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41.
Syed Siraj-ul-Islam Chintala V.N. Rao Atindra N. Chakraborty S. Ghosh Dastidar 《Carbohydrate research》1982,110(1):69-75
The lipopolysaccharide isolated from the cells of Shigella boydii type 8 bacteria gave precipitin bands against homologous antisera on Ouchterlony plates, whereas the carbohydrate-containing fractions obtained from it did not. One of the fractions was obtained in major proportion and contained 23.5% of sugars. A structure was assigned to the carbohydrate chain in this material by using the results of methylation, periodate oxidation, and deamination studies. 相似文献
42.
In this paper, a fractional complex transform (FCT) is used to convert the given fractional partial differential equations (FPDEs) into corresponding partial differential equations (PDEs) and subsequently Reduced Differential Transform Method (RDTM) is applied on the transformed system of linear and nonlinear time-fractional PDEs. The results so obtained are re-stated by making use of inverse transformation which yields it in terms of original variables. It is observed that the proposed algorithm is highly efficient and appropriate for fractional PDEs and hence can be extended to other complex problems of diversified nonlinear nature. 相似文献
43.
Mohyeddin Mandana Bonab Kamran Alimoghaddam Fatemeh Talebian Syed Hamid Ghaffari Ardeshir Ghavamzadeh Behrouz Nikbin 《BMC cell biology》2006,7(1):14-7
Background
A hot new topic in medical treatment is the use of mesenchymal stem cells (MSC) in therapy. The low frequency of this subpopulation of stem cells in bone marrow (BM) necessitates their in vitro expansion prior to clinical use. We evaluated the effect of long term culture on the senescence of these cells. 相似文献44.
Syed Mohsin Waheed Arnab Ghosh Ritu Chakravarti Ashis Biswas Mohammad Mahfuzul Haque Koustubh Panda Dennis J. Stuehr 《Free radical biology & medicine》2010,48(11):1548-1558
Although the insertion of heme into proteins enables their function in bioenergetics, metabolism, and signaling, the mechanisms and regulation of this process are not fully understood. We developed a means to study cellular heme insertion into apo-protein targets over a 3-h period and then investigated how nitric oxide (NO) released from a chemical donor (NOC-18) might influence heme (protoporphyrin IX) insertion into seven targets that present a range of protein structures, heme ligation states, and functions (three NO synthases, two cytochrome P450's, catalase, and hemoglobin). NO blocked cellular heme insertion into all seven apo-protein targets. The inhibition occurred at relatively low (nM/min) fluxes of NO, was reversible, and did not involve changes in intracellular heme levels, activation of guanylate cyclase, or inhibition of mitochondrial ATP production. These aspects and the range of protein targets suggest that NO can act as a global inhibitor of heme insertion, possibly by inhibiting a common step in the process. 相似文献
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Senthilkumar Nangan Aziz Md. Abdul Pannipara Mehboobali Alphonsa A. Therasa Al-Sehemi Abdullah G. Balasubramani A. Gnana kumar G. 《Bioprocess and biosystems engineering》2020,43(1):97-109
Bioprocess and Biosystems Engineering - Despite the green energy generation with low cost compared to conventional fuel cells, microbial fuel cells (MFCs) still suffer with anode related... 相似文献
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Syed Muhammad Hamid Mevlut Citir Erdem Murat Terzi Ismail Cimen Zehra Yildirim Asli Ekin Dogan Begum Kocaturk Umut Inci Onat Moshe Arditi Christian Weber Alexis TraynorKaplan Carsten Schultz Ebru Erbay 《EMBO reports》2020,21(12)
The ER‐bound kinase/endoribonuclease (RNase), inositol‐requiring enzyme‐1 (IRE1), regulates the phylogenetically most conserved arm of the unfolded protein response (UPR). However, the complex biology and pathology regulated by mammalian IRE1 cannot be fully explained by IRE1’s one known, specific RNA target, X box‐binding protein‐1 (XBP1) or the RNA substrates of IRE1‐dependent RNA degradation (RIDD) activity. Investigating other specific substrates of IRE1 kinase and RNase activities may illuminate how it performs these diverse functions in mammalian cells. We report that macrophage IRE1 plays an unprecedented role in regulating phosphatidylinositide‐derived signaling lipid metabolites and has profound impact on the downstream signaling mediated by the mammalian target of rapamycin (mTOR). This cross‐talk between UPR and mTOR pathways occurs through the unconventional maturation of microRNA (miR) 2137 by IRE1’s RNase activity. Furthermore, phosphatidylinositol (3,4,5) phosphate (PI(3,4,5)P3) 5‐phosphatase‐2 (INPPL1) is a direct target of miR‐2137, which controls PI(3,4,5)P3 levels in macrophages. The modulation of cellular PI(3,4,5)P3/PIP2 ratio and anabolic mTOR signaling by the IRE1‐induced miR‐2137 demonstrates how the ER can provide a critical input into cell growth decisions. 相似文献
49.
Russian Journal of Bioorganic Chemistry - Pyridazines hold considerable interest relative to pharmacologically active molecules. The pyridazine compounds are exhibited different types of... 相似文献
50.
Abdullah Al Emran Hsin‐Yi Tseng Mikaela C. Coleman Jessamy Tiffen Stuart Cook Helen M. McGuire Stuart Gallagher Carl Feng Peter Hersey 《Pigment cell & melanoma research》2020,33(5):660-670
Melanoma, as for many other cancers, undergoes a selection process during progression that limits many innate and adaptive tumor control mechanisms. Immunotherapy with immune checkpoint blockade overcomes one of the escape mechanisms but if the tumor is not eliminated other escape mechanisms evolve that require new approaches for tumor control. Some of the innate mechanisms that have evolved against infections with microorganisms and viruses are proving to be active against cancer cells but require better understanding of how they are activated and what inhibitory mechanisms may need to be targeted. This is particularly so for inflammasomes which have evolved against many different organisms and which recruit a number of cytotoxic mechanisms that remain poorly understood. Equally important is understanding of where these mechanisms will fit into existing treatment strategies and whether existing strategies already involve the innate killing mechanisms. 相似文献