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The human genome also contains a gene homologous to the rodent IIb gene (Weiss, Schiaffino & Leinwand, 1999), but so far protein expression from this gene has not been demonstrated.
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So far, TKTL1 protein expression was described primarily in paraffin-embedded tumor tissue.
Transduction of normal hepatocytes with Ad[CgA-E1A] resulted in far lower E1A protein expression than wild-type Ad5 (Ad5 wt) and E1A expression was completely suppressed after transduction with Ad[CgA-E1A-miR122] Ad[CgA-E1A-miR122] Ad[CgA-E1A-miR122]gure 3and indicating very efficient silencing.
Only one study has so far determined the protein expression of components of the uPA system and evaluated its impact on prognosis for soft-tissue sarcoma (STS) patients.
As far as SREBP1 protein expression is concerned, interaction with fibroblasts seemed to produce a divergent effect in the two cancer cell models.
So far studies of S100A protein expression in inflammatory cells infiltrating cancer have been rare due to lack of appropriate way to quantify the S100A expression by inflammatory cells.
Having these advantages, the level of protein expression is far enhanced as comparable to that of viral expression systems.
Indeed, the increase in TMIGD1 protein expression was far more modest.
As far as we know, hOGG1 protein expression has not been studied in breast cancer in vivo.
So far, however, data on the protein expression of molecules involved in oxidative burst in multiple sclerosis lesions are not available.
As far as immunohistochemistry for Hiwi protein expression is concerned, a strong positive staining in 26.9% of the carcinomas (21 out of 78 patients) was observed, a rate substantially lower than for mRNA transcript levels.
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