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L Merlini

Showing results (171-180 of 209) with videos related to

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Acta Neuropathologica|August 31, 2000
Emerin presence in plateletsS Squarzoni, P Sabatelli, C Capanni, et al.
Nature Genetics|August 31, 2001
Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndromeB Moghadaszadeh, N Petit, C Jaillard, et al.
Human Mutation|July 5, 2001
Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian familiesM L Mostacciuolo, E Righetti, M Zortea, et al.
British Journal of Pharmacology|June 13, 2009
The cyclophilin inhibitor Debio 025 normalizes mitochondrial function, muscle apoptosis and ultrastructural defects in Col6a1-/- myopathic miceT Tiepolo, A Angelin, E Palma, et al.
FEBS Letters|February 26, 1996
Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12D Jung, F Leturcq, Y Sunada, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|November 3, 2001
Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblastsP Sabatelli, P Bonaldo, G Lattanzi, et al.
Biochimica Et Biophysica Acta|June 8, 2014
Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathiesF Tagliavini, C Pellegrini, F Sardone, et al.
Human Molecular Genetics|March 21, 1998
Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophyL Cartegni, M R di Barletta, R Barresi, et al.
Cancer Research|October 5, 2001
Potent antitumor activity and improved pharmacological profile of ST1481, a novel 7-substituted camptothecinM De Cesare, G Pratesi, P Perego, et al.
Human Mutation|August 19, 2006
Mutation profile of the GAA gene in 40 Italian patients with late onset glycogen storage disease type IIA L E Montalvo, B Bembi, M Donnarumma, et al.
Pageof 21

Showing results (171-180 of 209) with videos related to

Sort By:
Pageof 21
Acta Neuropathologica|August 31, 2000
Emerin presence in plateletsS Squarzoni, P Sabatelli, C Capanni, et al.
Nature Genetics|August 31, 2001
Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndromeB Moghadaszadeh, N Petit, C Jaillard, et al.
Human Mutation|July 5, 2001
Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian familiesM L Mostacciuolo, E Righetti, M Zortea, et al.
British Journal of Pharmacology|June 13, 2009
The cyclophilin inhibitor Debio 025 normalizes mitochondrial function, muscle apoptosis and ultrastructural defects in Col6a1-/- myopathic miceT Tiepolo, A Angelin, E Palma, et al.
FEBS Letters|February 26, 1996
Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12D Jung, F Leturcq, Y Sunada, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|November 3, 2001
Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblastsP Sabatelli, P Bonaldo, G Lattanzi, et al.
Biochimica Et Biophysica Acta|June 8, 2014
Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathiesF Tagliavini, C Pellegrini, F Sardone, et al.
Human Molecular Genetics|March 21, 1998
Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophyL Cartegni, M R di Barletta, R Barresi, et al.
Cancer Research|October 5, 2001
Potent antitumor activity and improved pharmacological profile of ST1481, a novel 7-substituted camptothecinM De Cesare, G Pratesi, P Perego, et al.
Human Mutation|August 19, 2006
Mutation profile of the GAA gene in 40 Italian patients with late onset glycogen storage disease type IIA L E Montalvo, B Bembi, M Donnarumma, et al.
Pageof 21