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However, we revealed that NGH particles with diameters of more than 0.50 mm were preserved for two weeks.
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The primary urologic objectives for lipomyelomeningocele (LMM) and myelomeningocele (MM) are preserving renal integrity and achieving continence.
Samples of mouse livers (5 mm × 6 mm size) were preserved in 4% paraformaldehyde (PFA) for histological analysis, while other samples (100-200 mg) were immediately frozen in liquid nitrogen.
After 2 h of an IAH of 20 mm Hg and a mean final APP lower than 50 mm Hg, all variable values were preserved.
Surgical waste obtained from the anterior portion of the superior temporal gyrus, an area some distance from sclerotic areas and epileptogenic foci, was dissected at 4 mm intervals, and alternate sections were preserved by flash freezing for molecular analyses and by formalin fixation for histological evaluation.
After agitation, leachates were collected by 0.8-mm glass fiber filters and the leachates were preserved in 2 % HNO3.
All purified enzymes were preserved in a 20-mM sodium acetate buffer (pH 5.5) containing 0.01% NaN3 at 4°C.
None were preserved.
In an earlier work by Min et al [14] it was showed that the for a simple enzyme catalyzed reaction (1), the classical MM mass action kinetics is preserved in the quasi-equilibrium limit even in the presence of conformational fluctuations which are slower or comparable to other binding- dissociation processes.
When GSH concentration is high (>1 mM), all cell functions are preserved from oxidative inhibition.
At least 5 mm of gingival cuff is preserved to allow for closure.
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