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
Main Authors:	Frock, Richard L., Chen, Steven C., Dai, Dao-Fu, Frett, Ellie, Lau, Carmen, Brown, Christina, Pak, Diana N., Wang, Yuexia, Muchir, Antoine, Worman, Howard J., Santana, Luis F., Ladiges, Warren C., Rabinovitch, Peter S., Kennedy, Brian K.
Format:	Online
Language:	English
Published:	Public Library of Science 2012
Online Access:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3465171/

Similar Items

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

LMNA cardiomyopathy: cell biology and genetics meet clinical medicine
by: Lu, Jonathan T., et al.
Published: (2011)

Inhibition of extracellular signal-regulated kinase 1/2 signaling has beneficial effects on skeletal muscle in a mouse model of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutation
by: Muchir, Antoine, et al.
Published: (2013)

A truncated lamin A in the Lmna−/− mouse line: Implications for the understanding of laminopathies
by: Jahn, Daniel, et al.
Published: (2012)

The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stress
by: Verstraeten, Valerie LRM, et al.
Published: (2009)

LMNA-related dilated cardiomyopathy
by: Vaikhanskaya, Tatiyana, et al.
Published: (2014)

Mutations in LMNA Modulate the Lamin A - Nesprin-2 Interaction and Cause LINC Complex Alterations
by: Yang, Liu, et al.
Published: (2013)

Metreleptin therapy in LMNA-linked lipodystrophies
by: Vatier, Camille, et al.
Published: (2015)

Mandibuloacral Dysplasia Caused by LMNA Mutations and Uniparental Disomy
by: Bai, Shaochun, et al.
Published: (2014)

Irisin levels in LMNA-mutated lipodystrophic syndromes
by: Bensmaine, Faiza, et al.
Published: (2015)

Investigation of pathomechanisms of ventricular arrhythmias in cardiac laminopathies
by: Muchir, Antoine
Published: (2015)

Altered protein dynamics of disease-associated lamin A mutants
by: Gilchrist, Susan, et al.
Published: (2004)

Hutchinson-Gilford Progeria Syndrome with G608G LMNA Mutation
by: Kim, Hui Kwon, et al.
Published: (2011)

Low and High Expressing Alleles of the LMNA Gene: Implications for Laminopathy Disease Development
by: Rodríguez, Sofía, et al.
Published: (2011)

Abberent expression analysis of LMNA gene in hutchinson-gilford progeria syndrome
by: Navid, Afifa, et al.
Published: (2012)

LMNA Knock-Down Affects Differentiation and Progression of Human Neuroblastoma Cells
by: Maresca, Giovanna, et al.
Published: (2012)

Potential association of LMNA-associated generalized lipodystrophy with juvenile dermatomyositis
by: Melis Sahinoz, et al.
Published: (2018-03-01)

Novel mutations in LMNA A/C gene and associated phenotypes
by: Petillo, Roberta, et al.
Published: (2015)

LMNA-associated myopathies: the Italian experience in a large cohort of patients
by: Maggi, Lorenzo
Published: (2015)

Management of congenital muscular dystrophies related to defects in the LMNA gene
by: Quijano-Roy, Susana, et al.
Published: (2015)

Porcine LMNA Is a Positional Candidate Gene Associated with Growth and Fat Deposition
by: Choi, Bong Hwan, et al.
Published: (2012)

Decreased Proliferation Kinetics of Mouse Myoblasts Overexpressing FRG1
by: Chen, Steven C., et al.
Published: (2011)

Mitochondrial catalase suppresses naturally occurring lung cancer in old mice
by: Ge, Xuang, et al.
Published: (2015)

Animal models play a vital role in translational aging research
by: Ladiges, Warren C.
Published: (2015)

Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress
by: Paradisi, Mauro, et al.
Published: (2005)

Pathobiology of aging: an old problem gets a new look
by: Ladiges, Warren
Published: (2011)

The quality control theory of aging
by: Ladiges, Warren
Published: (2014)

Pathology assessment is necessary to validate translational endpoints in preclinical aging studies
by: Ladiges, Warren
Published: (2016)

Geropathology Research Network Symposium 2015
by: Ladiges, Warren
Published: (2015)

Strain concentrations in notched laminates under bending
by: Timothy C., Kennedy, et al.
Published: (2009)

A novel long term short interval physical activity regime improves body composition in mice
by: Goh, Jorming, et al.
Published: (2013)

Grip strength is potentially an early indicator of age-related decline in mice
by: Ge, Xuan, et al.
Published: (2016)

Progeroid laminopathy with restrictive dermopathy-like features caused by an isodisomic LMNA mutation p.R435C
by: Starke, Sven, et al.
Published: (2013)

LMNA p.R482W mutation related to FPLD2 alters SREBP1-A type lamin interactions in human fibroblasts and adipose stem cells
by: Buendia, Brigitte
Published: (2015)

Mitotic Defects Lead to Pervasive Aneuploidy and Accompany Loss of RB1 Activity in Mouse LmnaDhe Dermal Fibroblasts
by: Pratt, C. Herbert, et al.
Published: (2011)

Deletion of the Lmna Gene Induces Growth Delay and Serum Biochemical Changes in C57BL/6 Mice
by: Ruan, J., et al.
Published: (2014)

A novel radial water tread maze tracks age-related cognitive decline in mice
by: Pettan-Brewer, Christina, et al.
Published: (2013)

Identifying mentors for student employees on campus
by: David, Frock
Published: (2015)

Lamin A, lamin B, and lamin B receptor analogues in yeast
Published: (1989)

Involvement of the Lamin Rod Domain in Heterotypic Lamin Interactions Important for Nuclear Organization
by: Schirmer, Eric C., et al.
Published: (2001)