Abstract
In order to investigate the kinetics of vocal fold epithelium a bromodeoxyuridine-anti bromodeoxyuridine method has been applied in vivo at both light and electron microscopy level. This method is able to define the length of both epithelium turnover and cell-cycle in basal elements, as well as the existence of a higher proliferation rate during night time in comparison with day time. Moreover distinct labeling patterns observed in incorporating cells allow us to define the precise localization in S-phase of cycling elements.
| Original language | English |
|---|---|
| Pages (from-to) | 1081-1088 |
| Number of pages | 8 |
| Journal | Bollettino della Societa Italiana di Biologia Sperimentale |
| Volume | 67 |
| Issue number | 12 |
| Publication status | Published - Dec 1991 |
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ASJC Scopus subject areas
- Medicine(all)
Cite this
Cell kinetics of vocal fold epithelium in rats. / Savelli, V.; Rizzoli, R.; Rizzi, E.; Galanzi, A.; Buffa, A.; Rana, R.; Lattanzi, G.; Baratta, B.
In: Bollettino della Societa Italiana di Biologia Sperimentale, Vol. 67, No. 12, 12.1991, p. 1081-1088.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Cell kinetics of vocal fold epithelium in rats.
AU - Savelli, V.
AU - Rizzoli, R.
AU - Rizzi, E.
AU - Galanzi, A.
AU - Buffa, A.
AU - Rana, R.
AU - Lattanzi, G.
AU - Baratta, B.
PY - 1991/12
Y1 - 1991/12
N2 - In order to investigate the kinetics of vocal fold epithelium a bromodeoxyuridine-anti bromodeoxyuridine method has been applied in vivo at both light and electron microscopy level. This method is able to define the length of both epithelium turnover and cell-cycle in basal elements, as well as the existence of a higher proliferation rate during night time in comparison with day time. Moreover distinct labeling patterns observed in incorporating cells allow us to define the precise localization in S-phase of cycling elements.
AB - In order to investigate the kinetics of vocal fold epithelium a bromodeoxyuridine-anti bromodeoxyuridine method has been applied in vivo at both light and electron microscopy level. This method is able to define the length of both epithelium turnover and cell-cycle in basal elements, as well as the existence of a higher proliferation rate during night time in comparison with day time. Moreover distinct labeling patterns observed in incorporating cells allow us to define the precise localization in S-phase of cycling elements.
UR - http://www.scopus.com/inward/record.url?scp=0026290525&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0026290525&partnerID=8YFLogxK
M3 - Article
VL - 67
SP - 1081
EP - 1088
JO - Bollettino della Societa Italiana di Biologia Sperimentale
JF - Bollettino della Societa Italiana di Biologia Sperimentale
SN - 0037-8771
IS - 12
ER -