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Kati Donner

Showing results (11-20 of 26) with videos related to

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Plos One|July 28, 2015
Genetic Loci Associated with Allergic Sensitization in LithuaniansIngrida Šaulienė, Jūratė Greičiuvienė, Laura Šukienė, et al.
Epigenetics|February 25, 2022
Pharmacoepigenetics of hypertension: genome-wide methylation analysis of responsiveness to four classes of antihypertensive drugs using a double-blind crossover study designMarja-Liisa Nuotio, Heini Sánez Tähtisalo, Alexandra Lahtinen, et al.
Neuromuscular Disorders : NMD|December 12, 2001
Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathyKati Donner, Miina Ollikainen, Maaret Ridanpää, et al.
The Biochemical Journal|November 17, 2011
Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemaline and cap myopathyMinttu Marttila, Elina Lemola, William Wallefeld, et al.
Human Mutation|April 14, 2025
Characterisation of a LINE-1 Insertion in the <i>RP1</i> Gene by Targeted Adaptive Nanopore Sequencing in a Family with Retinitis PigmentosaMichael P Backlund, Pauliina Repo, Harri Kangas, et al.
European Journal of Human Genetics : EJHG|April 3, 2008
Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish originVilma-Lotta Lehtokari, Katarina Pelin, Kati Donner, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|January 14, 2024
High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human DiseasesOmar Youssef, Anu Loukola, Yossra H S Zidi-Mouaffak, et al.
Clinical and Translational Allergy|November 2, 2020
Genomics of asthma, allergy and chronic rhinosinusitis: novel concepts and relevance in airway mucosaAnu Laulajainen-Hongisto, Annina Lyly, Tanzeela Hanif, et al.
Journal of Hypertension|May 14, 2008
Laboratory tests as predictors of the antihypertensive effects of amlodipine, bisoprolol, hydrochlorothiazide and losartan in men: results from the randomized, double-blind, crossover GENRES StudyTimo Suonsyrjä, Tuula Hannila-Handelberg, Kristian J Paavonen, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Mutations in the nebulin gene can cause severe congenital nemaline myopathyCarina Wallgren-Pettersson, Kati Donner, Caroline Sewry, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Plos One|July 28, 2015
Genetic Loci Associated with Allergic Sensitization in LithuaniansIngrida Šaulienė, Jūratė Greičiuvienė, Laura Šukienė, et al.
Epigenetics|February 25, 2022
Pharmacoepigenetics of hypertension: genome-wide methylation analysis of responsiveness to four classes of antihypertensive drugs using a double-blind crossover study designMarja-Liisa Nuotio, Heini Sánez Tähtisalo, Alexandra Lahtinen, et al.
Neuromuscular Disorders : NMD|December 12, 2001
Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathyKati Donner, Miina Ollikainen, Maaret Ridanpää, et al.
The Biochemical Journal|November 17, 2011
Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemaline and cap myopathyMinttu Marttila, Elina Lemola, William Wallefeld, et al.
Human Mutation|April 14, 2025
Characterisation of a LINE-1 Insertion in the <i>RP1</i> Gene by Targeted Adaptive Nanopore Sequencing in a Family with Retinitis PigmentosaMichael P Backlund, Pauliina Repo, Harri Kangas, et al.
European Journal of Human Genetics : EJHG|April 3, 2008
Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish originVilma-Lotta Lehtokari, Katarina Pelin, Kati Donner, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|January 14, 2024
High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human DiseasesOmar Youssef, Anu Loukola, Yossra H S Zidi-Mouaffak, et al.
Clinical and Translational Allergy|November 2, 2020
Genomics of asthma, allergy and chronic rhinosinusitis: novel concepts and relevance in airway mucosaAnu Laulajainen-Hongisto, Annina Lyly, Tanzeela Hanif, et al.
Journal of Hypertension|May 14, 2008
Laboratory tests as predictors of the antihypertensive effects of amlodipine, bisoprolol, hydrochlorothiazide and losartan in men: results from the randomized, double-blind, crossover GENRES StudyTimo Suonsyrjä, Tuula Hannila-Handelberg, Kristian J Paavonen, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Mutations in the nebulin gene can cause severe congenital nemaline myopathyCarina Wallgren-Pettersson, Kati Donner, Caroline Sewry, et al.
Pageof 3