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Together, these data indicate that bone marrow stroma has no protective activity against HM1.24-ETA′-mediated induction of apoptosis.
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Mesenchymal stem cells (MSC) from bone marrow stroma have been broadly studied for use in the therapy of neurological disorders.
Anatomical relationships of HSCs with bone marrow stroma cells have also implied vascular endothelial-cadherin+ sinusoidal endothelial cells (SECs) [ 19, 20], perivascular cells and mesenchymal stem cells (MSCs) [ 15, 21] as additional components of the niche.
Thus, disseminated cancer cells expressing the appropriate receptor arsenal for the trophic factors locally produced by the bone marrow stroma will have a major advantage in supporting their survival and growth into clinically evident tumors.
Today, Stroma has no regular communications with the mainland.
The donor (human) origin of osteocytes and myelosupportive stroma have been determined by various methods, whereas the donor origin of marrow adipocytes has long been suspected and even assumed, but never proven owing to their large cytoplasmic to nuclear ratio, making detection with nuclear markers difficult.
In our study, cells grown in standard media showed spindle-shaped and flattened cells and had the ability to continuously divide, as has been observed for bone marrow stroma and tissue-specific MSCs from other species [ 39, 40].
The identification of multipotential mesenchymal stem cells (MSCs) derived from adult human tissues, including bone marrow stroma and a number of connective tissues, has provided exciting prospects for cell-based tissue engineering and regeneration.
MMP-7 (matrilysin) exhibits high activity against collagen IV, a major component of bone marrow stroma (BMS) and other basement membranes and has been found previously in carcinoma cells of many cancers including prostate and their metastases (Pajouh et al, 1991).
Some of the bone marrow stroma at the interface with the PEC (orange/yellow) had retracted away and showed intense MMP-1 green staining (arrows).
For example, αvβ3 has high affinity binding with the bone marrow stroma ligands, osteopontin and vitronectin, to promote prostate bone metastasis [ 49].
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