Finnish neuroscience from past to present

doi:10.1111/ejn.14693

Editorial

. 2020 Sep;52(5):3273-3289.

doi: 10.1111/ejn.14693. Epub 2020 Feb 18.

Finnish neuroscience from past to present

Esa R Korpi¹, Dan Lindholm^{2

3}, Pertti Panula⁴, Pentti J Tienari^{5

6}, Matti Haltia⁷

Affiliations

¹ Department of Pharmacology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
² Department of Biochemistry and Developmental Biology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
³ Minerva Foundation Institute for Medical Research, Helsinki, Finland.
⁴ Department of Anatomy, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
⁵ Research Programs Unit, Translational Immunology, University of Helsinki, Helsinki, Finland.
⁶ Department of Neurology, Neurocenter, Helsinki University Hospital, Helsinki, Finland.
⁷ Department of Pathology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.

PMID: 32017266
DOI: 10.1111/ejn.14693

Editorial

Finnish neuroscience from past to present

Esa R Korpi et al. Eur J Neurosci. 2020 Sep.

. 2020 Sep;52(5):3273-3289.

doi: 10.1111/ejn.14693. Epub 2020 Feb 18.

Authors

Esa R Korpi¹, Dan Lindholm^{2

3}, Pertti Panula⁴, Pentti J Tienari^{5

6}, Matti Haltia⁷

Affiliations

¹ Department of Pharmacology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
² Department of Biochemistry and Developmental Biology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
³ Minerva Foundation Institute for Medical Research, Helsinki, Finland.
⁴ Department of Anatomy, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
⁵ Research Programs Unit, Translational Immunology, University of Helsinki, Helsinki, Finland.
⁶ Department of Neurology, Neurocenter, Helsinki University Hospital, Helsinki, Finland.
⁷ Department of Pathology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.

PMID: 32017266
DOI: 10.1111/ejn.14693

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References

REFERENCES

1. Aho, A. C., Donner, K., Hyden, C., Larsen, L. O., & Reuter, T. (1988). Low retinal noise in animals with low body temperature allows high visual sensitivity. Nature, 334, 348-350. https://doi.org/10.1038/334348a0
1. Airaksinen, M. S., & Saarma, M. (2002). The GDNF family: Signalling, biological functions and therapeutic value. Nature Reviews Neuroscience, 3, 383-394. https://doi.org/10.1038/nrn812
1. Alzheimer's Disease Collaborative, Group (1995). The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families. Nature Genetics, 11, 219-222. https://doi.org/10.1038/ng1095-219
1. Anttonen, A.-K., Laari, A., Kousi, M., Yang, Y. J., Jääskeläinen, T., Somer, M., … Lehesjoki, A.-E. (2017). ZNHIT3 is defective in PEHO syndrome, a severe encephalopathy with cerebellar granule neuron loss. Brain, 140, 1267-1279. https://doi.org/10.1093/brain/awx040
1. Bevilacqua, L., Doly, S., Kaprio, J., Yuan, Q., Tikkanen, R., Paunio, T., … Goldman, D. (2010). A population-specific HTR2B stop codon predisposes to severe impulsivity. Nature, 468, 1061-1066. https://doi.org/10.1038/nature09629

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[1] Aho, A. C., Donner, K., Hyden, C., Larsen, L. O., & Reuter, T. (1988). Low retinal noise in animals with low body temperature allows high visual sensitivity. Nature, 334, 348-350. https://doi.org/10.1038/334348a0

[2] Aho, A. C., Donner, K., Hyden, C., Larsen, L. O., & Reuter, T. (1988). Low retinal noise in animals with low body temperature allows high visual sensitivity. Nature, 334, 348-350. https://doi.org/10.1038/334348a0

[3] Airaksinen, M. S., & Saarma, M. (2002). The GDNF family: Signalling, biological functions and therapeutic value. Nature Reviews Neuroscience, 3, 383-394. https://doi.org/10.1038/nrn812

[4] Airaksinen, M. S., & Saarma, M. (2002). The GDNF family: Signalling, biological functions and therapeutic value. Nature Reviews Neuroscience, 3, 383-394. https://doi.org/10.1038/nrn812

[5] Alzheimer's Disease Collaborative, Group (1995). The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families. Nature Genetics, 11, 219-222. https://doi.org/10.1038/ng1095-219

[6] Alzheimer's Disease Collaborative, Group (1995). The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families. Nature Genetics, 11, 219-222. https://doi.org/10.1038/ng1095-219

[7] Anttonen, A.-K., Laari, A., Kousi, M., Yang, Y. J., Jääskeläinen, T., Somer, M., … Lehesjoki, A.-E. (2017). ZNHIT3 is defective in PEHO syndrome, a severe encephalopathy with cerebellar granule neuron loss. Brain, 140, 1267-1279. https://doi.org/10.1093/brain/awx040

[8] Anttonen, A.-K., Laari, A., Kousi, M., Yang, Y. J., Jääskeläinen, T., Somer, M., … Lehesjoki, A.-E. (2017). ZNHIT3 is defective in PEHO syndrome, a severe encephalopathy with cerebellar granule neuron loss. Brain, 140, 1267-1279. https://doi.org/10.1093/brain/awx040

[9] Bevilacqua, L., Doly, S., Kaprio, J., Yuan, Q., Tikkanen, R., Paunio, T., … Goldman, D. (2010). A population-specific HTR2B stop codon predisposes to severe impulsivity. Nature, 468, 1061-1066. https://doi.org/10.1038/nature09629

[10] Bevilacqua, L., Doly, S., Kaprio, J., Yuan, Q., Tikkanen, R., Paunio, T., … Goldman, D. (2010). A population-specific HTR2B stop codon predisposes to severe impulsivity. Nature, 468, 1061-1066. https://doi.org/10.1038/nature09629

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Finnish neuroscience from past to present

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Finnish neuroscience from past to present

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