Manuela Morleo

An organelle-specific protein landscape identifies novel diseases and molecular mechanisms

Karsten Boldt, Jeroen van Reeuwijk, Qianhao Lu et al. · Nature Communications · 2016 · 255 citations · Full text

Mutations in COX7B Cause Microphthalmia with Linear Skin Lesions, an Unconventional Mitochondrial Disease

Alessia Indrieri, Vanessa A. van Rahden, Valeria Tiranti et al. · The American Journal of Human Genetics · 2012 · 170 citations · Full text

Disease Mechanism, Mitochondrial Function, Cutaneous Biology +9

Mutations of the Mitochondrial Holocytochrome c–Type Synthase in X-Linked Dominant Microphthalmia with Linear Skin Defects Syndrome

Isabella Wimplinger, Manuela Morleo, Georg Rosenberger et al. · The American Journal of Human Genetics · 2006 · 161 citations · Full text

Skin Development, Mendelian Disorder, Genetic Disorder +8

Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators

Yangfan P. Liu, I-Chun Tsai, Manuela Morleo et al. · Journal of Clinical Investigation · 2014 · 95 citations · Full text

Proteasomal Degradation, Signal Transduction, Developmental Biology +14

Regulation of autophagosome biogenesis by OFD1‐mediated selective autophagy

Manuela Morleo, Simona Brillante, Umberto Formisano et al. · The EMBO Journal · 2020 · 53 citations · Full text

Cell Autophagy, Autophagy, Autophagosome Biogenesis +2