CNR Institutional Research Information System

RISTALDI, MARIA SERAFINA
 Distribuzione geografica
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Continente #
AS - Asia 1.684
NA - Nord America 950
EU - Europa 422
SA - Sud America 253
AF - Africa 23
OC - Oceania 3
Totale 3.335
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Nazione #
US - Stati Uniti d'America 923
SG - Singapore 760
CN - Cina 380
BR - Brasile 216
VN - Vietnam 187
HK - Hong Kong 171
IT - Italia 115
FR - Francia 104
KR - Corea 72
NL - Olanda 51
DE - Germania 39
GB - Regno Unito 33
IN - India 29
FI - Finlandia 20
AR - Argentina 17
BD - Bangladesh 16
CA - Canada 12
JP - Giappone 12
IL - Israele 8
MX - Messico 8
PK - Pakistan 7
UZ - Uzbekistan 7
CO - Colombia 6
ID - Indonesia 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
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
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 3.335
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Città #
Singapore 435
Santa Clara 300
Hong Kong 166
San Jose 150
Hefei 115
Beijing 111
Ashburn 103
Lauterbourg 85
Ho Chi Minh City 77
Seoul 72
Los Angeles 49
Hanoi 47
Assemini 41
Cagliari 36
Buffalo 23
São Paulo 20
Dallas 14
Helsinki 13
New York 13
Orem 12
Düsseldorf 11
Frankfurt am Main 11
London 9
Minamishinagawa 8
Selargius 8
Bengaluru 7
Chennai 7
Falkenstein 7
Portsmouth 7
Tashkent 7
Belo Horizonte 6
Chicago 6
Council Bluffs 6
Da Nang 6
Haiphong 6
Lappeenranta 6
Newark 6
Porto Alegre 6
Stockholm 6
Biên Hòa 5
Manchester 5
Milan 5
Mumbai 5
Queens 5
Bogotá 4
Cleveland 4
Fortaleza 4
Ha Long 4
Hải Dương 4
Montreal 4
Nuremberg 4
Phoenix 4
Quito 4
San Francisco 4
Thái Nguyên 4
Tokyo 4
Toronto 4
Turin 4
Zurich 4
Atlanta 3
Brasília 3
Brescia 3
Caruaru 3
Curitiba 3
Dhaka 3
Giza 3
Glasgow 3
Guangzhou 3
Guarulhos 3
Lahore 3
Lisbon 3
Paris 3
Riga 3
Rio de Janeiro 3
Vũng Tàu 3
Amman 2
Amsterdam 2
Athens 2
Auckland 2
Belém 2
Birmingham 2
Bishkek 2
Boston 2
Brooklyn 2
Bắc Ninh 2
Campinas 2
Carapicuíba 2
Charlotte 2
Columbus 2
Goiânia 2
Hamburg 2
Istanbul 2
Johannesburg 2
Karachi 2
Kyiv 2
Las Vegas 2
Lima 2
Luxembourg 2
Madrid 2
Marseille 2
Totale 2.201
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Nome #
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome. 96
In vivo activation of the human delta globin gene promoter 69
?-Thalassemia mutations in Corsica 68
miR-365-3p mediates BCL11A and SOX6 erythroid-specific coregulation: A new player in HbF activation 66
beta-thalassemia in the Italian population 62
Post-GWAS Validation of Target Genes Associated with HbF and HbA2 Levels 62
Delayed Embryonic to Adult Globin Switching in HMGB2 Knock Out Mice 61
Delta-Globin Gene Expression Is Enhanced in vivo by Interferon Type I 55
An alternative approach to beta thalassemia therapy: human delta globin gene activation in transgenic mice 54
Variability of the CD4 and F13A1 short tandem repeats in Corsicans, Sardinians and Piaroa 53
AN ALTERNATIVE APPROACH TO BETA THALASSEMIA THERAPY: HUMAN DELTA GLOBIN GENE ACTIVATION 53
Regulation of the human HBA genes by KLF4 in erythroid cell lines. 52
Post GWAS analysis of a BCL11A intronic region to define its role in regulating HbF levels 52
Delta-globin gene expression improves sickle cell disease in a humanised mouse model 51
Krüppel-Like Factor 1: A Pivotal Gene Regulator in Erythropoiesis 51
Deficiency in interferon type 1 receptor improves definitive erythropoiesis in Klf1 null mice 51
Differentiation of single cell derived human mesenchymal stem cells into cells with a neuronal phenotype: RNA and microRNA expression profile. 51
Normal delta globin gene sequence in carrier of the silent -101 (C-T) beta talassemia mutation with normal HbA2 level 50
Multi-Organ Morphological Findings in a Humanized Murine Model of Sickle Cell Trait 50
Post GWAS analysis of the BCL11A intronic region to define its role in regulating HbF levels. 49
Analysis of the Linkage Disequilibrium (LD) extension in three sub-isolated population of Corsica. 48
Differentiation of single cell derived human mesenchymal stem cells into cells with a neuronal phenotype: RNA and microRNA expression profile. 48
Beta minor gene expression is preferentially reduced in EKLF Knock-out mice 47
The therapeutic potential of delta globin genein Th3/+ mice. Europ. Journal of Human Genetics. 46
In vivo activation of the human delta-globin gene: the therapeutic potential in beta-thalassemic mice 46
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
Different Hemoglobin switching pattern of beta-thalassemia mutations at the proximal and distal human beta globin CACCC box 45
Clonal mesenchymal stem cells transdifferentiation: expression profile 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
The proximal and distal human b globin CACCC box: a different effect in the hemoglobin switching of the -87 and -101 b thalassemia mutations. 40
Different Hemoglobin switching pattern of beta-thalassemia mutations at the proximal and distal human beta globin CACCC box. 39
Genetic isolates in Corsica (France): linkage disequilibrium extension analysis on the Xq13 region. 39
Delta-globin gene structure and expression in K562 38
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. 36
Reversible Disruption of Pre-Pulse Inhibition (PPI) in Hypomorphic-Inducible and Reversible CB1-/- Mice 36
Linkage Disequilibrium extension analysis on the Xq13 region in the island of Corsica 36
A Novel delta-thalassemica mutation a G-C substitution at codon 30 of the delta-globin gene in a person of southern Italian origin 35
Temporal and tissue-specific inducible CB1 knockout mice: generation and behavioral characterization. 34
Linkage Disequilibrium's extension in Corsica. Looking for genetic isolates. 32
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 31
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
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
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
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 29
Genetic isolates in Corsica (France): Linkage disequilibrium extension analysis on the Xq13 region 28
Prenatal diagnosis of ?-thalassaemia in Mediterranean populations by dot blot analysis with DNA amplification and allele specific oligonucleotide probes 28
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
delta-globin gene structure and expression in the K562 cell line 27
?-Globin Gene Cluster Haplotypes in the Corsican and Sardinian Populations 27
The role of the -50 region of the human ?-globin gene in switching 26
Role of the -50 gamma globin region in haemoglobin switching. 26
Beta Globin haplotype frequencies and distribution in Sardinian and Corsican populations 26
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
Sheep alpha-globin gene sequences: implications for their concerted evolution and for the down-regulation of the 3' genes 25
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
Beta-Globin gene cluster haplotypes in the Corsican and Sardinian populations 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
Prenatal diagnosis of ß-thalassemia in Mediterranean Population by Dot Blot Analysis with Allelyc specific Oligonucleotide-Probes. 23
Temporal and tissue specific inducible KnockOut mice : Generation and behavioral characterization. 23
Molecualar Basis of ?delta ß-thalassemia with normal HbF. 23
Beta-min Globin gene expression is preferentially reduced in EKLF KO mice. 22
A novel ?-thalassemia mutation A G->C substitution at codon 30 of the ?-globin gene in a person of Southern Italian origin 22
Recurrent mutations and three novel rearrangements in the factor VIII gene of hemophilia 22
In vitro expression of the -87 beta thalassemic mutation 22
Prenatal Diagnosis of ß thalassenia in Italian Population. Haematologica 21
Expression gradient in sheep alpha alpha and alpha alpha alpha globin gene haplotypes: mRNA levels 21
Beta-thalassemia mutations in Corsica 21
AcP and EsD polymorphisms in Sardinia 20
Globin gene expression is preferentially reduced in EKLF KO mice 20
Drugs Repurposing of Molecules Modulating Human Delta Globin Gene Expression via a Model of Transgenic Foetal Liver Cells: Implications for Beta-Hemoglobinopathy Therapeutics 20
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 20
Gc and C3 polymorphisms in Sardinia 19
Carrier detection and early diagnosis of Wilson's disease by restriction lenght polymorphism analysis. 19
Sheep ?-globin gene sequences: Implications for their concerted evolution and for the down-regulation of the 3? genes 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
Etude genetique des beta thalassemies en Corse: aspects anthropologiques. 18
Variability of Linkage Disequilibrium (LD) among Corsican populations 17
Beta-globin cluster haplotypes in normal individuals and beta(0)39-thalassemia carriers from Sardinia, Italy. 17
Prenatal Diagnosis of inherited Hemoglobinopathies 17
Prenatal diagnosis of inherited hemoglobinopathies 16
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
Generation and characterization of temporal tissue-specific inducible CB1 knockout mice 16
Molecular Analysis of atypical ß thalassemia heterozygous 15
Differentiation of human bone marrow stem cells into neural cells: diverse effects of two specific treatments . 13
Totale 3.376
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Categoria #
all - tutte 11.477
article - articoli 8.966
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 20.443
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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
2025/20261.929 105 154 146 245 436 83 400 85 106 115 54 0
Totale 3.376