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Per Zetterström
Kontakt
E-post
per.zetterstrom@umu.se
Telefon
090-785 29 50
Verksam vid
Anknytning
Biträdande universitetslektor, ST-läkare vid
Institutionen för medicinsk biovetenskap
Enhet: Klinisk kemi
Plats
By 6M, vån 2, Sjukhusområdet
Umeå universitet, 901 85 Umeå
Publikationer
Publikationer
Forskning
Forskning
Omnämnanden
Omnämnanden
2023
Mutant SOD1 aggregates formed in vitro and in cultured cells are polymorphic and differ from those arising in the CNS
Journal of Neurochemistry
, John Wiley & Sons 2023, Vol. 164, (1) : 77-93
Nordström, Ulrika; Lang, Lisa; Ekhtiari Bidhendi, Elaheh; et al.
2023
The motor system is exceptionally vulnerable to absence of the ubiquitously expressed superoxide dismutase-1
Brain Communications
, Oxford University Press 2023, Vol. 5, (1)
Park, Julien H.; Nordström, Ulrika; Tsiakas, Konstantinos; et al.
2020
ALS kan vara en prionsjukdom: Inklusioner av felvecklat SOD1-protein tycks finnas hos patienter med alla typer av ALS
Läkartidningen
, Läkartidningen Förlag AB 2020, Vol. 117
Forsberg, Karin; Tjust, Anton E.; Zetterström, Per; et al.
2020
Aggregate-selective antibody attenuates seeded aggregation but not spontaneously evolving disease in SOD1 ALS model mice
Acta neuropathologica communications
, BMC 2020, Vol. 8, (1)
Lehmann, Manuela; Marklund, Matthew; Bolender, Anna-Lena; et al.
2019
Phenotype in an Infant with
SOD1
Homozygous Truncating Mutation
New England Journal of Medicine
, Massachusetts Medical Society 2019, Vol. 381, (5) : 486-488
Andersen, Peter M.; Hempel, Maja; Santer, René; et al.
2019
The molecular pathogenesis of superoxide dismutase 1-linked ALS is promoted by low oxygen tension
Acta Neuropathologica
, New York: Springer 2019, Vol. 138, (1) : 85-101
Keskin, Isil; Forsgren, Elin; Lehmann, Manuela; et al.
2018
Mutant superoxide dismutase aggregates from human spinal cord transmit amyotrophic lateral sclerosis
Acta Neuropathologica
, Springer 2018, Vol. 136, (6) : 939-953
Ekhtiari Bidhendi, Elaheh; Bergh, Johan; Zetterström, Per; et al.
2016
Two superoxide dismutase prion strains transmit amyotrophic lateral sclerosis-like disease
Journal of Clinical Investigation
, Vol. 126, (6) : 2249-2253
Ekhtiari Bidhendi, Elaheh; Bergh, Johan; Zetterström, Per; et al.
2015
Structural and kinetic analysis of protein-aggregate strains in vivo using binary epitope mapping
Proceedings of the National Academy of Sciences of the United States of America
, National Academy of Sciences 2015, Vol. 112, (14) : 4489-4494
Bergh, Johan; Zetterström, Per; Andersen, Peter M.; et al.
2015
SOD1 aggregation in ALS mice shows simplistic test tube behavior
Proceedings of the National Academy of Sciences of the United States of America
, Vol. 112, (32) : 9878-9883
Lang, Lisa; Zetterström, Per; Brännström, Thomas; et al.
2013
Expression of wild-type human superoxide dismutase-1 in mice causes amyotrophic lateral sclerosis
Human Molecular Genetics
, Vol. 22, (1) : 51-60
Graffmo, Karin S.; Forsberg, Karin; Bergh, Johan; et al.
2013
Composition of soluble misfolded superoxide Dismutase-1 in murine models of Amyotrophic Lateral Sclerosis
Neuromolecular medicine
, Vol. 15, (1) : 147-158
Zetterström, Per; Graffmo, Karin S.; Andersen, Peter M; et al.
2012
Cytotoxicity of Superoxide Dismutase 1 in Cultured Cells Is Linked to Zn2+ Chelation
PLOS ONE
, Vol. 7, (4) : e36104-
Johansson, Ann-Sofi; Vestling, Monika; Zetterström, Per; et al.
2011
Misfolded superoxide dismutase-1 in amyotrophic lateral sclerosis
Umeå University medical dissertations
, 1421
Zetterström, Per
2011
Misfolded superoxide dismutase-1 in CSF from amyotrophic lateral sclerosis patients
Journal of Neurochemistry
, Vol. 117, (1) : 91-99
Zetterström, Per; Andersen, Peter M; Brännström, Thomas; et al.
2011
Proteins that bind to misfolded mutant superoxide dismutase-1 in spinal cords from transgenic ALS model mice
Journal of Biological Chemistry
, American Society for Biochemistry and Molecular Biology 2011, Vol. 286, (23) : 20130-20136
Zetterström, Per; Graffmo, Karin S; Andersen, Peter M; et al.
2009
Functional features cause misfolding of the ALS-provoking enzyme SOD1
Proceedings of the National Academy of Sciences of the United States of America
, National Academy of Sciences 2009, Vol. 106, (24) : 9667-9672
Nordlund, Anna; Leinartaitė, Lina; Saraboji, Kadhirvel; et al.
2007
Soluble misfolded subfractions of mutant superoxide dismutase-1s are enriched in spinal cords throughout life in murine ALS models
Proceedings of the National Academy of Sciences of the United States of America
, Vol. 104, (35) : 14157-14162
Zetterström, Per; Stewart, Heather G; Bergemalm, Daniel; et al.
Superoxide dismutase prions transmit fatal ALS to transgenic mice which do not spontaneously develop symptoms
Ekhtiari Bidhendi, Elaheh; Zetterström, Per; Andersen, Peter M.; et al.
High expression of wild-type human superoxide dismutase-1 gives a model of sporadic ALS
Forsberg, Karin; Graffmo, Karin S; Zetterström, Per; et al.
Enhanced protein misfolding in patient-derived models of amyotrophic lateral sclerosis
Forsgren, Elin; Lehmann, Manuela; Weygandt Mathis, Mackenzie; et al.
Low oxygen tension induces misfolding and aggregation of superoxide dismutase in ALS patient-derived motor neurons
Keskin, Isil; Forsgren, Elin; Andersen, Peter M.; et al.
Structure of soluble misfolded superoxide dismutase-1 in murine ALS models
Zetterström, Per; Graffmo, Karin S; Andersen, Peter M; et al.
Visa publikationer i DiVA
Forskargrupper
Forskningsledare
ALS-forskning Umeå
Forskningsledare
Per Zetterströms labb
Publicerad: 18 jul, 2019
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