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Human Gene Therapy|February 15, 2022
Long-Term Disease Prevention with a Gene Therapy Targeting Oligodendrocytes in a Mouse Model of AdrenomyeloneuropathyYasemin Özgür-Günes, Malha Chedik, Catherine Le Stunff, et al.
Physiological Genomics|March 30, 2006
Heterogeneity of class I INS VNTR allele association with insulin secretion in obese childrenSophie Le Fur, Cédric Auffray, Franck Letourneur, et al.
Clinical Epigenetics|May 18, 2022
Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short statureXiaojian Shao, Catherine Le Stunff, Warren Cheung, et al.
The Journal of Clinical Endocrinology and Metabolism|February 7, 2008
Akt phosphorylation in lymphocytes provides an index of in vitro insulin-like growth factor I sensitivity associated with growth hormone-induced growthChantal Lotton, Danielle Rodrigue, Caroline Elie, et al.
Gene Therapy|October 2, 2021
Correction of a knock-in mouse model of acrodysostosis with gene therapy using a rAAV9-CAG-human PRKAR1A vectorYasemin Özgür-Günes, Catherine Le Stunff, Malha Chedik, et al.
Diabetes|November 25, 2003
The human MC4R promoter: characterization and role in obesityCecile Lubrano-Berthelier, Martha Cavazos, Catherine Le Stunff, et al.
Stem Cell Reports|September 23, 2014
Methylation and transcripts expression at the imprinted GNAS locus in human embryonic and induced pluripotent stem cells and their derivativesVirginie Grybek, Laetitia Aubry, Stéphanie Maupetit-Méhouas, et al.
Molecular Genetics and Metabolism|December 23, 2008
In obese and non-obese adults, the cis-regulatory rs361072 promoter variant of PIK3CB is associated with insulin resistance not with type 2 diabetesKarine Clément, Catherine Le Stunff, Aline Meirhaeghe, et al.
The Journal of Biological Chemistry|September 26, 2015
Functional Characterization of PRKAR1A Mutations Reveals a Unique Molecular Mechanism Causing Acrodysostosis but Multiple Mechanisms Causing Carney ComplexYara Rhayem, Catherine Le Stunff, Waed Abdel Khalek, et al.
Human Molecular Genetics|October 11, 2017
Mutations causing acrodysostosis-2 facilitate activation of phosphodiesterase 4D3Claire Briet, Arrate Pereda, Catherine Le Stunff, et al.
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