Depletion of lamina-associated polypeptide 1 from cardiomyocytes causes cardiac dysfunction in mice

Mutation in TOR1AIP1 encoding LAP1B in a form of muscular dystrophy: A novel gene related to nuclear envelopathies

(2014) Gulsum Kayman-Kurekci et al.   NEUROMUSCULAR DISORDERS

Lamina-associated polypeptide 1: Protein interactions and tissue-selective functions

(2014) Ji-Yeon Shin et al.   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY

Multiple novel functions of Lamina associated polypeptide 2α in striated muscle

(2014) Ivana Gotic et al.   Nucleus

Lamina-Associated Polypeptide-1 Interacts with the Muscular Dystrophy Protein Emerin and Is Essential for Skeletal Muscle Maintenance

(2013) Ji-Yeon Shin et al.   DEVELOPMENTAL CELL

Depletion of extracellular signal-regulated kinase 1 in mice with cardiomyopathy caused by lamin A/C gene mutation partially prevents pathology before isoenzyme activation

(2013) W. Wu et al.   HUMAN MOLECULAR GENETICS

Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity

(2013) Marie-Elodie Cattin et al.   HUMAN MOLECULAR GENETICS

The Nuclear Envelope Protein, LAP1B, Is a Novel Protein Phosphatase 1 Substrate

(2013) Mariana Santos et al.   PLoS One

Abnormal p38  mitogen-activated protein kinase signaling in dilated cardiomyopathy caused by lamin A/C gene mutation

(2012) A. Muchir et al.   HUMAN MOLECULAR GENETICS

Mouse fukutin deletion impairs dystroglycan processing and recapitulates muscular dystrophy

(2012) Aaron M. Beedle et al.   JOURNAL OF CLINICAL INVESTIGATION

Treatment with selumetinib preserves cardiac function and improves survival in cardiomyopathy caused by mutation in the lamin A/C gene

(2011) A. Muchir et al.   CARDIOVASCULAR RESEARCH

Defective Tbx2-dependent patterning of the atrioventricular canal myocardium causes accessory pathway formation in mice

(2011) Wim T.J. Aanhaanen et al.   JOURNAL OF CLINICAL INVESTIGATION

Nuclear lamins and laminopathies

(2011) Howard J. Worman   JOURNAL OF PATHOLOGY

Mitogen-Activated Protein Kinase Inhibitors Improve Heart Function and Prevent Fibrosis in Cardiomyopathy Caused by Mutation in Lamin A/C Gene

(2010) Wei Wu et al.   CIRCULATION

X-linked muscular dystrophy with early contractures and cardiomyopathy (Emery-Dreifuss type)

(2010) Alan E. H. Emery   CLINICAL GENETICS

A molecular mechanism underlying the neural-specific defect in torsinA mutant mice

(2010) C. E. Kim et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Lamina-Associated Polypeptide 2α Loss Impairs Heart Function and Stress Response in Mice

(2009) Ivana Gotic et al.   CIRCULATION RESEARCH

The Nuclear Envelope as a Signaling Node in Development and Disease

(2009) William T. Dauer et al.   DEVELOPMENTAL CELL

Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins

(2008) A. Muchir et al.   HUMAN MOLECULAR GENETICS