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Jacques Drouin

Showing results (81-90 of 85) with videos related to

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BMC Medical Genetics|December 20, 2014
Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficienciesThierry Brue, Marie-Hélène Quentien, Konstantin Khetchoumian, et al.
Nature Communications|July 2, 2025
O-GlcNAcylation of FOXK1 co-opts BAP1 to orchestrate the E2F pathway and promotes oncogenesisOumaima Ahmed, Louis Masclef, Nicholas Iannantuono, et al.
Biorxiv : the Preprint Server for Biology|March 11, 2024
O-GlcNAcylation of FOXK1 orchestrates the E2F pathway and promotes oncogenesisLouis Masclef, Oumaima Ahmed, Nicholas Iannantuono, et al.
Endocrine-Related Cancer|May 24, 2017
Loss-of-function mutations in the <i>CABLES1</i> gene are a novel cause of Cushing's diseaseLaura C Hernández-Ramírez, Ryhem Gam, Nuria Valdés, et al.
The Journal of Clinical Endocrinology and Metabolism|December 23, 2004
Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutationsSophie Vallette-Kasic, Thierry Brue, Anne-Marie Pulichino, et al.
Pageof 9

Showing results (81-90 of 85) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 85 results.
BMC Medical Genetics|December 20, 2014
Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficienciesThierry Brue, Marie-Hélène Quentien, Konstantin Khetchoumian, et al.
Nature Communications|July 2, 2025
O-GlcNAcylation of FOXK1 co-opts BAP1 to orchestrate the E2F pathway and promotes oncogenesisOumaima Ahmed, Louis Masclef, Nicholas Iannantuono, et al.
Biorxiv : the Preprint Server for Biology|March 11, 2024
O-GlcNAcylation of FOXK1 orchestrates the E2F pathway and promotes oncogenesisLouis Masclef, Oumaima Ahmed, Nicholas Iannantuono, et al.
Endocrine-Related Cancer|May 24, 2017
Loss-of-function mutations in the <i>CABLES1</i> gene are a novel cause of Cushing's diseaseLaura C Hernández-Ramírez, Ryhem Gam, Nuria Valdés, et al.
The Journal of Clinical Endocrinology and Metabolism|December 23, 2004
Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutationsSophie Vallette-Kasic, Thierry Brue, Anne-Marie Pulichino, et al.
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