Jenni M Laitila - JoVE Visualize

Showing results (1-10 of 4) with videos related to

Pageof 1

Sort By:

Journal of Muscle Research and Cell Motility|June 23, 2019

Nemaline myopathies: a current viewCaroline A Sewry, Jenni M Laitila, Carina Wallgren-Pettersson

JCI Insight|April 17, 2019

Cullin-3 dependent deregulation of ACTN1 represents a new pathogenic mechanism in nemaline myopathyJordan Blondelle, Kavya Tallapaka, Jane T Seto, et al.

Neuromuscular Disorders : NMD|January 26, 2019

Dominantly inherited distal nemaline/cap myopathy caused by a large deletion in the nebulin geneKirsi J Kiiski, Vilma-Lotta Lehtokari, Anna K Vihola, et al.

Acta Neuropathologica Communications|February 19, 2020

Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in NebJenni M Laitila, Elyshia L McNamara, Catherine D Wingate, et al.

Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:

Pageof 1

Journal of Muscle Research and Cell Motility|June 23, 2019

Nemaline myopathies: a current viewCaroline A Sewry, Jenni M Laitila, Carina Wallgren-Pettersson

JCI Insight|April 17, 2019

Cullin-3 dependent deregulation of ACTN1 represents a new pathogenic mechanism in nemaline myopathyJordan Blondelle, Kavya Tallapaka, Jane T Seto, et al.

Neuromuscular Disorders : NMD|January 26, 2019

Dominantly inherited distal nemaline/cap myopathy caused by a large deletion in the nebulin geneKirsi J Kiiski, Vilma-Lotta Lehtokari, Anna K Vihola, et al.

Acta Neuropathologica Communications|February 19, 2020

Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in NebJenni M Laitila, Elyshia L McNamara, Catherine D Wingate, et al.

Pageof 1