279) factor (NF)-κB and p38 mitogen-activated protein kinases (MAPK) signaling pathway. |
280) 6, IL-8), activation of mitogen-activated protein kinases (MAPKs) and expression of |
281) e stress, apoptosis and mitogen-activated protein kinases (MAPKs) in lead-exposed li |
282) The Akt, family of serine/threonine protein kinases functions as key regulator |
283) mportant function of CDC37 in chaperoning protein kinases. |
284) Upon culturing for 48 h, mRNA, protein levels, and caspase 3 activity wer |
285) NFAT1, reduced E-cadherin and α-catenin protein levels, and increased protein leve |
286) increases MMP expression at both mRNA and protein levels, and promotes invasion pote |
287) n human colon cancer cells increased CDK4 protein levels, which was negated upon CDC |
288) n mice can attenuate caspase-3 and PARP-1 protein expression, and improve mouse surv |
289) terized by histology, gene expression and protein expression, in the absence of key |
290) L6-expressing cells reduced BCL6 mRNA and protein expression, which is sufficient to |
291) The superoxide-scavenging activity of the protein has also been measured. |
292) tions, the precise localization of SUCLA2 protein has never been investigated. |
293) rovide evidence that the synthetic matrix protein has the ability to function as an |
294) ther ectopically expressed NLS-containing protein is able to adopt a nuclear localis |
295) f proteinopathies as the aggregated prion protein is highly infectious and can self- |
296) This protein is released from its parent molecu |
297) eukin-6, lactate dehydrogenase, and total protein of BALF. |
298) Milk protein of farm animals is difficult to is |
299) inidase (iNA) is a homotetrameric surface protein of the influenza virus and an esta |
300) with the decrease in lipid peroxidation, protein oxidation, and collagen content. |
301) We examined protein oxidation, expressed as concentrat |
302) age of protein, lipid, and DNA and causes protein oxidation, lipid peroxidation, and |
303) Protein stability was evaluated functional |
304) and M6 loop play an important role in the protein stability and function and is resp |
305) The effect of annealing on both protein stability and the physical state o |
306) A number of additional protein thiol differences in GDFs were ide |
307) eficient expression of an apparent 55 kDa protein thiol in GDFs from independent Gor |
308) hiol reactive probes to define changes in protein thiol profiles in live cell studie |
309) analyses conducted included Kjeldhal for protein, acid hydrolysis and extraction fo |
310) al for hydrophobic interfaces of specific protein-nucleic acid interactions, that th |
311) vegetable-based) was with respect to the protein content (P=0.04) per 100 g of food |
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