Normal and aberrant splicing ofLMNA

A Novel Mutation in a Large French-Canadian Family with LGMD1B

(2014) Nicolas Chrestian et al.   CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES

Dynamic Integration of Splicing within Gene Regulatory Pathways

(2013) Ulrich Braunschweig et al.   CELL

Single-Cell Dynamics of Genome-Nuclear Lamina Interactions

(2013) Jop Kind et al.   CELL

Adult-onset autosomal dominant leukodystrophy without early autonomic dysfunctions linked to lamin B1 duplication: a phenotypic variant

(2013) Ana Potic et al.   JOURNAL OF NEUROLOGY

Reflections on the history of pre-mRNA processing and highlights of current knowledge: A unified picture

(2013) J. E. Darnell   RNA

Nuclear Lamin-A Scales with Tissue Stiffness and Enhances Matrix-Directed Differentiation

(2013) J. Swift et al.   SCIENCE

The Meiotic Nuclear Lamina Regulates Chromosome Dynamics and Promotes Efficient Homologous Recombination in the Mouse

(2013) Jana Link et al.   PLoS Genetics

Neonatal progeria: increased ratio of progerin to lamin A leads to progeria of the newborn

(2012) Janine Reunert et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Identification of Novel Mutations in LMNA Associated with Familial Forms of Dilated Cardiomyopathy

(2012) Birgit Stallmeyer et al.   Genetic Testing and Molecular Biomarkers

Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia

(2012) Brent L. Fogel et al.   MOVEMENT DISORDERS

Regulation of prelamin A but not lamin C by miR-9, a brain-specific microRNA

(2012) H.-J. Jung et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A Bioinformatics Analysis of Lamin-A Regulatory Network: A Perspective on Epigenetic Involvement in Hutchinson–Gilford Progeria Syndrome

(2012) Walter Arancio   REJUVENATION RESEARCH

Unique Preservation of Neural Cells in Hutchinson- Gilford Progeria Syndrome Is Due to the Expression of the Neural-Specific miR-9 MicroRNA

(2012) Xavier Nissan et al.   Cell Reports

Evolution of the lamin protein family

(2012) Annette Peter et al.   Nucleus

Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A

(2011) Fuki M. Hisama et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A Complex Double Deletion in LMNA Underlies Progressive Cardiac Conduction Disease, Atrial Arrhythmias, and Sudden Death

(2011) Roos F. Marsman et al.   Circulation-Cardiovascular Genetics

A conserved splicing mechanism of the LMNA gene controls premature aging

(2011) Isabel C. Lopez-Mejia et al.   HUMAN MOLECULAR GENETICS

Nuclear lamins and laminopathies

(2011) Howard J. Worman   JOURNAL OF PATHOLOGY

Filaments assembly of ectopically expressed Caenorhabditis elegans lamin within Xenopus oocytes

(2011) Einat Grossman et al.   JOURNAL OF STRUCTURAL BIOLOGY

Aberrant splicing in the LMNA gene caused by a novel mutation on the polypyrimidine tract of intron 5

(2011) Nicola Carboni et al.   MUSCLE & NERVE

P5.34 Alternative splicing of lamin A leads to age-dependent accumulation of progerin transcript in normal human muscle and sporadic IBM

(2011) Y.B. Luo et al.   NEUROMUSCULAR DISORDERS

Embryonic Senescence and Laminopathies in a Progeroid Zebrafish Model

(2011) Eriko Koshimizu et al.   PLoS One

Low and High Expressing Alleles of the LMNA Gene: Implications for Laminopathy Disease Development

(2011) Sofía Rodríguez et al.   PLoS One

Differential Temporal and Spatial Progerin Expression during Closure of the Ductus Arteriosus in Neonates

(2011) Regina Bökenkamp et al.   PLoS One

Interaction between the RNA binding domains of Ser-Arg splicing factor 1 and U1-70K snRNP protein determines early spliceosome assembly

(2011) S. Cho et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Splicing-Directed Therapy in a New Mouse Model of Human Accelerated Aging

(2011) F. G. Osorio et al.   Science Translational Medicine

Understanding splicing regulation through RNA splicing maps

(2011) Joshua T. Witten et al.   TRENDS IN GENETICS

Evolution of SR protein and hnRNP splicing regulatory factors

(2011) Anke Busch et al.   Wiley Interdisciplinary Reviews-RNA

Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption

(2010) Pallavi Gupta et al.   BASIC RESEARCH IN CARDIOLOGY

Lamin A-linked progerias: is farnesylation the be all and end all?

(2010) Dawn T. Smallwood et al.   BIOCHEMICAL SOCIETY TRANSACTIONS

A Human iPSC Model of Hutchinson Gilford Progeria Reveals Vascular Smooth Muscle and Mesenchymal Stem Cell Defects

(2010) Jinqiu Zhang et al.   Cell Stem Cell

Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations

(2010) Juergen Scharner et al.   HUMAN MUTATION

Direct Synthesis of Lamin A, Bypassing Prelamin A Processing, Causes Misshapen Nuclei in Fibroblasts but No Detectable Pathology in Mice

(2010) Catherine Coffinier et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

LMNArs4641 and the Muscle Lamin A and C Isoforms in Twins—Metabolic Implications and Transcriptional Regulation

(2010) L. Wegner et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Cap and cap-binding proteins in the control of gene expression

(2010) Ivan Topisirovic et al.   Wiley Interdisciplinary Reviews-RNA

Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging

(2009) Sofia Rodriguez et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Activating the synthesis of progerin, the mutant prelamin A in Hutchinson–Gilford progeria syndrome, with antisense oligonucleotides

(2009) Loren G. Fong et al.   HUMAN MOLECULAR GENETICS

Heart transplantation in 7 patients from a single family with limb-girdle muscular dystrophy caused by lamin A/C mutation

(2009) Pierre Ambrosi et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Partial Epilepsy in an Adolescent Male With Limb-Girdle Muscular Dystrophy 1B

(2009) Chang-Yong Tsao et al.   JOURNAL OF CHILD NEUROLOGY

Emery-Dreifuss Muscular Dystrophy: A Novel Mutation in the LMNA Gene

(2009) Petra Laššuthová et al.   PEDIATRIC NEUROLOGY

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

(2008) Sharie B. Parks et al.   AMERICAN HEART JOURNAL

De novoLMNAmutations cause a new form of congenital muscular dystrophy

(2008) Susana Quijano-Roy et al.   ANNALS OF NEUROLOGY

Cryptic splicing sites are differentially utilized in vivo

(2008) Amel Haj Khelil et al.   FEBS Journal

The A- and B-type nuclear lamin networks: microdomains involved in chromatin organization and transcription

(2008) T. Shimi et al.   GENES & DEVELOPMENT

Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies

(2008) Michele Pasotti et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Alternative isoform regulation in human tissue transcriptomes

(2008) Eric T. Wang et al.   NATURE

Phenotype and Course of Hutchinson–Gilford Progeria Syndrome

(2008) Melissa A. Merideth et al.   NEW ENGLAND JOURNAL OF MEDICINE