Anna Birve

Senior research engineer (absence) at Department of Pharmacology and Clinical Neuroscience
Clinical Neuroscience

Publications

Author

Title

Year sorteringsordning

Fulltext

Keskin, Isil
Birve, Anna
Berdynski, Mariusz; et al.

Comprehensive analysis to explain reduced or increased SOD1 enzymatic activity in ALS patients and their relatives
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 18(5-6): 457-463

2017

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Keskin, Isil
Forsgren, Elin
Lange, Dale J.; et al.

Effects of Cellular Pathway Disturbances on Misfolded Superoxide Dismutase-1 in Fibroblasts Derived from ALS Patients
PLoS ONE, 11(2)

2016

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Ingre, Caroline
Wuolikainen, Anna
Marklund, Stefan L.; et al.

A 50bp deletion in the SOD1 promoter lowers enzyme expression but is not associated with ALS in Sweden
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 17(5-6): 452-457

2016

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Nordin, Angelica
Akimoto, Chizuru
Wuolikainen, Anna; et al.

Extensive size variability of the GGGGCC expansion in C9orf72 in both neuronal and non-neuronal tissues in 18 patients with ALS or FTD
Human Molecular Genetics, 24(11): 3133-3142

2015

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Hugosson, Fredrik
Sjögren, Camilla
Birve, Anna; et al.

The Drosophila Midkine/Pleiotrophin Homologues Miple1 and Miple2 Affect Adult Lifespan but Are Dispensable for Alk Signaling during Embryonic Gut Formation
PLoS ONE, 9(11): e112250-

2014

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Van Doormaal, Perry T. C.
Ticozzi, Nicola
Gellera, Cinzia; et al.

Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study
Neurobiology of Aging, 35(10): 2420.e13-

2014

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Akimoto, Chizuru
Volk, Alexander E.
van Blitterswijk, Marka; et al.

A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories
Journal of Medical Genetics, 51(6): 419-424

2014

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Graffmo, Karin S.
Forsberg, Karin
Bergh, Johan; et al.

Expression of wild-type human superoxide dismutase-1 in mice causes amyotrophic lateral sclerosis
Human Molecular Genetics, 22(1): 51-60

2013

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Akimoto, Chizuru
Forsgren, Lars
Linder, Jan; et al.

No GGGGCC-hexanucleotide repeat expansion in C9ORF72 in parkinsonism patients in Sweden
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 14(1): 26-29

2013

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Ingre, Caroline
Landers, John E
Rizik, Naji; et al.

A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts
Neurobiology of Aging, 34(6): 1708.e1-1708.e6

2013

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