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Germana Meroni

Showing results (41-50 of 52) with videos related to

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Experimental Cell Research|July 25, 2003
BTBD1 and BTBD2 colocalize to cytoplasmic bodies with the RBCC/tripartite motif protein, TRIM5deltaLixin Xu, Lihong Yang, Prasun K Moitra, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
X-linked recessive chondrodysplasia punctata: spectrum of arylsulfatase E gene mutations and expanded clinical variabilityNicola Brunetti-Pierri, Maria Vittoria Andreucci, Rosaria Tuzzi, et al.
Archives of Toxicology|March 4, 2025
Comprehensive ubiquitome analysis reveals persistent mitochondrial remodeling disruptions from doxorubicin-induced cardiotoxicity in aged CD-1 male miceSofia Reis Brandão, Elisa Lazzari, Rui Vitorino, et al.
Plos One|July 26, 2012
TRIM27 negatively regulates NOD2 by ubiquitination and proteasomal degradationBirte Zurek, Ida Schoultz, Andreas Neerincx, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|September 29, 2007
Molecular classification of nodal metastasis in primary larynx squamous cell carcinomaFrancesco Carinci, Diego Arcelli, Lorenzo Lo Muzio, et al.
European Journal of Medical Genetics|June 25, 2013
Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterationsChiara Migliore, Emmanouil Athanasakis, Sophie Dahoun, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 11, 2007
Pharmacological enhancement of mutated alpha-glucosidase activity in fibroblasts from patients with Pompe diseaseGiancarlo Parenti, Alfredo Zuppaldi, M Gabriela Pittis, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 10, 2017
Pharmacological Enhancement of Mutated α-Glucosidase Activity in Fibroblasts from Patients with Pompe DiseaseGiancarlo Parenti, Alfredo Zuppaldi, M Gabriela Pittis, et al.
American Journal of Human Genetics|May 11, 2006
A mutation of beta -actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystoniaVincent Procaccio, Gloria Salazar, Shoichiro Ono, et al.
European Journal of Immunology|July 22, 2014
Midline 1 directs lytic granule exocytosis and cytotoxicity of mouse killer T cellsLasse Boding, Ann K Hansen, Germana Meroni, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Experimental Cell Research|July 25, 2003
BTBD1 and BTBD2 colocalize to cytoplasmic bodies with the RBCC/tripartite motif protein, TRIM5deltaLixin Xu, Lihong Yang, Prasun K Moitra, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
X-linked recessive chondrodysplasia punctata: spectrum of arylsulfatase E gene mutations and expanded clinical variabilityNicola Brunetti-Pierri, Maria Vittoria Andreucci, Rosaria Tuzzi, et al.
Archives of Toxicology|March 4, 2025
Comprehensive ubiquitome analysis reveals persistent mitochondrial remodeling disruptions from doxorubicin-induced cardiotoxicity in aged CD-1 male miceSofia Reis Brandão, Elisa Lazzari, Rui Vitorino, et al.
Plos One|July 26, 2012
TRIM27 negatively regulates NOD2 by ubiquitination and proteasomal degradationBirte Zurek, Ida Schoultz, Andreas Neerincx, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|September 29, 2007
Molecular classification of nodal metastasis in primary larynx squamous cell carcinomaFrancesco Carinci, Diego Arcelli, Lorenzo Lo Muzio, et al.
European Journal of Medical Genetics|June 25, 2013
Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterationsChiara Migliore, Emmanouil Athanasakis, Sophie Dahoun, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 11, 2007
Pharmacological enhancement of mutated alpha-glucosidase activity in fibroblasts from patients with Pompe diseaseGiancarlo Parenti, Alfredo Zuppaldi, M Gabriela Pittis, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 10, 2017
Pharmacological Enhancement of Mutated α-Glucosidase Activity in Fibroblasts from Patients with Pompe DiseaseGiancarlo Parenti, Alfredo Zuppaldi, M Gabriela Pittis, et al.
American Journal of Human Genetics|May 11, 2006
A mutation of beta -actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystoniaVincent Procaccio, Gloria Salazar, Shoichiro Ono, et al.
European Journal of Immunology|July 22, 2014
Midline 1 directs lytic granule exocytosis and cytotoxicity of mouse killer T cellsLasse Boding, Ann K Hansen, Germana Meroni, et al.
Pageof 6