Correction: Cardiomyocyte-Specific Expression of Lamin A Improves Cardiac Function in Lmna−/− Mice

Correction: Cardiomyocyte-Specific Expression of Lamin A Improves Cardiac Function in Lmna−/− Mice

Bibliographic Details
Format:	Article
Language:	English
Published:	Public Library of Science (PLoS) 2012-01-01
Series:	PLoS ONE
Online Access:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3465171/?tool=EBI

Similar Items

Cardiomyocyte-specific expression of lamin a improves cardiac function in Lmna-/- mice.
by: Richard L Frock, et al.
Published: (2012-01-01)

Correction: Cardiomyocyte-Specific Expression of Lamin A Improves Cardiac Function in Mice.
by: Richard L. Frock, et al.
Published: (2012-01-01)

Cardiomyocyte Proliferative Capacity Is Restricted in Mice With Lmna Mutation
by: Kenji Onoue, et al.
Published: (2021-06-01)

Phenotypic Variability in iPSC-Induced Cardiomyocytes and Cardiac Fibroblasts Carrying Diverse LMNA Mutations
by: Jiajia Yang, et al.
Published: (2021-12-01)

Revisiting the truncated lamin A produced by a commonly used strain of Lmna knockout mice
by: Joonyoung R. Kim, et al.
Published: (2023-12-01)

Corrigendum: Phenotypic variability in iPSC-induced cardiomyocytes and cardiac fibroblasts carrying diverse LMNA mutations
by: Jiajia Yang, et al.
Published: (2022-08-01)

The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype
by: Rafael D. González-Cruz, et al.
Published: (2018-11-01)

Correction: Trastuzumab Alters the Expression of Genes Essential for Cardiac Function and Induces Ultrastructural Changes of Cardiomyocytes in Mice
Published: (2014-01-01)

Correction: Trastuzumab Alters the Expression of Genes Essential for Cardiac Function and Induces Ultrastructural Changes of Cardiomyocytes in Mice.
by: M. Khair ElZarrad, et al.
Published: (2014-01-01)

LAMIN A/C GENE (LMNA) MUTATIONS IN PATIENTS WITH DILATED CARDIOMYOPATHY AND THEIR PHENOTYPIC MANIFESTATION
by: T. G. Vaikhanskaya, et al.
Published: (2016-03-01)

Effects of mutant lamins on nucleo-cytoskeletal coupling in Drosophila models of LMNA muscular dystrophy
by: Nicholas M. Shaw, et al.
Published: (2022-08-01)

Cell-extrinsic defective lymphocyte development in Lmna(-/-) mice.
by: J Scott Hale, et al.
Published: (2010-04-01)

Characterization of cardiac involvement in children with LMNA-related muscular dystrophy
by: Sergi Cesar, et al.
Published: (2023-03-01)

Genome organization in cardiomyocytes expressing mutated A-type lamins
by: Marie Kervella, et al.
Published: (2022-10-01)

Trastuzumab alters the expression of genes essential for cardiac function and induces ultrastructural changes of cardiomyocytes in mice.
by: M Khair ElZarrad, et al.
Published: (2013-01-01)

Systematic in vivo candidate evaluation uncovers therapeutic targets for LMNA dilated cardiomyopathy and risk of Lamin A toxicity
by: Chia Yee Tan, et al.
Published: (2023-10-01)

Investigating <i>LMNA</i>-Related Dilated Cardiomyopathy Using Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
by: Yuval Shemer, et al.
Published: (2021-07-01)

Activation of sarcolipin expression and altered calcium cycling in LMNA cardiomyopathy
by: Blanca Morales Rodriguez, et al.
Published: (2020-07-01)

The Broad Spectrum of LMNA Cardiac Diseases: From Molecular Mechanisms to Clinical Phenotype
by: Silvia Crasto, et al.
Published: (2020-07-01)

<i>LMNA</i> Co-Regulated Gene Expression as a Suitable Readout after Precise Gene Correction
by: Haicui Wang, et al.
Published: (2022-12-01)

Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: association analyses in 9,518 subjects.
by: Owen, K, et al.
Published: (2007)

Can Circulating Cardiac Biomarkers Be Helpful in the Assessment of <i>LMNA</i> Mutation Carriers?
by: Przemyslaw Chmielewski, et al.
Published: (2020-05-01)

<i>LMNA</i> Mutation in a Family with a Strong History of Sudden Cardiac Death
by: Laura Keil, et al.
Published: (2022-01-01)

Characterization of cardiac involvement in patients with LMNA splice-site mutation–related dilated cardiomyopathy and sudden cardiac death
by: Xuebin Ling, et al.
Published: (2024-01-01)

Deficiency of emerin contributes differently to the pathogenesis of skeletal and cardiac muscles in LmnaH222P/H222P mutant mice.
by: Eiji Wada, et al.
Published: (2019-01-01)

Lamin A/C Ablation Restricted to Vascular Smooth Muscle Cells, Cardiomyocytes, and Cardiac Fibroblasts Causes Cardiac and Vascular Dysfunction
by: Alberto Del Monte-Monge, et al.
Published: (2023-07-01)

Mechanisms of A-Type Lamin Targeting to Nuclear Ruptures Are Disrupted in <i>LMNA-</i> and <i>BANF1-</i>Associated Progerias
by: Rhiannon M. Sears, et al.
Published: (2022-03-01)

Consequences of <i>Lmna</i> Exon 4 Mutations in Myoblast Function
by: Déborah Gómez-Domínguez, et al.
Published: (2020-05-01)

Heterozygous LMNA mutation-carrying iPSC lines from three cardiac laminopathy patients
by: Sangkyun Cho, et al.
Published: (2022-03-01)

LMNA mutation leads to cardiac sodium channel dysfunction in the Emery-Dreifuss muscular dystrophy patient
by: Kseniya Perepelina, et al.
Published: (2022-07-01)

Low and high expressing alleles of the LMNA gene: implications for laminopathy disease development.
by: Sofía Rodríguez, et al.
Published: (2011-01-01)

Sudden Cardiac Arrest in a Patient With Mitral Valve Prolapse and LMNA and SCN5A Mutations
by: Asha M. Mahajan, MD, et al.
Published: (2021-02-01)

Epigenetics in <i>LMNA</i>-Related Cardiomyopathy
by: Yinuo Wang, et al.
Published: (2023-03-01)

A heterozygous p.S143P mutation in LMNA associates with proteasome dysfunction and enhanced autophagy-mediated degradation of mutant lamins A and C
by: Gun West, et al.
Published: (2022-08-01)

Effect of Occurrence of Lamin A/C (LMNA) Genetic Variants in a Cohort of 101 Consecutive Apparent “Lone AF” Patients: Results and Insights
by: Gabrielle D'Arezzo Pessente, et al.
Published: (2022-04-01)

The relative contributions of cardiomyocytes versus endothelial cells to cardiac BH4 production; studies in novel cardiomyocyte- and endothelial-specific GTPCH I-deficient mice
by: Bendall, J, et al.
Published: (2012)

Construction of HEK293 and C2C12 cell models transfected by LMNA mutant and related intracellular sublocalization of lamin A/C
by: TAN Dan-dan, CHAI Jing-yan, LIU Jian-yun, NIE Hong-bing, XIONG Hui, WU Xiang-bin
Published: (2020-04-01)

Deletion of entire LMNA gene as a cause of cardiomyopathy
by: Allison L. Cirino, MS, et al.
Published: (2020-07-01)

Whole-exome sequencing to identify a novel LMNA gene mutation associated with inherited cardiac conduction disease.
by: Chun-Chi Lai, et al.
Published: (2013-01-01)

Pregnancy and Progression of Cardiomyopathy in Women With LMNA Genotype‐Positive
by: Anna I. Castrini, et al.
Published: (2022-04-01)