none6noneMaraldi NM; Capanni C; Lattanzi G; Camozzi D; Facchini A; Manzoli FA.Maraldi NM; Capanni C; Lattanzi G; Camozzi D; Facchini A; Manzoli FA
LMNA p.R482W mutation related to FPLD2 alters SREBP1-A type lamin interactions in human fibroblasts ...
International audienceMutations in LMNA, encoding A-type lamins, are responsible for laminopathies i...
Familial partial lipodystrophy (FPLD) is an inherited condition in which regional fat loss occurs at...
International audienceLamins A and C are nuclear intermediate filament proteins expressed in most di...
Lipodystrophies are a heterogeneous group of human disorders characterized by the anomalous distribu...
Lipodystrophies are a heterogeneous group of human disorders characterized by the anomalous distribu...
The p.R482W substitution in A-type lamins deregulates SREBP1 activity in Dunnigan-type familial part...
Laminopathies belong to the group of diseases caused by mutations in genes encoding nuclear envelope...
Lamin A is a component of the nuclear lamina mutated in a group of human inherited disorders known a...
Lamin A is a component of the nuclear lamina mutated in a group of human inherited disorders known a...
Lamin A is a component of the nuclear lamina mutated in a group of human inherited disorders known a...
Failure to process prelamin A, by the enzyme ZMPSTE24, leads to the build up of farnesylated prelami...
Mutations in A-type lamins or lamin-binding proteins are involved in the pathogenesis of diseases re...
LMNA p.R482W mutation related to FPLD2 alters SREBP1-A type lamin interactions in human fibroblasts ...
International audienceMutations in LMNA, encoding A-type lamins, are responsible for laminopathies i...
Familial partial lipodystrophy (FPLD) is an inherited condition in which regional fat loss occurs at...
International audienceLamins A and C are nuclear intermediate filament proteins expressed in most di...
Lipodystrophies are a heterogeneous group of human disorders characterized by the anomalous distribu...
Lipodystrophies are a heterogeneous group of human disorders characterized by the anomalous distribu...
The p.R482W substitution in A-type lamins deregulates SREBP1 activity in Dunnigan-type familial part...
Laminopathies belong to the group of diseases caused by mutations in genes encoding nuclear envelope...
Lamin A is a component of the nuclear lamina mutated in a group of human inherited disorders known a...
Lamin A is a component of the nuclear lamina mutated in a group of human inherited disorders known a...
Lamin A is a component of the nuclear lamina mutated in a group of human inherited disorders known a...
Failure to process prelamin A, by the enzyme ZMPSTE24, leads to the build up of farnesylated prelami...
Mutations in A-type lamins or lamin-binding proteins are involved in the pathogenesis of diseases re...
LMNA p.R482W mutation related to FPLD2 alters SREBP1-A type lamin interactions in human fibroblasts ...
International audienceMutations in LMNA, encoding A-type lamins, are responsible for laminopathies i...
Familial partial lipodystrophy (FPLD) is an inherited condition in which regional fat loss occurs at...
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