SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

TRABANELLI, Cecilia
 Distribuzione geografica
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Continente #
NA - Nord America 3.716
AS - Asia 1.942
EU - Europa 1.163
SA - Sud America 280
AF - Africa 45
Continente sconosciuto - Info sul continente non disponibili 42
OC - Oceania 6
Totale 7.194
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Nazione #
US - Stati Uniti d'America 3.613
SG - Singapore 727
CN - Cina 486
DE - Germania 326
VN - Vietnam 251
BR - Brasile 216
IT - Italia 177
UA - Ucraina 146
HK - Hong Kong 138
GB - Regno Unito 133
TR - Turchia 111
FI - Finlandia 73
SE - Svezia 62
FR - Francia 53
CA - Canada 48
RU - Federazione Russa 48
BD - Bangladesh 46
IN - India 45
MX - Messico 36
JP - Giappone 33
PL - Polonia 27
AR - Argentina 25
ES - Italia 21
ID - Indonesia 21
NL - Olanda 19
ZA - Sudafrica 15
BE - Belgio 13
VE - Venezuela 13
AT - Austria 12
PK - Pakistan 12
LT - Lituania 11
CO - Colombia 9
MY - Malesia 9
PH - Filippine 9
CZ - Repubblica Ceca 8
IE - Irlanda 8
UZ - Uzbekistan 8
IQ - Iraq 7
MA - Marocco 7
SA - Arabia Saudita 7
EC - Ecuador 5
EG - Egitto 5
HU - Ungheria 5
JM - Giamaica 5
AE - Emirati Arabi Uniti 4
AU - Australia 4
CH - Svizzera 4
CL - Cile 4
CR - Costa Rica 4
DZ - Algeria 4
IL - Israele 4
IR - Iran 4
JO - Giordania 4
KE - Kenya 4
TN - Tunisia 4
BY - Bielorussia 3
NP - Nepal 3
OM - Oman 3
PY - Paraguay 3
RO - Romania 3
SI - Slovenia 3
ET - Etiopia 2
GT - Guatemala 2
KR - Corea 2
LV - Lettonia 2
NZ - Nuova Zelanda 2
UY - Uruguay 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AZ - Azerbaigian 1
BB - Barbados 1
BO - Bolivia 1
BS - Bahamas 1
CM - Camerun 1
CY - Cipro 1
DO - Repubblica Dominicana 1
GP - Guadalupe 1
GR - Grecia 1
KH - Cambogia 1
KZ - Kazakistan 1
LK - Sri Lanka 1
MK - Macedonia 1
MQ - Martinica 1
MR - Mauritania 1
NI - Nicaragua 1
NO - Norvegia 1
PA - Panama 1
PE - Perù 1
PR - Porto Rico 1
PS - Palestinian Territory 1
PT - Portogallo 1
QA - Qatar 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
SR - Suriname 1
TH - Thailandia 1
TZ - Tanzania 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 7.154
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Città #
Singapore 458
Ashburn 438
San Jose 314
Fairfield 258
Woodbridge 258
Chandler 225
Beijing 199
Ann Arbor 182
Houston 182
Jacksonville 144
Santa Clara 140
Hong Kong 135
Ho Chi Minh City 92
Wilmington 91
Seattle 90
Los Angeles 89
Munich 84
Cambridge 80
New York 70
Dallas 59
Hanoi 52
Izmir 50
Council Bluffs 49
Nanjing 44
Princeton 38
Milan 34
Lauterbourg 32
San Diego 32
Tokyo 31
Shanghai 30
Buffalo 29
Orem 29
Ferrara 27
London 25
Turku 25
Boardman 24
Bremen 24
Warsaw 23
São Paulo 21
Toronto 20
Frankfurt am Main 19
Da Nang 18
Helsinki 18
Montreal 18
Brooklyn 17
Chicago 17
Mexico City 16
Stockholm 16
Jiaxing 14
The Dalles 14
Tianjin 14
Chennai 13
Falkenstein 13
Jakarta 12
Poplar 12
Rome 12
Brussels 11
Falls Church 11
Dearborn 10
Jinan 10
Johannesburg 10
Nanchang 10
San Mateo 10
Shenyang 10
Denver 9
Nuremberg 9
Redwood City 9
Amsterdam 8
Atlanta 8
Changsha 8
Haiphong 8
Hebei 8
Hefei 8
Phoenix 8
Addison 7
Ankara 7
Dublin 7
Mountain View 7
Tashkent 7
Guangzhou 6
Milwaukee 6
Norwalk 6
Nürnberg 6
Osasco 6
Rio de Janeiro 6
Thái Bình 6
Washington 6
Zhengzhou 6
Auburn Hills 5
Belo Horizonte 5
Bologna 5
Brno 5
Des Moines 5
Kunming 5
Lanzhou 5
Moscow 5
Mumbai 5
Ottawa 5
Vienna 5
Boston 4
Totale 4.783
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Nome #
Reactivation of infectious simian virus 40 from normal human tissues 284
Paternal germline mosaicism in collagen VI related myopathies 279
G.P.12.06 A comprehensive molecular characterisation of dystrophinopathies 272
A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies 267
GENETIC, CLINICAL AND NEUROPATHOLOGICAL INSIGHTS INTO PATIENTS WITH ASCERTAINED DIAGNOSIS OF HUNTINGTON DISEASE 259
Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-terminal domain: a case report 257
Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5′ mutation hot spot of the dystrophin gene 250
Exon skipping-mediated dystrophin reading frame restoration for small mutations 248
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies 239
Mutation Load of Multiple Ion Channel Gene Mutations in Brugada Syndrome 235
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation 231
Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies. 227
Chromosomal aberrations induced by BK virus T antigen in human fibroblasts 220
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females 219
Commercial kit-based diagnosis is not enough for prenatal testing of beta-thalassemia: pitfalls in diagnostic mutation analysis raises the need for reference laboratories 217
Exploring the clinical and epidemiological complexity of GJB2-linked deafness 216
Morphological, histochemical, immunohistochemical, and ultrastructural characterization of tumors and dysplastic and non-neoplastic lesions arising in BK virus/tat transgenic mice 214
Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries 213
Characterization of a 4-Mb region at chromosome 6q21 harboring a replicative senescence gene 208
Antiangiogenic, antitumoural and antimetastatic effects of two distamycin A derivatives with anti-HIV-1 Tat activity in a Kaposi's sarcoma-like murine model 201
Becker muscular dystrophy due to an intronic splicing mutation inducing a dual dystrophin transcript 195
DMD gene molecular genetic characterization in Eastern Europe and non European countries 190
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study 181
Prevalence of liver tumours in HIV-1 tat-transgenic mice treated with urethane 177
Left ventricular myocardial noncompaction with advanced atrioventricular conduction disorder and ventricular arrhythmias in a young patient: Role of MIB1 gene 170
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies 169
Simian virus 40 fotprints in normal human tissues, brain and bone tumors of different histotypes 159
Simian virus 40 footprints in normal human tissues, brain and bone tumours of different histotypes. In: SIMIAN VIRUS 40 (SV40): A POSSIBLE HUMAN POLYOMAVIRUS. 153
Genetic analysis of a 6q21 region harboring a senescence gene: construction of a 4 megabase yeast artificial chromosome contig 148
Simian virus 40 footprints in normal human tissues, brain and bone tumors of different histotypes 145
SV40 as a possible cofactor in the etiopathogenesis of mesothelioma and other human tumors 139
SV40 e Papovavirus umani BK e JC nell'oncogenesi sperimentale e umana: aspetti patogenetici ed epidemiologici. 117
Riflessioni sul possibile ruolo di SV40 nell'eziopatogenesi dei tumori umani. 114
Oncogenesi virale 111
null 92
Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion. 74
Tumor-host interaction mediates the regression of BK virus-induced vascular tumors in mice: involvement of transforming growth factor-beta 1 54
null 50
Totale 7.194
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Categoria #
all - tutte 31.986
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.390
Totale 33.376
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022422 0 35 26 24 20 16 20 24 19 29 42 167
2022/2023471 49 52 13 54 88 60 22 43 62 6 17 5
2023/2024264 23 24 13 6 20 72 8 15 4 7 7 65
2024/20251.033 18 24 66 59 128 78 62 35 191 104 146 122
2025/20262.798 303 96 243 338 449 172 368 137 252 279 120 41
2026/2027145 69 76 0 0 0 0 0 0 0 0 0 0
Totale 7.194