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Germana Meroni

Showing results (21-30 of 52) with videos related to

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The Biochemical Journal|December 15, 2010
Functional interactions between ubiquitin E2 enzymes and TRIM proteinsLuisa M Napolitano, Ellis G Jaffray, Ronald T Hay, et al.
Clinical Dysmorphology|July 31, 2010
A MID1 mutation associated with reduced penetrance of X-linked Opitz G/BBB syndromeMariken Ruiter, Erik-Jan Kamsteeg, Germana Meroni, et al.
Molecular Genetics and Metabolism|December 28, 2005
A structure-function study of MID1 mutations associated with a mild Opitz phenotypeLaila Mnayer, Sawsan Khuri, Hassan Al-Ali Merheby, et al.
Biotechniques|November 30, 2020
An online tool for fetal fraction prediction based on direct size distribution analysis of maternal cell-free DNALuca Bedon, Josef Vuch, Simeone Dal Monego, et al.
Oncogene|March 1, 2005
PML interacts with Myc, and Myc target gene expression is altered in PML-null fibroblastsStefano Cairo, Francesca De Falco, Mariateresa Pizzo, et al.
Human Mutation|November 13, 2007
Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2HValentina Saccone, Michela Palmieri, Luigia Passamano, et al.
Cells|April 30, 2021
TRIM32 and Malin in Neurological and Neuromuscular Rare DiseasesLorena Kumarasinghe, Lu Xiong, Maria Adelaida Garcia-Gimeno, et al.
The FEBS Journal|June 16, 2026
TRIM32 controls timely cell cycle exit in muscular differentiation through downregulation of c-Myc mRNALu Xiong, Elisa Lazzari, Sabrina Pacor, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 20, 2024
A unique missense mutation in the RING domain impairs MID1 E3 ubiquitin ligase activity and localisation and is associated with uncommon Opitz Syndrome-like signsMartina Mascaro, Luigi D'Ambrosio, Elisa Lazzari, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 26, 2010
Lack of Mid1, the mouse ortholog of the Opitz syndrome gene, causes abnormal development of the anterior cerebellar vermisAlessio Lancioni, Mariateresa Pizzo, Bianca Fontanella, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
The Biochemical Journal|December 15, 2010
Functional interactions between ubiquitin E2 enzymes and TRIM proteinsLuisa M Napolitano, Ellis G Jaffray, Ronald T Hay, et al.
Clinical Dysmorphology|July 31, 2010
A MID1 mutation associated with reduced penetrance of X-linked Opitz G/BBB syndromeMariken Ruiter, Erik-Jan Kamsteeg, Germana Meroni, et al.
Molecular Genetics and Metabolism|December 28, 2005
A structure-function study of MID1 mutations associated with a mild Opitz phenotypeLaila Mnayer, Sawsan Khuri, Hassan Al-Ali Merheby, et al.
Biotechniques|November 30, 2020
An online tool for fetal fraction prediction based on direct size distribution analysis of maternal cell-free DNALuca Bedon, Josef Vuch, Simeone Dal Monego, et al.
Oncogene|March 1, 2005
PML interacts with Myc, and Myc target gene expression is altered in PML-null fibroblastsStefano Cairo, Francesca De Falco, Mariateresa Pizzo, et al.
Human Mutation|November 13, 2007
Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2HValentina Saccone, Michela Palmieri, Luigia Passamano, et al.
Cells|April 30, 2021
TRIM32 and Malin in Neurological and Neuromuscular Rare DiseasesLorena Kumarasinghe, Lu Xiong, Maria Adelaida Garcia-Gimeno, et al.
The FEBS Journal|June 16, 2026
TRIM32 controls timely cell cycle exit in muscular differentiation through downregulation of c-Myc mRNALu Xiong, Elisa Lazzari, Sabrina Pacor, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 20, 2024
A unique missense mutation in the RING domain impairs MID1 E3 ubiquitin ligase activity and localisation and is associated with uncommon Opitz Syndrome-like signsMartina Mascaro, Luigi D'Ambrosio, Elisa Lazzari, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 26, 2010
Lack of Mid1, the mouse ortholog of the Opitz syndrome gene, causes abnormal development of the anterior cerebellar vermisAlessio Lancioni, Mariateresa Pizzo, Bianca Fontanella, et al.
Pageof 6