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The technique devised by Jacob W. Petrich and colleagues takes advantage of the fact that nervous system tissues contain high concentrations of a compound, lipofuscin, that fluoresces when exposed to light.
Many diseases require replacement of respiratory system tissues, organs, or both.
This is particularly true for nervous system tissues, where information processing function depends on intricate circuit and synaptic architectures.
Our results demonstrated that astrocyte activation occurred and was accompanied by elevated TNF-α levels in central nervous system tissues following CCI.
Here, we review current experimental models that promote the development of novel bio-nanotechnology tools to help repair damaged nervous system tissues.
In a multidisciplinary approach, bone marrow derived mesenchymal stem cells (BMSCs) are genetically engineered to overexpress neurotrophin-3 (nt-3 gene) that protect central nervous system tissues and stimulates neuronal-like differentiation of BMSCs.
Peripheral benzodiazepine receptors are present in peripheral nervous system tissues, glial cells, and to a lesser extent the central nervous system.
Central nervous system tissues were collected and stored at -80°C.
The majority of tissue-selective genes shared by ten or more tissues were expressed in neural system tissues.
The isoform was found in some but not all nervous system tissues, and in embryonic nervous system but not whole embryo.
Fresh necropsy instruments were used for each necropsy, with the central nervous system tissues removed at the completion of the necropsy.
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