Search Results - "Vallone, Sabrina"

Ret Receptor Has Distinct Alterations and Functions in Breast Cancer by Gattelli, Albana, Hynes, Nancy E., Schor, Ignacio E., Vallone, Sabrina A.

“…Ret receptor tyrosine kinase is a proto-oncogene that participates in development of various cancers. Several independent studies have recently identified Ret…”
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Aberrant RET expression affects normal mammary gland post-lactation transition, enhancing cancer potential by Vallone, Sabrina A, García Solá, Martín, Schere-Levy, Carolina, Meiss, Roberto P, Hermida, Gladys N, Chodosh, Lewis A, Kordon, Edith C, Hynes, Nancy E, Gattelli, Albana

“…RET is a receptor tyrosine kinase with oncogenic potential in the mammary epithelium. Several receptors with oncogenic activity in the breast are known to…”
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De Novo Large Deletions in the PHEX Gene Caused X-Linked Hypophosphataemic Rickets in Two Italian Female Infants Successfully Treated with Burosumab by Pecoraro, Carmine, Fioretti, Tiziana, Perruno, Assunta, Klain, Antonella, Cioffi, Daniela, Ambrosio, Adelaide, Passaro, Diego, Annicchiarico Petruzzelli, Luigi, Di Domenico, Carmela, de Girolamo, Domenico, Vallone, Sabrina, Cattaneo, Fabio, Ammendola, Rosario, Esposito, Gabriella

“…Pathogenic variants in the gene cause rare and severe X-linked dominant hypophosphataemia (XLH), a form of heritable hypophosphatemic rickets (HR)…”
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Comprehensive Molecular Analysis of Disease-Related Genes as First-Tier Test for Early Diagnosis, Classification, and Management of Patients Affected by Nonsyndromic Ichthyosis by Fioretti, Tiziana, Martora, Fabrizio, De Maggio, Ilaria, Ambrosio, Adelaide, Piscopo, Carmelo, Vallone, Sabrina, Amato, Felice, Passaro, Diego, Acquaviva, Fabio, Gaudiello, Francesca, Di Girolamo, Daniela, Maiolo, Valeria, Zarrilli, Federica, Esposito, Speranza, Vitiello, Giuseppina, Auricchio, Luigi, Sammarco, Elena, Brasi, Daniele De, Petillo, Roberta, Gambale, Antonella, Cattaneo, Fabio, Ammendola, Rosario, Nappa, Paola, Esposito, Gabriella

“…Inherited ichthyoses are a group of clinically and genetically heterogeneous rare disorders of skin keratinization with overlapping phenotypes. The clinical…”
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Abstract 3685: Sustained Ret expression during mammary gland post-lactation induces premature involution and enhances cancer potential by Vallone, Sabrina A., Solá, Martín García, Cardiff, Robert D., Meiss, Roberto P., Chodosh, Lewis A., Shere-Levy, Carolina, Kordon, Edith C C., Hynes, Nancy E., Gattelli, Albana

“…Loss of normal development is a hallmark of cancer. Thus, understanding the mechanisms of tissue-specific developmental regulation and the changes that occur…”
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De Novo Large Deletions in the IPHEX/I Gene Caused X-Linked Hypophosphataemic Rickets in Two Italian Female Infants Successfully Treated with Burosumab by Pecoraro, Carmine, Fioretti, Tiziana, Perruno, Assunta, Klain, Antonella, Cioffi, Daniela, Ambrosio, Adelaide, Passaro, Diego, Annicchiarico Petruzzelli, Luigi, Di Domenico, Carmela, de Girolamo, Domenico, Vallone, Sabrina, Cattaneo, Fabio, Ammendola, Rosario, Esposito, Gabriella

“…Pathogenic variants in the PHEX gene cause rare and severe X-linked dominant hypophosphataemia (XLH), a form of heritable hypophosphatemic rickets (HR)…”
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