CATALOGO DEI PRODOTTI DELLA RICERCA

GANDINI, Alberto
 Distribuzione geografica
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Continente #
AS - Asia 3.360
NA - Nord America 2.466
EU - Europa 2.160
SA - Sud America 170
AF - Africa 62
Continente sconosciuto - Info sul continente non disponibili 60
OC - Oceania 11
Totale 8.289
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Nazione #
CN - Cina 2.480
US - Stati Uniti d'America 2.376
RU - Federazione Russa 754
SG - Singapore 434
GB - Regno Unito 379
IT - Italia 361
VN - Vietnam 136
BR - Brasile 119
IE - Irlanda 109
SE - Svezia 109
DE - Germania 107
HK - Hong Kong 89
FI - Finlandia 86
FR - Francia 77
CA - Canada 46
KR - Corea 43
NL - Olanda 33
IN - India 32
TR - Turchia 29
ID - Indonesia 22
BE - Belgio 20
UA - Ucraina 20
JP - Giappone 19
AR - Argentina 18
PL - Polonia 18
AT - Austria 14
BD - Bangladesh 14
ES - Italia 14
ZA - Sudafrica 14
NG - Nigeria 13
MX - Messico 12
AU - Australia 10
PK - Pakistan 10
CO - Colombia 9
LT - Lituania 9
RO - Romania 9
GR - Grecia 8
IQ - Iraq 8
IR - Iran 7
MA - Marocco 7
PE - Perù 6
PH - Filippine 6
SA - Arabia Saudita 6
SC - Seychelles 6
CZ - Repubblica Ceca 5
EC - Ecuador 5
GT - Guatemala 5
HU - Ungheria 5
JO - Giordania 5
NI - Nicaragua 5
PY - Paraguay 5
TT - Trinidad e Tobago 5
AE - Emirati Arabi Uniti 4
BJ - Benin 4
CH - Svizzera 4
CR - Costa Rica 4
EG - Egitto 4
JM - Giamaica 4
SV - El Salvador 4
UZ - Uzbekistan 4
BO - Bolivia 3
CL - Cile 3
CW - ???statistics.table.value.countryCode.CW??? 3
SI - Slovenia 3
TG - Togo 3
BB - Barbados 2
DK - Danimarca 2
LV - Lettonia 2
PT - Portogallo 2
RS - Serbia 2
SN - Senegal 2
TH - Thailandia 2
TJ - Tagikistan 2
TW - Taiwan 2
AL - Albania 1
AM - Armenia 1
AO - Angola 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BY - Bielorussia 1
CG - Congo 1
CI - Costa d'Avorio 1
DZ - Algeria 1
ET - Etiopia 1
GE - Georgia 1
GY - Guiana 1
IL - Israele 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
PR - Porto Rico 1
RW - Ruanda 1
Totale 8.229
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Città #
Ashburn 364
Southend 285
Moscow 267
Singapore 241
Chandler 229
San Jose 212
Verona 198
Dallas 162
Jacksonville 135
Dublin 108
Hong Kong 80
Woodbridge 79
Beijing 77
Council Bluffs 77
New York 71
Houston 63
Ann Arbor 52
The Dalles 52
Ho Chi Minh City 41
Los Angeles 41
Helsinki 34
Jinan 28
Munich 28
Princeton 27
Lawrence 26
Nanjing 26
Shenyang 25
Wilmington 24
Santa Clara 23
Brussels 19
Buffalo 18
Montreal 18
Tokyo 17
Hanoi 16
Lancaster 16
São Paulo 16
Dong Ket 15
Frankfurt am Main 15
Guangzhou 15
San Francisco 15
Turku 15
Jakarta 14
London 14
Sindelfingen 14
Orem 13
Phoenix 13
Redmond 13
Toronto 13
Abuja 12
Warsaw 12
Johannesburg 11
Ningbo 11
Redondo Beach 11
Seoul 11
Vienna 11
Amsterdam 10
Boston 10
Changsha 10
Milan 10
Tianjin 10
Brescia 9
Chicago 9
Haikou 9
Hangzhou 9
Hebei 9
Lanzhou 9
Nanchang 9
Brooklyn 8
Chennai 8
Denver 8
Haiphong 8
Manchester 8
Atlanta 7
Boardman 7
Bologna 7
Columbus 7
Jiaxing 7
Lappeenranta 7
Redwood City 7
Zhengzhou 7
Ankara 6
Barnet 6
Da Nang 6
Des Moines 6
Kent 6
Mahé 6
Mumbai 6
Naples 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
Lima 5
Saint-Etienne 5
Totale 3.765
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Nome #
CRISPR/Cas9 mediated knock-out of RUNX2 in melanoma cells 1.347
CRISPR/Cas9 genome editing in melanoma cells: new insight of RUNT domain 1.308
Apparent Mineralocorticoid Excess by a Novel Mutation and Epigenetic Modulation by HSD11B2 Promoter Methylation 328
A novel splicing mutation in FKBP10 causing osteogenesis imperfecta with a possible mineralization defect 263
Type VI Osteogenesis imperfecta: effect of plasma transfusion on bone metabolism 248
Analysis of the d3-growth hormone receptor polymorphism in large cohorts of small, appropriate and large for gestational age newborns. 241
A Novel Splicing Mutation in FKBP10 in a patient with a moderate Osteogenesis Imperfecta histologically classificable as type VI 236
Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal Collagen I 233
How to cope with a severe skeletal dysplasia 229
Lack of expression of SERPINF1, the gene coding for pigment epithelium derived factor, causes progressively deforming Osteogenesis Imperfecta with normal type I collagen 227
A potential role of RUNX2- RUNT domain in modulating the expression of genes involved in bone metastases: an in vitro study with melanoma cells 223
Runx2 stimulates neoangiogenesis through the Runt domain in melanoma 222
The Runt domain of RUNX2 induces the migration of melanoma cells to bone 206
Genetic analysis carried out on blood-spots of phenylalanine hydroxylase-deficient newborns detected by northeastern italian neonatal screening 201
New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and Migration 192
No osteonecrosis of the jaw in children and adolescents treated with Neridronate for osteogenesis imperfecta. 186
Polymorphisms of the TSH Receptor gene in children with resistance to TSH and in helthy young controls 183
The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene 182
Two novel C-terminus RUNX2 mutations in two cleidocranial dysplasia (CCD) patients impairing p53 expression 177
Novel Splicing Mutation in FKBP10 gene in a patient with moderate-severe form of Osteogenesis imperfecta 176
Hypercalciuria and renal function in children affected by Osteogenesis Imperfecta 173
Fisetin: an integrated approach to identify a strategy promoting osteogenesis 173
Hypophosphatasia in adults: A new manifestation, a new mutation. A case report 173
A technique of mRNA extraction and labeling from circulating lymphocytes of children treated with growth hormone replacement therapy for microarray analysis 161
Exploring the Interplay of RUNX2 and CXCR4 in Melanoma Progression 158
Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes. 148
Expression of FBXW11 in normal and disease-associated osteogenic cells 144
Role of genetic investigation in the diagnosis of short stature in a cohort of Italian children 143
West Nile Virus Encephalitis in Haematological Setting: Report of Two Cases and a Brief Review of the Literature 126
Unraveling RUNX2 mutation in a cleidocranial dysplasia patient: Molecular insights into osteogenesis and proteostasis 110
Prostaglandin D2 synthase and its post-translational modifications in neurological disorders 107
Extracellular Vesicles in Osteogenesis: Comparative Analysis of Stem Cell Sources, Conditioning Strategies, and In Vitro Models Toward Advanced Bone Regeneration 65
Totale 8.289
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Categoria #
all - tutte 22.390
article - articoli 14.097
book - libri 0
conference - conferenze 8.293
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 44.780
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022145 0 0 0 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
2026/2027436 33 51 97 255 0 0 0 0 0 0 0 0
Totale 8.289