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T Paunio

Showing results (11-20 of 49) with videos related to

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FEBS Letters|April 7, 1997
Tissue distribution and levels of gelsolin mRNA in normal individuals and patients with gelsolin-related amyloidosisT Paunio, H Kangas, S Kiuru, et al.
Sleep Medicine|September 7, 2021
Corrigendum to "Maternal and paternal sleep during pregnancy in the CHILD-SLEEP cohort" [Sleep Med 29 (2017) 47-56]E J Paavonen, O Saarenpää-Heikkilä, P Pölkki, et al.
Gene Therapy|January 16, 2004
Delivery of GDNF by an E1,E3/E4 deleted adenoviral vector and driven by a GFAP promoter prevents dopaminergic neuron degeneration in a rat model of Parkinson's diseaseN A Do Thi, P Saillour, L Ferrero, et al.
FEBS Letters|August 4, 1999
Functional consequences of amyloidosis mutation for gelsolin polypeptide -- analysis of gelsolin-actin interaction and gelsolin processing in gelsolin knock-out fibroblastsH Kangas, I Ulmanen, T Paunio, et al.
Human Mutation|January 1, 1995
Haplotype analysis in gelsolin-related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and JapanT Paunio, Y Sunada, S Kiuru, et al.
Gene Therapy|February 4, 1999
Adenovirus-mediated gene transfer results in decreased lysosomal storage in brain and total correction in liver of aspartylglucosaminuria (AGU) mouseM Peltola, A Kyttälä, O Heinonen, et al.
Translational Psychiatry|November 18, 2015
Impulsive alcohol-related risk-behavior and emotional dysregulation among individuals with a serotonin 2B receptor stop codonR Tikkanen, J Tiihonen, M R Rautiainen, et al.
Genomics|May 1, 1992
Solid-phase minisequencing test reveals Asp187----Asn (G654----A) mutation of gelsolin in all affected individuals with Finnish type of familial amyloidosisT Paunio, S Kiuru, V Hongell, et al.
Heliyon|May 8, 2023
Moderate associations between <i>BDNF</i> Val66Met gene polymorphism, musical expertise, and mismatch negativityL Bonetti, S E P Bruzzone, T Paunio, et al.
Molecular Psychiatry|August 17, 2005
A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophreniaW Hennah, A Tuulio-Henriksson, T Paunio, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
FEBS Letters|April 7, 1997
Tissue distribution and levels of gelsolin mRNA in normal individuals and patients with gelsolin-related amyloidosisT Paunio, H Kangas, S Kiuru, et al.
Sleep Medicine|September 7, 2021
Corrigendum to "Maternal and paternal sleep during pregnancy in the CHILD-SLEEP cohort" [Sleep Med 29 (2017) 47-56]E J Paavonen, O Saarenpää-Heikkilä, P Pölkki, et al.
Gene Therapy|January 16, 2004
Delivery of GDNF by an E1,E3/E4 deleted adenoviral vector and driven by a GFAP promoter prevents dopaminergic neuron degeneration in a rat model of Parkinson's diseaseN A Do Thi, P Saillour, L Ferrero, et al.
FEBS Letters|August 4, 1999
Functional consequences of amyloidosis mutation for gelsolin polypeptide -- analysis of gelsolin-actin interaction and gelsolin processing in gelsolin knock-out fibroblastsH Kangas, I Ulmanen, T Paunio, et al.
Human Mutation|January 1, 1995
Haplotype analysis in gelsolin-related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and JapanT Paunio, Y Sunada, S Kiuru, et al.
Gene Therapy|February 4, 1999
Adenovirus-mediated gene transfer results in decreased lysosomal storage in brain and total correction in liver of aspartylglucosaminuria (AGU) mouseM Peltola, A Kyttälä, O Heinonen, et al.
Translational Psychiatry|November 18, 2015
Impulsive alcohol-related risk-behavior and emotional dysregulation among individuals with a serotonin 2B receptor stop codonR Tikkanen, J Tiihonen, M R Rautiainen, et al.
Genomics|May 1, 1992
Solid-phase minisequencing test reveals Asp187----Asn (G654----A) mutation of gelsolin in all affected individuals with Finnish type of familial amyloidosisT Paunio, S Kiuru, V Hongell, et al.
Heliyon|May 8, 2023
Moderate associations between <i>BDNF</i> Val66Met gene polymorphism, musical expertise, and mismatch negativityL Bonetti, S E P Bruzzone, T Paunio, et al.
Molecular Psychiatry|August 17, 2005
A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophreniaW Hennah, A Tuulio-Henriksson, T Paunio, et al.
Pageof 5