List of works - Nadir Mario Maraldi

A pathogenic mechanism leading to partial lipodistrophy and prospects for pharmacological treatment of insulin resistance syndrome

scientific article published on 01 January 2007

A-type lamins and signaling: the PI 3-kinase/Akt pathway moves forward

scientific article published on September 2009

Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy

scientific article published on 26 July 2005

Altered chromatin organization and SUN2 localization in mandibuloacral dysplasia are rescued by drug treatment.

scientific article

Altered pre-lamin A processing is a common mechanism leading to lipodystrophy.

scientific article published on 20 April 2005

Ankrd2/ARPP is a novel Akt2 specific substrate and regulates myogenic differentiation upon cellular exposure to H(2)O(2)

scientific article

Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts

scientific article (publication date: 11 April 2003)

At the nucleus of the problem: nuclear proteins and disease

scientific article

Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblasts

article

Drugs affecting prelamin A processing: effects on heterochromatin organization

scientific article

Dysferlin in a hyperCKaemic patient with caveolin 3 mutation and in C2C12 cells after p38 MAP kinase inhibition

scientific article (publication date: 31 December 2003)

Effects of prelamin A processing inhibitors on the differentiation and activity of human osteoclasts

scientific article published in September 2008

Emerin-prelamin A interplay in human fibroblasts

scientific article

Emery-Dreifuss muscular dystrophy, nuclear cell signaling and chromatin remodeling

scientific article

Extracellular matrix and nuclear abnormalities in skeletal muscle of a patient with Walker-Warburg syndrome caused by POMT1 mutation

scientific article

Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: altered intermolecular interaction with emerin and implications for gene transcription

scientific article published in November 2003

Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistribution

scientific article

Implications for nuclear organization and gene transcription of lamin A/C specific mutations

article

Lamin A Ser404 is a nuclear target of Akt phosphorylation in C2C12 cells

scientific article published on 23 September 2008

Lamin A precursor induces barrier-to-autointegration factor nuclear localization.

scientific article published in July 2010

Laminopathies and A-type lamin-associated signalling pathways.

scientific article

Laminopathies and lamin-associated signaling pathways

scientific article

Laminopathies: a chromatin affair

scientific article published on 18 July 2006

Laminopathies: involvement of structural nuclear proteins in the pathogenesis of an increasing number of human diseases

scientific article published in May 2005

Lamins are rapamycin targets that impact human longevity: a study in centenarians

scientific article published on 23 October 2013

Muscular laminopathies: role of prelamin A in early steps of muscle differentiation

scientific article published on 28 October 2010

Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy

article published in 2001

Osteoblasts from a mandibuloacral dysplasia patient induce human blood precursors to differentiate into active osteoclasts

scientific article published on 16 March 2011

Pre-Lamin A processing is linked to heterochromatin organization.

scientific article published in December 2007

Prelamin A is involved in early steps of muscle differentiation.

scientific article

Prelamin A processing and heterochromatin dynamics in laminopathies.

scientific article published on 23 December 2006

Rapamycin treatment of Mandibuloacral dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamics

scientific article

SREBP1 interaction with prelamin A forms: a pathogenic mechanism for lipodystrophic laminopathies

scientific article published on 19 November 2007

The empowerment of translational research: lessons from laminopathies.

scientific article

Ultrastructural defects of collagen VI filaments in an Ullrich syndrome patient with loss of the alpha3(VI) N10-N7 domains

scientific article published on 01 January 2006

List of works by Nadir Mario Maraldi

A pathogenic mechanism leading to partial lipodistrophy and prospects for pharmacological treatment of insulin resistance syndrome

A-type lamins and signaling: the PI 3-kinase/Akt pathway moves forward

Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy

Altered chromatin organization and SUN2 localization in mandibuloacral dysplasia are rescued by drug treatment.

Altered pre-lamin A processing is a common mechanism leading to lipodystrophy.

Ankrd2/ARPP is a novel Akt2 specific substrate and regulates myogenic differentiation upon cellular exposure to H(2)O(2)

Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts

At the nucleus of the problem: nuclear proteins and disease

Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblasts

Drugs affecting prelamin A processing: effects on heterochromatin organization

Dysferlin in a hyperCKaemic patient with caveolin 3 mutation and in C2C12 cells after p38 MAP kinase inhibition

Effects of prelamin A processing inhibitors on the differentiation and activity of human osteoclasts

Emerin-prelamin A interplay in human fibroblasts

Emery-Dreifuss muscular dystrophy, nuclear cell signaling and chromatin remodeling

Extracellular matrix and nuclear abnormalities in skeletal muscle of a patient with Walker-Warburg syndrome caused by POMT1 mutation

Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: altered intermolecular interaction with emerin and implications for gene transcription

Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistribution

Implications for nuclear organization and gene transcription of lamin A/C specific mutations

Lamin A Ser404 is a nuclear target of Akt phosphorylation in C2C12 cells

Lamin A precursor induces barrier-to-autointegration factor nuclear localization.

Laminopathies and A-type lamin-associated signalling pathways.

Laminopathies and lamin-associated signaling pathways

Laminopathies: a chromatin affair

Laminopathies: involvement of structural nuclear proteins in the pathogenesis of an increasing number of human diseases

Lamins are rapamycin targets that impact human longevity: a study in centenarians

Muscular laminopathies: role of prelamin A in early steps of muscle differentiation

Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy

Osteoblasts from a mandibuloacral dysplasia patient induce human blood precursors to differentiate into active osteoclasts

Pre-Lamin A processing is linked to heterochromatin organization.

Prelamin A is involved in early steps of muscle differentiation.

Prelamin A processing and heterochromatin dynamics in laminopathies.

Rapamycin treatment of Mandibuloacral dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamics

SREBP1 interaction with prelamin A forms: a pathogenic mechanism for lipodystrophic laminopathies

The empowerment of translational research: lessons from laminopathies.

Ultrastructural defects of collagen VI filaments in an Ullrich syndrome patient with loss of the alpha3(VI) N10-N7 domains