RISTALDI, MARIA SERAFINA
 Distribuzione geografica
Continente #
AS - Asia 1.701
NA - Nord America 1.056
EU - Europa 436
SA - Sud America 255
AF - Africa 23
OC - Oceania 3
Totale 3.474
Nazione #
US - Stati Uniti d'America 1.019
SG - Singapore 760
CN - Cina 382
BR - Brasile 217
VN - Vietnam 189
HK - Hong Kong 171
IT - Italia 129
FR - Francia 104
KR - Corea 72
NL - Olanda 51
DE - Germania 39
GB - Regno Unito 33
IN - India 29
BD - Bangladesh 28
FI - Finlandia 20
AR - Argentina 18
CA - Canada 18
JP - Giappone 12
MX - Messico 9
IL - Israele 8
ID - Indonesia 7
PK - Pakistan 7
UZ - Uzbekistan 7
CO - Colombia 6
SE - Svezia 6
EC - Ecuador 5
LT - Lituania 5
ZA - Sudafrica 5
CH - Svizzera 4
DZ - Algeria 4
ES - Italia 4
MA - Marocco 4
TR - Turchia 4
UA - Ucraina 4
AT - Austria 3
CR - Costa Rica 3
CZ - Repubblica Ceca 3
EG - Egitto 3
KE - Kenya 3
LV - Lettonia 3
PL - Polonia 3
PT - Portogallo 3
RS - Serbia 3
SA - Arabia Saudita 3
VE - Venezuela 3
AE - Emirati Arabi Uniti 2
CL - Cile 2
CY - Cipro 2
GR - Grecia 2
HR - Croazia 2
IQ - Iraq 2
JM - Giamaica 2
JO - Giordania 2
KG - Kirghizistan 2
KH - Cambogia 2
LU - Lussemburgo 2
NG - Nigeria 2
NZ - Nuova Zelanda 2
OM - Oman 2
PE - Perù 2
PH - Filippine 2
AD - Andorra 1
AL - Albania 1
AU - Australia 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EE - Estonia 1
GE - Georgia 1
GT - Guatemala 1
HN - Honduras 1
IE - Irlanda 1
KZ - Kazakistan 1
LY - Libia 1
MK - Macedonia 1
MT - Malta 1
PY - Paraguay 1
RE - Reunion 1
RO - Romania 1
RU - Federazione Russa 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
SV - El Salvador 1
TH - Thailandia 1
TJ - Tagikistan 1
TT - Trinidad e Tobago 1
Totale 3.474
Città #
Singapore 435
Santa Clara 300
Hong Kong 166
San Jose 151
Ashburn 141
Hefei 115
Beijing 111
Lauterbourg 85
Ho Chi Minh City 77
Seoul 72
Los Angeles 50
Hanoi 49
Assemini 41
Cagliari 36
Buffalo 25
São Paulo 20
Dallas 14
Helsinki 13
New York 13
Orem 12
Düsseldorf 11
Frankfurt am Main 11
London 9
Milan 8
Minamishinagawa 8
Selargius 8
Bengaluru 7
Chennai 7
Chicago 7
Falkenstein 7
Portsmouth 7
Tashkent 7
Belo Horizonte 6
Council Bluffs 6
Da Nang 6
Haiphong 6
Lappeenranta 6
Newark 6
Porto Alegre 6
Stockholm 6
Toronto 6
Biên Hòa 5
Manchester 5
Montreal 5
Mumbai 5
Queens 5
Turin 5
Bogotá 4
Cleveland 4
Fortaleza 4
Ha Long 4
Hải Dương 4
Nuremberg 4
Phoenix 4
Quito 4
San Francisco 4
Thái Nguyên 4
Tokyo 4
Zurich 4
Atlanta 3
Bari 3
Brasília 3
Brescia 3
Brooklyn 3
Caruaru 3
Charlotte 3
Curitiba 3
Dhaka 3
Giza 3
Glasgow 3
Guangzhou 3
Guarulhos 3
Houston 3
Lahore 3
Lisbon 3
Paris 3
Philadelphia 3
Riga 3
Rio de Janeiro 3
Vũng Tàu 3
Amman 2
Amsterdam 2
Athens 2
Auckland 2
Austin 2
Belém 2
Birmingham 2
Bishkek 2
Boston 2
Brookfield 2
Bắc Ninh 2
Campinas 2
Carapicuíba 2
Columbus 2
Dayton 2
Denver 2
Endicott 2
Goiânia 2
Greenwood 2
Hamburg 2
Totale 2.258
Nome #
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome. 100
An alternative approach to beta thalassemia therapy: human delta globin gene activation in transgenic mice 75
Post-GWAS Validation of Target Genes Associated with HbF and HbA2 Levels 72
In vivo activation of the human delta globin gene promoter 71
?-Thalassemia mutations in Corsica 69
miR-365-3p mediates BCL11A and SOX6 erythroid-specific coregulation: A new player in HbF activation 68
beta-thalassemia in the Italian population 62
Delayed Embryonic to Adult Globin Switching in HMGB2 Knock Out Mice 62
Delta-Globin Gene Expression Is Enhanced in vivo by Interferon Type I 57
Post GWAS analysis of a BCL11A intronic region to define its role in regulating HbF levels 56
AN ALTERNATIVE APPROACH TO BETA THALASSEMIA THERAPY: HUMAN DELTA GLOBIN GENE ACTIVATION 54
Deficiency in interferon type 1 receptor improves definitive erythropoiesis in Klf1 null mice 54
Variability of the CD4 and F13A1 short tandem repeats in Corsicans, Sardinians and Piaroa 53
Regulation of the human HBA genes by KLF4 in erythroid cell lines. 53
Delta-globin gene expression improves sickle cell disease in a humanised mouse model 52
Krüppel-Like Factor 1: A Pivotal Gene Regulator in Erythropoiesis 52
Beta minor gene expression is preferentially reduced in EKLF Knock-out mice 52
Normal delta globin gene sequence in carrier of the silent -101 (C-T) beta talassemia mutation with normal HbA2 level 51
Differentiation of single cell derived human mesenchymal stem cells into cells with a neuronal phenotype: RNA and microRNA expression profile. 51
Post GWAS analysis of the BCL11A intronic region to define its role in regulating HbF levels. 50
Multi-Organ Morphological Findings in a Humanized Murine Model of Sickle Cell Trait 50
Analysis of the Linkage Disequilibrium (LD) extension in three sub-isolated population of Corsica. 49
Different Hemoglobin switching pattern of beta-thalassemia mutations at the proximal and distal human beta globin CACCC box 49
Differentiation of single cell derived human mesenchymal stem cells into cells with a neuronal phenotype: RNA and microRNA expression profile. 49
The therapeutic potential of delta globin genein Th3/+ mice. Europ. Journal of Human Genetics. 48
In vivo activation of the human delta-globin gene: the therapeutic potential in beta-thalassemic mice 47
The C-T substitution in the distal CACCC box of the beta-globin gene promoter is a common cause of silent beta-thalassemia in the italian population 45
Clonal mesenchymal stem cells transdifferentiation: expression profile 45
The proximal and distal human b globin CACCC box: a different effect in the hemoglobin switching of the -87 and -101 b thalassemia mutations. 44
Genetic isolates in Corsica (France): linkage disequilibrium extension analysis on the Xq13 region. 44
Klf1 affects DNase II-alpha expression in the central macrophage of a fetal liver erythroblastic island: a non-cell-autonomous role in definitive erythropoiesis 43
The therapeutic potential of delta globin gene in Th3/+ mouse 42
Different switching patterns of beta-thalassaemic mutations at the proximal and distal CACCC box of the human HBB (beta-globin) gene 42
Disequilibrium extension analysis on the Xq13 region in Corsica 42
Differentiation of single cell derived human mesenchymal stem cells into cells with a neuronal phenotype: RNA and microRNA expression profile 41
Reversible disruption of pre-pulse inhibition in hypomorphic-inducible and reversible CB1-/- mice 41
Delta-globin gene structure and expression in K562 40
Different Hemoglobin switching pattern of beta-thalassemia mutations at the proximal and distal human beta globin CACCC box. 39
Reversible Disruption of Pre-Pulse Inhibition (PPI) in Hypomorphic-Inducible and Reversible CB1-/- Mice 39
Differentiation of human adult CD34+ stem cells into cells wih a neural phenotype: role of astrocytes 37
Isolation rearing-induced reduction of brain 5±-reductase expression: Relevance to dopaminergic impairments. 37
A Novel delta-thalassemica mutation a G-C substitution at codon 30 of the delta-globin gene in a person of southern Italian origin 36
Linkage Disequilibrium extension analysis on the Xq13 region in the island of Corsica 36
Temporal and tissue-specific inducible CB1 knockout mice: generation and behavioral characterization. 35
Linkage Disequilibrium's extension in Corsica. Looking for genetic isolates. 33
The C-T substitution in the distal CACCC box of the ?-globin gene promoter is a common cause of silent ? thalassaemia in the Italian population 32
The C-T substitution in the distal CACCC box of the beta-globin gene promoter is a common cause of silent beta thalassemia in the italian population 32
The prevention of thalassemia in Sardinia 31
A spontaneous mutation produced a novel elongated ?-globin chain structural variant (Hb Agnana) with a thalassemia-like phenotype 30
Genetic isolates in Corsica (France): Linkage disequilibrium extension analysis on the Xq13 region 30
Prenatal diagnosis of ?-thalassaemia in Mediterranean populations by dot blot analysis with DNA amplification and allele specific oligonucleotide probes 30
Cri Du Chat mosaicism: a new case with partial deletion and partial deletion/duplication of the short arm of chromosome 5, leading to an unusual phenotype. 30
Role of the -50 gamma globin region in haemoglobin switching. 30
Isolation rearing-induced reduction of brain 5?-reductase expression: Relevance to dopaminergic impairments 29
Role of the microinvionement in neural distribution of bone marrow stem cells 29
Cri Du Chat Mosaicism: An Unusual Case Of Partial Deletion And Partial Deletion/Duplication Of The Short Arm Of Chromosome 5,Leading To An Unusual Cri Du Chat Phenotype 28
Prenatal diagnosis of ß-thalassemia in Mediterranean Population by Dot Blot Analysis with Allelyc specific Oligonucleotide-Probes. 27
delta-globin gene structure and expression in the K562 cell line 27
?-Globin Gene Cluster Haplotypes in the Corsican and Sardinian Populations 27
Beta Globin haplotype frequencies and distribution in Sardinian and Corsican populations 27
Sheep alpha-globin gene sequences: implications for their concerted evolution and for the down-regulation of the 3' genes 27
The role of the -50 region of the human ?-globin gene in switching 26
Temporal and tissue specific inducible KnockOut mice : Generation and behavioral characterization. 25
Activation of the delta-globin gene by the beta-globin CACCC motif 25
Prenatal diagnosis of ß thalassaemia based on restriction endonuclease analysis of amplified fetal DNA. 25
Beta-min Globin gene expression is preferentially reduced in EKLF KO mice. 24
The effect of ß thalassemia mutations on the clinical severity of the sickle-ßthalassemia syndrome 24
Micro-differentation among different sub-populations in Corsica 24
Recurrent mutations and three novel rearrangements in the factor VIII gene of hemophilia 24
Beta-Globin gene cluster haplotypes in the Corsican and Sardinian populations 24
Molecualar Basis of ?delta ß-thalassemia with normal HbF. 24
Linkage disequilibrium extension analysis in Corsica. 24
Generation and characterization of temporal tissue-specific inducible CB1 knockout mice 24
In vitro expression of the -87 ?-globin thalassemic mutations [5] 24
CRI du chat mosaicism: An unusual case of partial deletion and partial deletion/duplication of the short arm of chromosome 5, leading to an unusual CRI du chat phenotype 24
Prenatal Diagnosis of ß thalassenia in Italian Population. Haematologica 22
A novel ?-thalassemia mutation A G->C substitution at codon 30 of the ?-globin gene in a person of Southern Italian origin 22
Carrier detection and early diagnosis of Wilson's disease by restriction lenght polymorphism analysis. 22
Expression gradient in sheep alpha alpha and alpha alpha alpha globin gene haplotypes: mRNA levels 22
In vitro expression of the -87 beta thalassemic mutation 22
Beta-thalassemia mutations in Corsica 22
Sheep ?-globin gene sequences: Implications for their concerted evolution and for the down-regulation of the 3? genes 21
Drugs Repurposing of Molecules Modulating Human Delta Globin Gene Expression via a Model of Transgenic Foetal Liver Cells: Implications for Beta-Hemoglobinopathy Therapeutics 21
AcP and EsD polymorphisms in Sardinia 20
Gc and C3 polymorphisms in Sardinia 20
Globin gene expression is preferentially reduced in EKLF KO mice 20
Variability of Linkage Disequilibrium (LD) among Corsican populations 19
Etude genetique des beta thalassemies en Corse: aspects anthropologiques. 19
Prenatal Diagnosis of inherited Hemoglobinopathies 19
A spontaneous mutation produced a novel elongated ß globin chain structural variant (Hb Agnana) with a thalassemia like phenotype 18
AK, PGM and 6PGD Polymorphisms in Central Sardinia. 18
Prenatal diagnosis of inherited hemoglobinopathies 17
Molecular Analysis of atypical ß thalassemia heterozygous 17
Beta-globin cluster haplotypes in normal individuals and beta(0)39-thalassemia carriers from Sardinia, Italy. 17
Generation and characterization of temporal tissue-specific inducible CB1 knockout mice 17
Different pattern of Linkage disequilibrium (LD) among Corsica sub-populations 16
A novel delta-thalassemia mutation, a G-C substitution at codon 30 of the delta-globin gene in a Person of Southern Italian origin 16
Differentiation of human bone marrow stem cells into neural cells: diverse effects of two specific treatments . 14
Totale 3.515
Categoria #
all - tutte 12.764
article - articoli 10.011
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 22.775


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202426 0 0 0 0 0 0 0 0 1 0 16 9
2024/20251.421 2 15 107 54 283 80 45 74 64 89 321 287
2025/20262.013 105 154 146 245 436 83 400 85 106 115 105 33
2026/202755 55 0 0 0 0 0 0 0 0 0 0 0
Totale 3.515