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161.
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy 总被引:20,自引:0,他引:20
Strømme P Mangelsdorf ME Shaw MA Lower KM Lewis SM Bruyere H Lütcherath V Gedeon AK Wallace RH Scheffer IE Turner G Partington M Frints SG Fryns JP Sutherland GR Mulley JC Gécz J 《Nature genetics》2002,30(4):441-445
Mental retardation and epilepsy often occur together. They are both heterogeneous conditions with acquired and genetic causes. Where causes are primarily genetic, major advances have been made in unraveling their molecular basis. The human X chromosome alone is estimated to harbor more than 100 genes that, when mutated, cause mental retardation. At least eight autosomal genes involved in idiopathic epilepsy have been identified, and many more have been implicated in conditions where epilepsy is a feature. We have identified mutations in an X chromosome-linked, Aristaless-related, homeobox gene (ARX), in nine families with mental retardation (syndromic and nonspecific), various forms of epilepsy, including infantile spasms and myoclonic seizures, and dystonia. Two recurrent mutations, present in seven families, result in expansion of polyalanine tracts of the ARX protein. These probably cause protein aggregation, similar to other polyalanine and polyglutamine disorders. In addition, we have identified a missense mutation within the ARX homeodomain and a truncation mutation. Thus, it would seem that mutation of ARX is a major contributor to X-linked mental retardation and epilepsy. 相似文献
162.
Genome-wide retroviral insertional tagging of genes involved in cancer in Cdkn2a-deficient mice 总被引:17,自引:0,他引:17
Lund AH Turner G Trubetskoy A Verhoeven E Wientjens E Hulsman D Russell R DePinho RA Lenz J van Lohuizen M 《Nature genetics》2002,32(1):160-165
We have used large-scale insertional mutagenesis to identify functional landmarks relevant to cancer in the recently completed mouse genome sequence. We infected Cdkn2a(-/-) mice with Moloney murine leukemia virus (MoMuLV) to screen for loci that can participate in tumorigenesis in collaboration with loss of the Cdkn2a-encoded tumor suppressors p16INK4a and p19ARF. Insertional mutagenesis by the latent retrovirus was synergistic with loss of Cdkn2a expression, as indicated by a marked acceleration in the development of both myeloid and lymphoid tumors. We isolated 747 unique sequences flanking retroviral integration sites and mapped them against the mouse genome sequence databases from Celera and Ensembl. In addition to 17 insertions targeting gene loci known to be cancer-related, we identified a total of 37 new common insertion sites (CISs), of which 8 encode components of signaling pathways that are involved in cancer. The effectiveness of large-scale insertional mutagenesis in a sensitized genetic background is demonstrated by the preference for activation of MAP kinase signaling, collaborating with Cdkn2a loss in generating the lymphoid and myeloid tumors. Collectively, our results show that large-scale retroviral insertional mutagenesis in genetically predisposed mice is useful both as a system for identifying genes underlying cancer and as a genetic framework for the assignment of such genes to specific oncogenic pathways. 相似文献
163.
F. Steckerl A. Ofodile M. L. Turner G. H. Friedell 《Cellular and molecular life sciences : CMLS》1963,19(12):643-644
Zusammenfassung Nachweis, dass Ehrlich-Ascites-Tumorzellen, die in Phosphat-Puffer bei einer Temperatur von 37°C inkubiert werden, in saurem pH des Milieus viel länger leben als beim neutralen.Morphologische Kriterien für Zellschädigung werden diskutiert und erweisen sich als unzulänglich zu Voraussagen über die biologische Wachstumsfähigkeit dieser Krebszellen. 相似文献
164.
Zusammenfassung Nachweis, dass der gesamte DNS-Gehalt in der Brustdrüse bei Tieren mit proteinfreier oder 5% iger Proteinnahrung im Vergleich zu der Kontroll-gruppe herabgesetzt ist. Wird Protein in der Nahrung um 10–20% erhöht, so bleiben DNS-Gehalt und Körperwachstum konstant. 相似文献
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Anabolism. Low mechanical signals strengthen long bones 总被引:17,自引:0,他引:17
Although the skeleton's adaptability to load-bearing has been recognized for over a century, the specific mechanical components responsible for strengthening it have not been identified. Here we show that after mechanically stimulating the hindlimbs of adult sheep on a daily basis for a year with 20-minute bursts of very-low-magnitude, high-frequency vibration, the density of the spongy (trabecular) bone in the proximal femur is significantly increased (by 34.2%) compared to controls. As the strain levels generated by this treatment are three orders of magnitude below those that damage bone tissue, this anabolic, non-invasive stimulus may have potential for treating skeletal conditions such as osteoporosis. 相似文献