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Dr. Ernst Sklarz 《Journal of molecular medicine (Berlin, Germany)》1922,1(28):1414-1415
Ohne Zusammenfassung 相似文献
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E Neufeld B Sklarz S Goldberg S Gilad H Goldfarb L Laurian D S Silverberg R Chayen 《Nephron》1985,39(2):146-148
Urodiolenone is a substance that appears as the glucuronide in the urine of 1 in 3 hypertensive subjects. It is a potent inhibitor of Na+, K+-ATPase in kidney tissue of the guinea pig, as measured by cytochemical assay. Chemical and mass spectrometric evidence is presented, from which it is concluded that urodiolenone is a sesquiterpenoid substance, is a bicyclic enone with a vicinal diol side chain, and has molecular formula C15H24O3. 相似文献
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Herr Ernst Sklarz 《Archives of dermatological research》1924,145(1):321-324
Ohne Zusammenfassung 相似文献
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Ohne Zusammenfassung 相似文献
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Dr. Ernst Sklarz 《Archives of dermatological research》1923,142(1):1-5
Ohne Zusammenfassung 相似文献
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Tammarah Sklarz Peng Guan Mercy Gohil Renee M. Cotton Moyar Q. Ge Angela Haczku Rupali Das Martha S. Jordan 《European journal of immunology》2017,47(3):516-526
Invariant NKT (iNKT) cells bridge innate and adaptive immunity by rapidly secreting cytokines and lysing targets following TCR recognition of lipid antigens. Based on their ability to secrete IFN‐γ, IL‐4 and IL‐17A, iNKT‐cells are classified as NKT‐1, NKT‐2, and NKT‐17 subsets, respectively. The molecular pathways regulating iNKT‐cell fate are not fully defined. Recent studies implicate Rictor, a required component of mTORC2, in the development of select iNKT‐cell subsets, however these reports are conflicting. To resolve these questions, we used Rictorfl/fl CD4cre+ mice and found that Rictor is required for NKT‐17 cell development and normal iNKT‐cell cytolytic function. Conversely, Rictor is not absolutely required for IL‐4 and IFN‐γ production as peripheral iNKT‐cells make copious amounts of these cytokines. Overall iNKT‐cell numbers are dramatically reduced in the absence of Rictor. We provide data indicating Rictor regulates cell survival as well as proliferation of developing and mature iNKT‐cells. Thus, mTORC2 regulates multiple aspects of iNKT‐cell development and function. 相似文献
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Dr. Ernst Sklarz 《Archives of dermatological research》1923,144(2):295-301
Ohne ZusammenfassungMit 3 Textabbildungen. 相似文献
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Dr. Ernst Sklarz 《Archives of dermatological research》1921,132(1):238-249
Ohne Zusammenfassung 相似文献
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