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Furthermore (and potentially of greater interest), we will determine the ability of CD4+CD45RO+VLA-4high CD4+CD45RO+VLA-4high Tcksynovial grafts in the RA/severe cellsned immunodeficientomouse model, trafficr wito their potential to upregulate cytokinesynovialy in this tissue.
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The combined use of transformation strategies in cell culture and mouse models together with molecular definition of human breast cancer subtypes should help to elucidate the nature of breast cancer diversity and to develop individualized therapies.
Injection of TG1050 induced both splenic and intrahepatic functional T cells producing cytokines and displaying cytolytic activity in HBV-naïve and HBV-persistent mouse models together with significant reduction of circulating viral parameters.
Recently, we resolved the minimal docking machinery in adrenal medullary chromaffin cells using embryonic mouse model systems together with electron-microscopic analyses and also found that docking is controlled by the sub-membrane filamentous (F- actin.
As a result, rat-based disease models will complement existing mouse models and together they may provide new insight into mechanisms and behavioural outcomes of FMRP dysregulation in humans.
In view of these observations in mouse models systems, together with the widespread occurrence of mutations that activate Wnt signaling in human cancers of other tissues, it is particularly surprising that equivalent mutations have generally not been detected in human breast cancers.
Using genetically engineered mouse models (GEM) together with molecular analysis, it has been well documented that COUP-TFII serves as one of the master regulators to control developmental programs, including organogenesis, angiogenesis, cardiovascular development, reproduction, neuronal development and metabolic homeostasis [ 7– 15].
We found increased BAL fluid activin A levels in a mouse model of chronic asthma together with induction of airway remodelling (airway mucus production, subepithelial collagen and smooth muscle deposition), and these changes were inhibited by follistatin instillation into the lung prior to allergen challenge [ 18].
Taken together, this mouse model may serve as an alternative noninvasive, cost-effective and accurate in vivo representative model of a post-arthroplasty S. aureus infection.
Taken together, this mouse model may represent an alternative pre-clinical screening tool to evaluate novel in vivo therapeutic strategies before studies in larger animals and in human subjects.
Taken together, this mouse model of post-arthroplasty infection provides longitudinal tracking of both bacterial burden and inflammatory response while substantially reducing animal usage, labor, material and experimental costs.
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