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  4. p27(Kip1) down-regulation as achieved by two clinically feasible means did not induce proliferation of supporting cells in the rat neonatal cochlea in vivo
Details

p27(Kip1) down-regulation as achieved by two clinically feasible means did not induce proliferation of supporting cells in the rat neonatal cochlea in vivo

Journal
Hearing Research
ISSN
0378-5955
Date Issued
2019
Author(s)
Sebastián A. Silva
Juan C. Maass
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Type
Resource Types::text::journal::journal article
Scopus ID
2-s2.0-85058647142
WoS ID
WOS:000458710100002
DOI
10.1016/j.heares.2018.12.002
URL
https://investigadores.udd.cl/handle/123456789/2504
URL Institutional Repository
http://hdl.handle.net/11447/6292
Subjects
inner ear

; 

labyrinth supporting cells

; 

cell proliferation

; 

cdkn1b protein

; 

shrna

; 

alsterpaullone

; 

animals

; 

animals, newborn

; 

benzazepines

; 

cell proliferation

; 

cochlea

; 

cyclin-dependent kinase inhibitor p27

; 

down-regulation

; 

indoles

; 

labyrinth supporting cells

; 

rats, sprague-dawley

; 

rna interference

; 

rna, small interfering

; 

signal transduction

; 

tissue culture techniques

; 

alsterpaullone

; 

cell marker

; 

cyclin dependent kinase inhibitor 1b

; 

lentivirus vector

; 

short hairpin rna

; 

benzazepine derivative

; 

cdkn1b protein, rat

; 

cyclin dependent kinase inhibitor 1b

; 

indole derivative

; 

small interfering rna

; 

animal cell

; 

animal experiment

; 

article

; 

cell proliferation

; 

cochlea

; 

cochlea duct

; 

cochlea fenestra

; 

cochlea injury

; 

controlled study

; 

corti organ

; 

down regulation

; 

feasibility study

; 

gene expression

; 

immunohistochemistry

; 

in vitro study

; 

in vivo study

; 

newborn

; 

nonhuman

; 

priority journal

; 

protein expression

; 

protein modification

; 

rat

; 

reverse transcription polymerase chain reaction

; 

sustentacular cell

; 

animal

; 

cochlea

; 

drug effect

; 

genetics

; 

labyrinth supporting cells

; 

metabolism

; 

pathology

; 

rna interference

; 

signal transduction

; 

sprague dawley rat

; 

tissue culture technique
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