相似文献
5.
Joseph H. Fleisher Klaus Brendel Milos Chvapil Erle E. Peacock 《Analytical biochemistry》1976,74(1):254-259
Thin-layer chromatography of β-aminopropionitrile (BAPN) in acetone and 1 m ammonium hydroxide (9:1) allowed separation of that compound from amino acids present in rat-liver perfusion fluid without prior solvent extraction. Direct densitometry of the spots obtained with ninhydrin yielded satisfactory quantitation of β-aminopropionitrile present. Utilization of [14C]nitrile-labeled β-aminopropionitrile and concurrent analysis of cyanoacetic acid allowed almost complete accountability of BAPN added to isolated rat liver. 相似文献
6.
Susanne Siebentritt Enrico Avancini Marcus Br Jakob Bombsch Emilie Bourgeois Stephan Buecheler Romain Carron Celia Castro Sebastien Duguay Roberto Flix Evelyn Handick Dimitrios Hariskos Ville Havu Philip Jackson Hannu‐Pekka Komsa Thomas Kunze Maria Malitckaya Roberto Menozzi Milos Nesladek Nicoleta Nicoara Martti Puska Mohit Raghuwanshi Philippe Pareige Sascha Sadewasser Giovanna Sozzi Ayodhya Nath Tiwari Shigenori Ueda Arantxa Vilalta‐Clemente Thomas Paul Weiss Florian Werner Regan G. Wilks Wolfram Witte Max Hilaire Wolter 《Liver Transplantation》2020,10(8)
7.
8.
Emmet McCormack Katherine J. Adams Namir J. Hassan Akhil Kotian Nikolai M. Lissin Malkit Sami Maja Mujić Tereza Osdal Bjørn Tore Gjertsen Deborah Baker Alex S. Powlesland Milos Aleksic Annelise Vuidepot Olivier Morteau Deborah H. Sutton Carl H. June Michael Kalos Rebecca Ashfield Bent K. Jakobsen 《Cancer immunology, immunotherapy : CII》2013,62(4):773-785
NY-ESO-1 and LAGE-1 are cancer testis antigens with an ideal profile for tumor immunotherapy, combining up-regulation in many cancer types with highly restricted expression in normal tissues and sharing a common HLA-A*0201 epitope, 157–165. Here, we present data to describe the specificity and anti-tumor activity of a bifunctional ImmTAC, comprising a soluble, high-affinity T-cell receptor (TCR) specific for NY-ESO-1157–165 fused to an anti-CD3 scFv. This reagent, ImmTAC-NYE, is shown to kill HLA-A2, antigen-positive tumor cell lines, and freshly isolated HLA-A2- and LAGE-1-positive NSCLC cells. Employing time-domain optical imaging, we demonstrate in vivo targeting of fluorescently labelled high-affinity NYESO-specific TCRs to HLA-A2-, NY-ESO-1157–165-positive tumors in xenografted mice. In vivo ImmTAC-NYE efficacy was tested in a tumor model in which human lymphocytes were stably co-engrafted into NSG mice harboring tumor xenografts; efficacy was observed in both tumor prevention and established tumor models using a GFP fluorescence readout. Quantitative RT-PCR was used to analyze the expression of both NY-ESO-1 and LAGE-1 antigens in 15 normal tissues, 5 cancer cell lines, 10 NSCLC, and 10 ovarian cancer samples. Overall, LAGE-1 RNA was expressed at a greater frequency and at higher levels than NY-ESO-1 in the tumor samples. These data support the clinical utility of ImmTAC-NYE as an immunotherapeutic agent for a variety of cancers. 相似文献
9.
Xin Hu Milos Vujanac Noel Southall C. Erec Stebbins 《Bioorganic & medicinal chemistry letters》2013,23(4):1056-1062
The bacterial protein tyrosine phosphatase YopH is an essential virulence determinant in Yersinia pestis and a potential antibacterial drug target. Here we report our studies of screening for small molecule inhibitors of YopH using both high throughput and in silico approaches. The identified inhibitors represent a diversity of chemotypes and novel pTyr mimetics, providing a starting point for further development and fragment-based design of multi-site binding inhibitors. We demonstrate that the applications of high throughput and virtual screening, when guided by structural binding mode analysis, is an effective approach for identifying potent and selective inhibitors of YopH and other protein phosphatases for rational drug design. 相似文献
10.
Ankita Singhal Ying Guo Milos Matkovic Gebhard Schertler Xavier Deupi Elsa CY Yan Joerg Standfuss 《EMBO reports》2016,17(10):1431-1440
Congenital stationary night blindness (CSNB) is an inherited and non‐progressive retinal dysfunction. Here, we present the crystal structure of CSNB‐causing T94I2.61 rhodopsin in the active conformation at 2.3 Å resolution. The introduced hydrophobic side chain prolongs the lifetime of the G protein activating metarhodopsin‐II state by establishing a direct van der Waals contact with K2967.43, the site of retinal attachment. This is in stark contrast to the light‐activated state of the CSNB‐causing G90D2.57 mutation, where the charged mutation forms a salt bridge with K2967.43. To find the common denominator between these two functional modifications, we combined our structural data with a kinetic biochemical analysis and molecular dynamics simulations. Our results indicate that both the charged G90D2.57 and the hydrophobic T94I2.61 mutation alter the dark state by weakening the interaction between the Schiff base (SB) and its counterion E1133.28. We propose that this interference with the tight regulation of the dim light photoreceptor rhodopsin increases background noise in the visual system and causes the loss of night vision characteristic for CSNB patients. 相似文献