Olivier Feraud
Villejuif, 94800, France
Last Updated: 09/26/2026
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Found 28 publications
Comparative Evaluation of Endothelial Colony-Forming Cells from Cord and Adult Blood vs. Human Embryonic Stem Cell-Derived Endothelial Cells: Insights into Therapeutic Angiogenesis Potential.
Journal: Stem cell reviews and reports
Published: November 25, 2024
iPSC-Derived Embryoid Bodies as Models of c-Met-Mutated Hereditary Papillary Renal Cell Carcinoma.
Journal: International journal of molecular sciences
Published: September 02, 2019
Long-term development of human iPSC-derived pyramidal neurons quantified after transplantation into the neonatal mouse cortex.
Journal: Developmental biology
Published: July 06, 2019
Global MicroRNA Profiling Uncovers miR-206 as a Negative Regulator of Hematopoietic Commitment in Human Pluripotent Stem Cells.
Journal: International journal of molecular sciences
Published: February 22, 2019
Genomic landscape analyses of reprogrammed cells using integrative and non-integrative methods reveal variable cancer-associated alterations.
Journal: Oncotarget
Published: September 25, 2018
Direct and rapid identification of T315I-Mutated BCR-ABL expressing leukemic cells using infrared microspectroscopy.
Journal: Biochemical and biophysical research communications
Published: July 10, 2018
Corrigendum: Non integrative strategy decreases chromosome instability and improves endogenous pluripotency genes reactivation in porcine induced pluripotent-like stem cells.
Journal: Scientific reports
Published: January 09, 2018
Generation of an induced pluripotent stem cell (iPSC) line from a patient with maturity-onset diabetes of the young type 3 (MODY3) carrying a hepatocyte nuclear factor 1-alpha (HNF1A) mutation.
Journal: Stem cell research
Published: November 24, 2017
Generation of induced pluripotent stem cell (iPSC) line from a patient with triple negative breast cancer with hereditary exon 17 deletion of BRCA1 gene.
Journal: Stem cell research
Published: August 03, 2017
Generation of an induced pluripotent stem cell line from a patient with hereditary multiple endocrine neoplasia 2B (MEN2B) syndrome with "highest risk" RET mutation.
Journal: Stem cell research
Published: July 08, 2017
Last Updated: 09/26/2026