The effect of the lamin A and its mutants on nuclear structure, cell proliferation, protein stability, and mobility in embryonic cells

Deleterious assembly of the lamin A/C mutant p.S143P causes ER stress in familial dilated cardiomyopathy

(2016) Gun West et al.   JOURNAL OF CELL SCIENCE

A novel lamin A/C gene missense mutation (445 V > E) in immunoglobulin-like fold associated with left ventricular non-compaction

(2015) Zhouying Liu et al.   EUROPACE

Emery-Dreifuss muscular dystrophy type 2 associated (?) with mild peripheral polyneuropathy

(2015) Agnieszka Madej-Pilarczyk et al.   FOLIA NEUROPATHOLOGICA

Proliferation of progeria cells is enhanced by lamina-associated polypeptide 2α (LAP2α) through expression of extracellular matrix proteins

(2015) Sandra Vidak et al.   GENES & DEVELOPMENT

LMNAMutation c.917T>G (p.L306R) Leads to Deleterious Hyper-Assembly of Lamin A/C and Associates with Severe Right Ventricular Cardiomyopathy and Premature Aging

(2015) Tero-Pekka Alastalo et al.   HUMAN MUTATION

Various lamin A/C mutations alter expression profile of mesenchymal stem cells in mutation specific manner

(2015) Anna Malashicheva et al.   MOLECULAR GENETICS AND METABOLISM

Autophagy mediates degradation of nuclear lamina

(2015) Zhixun Dou et al.   NATURE

Regulation of lamin properties and functions: does phosphorylation do it all?

(2015) Magdalena Machowska et al.   Open Biology

Phenotype–Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy

(2015) Dandan Tan et al.   PLoS One

Do lamin A and lamin C have unique roles?

(2014) Rasha Al-Saaidi et al.   CHROMOSOMA

Antagonistic functions of LMNA isoforms in energy expenditure and lifespan

(2014) I. C. Lopez-Mejia et al.   EMBO REPORTS

Systematic identification of pathological lamin A interactors

(2014) Travis A. Dittmer et al.   MOLECULAR BIOLOGY OF THE CELL

Striated muscle laminopathies

(2014) Feriel Azibani et al.   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY

Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations

(2014) Yao-Cheng Lin et al.   Nature Communications

MicroRNA-9 controls dendritic development by targeting REST

(2014) Sebastian A Giusti et al.   eLife

Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations

(2013) Takuro Arimura et al.   CARDIOVASCULAR RESEARCH

When Lamins Go Bad: Nuclear Structure and Disease

(2013) Katherine H. Schreiber et al.   CELL

The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteins

(2013) Rasha Al-Saaidi et al.   EXPERIMENTAL CELL RESEARCH

The protein kinase Akt/PKB regulates both prelamin A degradation and Lmna gene expression

(2013) Jessika Bertacchini et al.   FASEB JOURNAL

Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α

(2013) Tatiana V. Cohen et al.   HUMAN MOLECULAR GENETICS

Lamin A/C Haploinsufficiency Modulates the Differentiation Potential of Mouse Embryonic Stem Cells

(2013) Poonam Sehgal et al.   PLoS One

Mapping disease-related missense mutations in the immunoglobulin-like fold domain of lamin A/C reveals novel genotype-phenotype associations for laminopathies

(2013) Juergen Scharner et al.   PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS

Lamin A/C is Expressed in Pluripotent Mouse Embryonic Stem Cells

(2013) Melanie A. Eckersley-Maslin et al.   Nucleus

The nuclear envelope LEM-domain protein emerin

(2013) Jason M Berk et al.   Nucleus

Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistribution

(2012) Cristina Capanni et al.   CELL CYCLE

Muscle development, regeneration and laminopathies: how lamins or lamina-associated proteins can contribute to muscle development, regeneration and disease

(2012) Magda Dubinska-Magiera et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

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

Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria

(2011) V. Cenni et al.   EUROPEAN JOURNAL OF HISTOCHEMISTRY

DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death

(2011) Anne T. Bertrand et al.   HUMAN MOLECULAR GENETICS

Post-natal myogenic and adipogenic developmental

(2011) Nard Kubben et al.   Nucleus

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

Emerin-prelamin A interplay in human fibroblasts

(2009) Cristina Capanni et al.   BIOLOGY OF THE CELL

Adenoviral E1A Function through Myc

(2008) A. A. Chakraborty et al.   CANCER RESEARCH

Specific contribution of lamin A and lamin C in the development of laminopathies

(2008) N SYLVIUS et al.   EXPERIMENTAL CELL RESEARCH

NEP-A and NEP-B both contribute to nuclear pore formation in Xenopus eggs and oocytes

(2008) G. Salpingidou et al.   JOURNAL OF CELL SCIENCE

Lamin A Ser404 Is a Nuclear Target of Akt Phosphorylation in C2C12 Cells

(2008) Vittoria Cenni et al.   JOURNAL OF PROTEOME RESEARCH

Suppression of Proliferative Defects Associated with Processing-defective Lamin A Mutants by hTERT or Inactivation of p53

(2008) Brian A. Kudlow et al.   MOLECULAR BIOLOGY OF THE CELL