Lamin A Truncation in Hutchinson-Gilford Progeria

Annachiara De Sandre‐Giovannoli, Rafaëlle Bernard, Pierre Cau, +8

Science

BiologyUnicellular OrganismEngineeringData ScienceMeasurement +6

Combined treatment with statins and aminobisphosphonates extends longevity in a mouse model of human premature aging

Ignacio Varela, Sandrine Pereira, Alejandro P. Ugalde, +11

Nature Medicine

Lifespan ExtensionHuman PrematureAgingAnti-agingGeriatrics +10

Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy

Claire Navarro, Annachiara De Sandre‐Giovannoli, Rafaëlle Bernard, +17

Human Molecular Genetics

Restrictive DermopathyGeneticsNuclear LaminaPathologyLethal Neonatal Laminopathy +15

Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors

Claire Navarro, Juan Cadiñanos, Annachiara De Sandre‐Giovannoli, +14

Human Molecular Genetics

SRPX2 mutations in disorders of language cortex and cognition

Patrice Roll, Gabrielle Rudolf, Sandrine Pereira, +23

Human Molecular Genetics

Neurological DisorderNeurolinguisticsGeneticsSocial SciencesSylvian Fissures +15

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

Philippe Jay, Claire Rougeulle, Annick Massacrier, +10

Nature Genetics

Developmental BiologyGenetic DisorderMedicineGeneticsGenomic Mechanism +6

Texture Indexes and Gray Level Size Zone Matrix Application to Cell Nuclei Classification

Guillaume Thibault, Bernard Fertil, Claire Navarro, +5

Digital Library of the Belarusian State University (Belarusian State University)

<scp>MG</scp> 132‐induced progerin clearance is mediated by autophagy activation and splicing regulation

Karim Harhouri, Claire Navarro, D. Depétris, +5

EMBO Molecular Medicine

Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR

Barbara Royer-Zemmour, Magali Ponsole-Lenfant, Hyam Gara, +9

Human Molecular Genetics

Molecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areas

Barbara Royer, Dinesh C. Soares, Paul N. Barlow, +8

BMC Genetics