Results 41 to 50 of about 1,480,665 (235)

A novel role of lamins from genetic disease to cancer biomarkers

open access: yesOncology Reviews, 2016
Lamins are the key components of the nuclear lamina and by virtue of their interactions with chromatin and binding partners act as regulators of cell proliferation and differentiation.
Kunnathur Murugesan Sakthivel   +1 more
doaj   +1 more source

Regulation of Lipid Metabolism by Lamin in Mutation-Related Diseases

open access: yesFrontiers in Pharmacology, 2022
Nuclear lamins, known as type 5 intermediate fibers, are composed of lamin A, lamin C, lamin B1, and lamin B2, which are encoded by LMNA and LMNB genes, respectively.
Yue Peng   +4 more
doaj   +1 more source

Recent advances in understanding the role of lamins in health and disease [version 1; referees: 2 approved]

open access: yesF1000Research, 2016
Lamins are major components of the nuclear lamina, a network of proteins that supports the nuclear envelope in metazoan cells. Over the past decade, biochemical studies have provided support for the view that lamins are not passive bystanders providing ...
Sita Reddy, Lucio Comai
doaj   +1 more source

A heterozygous p.S143P mutation in LMNA associates with proteasome dysfunction and enhanced autophagy-mediated degradation of mutant lamins A and C

open access: yesFrontiers in Cell and Developmental Biology, 2022
Lamins A and C are nuclear intermediate filament proteins that form a proteinaceous meshwork called lamina beneath the inner nuclear membrane. Mutations in the LMNA gene encoding lamins A and C cause a heterogenous group of inherited degenerative ...
Gun West   +15 more
doaj   +1 more source

Nuclear Lamins a and B1 [PDF]

open access: yesThe Journal of Cell Biology, 2000
At the end of mitosis, the nuclear lamins assemble to form the nuclear lamina during nuclear envelope formation in daughter cells. We have fused A- and B-type nuclear lamins to the green fluorescent protein to study this process in living cells. The results reveal that the A- and B-type lamins exhibit different pathways of assembly. In the early stages
R D, Moir   +3 more
openaire   +2 more sources

Lamins in Lung Cancer: Biomarkers and Key Factors for Disease Progression through miR-9 Regulation?

open access: yesCells, 2018
Lung cancer represents the primary cause of cancer death in the world. Malignant cells identification and characterization are crucial for the diagnosis and management of patients with primary or metastatic cancers. In this context, the identification of
Julien Guinde   +8 more
doaj   +1 more source

Genome organization in cardiomyocytes expressing mutated A-type lamins

open access: yesFrontiers in Cell and Developmental Biology, 2022
Cardiomyopathy is a myocardial disorder, in which the heart muscle is structurally and functionally abnormal, often leading to heart failure. Dilated cardiomyopathy is characterized by a compromised left ventricular function and contributes significantly
Marie Kervella   +3 more
doaj   +1 more source

Need for NAD+: Focus on Striated Muscle Laminopathies

open access: yesCells, 2020
Laminopathies are a heterogeneous group of rare diseases caused by genetic mutations in the LMNA gene, encoding A-type lamins. A-type lamins are nuclear envelope proteins which associate with B-type lamins to form the nuclear lamina, a meshwork ...
Déborah Cardoso, Antoine Muchir
doaj   +1 more source

Nuclear lamins: key regulators of nuclear structure and activities [PDF]

open access: yesJournal of Cellular and Molecular Medicine, 2009
The lamin molecule The supramolecular assembly of lamins Lamin‐binding proteins Lamins and aging Lamins and stem cells Lamins and cancer Lamin and viruses AbstractThe nuclear lamina is a proteinaceous structure located underneath the inner nuclear membrane (INM), where it associates with the peripheral chromatin.
Prokocimer, Miron   +7 more
openaire   +2 more sources

Structure of the Globular Tail of Nuclear Lamin [PDF]

open access: yesJournal of Biological Chemistry, 2002
The nuclear lamins form a two-dimensional matrix that provides integrity to the cell nucleus and participates in nuclear activities. Mutations in the region of human LMNA encoding the carboxyl-terminal tail Lamin A/C are associated with forms of muscular dystrophy and familial partial lipodystrophy (FPLD).
Sirano, Dhe-Paganon   +3 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy