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However, the above described modeling procedure employed a single data processing algorithm, namely PLS.
The analytical procedure employed a multicommuted flow analysis manifold, using solenoid mini-pumps for fluid propulsion.
The first method we implemented [4] that allows this procedure employed a standard known as 10320/loc [10320/loc
The procedure employed a concentrate of autologous bone marrow-derived stem cells harvested from the patient's posterior iliac crest, biological and biodegradable scaffold (hyaluronic acid) and platelet-rich fibrin (PRF), used as a source of growth factors (such as TGF-B1 and PDGF) to improve the healing process.
The model-building procedure employed a multimodel inference approach [59], [60] to address hypotheses about temporal and weather-related patterns in shift length.
The entire immunoblotting procedure employed a commercial standardised technique (BM Chemiluminescence Western Blotting Kit, Roche Applied Science; Mannheim, Germany) with rabbit antibodies against human H-Ras (clone C-20), c-Fos (4), and Egr-1 (588) proteins that were purchased from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA, USA).
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The staining procedure employed an HMGCR antibody (Cat. No HPA008338, Atlas Antibodies AB, Stockholm, Sweden) (diluted 1 100) and an EnVision FLEX high-pH kit.
The calibration procedure employs a three-parameter Weibull stress model which includes the effects of a minimum (threshold) toughness, Kmin.
The calibration procedure employs a combination of linear and polynomial functions allowing correction of both lens and parallax distortions.
Optimization procedure employing a simplified gradient technique is used to calculate predictions of the future control actions.
The ranking procedure employs a robust principal component analysis and statistics used as the measures of fit.
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