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pesek Revizija Vrtovi mutations of lamins Ponosni Zelena Ojačaj

Broken nuclei--lamins, nuclear mechanics, and disease. - Abstract - Europe  PMC
Broken nuclei--lamins, nuclear mechanics, and disease. - Abstract - Europe PMC

Frontiers | Post-Translational Modification of Lamins: Mechanisms and  Functions
Frontiers | Post-Translational Modification of Lamins: Mechanisms and Functions

Mutant lamins cause nuclear envelope rupture and DNA damage in skeletal  muscle cells | Nature Materials
Mutant lamins cause nuclear envelope rupture and DNA damage in skeletal muscle cells | Nature Materials

A progeria mutation reveals functions for lamin A in nuclear assembly,  architecture, and chromosome organization | PNAS
A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS

Pushing the Envelope | Science of Aging Knowledge Environment
Pushing the Envelope | Science of Aging Knowledge Environment

The lamin protein family | Genome Biology | Full Text
The lamin protein family | Genome Biology | Full Text

Progerin - Wikipedia
Progerin - Wikipedia

Unweaving the role of nuclear Lamins in neural circuit integrity
Unweaving the role of nuclear Lamins in neural circuit integrity

A progeria mutation reveals functions for lamin A in nuclear assembly,  architecture, and chromosome organization | PNAS
A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS

Cells | Free Full-Text | Consequences of Lmna Exon 4 Mutations in Myoblast  Function
Cells | Free Full-Text | Consequences of Lmna Exon 4 Mutations in Myoblast Function

Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes |  Journal of Medical Genetics
Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes | Journal of Medical Genetics

Research Summary | The Lammerding Lab
Research Summary | The Lammerding Lab

Aging: Progeria and the Lamin Connection - ScienceDirect
Aging: Progeria and the Lamin Connection - ScienceDirect

Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in  Mechanophenotype
Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype

CRISPR base editor treats premature-aging syndrome | Signal Transduction  and Targeted Therapy
CRISPR base editor treats premature-aging syndrome | Signal Transduction and Targeted Therapy

The wide and growing range of lamin B-related diseases: from laminopathies  to cancer | Cellular and Molecular Life Sciences
The wide and growing range of lamin B-related diseases: from laminopathies to cancer | Cellular and Molecular Life Sciences

PDF] The structural and gene expression hypotheses in laminopathic  diseases—not so different after all | Semantic Scholar
PDF] The structural and gene expression hypotheses in laminopathic diseases—not so different after all | Semantic Scholar

Schematic of the LMNA gene and lamin A protein indicating... | Download  Scientific Diagram
Schematic of the LMNA gene and lamin A protein indicating... | Download Scientific Diagram

Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers  Associated with Abnormal Transcription in Progeria - ScienceDirect
Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers Associated with Abnormal Transcription in Progeria - ScienceDirect

Lamin mutation location predicts cardiac phenotype severity: combined  analysis of the published literature | Open Heart
Lamin mutation location predicts cardiac phenotype severity: combined analysis of the published literature | Open Heart

JCI - How do mutations in lamins A and C cause disease?
JCI - How do mutations in lamins A and C cause disease?

Distribution of laminopathy-causing mutations causing mutations in the... |  Download Scientific Diagram
Distribution of laminopathy-causing mutations causing mutations in the... | Download Scientific Diagram

Frontiers | The Broad Spectrum of LMNA Cardiac Diseases: From Molecular  Mechanisms to Clinical Phenotype
Frontiers | The Broad Spectrum of LMNA Cardiac Diseases: From Molecular Mechanisms to Clinical Phenotype