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11.
Background
Existing cut-offs for fasting plasma glucose (FPG) and post-load glucose (2hPG) criteria are not equivalent in the diagnosis of diabetes and glucose intolerance. Adjusting cut-offs of single measurements have not helped so we undertook this project to see if they could be complementary. 相似文献12.
Guo-Ling Nan Adelheid R. Kuehnle 《In vitro cellular & developmental biology. Plant》1995,31(3):131-136
Summary Five parameters were examined for their effect on transformation ofDendrobium tissues by microprojectile bombardment. The superpromoter in pBI426 produced at least 1.5 times as many transient transformants
as the single cauliflower mosaic virus 35S promoter in pBI121 (37 to 69% vs. 0 to 44%) with dark and frequent GUS (β-glucuronidase) staining. Tissue, genotype, and type of microparticle significantly affected transient GUS activity. Higher
expression was seen in protocormlike bodies and in hybrid UH44 compared to etiolated shoots and protocorms and to hybrids
M61 and K1329-39. Microparticles of 1.6-μm Bio-Rad gold were more effective than 1.0-μm ASI gold. Transient GUS activity did
not differ among protocormlike bodies bombarded using helium propellant pressures of 650, 900, or 1100 psi. Transgenic plants
were recovered fromDendrobium UH800 protocormlike bodies bombarded with pBI426-coated, 1.1-μm tungsten particles using an early-model gunpowder-driven
apparatus with an estimated stable transformation rate of 11.7%. One transgenic plant ofDendrobium UH44 was recovered from etiolated shoot explants bombarded with pBI121-coated, 1.1-μm tungsten particles using the Dupont
PDS-1000 with a stable transformation rate of 0.17%. Positive selection results showed 100 to 200 mg·liter−1 kanamycin to be appropriate for regeneration of transgenic plants from protocormlike bodies, protocorms, and etiolated shoot
explants over a 3- to 9.5-mo. period. 相似文献
13.
Dr AR Holmes RD Cannon HF Jenkinson 《Journal of industrial microbiology & biotechnology》1995,15(3):208-213
The yeastCandida albicans coaggregates with a variety of streptococcal species, an interaction that may promote oral colonization by yeast cells.C. albicans andCandida tropicalis are the yeasts most frequently isolated from the human oral cavity and our data demonstrate that both these species bind toStreptococcus gordonii NCTC 7869 while two otherCandida species (Candida krusei andCandida kefyr) do not. Adherence ofC. albicans was greatest when the yeast had been grown at 30° C to mid-exponential growth phase. For 21 strains ofC. albicans there was a positive correlation between the ability to adhere toS. gordonii and adherence to experimental salivary pellicle. Whole saliva either stimulated or slightly inhibited adherence ofC. albicans toS. gordonii depending on the streptococcal growth conditions. The results suggest that the major salivary adhesins and coaggregation adhesins ofC. albicans are co-expressed. 相似文献
14.
Chen Fure-Chyi Kuehnle Adelheid R. Sugii Nellie 《Plant Cell, Tissue and Organ Culture》1997,50(1):71-74
Growth of Blechnum spicant gametophytes was optimal in MS liquid medium, a 16-h photoperiod, and it was unaffected by variation
of the pH between 4.7 and 8.7. Antheridia were observed during all developmental stages of the gametophyte: filamentous, spatulate
or cordate and their formation was induced by compounds excreted into the culture medium by mature gametophytes. This antheridiogen
activity was found in the fractions corresponding to free and apolar esters of gibberellins. IBA at 5 μM and 50 μM, and BA
at 50 μM inhibited antheridiogen. Exogenous application of GA3 allowed spore germination but strongly inhibited gametophyte development; the two dimensional state was not reached.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
15.
16.
17.
A Sahaboglu O Paquet-Durand J Dietter K Dengler S Bernhard-Kurz P AR Ekstr?m B Hitzmann M Ueffing F Paquet-Durand 《Cell death & disease》2013,4(2):e488
For most neurodegenerative diseases the precise duration of an individual cell''s death is unknown, which is an obstacle when counteractive measures are being considered. To address this, we used the rd1 mouse model for retinal neurodegeneration, characterized by phosphodiesterase-6 (PDE6) dysfunction and photoreceptor death triggered by high cyclic guanosine-mono-phosphate (cGMP) levels. Using cellular data on cGMP accumulation, cell death, and survival, we created mathematical models to simulate the temporal development of the degeneration. We validated model predictions using organotypic retinal explant cultures derived from wild-type animals and exposed to the selective PDE6 inhibitor zaprinast. Together, photoreceptor data and modeling for the first time delineated three major cell death phases in a complex neuronal tissue: (1) initiation, taking up to 36 h, (2) execution, lasting another 40 h, and finally (3) clearance, lasting about 7 h. Surprisingly, photoreceptor neurodegeneration was noticeably slower than necrosis or apoptosis, suggesting a different mechanism of death for these neurons. 相似文献
18.
Conserved sequences in enzymes of the UDP-GlcNAc/MurNAc family are essential in hamster UDP-GlcNAc:dolichol-P GlcNAc-1-P transferase 总被引:1,自引:0,他引:1
The UDP-GlcNAc/MurNAc family of eukaryotic and prokaryotic enzymes use
UDP-GlcNAc or UDP-MurNAc-pentapeptide as donors, dolichol-P or polyprenol-P
as acceptors, and generate sugar-P-P-polyisoprenols. A series of six
conserved sequences, designated A through F and ranging from 5 to 13 amino
acid residues, has been identified in this family. To determine whether
these conserved sequences are required for enzyme function, various
mutations were examined in hamster UDP- GlcNAc:dolichol-P GlcNAc-1-P
transferase (GPT). Scramble mutations of sequences B-F, generated by
scrambling the residues within each sequence, demonstrated that each is
important in GPT. While E and F scrambles appeared to prevent stable
expression of GPT, scrambling of B- D resulted in GPT mutants that could be
stably expressed and bound tunicamycin, but lacked enzymatic activity.
Further, the C and D scramble mutants had an unexpected sorting defect.
Replacement of sequences B-F with prokaryotic counterparts from either the
B.subtilis mraY or E.coli rfe genes also affected GPT by preventing
expression of the mutant protein (B, F) or inhibiting its enzymatic
activity (C-E). For the C-E replacements, no acquisition of acceptor
activity for polyprenol-P, the fully unsaturated natural bacterial
acceptor, was detected. These studies show that the conserved sequences of
the UDP- GlcNAc/MurNAc family are important, and that the eukaryotic and
prokaryotic counterparts are not freely interchangeable. Since several
mutants were efficiently expressed and bound tunicamycin, yet lacked
enzymatic activity, the data are consistent with these sequences having a
direct role in product formation.
相似文献
19.
20.
Katrin Kuehnle Maria D. Ledesma Lucie Kalvodova Alicia E. Smith Arames Crameri Fabienne Skaanes-Brunner Karin M. Thelen Luka Kulic Dieter Lütjohann Frank L. Heppner Roger M. Nitsch M. Hasan Mohajeri 《Neurochemical research》2009,34(6):1167-1182
Cholesterol is a prominent modulator of the integrity and functional activity of physiological membranes and the most abundant
sterol in the mammalian brain. DHCR24-knock-out mice lack cholesterol and accumulate desmosterol with age. Here we demonstrate
that brain cholesterol deficiency in 3-week-old DHCR24−/− mice was associated with altered membrane composition including disrupted detergent-resistant membrane domain (DRM) structure.
Furthermore, membrane-related functions differed extensively in the brains of these mice, resulting in lower plasmin activity,
decreased β-secretase activity and diminished Aβ generation. Age-dependent accumulation and integration of desmosterol in
brain membranes of 16-week-old DHCR24−/− mice led to the formation of desmosterol-containing DRMs and rescued the observed membrane-related functional deficits. Our
data provide evidence that an alternate sterol, desmosterol, can facilitate processes that are normally cholesterol-dependent
including formation of DRMs from mouse brain extracts, membrane receptor ligand binding and activation, and regulation of
membrane protein proteolytic activity. These data indicate that desmosterol can replace cholesterol in membrane-related functions
in the DHCR24−/− mouse.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.
An erratum to this article can be found at 相似文献