Normal bone marrow was exposed to various doses of OSCs for 48 hours, washed, and counted.
In an in vitro erythropoietic micronucleus assay, rat bone marrow cells were exposed to DMF at a concentration of 0.1 mM for 1 h.
Female mice receiving bone marrow transplantation were exposed to either normal room air (20.8% O2) or 10% O2 for 7 days as we have described [3], [7], [15] [18].
When bone marrow cells were exposed to CP in the presence of induced S9 mix, the stem cell population, enumerated by colonization in semisolid medium, was reduced in a dose-dependent manner, with an ED50 of 5.2 microgram/ml.
To destroy the bone marrow, APP/PS1 mice were exposed to a lethal dose of X-ray irradiation (900 rad).
Cultured human bone marrow hTERT-MSCs were exposed to 0.5 mg/ml of QMix™ and NaOCl for 2 hrs.
Bone marrow MSCs (BM-MSC) were exposed to four different cell culture conditions: 1.
MM cell lines and primary bone marrow CD138+ MM cells were exposed to the pan-PI3K/mTOR inhibitor, PI-103, and assessed for cell cycle profiles, [H]-thymidine uptake and cell cycle proteins.
DCs derived from the bone marrow of BALB/c mice were exposed to chymotrypsin-treated gluten, which induced DC maturation with upregulation of MHC II, co-stimulatory molecules (CD86, CD40, CD54) and high production of MIP-2 and keratinocyte-derived cytokine (KC).
The sections of implant, which were exposed to the marrow spaces, displayed either no bone deposition or very thin bone tissue.
