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  4. Comparative study of the neural differentiation capacity of mesenchymal stromal cells from different tissue sources: An approach for their use in neural regeneration therapies
Details

Comparative study of the neural differentiation capacity of mesenchymal stromal cells from different tissue sources: An approach for their use in neural regeneration therapies

Journal
PLOS ONE
ISSN
1932-6203
Date Issued
2019
Author(s)
Daniela N. Urrutia
Pablo Caviedes
Rodrigo Mardones
José J. Minguell
ANA MARIA FERNANDA VEGA LETTER
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Claudio M. Jofre
Type
Resource Types::text::journal::journal article
Scopus ID
2-s2.0-85062845941
WoS ID
WOS:000461030300020
DOI
10.1371/journal.pone.0213032
URL
https://investigadores.udd.cl/handle/123456789/2509
URL Institutional Repository
http://hdl.handle.net/11447/6289
Cite this document
Urrutia, D. N., Caviedes, P., Mardones, R., Minguell, J. J., Vega-Letter, A. M., & Jofre, C. M. (2019). Comparative study of the neural differentiation capacity of mesenchymal stromal cells from different tissue sources: An approach for their use in neural regeneration therapies. PLOS ONE, 14(3), e0213032. https://doi.org/10.1371/journal.pone.0213032
Subjects
human bone-marrow

; 

stem-cells

; 

progenitor cells

; 

adipose-tissue

; 

rat model

; 

in-vitro

; 

expression

; 

transplantation

; 

populations

; 

precursors

; 

adipose tissue

; 

adult

; 

bone marrow cells

; 

cell proliferation

; 

cell- and tissue-based therapy

; 

cells, cultured

; 

central nervous system diseases

; 

chile

; 

female

; 

humans

; 

male

; 

mesenchymal stem cells

; 

nerve regeneration

; 

neurogenesis

; 

primary cell culture

; 

regenerative medicine

; 

skin

; 

umbilical cord

; 

young adult

; 

5' nucleotidase

; 

beta tubulin

; 

beta1 integrin

; 

cd11b antigen

; 

cd19 antigen

; 

cd34 antigen

; 

cell marker

; 

cell protein

; 

disks large homolog 4

; 

endoglin

; 

hla dr antigen

; 

messenger rna

; 

nestin

; 

neurotrophin 3

; 

nuclear receptor related factor 1

; 

protein nefl

; 

protein nefm

; 

protein s100b

; 

receptor type tyrosine protein phosphatase c

; 

synaptophysin

; 

thy 1 membrane glycoprotein

; 

tyrosine 3 monooxygenase

; 

unclassified drug

; 

adipogenesis

; 

adipose tissue

; 

adult

; 

article

; 

bone development

; 

bone marrow

; 

cell count

; 

cell expansion

; 

cell function

; 

cell isolation

; 

cell lineage

; 

cell maturation

; 

cell population

; 

cell proliferation

; 

cell selection

; 

cell size

; 

cell structure

; 

cell therapy

; 

cell transdifferentiation

; 

cellular distribution

; 

chondrogenesis

; 

comparative study

; 

controlled study

; 

degenerative disease

; 

ex vivo study

; 

feasibility study

; 

female

; 

flow cytometry

; 

gene

; 

gene expression

; 

human

; 

human cell

; 

human tissue

; 

immunophenotyping

; 

male

; 

mesenchymal stem cell

; 

mesenchymal stroma cell

; 

nefl gene

; 

nefm gene

; 

nerve cell differentiation

; 

nerve regeneration

; 

nervous system development

; 

neural stem cell

; 

neurite outgrowth

; 

neurofilament

; 

newborn

; 

nt 3 gene

; 

nurr1 gene

; 

protein expression

; 

s100b gene

; 

skin

; 

spindle cell

; 

synapse vesicle

; 

tissue differentiation

; 

tissue distribution

; 

umbilical cord

; 

biological therapy

; 

bone marrow cell

; 

cell culture

; 

central nervous system disease

; 

chile

; 

cytology

; 

nervous system development

; 

physiology

; 

primary cell culture

; 

procedures

; 

regenerative medicine

; 

young adult
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