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Hypoxia sustains glioblastoma radioresistance through ERKs/DNA-PKcs/HIF-1α functional interplay.
Published in:
International Journal of Oncology, 2014, v. 44, n. 6, p. 2121, doi. 10.3892/ijo.2014.2358
By:
- MARAMPON, FRANCESCO;
- GRAVINA, GIOVANNI LUCA;
- ZANI, BIANCA MARIA;
- POPOV, VLADIMIR M.;
- FRATTICCI, AMATO;
- CERASANI, MANUELA;
- DI GENOVA, DANIELA;
- MANCINI, MARTA;
- CICCARELLI, CARMELA;
- FICORELLA, CORRADO;
- DI CESARE, ERNESTO;
- FESTUCCIA, CLAUDIO
Publication type:
Article
A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia.
Published in:
Nature Genetics, 2006, v. 38, n. 7, p. 794, doi. 10.1038/ng1809
By:
- Horvath, Anelia;
- Boikos, Sosipatros;
- Giatzakis, Christoforos;
- Robinson-White, Audrey;
- Groussin, Lionel;
- Griffin, Kurt J.;
- Stein, Erica;
- Levine, Elizabeth;
- Delimpasi, Georgia;
- Hui Pin Hsiao;
- Keil, Meg;
- Heyerdahl, Sarah;
- Matyakhina, Ludmila;
- Libè, Rossella;
- Fratticci, Amato;
- Kirschner, Lawrence S.;
- Cramer, Kevin;
- Gaillard, Rolf C.;
- Bertagna, Xavier;
- Carney, J. Aidan
Publication type:
Article
Frequent phosphodiesterase 11A gene (PDE11A) defects in patients with Carney complex (CNC) caused by PRKAR1A mutations: PDE11A may contribute to adrenal and testicular tumors in CNC as a modifier of the phenotype.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 1, p. E208, doi. 10.1210/jc.2010-1704
By:
- Libé, Rossella;
- Horvath, Anelia;
- Vezzosi, Delphine;
- Fratticci, Amato;
- Coste, Joel;
- Perlemoine, Karine;
- Ragazzon, Bruno;
- Guillaud-Bataille, Marine;
- Groussin, Lionel;
- Clauser, Eric;
- Raffin-Sanson, Marie-Laure;
- Siegel, Jennifer;
- Moran, Jason;
- Drori-Herishanu, Limor;
- Rueda Faucz, Fabio;
- Lodish, Maya;
- Nesterova, Maria;
- Bertagna, Xavier;
- Bertherat, Jerome;
- Stratakis, Constantine A.
Publication type:
Article
Identification of novel genetic variants in phosphodiesterase 8B ( PDE8B), a cAMP-specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort of patients with adrenal tumours.
Published in:
Clinical Endocrinology, 2012, v. 77, n. 2, p. 195, doi. 10.1111/j.1365-2265.2012.04366.x
By:
- Rothenbuhler, Anya;
- Horvath, Anelia;
- Libé, Rossella;
- Faucz, Fabio R.;
- Fratticci, Amato;
- Raffin Sanson, Marie L.;
- Vezzosi, Delphine;
- Azevedo, Monalisa;
- Levy, Isaak;
- Almeida, Madson Q.;
- Lodish, Maya;
- Nesterova, Maria;
- Bertherat, Jérôme;
- Stratakis, Constantine A.
Publication type:
Article

Found: 4

Hypoxia sustains glioblastoma radioresistance through ERKs/DNA-PKcs/HIF-1α functional interplay.

A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia.

Frequent phosphodiesterase 11A gene (PDE11A) defects in patients with Carney complex (CNC) caused by PRKAR1A mutations: PDE11A may contribute to adrenal and testicular tumors in CNC as a modifier of the phenotype.

Identification of novel genetic variants in phosphodiesterase 8B ( PDE8B), a cAMP-specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort of patients with adrenal tumours.