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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1989 1
1990 1
1991 3
1992 4
1993 4
1994 1
1995 5
1996 3
1997 2
1999 1
2000 3
2001 1
2002 4
2003 2
2004 3
2005 3
2006 1
2008 2
2009 2
2010 3
2011 2
2012 3
2013 1
2014 2
2015 2
2016 1
2017 1
2018 1
2021 0
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57 results
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Page 1
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. Ylä-Anttila T, et al. Among authors: vesa j. Eur J Commun. 2018 Dec;33(6):587-603. doi: 10.1177/0267323118790155. Epub 2018 Jul 30. Eur J Commun. 2018. PMID: 30587880 Free PMC article.
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. Nalbandian A, et al. Among authors: vesa j. J Mol Neurosci. 2011 Nov;45(3):522-31. doi: 10.1007/s12031-011-9627-y. Epub 2011 Sep 3. J Mol Neurosci. 2011. PMID: 21892620 Review.
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. Vesa J, et al. AIDS. 2017 May 15;31(8):1149-1158. doi: 10.1097/QAD.0000000000001445. AIDS. 2017. PMID: 28244954 Free PMC article.
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. Kimonis VE, et al. Among authors: vesa j. Biochim Biophys Acta. 2008 Dec;1782(12):744-8. doi: 10.1016/j.bbadis.2008.09.003. Epub 2008 Sep 18. Biochim Biophys Acta. 2008. PMID: 18845250 Free article. Review.
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. Nalbandian A, et al. Among authors: vesa j. Clin Transl Sci. 2012 Jun;5(3):226-34. doi: 10.1111/j.1752-8062.2012.00407.x. Epub 2012 Apr 4. Clin Transl Sci. 2012. PMID: 22686199 Free PMC article.
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. Nalbandian A, et al. Among authors: vesa j. Mitochondrion. 2015 May;22:1-8. doi: 10.1016/j.mito.2015.02.004. Epub 2015 Feb 25. Mitochondrion. 2015. PMID: 25724235 Free PMC article.
Mutated genes in juvenile and variant late infantile neuronal ceroid lipofuscinoses encode lysosomal proteins.
Vesa J, Peltonen L. Vesa J, et al. Curr Mol Med. 2002 Aug;2(5):439-44. doi: 10.2174/1566524023362311. Curr Mol Med. 2002. PMID: 12125809 Review.
Molecular genetics of neuronal ceroid lipofuscinoses.
Järvelä I, Vesa J, Santavuori P, Hellsten E, Peltonen L. Järvelä I, et al. Among authors: vesa j. Pediatr Res. 1992 Dec;32(6):645-8. doi: 10.1203/00006450-199212000-00003. Pediatr Res. 1992. PMID: 1287553 Review.
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. Nalbandian A, et al. Among authors: vesa j. Clin Transl Sci. 2015 Feb;8(1):8-16. doi: 10.1111/cts.12241. Epub 2014 Nov 12. Clin Transl Sci. 2015. PMID: 25388089 Free PMC article.
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. Nalbandian A, et al. Among authors: vesa j. Muscle Nerve. 2013 Feb;47(2):260-70. doi: 10.1002/mus.23522. Epub 2012 Nov 21. Muscle Nerve. 2013. PMID: 23169451 Free PMC article.
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