Rezultati - Giuseppe Merla
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1
E3 Ubiquitin Ligase TRIM Proteins, Cell Cycle and Mitosis od Santina Venuto, Giuseppe Merla
Izdano 2019Revisão -
2
Supravalvular Aortic Stenosis od Giuseppe Merla, Nicola Brunetti‐Pierri, Pasquale Piccolo, Lucia Micale, Maria Nicla Loviglio
Izdano 2012Revisão -
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Submicroscopic Deletion in Patients with Williams-Beuren Syndrome Influences Expression Levels of the Nonhemizygous Flanking Genes od Giuseppe Merla, Cédric Howald, Charlotte N. Henrichsen, Robert Lyle, Carine Wyss, M. T. Zabot, Stylianos E. Antonarakis, Alexandre Reymond
Izdano 2006Artigo -
5
An atypical 7q11.23 deletion in a normal IQ Williams–Beuren syndrome patient od Giovanni Battista Ferrero, Cédric Howald, Lucia Micale, Elisa Biamino, Bartolomeo Augello, Carmela Fusco, Maria Giuseppina Turturo, Serena Forzano, Alexandre Reymond, Giuseppe Merla
Izdano 2009Artigo -
6
Prevalence of Apolipoprotein E Alleles in Healthy Subjects and Survivors of Ischemic Stroke od Maurizio Margaglione, Davide Seripa, Carolina Gravina, Elvira Grandone, Gennaro Vecchione, Giuseppe Cappucci, Giuseppe Merla, Sara Papa, Alfredo Postiglione, Giovanni Di Minno, Vito Michele Fazio
Izdano 1998Artigo -
7
Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases od Mirella Filocamo, Chiara Baldo, Stefano Goldwurm, Alessandra Renieri, C. Angelini, Maurizio Moggio, Marina Mora, Giuseppe Merla, Luisa Politano, Barbara Garavaglia, Lorena Casareto, Francesca Bricarelli
Izdano 2013Artigo -
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Schilbach–Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene od Paolo Prontera, Daniela Rogaia, Ester Sallicandro, Amedea Mencarelli, Valentina Imperatore, Gabriella Maria Squeo, Giuseppe Merla, Sandro Elisei, Danilo Moretti‐Ferreira, Susanna Esposito, Gabriela Stangoni
Izdano 2019Artigo -
10
Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits od Carmela Fusco, Lucia Micale, Bartolomeo Augello, Maria Teresa Pellico, Deny Menghini, Paolo Alfieri, M. Cristina Digilio, Barbara Mandriani, Massimo Carella, Orazio Palumbo, Stefano Vicari, Giuseppe Merla
Izdano 2013Artigo -
11
Identification and characterization of seven novel mutations of elastin gene in a cohort of patients affected by supravalvular aortic stenosis od Lucia Micale, Maria Giuseppina Turturo, Carmela Fusco, Bartolomeo Augello, L.A. Pérez Jurado, Claudia Izzi, M. Cristina Digilio, Donatella Milani, Elisabetta Lapi, Leopoldo Zelante, Giuseppe Merla
Izdano 2009Artigo -
12
Two high throughput technologies to detect segmental aneuploidies identify new Williams-Beuren syndrome patients with atypical deletions od Cédric Howald, Giuseppe Merla, M. Cristina Digilio, Styliani Amenta, Robert Lyle, Samuel Deutsch, Urmila Choudhury, Armand Bottani, Stylianos E. Antonarakis, Helen Fryssira, Bruno Dallapiccola, Alexandre Reymond
Izdano 2005Carta -
13
Clock-genes and mitochondrial respiratory activity: Evidence of a reciprocal interplay od Rosella Scrima, Olga Cela, Giuseppe Merla, Bartolomeo Augello, Rosa Rubino, Giovanni Quarato, Sabino Fugetto, Marta Menga, Luise Fuhr, Angela Relógio, Cláudia Piccoli, Gianluigi Mazzoccoli, Nazzareno Capitanio
Izdano 2016Artigo -
14
The ubiquitin ligase TRIM32 promotes the autophagic response to Mycobacterium tuberculosis infection in macrophages od Alessandra Romagnoli, Martina Di Rienzo, Elisa Petruccioli, Carmela Fusco, Ivana Palucci, Lucia Micale, Tommaso Mazza, Giovanni Delogu, Giuseppe Merla, Delia Goletti, Mauro Piacentini, Gian María Fimia
Izdano 2023Artigo -
15
Dissecting KMT2D missense mutations in Kabuki syndrome patients od Dario Cocciadiferro, Bartolomeo Augello, Pasquelena De Nittis, Jiyuan Zhang, Barbara Mandriani, Natascia Malerba, Gabriella Maria Squeo, Alessandro Romano, Barbara Piccinni, Tiziano Verri, Lucia Micale, Laura Pasqualucci, Giuseppe Merla
Izdano 2018Artigo -
16
TRIM8 modulates p53 activity to dictate cell cycle arrest od Mariano Francesco Caratozzolo, Lucia Micale, Maria Giuseppina Turturo, S Cornacchia, Carmela Fusco, Flaviana Marzano, Bartolomeo Augello, Anna Maria D’Erchia, Luisa Guerrini, Graziano Pesole, Elisabetta Sbisà, Giuseppe Merla, Apollonia Tullo
Izdano 2012Artigo -
17
The tripartite motif family identifies cell compartments od Alexandre Reymond, Germana Meroni, Anna Fantozzi, Giuseppe Merla, Stefano Cairo, Lucilla Luzi, Daniela Riganelli, Elena Zanaria, Silvia Messali, Silvia Cainarca, Alessandro Guffanti, Saverio Minucci, Pier Giuseppe Pelicci, Andrea Ballabio
Izdano 2001Artigo -
18
The E3-Ubiquitin Ligase TRIM50 Interacts with HDAC6 and p62, and Promotes the Sequestration and Clearance of Ubiquitinated Proteins into the Aggresome od Carmela Fusco, Lucia Micale, Mikhail V. Egorov, Maria Monti, Ester Valentina D’Addetta, Bartolomeo Augello, Flora Cozzolino, Alessia Calcagnì, Andrea Fontana, Roman Polishchuk, Gérard Didelot, Alexandre Reymond, Piero Pucci, Giuseppe Merla
Izdano 2012Artigo -
19
TRIM50 regulates Beclin 1 proautophagic activity od Carmela Fusco, Barbara Mandriani, Martina Di Rienzo, Lucia Micale, Natascia Malerba, Dario Cocciadiferro, Eva Sjøttem, Bartolomeo Augello, Gabriella Maria Squeo, Maria Teresa Pellico, Ashish Jain, Terje Johansen, Gian María Fimia, Giuseppe Merla
Izdano 2018Artigo -
20
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors od Francesca Cillo, Emma Coppola, Federico Habetswallner, Francesco Cecere, Laura Pignata, Elisabetta Toriello, A. De Rosa, Laura Grilli, Antonio Ammendola, Paolo Salerno, Roberta Romano, Emilia Cirillo, Giuseppe Merla, Andrea Riccio, Claudio Pignata, Giuliana Giardino
Izdano 2024Artigo
Iskalna orodja:
Sorodne teme
Biology
Gene
Genetics
Medicine
Phenotype
Internal medicine
Allele
Gene expression
Cell biology
Mutation
Bioinformatics
Cancer research
DNA methylation
Haploinsufficiency
Apoptosis
Methylation
Missense mutation
Neuroscience
Chromosome
Computational biology
DNA
Genome
Genotype
Pathology
Autophagy
Biochemistry
Cancer
Cognition
Copy-number variation
Disease