Get started
Award

GGP13222

Funded outputs count: 10
Funder award ID: GGP13222
OpenAlex ID: G1308648708
Age-Associated Loss of OPA1 in Muscle Impacts Muscle Mass, Metabolic Homeostasis, Systemic Inflammation, and Epithelial Senescence
2017 · Caterina Tezze, Vanina Romanello, et al. · Cell Metabolism · 568
PDF
MCM5: a new actor in the link between DNA replication and Meier-Gorlin syndrome
2017 · Annalisa Vetro, Salvatore Savasta, et al. · European Journal of Human Genetics · 77
Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients
2017 · Doriana Borgia, Adriana Malena, et al. · Human Molecular Genetics · 62
PDF
TheCOQ2genotype predicts the severity of coenzyme Q10deficiency
2016 · Maria Andrea Desbats, Valeria Morbidoni, et al. · Human Molecular Genetics · 67
Coenzyme Q biosynthesis in health and disease
2016 · Manuel Jesús Acosta, Luis Vazquez Fonseca, et al. · Biochimica et Biophysica Acta (BBA) - Bioenergetics · 236
PDF
Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations
2015 · Michelangelo Cao, Marta Donà, et al. · Neurogenetics · 35
Severe encephalopathy associated to pyruvate dehydrogenase mutations and unbalanced coenzyme Q10 content
2015 · Claudio Asencio, María A Rodríguez-Hernandez, et al. · European Journal of Human Genetics · 16
Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure
2015 · Maria Andrea Desbats, Annalisa Vetro, et al. · European Journal of Human Genetics · 51
PDF
Molecular characterization of the human COQ5 C-methyltransferase in coenzyme Q10 biosynthesis
2014 · Theresa P.T. Nguyen, Alberto Casarin, et al. · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · 58
PDF
Primary Coenzyme Q 10 Deficiency
1993 · Adam Mp, Ardinger Hh, et al. · Padua Research Archive (University of Padova) · 38
PDF
Year
Topic