Results 1 to 10 of about 14,738 (282)

Modulation of muscle redox and protein aggregation rescues lethality caused by mutant lamins

open access: yesRedox Biology, 2021
Mutations in the human LMNA gene cause a collection of diseases called laminopathies, which includes muscular dystrophy and dilated cardiomyopathy. The LMNA gene encodes lamins, filamentous proteins that form a meshwork on the inner side of the nuclear ...
Shuping Lai, Qiang Dai, Nnamdi Uche
exaly   +3 more sources

Drosophila as a Model for Studying the Roles of Lamins in Normal Tissues and Laminopathies [PDF]

open access: yesCells
Nuclear processes are fundamental to the regulation of cellular, tissue, and organismal function, especially in complex multicellular systems. Central to these processes are lamins and lamin-associated proteins, which contribute to nuclear structure ...
Aleksandra Zielińska   +3 more
doaj   +2 more sources

Nuclear Mechanics and Nuclear Mechanotransduction in Cancer Cell Migration and Invasion [PDF]

open access: yesBiomolecules
Nuclear mechanics and mechanotransduction are involved in the migration and invasion process, such as those in which the cells need to deform themselves to pass through constrictions.
Claudia Tanja Mierke
doaj   +2 more sources

The relationship of lamins with epigenetic factors during aging

open access: yesВавиловский журнал генетики и селекции, 2022
The key factor of genome instability during aging is transposon dysregulation. This may be due to senile changes in the expression of lamins, which epigenetically modulate transposons. Lamins directly physically interact with transposons.
R. N. Mustafin, E. K. Khusnutdinova
doaj   +1 more source

Diversity of Nuclear Lamin A/C Action as a Key to Tissue-Specific Regulation of Cellular Identity in Health and Disease

open access: yesFrontiers in Cell and Developmental Biology, 2021
A-type lamins are the main structural components of the nucleus, which are mainly localized at the nucleus periphery. First of all, A-type lamins, together with B-type lamins and proteins of the inner nuclear membrane, form a stiff structure—the nuclear ...
Anna Malashicheva, Kseniya Perepelina
doaj   +1 more source

Lamins [PDF]

open access: yesCurrent Biology, 2016
Xie and Burke discuss the roles of lamins in nuclear morphology and the pathological consequences of defects in these nuclear envelope proteins.
Wei, Xie, Brian, Burke
openaire   +2 more sources

A comparative study of Drosophila and human A-type lamins. [PDF]

open access: yesPLoS ONE, 2009
Nuclear intermediate filament proteins, called lamins, form a meshwork that lines the inner surface of the nuclear envelope. Lamins contain three domains: an N-terminal head, a central rod and a C-terminal tail domain possessing an Ig-fold structural ...
Sandra R Schulze   +10 more
doaj   +1 more source

Mechanisms of A-Type Lamin Targeting to Nuclear Ruptures Are Disrupted in LMNA- and BANF1-Associated Progerias

open access: yesCells, 2022
Mutations in the genes LMNA and BANF1 can lead to accelerated aging syndromes called progeria. The protein products of these genes, A-type lamins and BAF, respectively, are nuclear envelope (NE) proteins that interact and participate in various cellular ...
Rhiannon M. Sears, Kyle J. Roux
doaj   +1 more source

Nuclear Lamins: Key Proteins for Embryonic Development

open access: yesBiology, 2022
Lamins are essential components of the nuclear envelope and have been studied for decades due to their involvement in several devastating human diseases, the laminopathies.
Jasper Chrysolite Paul, Helena Fulka
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

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