Lista de obras -

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

artículo científico publicado en 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

artículo científico publicado en 2005

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

artículo científico publicado en 2012

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

artículo científico publicado en 2005

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

artículo científico publicado en 2011

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

artículo científico publicado en 2003

At the nucleus of the problem: nuclear proteins and disease

artículo científico publicado en 2003

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

artículo científico publicado en 2007

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

artículo científico publicado en 2003

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

artículo científico publicado en 2008

Emerin-prelamin A interplay in human fibroblasts

artículo científico publicado en 2009

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

artículo científico publicado en 2002

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

artículo científico publicado en 2003

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

artículo científico publicado en 2003

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

artículo científico publicado en 2012

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

artículo científico publicado en 2008

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

artículo científico publicado en 2010

Laminopathies and A-type lamin-associated signalling pathways.

artículo científico publicado en 2009

Laminopathies and lamin-associated signaling pathways

artículo científico publicado en 2011

Laminopathies: a chromatin affair

artículo científico publicado en 2006

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

artículo científico publicado en 2005

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

artículo científico publicado en 2013

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

artículo científico publicado en 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

artículo científico publicado en 2011

Pre-Lamin A processing is linked to heterochromatin organization.

artículo científico publicado en 2007

Prelamin A is involved in early steps of muscle differentiation.

artículo científico publicado en 2008

Prelamin A processing and heterochromatin dynamics in laminopathies.

artículo científico publicado en 2006

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

artículo científico publicado en 2014

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

artículo científico publicado en 2007

The empowerment of translational research: lessons from laminopathies.

artículo científico publicado en 2012

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

Lista de obras de

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