MERONI, GERMANA
MERONI, GERMANA
Dipartimento di Scienze della Vita
Docenti di ruolo di IIa fascia
A CLUSTER OF SULFATASE GENES ON XP22.3 - MUTATIONS IN CHONDRODYSPLASIA PUNCTATA (CDPX) AND IMPLICATIONS FOR WARFARIN EMBRYOPATHY
1995-01-01 Franco, Brunella; Meroni, Germana; Parenti, Giancarlo; Levilliers, Jaqueline; Bernard, Loris; Gebbia, Marinella; Cox, Liza; Maroteaux, Pierre; Sheffield, Leslie; Rappold, Gudrun A; Andria, Generoso; Petit, Christine; Ballabio, Andrea
A MID1 mutation associated with reduced penetrance of X-linked Opitz G/BBB syndrome
2010-01-01 Ruiter, Marikena; Kamsteeg, Erik Jana; Meroni, Germana; de Vries, Bert B. A.
A mutation of beta-actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia
2006-01-01 Procaccio, V; Salazar, G; Ono, S; Styers, Ml; Gearing, M; Davila, A; Jimenez, R; Juncos, J; Gutekunst, Ca; Meroni, Germana; Fontanella, B; Sontag, E; Sontag, Jm; Faundez, V; Wainer, B. H.
A structure-function study of MID1 mutations associated with a mild Opitz phenotype
2006-01-01 Mnayer, Laila; Khuri, Sawsan; Merheby, Hassan AA; Meroni, Germana; Elsas, Louis J.
A unique missense mutation in the RING domain impairs MID1 E3 ubiquitin ligase activity and localisation and is associated with uncommon Opitz Syndrome-like signs
2024-01-01 Mascaro, Martina; D'Ambrosio, Luigi; Lazzari, Elisa; Almoguera, Berta; Swafiri, Saoud Tahsin; Zanchetta, Melania Eva; Meroni, Germana
An online tool for fetal fraction prediction based on direct size distribution analysis of maternal cell-free DNA
2020-01-01 Bedon, Luca; Vuch, Josef; Monego, Simeone Dal; Meroni, Germana; Pecile, Vanna; Licastro, Danilo
Analysis of candidate genes at the IBGC1 locus associated with idiopathic basal ganglia calcification ("Fahr's disease")
2007-01-01 Oliveira, Jrm; Sobrido, Mj; Spiteri, E; Hopfer, S; Meroni, Germana; Petek, E; Baquero, M; Geschwind, Dh
Analysis of the Zn-Binding Domains of TRIM32, the E3 Ubiquitin Ligase Mutated in Limb Girdle Muscular Dystrophy 2H
2019-01-01 Lazzari, Elisa; El-Halawany, Medhat; De March, Matteo; Valentino, Floriana; Cantatore, Francesco; Migliore, Chiara; Onesti, Silvia; Meroni, Germana
Assignement of the E1A-regulated transcription factor gene(E4F17 to human chromosome band 16p13.3 by in situ hybridization and somatic cell hybrids
1998-01-01 Saccone, S.; Sandy, P.; Meroni, Germana; Gostissa, M.; DEL SAL, Giannino
Biochemical characterization of arylsulfatase E and functional analysis of mutations found in patients with X-linked chondrodysplasia punctata
1998-01-01 Daniele, Aurora; Parenti, Giancarlo; D'Addio, Maddalena; Andria, Generoso; Ballabio, Andrea; Meroni, Germana
BTBD1 and BTBD2 colocalize to cytoplasmic bodies with the RBCC/tripartite motif protein, TRIM5 delta
2003-01-01 Xu, Lx; Yang, Lh; Moitra, Pk; Hashimoto, K; Rallabhandi, P; Kaul, S; Meroni, Germana; Jensen, Jp; Weissman, Am; D'Arpa, P.
Cellular Function of TRIM E3 Ubiquitin Ligases in Health and Disease
2022-01-01 Meroni, G.; Desagher, S.
Cellular TRIM33 restrains HIV-1 infection by targeting viral integrase for proteasomal degradation.
2019-01-01 Ali, Hashim; Mano, Miguel; Braga, Luca; Naseem, Asma; Marini, Bruna; My Vu, Diem; Collesi, Chiara; Meroni, Germana; Lusic, Marina; Giacca, Mauro
Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region
1996-01-01 Meroni, Germana; Franco, Brunella; Archidiacono, Nicoletta; Messali, Silvia; Andolfi, Grazia; Rocchi, Mariano; Ballabio, Andrea
Comparative mapping of Xp22 genes in hominoids - Evolutionary linear instability of their Y homologues
1997-01-01 Glaser, B; Grutzner, F; Taylor, K; Schiebel, K; Meroni, Germana; Tsioupra, K; Pasantes, J; Rietschel, W; Toder, R; Willmann, U; Zeitler, S; Yen, P; Ballabio, A; Rappold, G; Schempp, W.
Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations
2013-01-01 Migliore, CHIARA MARIA; Athanasakis, Emmanouil; Dahoun, S; Wonkam, A; Lees, M; Calabrese, O; Connell, F; Lynch, Sa; Izzi, C; Pompilii, E; Thakur, S; van Maarle, M; Wilson, Lc; Meroni, Germana
DEFINITION OF THE TRANSCRIPTION INITIATION SITE OF HUMAN PLASMINOGEN GENE IN LIVER AND NON HEPATIC CELL-LINES
1990-01-01 Malgaretti, N; Bruno, L; Pontoglio, M; Candiani, G; Meroni, Germana; Ottolenghi, S; Taramelli, R.
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome
2004-01-01 Pinson, L; Auge, J; Audollent, S; Mattei, G; Etchevers, H; Gigarel, N; Razavi, F; Lacombe, D; Odent, S; Le Merrer, M; Amiel, J; Munnich, A; Meroni, Germana; Lyonnet, S; Vekemans, M; Attie Bitach, T.
Emerging Roles of the TRIM E3 Ubiquitin Ligases MID1 and MID2 in Cytokinesis
2019-01-01 Zanchetta, Melania Eva; Meroni, Germana
Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle
1999-01-01 Cainarca, Silvia; Messali, Silvia; Ballabio, Andrea; Meroni, Germana