The p.R482W substitution in A-type lamins deregulates SREBP1 activity in Dunnigan-type familial partial lipodystroph
A-type lamin mutations are associated with degenerative disorders causing dilated cardiomyopathy, Ch...
: Laminopathies are disorders caused by LMNA gene mutations, which selectively affect different tiss...
PubMed ID: 26775134Background Familial partial lipodystrophy (FPL) is a rare genetic disorder charac...
none6noneMaraldi NM; Capanni C; Lattanzi G; Camozzi D; Facchini A; Manzoli FA.Maraldi NM; Capanni C;...
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...
Familial partial lipodystrophy (FPLD) is an inherited condition in which regional fat loss occurs at...
Familial partial lipodystrophy (FPLD), Dunnigan variety, is an autosomal dominant disorder character...
LMNA p.R482W mutation related to FPLD2 alters SREBP1-A type lamin interactions in human fibroblasts ...
The familial partial Dunnigan lipodystrophy, characterized by subcutaneous fat loss, is frequently c...
The understanding of a common complex phenotype such as insulin resistance can be favoured by evalua...
Background: Familial partial lipodystrophy (FPL) is a rare genetic disorder characterized by selecti...
International audienceMutations in LMNA, encoding A-type lamins, are responsible for laminopathies i...
Dunnigan-type familial partial lipodystrophy (FPLD) is a laminopathy characterized by an aberrant fa...
A-type lamin mutations are associated with degenerative disorders causing dilated cardiomyopathy, Ch...
: Laminopathies are disorders caused by LMNA gene mutations, which selectively affect different tiss...
PubMed ID: 26775134Background Familial partial lipodystrophy (FPL) is a rare genetic disorder charac...
none6noneMaraldi NM; Capanni C; Lattanzi G; Camozzi D; Facchini A; Manzoli FA.Maraldi NM; Capanni C;...
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...
Familial partial lipodystrophy (FPLD) is an inherited condition in which regional fat loss occurs at...
Familial partial lipodystrophy (FPLD), Dunnigan variety, is an autosomal dominant disorder character...
LMNA p.R482W mutation related to FPLD2 alters SREBP1-A type lamin interactions in human fibroblasts ...
The familial partial Dunnigan lipodystrophy, characterized by subcutaneous fat loss, is frequently c...
The understanding of a common complex phenotype such as insulin resistance can be favoured by evalua...
Background: Familial partial lipodystrophy (FPL) is a rare genetic disorder characterized by selecti...
International audienceMutations in LMNA, encoding A-type lamins, are responsible for laminopathies i...
Dunnigan-type familial partial lipodystrophy (FPLD) is a laminopathy characterized by an aberrant fa...
A-type lamin mutations are associated with degenerative disorders causing dilated cardiomyopathy, Ch...
: Laminopathies are disorders caused by LMNA gene mutations, which selectively affect different tiss...
PubMed ID: 26775134Background Familial partial lipodystrophy (FPL) is a rare genetic disorder charac...