Article

LMNA p.R482W mutation related to FPLD2 alters SREBP1-A type lamin interactions in human fibroblasts and adipose stem cells

2015-01-01

Abstract excerpt

No abstract is available from the source.

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: a03eec31-0375-5b7e-a12b-905340fffce3
DOI: 10.1186/1750-1172-10-s2-o13
PMCID: PMC4652467

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

LMNA p.R482W mutation related to FPLD2 alters SREBP1-A type lamin interactions in human fibroblasts and adipose stem cellsDOI 10.1186/1750-1172-10-s2-o13Read

Lipodystrophic Laminopathies: From Dunnigan Disease to Progeroid Syndromes.Semantic proximity Read

A Rare Mutation in LMNB2 Associated with Lipodystrophy Drives Premature Cell Senescence.Semantic proximity Read

Lipodystrophic syndromes due to LMNA mutations: recent developments on biomolecular aspects, pathophysiological hypotheses and therapeutic perspectives.Semantic proximity Read

Novel LMNA mutations seen in patients with familial partial lipodystrophy subtype 2 (FPLD2; MIM 151660).Semantic proximity Read

<i>LMNA</i>R644C associates with hepatic steatosis in a large cohort and increases cellular lipid droplet accumulation<i>in vitro</i>Semantic proximity Read

A subtype of laminopathies: Generalized lipodystrophy-associated progeroid syndrome caused by LMNA gene c.29C>T mutation.Semantic proximity Read

A recurrent familial partial lipodystrophy due to a monoallelic or biallelic LMNA founder variant highlights the multifaceted cardiac manifestations of metabolic laminopathies.Semantic proximity Read

Advances in lipodystrophy syndrome caused by LMNA gene mutation.Semantic proximity Read

The Clinical Characteristics and Potential Molecular Mechanism of LMNA Mutation-Related Lipodystrophy.Semantic proximity Read

Navigating Lipodystrophy: Insights from Laminopathies and Beyond.Semantic proximity Read

Deregulation of Fragile X-related protein 1 by the lipodystrophic lamin A p.R482W mutation elicits a myogenic gene expression program in preadipocytes.Semantic proximity Read

Laminopathies; Mutations on single gene and various human genetic diseases.Semantic proximity Read