Lista de obras - Elisabetta Mattioli - Dominio Público Uruguay

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

artículo científico publicado en 2007

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

artículo científico publicado en 2005

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

artículo científico publicado en 2005

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

artículo científico publicado en 2003

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

article

Diverse lamin-dependent mechanisms interact to control chromatin dynamics. Focus on laminopathies

artículo científico publicado en 2014

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 on Collagen VI mRNA Stability and Microfibrillar Assembly of ThreeCOL6A2Mutations in Two Families with Ullrich Congenital Muscular Dystrophy

artículo científico publicado en 2002

Emerin Phosphorylation during the Early Phase of the Oxidative Stress Response Influences Emerin-BAF Interaction and BAF Nuclear Localization

artículo científico publicado en 2020

Emerin increase in regenerating muscle fibers

article

Emerin-prelamin A interplay in human fibroblasts

artículo científico publicado en 2009

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

Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology.

artículo científico publicado en 2003

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

Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins

artículo científico publicado en 2007

Muscular dystrophy-associated SUN1 and SUN2 variants disrupt nuclear-cytoskeletal connections and myonuclear organization

artículo científico publicado en 2014

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

artículo científico publicado en 2010

Normal calpain expression in genetically confirmed limb-girdle muscular dystrophy type 2A

artículo científico publicado en 2001

Nuclear envelope proteins and chromatin arrangement: a pathogenic mechanism for laminopathies.

artículo científico publicado en 2006

Oct-1 recruitment to the nuclear envelope in adult-onset autosomal dominant leukodystrophy

scientific article published on 20 December 2012

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

artículo científico publicado en 2011

PCAF Involvement in Lamin A/C-HDAC2 Interplay during the Early Phase of Muscle Differentiation

artículo científico publicado en 2020

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

Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle.

artículo científico publicado en 2011

Progeroid laminopathy with restrictive dermopathy-like features caused by an isodisomic LMNA mutation p.R435C.

artículo científico publicado en 2013

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

artículo científico publicado en 2014

Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment

artículo científico publicado en 2005

Site-dependent differences in both prelamin A and adipogenic genes in subcutaneous adipose tissue of patients with type 2 familial partial lipodystrophy

article

Ullrich myopathy phenotype with secondary ColVI defect identified by confocal imaging and electron microscopy analysis

artículo científico publicado en 2007

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 Elisabetta Mattioli

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

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

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

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

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

Diverse lamin-dependent mechanisms interact to control chromatin dynamics. Focus on laminopathies

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 on Collagen VI mRNA Stability and Microfibrillar Assembly of ThreeCOL6A2Mutations in Two Families with Ullrich Congenital Muscular Dystrophy

Emerin Phosphorylation during the Early Phase of the Oxidative Stress Response Influences Emerin-BAF Interaction and BAF Nuclear Localization

Emerin increase in regenerating muscle fibers

Emerin-prelamin A interplay in human fibroblasts

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

Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology.

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

Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins

Muscular dystrophy-associated SUN1 and SUN2 variants disrupt nuclear-cytoskeletal connections and myonuclear organization

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

Normal calpain expression in genetically confirmed limb-girdle muscular dystrophy type 2A

Nuclear envelope proteins and chromatin arrangement: a pathogenic mechanism for laminopathies.

Oct-1 recruitment to the nuclear envelope in adult-onset autosomal dominant leukodystrophy

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

PCAF Involvement in Lamin A/C-HDAC2 Interplay during the Early Phase of Muscle Differentiation

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.

Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle.

Progeroid laminopathy with restrictive dermopathy-like features caused by an isodisomic LMNA mutation p.R435C.

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

Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment

Site-dependent differences in both prelamin A and adipogenic genes in subcutaneous adipose tissue of patients with type 2 familial partial lipodystrophy

Ullrich myopathy phenotype with secondary ColVI defect identified by confocal imaging and electron microscopy analysis

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