Mdc1a | List of Frontiers open access articles

Original Research

Published on 03 Jul 2014

Laminin α2 Chain-Deficiency is Associated with microRNA Deregulation in Skeletal Muscle and Plasma

in Cellular and Molecular Mechanisms of Brain-aging

Johan Holmberg
Azra Alajbegovic
Kinga Izabela Gawlik
Linda Elowsson
Madeleine Durbeej

Frontiers in Aging Neuroscience

doi 10.3389/fnagi.2014.00155

6,654 views
26 citations

Review

Published on 23 Jul 2020

Brain Dysfunction in LAMA2-Related Congenital Muscular Dystrophy: Lessons From Human Case Reports and Mouse Models

in Molecular Signalling and Pathways

Andrea J. Arreguin
Holly Colognato

Frontiers in Molecular Neuroscience

doi 10.3389/fnmol.2020.00118

9,916 views
27 citations

Original Research

Published on 07 May 2019

Identification of Candidate Protein Markers in Skeletal Muscle of Laminin-211-Deficient CMD Type 1A-Patients

in Movement Disorders

Heike Kölbel
Denisa Hathazi
Matthew Jennings
Rita Horvath
Andreas Roos
Ulrike Schara

Frontiers in Neurology

doi 10.3389/fneur.2019.00470

6,225 views
18 citations

Review

Published on 04 Feb 2020

Fibrogenesis in LAMA2-Related Muscular Dystrophy Is a Central Tenet of Disease Etiology

in Brain Disease Mechanisms

Anthony Accorsi
Megan L. Cramer
Mahasweta Girgenrath

Frontiers in Molecular Neuroscience

doi 10.3389/fnmol.2020.00003

9,739 views
28 citations

Review

Published on 09 Jul 2020

Zebrafish Models of LAMA2-Related Congenital Muscular Dystrophy (MDC1A)

in Methods and Model Organisms

Lacramioara Fabian
James J. Dowling

Frontiers in Molecular Neuroscience

doi 10.3389/fnmol.2020.00122

5,871 views
7 citations

Original Research

Published on 25 Jul 2019

Molecular Genetics Analysis of 70 Chinese Families With Muscular Dystrophy Using Multiplex Ligation-Dependent Probe Amplification and Next-Generation Sequencing

in Translational Pharmacology

Dong Wang
Min Gao
Kaihui Zhang
Ruifeng Jin
Yuqiang Lv
Yong Liu
Jian Ma
Ya Wan
Zhongtao Gai
Yi Liu

Frontiers in Pharmacology

doi 10.3389/fphar.2019.00814

6,639 views
13 citations

Case Report

Published on 13 Feb 2018

Identification of Two Novel LAMA2 Mutations in a Chinese Patient with Congenital Muscular Dystrophy

in Genetics of Common and Rare Diseases

Jing Zhou
Jianxin Tan
Dingyuan Ma
Jingjing Zhang
Jian Cheng
Chunyu Luo
Gang Liu
Yuguo Wang
Zhengfeng Xu

Frontiers in Genetics

doi 10.3389/fgene.2018.00043

4,166 views
6 citations

Articles

Laminin α2 Chain-Deficiency is Associated with microRNA Deregulation in Skeletal Muscle and Plasma

Brain Dysfunction in LAMA2-Related Congenital Muscular Dystrophy: Lessons From Human Case Reports and Mouse Models

Identification of Candidate Protein Markers in Skeletal Muscle of Laminin-211-Deficient CMD Type 1A-Patients

Fibrogenesis in LAMA2-Related Muscular Dystrophy Is a Central Tenet of Disease Etiology

Zebrafish Models of LAMA2-Related Congenital Muscular Dystrophy (MDC1A)

Molecular Genetics Analysis of 70 Chinese Families With Muscular Dystrophy Using Multiplex Ligation-Dependent Probe Amplification and Next-Generation Sequencing

Identification of Two Novel LAMA2 Mutations in a Chinese Patient with Congenital Muscular Dystrophy