Lista de obras - Giovanna Lattanzi - Dominio Público Uruguay

108th ENMC International Workshop, 3rd Workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) Workshop, 13-15 September 2002, Naarden, The Netherlands

artículo científico publicado en 2003

A novel phenotypic expression associated with a new mutation in LMNA gene, characterized by partial lipodystrophy, insulin resistance, aortic stenosis and hypertrophic cardiomyopathy

artículo científico publicado en 2008

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

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 adipocyte differentiation and unbalanced autophagy in type 2 Familial Partial Lipodystrophy: an in vitro and in vivo study of adipose tissue browning

scientific article published on 02 August 2019

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

artículo científico publicado en 2012

Altered modulation of lamin A/C-HDAC2 interaction and p21 expression during oxidative stress response in HGPS

artículo científico publicado en 2018

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

artículo científico publicado en 2005

An overview of new translational, clinical and therapeutic perspectives in laminopathies and other nuclear envelope-related diseases.

artículo científico publicado en 2015

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

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

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

artículo científico publicado en 2011

BK channel overexpression on plasma membrane of fibroblasts from Hutchinson-Gilford progeria syndrome

artículo científico publicado en 2018

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

artículo científico publicado en 2015

Bethlem myopathy (BETHLEM) 86th ENMC international workshop, 10-11 November 2000, Naarden, The Netherlands

artículo científico publicado en 2002

Bethlem myopathy (BETHLEM) and Ullrich scleroatonic muscular dystrophy: 100th ENMC international workshop, 23-24 November 2001, Naarden, The Netherlands

artículo científico publicado en 2002

Binding of hexachloroethane to biological macromolecules from rat and mouse organs

artículo científico publicado en 1988

CD99 acts as an oncosuppressor in osteosarcoma

artículo científico publicado en 2006

Cardiolaminopathies from bench to bedside: challenges in clinical decision-making with focus on arrhythmia-related outcomes

artículo científico publicado en 2018

Changes in polyphosphoinositide levels in rat liver nuclei in response to prolactin, a known hepatic mitogen

artículo científico publicado en 1992

Chloroform Bioactivation Leading to Nucleic Acids Binding ⬇️

artículo científico publicado el 31 de agosto de 1991

Chromatin dynamics and in vitro biomarkers in laminopathies: an overview.

artículo científico publicado en 2015

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

article

Compound Heterozygosity for Mutations inLMNAin a Patient with a Myopathic and Lipodystrophic Mandibuloacral Dysplasia Type A Phenotype

artículo científico publicado en 2007

Constitutive heterochromatin: a surprising variety of expressed sequences.

artículo científico publicado en 2009

Covalent binding of 1,1,1,2‐tetrachloroethane to nucleic acids as evidence of genotoxic activity

artículo científico publicado en 1989

Cytokine Profile in Striated Muscle Laminopathies: New Promising Biomarkers for Disease Prediction

artículo científico publicado en 2020

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

Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy

artículo científico publicado en 2013

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

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

artículo científico publicado en 2008

Elevated TGF β2 serum levels in Emery-Dreifuss muscular dystrophy: implications for myocyte and tenocyte differentiation and fibrogenic processes.

artículo científico publicado en 2018

Emerging perspectives on laminopathies

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

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

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

Functional domains of the nucleus: implications for Emery-Dreifuss muscular dystrophy

artículo científico publicado en 2002

Genotoxic and biochemical effects of dimethylamine

scientific article published on 01 May 1993

High resolution detection of uncoated metaphase chromosomes by means of field emission scanning electron microscopy

artículo científico publicado en 1994

High-resolution FEISEM detection of DNA centromeric probes in HeLa metaphase chromosomes

artículo científico publicado en 1995

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

Improvement of short-term tests for mutagenicity: on the optimal pH for the liver microsomal assay

scientific article published on 01 December 1988

In vivo and in vitro interaction of trichloroethylene with macromolecules from various organs of rat and mouse

artículo científico publicado en 1992

Interleukin-6 neutralization ameliorates symptoms in prematurely aged mice

artículo científico publicado en 2021

LMNA-associated myopathies: the Italian experience in a large cohort of patients.

artículo científico publicado en 2014

Lamin A Ser404 is a nuclear target of Akt phosphorylation in C2C12 cells

artículo científico publicado en 2008

Lamin A and Prelamin A Counteract Migration of Osteosarcoma Cells

scientific article published on 22 March 2020

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

artículo científico publicado en 2010

Laminopathies

artículo científico publicado en 2018

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

Laminopathies: many diseases, one gene. Report of the first Italian Meeting Course on Laminopathies.

artículo científico publicado en 2011

Lamins and bone disorders: current understanding and perspectives.

artículo científico publicado en 2018

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

artículo científico publicado en 2013

Linkage of lamins to fidelity of gene transcription

artículo científico publicado en 2005

Mandibuloacral dysplasia: A premature ageing disease with aspects of physiological ageing

artículo científico publicado en 2017

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

artículo científico publicado en 2015

Molecular mechanisms of CD99-induced caspase-independent cell death and cell-cell adhesion in Ewing's sarcoma cells: actin and zyxin as key intracellular mediators.

artículo científico publicado en 2004

Morphological study of TNPO3 and SRSF1 interaction during myogenesis by combining confocal, structured illumination and electron microscopy analysis

artículo científico publicado en 2021

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

Network assessment of demethylation treatment in melanoma: Differential transcriptome-methylome and antigen profile signatures

scientific article published in PLoS ONE

Novel COL6A1 splicing mutation in a family affected by mild Bethlem myopathy

artículo científico publicado en 2002

Novel histone deacetylase inhibitors induce growth arrest, apoptosis, and differentiation in sarcoma cancer stem cells

artículo científico publicado en 2015

Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy

article published in 2001

Nuclear damages and oxidative stress: new perspectives for laminopathies

artículo científico

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

artículo científico publicado en 2006

O-4The Italian Network for Laminopathies.

artículo científico publicado en 2011

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

Partial lipodystrophy associated with muscular dystrophy of unknown genetic origin

scientific article published on 01 June 2014

Potential therapeutic effects of the MTOR inhibitors for preventing ageing and progeria-related disorders

artículo científico publicado en 2016

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 nuclear envelope dynamics in normal and laminopathic cells ⬇️

artículo científico publicado el 1 de diciembre de 2011

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

artículo científico publicado en 2011

Prevalent cardiac phenotype resulting in heart transplantation in a novel LMNA gene duplication

artículo científico publicado en 2010

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

Reduced adipogenic gene expression in fibroblasts from a patient with type 2 congenital generalized lipodystrophy.

artículo científico publicado en 2010

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

Samp1 Mislocalization in Emery-Dreifuss Muscular Dystrophy

artículo científico publicado en 2018

Satellite cell characterization from aging human muscle.

artículo científico publicado en 2010

Short-term tests of genotoxicity for 1,1,1-trichloroethane

artículo científico publicado en 1986

Silencing of Euchromatic Transposable Elements as a Consequence of Nuclear Lamina Dysfunction

artículo científico publicado en 2020

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

article

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

artículo científico publicado en 2015

Statins and Histone Deacetylase Inhibitors Affect Lamin A/C - Histone Deacetylase 2 Interaction in Human Cells

artículo científico publicado en 2019

Staurosporine treatment and serum starvation promote the cleavage of emerin in cultured mouse myoblasts: involvement of a caspase-dependent mechanism

artículo científico publicado en 2001

Strategies for optimization of short-term genotoxicity tests: the synergistic effect of NADPH and NADH on P450 function in processing pre mutagens

artículo científico publicado en 1990

Targeting of the Akt/PKB kinase to the actin skeleton.

artículo científico publicado en 2003

The Cutting Edge: The Role of mTOR Signaling in Laminopathies

scientific article published on 15 February 2019

The accumulation of un-repairable DNA damage in laminopathy progeria fibroblasts is caused by ROS generation and is prevented by treatment with N-acetyl cysteine ⬇️

artículo científico publicado el 15 de octubre de 2011

The covalent binding of 1, 1,2,2-tetrachloroethane to macromolecules of rat and mouse organs

artículo científico publicado en 1987

The different genotoxicity of p-dichlorobenzene in mouse and rat: measurement of the in vivo and in vitro covalent interaction with nucleic acids.

artículo científico publicado en 1989

The empowerment of translational research: lessons from laminopathies.

artículo científico publicado en 2012

The telomeric protein AKTIP interacts with A- and B-type lamins and is involved in regulation of cellular senescence.

artículo científico publicado en 2016

Troglitazione affects survival of human osteosarcoma cells

artículo científico publicado en 2002

Ultrastructural aspects of the DNA polymerase alpha distribution during the cell cycle

artículo científico publicado en 1998

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

Up-regulation of nuclear PLCbeta1 in myogenic differentiation

artículo científico publicado en 2003

Lista de obras de Giovanna Lattanzi

108th ENMC International Workshop, 3rd Workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) Workshop, 13-15 September 2002, Naarden, The Netherlands

A novel phenotypic expression associated with a new mutation in LMNA gene, characterized by partial lipodystrophy, insulin resistance, aortic stenosis and hypertrophic cardiomyopathy

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

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 adipocyte differentiation and unbalanced autophagy in type 2 Familial Partial Lipodystrophy: an in vitro and in vivo study of adipose tissue browning

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

Altered modulation of lamin A/C-HDAC2 interaction and p21 expression during oxidative stress response in HGPS

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

An overview of new translational, clinical and therapeutic perspectives in laminopathies and other nuclear envelope-related diseases.

Ankrd2 in Mechanotransduction and Oxidative Stress Response in Skeletal Muscle: New Cues for the Pathogenesis of Muscular Laminopathies

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

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

BK channel overexpression on plasma membrane of fibroblasts from Hutchinson-Gilford progeria syndrome

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

Bethlem myopathy (BETHLEM) 86th ENMC international workshop, 10-11 November 2000, Naarden, The Netherlands

Bethlem myopathy (BETHLEM) and Ullrich scleroatonic muscular dystrophy: 100th ENMC international workshop, 23-24 November 2001, Naarden, The Netherlands

Binding of hexachloroethane to biological macromolecules from rat and mouse organs

CD99 acts as an oncosuppressor in osteosarcoma

Cardiolaminopathies from bench to bedside: challenges in clinical decision-making with focus on arrhythmia-related outcomes

Changes in polyphosphoinositide levels in rat liver nuclei in response to prolactin, a known hepatic mitogen

Chloroform Bioactivation Leading to Nucleic Acids Binding ⬇️

Chromatin dynamics and in vitro biomarkers in laminopathies: an overview.

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

Compound Heterozygosity for Mutations inLMNAin a Patient with a Myopathic and Lipodystrophic Mandibuloacral Dysplasia Type A Phenotype

Constitutive heterochromatin: a surprising variety of expressed sequences.

Covalent binding of 1,1,1,2‐tetrachloroethane to nucleic acids as evidence of genotoxic activity

Cytokine Profile in Striated Muscle Laminopathies: New Promising Biomarkers for Disease Prediction

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

Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy

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

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

Elevated TGF β2 serum levels in Emery-Dreifuss muscular dystrophy: implications for myocyte and tenocyte differentiation and fibrogenic processes.

Emerging perspectives on laminopathies

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

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.

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

Functional domains of the nucleus: implications for Emery-Dreifuss muscular dystrophy

Genotoxic and biochemical effects of dimethylamine

High resolution detection of uncoated metaphase chromosomes by means of field emission scanning electron microscopy

High-resolution FEISEM detection of DNA centromeric probes in HeLa metaphase chromosomes

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

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

Improvement of short-term tests for mutagenicity: on the optimal pH for the liver microsomal assay

In vivo and in vitro interaction of trichloroethylene with macromolecules from various organs of rat and mouse

Interleukin-6 neutralization ameliorates symptoms in prematurely aged mice

LMNA-associated myopathies: the Italian experience in a large cohort of patients.

Lamin A Ser404 is a nuclear target of Akt phosphorylation in C2C12 cells

Lamin A and Prelamin A Counteract Migration of Osteosarcoma Cells

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

Laminopathies

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

Laminopathies: many diseases, one gene. Report of the first Italian Meeting Course on Laminopathies.

Lamins and bone disorders: current understanding and perspectives.

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

Linkage of lamins to fidelity of gene transcription

Mandibuloacral dysplasia: A premature ageing disease with aspects of physiological ageing

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

Molecular mechanisms of CD99-induced caspase-independent cell death and cell-cell adhesion in Ewing's sarcoma cells: actin and zyxin as key intracellular mediators.

Morphological study of TNPO3 and SRSF1 interaction during myogenesis by combining confocal, structured illumination and electron microscopy analysis

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

Network assessment of demethylation treatment in melanoma: Differential transcriptome-methylome and antigen profile signatures