Rezultati pretrage - Salpea, Paraskevi

Carney Complex and McCune Albright Syndrome: An overview of clinical manifestations and human molecular genetics od Salpea, Paraskevi, Stratakis, Constantine A.

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Carney Complex: an update od Correa, Ricardo, Salpea, Paraskevi, Stratakis, Constantine

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Endoplasmic reticulum stress and eIF2α phosphorylation: The Achilles heel of pancreatic β cells od Cnop, Miriam, Toivonen, Sanna, Igoillo-Esteve, Mariana, Salpea, Paraskevi

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Postnatal development- and age-related changes in DNA-methylation patterns in the human genome od Salpea, Paraskevi, Russanova, Valya R., Hirai, Tazuko H., Sourlingas, Thomae G., Sekeri-Pataryas, Kalliope E., Romero, Roberto, Epstein, Jonathan, Howard, Bruce H.

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Celecoxib treatment of fibrous dysplasia (FD) in a human FD cell line and FD-like lesions in mice with protein kinase A (PKA) defects od Saloustros, Emmanouil, Liu, Sisi, Mertz, Edward L., Bhattacharyya, Nisan, Starost, Matthew F., Salpea, Paraskevi, Nesterova, Maria, Collins, Michael, Leikin, Sergey, Stratakis, Constantine A.

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Prkar1a gene knockout in the pancreas leads to neuroendocrine tumorigenesis od Saloustros, Emmanouil, Salpea, Paraskevi, Starost, Matthew, Liu, Sissi, Faucz, Fabio R., London, Edra, Szarek, Eva, Song, Woo-Jin, Hussain, Mehboob, Stratakis, Constantine A.

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Developmental and epigenetic regulation of the human TLR3 gene od Porrás, Analia, Kozar, Sarah, Russanova, Valya, Salpea, Paraskevi, Hirai, Tazuko, Sammons, Nicholas, Mittal, Pooja, Kim, Ji Young, Ozato, Keiko, Romero, Roberto, Howard, Bruce H.

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Germline PRKACA amplification causes variable phenotypes that may depend on the extent of the genomic defect: molecular mechanisms and clinical presentations od Lodish, 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.

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Deletions of the PRKAR1A Locus at 17q24.2-q24.3 in Carney Complex: Genotype-Phenotype Correlations and Implications for Genetic Testing od Salpea, 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.

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