CNR Institutional Research Information System

CAPANNI, CRISTINA
 Distribuzione geografica
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Continente #
AS - Asia 1.611
NA - Nord America 1.149
EU - Europa 397
SA - Sud America 287
Continente sconosciuto - Info sul continente non disponibili 112
AF - Africa 34
OC - Oceania 3
Totale 3.593
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Nazione #
US - Stati Uniti d'America 1.092
SG - Singapore 717
CN - Cina 355
BR - Brasile 232
HK - Hong Kong 168
VN - Vietnam 157
FR - Francia 124
IT - Italia 91
KR - Corea 60
IN - India 37
DE - Germania 33
FI - Finlandia 33
NL - Olanda 29
GB - Regno Unito 28
CA - Canada 26
JP - Giappone 23
BD - Bangladesh 22
AR - Argentina 19
IQ - Iraq 13
ZA - Sudafrica 12
MX - Messico 11
EC - Ecuador 9
ID - Indonesia 9
SE - Svezia 9
IL - Israele 8
PT - Portogallo 8
EG - Egitto 7
ES - Italia 7
PL - Polonia 7
CO - Colombia 6
RU - Federazione Russa 6
VE - Venezuela 6
BO - Bolivia 4
CL - Cile 4
DO - Repubblica Dominicana 4
JM - Giamaica 4
MA - Marocco 4
MY - Malesia 4
NP - Nepal 4
TR - Turchia 4
AT - Austria 3
AU - Australia 3
AZ - Azerbaigian 3
GR - Grecia 3
HN - Honduras 3
PA - Panama 3
PK - Pakistan 3
PY - Paraguay 3
TT - Trinidad e Tobago 3
TW - Taiwan 3
AE - Emirati Arabi Uniti 2
AL - Albania 2
CR - Costa Rica 2
CY - Cipro 2
CZ - Repubblica Ceca 2
DZ - Algeria 2
IE - Irlanda 2
JO - Giordania 2
KE - Kenya 2
KZ - Kazakistan 2
OM - Oman 2
PH - Filippine 2
RO - Romania 2
SA - Arabia Saudita 2
SK - Slovacchia (Repubblica Slovacca) 2
TN - Tunisia 2
UA - Ucraina 2
UY - Uruguay 2
UZ - Uzbekistan 2
BG - Bulgaria 1
BW - Botswana 1
DK - Danimarca 1
GY - Guiana 1
HR - Croazia 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
NG - Nigeria 1
NI - Nicaragua 1
PE - Perù 1
QA - Qatar 1
RE - Reunion 1
RS - Serbia 1
SC - Seychelles 1
SN - Senegal 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
Totale 3.481
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Città #
Santa Clara 458
Singapore 413
Hefei 166
Hong Kong 164
San Jose 112
Ashburn 86
Lauterbourg 79
Beijing 74
Seoul 59
Ho Chi Minh City 53
Los Angeles 44
Hanoi 40
Pavia 28
São Paulo 27
Helsinki 22
Dallas 17
Tokyo 14
Düsseldorf 13
Frankfurt am Main 13
Rio de Janeiro 13
New York 12
Phoenix 12
Montreal 11
Bologna 10
Buffalo 10
Da Nang 10
Lappeenranta 10
London 10
Biên Hòa 9
Orem 9
Milan 8
Minamishinagawa 8
Amsterdam 7
Bengaluru 7
Chennai 7
Atlanta 6
Baghdad 6
Chicago 6
Denver 6
Dhaka 6
Haiphong 6
Houston 6
Lisbon 6
Stockholm 6
Brasília 5
Campinas 5
Elk Grove Village 5
Johannesburg 5
Piscataway 5
Portsmouth 5
Saint-Martin-d'Hères 5
San Francisco 5
Tampa 5
Belo Horizonte 4
Boston 4
Guayaquil 4
Mumbai 4
Sorocaba 4
Thái Bình 4
Baku 3
Brooklyn 3
Cairo 3
Cincinnati 3
City of London 3
Curitiba 3
Dayton 3
Fort Worth 3
Greensboro 3
Guarulhos 3
Hollywood 3
Hải Dương 3
Jacksonville 3
Livorno 3
New Delhi 3
Panama City 3
Roubaix 3
Vienna 3
Washington 3
Wroclaw 3
Acalanes Ridge 2
Alexandria 2
Algiers 2
Americana 2
Amman 2
Anápolis 2
Assago 2
Athens 2
Avellaneda 2
Birmingham 2
Boardman 2
Bogotá 2
Bratislava 2
Bridgeport 2
Bullhead City 2
Can Tho 2
Casablanca 2
Caxias do Sul 2
Chaguanas 2
Chandigarh 2
Chengdu 2
Totale 2.260
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Nome #
Long term breeding of the Lmna G609G progeric mouse: Characterization of homozygous and heterozygous models 105
Characterization of new genetic defects in mad 99
PCAF Involvement in Lamin A/C-HDAC2 Interplay during the Early Phase of Muscle Differentiation 96
Barrier-to-Autointegration Factor (BAF) evaluation during DNA-damage response. 87
Emerin increase in regenerating muscle fibers, 85
Lamin A Involvement in Ageing Processes 78
Interleukin-6 neutralization ameliorates symptoms in prematurely aged mice 76
Dysferlin in a hyperCKaemic patient with caveolin 3 mutation and in C2C12 cells after p38 MAP kinase inhibition. 70
Lamin A-dependent heterochromatin dynamics in control and progeria syndrome fibroblasts, 70
The Italian Network for Laminopathies. 69
The empowerment of translational research: lessons from laminopathies. 69
Ankrd2 in Mechanotransduction and Oxidative Stress Response in Skeletal Muscle: New Cues for the Pathogenesis of Muscular Laminopathies 68
Ectopic expression of Ankrd2 affects proliferation, motility and clonogenic potential of human osteosarcoma cells 64
Morphological study of TNPO3 and SRSF1 interaction during myogenesis by combining confocal, structured illumination and electron microscopy analysis 61
Emerin Phosphorylation during the Early Phase of the Oxidative Stress Response Influences Emerin-BAF Interaction and BAF Nuclear Localization 58
Lamin A and the LINC complex act as potential tumor suppressors in Ewing Sarcoma 58
Altered Mitochondrial Dynamic in Lymphoblasts and Fibroblasts Mutated for FANCA-A Gene: The Central Role of DRP1 57
The NFATc1/P2X7 receptor relationship in human intervertebral disc cells 54
Combined alteration of lamin and nuclear morphology influences the localization of the tumor-associated factor AKTIP 51
Altered pre-lamin A processing is a common mechanism leading to lipodystrophy, 49
Prelamin A processing and functional effects in restrictive dermopathy. 47
Prelamin A forms accumulated in laminopathies 46
Emerin-prelamin A interplay in human fibroblasts. 45
Pre-Lamin A processing is linked to heterochromatin organization 44
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 44
Altered chromatin organization and SUN2 localization in mandibuloacral dysplasia are rescued by drug treatment. 44
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. 44
Altered lamin A/C phosphorylation in Emery-Dreifuss muscle, 44
Inhibition of metalloproteinase activity in FANCA is linked to altered oxygen metabolism. 43
Barrier-to-Autointegration Factor (BAF) involvement in prelamin A-related chromatin organization changes. 43
Statins and Histone Deacetylase Inhibitors Affect Lamin A/C - Histone Deacetylase 2 Interaction in Human Cells. 42
Altered adipocyte differentiation and unbalanced autophagy in type 2 Familial Partial Lipodystrophy: an in vitro and in vivo study of adipose tissue browning 42
Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy. 42
Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy, 41
The role of prelamin A post-translational maturation in stress response and 53BP1 recruitment 40
Characterization of prelamin A forms accumulated in Mandibuloacral Dysplasia and prospects for therapy 40
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment, 40
Muscular laminopathies: role of prelamin a in early steps of muscle differentiation 40
Detection of mesenchymal stem cells senescence by prelamin A accumulation at the nuclear level 40
Laminopathies: involvement of structural nuclear proteins in the pathogenesis of an increasing number of human diseases, 38
Diverse lamin-dependent mechanisms interact to control chromatin dynamics: Focus on laminopathies 37
Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria. 36
Laminopathies and lamin-associated signaling pathways. 36
Laminopathies: a chromatin affair, 36
Prelamin A is involved in early steps of muscle differentiation. 36
Ultrastructural defects of collagen VI filaments in an Ullrich syndrome patient with loss of the alpha3(VI) N10-N7 domains, 35
All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype. 35
Lamin A precursor induces barrier-to-autointegration factor nuclear localization. 35
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria. 35
Lamins are rapamycin targets that impact human longevity: A study in centenarians 34
Rapamycin treatment of Mandibuloacral Dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamics 34
Nuclear envelope proteins and chromatin arrangem ent: a pathogenic mechanism for laminopathies, 34
Prelamin A degradation pathways and progeria 34
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. 33
Lamin A-dependent heterochromatin dynamics in control and progeria syndrome fibroblasts, 33
Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy, 33
Extracellular matrix and nuclear abnormalities in skeletal muscle of a patient with Walker-Warburg syndrome caused by POMT1 mutation 33
Changes in vimentin, lamin A/C and mitofilin induce aberrant cell organization in fibroblasts from Fanconi anemia complementation group A (FA-A) patients 30
Barrier-to-autointegration factors nuclear localization and LAP2alpha mislocalization are a common features in laminopathies with defective prelamin A processing. 29
Apoptotic genes as potential markers of metastatic phenotype in human osteosarcoma cell lines. 29
Prelamin A is involved in early steps of muscle differentiation 29
Barrier-to-autointegration factor nuclear localization is a common feature in prelamin A accumulating cells under pathological or physiological conditions. 29
Pre-Lamin A processing is linked to heterochromatin organization. 29
Lamin A precursor induces barrier-to-autointegration factor nuclear localization. 29
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. 29
Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology 28
Slug transcription factor and nuclear Lamin B1 are upregulated in osteoarthritic chondrocytes 28
SREBP1 interaction with prelamin A forms: a pathogenic mechanism for lipodystrophic laminopathies. 28
Heterochromatin dynamics in hutchinson-gilford progeria sindrome fibroblasts, 28
Osteoblasts from a Mandibuloacral dysplasia patient induce human blood precursors to differentiate into active osteoclasts 28
Implications for nuclear organization and gene transcription of lamin A/C specific mutations, 27
Barrier-to-autointegration factor involvement in prelamin A-related chromatin remodeling 27
Barrier-to-autointegration factor involvement in prelamin A-related chromatin remodeling 26
Mitochondrial respiratory chain Complex I defects in Fanconi anemia complementation group A 26
Drugs affecting prelamin A processing: Effects on heterochromatin organization 26
Altered pre-lamin A processing in laminopathies featuring lipodystrophy 25
Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts. 25
Treatment of FANCA Cells with Resveratrol and N-Acetylcysteine: A Comparative Study 24
Prelamin A in diverse tissues. What happens in health and disease? 24
Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistribution. 23
Localization of SUNs and LAP2alpha in the human myocardium 23
Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle. 22
Time-course of apoptosis by in situ nick translation in adherent tumor cell lines. 22
Leupeptin preserves cardiac nitric oxide synthase 3 during reperfusion following long-term cardioplegia. 20
null 18
Totale 3.593
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Categoria #
all - tutte 12.125
article - articoli 9.515
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 21.640
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/20243 0 0 0 0 0 0 0 0 3 0 0 0
2024/20251.588 1 8 112 47 425 123 35 104 69 68 318 278
2025/20261.860 88 200 168 346 311 100 293 68 92 93 60 41
2026/2027142 135 7 0 0 0 0 0 0 0 0 0 0
Totale 3.593