List of works - Stefano Squarzoni

82nd ENMC international workshop, 5th international Emery-Dreifuss muscular dystrophy (EDMD) workshop, 1st Workshop of the MYO-CLUSTER project EUROMEN (European muscle envelope nucleopathies), 15-16 September 2000, Naarden, The Netherlands.

scientific article published in February 2002

98th ENMC International Workshop on Congenital Muscular Dystrophy (CMD), 7th Workshop of the International Consortium on CMD, 2nd Workshop of the MYO CLUSTER project GENRE. 26-28th October, 2001, Naarden, The Netherlands.

scientific article published in November 2002

A case report of fracture of ceramic head in total hip arthroplasty: histological and biochemical features of perimplant tissues

scientific article published in August 2006

A new method for isolation of polyethylene wear debris from tissue and synovial fluid

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

scientific article published on 01 January 2007

A recently developed bifacial platelet-rich fibrin matrix

scientific article published on 01 July 2010

All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype.

scientific article published on 13 August 2015

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

Antisense-induced messenger depletion corrects a COL6A2 dominant mutation in Ullrich myopathy

scientific article published on 6 November 2012

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

Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria.

scientific article published on 19 October 2011

Autosomal recessive Bethlem myopathy

scientific article

Autosomal recessive myosclerosis myopathy is a collagen VI disorder

scientific article published on 01 October 2008

Barrier-to-autointegration factor (BAF) involvement in prelamin A-related chromatin organization changes

scientific article published on 20 December 2015

Ceramic debris in hip prosthesis: correlation between synovial fluid and joint capsule

scientific article published on 13 March 2013

Chromosome spread for confocal microscopy

scientific article published on 01 January 1999

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

article

Collagen VI-NG2 axis in human tendon fibroblasts under conditions mimicking injury response

article

Considerations on ceramic prosthesis explants

scientific article published on 01 October 1992

Critical evaluation of the use of cell cultures for inclusion in clinical trials of patients affected by collagen VI myopathies

scientific article

Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies

scientific article

Determination of crystallinity and crystal structure of Hylamer polyethylene after in vivo wear

scientific article published on 27 January 2006

Differential and restricted expression of novel collagen VI chains in mouse.

scientific article published on 6 April 2011

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

scientific article

Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy

scientific article published in September 2005

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)

Early diagnosis of ceramic liner fracture. Guidelines based on a twelve-year clinical experience.

scientific article published in December 2006

Effect of mechanical strain on the collagen VI pericellular matrix in anterior cruciate ligament fibroblasts.

scientific article published in July 2014

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

scientific article published in September 2008

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

scientific article published in Journal of Biological Chemistry

Electron microscopy microsampling of isolated nuclei sorted by flow cytometry

scientific article published on 01 November 1986

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

scientific article published on 06 June 2020

Emerin increase in regenerating muscle fibers

article

Emerin presence in platelets

scientific article (publication date: September 2000)

Emerin-prelamin A interplay in human fibroblasts

scientific article

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

scientific article

Experimental colitis increases small intestine permeability in the rat

scientific article published on 01 January 1999

Expression of collagen VI α5 and α6 chains in human muscle and in Duchenne muscular dystrophy-related muscle fibrosis

scientific article published on 30 December 2011

Expression of the collagen VI α5 and α6 chains in normal human skin and in skin of patients with collagen VI-related myopathies

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

Fretting wear in a modular neck hip prosthesis.

scientific article

Honey flavonoids inhibit Candida albicans morphogenesis by affecting DNA behavior and mitochondrial function

scientific article published on January 2014

Image analysis of the chromatin organization in the nuclear domains of freeze fractured hepatocytes and lymphocytes

scientific article published on 01 January 1990

Image analysis techniques. The problem of the quantitative evaluation of the chromatin ultrastructure

Immunocytochemical detection of emerin within the nuclear matrix

scientific article

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

scientific article

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

article

Increase of Neuronal Nitric Oxide Synthase in Rat Skeletal Muscle during Ageing

scientific article published on 01 April 1998

Intracellular detection of laminin alpha 2 chain in skin by electron microscopy immunocytochemistry: comparison between normal and laminin alpha 2 chain deficient subjects

scientific article (publication date: March 1997)

Intramembrane protein distribution in cell cultures is affected by 50 Hz pulsed magnetic fields.

scientific article published on January 1997

Intranuclear localization of phospholipids by ultrastructural cytochemistry

scientific article published on 01 September 1992

Isolation and characterization of wear debris generated in patients wearing polyethylene Hylamer inserts, gamma irradiated in air.

scientific article published in October 2005

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

scientific article published in July 2010

Lamin A/C sustains PcG protein architecture, maintaining transcriptional repression at target genes.

scientific article published on November 2015

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

Localization of laminin alpha 2 chain in normal human central nervous system: an immunofluorescence and ultrastructural study

scientific article published in December 1997

Localization of the laminin alpha 2 chain in normal human skeletal muscle and peripheral nerve: an ultrastructural immunolabeling study

scientific article published on February 1997

Metal-on-metal hip prostheses: correlation between debris in the synovial fluid and levels of cobalt and chromium ions in the bloodstream.

scientific article published on March 2014

Mineralization behavior with mesenchymal stromal cells in a biomimetic hyaluronic acid-based scaffold.

scientific article published on 20 February 2010

Mixing and matching in ceramic-on-metal hip arthroplasty: an in-vitro hip simulator study

scientific article published on 15 September 2009

Modulation of TGFbeta 2 levels by lamin A in U2-OS osteoblast-like cells: understanding the osteolytic process triggered by altered lamins

scientific article

Morphological evidence of function-related localization of phospholipids in the cell nucleus

scientific article

Morphometric and microanalytical analyses of alumina wear particles in hip prostheses

scientific article published on 01 July 1993

Morphometric study of chromatin pattern in freeze-fractured rat liver nuclei during malignancy evolution

scientific article published on 01 November 1989

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

scientific article published on 28 October 2010

New roles for lamins, nuclear envelope proteins and actin in the nucleus

scientific article

Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy

article published in 2001

Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophy

scientific article published on 01 July 1999

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

scientific article

Nuclear matrix involvement in sperm head structural organization.

scientific article published on January 1994

Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery–Dreifuss muscular dystrophy patients and carriers

scientific article published on 01 April 1998

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 functional effects in restrictive dermopathy

scientific article

Prelamin A processing and heterochromatin dynamics in laminopathies.

scientific article published on 23 December 2006

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

scientific article published on 11 February 2011

Preparation of chromosome spreads for electron (TEM, SEM, STEM), light and confocal microscopy

scientific article published on 01 October 1994

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

scientific article

Recessive COL6A2 C-globular missense mutations in Ullrich congenital muscular dystrophy: role of the C2a splice variant.

scientific article

Reduction of background labeling in colloidal gold-enzyme reactions

scientific article published on 01 January 1990

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

scientific article published on November 2005

Severe wear from retrieved alumina-on-alumina coupled implant: a case report

scientific article published on 01 September 2001

Synovial fluid microanalysis allows early diagnosis of ceramic hip prosthesis damage

scientific article published on 27 January 2012

Tendon Extracellular Matrix Remodeling and Defective Cell Polarization in the Presence of Collagen VI Mutations

scientific article published on 11 February 2020

The empowerment of translational research: lessons from laminopathies.

scientific article

Ultrastructural changes in muscle cells of patients with collagen VI-related myopathies

scientific article published on October 2013

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 Stefano Squarzoni

82nd ENMC international workshop, 5th international Emery-Dreifuss muscular dystrophy (EDMD) workshop, 1st Workshop of the MYO-CLUSTER project EUROMEN (European muscle envelope nucleopathies), 15-16 September 2000, Naarden, The Netherlands.

98th ENMC International Workshop on Congenital Muscular Dystrophy (CMD), 7th Workshop of the International Consortium on CMD, 2nd Workshop of the MYO CLUSTER project GENRE. 26-28th October, 2001, Naarden, The Netherlands.

A case report of fracture of ceramic head in total hip arthroplasty: histological and biochemical features of perimplant tissues

A new method for isolation of polyethylene wear debris from tissue and synovial fluid

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

A recently developed bifacial platelet-rich fibrin matrix

All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype.

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.

Antisense-induced messenger depletion corrects a COL6A2 dominant mutation in Ullrich myopathy

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

At the nucleus of the problem: nuclear proteins and disease

Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria.

Autosomal recessive Bethlem myopathy

Autosomal recessive myosclerosis myopathy is a collagen VI disorder

Barrier-to-autointegration factor (BAF) involvement in prelamin A-related chromatin organization changes

Ceramic debris in hip prosthesis: correlation between synovial fluid and joint capsule

Chromosome spread for confocal microscopy

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

Collagen VI-NG2 axis in human tendon fibroblasts under conditions mimicking injury response

Considerations on ceramic prosthesis explants

Critical evaluation of the use of cell cultures for inclusion in clinical trials of patients affected by collagen VI myopathies

Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies

Determination of crystallinity and crystal structure of Hylamer polyethylene after in vivo wear

Differential and restricted expression of novel collagen VI chains in mouse.

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

Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy

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

Early diagnosis of ceramic liner fracture. Guidelines based on a twelve-year clinical experience.

Effect of mechanical strain on the collagen VI pericellular matrix in anterior cruciate ligament fibroblasts.

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

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

Electron microscopy microsampling of isolated nuclei sorted by flow cytometry

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 presence in platelets

Emerin-prelamin A interplay in human fibroblasts

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

Experimental colitis increases small intestine permeability in the rat

Expression of collagen VI α5 and α6 chains in human muscle and in Duchenne muscular dystrophy-related muscle fibrosis

Expression of the collagen VI α5 and α6 chains in normal human skin and in skin of patients with collagen VI-related myopathies

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

Fretting wear in a modular neck hip prosthesis.

Honey flavonoids inhibit Candida albicans morphogenesis by affecting DNA behavior and mitochondrial function

Image analysis of the chromatin organization in the nuclear domains of freeze fractured hepatocytes and lymphocytes

Image analysis techniques. The problem of the quantitative evaluation of the chromatin ultrastructure

Immunocytochemical detection of emerin within the nuclear matrix

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

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

Increase of Neuronal Nitric Oxide Synthase in Rat Skeletal Muscle during Ageing

Intracellular detection of laminin alpha 2 chain in skin by electron microscopy immunocytochemistry: comparison between normal and laminin alpha 2 chain deficient subjects

Intramembrane protein distribution in cell cultures is affected by 50 Hz pulsed magnetic fields.

Intranuclear localization of phospholipids by ultrastructural cytochemistry

Isolation and characterization of wear debris generated in patients wearing polyethylene Hylamer inserts, gamma irradiated in air.

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

Lamin A/C sustains PcG protein architecture, maintaining transcriptional repression at target genes.

Laminopathies: a chromatin affair

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

Localization of laminin alpha 2 chain in normal human central nervous system: an immunofluorescence and ultrastructural study

Localization of the laminin alpha 2 chain in normal human skeletal muscle and peripheral nerve: an ultrastructural immunolabeling study

Metal-on-metal hip prostheses: correlation between debris in the synovial fluid and levels of cobalt and chromium ions in the bloodstream.

Mineralization behavior with mesenchymal stromal cells in a biomimetic hyaluronic acid-based scaffold.

Mixing and matching in ceramic-on-metal hip arthroplasty: an in-vitro hip simulator study

Modulation of TGFbeta 2 levels by lamin A in U2-OS osteoblast-like cells: understanding the osteolytic process triggered by altered lamins

Morphological evidence of function-related localization of phospholipids in the cell nucleus

Morphometric and microanalytical analyses of alumina wear particles in hip prostheses

Morphometric study of chromatin pattern in freeze-fractured rat liver nuclei during malignancy evolution

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

New roles for lamins, nuclear envelope proteins and actin in the nucleus

Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy

Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophy

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

Nuclear matrix involvement in sperm head structural organization.

Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery–Dreifuss muscular dystrophy patients and carriers

Pre-Lamin A processing is linked to heterochromatin organization.

Prelamin A is involved in early steps of muscle differentiation.