CNR Institutional Research Information System

CAPANNI, CRISTINA
 Distribuzione geografica
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Continente #
AS - Asia 1.600
NA - Nord America 989
EU - Europa 380
SA - Sud America 285
AF - Africa 33
OC - Oceania 3
Totale 3.290
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Nazione #
US - Stati Uniti d'America 943
SG - Singapore 717
CN - Cina 355
BR - Brasile 232
HK - Hong Kong 168
VN - Vietnam 155
FR - Francia 121
IT - Italia 81
KR - Corea 60
IN - India 37
DE - Germania 33
FI - Finlandia 33
NL - Olanda 29
GB - Regno Unito 28
JP - Giappone 23
AR - Argentina 18
CA - Canada 18
BD - Bangladesh 15
IQ - Iraq 13
ZA - Sudafrica 12
MX - Messico 10
EC - Ecuador 9
SE - Svezia 9
ID - Indonesia 8
IL - Israele 8
EG - Egitto 7
ES - Italia 7
PL - Polonia 7
PT - Portogallo 7
RU - Federazione Russa 6
VE - Venezuela 6
CO - Colombia 5
BO - Bolivia 4
CL - Cile 4
DO - Repubblica Dominicana 4
MA - Marocco 4
NP - Nepal 4
TR - Turchia 4
AT - Austria 3
AU - Australia 3
AZ - Azerbaigian 3
JM - Giamaica 3
MY - Malesia 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
GR - Grecia 2
HN - Honduras 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
UY - Uruguay 2
UZ - Uzbekistan 2
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
SN - Senegal 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
UA - Ucraina 1
Totale 3.290
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Città #
Santa Clara 455
Singapore 413
Hefei 166
Hong Kong 164
San Jose 112
Lauterbourg 79
Beijing 74
Seoul 59
Ho Chi Minh City 52
Ashburn 51
Los Angeles 41
Hanoi 40
Pavia 28
São Paulo 27
Helsinki 22
Dallas 14
Tokyo 14
Düsseldorf 13
Frankfurt am Main 13
Rio de Janeiro 13
Montreal 11
Da Nang 10
Lappeenranta 10
London 10
New York 10
Biên Hòa 9
Orem 9
Phoenix 9
Bologna 8
Minamishinagawa 8
Bengaluru 7
Chennai 7
Atlanta 6
Baghdad 6
Buffalo 6
Dhaka 6
Haiphong 6
Lisbon 6
Milan 6
Stockholm 6
Amsterdam 5
Brasília 5
Campinas 5
Elk Grove Village 5
Houston 5
Johannesburg 5
Portsmouth 5
San Francisco 5
Belo Horizonte 4
Boston 4
Denver 4
Guayaquil 4
Mumbai 4
Saint-Martin-d'Hères 4
Sorocaba 4
Thái Bình 4
Baku 3
Brooklyn 3
Cairo 3
Chicago 3
City of London 3
Curitiba 3
Fort Worth 3
Guarulhos 3
Hải Dương 3
Livorno 3
New Delhi 3
Panama City 3
Roubaix 3
Vienna 3
Wroclaw 3
Acalanes Ridge 2
Algiers 2
Americana 2
Amman 2
Anápolis 2
Assago 2
Athens 2
Avellaneda 2
Bogotá 2
Bratislava 2
Bridgeport 2
Can Tho 2
Casablanca 2
Caxias do Sul 2
Chaguanas 2
Chandigarh 2
Chengdu 2
Contagem 2
Dublin 2
Duque de Caxias 2
Durban 2
Erbil 2
Falkenstein 2
Ferrara 2
Georgetown 2
Goiânia 2
Hortolândia 2
Jaboatão dos Guararapes 2
Jacobina 2
Totale 2.181
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Nome #
Long term breeding of the Lmna G609G progeric mouse: Characterization of homozygous and heterozygous models 101
Characterization of new genetic defects in mad 96
PCAF Involvement in Lamin A/C-HDAC2 Interplay during the Early Phase of Muscle Differentiation 95
Emerin increase in regenerating muscle fibers, 82
Barrier-to-Autointegration Factor (BAF) evaluation during DNA-damage response. 82
Lamin A Involvement in Ageing Processes 75
Interleukin-6 neutralization ameliorates symptoms in prematurely aged mice 75
The Italian Network for Laminopathies. 69
The empowerment of translational research: lessons from laminopathies. 68
Dysferlin in a hyperCKaemic patient with caveolin 3 mutation and in C2C12 cells after p38 MAP kinase inhibition. 67
Lamin A-dependent heterochromatin dynamics in control and progeria syndrome fibroblasts, 67
Ankrd2 in Mechanotransduction and Oxidative Stress Response in Skeletal Muscle: New Cues for the Pathogenesis of Muscular Laminopathies 62
Ectopic expression of Ankrd2 affects proliferation, motility and clonogenic potential of human osteosarcoma cells 60
Morphological study of TNPO3 and SRSF1 interaction during myogenesis by combining confocal, structured illumination and electron microscopy analysis 58
Emerin Phosphorylation during the Early Phase of the Oxidative Stress Response Influences Emerin-BAF Interaction and BAF Nuclear Localization 57
Lamin A and the LINC complex act as potential tumor suppressors in Ewing Sarcoma 55
Altered Mitochondrial Dynamic in Lymphoblasts and Fibroblasts Mutated for FANCA-A Gene: The Central Role of DRP1 53
Combined alteration of lamin and nuclear morphology influences the localization of the tumor-associated factor AKTIP 51
The NFATc1/P2X7 receptor relationship in human intervertebral disc cells 51
Altered pre-lamin A processing is a common mechanism leading to lipodystrophy, 48
Prelamin A forms accumulated in laminopathies 45
Prelamin A processing and functional effects in restrictive dermopathy. 44
Emerin-prelamin A interplay in human fibroblasts. 44
Pre-Lamin A processing is linked to heterochromatin organization 43
Altered chromatin organization and SUN2 localization in mandibuloacral dysplasia are rescued by drug treatment. 43
Altered lamin A/C phosphorylation in Emery-Dreifuss muscle, 43
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 41
Inhibition of metalloproteinase activity in FANCA is linked to altered oxygen metabolism. 41
Characterization of prelamin A forms accumulated in Mandibuloacral Dysplasia and prospects for therapy 40
Muscular laminopathies: role of prelamin a in early steps of muscle differentiation 40
Altered adipocyte differentiation and unbalanced autophagy in type 2 Familial Partial Lipodystrophy: an in vitro and in vivo study of adipose tissue browning 40
The role of prelamin A post-translational maturation in stress response and 53BP1 recruitment 39
Statins and Histone Deacetylase Inhibitors Affect Lamin A/C - Histone Deacetylase 2 Interaction in Human Cells. 39
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. 38
Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy, 38
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment, 36
Barrier-to-Autointegration Factor (BAF) involvement in prelamin A-related chromatin organization changes. 36
Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy. 36
Prelamin A is involved in early steps of muscle differentiation. 36
Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria. 35
All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype. 35
Diverse lamin-dependent mechanisms interact to control chromatin dynamics: Focus on laminopathies 35
Laminopathies and lamin-associated signaling pathways. 34
Detection of mesenchymal stem cells senescence by prelamin A accumulation at the nuclear level 34
Laminopathies: a chromatin affair, 34
Ultrastructural defects of collagen VI filaments in an Ullrich syndrome patient with loss of the alpha3(VI) N10-N7 domains, 33
Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy, 32
Laminopathies: involvement of structural nuclear proteins in the pathogenesis of an increasing number of human diseases, 32
Rapamycin treatment of Mandibuloacral Dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamics 32
Extracellular matrix and nuclear abnormalities in skeletal muscle of a patient with Walker-Warburg syndrome caused by POMT1 mutation 32
Prelamin A degradation pathways and progeria 32
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. 31
Lamins are rapamycin targets that impact human longevity: A study in centenarians 31
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria. 31
Lamin A-dependent heterochromatin dynamics in control and progeria syndrome fibroblasts, 30
Nuclear envelope proteins and chromatin arrangem ent: a pathogenic mechanism for laminopathies, 30
Apoptotic genes as potential markers of metastatic phenotype in human osteosarcoma cell lines. 29
Changes in vimentin, lamin A/C and mitofilin induce aberrant cell organization in fibroblasts from Fanconi anemia complementation group A (FA-A) patients 29
Lamin A precursor induces barrier-to-autointegration factor nuclear localization. 29
Barrier-to-autointegration factors nuclear localization and LAP2alpha mislocalization are a common features in laminopathies with defective prelamin A processing. 28
Lamin A precursor induces barrier-to-autointegration factor nuclear localization. 28
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. 28
Prelamin A is involved in early steps of muscle differentiation 27
Implications for nuclear organization and gene transcription of lamin A/C specific mutations, 27
Barrier-to-autointegration factor nuclear localization is a common feature in prelamin A accumulating cells under pathological or physiological conditions. 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
Slug transcription factor and nuclear Lamin B1 are upregulated in osteoarthritic chondrocytes 26
Pre-Lamin A processing is linked to heterochromatin organization. 26
Heterochromatin dynamics in hutchinson-gilford progeria sindrome fibroblasts, 26
Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology 25
SREBP1 interaction with prelamin A forms: a pathogenic mechanism for lipodystrophic laminopathies. 25
Osteoblasts from a Mandibuloacral dysplasia patient induce human blood precursors to differentiate into active osteoclasts 25
Mitochondrial respiratory chain Complex I defects in Fanconi anemia complementation group A 24
Treatment of FANCA Cells with Resveratrol and N-Acetylcysteine: A Comparative Study 23
Altered pre-lamin A processing in laminopathies featuring lipodystrophy 23
Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle. 22
Prelamin A in diverse tissues. What happens in health and disease? 22
Time-course of apoptosis by in situ nick translation in adherent tumor cell lines. 22
Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts. 22
Drugs affecting prelamin A processing: Effects on heterochromatin organization 21
Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistribution. 20
Localization of SUNs and LAP2alpha in the human myocardium 20
Leupeptin preserves cardiac nitric oxide synthase 3 during reperfusion following long-term cardioplegia. 20
null 18
Totale 3.402
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Categoria #
all - tutte 10.752
article - articoli 8.426
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 19.178
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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
2025/20261.811 88 200 168 346 311 100 293 68 92 93 52 0
Totale 3.402