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Sanna Seitsonen

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

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Acta Ophthalmologica|July 9, 2015
The genetic variant rs4073 A→T of the Interleukin-8 promoter region is associated with the earlier onset of exudative age-related macular degenerationAsta Hautamäki, Sanna Seitsonen, Juha M Holopainen, et al.
Neuroscience Letters|March 6, 2012
Adiponectin receptor 1 gene (ADIPOR1) variant is associated with advanced age-related macular degeneration in Finnish populationKai Kaarniranta, Jussi Paananen, Tanja Nevalainen, et al.
Ophthalmology|November 10, 2009
Vascular endothelial growth factor gene variation and the response to photodynamic therapy in age-related macular degenerationIlkka Immonen, Sanna Seitsonen, Petri Tommila, et al.
Acta Ophthalmologica|September 21, 2022
Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delGAnna Majander, Eeva-Marja Sankila, Aura Falck, et al.
Human Molecular Genetics|December 25, 2016
Protective coding variants in CFH and PELI3 and a variant near CTRB1 are associated with age-related macular degeneration†Yi Yu, Erin K Wagner, Eric H Souied, et al.
Molecular Vision|August 4, 2006
Analysis of variants in the complement factor H, the elongation of very long chain fatty acids-like 4 and the hemicentin 1 genes of age-related macular degeneration in the Finnish populationSanna Seitsonen, Susanna Lemmelä, Juha Holopainen, et al.
Retina (Philadelphia, Pa.)|April 16, 2013
Interleukin 8 promoter polymorphism predicts the initial response to bevacizumab treatment for exudative age-related macular degenerationAsta Hautamäki, Jarno Kivioja, Satu Vavuli, et al.
Ophthalmic Genetics|October 5, 2025
Long-read sequencing uncovers novel pathogenic duplications in the <i>PRPH2</i> gene in patients with macular dystrophyMichael P Backlund, Suzie A Gasparian, Pauliina E Repo, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 7, 2007
Y402H polymorphism of complement factor H affects binding affinity to C-reactive proteinMatti Laine, Hanna Jarva, Sanna Seitsonen, et al.
Biochemistry and Biophysics Reports|February 16, 2026
Functional polymorphisms in pigmentation-related genes <i>MC1R</i> and <i>DCT</i> display population-specific association with wet age-related macular degenerationMika Reinisalo, Seppo Helisalmi, Ali Koskela, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Acta Ophthalmologica|July 9, 2015
The genetic variant rs4073 A→T of the Interleukin-8 promoter region is associated with the earlier onset of exudative age-related macular degenerationAsta Hautamäki, Sanna Seitsonen, Juha M Holopainen, et al.
Neuroscience Letters|March 6, 2012
Adiponectin receptor 1 gene (ADIPOR1) variant is associated with advanced age-related macular degeneration in Finnish populationKai Kaarniranta, Jussi Paananen, Tanja Nevalainen, et al.
Ophthalmology|November 10, 2009
Vascular endothelial growth factor gene variation and the response to photodynamic therapy in age-related macular degenerationIlkka Immonen, Sanna Seitsonen, Petri Tommila, et al.
Acta Ophthalmologica|September 21, 2022
Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delGAnna Majander, Eeva-Marja Sankila, Aura Falck, et al.
Human Molecular Genetics|December 25, 2016
Protective coding variants in CFH and PELI3 and a variant near CTRB1 are associated with age-related macular degeneration†Yi Yu, Erin K Wagner, Eric H Souied, et al.
Molecular Vision|August 4, 2006
Analysis of variants in the complement factor H, the elongation of very long chain fatty acids-like 4 and the hemicentin 1 genes of age-related macular degeneration in the Finnish populationSanna Seitsonen, Susanna Lemmelä, Juha Holopainen, et al.
Retina (Philadelphia, Pa.)|April 16, 2013
Interleukin 8 promoter polymorphism predicts the initial response to bevacizumab treatment for exudative age-related macular degenerationAsta Hautamäki, Jarno Kivioja, Satu Vavuli, et al.
Ophthalmic Genetics|October 5, 2025
Long-read sequencing uncovers novel pathogenic duplications in the <i>PRPH2</i> gene in patients with macular dystrophyMichael P Backlund, Suzie A Gasparian, Pauliina E Repo, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 7, 2007
Y402H polymorphism of complement factor H affects binding affinity to C-reactive proteinMatti Laine, Hanna Jarva, Sanna Seitsonen, et al.
Biochemistry and Biophysics Reports|February 16, 2026
Functional polymorphisms in pigmentation-related genes <i>MC1R</i> and <i>DCT</i> display population-specific association with wet age-related macular degenerationMika Reinisalo, Seppo Helisalmi, Ali Koskela, et al.
Pageof 2