未登录Prkar1a gene knockout in the pancreas leads to neuroendocrine tumorigenesis
Saloustros, Emmanouil; Salpea, Paraskevi; Starost, Matthew; Liu, Sissi; Faucz, Fabio R.; London, Edra; Szarek, Eva; Song, Woo-Jin; Hussain, Mehboob; Stratakis, Constantine A. .png)
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收藏Celecoxib treatment of fibrous dysplasia (FD) in a human FD cell line and FD-like lesions in mice with protein kinase A (PKA) defectsSaloustros, Emmanouil; Liu, Sisi; Mertz, Edward L.; Bhattacharyya, Nisan; Starost, Matthew F.; Salpea, Paraskevi; Nesterova, Maria; Collins, Michael; Leikin, Sergey; Stratakis, Constantine A. 分享 收藏 Hematopoietic neoplasms in Prkar2a-deficient miceSaloustros, Emmanouil; Salpea, Paraskevi; Qi, Chen-Feng; Gugliotti, Lina A.; Tsang, Kitman; Liu, Sisi; Starost, Matthew F.; Morse, Herbert C., III; Stratakis, Constantine A. 分享 收藏 Celecoxib reduces glucocorticoids in vitro and in a mouse model with adrenocortical hyperplasiaLiu, Sisi; Saloustros, Emmanouil; Berthon, Annabel; Starost, Matthew F.; Sahut-Barnola, Isabelle; Salpea, Paraskevi; Szarek, Eva; Faucz, Fabio R.; Martinez, Antoine; Stratakis, Constantine A. 分享 收藏 分享 收藏 Haploinsufficiency for either one of the type-II regulatory subunits of protein kinase A improves the bone phenotype of Prkar1a+/- miceLiu, Sisi; Saloustros, Emmanouil; Mertz, Edward L.; Tsang, Kitman; Starost, Matthew F.; Salpea, Paraskevi; Faucz, Fabio R.; Szarek, Eva; Nesterova, Maria; Leikin, Sergey; Stratakis, Constantine A. 分享 收藏 Germline PRKACA amplification causes variable phenotypes that may depend on the extent of the genomic defect: molecular mechanisms and clinical presentationsLodish, Maya B.; Yuan, Bo; Levy, Isaac; Braunstein, Glenn D.; Lyssikatos, Charalampos; Salpea, Paraskevi; Szarek, Eva; Karageorgiadis, Alexander S.; Belyavskaya, Elena; Raygada, Margarita; Faucz, Fabio Rueda; Izatt, Louise; Brain, Caroline; Gardner, James; Quezado, Martha; Carney, J. Aidan; Lupski, James R.; Stratakis, Constantine A. 分享 收藏 Constitutive activation of PRKACA in adrenal Cushing's syndromeFaucz, Fabio R.; Beuschlei, Felix; Fassnacht, Martin; Assie, Guilaume; Calebiro, Davide; Stratakis, Constantine; Osswald, Andrea; Ronchi, Cristina L.; Wieland, Thomas; Sbiera, Silviu; Schaak, Katrin; Schmittfull, Anett; Schwarzmayr, Thomas; Barreau, Olivia; Vezzosi, Delphine; Rizk-Rabbin, Marthe; Zabel, Ulrike; Szarek, Eva; Salpea, Paraskevi; Forlino, Antonella; Vetro, Annalisa; Zuffardi, Orsetta; Kisker, Caroline; Diener, Susanne; Meitinger, Thomas; Lohse, Martin J.; Reincke, Martin; Bertherat, Jerome; Strom, Tim M.; Allolio, Bruno 分享 收藏 Deletions of the PRKAR1A Locus at 17q24.2-q24.3 in Carney Complex: Genotype-Phenotype Correlations and Implications for Genetic TestingSalpea, Paraskevi; Horvath, Anelia; London, Edra; Faucz, Fabio R.; Vetro, Annalisa; Levy, Isaac; Gourgari, Evgenia; Dauber, Andrew; Holm, Ingrid A.; Morrison, Patrick J.; Keil, Margaret F.; Lyssikatos, Charalampos; Smith, Eric D.; Sanidad, Marc A.; Kelly, Joann C.; Dai, Zunyan; Mowrey, Philip; Forlino, Antonella; Zuffardi, Orsetta; Stratakis, Constantine A. 分享 收藏 Novel hematopoietic neoplasms in prkar2a-deficient miceSaloustros, Emmanouil; Salpea, Paraskevi; Gugglioti, Lina; Tsang, Kittman; Horvath, Anelia; Nesterova, Maria; Qi, Chen-Feng; Morse, Herbert C., III; Stratakis, Constantine A. 分享 收藏 
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