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Germana Meroni

Showing results (11-20 of 52) with videos related to

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Cells|January 21, 2022
Microtubular TRIM36 E3 Ubiquitin Ligase in Embryonic Development and SpermatogenesisMartina Mascaro, Inês Lages, Germana Meroni
Human Mutation|March 25, 2008
MID1 mutations in patients with X-linked Opitz G/BBB syndromeBianca Fontanella, Giorgio Russolillo, Germana Meroni
Gene|April 14, 2020
The MID1 gene product in physiology and diseaseRossella Baldini, Martina Mascaro, Germana Meroni
BMC Cell Biology|April 9, 2004
Mig12, a novel Opitz syndrome gene product partner, is expressed in the embryonic ventral midline and co-operates with Mid1 to bundle and stabilize microtubulesCaterina Berti, Bianca Fontanella, Rosa Ferrentino, et al.
European Journal of Human Genetics : EJHG|December 4, 2002
Molecular and biochemical characterisation of a novel sulphatase gene: Arylsulfatase G (ARSG)Paola Ferrante, Silvia Messali, Germana Meroni, et al.
Gene|July 13, 2004
Identification and biochemical characterization of an avian sulfatase homologous to the human ARSE, the gene for X-linked chondrodysplasia punctataPaola Ferrante, Silvia Messali, Andrea Ballabio, et al.
Mechanisms of Development|April 19, 2002
TRIM9 is specifically expressed in the embryonic and adult nervous systemCaterina Berti, Silvia Messali, Andrea Ballabio, et al.
BMC Evolutionary Biology|August 5, 2008
Genomic analysis of the TRIM family reveals two groups of genes with distinct evolutionary propertiesMarco Sardiello, Stefano Cairo, Bianca Fontanella, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|August 2, 2017
The E3 ubiquitin ligase MID1/TRIM18 promotes atypical ubiquitination of the BRCA2-associated factor 35, BRAF35Melania E Zanchetta, Luisa M R Napolitano, Danilo Maddalo, et al.
Human Mutation|January 16, 2007
MID1 mutation screening in a large cohort of Opitz G/BBB syndrome patients: twenty-nine novel mutations identifiedRosa Ferrentino, Maria Teresa Bassi, David Chitayat, et al.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
Cells|January 21, 2022
Microtubular TRIM36 E3 Ubiquitin Ligase in Embryonic Development and SpermatogenesisMartina Mascaro, Inês Lages, Germana Meroni
Human Mutation|March 25, 2008
MID1 mutations in patients with X-linked Opitz G/BBB syndromeBianca Fontanella, Giorgio Russolillo, Germana Meroni
Gene|April 14, 2020
The MID1 gene product in physiology and diseaseRossella Baldini, Martina Mascaro, Germana Meroni
BMC Cell Biology|April 9, 2004
Mig12, a novel Opitz syndrome gene product partner, is expressed in the embryonic ventral midline and co-operates with Mid1 to bundle and stabilize microtubulesCaterina Berti, Bianca Fontanella, Rosa Ferrentino, et al.
European Journal of Human Genetics : EJHG|December 4, 2002
Molecular and biochemical characterisation of a novel sulphatase gene: Arylsulfatase G (ARSG)Paola Ferrante, Silvia Messali, Germana Meroni, et al.
Gene|July 13, 2004
Identification and biochemical characterization of an avian sulfatase homologous to the human ARSE, the gene for X-linked chondrodysplasia punctataPaola Ferrante, Silvia Messali, Andrea Ballabio, et al.
Mechanisms of Development|April 19, 2002
TRIM9 is specifically expressed in the embryonic and adult nervous systemCaterina Berti, Silvia Messali, Andrea Ballabio, et al.
BMC Evolutionary Biology|August 5, 2008
Genomic analysis of the TRIM family reveals two groups of genes with distinct evolutionary propertiesMarco Sardiello, Stefano Cairo, Bianca Fontanella, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|August 2, 2017
The E3 ubiquitin ligase MID1/TRIM18 promotes atypical ubiquitination of the BRCA2-associated factor 35, BRAF35Melania E Zanchetta, Luisa M R Napolitano, Danilo Maddalo, et al.
Human Mutation|January 16, 2007
MID1 mutation screening in a large cohort of Opitz G/BBB syndrome patients: twenty-nine novel mutations identifiedRosa Ferrentino, Maria Teresa Bassi, David Chitayat, et al.
Pageof 6