Jouni Vesa
University of California, Irvine(US)
Publications by Year
Research Areas
Lysosomal Storage Disorders Research, Cellular transport and secretion, Mitochondrial Function and Pathology, Autophagy in Disease and Therapy, Amyotrophic Lateral Sclerosis Research
Most-Cited Works
- → Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis(1995)737 cited
- → VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD(2010)438 cited
- → GRACILE Syndrome, a Lethal Metabolic Disorder with Iron Overload, Is Caused by a Point Mutation in BCS1L(2002)294 cited
- → VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: Review of a unique disorder(2008)231 cited
- → The Multiple Faces of Valosin-Containing Protein-Associated Diseases: Inclusion Body Myopathy with Paget’s Disease of Bone, Frontotemporal Dementia, and Amyotrophic Lateral Sclerosis(2011)135 cited
- → Neuronal Ceroid Lipofuscinoses Are Connected at Molecular Level: Interaction of CLN5 Protein with CLN2 and CLN3(2002)124 cited
- → VCP Associated Inclusion Body Myopathy and Paget Disease of Bone Knock-In Mouse Model Exhibits Tissue Pathology Typical of Human Disease(2010)122 cited
- → Two Motifs Target Batten Disease Protein CLN3 to Lysosomes in Transfected Nonneuronal and Neuronal Cells(2003)118 cited
- → Mice with Ppt1Δex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons(2004)90 cited
- → A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging(2004)86 cited