CNR Institutional Research Information System

RISTALDI, MARIA SERAFINA
 Distribuzione geografica
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Continente #
AS - Asia 1.726
NA - Nord America 1.295
EU - Europa 464
SA - Sud America 281
Continente sconosciuto - Info sul continente non disponibili 41
AF - Africa 24
OC - Oceania 3
Totale 3.834
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Nazione #
US - Stati Uniti d'America 1.239
SG - Singapore 761
CN - Cina 382
BR - Brasile 222
VN - Vietnam 195
HK - Hong Kong 171
IT - Italia 148
FR - Francia 106
KR - Corea 72
NL - Olanda 51
DE - Germania 39
GB - Regno Unito 39
BD - Bangladesh 33
IN - India 29
CA - Canada 22
FI - Finlandia 20
AR - Argentina 19
CO - Colombia 17
JP - Giappone 12
MX - Messico 11
ID - Indonesia 9
EC - Ecuador 8
IL - Israele 8
UZ - Uzbekistan 8
VE - Venezuela 8
CR - Costa Rica 7
PK - Pakistan 7
SE - Svezia 6
ZA - Sudafrica 6
LT - Lituania 5
PH - Filippine 5
TR - Turchia 5
CH - Svizzera 4
DZ - Algeria 4
ES - Italia 4
HN - Honduras 4
MA - Marocco 4
UA - Ucraina 4
AE - Emirati Arabi Uniti 3
AT - Austria 3
CZ - Repubblica Ceca 3
EG - Egitto 3
JM - Giamaica 3
KE - Kenya 3
LV - Lettonia 3
PL - Polonia 3
PT - Portogallo 3
RS - Serbia 3
SA - Arabia Saudita 3
CL - Cile 2
CY - Cipro 2
EE - Estonia 2
GR - Grecia 2
HR - Croazia 2
IQ - Iraq 2
JO - Giordania 2
KG - Kirghizistan 2
KH - Cambogia 2
KZ - Kazakistan 2
LU - Lussemburgo 2
MY - Malesia 2
NG - Nigeria 2
NZ - Nuova Zelanda 2
OM - Oman 2
PE - Perù 2
PR - Porto Rico 2
AD - Andorra 1
AL - Albania 1
AU - Australia 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BO - Bolivia 1
BS - Bahamas 1
BY - Bielorussia 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
GE - Georgia 1
GT - Guatemala 1
GY - Guiana 1
IE - Irlanda 1
KY - Cayman, isole 1
LY - Libia 1
MK - Macedonia 1
MT - Malta 1
NI - Nicaragua 1
NP - Nepal 1
PS - Palestinian Territory 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 3.793
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Città #
Singapore 435
Santa Clara 300
San Jose 180
Hong Kong 166
Ashburn 153
Hefei 115
Beijing 111
Lauterbourg 85
Ho Chi Minh City 80
Seoul 72
Los Angeles 53
Hanoi 50
Assemini 41
Cagliari 36
Buffalo 25
São Paulo 20
New York 16
Dallas 15
Milan 14
Helsinki 13
Orem 12
Chicago 11
Düsseldorf 11
Frankfurt am Main 11
London 10
Minamishinagawa 8
Portsmouth 8
Selargius 8
Tashkent 8
Bengaluru 7
Brooklyn 7
Charlotte 7
Chennai 7
Cleveland 7
Falkenstein 7
Newark 7
Phoenix 7
Porto Alegre 7
Queens 7
Quito 7
Atlanta 6
Belo Horizonte 6
Council Bluffs 6
Da Nang 6
Haiphong 6
Lappeenranta 6
Philadelphia 6
Stockholm 6
Toronto 6
Birmingham 5
Biên Hòa 5
Bogotá 5
Manchester 5
Montreal 5
Mumbai 5
Rome 5
Turin 5
Brasília 4
Fortaleza 4
Ha Long 4
Hải Dương 4
Nuremberg 4
San Francisco 4
San José 4
Thái Nguyên 4
Tokyo 4
Zurich 4
Bari 3
Boston 3
Brescia 3
Caracas 3
Caruaru 3
Columbus 3
Curitiba 3
Dayton 3
Dhaka 3
El Paso 3
Giza 3
Glasgow 3
Guangzhou 3
Guarulhos 3
Houston 3
Lahore 3
Las Vegas 3
Lisbon 3
Medellín 3
New Orleans 3
Orlando 3
Paris 3
Riga 3
Rio de Janeiro 3
San Pedro Sula 3
Vũng Tàu 3
Amman 2
Amsterdam 2
Athens 2
Auckland 2
Austin 2
Bakersfield 2
Belém 2
Totale 2.370
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Nome #
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome. 106
An alternative approach to beta thalassemia therapy: human delta globin gene activation in transgenic mice 91
Post-GWAS Validation of Target Genes Associated with HbF and HbA2 Levels 82
In vivo activation of the human delta globin gene promoter 75
miR-365-3p mediates BCL11A and SOX6 erythroid-specific coregulation: A new player in HbF activation 74
?-Thalassemia mutations in Corsica 72
Delayed Embryonic to Adult Globin Switching in HMGB2 Knock Out Mice 66
Deficiency in interferon type 1 receptor improves definitive erythropoiesis in Klf1 null mice 65
beta-thalassemia in the Italian population 63
Delta-Globin Gene Expression Is Enhanced in vivo by Interferon Type I 62
Regulation of the human HBA genes by KLF4 in erythroid cell lines. 59
Post GWAS analysis of a BCL11A intronic region to define its role in regulating HbF levels 59
AN ALTERNATIVE APPROACH TO BETA THALASSEMIA THERAPY: HUMAN DELTA GLOBIN GENE ACTIVATION 58
Delta-globin gene expression improves sickle cell disease in a humanised mouse model 57
Krüppel-Like Factor 1: A Pivotal Gene Regulator in Erythropoiesis 56
Beta minor gene expression is preferentially reduced in EKLF Knock-out mice 56
Variability of the CD4 and F13A1 short tandem repeats in Corsicans, Sardinians and Piaroa 55
Normal delta globin gene sequence in carrier of the silent -101 (C-T) beta talassemia mutation with normal HbA2 level 54
Differentiation of single cell derived human mesenchymal stem cells into cells with a neuronal phenotype: RNA and microRNA expression profile. 54
Multi-Organ Morphological Findings in a Humanized Murine Model of Sickle Cell Trait 54
Different Hemoglobin switching pattern of beta-thalassemia mutations at the proximal and distal human beta globin CACCC box 53
Post GWAS analysis of the BCL11A intronic region to define its role in regulating HbF levels. 53
Analysis of the Linkage Disequilibrium (LD) extension in three sub-isolated population of Corsica. 51
The therapeutic potential of delta globin genein Th3/+ mice. Europ. Journal of Human Genetics. 50
Differentiation of single cell derived human mesenchymal stem cells into cells with a neuronal phenotype: RNA and microRNA expression profile. 50
Different switching patterns of beta-thalassaemic mutations at the proximal and distal CACCC box of the human HBB (beta-globin) gene 49
In vivo activation of the human delta-globin gene: the therapeutic potential in beta-thalassemic mice 49
Delta-globin gene structure and expression in K562 48
Disequilibrium extension analysis on the Xq13 region in Corsica 48
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 47
The proximal and distal human b globin CACCC box: a different effect in the hemoglobin switching of the -87 and -101 b thalassemia mutations. 47
Clonal mesenchymal stem cells transdifferentiation: expression profile 47
Klf1 affects DNase II-alpha expression in the central macrophage of a fetal liver erythroblastic island: a non-cell-autonomous role in definitive erythropoiesis 47
Genetic isolates in Corsica (France): linkage disequilibrium extension analysis on the Xq13 region. 47
The therapeutic potential of delta globin gene in Th3/+ mouse 45
Differentiation of single cell derived human mesenchymal stem cells into cells with a neuronal phenotype: RNA and microRNA expression profile 45
Reversible disruption of pre-pulse inhibition in hypomorphic-inducible and reversible CB1-/- mice 45
Reversible Disruption of Pre-Pulse Inhibition (PPI) in Hypomorphic-Inducible and Reversible CB1-/- Mice 43
Different Hemoglobin switching pattern of beta-thalassemia mutations at the proximal and distal human beta globin CACCC box. 41
Isolation rearing-induced reduction of brain 5±-reductase expression: Relevance to dopaminergic impairments. 41
Differentiation of human adult CD34+ stem cells into cells wih a neural phenotype: role of astrocytes 40
A Novel delta-thalassemica mutation a G-C substitution at codon 30 of the delta-globin gene in a person of southern Italian origin 38
Linkage Disequilibrium extension analysis on the Xq13 region in the island of Corsica 38
Temporal and tissue-specific inducible CB1 knockout mice: generation and behavioral characterization. 37
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 36
The prevention of thalassemia in Sardinia 35
Prenatal diagnosis of ?-thalassaemia in Mediterranean populations by dot blot analysis with DNA amplification and allele specific oligonucleotide probes 35
Linkage Disequilibrium's extension in Corsica. Looking for genetic isolates. 35
Genetic isolates in Corsica (France): Linkage disequilibrium extension analysis on the Xq13 region 34
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 34
Role of the -50 gamma globin region in haemoglobin switching. 34
A spontaneous mutation produced a novel elongated ?-globin chain structural variant (Hb Agnana) with a thalassemia-like phenotype 33
Isolation rearing-induced reduction of brain 5?-reductase expression: Relevance to dopaminergic impairments 32
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. 31
delta-globin gene structure and expression in the K562 cell line 30
Role of the microinvionement in neural distribution of bone marrow stem cells 30
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 30
The role of the -50 region of the human ?-globin gene in switching 29
?-Globin Gene Cluster Haplotypes in the Corsican and Sardinian Populations 29
Beta Globin haplotype frequencies and distribution in Sardinian and Corsican populations 29
Sheep alpha-globin gene sequences: implications for their concerted evolution and for the down-regulation of the 3' genes 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 29
Prenatal diagnosis of ß-thalassemia in Mediterranean Population by Dot Blot Analysis with Allelyc specific Oligonucleotide-Probes. 28
Beta-min Globin gene expression is preferentially reduced in EKLF KO mice. 28
Prenatal diagnosis of ß thalassaemia based on restriction endonuclease analysis of amplified fetal DNA. 28
Linkage disequilibrium extension analysis in Corsica. 27
In vitro expression of the -87 ?-globin thalassemic mutations [5] 27
The effect of ß thalassemia mutations on the clinical severity of the sickle-ßthalassemia syndrome 26
Micro-differentation among different sub-populations in Corsica 26
Temporal and tissue specific inducible KnockOut mice : Generation and behavioral characterization. 26
Beta-Globin gene cluster haplotypes in the Corsican and Sardinian populations 26
Molecualar Basis of ?delta ß-thalassemia with normal HbF. 26
Activation of the delta-globin gene by the beta-globin CACCC motif 26
Recurrent mutations and three novel rearrangements in the factor VIII gene of hemophilia 25
Carrier detection and early diagnosis of Wilson's disease by restriction lenght polymorphism analysis. 25
Generation and characterization of temporal tissue-specific inducible CB1 knockout mice 25
Drugs Repurposing of Molecules Modulating Human Delta Globin Gene Expression via a Model of Transgenic Foetal Liver Cells: Implications for Beta-Hemoglobinopathy Therapeutics 25
Prenatal Diagnosis of ß thalassenia in Italian Population. Haematologica 24
A novel ?-thalassemia mutation A G->C substitution at codon 30 of the ?-globin gene in a person of Southern Italian origin 24
Sheep ?-globin gene sequences: Implications for their concerted evolution and for the down-regulation of the 3? genes 24
Expression gradient in sheep alpha alpha and alpha alpha alpha globin gene haplotypes: mRNA levels 24
In vitro expression of the -87 beta thalassemic mutation 24
Variability of Linkage Disequilibrium (LD) among Corsican populations 23
Gc and C3 polymorphisms in Sardinia 23
Beta-globin cluster haplotypes in normal individuals and beta(0)39-thalassemia carriers from Sardinia, Italy. 23
Beta-thalassemia mutations in Corsica 23
A spontaneous mutation produced a novel elongated ß globin chain structural variant (Hb Agnana) with a thalassemia like phenotype 22
AK, PGM and 6PGD Polymorphisms in Central Sardinia. 22
Etude genetique des beta thalassemies en Corse: aspects anthropologiques. 22
AcP and EsD polymorphisms in Sardinia 21
Globin gene expression is preferentially reduced in EKLF KO mice 21
Different pattern of Linkage disequilibrium (LD) among Corsica sub-populations 20
Prenatal Diagnosis of inherited Hemoglobinopathies 20
Prenatal diagnosis of inherited hemoglobinopathies 19
Molecular Analysis of atypical ß thalassemia heterozygous 19
Generation and characterization of temporal tissue-specific inducible CB1 knockout mice 19
A novel delta-thalassemia mutation, a G-C substitution at codon 30 of the delta-globin gene in a Person of Southern Italian origin 17
Differentiation of human bone marrow stem cells into neural cells: diverse effects of two specific treatments . 15
Totale 3.834
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Categoria #
all - tutte 14.298
article - articoli 11.235
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 25.533
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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
2025/20262.013 105 154 146 245 436 83 400 85 106 115 105 33
2026/2027374 101 82 191 0 0 0 0 0 0 0 0 0
Totale 3.834