Eugenia Flores-Figueroa

Dr. Eugenia Flores-Figueroa

orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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13 January 2020 in Nature Genetics
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Journal Article
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MCMichelle Chan-Seng-Yue
Michelle Chan-Seng-Yue
JKJaeseung C. Kim
Jaeseung C. Kim
GWGavin W. Wilson
Gavin W. Wilson
KNKaren Ng
Karen Ng
EFEugenia Flores-Figueroa
Eugenia Flores-Figueroa
FNFaiyaz Notta
Faiyaz Notta

1 February 2005 in Leukemia Research
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Journal Article
Closed access
EFEugenia Flores-Figueroa
Eugenia Flores-Figueroa
RARosa Maria Arana-Trejo
Rosa Maria Arana-Trejo
GGGuillermo Gutiérrez-Espíndola
Guillermo Gutiérrez-Espíndola
APAdrián Pérez-Cabrera
Adrián Pérez-Cabrera
HMHector Mayani
Hector Mayani

1 October 2018 in Cell Stem Cell
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Journal Article
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KGKarin Golan
Karin Golan
AKAnju Kumari
Anju Kumari
OKOrit Kollet
Orit Kollet
EKEman Khatib-Massalha
Eman Khatib-Massalha
MSMohana Devi Subramaniam
Mohana Devi Subramaniam
TLTsvee Lapidot
Tsvee Lapidot

1 July 2002 in Leukemia Research
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Journal Article
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EFEugenia Flores-Figueroa
Eugenia Flores-Figueroa
GGGuillermo Gutiérrez-Espı́ndola
Guillermo Gutiérrez-Espı́ndola
JMJuan José Montesinos
Juan José Montesinos
RARosa Marı́a Arana-Trejo
Rosa Marı́a Arana-Trejo
HMHector Mayani
Hector Mayani

1 January 2009 in Cytotherapy
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Journal Article
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JMJ.J. Montesinos
J.J. Montesinos
EFEugenia Flores-Figueroa
Eugenia Flores-Figueroa
SCS. Castillo-Medina
S. Castillo-Medina
PFP. Flores-Guzmán
P. Flores-Guzmán
EHE. Hernández-Estévez
E. Hernández-Estévez
HMH. Mayani
H. Mayani
Bone marrow (BM) has been recognized as the main source of mesenchymal stromal cells (MSC); however, MSC have also been detected in umbilical cord blood (UCB) and placenta (PL). In the present study, we obtained MSC from these three sources and characterized them in a comparative manner. MSC were obtained from BM, UCB and PL samples and analyzed to determine their morphology, cell-surface antigen (Ag) expression and differentiation potential. Particular emphasis was placed on the expression of neural markers. MSC were detected in 9/9, 11/104 and 5/5 samples from BM, UCB and PL, respectively. MSC populations comprised several morphologically distinct cell types, including neural-like cells. MSC were positive for ‘mesenchymal’ Ag (CD105, CD73 and CD90), although CD90 expression was very heterogeneous. Interestingly, CD13 expression was high in all three sources. In all cases, MSC showed osteogenic and chondrogenic differentiation; however, UCB MSC showed no adipogenic potential. Furthermore, MSC from UCB produced a different type of cartilage compared with MSC from BM and PL. It is noteworthy that in all three sources we detected the expression of neural proteins without any neural differentiation stimuli. A significant increase in the proportion of neural marker-positive MSC was observed in the presence of neural inducers. Our results indicate that PL may prove to be a more appropriate source for obtaining MSC than UCB, and suggest the possibility that a subpopulation of MSC may possess neural potential, which is favored by neural inducers.

1 September 2008 in Leukemia Research
Verified
Journal Article
Closed access
EFEugenia Flores-Figueroa
Eugenia Flores-Figueroa
JMJuan José Montesinos
Juan José Montesinos
PFPatricia Flores-Guzmán
Patricia Flores-Guzmán
GGGuillermo Gutiérrez-Espíndola
Guillermo Gutiérrez-Espíndola
RARosa María Arana-Trejo
Rosa María Arana-Trejo
HMHector Mayani
Hector Mayani