Valentina Muto

Mutations in PAX2 Associate with Adult-Onset FSGS

Moumita Barua, Emilia Stellacci, Lorenzo Stella et al. · Journal of the American Society of Nephrology · 2014 · 122 citations · Full text

Glomerulonephritis, Urology, Pax2 Associate +15

Mutations in ZBTB20 cause Primrose syndrome

Viviana Cordeddu, B. Redeker, Emilia Stellacci et al. · Nature Genetics · 2014 · 96 citations

Genetic Disorder, Genetics, Inherited Metabolic Disease +2

Receptor Recognition of and Immune Intracellular Pathways for <i>Veillonella parvula</i> Lipopolysaccharide

Giovanni Matera, Valentina Muto, M. Vinci et al. · Clinical and Vaccine Immunology · 2009 · 71 citations · Full text

Repression of Interferon Regulatory Factor 1 by Hepatitis C Virus Core Protein Results in Inhibition of Antiviral and Immunomodulatory Genes

Anna Rita Ciccaglione, Emilia Stellacci, Cinzia Marcantonio et al. · Journal of Virology · 2006 · 65 citations · Full text

Hcv Structural Proteins, Systems Biology, Molecular Virology +14

SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling

Yuh‐Charn Lin, Marcello Niceta, Valentina Muto et al. · The American Journal of Human Genetics · 2020 · 64 citations · Full text

Developmental Anomaly, Sclerostin, Developmental Biology +9