IRIS
RINALDI, Carmela
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 3.728
NA - Nord America 2.862
AS - Asia 1.798
SA - Sud America 628
AF - Africa 53
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 2
Totale 9.077
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 2.810
RU - Federazione Russa 1.780
SG - Singapore 742
CN - Cina 545
BR - Brasile 534
IE - Irlanda 407
SE - Svezia 382
IT - Italia 371
HK - Hong Kong 179
DE - Germania 175
PL - Polonia 145
UA - Ucraina 118
VN - Vietnam 105
GB - Regno Unito 90
FR - Francia 89
FI - Finlandia 77
IN - India 44
AR - Argentina 28
BD - Bangladesh 27
TR - Turchia 25
BE - Belgio 21
ID - Indonesia 20
EC - Ecuador 19
MX - Messico 19
CA - Canada 18
UZ - Uzbekistan 18
MA - Marocco 15
NL - Olanda 15
ZA - Sudafrica 14
CO - Colombia 13
CZ - Repubblica Ceca 13
AT - Austria 12
PK - Pakistan 12
IQ - Iraq 11
VE - Venezuela 11
JP - Giappone 10
CL - Cile 8
PY - Paraguay 8
PH - Filippine 7
IL - Israele 6
ES - Italia 5
LT - Lituania 5
NP - Nepal 5
OM - Oman 5
AZ - Azerbaigian 4
ET - Etiopia 4
GR - Grecia 4
JM - Giamaica 4
KE - Kenya 4
PE - Perù 4
RO - Romania 4
BG - Bulgaria 3
CR - Costa Rica 3
DO - Repubblica Dominicana 3
EG - Egitto 3
IR - Iran 3
KH - Cambogia 3
MY - Malesia 3
NZ - Nuova Zelanda 3
PT - Portogallo 3
SA - Arabia Saudita 3
TH - Thailandia 3
TN - Tunisia 3
AE - Emirati Arabi Uniti 2
AU - Australia 2
CI - Costa d'Avorio 2
DZ - Algeria 2
EU - Europa 2
JO - Giordania 2
KG - Kirghizistan 2
MD - Moldavia 2
MT - Malta 2
MU - Mauritius 2
PS - Palestinian Territory 2
RS - Serbia 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
UY - Uruguay 2
AO - Angola 1
BH - Bahrain 1
BO - Bolivia 1
CH - Svizzera 1
GA - Gabon 1
GE - Georgia 1
GT - Guatemala 1
HR - Croazia 1
KR - Corea 1
KW - Kuwait 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
LV - Lettonia 1
LY - Libia 1
MN - Mongolia 1
NG - Nigeria 1
NI - Nicaragua 1
NR - Nauru 1
PA - Panama 1
TJ - Tagikistan 1
Totale 9.077
Salva come PNG Salva come JPEG
Città #
Moscow 533
Ashburn 419
Singapore 408
Dublin 406
Dallas 380
Chandler 290
Jacksonville 230
Beijing 210
Nyköping 200
Messina 185
Hong Kong 178
Warsaw 136
The Dalles 113
San Jose 107
Ann Arbor 69
Princeton 66
Medford 63
Lauterbourg 58
New York 54
Los Angeles 53
Munich 51
Cambridge 50
Des Moines 47
Dearborn 43
São Paulo 41
Boardman 40
Bremen 33
Lancaster 31
Buffalo 29
Ho Chi Minh City 29
Wilmington 21
Brussels 20
Hanoi 20
Redondo Beach 20
Woodbridge 20
Tianjin 19
Council Bluffs 17
Orem 17
Jinan 16
Rio de Janeiro 16
Tashkent 16
Belo Horizonte 15
Turku 15
Brasília 14
Frankfurt am Main 13
Seattle 13
Brooklyn 12
Catania 12
Jakarta 12
Ningbo 12
Rome 12
Santa Clara 12
Dong Ket 11
Helsinki 10
Houston 10
Manchester 10
Milan 10
Shanghai 10
Shenyang 10
Shenzhen 10
Amsterdam 9
Boston 9
Chennai 9
Phoenix 9
Pune 9
San Mateo 9
Tokyo 9
Hyderabad 8
Toronto 8
Chicago 7
Düsseldorf 7
Guarulhos 7
Istanbul 7
London 7
Quito 7
San Francisco 7
São José dos Campos 7
Atlanta 6
Curitiba 6
Denver 6
Guangzhou 6
Johannesburg 6
Lappeenranta 6
Mexico City 6
Nanjing 6
Stockholm 6
Vienna 6
Baghdad 5
Casablanca 5
Contagem 5
Da Nang 5
Duque de Caxias 5
Guayaquil 5
Hefei 5
Lahore 5
Montreal 5
Muscat 5
New Delhi 5
Olomouc 5
Padova 5
Totale 5.237
Salva come PNG Salva come JPEG
Nome #
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype 260
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case-control study. 234
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study. 232
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens 204
CCR5Δ32 Polymorphism Associated with a Slower Rate DiseaseProgression in a Cohort of RR-MS Sicilian Patients 203
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome 193
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes 191
A MOLECULAR- GENETIC ANALYSIS OF FLAVIN-CONTAINING MONOOXYGENASE3 GENE (FMO3) IN AN ITALIAN CHILD WITH A TMAURIA LIKE-PHENOTYPE 186
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa 181
Age dependent switching role of ciclyn D1 in breast cancer 180
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions 179
Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis? 171
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study 169
Costameric proteins in human skeletal muscle during muscular inactivity. 168
FMO3 allelic variants in Sicilian and Sardinian populations: Trimethylaminuria and absence of fish-like body odor 165
An intronic variant in PTEN gene is probably involved in splicing alteration events 163
Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells 161
LITHIUM TRANSPORT PATHWAYS IN HUMAN, CHICKEN AND EEL ERYTHROCYTES 159
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies 159
CCR5Δ32 POLYMORPHISM ASSOCIATED WITH A SLOWER RATE DISEASE PROGRESSION IN A COHORT OF RR-MS SICILIAN PATIENTS 154
A rare case of TMAU associated with suspected Currarino triad 153
Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration 149
Glyoxalase I A111E, paraoxonase 1 q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? 146
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study 146
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations 144
Distribuzione dell'allele mutato Δ32 del gene CCR5 nella popolazione sana del bacino del mediterraneo. 140
Distribuzione dell'allele mutato delta 32 del gene CCR5 nella popolazione siciliana 140
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations 139
Distribution of the mutated delta32 allele of the CCR5 gene in a Sicilian population 139
Distribution of Δ32-CCR5 polymorphism in a mediterranean basin population. 132
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function? 129
The interaction of haemoglobin, magnesium, organic phosphates and band 3 protein in nucleated and anucleated erythrocytes 128
Effetti contrastanti di alcuni ossidanti sul trasporto di litio in globuli rossi umani 127
NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUSMALFORMATIONS 123
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations 122
Sarcoglycan complex in human normal and pathological prostatic tissue: An immunohistochemical and RT-PCR study 120
Oxidative Stress and the Neurovascular Unit 120
GENETICS OF CAVERNOMAS: A CASE REPORT 117
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study 115
Molecular analysis of CCM genes promoter regions 115
IL SUBCOMPLESSO DEI SARCOGLICANI NEL MUSCOLO LISCIO UMANO 109
The biological pathways of Alzheimer disease: a review 109
Screening genetico dei geni CCM in pazienti italiani affetti da angioma cavernoso cerebrale: un caso familiare 108
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation 106
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling 106
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa 105
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation 101
Is α- sarcoglycan a member of sarcoglycan complex in human smooth muscle? 100
PON I and GLO I Gene Polymorphisms and Their Association with Breast Cancer: A Case-Control Study in a Population from Southern Italy 99
Sarcoglycans in muscolar diseases of ureters: an immunohistochemical study. 97
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report 97
The impact of modifier genes on cone-rod dystrophy heterogeneity: An explorative familial pilot study and a hypothesis on neurotransmission impairment 94
Sarcoglycans and integrins in muscular inactivity 94
INFLUSSO DELLO IONE SOLFATO NEI GLOBULI ROSSI IN SOGGETTI SANI,IPERTESI E DIABETICI 92
POLIMORFISMI DELLA GLIOSSALASI I E DELLA PARAOXONASI I IN INDIVIDUI SANI ED INDIVIDUI AFFETTI DA SCLEROSI MULTIPLA.FATTORI DI SUSCETTIBILITA'? 91
IMMUNOHISTOCHEMICAL AND NUCLEOTIDE SEQUENCING ANALYSIS OF SARCOGLYCANS IN EPITHELIUM 88
EXPRESSION OF SARCOGLYCANS IN THE HUMAN CEREBRAL CORTEX: AN IMMUNOHISTOCHEMICAL AND MOLECULAR STUDY 88
Quantification of trimethylamine (TMA) and trimethylamine oxide (TMAO) for diagnostic and targeted diet purposes. 87
New evaluation methods of read mapping by 17 aligners on simulated and empirical NGS data: an updated comparison of DNA- and RNA-Seq data from Illumina and Ion Torrent technologies 85
interazioni farmaco-cinetiche sul trasporto di litio nei globuli rossi umani 84
IS α SARCOGLYCAN A MEMBER OF SARCOGLYCAN COMPLEX IN HUMAN SMOOTH MUSCLE ? 80
LITHIUM TRANSPORT PATHWAYS IN HUMAN CHICKEN AND EEL ERYTHROCYTES 79
Genetic and functional study of CCR5 gene in HIV-1 infection 78
Decoding pediatric inherited retinal dystrophies: Bridging genetic complexity and clinical heterogeneity 76
IMMUNOISTOCHEMICAL AND NUCLEOTIDE SEQUENCING ANALYSIS OF SARCOGLYCANS IN EPITHELIUM 76
OSMOREGULATION IN NORMAL AND ABNORMAL HUMAN ERYTHROCYTES 74
Sarcoglycan subcomplex expression in normal human smooth muscle 65
Further data on a 9.1-kb insertion-deletion polymorphism: Survey of Mediterranean populations 64
Investigating G-quadruplex structures in RPGR gene: Implications for understanding X-linked retinal degeneration 58
Human retinal secretome: A cross-link between mesenchymal and retinal cells 56
Multifaceted disruption of AMPA receptor signaling by CACNG8 variants: Integrated evidence from human genetics and molecular simulation 47
null 38
Nel labirinto delle distrofie retiniche ereditarie: alla scoperta delle Terapie innovative e delle visioni del futuro 36
Mechanotransduction in development: a focus on angiogenesis 31
null 31
null 31
null 29
null 23
Comprehensive transcriptomic analysis reveals canonical and novel pathways modulated by nanoceria in mammalian retinal degeneration 14
Circulating lncRNAs Remark Expression Profile of Cerebrovascular Malformation Endothelial Cells 13
null 1
Totale 9.296
Salva come PNG Salva come JPEG
Categoria #
all - tutte 29.133
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 29.133
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202194 0 0 0 0 0 0 0 0 0 54 21 19
2021/2022539 3 74 17 13 6 6 29 28 8 152 47 156
2022/20231.217 83 92 59 104 110 110 17 81 510 5 40 6
2023/2024342 33 57 8 31 29 64 0 15 2 18 11 74
2024/20251.502 29 10 41 111 43 60 45 334 361 94 134 240
2025/20264.316 181 344 409 310 385 903 522 523 539 200 0 0
Totale 9.296