Dysfunctional Polycomb Transcriptional Repression Contributes to Lamin a/C Dependent Muscular Dystrophy

Journal of Clinical Investigation - United States
doi 10.1172/jci128161
Full Text
Abstract

Available in full text

Categories
Medicine
Date
Authors
Publisher

American Society for Clinical Investigation

Related search

Dropped Head Related Lamin a/C Associated Congenital Muscular Dystrophy Case; Previously Defined as Emerydreifuss Muscular Dystrophy

Turkish Journal of Pediatrics
Child HealthPediatricsPerinatology
2020English

Identification of Lamin a/C ( LMNA ) Gene Mutations in Korean Patients With Autosomal Dominant Emery-Dreifuss Muscular Dystrophy and Limb-Girdle Muscular Dystrophy 1B

Journal of Human Genetics
Genetics
2002English

C-CRK Proto-Oncogene Contributes to Transcriptional Repression of P120-Catenin in Non-Small Cell Lung Cancer Cells

Clinical and Experimental Metastasis
MedicineCancer ResearchOncology
2011English

Lamin a N-Terminal Phosphorylation Is Associated With Myoblast Activation: Impairment in Emery-Dreifuss Muscular Dystrophy

Journal of Medical Genetics
Genetics
2005English

Muscular Dystrophy

BMJ
1963English

Facioscapulohumeral Muscular Dystrophy

Rare Diseases
2013English

Congenital Muscular Dystrophy

The Internet Journal of Radiology
2010English

Expression of a Mutant Lamin a That Causes Emery-Dreifuss Muscular Dystrophy Inhibits in Vitro Differentiation of C2C12 Myoblasts

Molecular and Cellular Biology
Cell BiologyMolecular Biology
2004English

Comparative Proteomic Analyses of Duchenne Muscular Dystrophy and Becker Muscular Dystrophy Muscles: Changes Contributing to Preserve Muscle Function in Becker Muscular Dystrophy Patients

Journal of Cachexia, Sarcopenia and Muscle
OrthopedicsSports MedicinePhysiology
2020English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy