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Twenty-seven patients (30 implants) were divided into three groups.
Implants were divided into two groups: no keratinized mucosa (NKM) and KM.
Implants were divided into two groups: no keratinized mucosa (NKM) = 0 mm of keratinized mucosa and KM > 0 mm of keratinized mucosa.
The implants were divided in 2 groups (n = 8): the one-piece implant group (solid implants that comprise implant and abutment in one piece) and the two-piece implant group (external hexagon with a healing abutment).
A total of 12 (n=12) surface-enhanced implants were divided into two subgroups (A and B) and biocoated with rhBMP-2 [BMP-A: noncovalently immobilized rhBMP-2 (596 ng/cm), BMP-B: covalently immobilized rhBMP-2 (819 ng/cm)] [ 40].
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Similar to the micro-morphological presentation, each implant was divided into comparable sites of interest.
Each implant was divided into quadrants and fixed by immersion in 4% paraformaldehyde diluted in phosphate buffered saline solution.
In this protocol, the length of the implant was divided into 2 parts and subdivided into 2 lateral, 2 medial, and 1 inferior ROI.
Based on the different implants, patients were divided into three groups: Group A: one-third tubular plate; Group B: locking compression (LCP) metaphyseal plate; Group C: LCP distal fibula plate.
In the most of the reported studies mentioned above, removal of the displaced implant, sinus bone grafting, and new implant placement were divided into two or three individual procedures.
When tumours reached a size of ∼70 mm (approximately 15 days after tumour cell implant), mice were divided into seven groups (n=7).
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CEO of Professional Science Editing for Scientists @ prosciediting.com