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241.
Estimation of DNA sequence diversity in bovine cytokine genes 总被引:4,自引:0,他引:4
Michael P. Heaton William M. Grosse Steven M. Kappes John W. Keele Carol G. Chitko-McKown Larry V. Cundiff Andreas Braun Daniel P. Little William W. Laegreid 《Mammalian genome》2001,12(1):32-37
DNA sequence variation provides the fundamental material for improving livestock through selection. In cattle, single nucleotide
polymorphisms and small insertions/deletions (collectively referred to here as SNPs) have been identified in cytokine genes
and scored in a reference population to determine linkage map positions. The aim of the present study was twofold: first,
to estimate the SNP frequency in a reference population of beef cattle, and second, to determine cytokine haplotypes in a
group of sires from commercial populations. Forty-five SNP markers in DNA segments from nine cytokine gene loci were analyzed
in 26 reference parents. Comparison of all 52 haploid genomes at each PCR amplicon locus revealed an average of one SNP per
143 bp of sequence, whereas comparison of any two chromosomes identified heterozygous sites, on average, every 443 bp. The
combination of these 45 SNP genotypes was sufficient to uniquely identify each of the 26 animals. The average number of haplotype
alleles (4.4) per PCR amplicon (688 bp) and the percentage heterozygosity among founding parents (50%) were similar to those
for microsatellite markers in the same population. For 49 sires from seven common breeds of beef cattle, SNP genotypes (1225
total) were obtained by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) at three
amplicon loci. All three of the amplicon haplotypes were correctly deduced for each sire without the use of parent or progeny
genotypes. The latter allows a wide range of genetic studies in commercial populations of cattle where genotypic information
from relatives may not be available.
Received: 16 June 2000 / Accepted: 23 August 2000 相似文献
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BLA Verçosa CM Lemos IL Mendonça SMMS Silva SM de Carvalho H Goto FAL Costa 《BMC veterinary research》2008,4(1):45
Background
Visceral leishmaniasis in Brazil is caused by the protozoan Leishmania (Leishmania) chagasi and it is transmitted by sandfly of the genus Lutzomyia. Dogs are an important domestic reservoir, and control of the transmission of visceral leishmaniasis (VL) to humans includes the elimination of infected dogs. However, though dogs are considered to be an important element in the transmission cycle of Leishmania, the identification of infected dogs representing an immediate risk for transmission has not been properly evaluated. Since it is not possible to treat infected dogs, they are sacrificed when a diagnosis of VL is established, a measure that is difficult to accomplish in highly endemic areas. In such areas, parameters that allow for easy identification of reservoirs that represents an immediate risk for transmission is of great importance for the control of VL transmission. In this study we aimed to identify clinical parameters, reinforced by pathological parameters that characterize dogs with potential to transmit the parasite to the vector.Results
The major clinical manifestations of visceral leishmaniasis in dogs from an endemic area were onicogriphosis, skin lesions, conjunctivitis, lymphadenopathy, and weight loss. The transmission potential of these dogs was assessed by xenodiagnosis using Lutzomyia longipalpis. Six of nine symptomatic dogs were infective to Lutzomyia longipalpis while none of the five asymptomatic dogs were infective to the sandfly. Leishmania amastigotes were present in the skin of all clinically symptomatic dogs, but absent in asymptomatic dogs. Higher parasite loads were observed in the ear and ungueal region, and lower in abdomen. The inflammatory infiltrate was more intense in the ears and ungueal regions of both symptomatic and asymptomatic dogs. In clinically affected dogs in which few or none Leishmania amastigotes were observed, the inflammatory infiltrate was constituted mainly of lymphocytes and macrophages. When many parasites were present, the infiltrate was also comprised of lymphocytes and macrophages, as well as a larger quantity of polymorphonuclear neutrophils (PMNs).Conclusion
Dogs that represent an immediate risk for transmission of Leishmania in endemic areas present clinical manifestations that include onicogriphosis, skin lesions, conjunctivitis, lymphadenopathy, and weight loss. Lymphadenopathy in particular was a positive clinical hallmark since it was closely related to the positive xenodiagnosis.245.
Single nucleotide polymorphism (SNP) discovery and linkage mapping of bovine cytokine genes 总被引:5,自引:1,他引:4
William M. Grosse Steven M. Kappes William W. Laegreid John W. Keele Carol G. Chitko-McKown Michael P. Heaton 《Mammalian genome》1999,10(11):1062-1069
Polymorphic markers at bovine gene loci facilitate the integration of cattle genetic maps with those of humans and mice.
To this end, 31 single nucleotide polymorphism (SNP) markers were developed for seven bovine chemokine genes. Loci were amplified
from bovine genomic DNA by the polymerase chain reaction, and candidate amplicons were sequenced to determine their identity.
Amplified loci from 24 founding parents and select progeny from a beef cattle reference population were sequenced and analyzed
for SNPs. SNP haplotype alleles were determined by examining segregation patterns and used to establish the locus position
on the bovine linkage map. Loci for growth-related proteins (GRO3, GRO1, and GROX) were clustered with the related CXC chemokine
genes, interleukin (IL) 8, and epithelial cell inflammatory protein 1, at 84 cM from the centromeric end of the bovine chromosome
(BTA) 6 linkage group. Bovine loci for a cluster of IL8 receptors, a stromal cell-derived factor 1, interferon-γ, and tumor
necrosis factor-α were mapped at 90, 55, 59, and 34 cM, respectively, from the centromeric ends of the BTA 2, 28, 5, and 23
linkage groups. The positions of these bovine loci were compared with those of orthologous loci on the human map to refine
the boundaries of conserved synteny. These seven loci provide examples of SNP development in which the efficiency was largely
dependent on the availability of bovine genomic or cDNA sequence. The polymorphic nature of these SNP haplotype markers suggests
that they will be useful for mapping complex traits in cattle, such as resistance to infectious disease.
Received: 30 April 1999 / Accepted: 12 July 1999 相似文献
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The growth of bivalve gills proceeds at the posterior end of the gill from a meristem-like budding zone, that is, an undifferentiated terminal organ, which continuously proliferates new gill elements in growing bivalves. In representatives of protobranch, filibranch, and eulamellibranch gills (13 species from Protobranchia, Pteriomorphia, Palaeoheterodonta, and Heterodonta), the first growth steps demonstrate a uniform basic pattern. The budding zone produces either transverse folds that split after a transition zone into parallel pairs of lobules (which themselves later differentiate into the inner and outer demibranchs), or it produces the lobules directly, without first forming a transition zone. The lobules elongate, differentiate into lobes, and transform into leaflet-like structures (protobranchs) or into filaments (filibranchs and eulamellibranchs). The filaments represent the differentiated outer margins of each lobe, of which the central tissue (interlamellar septum) becomes incised or fenestrated, or transformed by tissue junctions. A distally located main growth zone for each lobe is suggested. With regard to the delayed onset of the differentiation of the outer demibranch in juvenile unionids, an additional temporary growth zone for filaments is suggested to exist at the anterior end of the outer demibranch. 相似文献
250.
Evidence that stable retroviral transduction and cell survival following DNA integration depend on components of the nonhomologous end joining repair pathway 总被引:3,自引:0,他引:3
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Daniel R Greger JG Katz RA Taganov KD Wu X Kappes JC Skalka AM 《Journal of virology》2004,78(16):8573-8581
We have previously reported several lines of evidence that support a role for cellular DNA repair systems in completion of the retroviral DNA integration process. Failure to repair an intermediate in the process of integrating viral DNA into host DNA appears to trigger growth arrest or death of a large percentage of infected cells. Cellular proteins involved in the nonhomologous end joining (NHEJ) pathway (DNA-PK(CS)) and the damage-signaling kinases (ATM and ATR) have been implicated in this process. However, some studies have suggested that NHEJ proteins may not be required for the completion of lentiviral DNA integration. Here we provide additional evidence that NHEJ proteins are required for stable transduction by human immunodeficiency type 1 (HIV-1)-based vectors. Our analyses with two different reporters show that the number of stably transduced DNA-PK(CS)-deficient scid fibroblasts was reduced by 80 to 90% compared to the number of control cells. Furthermore, transduction efficiency can be restored to wild-type levels in scid cells that are complemented with a functional DNA-PK(CS) gene. The efficiency of stable transduction by an HIV-1-based vector is also reduced upon infection of Xrcc4 and ligase IV-deficient cells, implying a role for these components of the NHEJ repair pathway. Finally, we show that cells deficient in ligase IV are killed by infection with an integrase-competent but not an integrase-deficient HIV-1 vector. Results presented in this study lend further support to a general role for the NHEJ DNA repair pathway in completion of the retroviral DNA integration process. 相似文献