CNR Institutional Research Information System

LATTANZI, GIOVANNA
 Distribuzione geografica
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Continente #
NA - Nord America 828
AS - Asia 252
EU - Europa 117
SA - Sud America 1
Totale 1.198
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Nazione #
US - Stati Uniti d'America 828
SG - Singapore 249
IT - Italia 52
FI - Finlandia 44
FR - Francia 10
DE - Germania 6
AT - Austria 1
CN - Cina 1
CO - Colombia 1
HK - Hong Kong 1
ID - Indonesia 1
LT - Lituania 1
NL - Olanda 1
RU - Federazione Russa 1
SE - Svezia 1
Totale 1.198
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Città #
Santa Clara 764
Singapore 195
Helsinki 44
Bologna 15
Milan 8
Falkenstein 6
Ferrara 4
Phoenix 4
Saint-Martin-d'Hères 4
Genoa 3
Lyon 2
Reggio Emilia 2
Rimini 2
Ashburn 1
Biella 1
Cagliari 1
Cascina 1
Fort Worth 1
Grenoble 1
Hong Kong 1
Melegnano 1
Messina 1
Naples 1
Vienna 1
Totale 1.064
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Nome #
XVII Convegno Nazionale di "Il linguaggio della Ricerca" 33
Ectopic expression of Ankrd2 affects proliferation, motility and clonogenic potential of human osteosarcoma cells 17
Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson-Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies 17
Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria. 16
Lamin A and Prelamin a Counteract Migration of Osteosarcoma Cells 15
Emerin Phosphorylation during the Early Phase of the Oxidative Stress Response Influences Emerin-BAF Interaction and BAF Nuclear Localization 15
Interleukin-6 neutralization ameliorates symptoms in prematurely aged mice 15
PCAF Involvement in Lamin A/C-HDAC2 Interplay during the Early Phase of Muscle Differentiation 14
Lamin A and the LINC complex act as potential tumor suppressors in Ewing Sarcoma 14
The role of prelamin A post-translational maturation in stress response and 53BP1 recruitment 14
Long term breeding of the Lmna G609G progeric mouse: Characterization of homozygous and heterozygous models 13
Lamin A Involvement in Ageing Processes 13
Silencing of Euchromatic Transposable Elements as a Consequence of Nuclear Lamina Dysfunction. 13
Desmin and Plectin Recruitment to the Nucleus and Nuclei Orientation Are Lost in Emery-Dreifuss Muscular Dystrophy Myoblasts Subjected to Mechanical Stimulation 13
Mineralocorticoid receptor antagonism prevents type 2 Familial Partial Lipodystrophy brown adipocyte dysfunction 13
Genomic loci mispositioning in Tmem120a knockout mice yields latent lipodystrophy 13
Skeletal and cardiac muscle disorders caused by mutations in genes encoding intermediate filament proteins 12
Characterization of prelamin A forms accumulated in Mandibuloacral Dysplasia and prospects for therapy 12
Pre-Lamin A processing is linked to heterochromatin organization 12
The telomeric protein AKTIP interacts with A- and B-type lamins and is involved in regulation of cellular senescence 12
Compound heterozygosity for mutations in LMNA in a patient with myopathic and lipodystrophic Mandibuloacral Dysplasia type A phenotype. 12
Nuclear Defects In Syndromic Laminopathies With Muscle Involvement 12
The protein kinase Akt/PKB regulates both prelamin A degradation and Lmna gene expression 11
Emerin increase in regenerating muscle fibers, 11
Characterization of new genetic defects in mad 11
Prelamin A forms accumulated in laminopathies 11
"Doubly heterozygous LMNA and TTN Mutations Revealed by Exome Sequencing in a Severe Form of Dilated Cardiomyopathy". 11
Joining European Scientific Forces to Face Pandemics. 11
Inhibition of DNA damage response at telomeres improves the detrimental phenotypes of Hutchinson-Gilford Progeria Syndrome. 11
A pathogenic mechanism leading to partial lipodistrophy and prospects for pharmacological treatment of insulin resistance syndrome 11
Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy, 11
Clinical Profile, Arrhythmias, and Adverse Cardiac Outcomes in Emery-Dreifuss Muscular Dystrophies: A Systematic Review of the Literature 11
Epigenomic signature of accelerated ageing in progeroid Cockayne syndrome 11
Drugs affecting prelamin A processing: Effects on heterochromatin organization. 10
Altered pre-lamin A processing is a common mechanism leading to lipodystrophy, 10
Elevated TGF beta 2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes 10
Non-farnesylated prelamin A mislocalization and disorganization of heterochromatin marker trimethyl-K9-histone 3 in Emery-Dreifuss Muscular Dystrophy fibroblasts after prelamin A interfering drug treatment. 10
Morphological study of TNPO3 and SRSF1 interaction during myogenesis by combining confocal, structured illumination and electron microscopy analysis 10
Retrotransposons Down- and Up-Regulation in Aging Somatic Tissue 10
Prelamin A processing and functional effects in restrictive dermopathy. 10
European lipodystrophy registry: Background and structure 10
Emerin-prelamin A interplay in human fibroblasts. 10
Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy, 10
Muscular laminopathies: Role of prelamin A in early steps of muscle differentiation. 10
Laminopathies: a chromatin affair, 10
The wide and growing range of lamin B-related diseases: from laminopathies to cancer 10
Prelamin A is involved in early steps of muscle differentiation. 10
BK channel overexpression on plasma membrane of fibroblasts from Hutchinson-Gilford progeria syndrome 9
The Italian Network for Laminopathies. 9
Advances in understanding the mechanisms of evasive and innate resistance to mTOR inhibition in cancer cells. 9
Potential therapeutic effects of the mtor inhibitors for preventing ageing and progeria-related disorders. 9
Ankrd2/ARPP is a Novel Akt2 Specific Substrate and Regulates Myogenic Differentiation Upon Cellular Exposure to H2O2. 9
Laminopathies and A-type lamin-associated signalling pathways. 9
The Cutting Edge: The Role of mTOR Signaling in Laminopathies 9
Ultrastructural defects of collagen VI filaments in an Ullrich syndrome patient with loss of the alpha3(VI) N10-N7 domains, 9
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment, 9
Lamin A Ser404 Is a Nuclear Target of Akt Phosphorylation in C2C12 Cells. 9
Muscular laminopathies: role of prelamin a in early steps of muscle differentiation 9
Prelamin A processing and heterochromatin dynamics in laminopathies. 9
Lamin A Ser404 is a nuclear target of Akt phosphorylation in C2C12 cells. 9
A-type lamins and signaling: the PI 3-kinase/Akt pathway moves forward. 9
Muscular Dystrophy-Associated SUN1 and SUN2 Variants Disrupt Nuclear-Cytoskeletal Connections and Myonuclear Organization 9
Prelamin A-emerin interplay in human fibroblasts. 9
Proceedings of the annual meeting of the European Consortium of Lipodystrophies (ECLip), Pisa, Italy, 28–29 September 2023 9
Altered lamin A/C phosphorylation in Emery-Dreifuss muscle, 9
The role of transposable elements activity in aging and their possible involvement in laminopathic diseases 9
Pre-lamin A is modulated during muscle cell differentiation,. Implications for Emery-Dreifuss muscular dystrofy. 9
A-type lamins and signaling: The PI 3-kinase/Akt pathway moves forward 9
Targeting of the Akt/PKB kinase to the actin skeleton. 9
Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy. 9
Nuclear envelope proteins and chromatin arrangem ent: a pathogenic mechanism for laminopathies, 9
Dysferlin in a hyperCKaemic patient with caveolin 3 mutation and in C2C12 cells after p38 MAP kinase inhibition. 8
New roles for lamins, nuclear envelope proteins and actin in the nucleus, 8
The empowerment of translational research: lessons from laminopathies. 8
Lamin A-dependent heterochromatin dynamics in control and progeria syndrome fibroblasts, 8
Ankrd2 in Mechanotransduction and Oxidative Stress Response in Skeletal Muscle: New Cues for the Pathogenesis of Muscular Laminopathies 8
Detection of mitochondrial defects in collagen VI deficient muscle cultures from UCMD patients and Col6a1 knockout mice: an ultrastructural study, 8
Mandibuloacral dysplasia: A premature ageing disease with aspects of physiological ageing. 8
New drug treatments in progeria cells: modulating mutated lamins to improve cell quality 8
Elevated TGFbeta 2 levels in Emery-Dreifuss muscular dystrophy affect myocyte and tenocyte phenotype and favor the fibrogenic process 8
Implications for nuclear organization and gene transcription of lamin A/C specific mutations, 8
Network assessment of demethylation treatment in melanoma: Differential transcriptome-methylome and antigen profile signatures 8
Effects of prelamin A processing inhibitors on the differentiation and activity of human osteoclasts. 8
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. 8
Lamins are rapamycin targets that impact human longevity: A study in centenarians 8
Oct-1 recruitment to the nuclear envelope in adult-onset autosomal dominant leukodystrophy. 8
PCNA staining pattern is altered in Emery-Dreifuss fibroblasts. 8
Transcription of non-coding satellite III RNAs and assembly of nuclear stress bodies is a universal stress response. 8
Samp1 Mislocalization in Emery-Dreifuss Muscular Dystrophy 8
Rapamycin treatment of Mandibuloacral Dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamics 8
Modulation of TGFbeta 2 levels by lamin A in U2-OS osteoblast-like cells: understanding the osteolytic process triggered by altered lamins 8
Diverse lamin-dependent mechanisms interact to control chromatin dynamics: Focus on laminopathies 8
Extracellular matrix and nuclear abnormalities in skeletal muscle of a patient with Walker-Warburg syndrome caused by POMT1 mutation 8
Barrier-to-autointegration factors nuclear localization and LAP2alpha mislocalization are a common features in laminopathies with defective prelamin A processing. 7
Barrier-to-Autointegration Factor (BAF) evaluation during DNA-damage response. 7
Chromatin remodelling is involved in the pathogenesis of the mandibulocral dyspasia (MADA), 7
Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology 7
Site-dependent differences in both prelamin A and adipogenic genes in subcutaneous adipose tissue of patients with type 2 familial partial lipodystrophy. 7
Barrier-to-autointegration factor involvement in prelamin A-related chromatin remodeling 7
Laminopathies 7
Totale 1.022
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Categoria #
all - tutte 4.997
article - articoli 3.772
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 27
Totale 8.796
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202431 0 0 0 0 0 0 0 0 26 4 1 0
2024/20251.303 6 9 229 96 715 248 0 0 0 0 0 0
Totale 1.334