Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Aldo Mari"'
Autor:
Juan Cristóbal Guarello
Una crónica sobre la increíble trayectoria vital de Aldo Marín, un revolucionario chileno desconocido hasta hoy La madrugada del jueves 5 de agosto de 1977 dos jóvenes murieron en Turín mientras intentaban cometer un atentado contra el diario La
Autor:
Vincenzo Silani, Giuseppe Calabrese, L. Giardino, Bruno Dallapiccola, Alessia Colosimo, Antonio Pizzuti, Donata Penso, Francesca Amati, Laura Calzà, Antonia Ratti, Gugliemo Scarlato, Aldo Mari, Giandomenico Palka, Giuseppe Novelli
Publikováno v:
Human Molecular Genetics. 5:953-958
The Drosophila dishevelled gene (dsh) encodes a secreted glycoprotein, which regulates cell proliferation, acting as a transducer molecule for developmental processes, including segmentation and neuroblast specification. We have isolated and characte
Autor:
Mauro Magnani, Franco Pandolfi, Roberta Bordoni, Alessia Colosimo, Aldo Mari, Antonia Ratti, Antonio Baldini, Giuseppe Novelli, Francesca Amati, Rita Crinelli, Emanuela Conti, Bruno Dallapiccola, Mario Bengala, Antonio Pizzuti, Federica Sangiuolo
Publikováno v:
Biochimica et biophysica acta. 1396(2)
We report the genomic organization, RNA and protein expression patterns of the gene encoding for the human homolog of the yeast ubiquitin fusion-degradation protein-1 (UFD1L). This enzyme is involved in a ubiquitin-dependent proteolytic pathway (UFD)
Autor:
Aldo Mari, Mario Bengala, Bruno Dallapiccola, Francesca Amati, Giuseppe Novelli, Emanuela Conti
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42a61d253233fd059917b2931c3e2ad6
http://hdl.handle.net/2108/49661
http://hdl.handle.net/2108/49661
Autor:
Guglielmo Scarlato, Silvia K. Nicolis, Francesca Amati, Giuseppe Calabrese, Aldo Mari, Giuseppe Novelli, Sergio Ottolenghi, Antonio Pizzuti, Vincenzo Silani, Antonia Ratti, Bruno Dallapiccola, Bruno Marino
Publikováno v:
Human molecular genetics. 6(2)
The CATCH 22 acronym outlines the main clinical features of 22q11.2 deletions (cardiac defects, abnormal facies, thymic hypoplasia, cleft palate and hypocalcemia), usually found in DiGeorge (DGS) and velo-cardio-facial (VCFS) syndromes. Hemizygosity
Autor:
V. Colloridi, Bruno Dallapiccola, G. Sebastio, Giuseppe Novelli, Francesca Amati, Rita Mingarelli, Aldo Mari, Aldo Giannotti
Publikováno v:
Human genetics. 96(4)
Williams syndrome (WS) is caused by deletion of the elastin (ELN) gene. We have analyzed an intragenic restriction fragment length polymorphism (RFLP) and the gene dosage of ELN using a new probe (FP4) in a series of 60 sporadic patients with a clini
Autor:
Francesca Amati, Rita Mingarelli, Aldo Giannotti, Bruno Dallapiccola, Bruno Marino, Giuseppe Novelli, Aldo Mari, Massimo Gennarelli, Maria Cristina Digilio
Publikováno v:
American journal of medical genetics. 57(3)
Atrioventricular canal defects (AVCD) constitute the predominant congenital heart defect in Down`s syndrome. For this reason, a candidate gene involved in atrioventricular canal development was previously searched and excluded in dominant pedigrees o
Autor:
Bruno Dallapiccola, Bruno Marino, Aldo Giannotti, Francesca Amati, Rita Mingarelli, Giuseppe Novelli, Maria Cristina Digilio, Aldo Mari
Publikováno v:
Human Genetics. 95
Tetralogy of Fallot (TF) is a congenital conotruncal heart defect commonly found in DiGeorge (DGS) and velo-cardio-facial (VCFS) syndromes. The deletion of chromosome 22q11 (del22q11) is a well established cause of DGS and VCFS, and it has been demon
Autor:
de Rivero, Oscar Espinosa
Publikováno v:
Antropológica (02549212). 2009, Vol. 27 Issue 27, p123-168. 46p.