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Katarina Pelin

Showing results (1-10 of 49) with videos related to

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The Journal of General Physiology|February 3, 2021
Nebulin: Size matters for optimal muscle functionKatarina Pelin
Gene|July 7, 2012
Nebulin is not expressed in plantsKatarina Pelin
Seminars in Pediatric Neurology|May 8, 2019
Update on the Genetics of Congenital MyopathiesKatarina Pelin, Carina Wallgren-Pettersson
Advances in Experimental Medicine and Biology|February 3, 2009
Nebulin--a giant chameleonKatarina Pelin, Carina Wallgren-Pettersson
Genes|May 28, 2022
Array Comparative Genomic Hybridisation and Droplet Digital PCR Uncover Recurrent Copy Number Variation of the <i>TTN</i> Segmental Duplication RegionLydia Sagath, Vilma-Lotta Lehtokari, Katarina Pelin, et al.
Neuromuscular Disorders : NMD|February 14, 2018
Clinically variable nemaline myopathy in a three-generation family caused by mutation of the skeletal muscle alpha-actin geneVilma-Lotta Lehtokari, Maria Gardberg, Katarina Pelin, et al.
Journal of Human Genetics|January 16, 2015
A commentary on identification of the rare compound heterozygous variants in the NEB gene in a Korean family with intellectual disability, epilepsy and early-childhood-onset generalized muscle weaknessKatarina Pelin, Kirsi Kiiski, Vilma-Lotta Lehtokari, et al.
Genomics|July 25, 2006
Developmental and muscle-type-specific expression of mouse nebulin exons 127 and 128Kati Donner, Kristen J Nowak, Mimmi Aro, et al.
Plos One|May 16, 2022
A custom ddPCR method for the detection of copy number variations in the nebulin triplicate regionLydia Sagath, Vilma-Lotta Lehtokari, Carina Wallgren-Pettersson, et al.
European Journal of Human Genetics : EJHG|July 22, 2004
Complete genomic structure of the human nebulin gene and identification of alternatively spliced transcriptsKati Donner, Maria Sandbacka, Vilma-Lotta Lehtokari, et al.
Pageof 5

Showing results (1-10 of 49) with videos related to

Sort By:
Pageof 5
The Journal of General Physiology|February 3, 2021
Nebulin: Size matters for optimal muscle functionKatarina Pelin
Gene|July 7, 2012
Nebulin is not expressed in plantsKatarina Pelin
Seminars in Pediatric Neurology|May 8, 2019
Update on the Genetics of Congenital MyopathiesKatarina Pelin, Carina Wallgren-Pettersson
Advances in Experimental Medicine and Biology|February 3, 2009
Nebulin--a giant chameleonKatarina Pelin, Carina Wallgren-Pettersson
Genes|May 28, 2022
Array Comparative Genomic Hybridisation and Droplet Digital PCR Uncover Recurrent Copy Number Variation of the <i>TTN</i> Segmental Duplication RegionLydia Sagath, Vilma-Lotta Lehtokari, Katarina Pelin, et al.
Neuromuscular Disorders : NMD|February 14, 2018
Clinically variable nemaline myopathy in a three-generation family caused by mutation of the skeletal muscle alpha-actin geneVilma-Lotta Lehtokari, Maria Gardberg, Katarina Pelin, et al.
Journal of Human Genetics|January 16, 2015
A commentary on identification of the rare compound heterozygous variants in the NEB gene in a Korean family with intellectual disability, epilepsy and early-childhood-onset generalized muscle weaknessKatarina Pelin, Kirsi Kiiski, Vilma-Lotta Lehtokari, et al.
Genomics|July 25, 2006
Developmental and muscle-type-specific expression of mouse nebulin exons 127 and 128Kati Donner, Kristen J Nowak, Mimmi Aro, et al.
Plos One|May 16, 2022
A custom ddPCR method for the detection of copy number variations in the nebulin triplicate regionLydia Sagath, Vilma-Lotta Lehtokari, Carina Wallgren-Pettersson, et al.
European Journal of Human Genetics : EJHG|July 22, 2004
Complete genomic structure of the human nebulin gene and identification of alternatively spliced transcriptsKati Donner, Maria Sandbacka, Vilma-Lotta Lehtokari, et al.
Pageof 5