Related references
Note: Only part of the references are listed.LMNA Mutation c.917T>G (p.L306R) Leads to Deleterious Hyper-Assembly of Lamin A/C and Associates with Severe Right Ventricular Cardiomyopathy and Premature Aging
Tero-Pekka Alastalo et al.
HUMAN MUTATION (2015)
Gene-rich chromosomal regions are preferentially localized in the lamin B deficient nuclear blebs of atypical progeria cells
Katrin Bercht Pfleghaar et al.
NUCLEUS (2015)
Gene-rich chromosomal regions are preferentially localized in the lamin B deficient nuclear blebs of atypical progeria cells
Katrin Bercht Pfleghaar et al.
NUCLEUS (2015)
Interphase phosphorylation of lamin A
Vitaly Kochin et al.
JOURNAL OF CELL SCIENCE (2014)
OASIS regulates chondroitin 6-O-sulfotransferase 1 gene transcription in the injured adult mouse cerebral cortex
Hiroaki Okuda et al.
JOURNAL OF NEUROCHEMISTRY (2014)
The Reactome pathway knowledgebase
David Croft et al.
NUCLEIC ACIDS RESEARCH (2014)
Endoplasmic Reticulum Stress Induces Different Molecular Structural Alterations in Human Dilated and Ischemic Cardiomyopathy
Ana Ortega et al.
PLOS ONE (2014)
Reactivation of autophagy ameliorates LMNA cardiomyopathy
Jason C. Choi et al.
AUTOPHAGY (2013)
'State-of-the-heart' of cardiac laminopathies
Marie-Elodie Cattin et al.
CURRENT OPINION IN CARDIOLOGY (2013)
Lamin A/C and emerin regulate MKL1-SRF activity by modulating actin dynamics
Chin Yee Ho et al.
NATURE (2013)
Dilated cardiomyopathy: the complexity of a diverse genetic architecture
Ray E. Hershberger et al.
NATURE REVIEWS CARDIOLOGY (2013)
The nuclear lamins: flexibility in function
Brian Burke et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2013)
Modeling of lamin A/C mutation premature cardiac aging using patient-specific induced pluripotent stem cells
Chung-Wah Siu et al.
AGING-US (2012)
A Novel Feedback Loop Regulates the Response to Endoplasmic Reticulum Stress via the Cooperation of Cytoplasmic Splicing and mRNA Translation
Mithu Majumder et al.
MOLECULAR AND CELLULAR BIOLOGY (2012)
CDK5 and MEKK1 mediate pro-apoptotic signalling following endoplasmic reticulum stress in an autosomal dominant retinitis pigmentosa model
Min-Ji Kang et al.
NATURE CELL BIOLOGY (2012)
Annotating Cancer Variants and Anti-Cancer Therapeutics in Reactome
Marija Milacic et al.
Cancers (2012)
Mitogen-Activated Protein Kinase Inhibitors Improve Heart Function and Prevent Fibrosis in Cardiomyopathy Caused by Mutation in Lamin A/C Gene
Wei Wu et al.
CIRCULATION (2011)
Gene expression, chromosome position and lamin A/C mutations
Megan J. Puckelwartz et al.
NUCLEUS (2011)
Lamin A and lamin C form homodimers and coexist in higher complex forms both in the nucleoplasmic fraction and in the lamina of cultured human cells
Thorsten Kolb et al.
NUCLEUS (2011)
A Multifunctional Lentiviral-Based Gene Knockdown with Concurrent Rescue that Controls for Off-Target Effects of RNAi
Yunfeng Feng et al.
GENOMICS PROTEOMICS & BIOINFORMATICS (2011)
Genotype-phenotype correlations in laminopathies: how does fate translate?
Juergen Scharner et al.
BIOCHEMICAL SOCIETY TRANSACTIONS (2010)
A novel LMNA mutation (R189W) in familial dilated cardiomyopathy: evidence for a 'hot spot' region at exon 3: a case report
Nicoletta Botto et al.
CARDIOVASCULAR ULTRASOUND (2010)
Morphological Analysis of 13 LMNA Variants Identified in a Cohort of 324 Unrelated Patients With Idiopathic or Familial Dilated Cardiomyopathy
Jason Cowan et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2010)
Attenuated hypertrophic response to pressure overload in a lamin A/C haploinsufficiency mouse
Mihaela Cupesi et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2010)
Nuclear Lamins
Thomas Dechat et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2010)
Reduced expression of A-type lamins and emerin activates extracellular signal-regulated kinase in cultured cells
Antoine Muchir et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2009)
Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins
Antoine Muchir et al.
HUMAN MOLECULAR GENETICS (2009)
The Supramolecular Organization of the C. elegans Nuclear Lamin Filament
Kfir Ben-Harush et al.
JOURNAL OF MOLECULAR BIOLOGY (2009)
Amyloid precursor protein promotes endoplasmic reticulum stress-induced cell death via C/EBP homologous protein-mediated pathway
Keita Takahashi et al.
JOURNAL OF NEUROCHEMISTRY (2009)
A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization
Pekka Taimen et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
The A- and B-type nuclear lamin networks: microdomains involved in chromatin organization and transcription
Takeshi Shimi et al.
GENES & DEVELOPMENT (2008)
Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease
Cordula M. Wolf et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2008)
Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cells
Sebastian Kandert et al.
HUMAN MOLECULAR GENETICS (2007)
Endoplasmic reticulum stress in the heart
Christopher C. Glembotski
CIRCULATION RESEARCH (2007)
Activation of MAPK pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy
Antoine Muchir et al.
JOURNAL OF CLINICAL INVESTIGATION (2007)
Nucleoplasmic lamins and their interaction partners, LAP2 alpha, Rb, and BAF, in transcriptional regulation
Daniela Dorner et al.
FEBS JOURNAL (2007)
Solubility properties and specific assembly pathways of the B-type lamin from Caenorhabditis elegans
Nicole Foeger et al.
JOURNAL OF STRUCTURAL BIOLOGY (2006)
Impact of disease mutations on the desmin filament assembly process
Harald Baer et al.
JOURNAL OF MOLECULAR BIOLOGY (2006)
Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies
T Arimura et al.
HUMAN MOLECULAR GENETICS (2005)
A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy
S Kärkkäinen et al.
EUROPEAN HEART JOURNAL (2004)
Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice
V Nikolova et al.
JOURNAL OF CLINICAL INVESTIGATION (2004)
Dilated cardiomyopathy caused by aberrant endoplasmic reticulum quality control in mutant KDEL receptor transgenic mice
H Hamada et al.
MOLECULAR AND CELLULAR BIOLOGY (2004)
Dynamic interaction between BAF and emerin revealed by FRAP, FLIP, and FRET analyses in living HeLa cells
T Shimi et al.
JOURNAL OF STRUCTURAL BIOLOGY (2004)
Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations
P Sébillon et al.
JOURNAL OF MEDICAL GENETICS (2003)
Intermediate filaments: novel assembly models and exciting new functions for nuclear lamins
H Herrmann et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2003)
IREI-mediated unconventional mRNA splicing and S2P-mediated ATF6 cleavage merge to regulate XBP1 in signaling the unfolded protein response
K Lee et al.
GENES & DEVELOPMENT (2002)
IRE1 couples endoplasmic reticulum load to secretory capacity by processing the XBP-1 mRNA
M Calfon et al.
NATURE (2002)
Gene Expression Omnibus: NCBI gene expression and hybridization array data repository
R Edgar et al.
NUCLEIC ACIDS RESEARCH (2002)
XBP1 mRNA is induced by ATF6 and spliced by IRE1 in response to ER stress to produce a highly active transcription factor
H Yoshida et al.
CELL (2001)
Nuclear lamins A and B1: Different pathways of assembly during nuclear envelope formation in living cells
RD Moir et al.
JOURNAL OF CELL BIOLOGY (2000)