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Items: 1 to 20 of 57


Up with ecology, down with economy? The consolidation of the idea of climate change mitigation in the global public sphere.

Ylä-Anttila T, Vesa J, Eranti V, Kukkonen A, Lehtimäki T, Lonkila M, Luhtakallio E.

Eur J Commun. 2018 Dec;33(6):587-603. doi: 10.1177/0267323118790155. Epub 2018 Jul 30.


Increased HIV-1 superinfection risk in carriers of specific human leukocyte antigen alleles.

Vesa J, Chaillon A, Wagner GA, Anderson CM, Richman DD, Smith DM, Little SJ.

AIDS. 2017 May 15;31(8):1149-1158. doi: 10.1097/QAD.0000000000001445.


In vitro studies in VCP-associated multisystem proteinopathy suggest altered mitochondrial bioenergetics.

Nalbandian A, Llewellyn KJ, Gomez A, Walker N, Su H, Dunnigan A, Chwa M, Vesa J, Kenney MC, Kimonis VE.

Mitochondrion. 2015 May;22:1-8. doi: 10.1016/j.mito.2015.02.004. Epub 2015 Feb 25.


Global gene expression profiling in R155H knock-in murine model of VCP disease.

Nalbandian A, Ghimbovschi S, Wang Z, Knoblach S, Llewellyn KJ, Vesa J, Hoffman EP, Kimonis VE.

Clin Transl Sci. 2015 Feb;8(1):8-16. doi: 10.1111/cts.12241. Epub 2014 Nov 12.


Neuronal ceroid lipofuscinosis genes, CLN2, CLN3 and CLN5 are spatially and temporally co-expressed in a developing mouse brain.

Fabritius AL, Vesa J, Minye HM, Nakano I, Kornblum H, Peltonen L.

Exp Mol Pathol. 2014 Dec;97(3):484-91. doi: 10.1016/j.yexmp.2014.10.003. Epub 2014 Oct 7.


A progressive translational mouse model of human valosin-containing protein disease: the VCP(R155H/+) mouse.

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.

Muscle Nerve. 2013 Feb;47(2):260-70. doi: 10.1002/mus.23522. Epub 2012 Nov 21.


Global gene profiling of VCP-associated inclusion body myopathy.

Nalbandian A, Ghimbovschi S, Radom-Aizik S, Dec E, Vesa J, Martin B, Knoblach S, Smith C, Hoffman E, Kimonis VE.

Clin Transl Sci. 2012 Jun;5(3):226-34. doi: 10.1111/j.1752-8062.2012.00407.x. Epub 2012 Apr 4.


Neuronal ceroid lipofuscinosis protein CLN3 interacts with motor proteins and modifies location of late endosomal compartments.

Uusi-Rauva K, Kyttälä A, van der Kant R, Vesa J, Tanhuanpää K, Neefjes J, Olkkonen VM, Jalanko A.

Cell Mol Life Sci. 2012 Jun;69(12):2075-89. doi: 10.1007/s00018-011-0913-1. Epub 2012 Jan 20.


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, Nguyen C, Mukherjee J, Caiozzo V, Martin B, Watts GD, Vesa J, Smith C, Kimonis VE.

J Mol Neurosci. 2011 Nov;45(3):522-31. doi: 10.1007/s12031-011-9627-y. Epub 2011 Sep 3. Review.


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 GD, Vesa J, Kitazawa M, Su H, Tanaja J, Dec E, Wallace DC, Mukherjee J, Caiozzo V, Warman M, Kimonis VE.

PLoS One. 2010 Oct 5;5(10). pii: e13183. doi: 10.1371/journal.pone.0013183.


[Urinary incontinence and prostate cancer: A rehabilitation program design].

Serdà BC, Vesa J, del Valle A, Monreal P.

Actas Urol Esp. 2010 Jun;34(6):522-30. Spanish.


VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD.

Tresse E, Salomons FA, Vesa J, Bott LC, Kimonis V, Yao TP, Dantuma NP, Taylor JP.

Autophagy. 2010 Feb;6(2):217-27. Epub 2010 Feb 22.


Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts.

Vesa J, Su H, Watts GD, Krause S, Walter MC, Martin B, Smith C, Wallace DC, Kimonis VE.

Neuromuscul Disord. 2009 Nov;19(11):766-72. doi: 10.1016/j.nmd.2009.08.003. Epub 2009 Oct 13.


Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome.

Su H, Fan W, Coskun PE, Vesa J, Gold JA, Jiang YH, Potluri P, Procaccio V, Acab A, Weiss JH, Wallace DC, Kimonis VE.

Neurosci Lett. 2011 Jan 7;487(2):129-33. doi: 10.1016/j.neulet.2009.06.079. Epub 2009 Jun 27.


VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: review of a unique disorder.

Kimonis VE, Fulchiero E, Vesa J, Watts G.

Biochim Biophys Acta. 2008 Dec;1782(12):744-8. doi: 10.1016/j.bbadis.2008.09.003. Epub 2008 Sep 18. Review.


Segmental testicular infarction vs testicular tumour: the usefulness of the excisional frozen biopsy.

Hidalgo J, Rodríguez A, Canalias J, Muntané MJ, Huerta MV, Carrasco N, Vesa J.

Arch Esp Urol. 2008 Jan-Feb;61(1):92-3.


[Penis necrosis in a diabetic patient on hemodialysis].

Picazo M, Cuxart M, Vesa J, Urcelay ML.

Nefrologia. 2006;26(5):649-50. Spanish. No abstract available.


Hydrolethalus syndrome is caused by a missense mutation in a novel gene HYLS1.

Mee L, Honkala H, Kopra O, Vesa J, Finnilä S, Visapää I, Sang TK, Jackson GR, Salonen R, Kestilä M, Peltonen L.

Hum Mol Genet. 2005 Jun 1;14(11):1475-88. Epub 2005 Apr 20.


Molecular and cellular characterization of the Down syndrome critical region protein 2.

Vesa J, Brown Y, Greenfield D, Korenberg JR.

Biochem Biophys Res Commun. 2005 Mar 4;328(1):235-42.


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