Lista de obras - Cristina Capanni - Dominio Público Uruguay

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

artículo científico publicado en 2007

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

artículo científico publicado en 2015

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 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

artículo científico publicado en 2003

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

artículo científico publicado en 2011

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

artículo científico publicado en 2015

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

artículo científico publicado en 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.

artículo científico publicado en 2016

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

artículo científico publicado en 2009

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

artículo científico publicado en 2009

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

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

artículo científico publicado en 2021

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 presence in platelets

artículo científico publicado en 2000

Emerin-prelamin A interplay in human fibroblasts

artículo científico publicado en 2009

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.

artículo científico publicado en 2017

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

artículo científico publicado en 2002

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

artículo científico publicado en 2012

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

artículo científico publicado en 2003

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

artículo científico publicado en 1998

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

artículo científico publicado en 2015

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

artículo científico publicado en 2010

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

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

artículo científico publicado en 2010

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

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

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

artículo científico publicado en 2006

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

artículo científico publicado en 1998

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

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.

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

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

artículo científico publicado en 2014

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

artículo científico publicado en 2008

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

artículo científico publicado en 2005

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

artículo científico publicado en 2007

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

artículo científico publicado en 2015

The empowerment of translational research: lessons from laminopathies.

artículo científico publicado en 2012

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

artículo científico publicado en 2014

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

artículo científico publicado en 1999

Lista de obras de 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