E3 Ubiquitin Ligase TRIM Proteins, Cell Cycle and Mitosis

le Venuto, Santina, Merla, Giuseppe
Foilsithe in Cells (2019)

Rise of TRIM8: A Molecule of Duality

le Bhaduri, Utsa, Merla, Giuseppe
Foilsithe in Mol Ther Nucleic Acids (2020)

Ubiquitination, Biotech Startups, and the Future of TRIM Family Proteins: A TRIM-Endous Opportunity

le Bhaduri, Utsa, Merla, Giuseppe
Foilsithe in Cells (2021)

The Emerging Role of Gβ Subunits in Human Genetic Diseases

le Malerba, Natascia, De Nittis, Pasquelena, Merla, Giuseppe
Foilsithe in Cells (2019)

DNA damage response defect in Williams-Beuren syndrome

le Guenat, David, Merla, Giuseppe, Deconinck, Eric, Borg, Christophe, Rohrlich, Pierre-Simon
Foilsithe in Int J Mol Med (2017)

A NGS-Targeted Autism/ID Panel Reveals Compound Heterozygous GNB5 Variants in a Novel Patient

le Malerba, Natascia, Towner, Shelley, Keating, Katherine, Squeo, Gabriella Maria, Wilson, William, Merla, Giuseppe
Foilsithe in Front Genet (2018)

Using Transcription Modules to Identify Expression Clusters Perturbed in Williams-Beuren Syndrome

le Henrichsen, Charlotte N., Csárdi, Gábor, Zabot, Marie-Thérèse, Fusco, Carmela, Bergmann, Sven, Merla, Giuseppe, Reymond, Alexandre
Foilsithe 2011

Williams–Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase

le Micale, Lucia, Fusco, Carmela, Augello, Bartolomeo, Napolitano, Luisa MR, Dermitzakis, Emmanouil T, Meroni, Germana, Merla, Giuseppe, Reymond, Alexandre
Foilsithe 2008

MiR-578 and miR-573 as potential players in BRCA-related breast cancer angiogenesis

le Danza, Katia, Summa, Simona De, Pinto, Rosamaria, Pilato, Brunella, Palumbo, Orazio, Merla, Giuseppe, Simone, Gianni, Tommasi, Stefania
Foilsithe in Oncotarget (2014)

Clinical Genetics Can Solve the Pitfalls of Genome-Wide Investigations: Lesson from Mismapping a Loss-of-Function Variant in KANSL1

le Bigoni, Stefania, Marangi, Giuseppe, Frangella, Silvia, Panfili, Arianna, Ognibene, Davide, Squeo, Gabriella Maria, Merla, Giuseppe, Zollino, Marcella
Foilsithe in Genes (Basel) (2020)

Submicroscopic Deletion in Patients with Williams-Beuren Syndrome Influences Expression Levels of the Nonhemizygous Flanking Genes

le Merla, Giuseppe, Howald, Cédric, Henrichsen, Charlotte N., Lyle, Robert, Wyss, Carine, Zabot, Marie-Thérèse, Antonarakis, Stylianos E., Reymond, Alexandre
Foilsithe 2006

VHL Frameshift Mutation as Target of Nonsense-Mediated mRNA Decay in Drosophila melanogaster and Human HEK293 Cell Line

le Micale, Lucia, Muscarella, Lucia Anna, Marzulli, Marco, Augello, Bartolomeo, Tritto, Patrizia, D'Agruma, Leonardo, Zelante, Leopoldo, Palumbo, Gioacchino, Merla, Giuseppe
Foilsithe 2009

Bronchial isomerism in a Kabuki syndrome patient with a novel mutation in MLL2 gene

le Cappuccio, Gerarda, Rossi, Alessandro, Fontana, Paolo, Acampora, Emma, Avolio, Valeria, Merla, Giuseppe, Zelante, Leopoldo, Secinaro, Aurelio, Andria, Generoso, Melis, Daniela
Foilsithe 2014

Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the Literature

le Prontera, Paolo, Rogaia, Daniela, Mencarelli, Amedea, Ottaviani, Valentina, Sallicandro, Ester, Guercini, Giorgio, Esposito, Susanna, Bersano, Anna, Merla, Giuseppe, Stangoni, Gabriela
Foilsithe in Int J Mol Sci (2017)

A New Split Hand/Foot Malformation with Long Bone Deficiency Familial Case

le Fusco, Carmela, Nittis, Pasquelena De, Alfaiz, Ali Abdullah, Pellico, Maria Teresa, Augello, Bartolomeo, Malerba, Natascia, Zelante, Leopoldo, Reymond, Alexandre, Merla, Giuseppe
Foilsithe in J Pediatr Genet (2016)

An atypical 7q11.23 deletion in a normal IQ Williams–Beuren syndrome patient

le Ferrero, Giovanni Battista, Howald, Cédric, Micale, Lucia, Biamino, Elisa, Augello, Bartolomeo, Fusco, Carmela, Turturo, Maria Giuseppina, Forzano, Serena, Reymond, Alexandre, Merla, Giuseppe
Foilsithe 2010

A Fish-Specific Transposable Element Shapes the Repertoire of p53 Target Genes in Zebrafish

le Micale, Lucia, Loviglio, Maria Nicla, Manzoni, Marta, Fusco, Carmela, Augello, Bartolomeo, Migliavacca, Eugenia, Cotugno, Grazia, Monti, Eugenio, Borsani, Giuseppe, Reymond, Alexandre, Merla, Giuseppe
Foilsithe 2012

Identification of tumor-associated cassette exons in human cancer through EST-based computational prediction and experimental validation

le Valletti Alessio, Anselmo Anna, Mangiulli Marina, Boria Ilenia, Mignone Flavio, Merla Giuseppe, D'Angelo Vincenzo, Tullo Apollonia, Sbisà Elisabetta, D'Erchia Anna, Pesole Graziano
Foilsithe 2010-09-01

Schilbach–Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene

le Prontera, Paolo, Rogaia, Daniela, Sallicandro, Ester, Mencarelli, Amedea, Imperatore, Valentina, Squeo, Gabriella Maria, Merla, Giuseppe, Elisei, Sandro, Moretti-Ferreira, Danilo, Esposito, Susanna, Stangoni, Gabriela
Foilsithe in Eur J Hum Genet (2019)

GRB10 Gene and Type 2 Diabetes in Whites

le Di Paola, Rosa, Wojcik, Joanna, Succurro, Elena, Marucci, Antonella, Chandalia, Manisha, Padovano, Libera, Powers, Christine, Merla, Giuseppe, Abate, Nicola, Sesti, Giorgio, Doria, Alessandro, Trischitta, Vincenzo
Foilsithe 2009