List of works - Cristina Capanni

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

scientific article published on 01 January 2007

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

scientific article published on 13 August 2015

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 in Mechanotransduction and Oxidative Stress Response in Skeletal Muscle: New Cues for the Pathogenesis of Muscular Laminopathies

scientific article published on 24 July 2019

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

scientific article (publication date: 11 April 2003)

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

scientific article published on 19 October 2011

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

scientific article published on 20 December 2015

Changes in vimentin, lamin A/C and mitofilin induce aberrant cell organization in fibroblasts from Fanconi anemia complementation group A (FA-A) patients

scientific article published on 2 July 2013

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

article

Detection of mesenchymal stem cells senescence by prelamin A accumulation at the nuclear level.

scientific article published on 26 August 2016

Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria

scientific article published in January 2009

Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria.

scientific article published on 31 March 2009

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

scientific 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)

Ectopic Expression of Ankrd2 Affects Proliferation, Motility and Clonogenic Potential of Human Osteosarcoma Cells

scientific article published on 06 January 2021

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-Associated Mutant Forms of Lamin A Recruit the Stress Responsive Protein Ankrd2 into the Nucleus, Affecting the Cellular Response to Oxidative Stress.

scientific article published on 25 May 2017

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 isolated hyperCKaemia associated with a new mutation in the caveolin-3 (CAV-3) gene

scientific article published on July 2002

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

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

Inhibition of Metalloproteinase Activity in FANCA Is Linked to Altered Oxygen Metabolism

scientific article published on 01 March 2015

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

scientific article published in July 2010

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

Leupeptin preserves cardiac nitric oxide synthase 3 during reperfusion following long-term cardioplegia

scientific article published on 12 June 2010

Mitochondrial respiratory chain Complex I defects in Fanconi anemia complementation group A.

scientific article

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

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

scientific article

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

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

scientific article published on 16 March 2011

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

scientific article published on 20 July 2020

Phosphatidylinositol 3-Kinase Is Required for the Induction of Ornithine Decarboxylase in Leukemia Cells Stimulated to Growth

scientific article published on 01 October 1997

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

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

scientific article published on 11 February 2011

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

scientific article

Remodelling of the nuclear lamina during human cytomegalovirus infection: role of the viral proteins pUL50 and pUL53

scientific article published on 01 March 2008

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

scientific article published on November 2005

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

scientific article published on 19 November 2007

Slug transcription factor and nuclear Lamin B1 are upregulated in osteoarthritic chondrocytes

scientific article published on 20 March 2015

The empowerment of translational research: lessons from laminopathies.

scientific article

Treatment of FANCA cells with resveratrol and N-acetylcysteine: a comparative study

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

p44/42 mitogen-activated protein kinase is involved in the expression of ornithine decarboxylase in leukaemia L1210 cells

scientific article published on July 1999

List of works by Cristina Capanni

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

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

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 in Mechanotransduction and Oxidative Stress Response in Skeletal Muscle: New Cues for the Pathogenesis of Muscular Laminopathies

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

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

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

Changes in vimentin, lamin A/C and mitofilin induce aberrant cell organization in fibroblasts from Fanconi anemia complementation group A (FA-A) patients

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

Detection of mesenchymal stem cells senescence by prelamin A accumulation at the nuclear level.

Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria

Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria.

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

Ectopic Expression of Ankrd2 Affects Proliferation, Motility and Clonogenic Potential of Human Osteosarcoma Cells

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-Associated Mutant Forms of Lamin A Recruit the Stress Responsive Protein Ankrd2 into the Nucleus, Affecting the Cellular Response to Oxidative Stress.

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 isolated hyperCKaemia associated with a new mutation in the caveolin-3 (CAV-3) gene

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

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

Inhibition of Metalloproteinase Activity in FANCA Is Linked to Altered Oxygen Metabolism

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

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

Leupeptin preserves cardiac nitric oxide synthase 3 during reperfusion following long-term cardioplegia

Mitochondrial respiratory chain Complex I defects in Fanconi anemia complementation group A.

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

Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy

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

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

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

Phosphatidylinositol 3-Kinase Is Required for the Induction of Ornithine Decarboxylase in Leukemia Cells Stimulated to Growth

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.

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

Remodelling of the nuclear lamina during human cytomegalovirus infection: role of the viral proteins pUL50 and pUL53

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

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

Slug transcription factor and nuclear Lamin B1 are upregulated in osteoarthritic chondrocytes

The empowerment of translational research: lessons from laminopathies.

Treatment of FANCA cells with resveratrol and N-acetylcysteine: a comparative study

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

p44/42 mitogen-activated protein kinase is involved in the expression of ornithine decarboxylase in leukaemia L1210 cells