Age-dependent effects of Armc5 haploinsufficiency on adrenocortical function von Berthon, A., Faucz, F.R., Espiard, S., Drougat, L., Bertherat, J., Stratakis, C.A.

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Expression of Pancreatic Endocrine Markers by Mesenchymal Stem Cells From Human Umbilical Cord Vein von Santos, T.M, Percegona, L.S, González, P, Calil, A, Corradi Perini, C, Faucz, F.R, Câmara, N.O.S, Aita, C.A.M

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Age-dependent effects of Armc5 haploinsufficiency on adrenocortical function von Berthon, A, Faucz, F R, Espiard, S, Drougat, L, Bertherat, J, Stratakis, C A

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Spatial Multi-omics Reveals the Role of the Wnt Modulator, Dkk2, in Palatogenesis von Piña, J.O., Raju, R., Roth, D.M., Winchester, E.W., Padilla, C., Iben, J., Faucz, F.R., Cotney, J.L., D’Souza, R.N.

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Gigantism and Acromegaly Due to Xq26 Microduplications and GPR101 Mutation von Trivellin, Giampaolo, Daly, Adrian F, Faucz, Fabio R, Yuan, Bo, Rostomyan, Liliya, Larco, Darwin O, Schernthaner-Reiter, Marie Helene, Szarek, Eva, Leal, Letícia F, Caberg, Jean-Hubert, Castermans, Emilie, Villa, Chiara, Dimopoulos, Aggeliki, Chittiboina, Prashant, Xekouki, Paraskevi, Shah, Nalini, Metzger, Daniel, Lysy, Philippe A, Ferrante, Emanuele, Strebkova, Natalia, Mazerkina, Nadia, Zatelli, Maria Chiara, Lodish, Maya, Horvath, Anelia, de Alexandre, Rodrigo Bertollo, Manning, Allison D, Levy, Isaac, Keil, Margaret F, Sierra, Maria de la Luz, Palmeira, Leonor, Coppieters, Wouter, Georges, Michel, Naves, Luciana A, Jamar, Mauricette, Bours, Vincent, Wu, T. John, Choong, Catherine S, Bertherat, Jerome, Chanson, Philippe, Kamenický, Peter, Farrell, William E, Barlier, Anne, Quezado, Martha, Bjelobaba, Ivana, Stojilkovic, Stanko S, Wess, Jurgen, Costanzi, Stefano, Liu, Pengfei, Lupski, James R, Beckers, Albert, Stratakis, Constantine A

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Functional screen analysis reveals miR-26b and miR-128 as central regulators of pituitary somatomammotropin tumor growth through activation of the PTEN-AKT pathway von Palumbo, T, Faucz, F.R, Azevedo, M, Xekouki, P, Iliopoulos, D, Stratakis, C.A

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Les mutations germinales du gène CDKN1B sont une cause de maladie de Cushing chez l’enfant von Chasseloup, F., Hernández-Ramírez, L.C., Faucz, F.R., Lodish, M.B., Pankratz, N., Chittiboina, P., Kay, D.M., Giampaolo, T., Bertherat, J., Mills, J.L., Stratakis, C.

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HLA-DQA1 and HLA-DQB1 Alleles and Haplotypes in Two Brazilian Indian Tribes: Evidence of Conservative Evolution of HLA-DQ von SOTOMAIOR, V.S., FAUCZ, F.R., SCHAFHAUSER, C., JANZEN-DÜCK, M., BOLDT, A.B.W., PETZL-ERLER, M.L.

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Cystic Fibrosis Gene Variability in Two Southern Brazilian Amerindian Populations: Analysis of the ΔF508 Mutation and the KM19 and XV2C Haplotypes von Raskin, S., Petzl-Erler, M. L., Phillips, J. A., Pereira-Ferrari, L., Probst, C. M., Faucz, F. R., Sotomaior, V., Salzano, F. M., Culpi, L.

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