Colin McGuckin

Prof. Colin McGuckin

CTIBIOTECH, Lyon, Auvergne-Rhône-Alpes, France
orcid

Research Focus & Metrics

Academic Career Length

38Years (1989-Present)

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

Representative Publications

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11 August 2005 in Cell Proliferation
Verified
Journal Article
Closed access
CMColin McGuckin
Colin McGuckin
NFN. Forraz
N. Forraz
MBM.‐O. Baradez
M.‐O. Baradez
SNS. Navran
S. Navran
JZJ. Zhao
J. Zhao
LDL. Denner
L. Denner

1 May 2011 in Biomaterials
Verified
Journal Article
Closed access
MJMarcin Jurga
Marcin Jurga
MDMaria B. Dainiak
Maria B. Dainiak
ASAnna Sarnowska
Anna Sarnowska
AJAnna Jablonska
Anna Jablonska
ATAnuj Tripathi
Anuj Tripathi
CMColin McGuckin
Colin McGuckin

1 September 1996 in British Journal of Haematology
Verified
Journal Article
Closed access
PDF file
SBS. E. Ball
S. E. Ball
CMColin McGuckin
Colin McGuckin
GJG. Jenkins
G. Jenkins
EGE. C. Gordon‐Smith
E. C. Gordon‐Smith

1 February 2010 in Stem Cells and Development
Verified
Journal Article
Closed access
Ornella ParoliniOrnella Parolini
Ornella Parolini
FAFrancesco Alviano
Francesco Alviano
IBIrene Bergwerf
Irene Bergwerf
DBDiana Boraschi
Diana Boraschi
CBCosimo De Bari
Cosimo De Bari
Cesar BorlonganCesar Borlongan
Cesar Borlongan
Among the many cell types that may prove useful to regenerative medicine, mounting evidence suggests that human term placenta-derived cells will join the list of significant contributors. In making new cell therapy-based strategies a clinical reality, it is fundamental that no a priori claims are made regarding which cell source is preferable for a particular therapeutic application. Rather, ongoing comparisons of the potentiality and characteristics of cells from different sources should be made to promote constant improvement in cell therapies, and such comparisons will likely show that individually tailored cells can address disease-specific clinical needs. The principle underlying such an approach is resistance to the notion that comprehensive characterization of any cell type has been achieved, neither in terms of phenotype nor risks-to-benefits ratio. Tailoring cell therapy approaches to specific conditions also requires an understanding of basic disease mechanisms and close collaboration between translational researchers and clinicians, to identify current needs and shortcomings in existing treatments. To this end, the international workshop entitled “Placenta-derived stem cells for treatment of inflammatory diseases: moving toward clinical application” was held in Brescia, Italy, in March 2009, and aimed to harness an understanding of basic inflammatory mechanisms inherent in human diseases with updated findings regarding biological and therapeutic properties of human placenta-derived cells, with particular emphasis on their potential for treating inflammatory diseases. Finally, steps required to allow their future clinical application according to regulatory aspects including good manufacturing practice (GMP) were also considered. In September 2009, the International Placenta Stem Cell Society (IPLASS) was founded to help strengthen the research network in this field.

1 May 2004 in Experimental Cell Research
Verified
Journal Article
Closed access
CMColin McGuckin
Colin McGuckin
NFNicolas Forraz
Nicolas Forraz
QAQuentin Allouard
Quentin Allouard
RPRuth Pettengell
Ruth Pettengell

11 April 2011 in Cell Proliferation
Verified
Journal Article
Closed access
PDF file
NFN. Forraz
N. Forraz
CMColin McGuckin
Colin McGuckin