[HTML][HTML] Quantitative proteomic analysis reveals metabolic alterations, calcium dysregulation, and increased expression of extracellular matrix proteins in laminin α2 …

BM de Oliveira, CY Matsumura… - Molecular & Cellular …, 2014 - ASBMB
Congenital muscular dystrophy with laminin α2 chain deficiency (MDC1A) is one of the most
severe forms of muscular disease and is characterized by severe muscle weakness and …

[HTML][HTML] Quantitative Proteomic Analysis Reveals Metabolic Alterations, Calcium Dysregulation, and Increased Expression of Extracellular Matrix Proteins in Laminin …

BM de Oliveira, CY Matsumura… - Molecular & Cellular …, 2014 - Elsevier
Congenital muscular dystrophy with laminin α2 chain deficiency (MDC1A) is one of the most
severe forms of muscular disease and is characterized by severe muscle weakness and …

Quantitative proteomic analysis reveals metabolic alterations, calcium dysregulation, and increased expression of extracellular matrix proteins in laminin α2 chain …

BM de Oliveira, CY Matsumura… - Molecular & Cellular …, 2014 - europepmc.org
Congenital muscular dystrophy with laminin α2 chain deficiency (MDC1A) is one of the most
severe forms of muscular disease and is characterized by severe muscle weakness and …

Quantitative proteomic analysis reveals metabolic alterations, calcium dysregulation and increased expression of extracellular matrix proteins in laminin α2 chain …

B Menezes de Oliveira, C Matsumura… - Molecular & Cellular …, 2014 - lup.lub.lu.se
Congenital muscular dystrophy with laminin α2 chain-deficiency (MDC1A) is one of the most
severe forms of muscular disease and is characterized by severe muscle weakness and …

Quantitative proteomic analysis reveals metabolic alterations, calcium dysregulation and increased expression of extracellular matrix proteins in laminin α2 chain …

BM de Oliveira, C Matsumura… - Molecular & …, 2014 - portal.research.lu.se
Congenital muscular dystrophy with laminin α2 chain-deficiency (MDC1A) is one of the most
severe forms of muscular disease and is characterized by severe muscle weakness and …

[HTML][HTML] Quantitative Proteomic Analysis Reveals Metabolic Alterations, Calcium Dysregulation, and Increased Expression of Extracellular Matrix Proteins in Laminin …

BM de Oliveira, CY Matsumura… - Molecular & Cellular …, 2014 - ncbi.nlm.nih.gov
Congenital muscular dystrophy with laminin α2 chain deficiency (MDC1A) is one of the most
severe forms of muscular disease and is characterized by severe muscle weakness and …

[PDF][PDF] Quantitative Proteomic Analysis Reveals Metabolic Alterations, Calcium Dysregulation, and Increased Expression of Extracellular Matrix Proteins in Laminin 2 …

BM de Oliveira, CY Matsumura… - Molecular & Cellular …, 2014 - researchgate.net
Congenital muscular dystrophy with laminin 2 chain deficiency (MDC1A) is one of the most
severe forms of muscular disease and is characterized by severe muscle weakness and …

Quantitative proteomic analysis reveals metabolic alterations, calcium dysregulation, and increased expression of extracellular matrix proteins in Laminin α2 Chain …

BM de Oliveira, CY Matsumura… - Molecular and …, 2014 - repositorio.unicamp.br
Congenital muscular dystrophy with laminin α2 chain deficiency (MDC1A) is one of the most
severe forms of muscular disease and is characterized by severe muscle weakness and …

Quantitative proteomic analysis reveals metabolic alterations, calcium dysregulation, and increased expression of extracellular matrix proteins in laminin α2 chain …

BM de Oliveira, CY Matsumura… - Molecular & …, 2014 - pubmed.ncbi.nlm.nih.gov
Congenital muscular dystrophy with laminin α2 chain deficiency (MDC1A) is one of the most
severe forms of muscular disease and is characterized by severe muscle weakness and …

Quantitative proteomic analysis reveals metabolic alterations, calcium dysregulation, and increased expression of extracellular matrix proteins in laminin α2 chain …

BM de Oliveira, CY Matsumura… - Molecular & Cellular …, 2014 - europepmc.org
Congenital muscular dystrophy with laminin α2 chain deficiency (MDC1A) is one of the most
severe forms of muscular disease and is characterized by severe muscle weakness and …