CATALOGO DEI PRODOTTI DELLA RICERCA

GANDINI, Alberto
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
AS - Asia 3.352
NA - Nord America 2.173
EU - Europa 2.119
SA - Sud America 165
AF - Africa 59
Continente sconosciuto - Info sul continente non disponibili 57
OC - Oceania 11
Totale 7.936
Salva come PNG Salva come JPEG
Nazione #
CN - Cina 2.480
US - Stati Uniti d'America 2.108
RU - Federazione Russa 753
SG - Singapore 434
GB - Regno Unito 376
IT - Italia 338
VN - Vietnam 136
BR - Brasile 115
IE - Irlanda 109
SE - Svezia 109
DE - Germania 101
HK - Hong Kong 89
FI - Finlandia 86
FR - Francia 75
KR - Corea 43
CA - Canada 36
NL - Olanda 32
IN - India 31
TR - Turchia 29
ID - Indonesia 21
BE - Belgio 20
UA - Ucraina 20
AR - Argentina 18
PL - Polonia 18
JP - Giappone 17
AT - Austria 14
ES - Italia 14
BD - Bangladesh 13
NG - Nigeria 13
ZA - Sudafrica 13
MX - Messico 12
AU - Australia 10
PK - Pakistan 10
CO - Colombia 9
RO - Romania 9
IQ - Iraq 8
LT - Lituania 8
IR - Iran 7
MA - Marocco 6
PH - Filippine 6
SC - Seychelles 6
CZ - Repubblica Ceca 5
EC - Ecuador 5
GR - Grecia 5
HU - Ungheria 5
JO - Giordania 5
PE - Perù 5
PY - Paraguay 5
SA - Arabia Saudita 5
AE - Emirati Arabi Uniti 4
BJ - Benin 4
CH - Svizzera 4
EG - Egitto 4
JM - Giamaica 4
UZ - Uzbekistan 4
BO - Bolivia 3
CL - Cile 3
SI - Slovenia 3
TG - Togo 3
TT - Trinidad e Tobago 3
BB - Barbados 2
CR - Costa Rica 2
DK - Danimarca 2
LV - Lettonia 2
NI - Nicaragua 2
PT - Portogallo 2
RS - Serbia 2
SN - Senegal 2
TH - Thailandia 2
TJ - Tagikistan 2
TW - Taiwan 2
AL - Albania 1
AZ - Azerbaigian 1
BG - Bulgaria 1
BY - Bielorussia 1
CG - Congo 1
CI - Costa d'Avorio 1
DZ - Algeria 1
ET - Etiopia 1
GE - Georgia 1
GT - Guatemala 1
GY - Guiana 1
IM - Isola di Man 1
KE - Kenya 1
LB - Libano 1
LU - Lussemburgo 1
LY - Libia 1
MT - Malta 1
MY - Malesia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PA - Panama 1
RW - Ruanda 1
SV - El Salvador 1
TN - Tunisia 1
VE - Venezuela 1
VG - Isole Vergini Britanniche 1
Totale 7.879
Salva come PNG Salva come JPEG
Città #
Southend 285
Moscow 267
Ashburn 263
Singapore 241
Chandler 229
Verona 198
San Jose 189
Dallas 154
Jacksonville 135
Dublin 108
Hong Kong 80
Woodbridge 79
Beijing 77
Council Bluffs 77
New York 69
Houston 62
Ann Arbor 52
The Dalles 52
Ho Chi Minh City 41
Los Angeles 38
Helsinki 34
Jinan 28
Munich 28
Princeton 27
Lawrence 26
Nanjing 26
Shenyang 25
Wilmington 24
Brussels 19
Buffalo 18
Montreal 17
Santa Clara 17
Hanoi 16
Dong Ket 15
Guangzhou 15
Lancaster 15
Tokyo 15
Turku 15
Jakarta 14
London 14
Sindelfingen 14
Orem 13
Phoenix 13
Redmond 13
San Francisco 13
Abuja 12
São Paulo 12
Warsaw 12
Frankfurt am Main 11
Johannesburg 11
Ningbo 11
Redondo Beach 11
Seoul 11
Toronto 11
Vienna 11
Amsterdam 10
Boston 10
Changsha 10
Tianjin 10
Brescia 9
Haikou 9
Hangzhou 9
Hebei 9
Lanzhou 9
Nanchang 9
Brooklyn 8
Chennai 8
Haiphong 8
Manchester 8
Boardman 7
Bologna 7
Denver 7
Jiaxing 7
Lappeenranta 7
Redwood City 7
Zhengzhou 7
Ankara 6
Atlanta 6
Barnet 6
Chicago 6
Columbus 6
Da Nang 6
Des Moines 6
Kent 6
Mahé 6
Milan 6
Mumbai 6
Norwalk 6
Paris 6
Poplar 6
Rio de Janeiro 6
Venice 6
Amman 5
Auburn Hills 5
Belo Horizonte 5
Budapest 5
Buenos Aires 5
Saint-Etienne 5
Sant'Ambrogio di Valpolicella 5
Utrecht 5
Totale 3.594
Salva come PNG Salva come JPEG
Nome #
CRISPR/Cas9 mediated knock-out of RUNX2 in melanoma cells 1.328
CRISPR/Cas9 genome editing in melanoma cells: new insight of RUNT domain 1.303
Apparent Mineralocorticoid Excess by a Novel Mutation and Epigenetic Modulation by HSD11B2 Promoter Methylation 319
A novel splicing mutation in FKBP10 causing osteogenesis imperfecta with a possible mineralization defect 254
Type VI Osteogenesis imperfecta: effect of plasma transfusion on bone metabolism 235
Analysis of the d3-growth hormone receptor polymorphism in large cohorts of small, appropriate and large for gestational age newborns. 234
A Novel Splicing Mutation in FKBP10 in a patient with a moderate Osteogenesis Imperfecta histologically classificable as type VI 230
Lack of expression of SERPINF1, the gene coding for pigment epithelium derived factor, causes progressively deforming Osteogenesis Imperfecta with normal type I collagen 217
A potential role of RUNX2- RUNT domain in modulating the expression of genes involved in bone metastases: an in vitro study with melanoma cells 216
Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal Collagen I 215
Runx2 stimulates neoangiogenesis through the Runt domain in melanoma 211
How to cope with a severe skeletal dysplasia 210
The Runt domain of RUNX2 induces the migration of melanoma cells to bone 199
Genetic analysis carried out on blood-spots of phenylalanine hydroxylase-deficient newborns detected by northeastern italian neonatal screening 193
New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and Migration 185
The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene 174
No osteonecrosis of the jaw in children and adolescents treated with Neridronate for osteogenesis imperfecta. 171
Two novel C-terminus RUNX2 mutations in two cleidocranial dysplasia (CCD) patients impairing p53 expression 169
Hypercalciuria and renal function in children affected by Osteogenesis Imperfecta 168
Polymorphisms of the TSH Receptor gene in children with resistance to TSH and in helthy young controls 166
Fisetin: an integrated approach to identify a strategy promoting osteogenesis 163
Novel Splicing Mutation in FKBP10 gene in a patient with moderate-severe form of Osteogenesis imperfecta 159
Hypophosphatasia in adults: A new manifestation, a new mutation. A case report 157
A technique of mRNA extraction and labeling from circulating lymphocytes of children treated with growth hormone replacement therapy for microarray analysis 153
Exploring the Interplay of RUNX2 and CXCR4 in Melanoma Progression 149
Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes. 142
Expression of FBXW11 in normal and disease-associated osteogenic cells 135
Role of genetic investigation in the diagnosis of short stature in a cohort of Italian children 125
West Nile Virus Encephalitis in Haematological Setting: Report of Two Cases and a Brief Review of the Literature 120
Prostaglandin D2 synthase and its post-translational modifications in neurological disorders 98
Unraveling RUNX2 mutation in a cleidocranial dysplasia patient: Molecular insights into osteogenesis and proteostasis 96
Extracellular Vesicles in Osteogenesis: Comparative Analysis of Stem Cell Sources, Conditioning Strategies, and In Vitro Models Toward Advanced Bone Regeneration 42
Totale 7.936
Salva come PNG Salva come JPEG
Categoria #
all - tutte 21.294
article - articoli 13.330
book - libri 0
conference - conferenze 7.964
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 42.588
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022230 0 71 14 30 2 7 4 14 8 3 18 59
2022/2023604 37 82 47 102 50 155 6 28 74 5 8 10
2023/20242.491 13 28 44 30 48 2.148 11 28 2 37 75 27
2024/2025760 41 44 48 140 29 43 35 43 76 49 76 136
2025/20262.496 146 118 137 429 697 152 253 100 223 145 35 61
2026/202783 33 50 0 0 0 0 0 0 0 0 0 0
Totale 7.936