Homeostasis of eukaryotic cells is largely dependent on dynamic com-partmentalization of the endo-membrane system. The membrane traf-ficking linking different organelles is essential to maintain a proper composition of various compartments as well as to transport various molecules to appropriate compartments. Respect to other cell types nervous system is more sensitive to alterations of the membrane traf-ficking. In the last years, we studied the role of endosomal trafficking in neurodegeneration focusing on two nervous system disorders, Charcot-Marie Tooth disease 4 J (CMT4 J) and a new form of autosomal recessive early-onset parkinsonism (PARK20), both caused by muta-tions of an i...
Although the pathogenesis of Parkinson's disease (PD) is considered multifactorial, evidence from ge...
Abstract: Autosomal dominant mutations in LITAF are responsible for the rare demyelinating periphera...
Lysosomal storage disorders (LSDs) are rare diseases caused by inherited mutations in genes coding f...
Homeostasis of eukaryotic cells is largely dependent on dynamic com-partmentalization of the endo-me...
Recently, a new form of autosomal recessive early-onset parkinsonism (PARK20), due to mutations in t...
Homeostasis of eukaryotic cells is largely dependent on the dynamic compartmentalization of the endo...
Homeostasis of eukaryotic cells is largely dependent on dynamic compartmentalization of the endo-mem...
Endo-lysosomal pathways are essential in maintaining protein homeostasis in the cell. Numerous genes...
Increasingly, genetic, cell biological, and in vivo work emphasizes the role of the endolysosomal sy...
Abstract Defects in membrane trafficking and degrada-tion are hallmarks of most, and maybe all, neur...
Endo-lysosomal pathways are essential in maintaining protein homeostasis in the cell. Numerous genes...
Although the pathogenesis of Parkinson's disease (PD) is considered multifactorial, evidence from ge...
Abnormal accumulation of the protein α- synuclein (α-syn) into proteinaceous inclusions called Lewy ...
Lysosomal function has a central role in maintaining neuronal homeostasis, and, accordingly, lysosom...
The small GTPase RAB7A regulates late stages of the endocytic pathway and plays specific roles in ne...
Although the pathogenesis of Parkinson's disease (PD) is considered multifactorial, evidence from ge...
Abstract: Autosomal dominant mutations in LITAF are responsible for the rare demyelinating periphera...
Lysosomal storage disorders (LSDs) are rare diseases caused by inherited mutations in genes coding f...
Homeostasis of eukaryotic cells is largely dependent on dynamic com-partmentalization of the endo-me...
Recently, a new form of autosomal recessive early-onset parkinsonism (PARK20), due to mutations in t...
Homeostasis of eukaryotic cells is largely dependent on the dynamic compartmentalization of the endo...
Homeostasis of eukaryotic cells is largely dependent on dynamic compartmentalization of the endo-mem...
Endo-lysosomal pathways are essential in maintaining protein homeostasis in the cell. Numerous genes...
Increasingly, genetic, cell biological, and in vivo work emphasizes the role of the endolysosomal sy...
Abstract Defects in membrane trafficking and degrada-tion are hallmarks of most, and maybe all, neur...
Endo-lysosomal pathways are essential in maintaining protein homeostasis in the cell. Numerous genes...
Although the pathogenesis of Parkinson's disease (PD) is considered multifactorial, evidence from ge...
Abnormal accumulation of the protein α- synuclein (α-syn) into proteinaceous inclusions called Lewy ...
Lysosomal function has a central role in maintaining neuronal homeostasis, and, accordingly, lysosom...
The small GTPase RAB7A regulates late stages of the endocytic pathway and plays specific roles in ne...
Although the pathogenesis of Parkinson's disease (PD) is considered multifactorial, evidence from ge...
Abstract: Autosomal dominant mutations in LITAF are responsible for the rare demyelinating periphera...
Lysosomal storage disorders (LSDs) are rare diseases caused by inherited mutations in genes coding f...