Jouni Vesa

Title(s)	Specialist, Pediatrics
School	Vc-health Sciences-schools
Address	9500 Gilman Drive # La Jolla CA 92093
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Bibliographic

Publications

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.

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Increased HIV-1 superinfection risk in carriers of specific human leukocyte antigen alleles. AIDS. 2017 05 15; 31(8):1149-1158. Vesa J, Chaillon A, Wagner GA, Anderson CM, Richman DD, Smith DM, Little SJ. PMID: 28244954; PMCID: PMC5559224.

View in: PubMed Mentions: 4 Fields:
Acq Acquired Immunodeficiency Synd
Translation:Humans
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. Data Brief. 2016 Sep; 8:741-9. Minye HM, Fabritius AL, Vesa J, Peltonen L. PMID: 27508227; PMCID: PMC4950137.

View in: PubMed Mentions: 4
In vitro studies in VCP-associated multisystem proteinopathy suggest altered mitochondrial bioenergetics. Mitochondrion. 2015 May; 22:1-8. Nalbandian A, Llewellyn KJ, Gomez A, Walker N, Su H, Dunnigan A, Chwa M, Vesa J, Kenney MC, Kimonis VE. PMID: 25724235; PMCID: PMC7105354.

View in: PubMed Mentions: 13 Fields:
Cel Cell Biology
Translation:Humans Animals Cells
Global gene expression profiling in R155H knock-in murine model of VCP disease. Clin Transl Sci. 2015 Feb; 8(1):8-16. Nalbandian A, Ghimbovschi S, Wang Z, Knoblach S, Llewellyn KJ, Vesa J, Hoffman EP, Kimonis VE. PMID: 25388089; PMCID: PMC4329058.

View in: PubMed Mentions: 2 Fields:
Med Medicine (General)
Translation:Humans Animals
A progressive translational mouse model of human valosin-containing protein disease: the VCP(R155H/+) mouse. Muscle Nerve. 2013 Feb; 47(2):260-70. Nalbandian A, Llewellyn KJ, Badadani M, Yin HZ, Nguyen C, Katheria V, Watts G, Mukherjee J, Vesa J, Caiozzo V, Mozaffar T, Weiss JH, Kimonis VE. PMID: 23169451; PMCID: PMC3556223.

View in: PubMed Mentions: 34 Fields:
Neu Neurology Phy Physiology
Translation:Animals Cells
Global gene profiling of VCP-associated inclusion body myopathy. Clin Transl Sci. 2012 Jun; 5(3):226-34. Nalbandian A, Ghimbovschi S, Radom-Aizik S, Dec E, Vesa J, Martin B, Knoblach S, Smith C, Hoffman E, Kimonis VE. PMID: 22686199; PMCID: PMC3375869.

View in: PubMed Mentions: 7 Fields:
Med Medicine (General)
Translation:Humans Cells
Neuronal ceroid lipofuscinosis protein CLN3 interacts with motor proteins and modifies location of late endosomal compartments. Cell Mol Life Sci. 2012 Jun; 69(12):2075-89. Uusi-Rauva K, Kyttälä A, van der Kant R, Vesa J, Tanhuanpää K, Neefjes J, Olkkonen VM, Jalanko A. PMID: 22261744.

View in: PubMed Mentions: 39 Fields:
Cel Cell Biology Mol Molecular Biology
Translation:Humans Cells
The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis. J Mol Neurosci. 2011 Nov; 45(3):522-31. Nalbandian A, Donkervoort S, Dec E, Badadani M, Katheria V, Rana P, Nguyen C, Mukherjee J, Caiozzo V, Martin B, Watts GD, Vesa J, Smith C, Kimonis VE. PMID: 21892620.

View in: PubMed Mentions: 73 Fields:
Mol Molecular Biology Neu Neurology
Translation:Humans Animals
VCP associated inclusion body myopathy and paget disease of bone knock-in mouse model exhibits tissue pathology typical of human disease. PLoS One. 2010 Oct 05; 5(10). Badadani M, Nalbandian A, Watts GD, Vesa J, Kitazawa M, Su H, Tanaja J, Dec E, Wallace DC, Mukherjee J, Caiozzo V, Warman M, Kimonis VE. PMID: 20957154; PMCID: PMC2950155.

View in: PubMed Mentions: 66 Fields:
Med Medicine (General)Sci Science
Translation:Animals
VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD. Autophagy. 2010 Feb; 6(2):217-27. Tresse E, Salomons FA, Vesa J, Bott LC, Kimonis V, Yao TP, Dantuma NP, Taylor JP. PMID: 20104022; PMCID: PMC2929010.

View in: PubMed Mentions: 245 Fields:
Cel Cell Biology
Translation:Humans Animals Cells
Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts. Neuromuscul Disord. 2009 Nov; 19(11):766-72. Vesa J, Su H, Watts GD, Krause S, Walter MC, Martin B, Smith C, Wallace DC, Kimonis VE. PMID: 19828315; PMCID: PMC2782446.

View in: PubMed Mentions: 41 Fields:
Neu Neurology
Translation:Humans Cells
Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome. Neurosci Lett. 2011 Jan 07; 487(2):129-33. Su H, Fan W, Coskun PE, Vesa J, Gold JA, Jiang YH, Potluri P, Procaccio V, Acab A, Weiss JH, Wallace DC, Kimonis VE. PMID: 19563863; PMCID: PMC2888840.

View in: PubMed Mentions: 37 Fields:
Neu Neurology
Translation:Animals Cells
VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: review of a unique disorder. Biochim Biophys Acta. 2008 Dec; 1782(12):744-8. Kimonis VE, Fulchiero E, Vesa J, Watts G. PMID: 18845250.

View in: PubMed Mentions: 113 Fields:
Bio Biochemistry Bio Biophysics
Translation:Humans
Hydrolethalus syndrome is caused by a missense mutation in a novel gene HYLS1. Hum Mol Genet. 2005 Jun 01; 14(11):1475-88. Mee L, Honkala H, Kopra O, Vesa J, Finnilä S, Visapää I, Sang TK, Jackson GR, Salonen R, Kestilä M, Peltonen L. PMID: 15843405.

View in: PubMed Mentions: 18 Fields:
Gen Genetics Mol Molecular Biology
Translation:Humans Animals Cells
Molecular and cellular characterization of the Down syndrome critical region protein 2. Biochem Biophys Res Commun. 2005 Mar 04; 328(1):235-42. Vesa J, Brown Y, Greenfield D, Korenberg JR. PMID: 15670775.

View in: PubMed Mentions: 3 Fields:
Bio Biochemistry Bio Biophysics
Translation:Humans Animals Cells
Mice with Ppt1Deltaex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons. Neurobiol Dis. 2005 Feb; 18(1):226-41. Jalanko A, Vesa J, Manninen T, von Schantz C, Minye H, Fabritius AL, Salonen T, Rapola J, Gentile M, Kopra O, Peltonen L. PMID: 15649713.

View in: PubMed Mentions: 34 Fields:
Neu Neurology
Translation:Animals Cells
A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging. Hum Mol Genet. 2004 Dec 01; 13(23):2893-906. Kopra O, Vesa J, von Schantz C, Manninen T, Minye H, Fabritius AL, Rapola J, van Diggelen OP, Saarela J, Jalanko A, Peltonen L. PMID: 15459177.

View in: PubMed Mentions: 34 Fields:
Gen Genetics Mol Molecular Biology
Translation:Humans Animals Cells
Two motifs target Batten disease protein CLN3 to lysosomes in transfected nonneuronal and neuronal cells. Mol Biol Cell. 2004 Mar; 15(3):1313-23. Kyttälä A, Ihrke G, Vesa J, Schell MJ, Luzio JP. PMID: 14699076; PMCID: PMC363135.

View in: PubMed Mentions: 48 Fields:
Cel Cell Biology Mol Molecular Biology
Translation:Humans Animals Cells
GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L. Am J Hum Genet. 2002 Oct; 71(4):863-76. Visapää I, Fellman V, Vesa J, Dasvarma A, Hutton JL, Kumar V, Payne GS, Makarow M, Van Coster R, Taylor RW, Turnbull DM, Suomalainen A, Peltonen L. PMID: 12215968; PMCID: PMC378542.

View in: PubMed Mentions: 74 Fields:
Gen Genetics
Translation:Humans Animals Cells
Neuronal ceroid lipofuscinoses are connected at molecular level: interaction of CLN5 protein with CLN2 and CLN3. Mol Biol Cell. 2002 Jul; 13(7):2410-20. Vesa J, Chin MH, Oelgeschläger K, Isosomppi J, DellAngelica EC, Jalanko A, Peltonen L. PMID: 12134079; PMCID: PMC117323.

View in: PubMed Mentions: 36 Fields:
Cel Cell Biology Mol Molecular Biology
Translation:Humans Animals Cells
Lysosomal localization of the neuronal ceroid lipofuscinosis CLN5 protein. Hum Mol Genet. 2002 Apr 15; 11(8):885-91. Isosomppi J, Vesa J, Jalanko A, Peltonen L. PMID: 11971870.

View in: PubMed Mentions: 39 Fields:
Gen Genetics Mol Molecular Biology
Translation:Humans Cells