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» Authors » Jouni Vesa

Jouni Vesa

Explore the profile of Jouni Vesa including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 21
Citations 1034
Followers 0
Related Specialties
Molecular Biology
Neurology
Cell Biology
Top 10 Co-Authors
Virginia E Kimonis
Leena Peltonen
Angele Nalbandian
Anu Jalanko
Hailing Su
Barbara Martin
Eric Dec
Anna-Liisa Fabritius
Outi Kopra
Vincent Caiozzo
Published In
Hum Mol Genet
Clin Transl Sci
Mol Biol Cell
Neurobiol Dis
Neurosci Lett
Affiliations
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Recent Articles
1.
Increased HIV-1 superinfection risk in carriers of specific human leukocyte antigen alleles
Vesa J, Chaillon A, Wagner G, Anderson C, Richman D, Smith D, et al.
AIDS . 2017 Mar; 31(8):1149-1158. PMID: 28244954
Objective: The aim of this study was to characterize the demographic, behavioural, clinical and immunogenetic determinants of HIV-1 superinfection in a high-risk cohort of MSM. Design: A retrospective cohort study...
2.
Data on characterizing the gene expression patterns of neuronal ceroid lipofuscinosis genes: CLN1, CLN2, CLN3, CLN5 and their association to interneuron and neurotransmission markers: Parvalbumin and Somatostatin
Minye H, Fabritius A, Vesa J, Peltonen L
Data Brief . 2016 Aug; 8:741-9. PMID: 27508227
The article contains raw and analyzed data related to the research article "Neuronal ceroid lipofuscinosis genes, CLN2, CLN3, CLN5 are spatially and temporally co-expressed in a developing mouse brain" (Fabritius...
3.
In vitro studies in VCP-associated multisystem proteinopathy suggest altered mitochondrial bioenergetics
Nalbandian A, Llewellyn K, Gomez A, Walker N, Su H, Dunnigan A, et al.
Mitochondrion . 2015 Mar; 22:1-8. PMID: 25724235
Mitochondrial dysfunction has recently been implicated as an underlying factor to several common neurodegenerative diseases, including Parkinson's disease, Alzheimer's and amyotrophic lateral sclerosis (ALS). Valosin containing protein (VCP)-associated multisystem proteinopathy...
4.
Global gene expression profiling in R155H knock-in murine model of VCP disease
Nalbandian A, Ghimbovschi S, Wang Z, Knoblach S, Llewellyn K, Vesa J, et al.
Clin Transl Sci . 2014 Nov; 8(1):8-16. PMID: 25388089
Dominant mutations in the valosin-containing protein (VCP) gene cause inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia, which is characterized by progressive muscle weakness, dysfunction in...
5.
A progressive translational mouse model of human valosin-containing protein disease: the VCP(R155H/+) mouse
Nalbandian A, Llewellyn K, Badadani M, Yin H, Nguyen C, Katheria V, et al.
Muscle Nerve . 2012 Nov; 47(2):260-70. PMID: 23169451
Introduction: Mutations in the valosin-containing protein (VCP) gene cause hereditary inclusion body myopathy (IBM) associated with Paget disease of bone (PDB), and frontotemporal dementia (FTD). More recently, these mutations have...
6.
Global gene profiling of VCP-associated inclusion body myopathy
Nalbandian A, Ghimbovschi S, Radom-Aizik S, Dec E, Vesa J, Martin B, et al.
Clin Transl Sci . 2012 Jun; 5(3):226-34. PMID: 22686199
Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder caused by mutations in the Valosin-containing protein (VCP) gene on chromosome 9p12-13....
7.
Neuronal ceroid lipofuscinosis protein CLN3 interacts with motor proteins and modifies location of late endosomal compartments
Uusi-Rauva K, Kyttala A, van der Kant R, Vesa J, Tanhuanpaa K, Neefjes J, et al.
Cell Mol Life Sci . 2012 Jan; 69(12):2075-89. PMID: 22261744
CLN3 is an endosomal/lysosomal transmembrane protein mutated in classical juvenile onset neuronal ceroid lipofuscinosis, a fatal inherited neurodegenerative lysosomal storage disorder. The function of CLN3 in endosomal/lysosomal events has remained...
8.
The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis
Nalbandian A, Donkervoort S, Dec E, Badadani M, Katheria V, Rana P, et al.
J Mol Neurosci . 2011 Sep; 45(3):522-31. PMID: 21892620
Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is a progressive, fatal genetic disorder with variable penetrance, predominantly affecting three main tissue types: muscle (IBM),...
9.
VCP associated inclusion body myopathy and paget disease of bone knock-in mouse model exhibits tissue pathology typical of human disease
Badadani M, Nalbandian A, Watts G, Vesa J, Kitazawa M, Su H, et al.
PLoS One . 2010 Oct; 5(10). PMID: 20957154
Dominant mutations in the valosin containing protein (VCP) gene cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD). We have generated a knock-in mouse model...
10.
VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD
Tresse E, Salomons F, Vesa J, Bott L, Kimonis V, Yao T, et al.
Autophagy . 2010 Jan; 6(2):217-27. PMID: 20104022
VCP (VCP/p97) is a ubiquitously expressed member of the AAA(+)-ATPase family of chaperone-like proteins that regulates numerous cellular processes including chromatin decondensation, homotypic membrane fusion and ubiquitin-dependent protein degradation by...