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Jouni Vesa

Title(s)Specialist, Pediatrics
SchoolVc-health Sciences-schools
Address9500 Gilman Drive #
La Jolla CA 92093
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    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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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. 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.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    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. Data Brief. 2016 Sep; 8:741-9. Minye HM, Fabritius AL, Vesa J, Peltonen L. PMID: 27508227.
      View in: PubMed   Mentions:
    3. 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.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansAnimalsCells
    4. 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.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansAnimals
    5. 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.
      View in: PubMed   Mentions: 24     Fields:    Translation:AnimalsCells
    6. 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.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    7. 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: 30     Fields:    Translation:HumansCells
    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. 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: 51     Fields:    Translation:HumansAnimals
    9. 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.
      View in: PubMed   Mentions: 49     Fields:    Translation:Animals
    10. 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.
      View in: PubMed   Mentions: 179     Fields:    Translation:HumansAnimalsCells
    11. 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.
      View in: PubMed   Mentions: 32     Fields:    Translation:HumansCells
    12. 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.
      View in: PubMed   Mentions: 27     Fields:    Translation:AnimalsCells
    13. 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: 75     Fields:    Translation:Humans
    14. 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: 12     Fields:    Translation:HumansAnimalsCells
    15. 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:    Translation:HumansAnimalsCells
    16. 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: 26     Fields:    Translation:AnimalsCells
    17. 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: 23     Fields:    Translation:HumansAnimalsCells
    18. 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.
      View in: PubMed   Mentions: 36     Fields:    Translation:HumansAnimalsCells
    19. 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.
      View in: PubMed   Mentions: 49     Fields:    Translation:HumansAnimalsCells
    20. 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.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansAnimalsCells
    21. 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: 23     Fields:    Translation:HumansCells
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