Laminopathies, caused by mutations in A-type nuclear lamins, encompass a range of diseases, including forms of progeria and muscular dystrophy. In this issue, Chen et al. provide evidence that elevated expression of the nuclear inner membrane protein SUN1 drives pathology in multiple laminopathies
In the last 5 years, an impressive series of genetic diseases (16 distinct diseased phenotypes have ...
lamina is a filamentous protein structure that is proximal to the inner nuclear membrane in multicel...
Lamin A/C belongs to type V intermediate filaments and constitutes the nuclear lamina and nuclear ma...
[[abstract]]Mutations in the LMNA gene are associated with a spectrum of human dystrophic diseases t...
Abstract Mutations in LMNA encoding lamins A and C are associated with at least 10 different degener...
SummaryHuman LMNA gene mutations result in laminopathies that include Emery-Dreifuss muscular dystro...
[[abstract]]The inner nuclear envelope protein Sun1 interacts with the nuclear lamina and participat...
The Publisher's final version can be found by following the DOI link.The nuclear envelope (NE) LINC ...
Laminopathies, caused by mutations in A-type nuclear lamins, encompass a range of diseases, includin...
[[abstract]]Human LMNA gene mutations result in laminopathies that include Emery-Dreifuss muscular d...
The nuclear envelope (NE) LINC complex, in mammals comprised of SUN domain and nesprin proteins, pro...
[[abstract]]Hutchinson-Gilford progeria syndrome (HGPS) is a human progeroid disease caused by a poi...
[[abstract]]Hutchinson-Gilford progeria syndrome (HGPS) is a human progeroid disease caused by a poi...
Laminopathies are genetic diseases due to mutations or altered post-translational processing of nucl...
Mutations in several genes encoding nuclear envelope (NE) associated proteins cause Emery-Dreifuss m...
In the last 5 years, an impressive series of genetic diseases (16 distinct diseased phenotypes have ...
lamina is a filamentous protein structure that is proximal to the inner nuclear membrane in multicel...
Lamin A/C belongs to type V intermediate filaments and constitutes the nuclear lamina and nuclear ma...
[[abstract]]Mutations in the LMNA gene are associated with a spectrum of human dystrophic diseases t...
Abstract Mutations in LMNA encoding lamins A and C are associated with at least 10 different degener...
SummaryHuman LMNA gene mutations result in laminopathies that include Emery-Dreifuss muscular dystro...
[[abstract]]The inner nuclear envelope protein Sun1 interacts with the nuclear lamina and participat...
The Publisher's final version can be found by following the DOI link.The nuclear envelope (NE) LINC ...
Laminopathies, caused by mutations in A-type nuclear lamins, encompass a range of diseases, includin...
[[abstract]]Human LMNA gene mutations result in laminopathies that include Emery-Dreifuss muscular d...
The nuclear envelope (NE) LINC complex, in mammals comprised of SUN domain and nesprin proteins, pro...
[[abstract]]Hutchinson-Gilford progeria syndrome (HGPS) is a human progeroid disease caused by a poi...
[[abstract]]Hutchinson-Gilford progeria syndrome (HGPS) is a human progeroid disease caused by a poi...
Laminopathies are genetic diseases due to mutations or altered post-translational processing of nucl...
Mutations in several genes encoding nuclear envelope (NE) associated proteins cause Emery-Dreifuss m...
In the last 5 years, an impressive series of genetic diseases (16 distinct diseased phenotypes have ...
lamina is a filamentous protein structure that is proximal to the inner nuclear membrane in multicel...
Lamin A/C belongs to type V intermediate filaments and constitutes the nuclear lamina and nuclear ma...
DOI
Add to ORKG