Sage Journals: Discover world-class research

Free access

Case report

First published 2022

A Single mtDNA Deletion in Association with a LMNA Gene New Frameshift Variant: A Case Report

Vincenzo Montano, Michelangelo Mancuso, Costanza Simoncini [...]

Journal of Neuromuscular Diseases

Retricted access

Case report

First published 2020-12

Hypopharyngeal Squamous Cell Carcinoma in Sisters with LMNA Associated Familial Partial Lipodystrophy: A Case Report and Review of the Literature

Stephanie J. Youssef, Robert J. Macielak, Lisa A. Schimmenti [...]

Annals of Otology,Rhinology & Laryngology

Retricted access

Research article

First published 2009-10

LMNA,ZMPSTE24,and LBR Are Not Mutated in Scleroderma

Caroline Gaudy-Marqueste, Amandine Boyer, Claire Navarro [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Research article

First published 2012-06

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

Birgit Stallmeyer, Matthias Koopmann, Eric Schulze-Bahr

Genetic Testing and Molecular Biomarkers

Free access

Research article

First published 2004-10

Analysis of Genetic Variations of Lamin A/C Gene (LMNA) by Denaturing High-Performance Liquid Chromatography

Matthew R. G. Taylor, Misi L. Robinson, Luisa Mestroni

Journal of Biomolecular Screening

Retricted access

Research article

First published 2020-2

Viscoelastic behavior of cardiomyocytes carrying LMNA mutations

Daniele Borin, Brisa Peña, Matthew R.G. Taylor [...]

Biorheology

Retricted access

Case report

First published 2020-8

Myxoid Spindle Cell Sarcoma With LMNA-NTRK Fusion: Expanding the Morphologic Spectrum of NTRK -Rearranged Tumors

Yik Ka So, Chit Chow, Ka Fai To [...]

International Journal of Surgical Pathology

Retricted access

Research article

First published 2025

Clinical and Genetic Landscape of Children With Congenital Muscular Dystrophies From North India

Anirban Basu, Renu Suthar, Abhishek Pandey [...]

Journal of Child Neurology

Retricted access

Research article

First published 2023-5

A novel deletion mutation accompanied by a point mutation in Lamin A/C gene: Screened from a dilated cardiomyopathy family

Hao Jia, Yongxin Sun, Wangchao Yao [...]

Perfusion

Retricted access

Research article

First published 2012-04

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

Walter Arancio

Rejuvenation Research

Search results