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41.
Dianna M. Milewicz Peter H. Byers John Reveille Austin L. Hughes Madeleine Duvic 《Journal of molecular evolution》1996,42(2):117-123
Alu elements are a class of repetitive DNA sequences found throughout the human genome that are thought to be duplicated via an RNA intermediate in a process termed retroposition. Recently inserted Alu elements are closely related, suggesting that they are derived from a single source gene or closely related source genes. Analysis of the type III collagen gene (COL3A1) revealed a polymorphic Alu insertion in intron 8 of the gene. The Alu insertion in the COL3A1 gene had a high degree of nucleotide identity to the Sb family of Alu elements, a family of older Alu elements. The Alu sequence was less similar to the consensus sequence for the PV or Sb2 subfamilies, subfamilies of recently inserted Alu elements. These data support the observations that at least three source genes are active in the human genome, one of which is distinct from the PV and Sb2 subfamilies and predates either of these two subfamilies. Appearance of the Alu insertion in different ethnic populations suggests that the insertion may have occurred in the last 100,000 years. This Alu insert should be a useful marker for population studies and for marking COL3A1 alleles. 相似文献
42.
Walter K. F. Seelentag Ursula Günthert Parvin Saremaslani Eva Futo Madeleine Pfaltz Philipp U. Heitz Jürgen Roth 《Histochemistry and cell biology》1996,106(3):283-289
CD44 isoforms have been implicated in tumor progression and metastasis formation. This study presents a thorough immunohistochemical
analysis of CD44 standard and isoform expression in normal human skin appendages and epidermis applying monoclonal antibodies
against CD44s, CD44v3, -v4, -v5, -v6, and -v9. An improved immunohistochemical protocol with microwave-based antigen retrieval
in paraffin sections and heavy metal amplification of the diaminobenzidine reaction product provided enhanced resolution and
sensitivity as compared to studies on frozen sections. The hair follicle, the seborrheic and eccrine sweat glands were strongly
positive for all CD44 isoforms studied. In the latter, the clear cells but not the dark (intercalated) cells were positive.
The sudoriferous ducts adjacent to the glands were weakly positive for all CD44 isoforms and strongly positive near the skin
surface. In the apocrine glands, the basal cells showed only a moderate positivity. The myoepithelial cells expressed only
CD44s. In the epidermis, all CD44 isoforms were detectable, with strongest CD44 immunostaining in the lower third of the stratum
spinosum and weaker staining in the stratum basale and the upper two-thirds of the stratum granulosum. The stratum granulosum
and corneum were unreactive. Thus, a regional and cell type-specific CD44 expression was revealed.
Accepted: 10 May 1996 相似文献
43.
MICROTUBULE ORGANIZATION 1 regulates structure and function of microtubule arrays during mitosis and cytokinesis in the Arabidopsis root 下载免费PDF全文
Kawamura E Himmelspach R Rashbrooke MC Whittington AT Gale KR Collings DA Wasteneys GO 《Plant physiology》2006,140(1):102-114
MICROTUBULE ORGANIZATION 1 (MOR1) is a plant member of the highly conserved MAP215/Dis1 family of microtubule-associated proteins. Prior studies with the temperature-sensitive mor1 mutants of Arabidopsis (Arabidopsis thaliana), which harbor single amino acid substitutions in an N-terminal HEAT repeat, proved that MOR1 regulates cortical microtubule organization and function. Here we demonstrate by use of live cell imaging and immunolabeling that the mor1-1 mutation generates specific defects in the microtubule arrays of dividing vegetative cells. Unlike the universal cortical microtubule disorganization in elongating mor1-1 cells, disruption of mitotic and cytokinetic microtubule arrays was not detected in all dividing cells. Nevertheless, quantitative analysis identified distinct defects in preprophase bands (PPBs), spindles, and phragmoplasts. In nearly one-half of dividing cells at the restrictive temperature of 30 degrees C, PPBs were not detected prior to spindle formation, and those that did form were often disrupted. mor1-1 spindles and phragmoplasts were short and abnormally organized and persisted for longer times than in wild-type cells. The reduced length of these arrays predicts that the component microtubule lengths are also reduced, suggesting that microtubule length is a critical determinant of spindle and phragmoplast structure, orientation, and function. Microtubule organizational defects led to aberrant chromosomal arrangements, misaligned or incomplete cell plates, and multinucleate cells. Antiserum raised against an N-terminal MOR1 sequence labeled the full length of microtubules in interphase arrays, PPBs, spindles, and phragmoplasts. Continued immunolabeling of the disorganized and short microtubules of mor1-1 at the restrictive temperature demonstrated that the mutant mor1-1(L174F) protein loses function without dissociating from microtubules, providing important insight into the mechanism by which MOR1 may regulate microtubule length. 相似文献
44.
Grit Nebrich Marion Herrmann Daniela Hartl Madeleine Diedrich Thomas Kreitler Christoph Wierling Joachim Klose Patrick Giavalisco Claus Zabel Dr. Lei Mao 《Proteomics》2009,9(7):1795-1808
In recent years proteomics became increasingly important to functional genomics. Although a large amount of data is generated by high throughput large‐scale techniques, a connection of these mostly heterogeneous data from different analytical platforms and of different experiments is limited. Data mining procedures and algorithms are often insufficient to extract meaningful results from large datasets and therefore limit the exploitation of the generated biological information. In our proteomic core facility, which almost exclusively focuses on 2‐DE/MS‐based proteomics, we developed a proteomic database custom tailored to our needs aiming at connecting MS protein identification information to 2‐DE derived protein expression profiles. The tools developed should not only enable an automatic evaluation of single experiments, but also link multiple 2‐DE experiments with MS‐data on different levels and thereby helping to create a comprehensive network of our proteomics data. Therefore the key feature of our “PROTEOMER” database is its high cross‐referencing capacity, enabling integration of a wide range of experimental data. To illustrate the workflow and utility of the system, two practical examples are provided to demonstrate that proper data cross‐referencing can transform information into biological knowledge. 相似文献
45.
Robyn L. Poerschke Karen White Scott R. Florell Robert H. I. Andtbacka Joycelyn Tross Madeleine Anderson Sancy A. Leachman Philip J. Moos 《Pigment cell & melanoma research》2015,28(6):685-695
Although significant progress has been made in targeted and immunologic therapeutics for melanoma, many tumors fail to respond, and most eventually progress when treated with the most efficacious targeted combination therapies thus far identified. Therefore, alternative approaches that exploit distinct melanoma phenotypes are necessary to develop new approaches for therapeutic intervention. Tissue microarrays containing human nevi and melanomas were used to evaluate levels of the antioxidant protein thioredoxin reductase 1 (TR1), which was found to increase as a function of disease progression. Melanoma cell lines revealed metabolic differences that correlated with TR1 levels. We used this new insight to design a model treatment strategy that creates a synthetic lethal interaction wherein targeting TR1 sensitizes melanoma to inhibition of glycolytic metabolism, resulting in a decrease in metastases in vivo. This approach holds the promise of a new clinical therapeutic strategy, distinct from oncoprotein inhibition. 相似文献
46.
Madeleine Olivereau 《Cell and tissue research》1964,63(4):496-505
Conclusion La technique à l'hématoxyline au plomb de Mac Conaill permet l'identification d'un type cellulaire situé dans la pars distalis rostrale, en bordure des ramifications de la neurohypophyse dans l'hypophyse de plusieurs Poissons Téléostéens; il est également colorable par le bleu d'alizarine d'Herlant; toutefois, l'intensité de ces deux réactions tinctoriales est très variable selon les espèces. Chez l'Anguille, les Salmonidés et le Cyprin, la nature corticotrope de ces cellules est établie expérimentalement. La colorabilité par l'hématoxyline d'une autre catégorie cellulaire dans la pars intermedia laisse supposer l'existence de constituants communs aux deux types cellulaires, et peut-être même à leurs produits d'élaboration. Cette communauté de certains aminoacides entre l'ACTH et l'intermédine a déjà été démontrée chez divers Mammifères. 相似文献
47.
Sporulation and Enterotoxin Production by Mutants of Clostridium perfringens 总被引:34,自引:4,他引:34 下载免费PDF全文
The ability of Clostridium perfringens type A to produce an enterotoxin active in human food poisoning has been shown to be directly related to the ability of the organism to sporulate. Enterotoxin was produced only in a sporulation medium and not in a growth medium in which sporulation was repressed. Mutants with an altered ability to sporulate were isolated from an sp(+) ent(+) strain either as spontaneous mutants or after mutagenesis with acridine orange or nitrosoguanidine. All sp(0) (-) mutants were ent(-). Except for one isolate, these mutants were not disturbed in other toxic functions characteristic of the wild type and unrelated to sporulation. A total of four of seven osp(0) mutants retained the ability to produce detectable levels of enterotoxin. None of the ent(-) mutants produced gene products serologically homologous to enterotoxin. A total of three sp(-) mutants, blocked at intermediate stages of sporulation, produced enterotoxin. Of these mutants, one was blocked at stage III, one probably at late stage IV, and one probably at stage V. A total of three sp(+) revertants isolated from an sp(-) ent(-) mutant regained not only the ability to sporulate but also the ability to produce enterotoxin. The enterotoxin appears to be a sporulation-specific gene product; however, the function of the enterotoxin in sporulation is unknown. 相似文献
48.
Spermidine is the most abundant polyamine in dormant turions of Hydrocharis morsus-ranae and Utricularia intermedia, and it is also the dominant polyamine in sprouts of U. intermedia. The putrescine level is high in young leaves of H. morsus-ranae. Cadaverine and homospermidine occur respectively in vernalized turions of H. morsus-ranae and of U. intermedia. 相似文献
49.
Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata 下载免费PDF全文
Martinez-Mir A Zlotogorski A Gordon D Petukhova L Mo J Gilliam TC Londono D Haynes C Ott J Hordinsky M Nanova K Norris D Price V Duvic M Christiano AM 《American journal of human genetics》2007,80(2):316-328
Alopecia areata (AA) is a genetically determined, immune-mediated disorder of the hair follicle that affects 1%-2% of the U.S. population. It is defined by a spectrum of severity that ranges from patchy localized hair loss on the scalp to the complete absence of hair everywhere on the body. In an effort to define the genetic basis of AA, we performed a genomewide search for linkage in 20 families with AA consisting of 102 affected and 118 unaffected individuals from the United States and Israel. Our analysis revealed evidence of at least four susceptibility loci on chromosomes 6, 10, 16 and 18, by use of several different statistical approaches. Fine-mapping analysis with additional families yielded a maximum multipoint LOD score of 3.93 on chromosome 18, a two-point affected sib pair (ASP) LOD score of 3.11 on chromosome 16, several ASP LOD scores >2.00 on chromosome 6q, and a haplotype-based relative risk LOD of 2.00 on chromosome 6p (in the major histocompatibility complex locus). Our findings confirm previous studies of association of the human leukocyte antigen locus with human AA, as well as the C3H-HeJ mouse model for AA. Interestingly, the major loci on chromosomes 16 and 18 coincide with loci for psoriasis reported elsewhere. These results suggest that these regions may harbor gene(s) involved in a number of different skin and hair disorders. 相似文献
50.
Donovan P. German Kathleen R. B. Marcelo Madeleine M. Stone Steven D. Allison 《Global Change Biology》2012,18(4):1468-1479
Decomposition of soil organic matter (SOM) is mediated by microbial extracellular hydrolytic enzymes (EHEs). Thus, given the large amount of carbon (C) stored as SOM, it is imperative to understand how microbial EHEs will respond to global change (and warming in particular) to better predict the links between SOM and the global C cycle. Here, we measured the Michaelis–Menten kinetics [maximal rate of velocity (Vmax) and half‐saturation constant (Km)] of five hydrolytic enzymes involved in SOM degradation (cellobiohydrolase, β‐glucosidase, β‐xylosidase, α‐glucosidase, and N‐acetyl‐β‐d ‐glucosaminidase) in five sites spanning a boreal forest to a tropical rainforest. We tested the specific hypothesis that enzymes from higher latitudes would show greater temperature sensitivities than those from lower latitudes. We then used our data to parameterize a mathematical model to test the relative roles of Vmax and Km temperature sensitivities in SOM decomposition. We found that both Vmax and Km were temperature sensitive, with Q10 values ranging from 1.53 to 2.27 for Vmax and 0.90 to 1.57 for Km. The Q10 values for the Km of the cellulose‐degrading enzyme β‐glucosidase showed a significant (P = 0.004) negative relationship with mean annual temperature, indicating that enzymes from cooler climates can indeed be more sensitive to temperature. Our model showed that Km temperature sensitivity can offset SOM losses due to Vmax temperature sensitivity, but the offset depends on the size of the SOM pool and the magnitude of Vmax. Overall, our results suggest that there is a local adaptation of microbial EHE kinetics to temperature and that this should be taken into account when making predictions about the responses of C cycling to global change. 相似文献