IRIS
RINALDI, Carmela
 Distribuzione geografica
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Continente #
EU - Europa 1.586
NA - Nord America 1.451
AS - Asia 280
SA - Sud America 5
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 2
AF - Africa 1
Totale 3.329
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Nazione #
US - Stati Uniti d'America 1.444
IE - Irlanda 405
SE - Svezia 375
IT - Italia 299
CN - Cina 204
PL - Polonia 127
UA - Ucraina 110
DE - Germania 102
GB - Regno Unito 56
FI - Finlandia 54
SG - Singapore 41
BE - Belgio 20
IN - India 16
VN - Vietnam 11
FR - Francia 9
CZ - Repubblica Ceca 8
NL - Olanda 7
CA - Canada 5
BR - Brasile 3
NZ - Nuova Zelanda 3
PK - Pakistan 3
RO - Romania 3
RU - Federazione Russa 3
CL - Cile 2
ES - Italia 2
EU - Europa 2
MT - Malta 2
MX - Messico 2
PH - Filippine 2
PT - Portogallo 2
AU - Australia 1
EG - Egitto 1
IR - Iran 1
JP - Giappone 1
KR - Corea 1
LT - Lituania 1
MD - Moldavia 1
Totale 3.329
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Città #
Dublin 404
Chandler 290
Jacksonville 228
Nyköping 200
Messina 154
Warsaw 127
Beijing 111
Ann Arbor 69
Princeton 66
Ashburn 64
Medford 63
Cambridge 50
Des Moines 45
Dearborn 43
Boardman 40
Bremen 33
Lancaster 31
New York 24
Singapore 22
Wilmington 21
Woodbridge 20
Brussels 19
Jinan 16
Ningbo 12
Dong Ket 11
Catania 10
Seattle 10
Shenyang 10
Rome 9
San Mateo 9
Pune 8
Hyderabad 6
Nanjing 6
Helsinki 5
Padova 5
Taizhou 5
Ancona 4
Fuzhou 4
Hefei 4
Milan 4
Norwalk 4
Prague 4
Rosolini 4
Taiyuan 4
Amsterdam 3
Auburn Hills 3
Brno 3
Changsha 3
Clearwater 3
Falls Church 3
Hebei 3
Islamabad 3
Lago 3
Lappeenranta 3
Munich 3
Ottawa 3
Shanghai 3
Tianjin 3
Vicosa 3
Washington 3
Whakatane 3
Alcamo 2
Cagliari 2
Chicago 2
Edinburgh 2
Ferrandina 2
Hangzhou 2
Houston 2
Jiaxing 2
Lisbon 2
Los Angeles 2
Manila 2
Milazzo 2
Mineo 2
Mountain View 2
Napoli 2
Odesa 2
Perugia 2
Pietà 2
Riva 2
Salerno 2
San Giovanni La Punta 2
Terlizzi 2
Trento 2
Zhengzhou 2
Atlanta 1
Baltimore 1
Boston 1
Bovezzo 1
Brooklyn 1
Cairo 1
Caltagirone 1
Caluso 1
Chieti 1
Chongqing 1
Downers Grove 1
Enna 1
Ercolano 1
Fort Worth 1
Fremont 1
Totale 2.392
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Nome #
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome 104
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study. 104
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study 95
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions 91
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case-control study. 90
CCR5Δ32 Polymorphism Associated with a Slower Rate DiseaseProgression in a Cohort of RR-MS Sicilian Patients 81
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens 80
Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis? 80
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype 75
Screening genetico dei geni CCM in pazienti italiani affetti da angioma cavernoso cerebrale: un caso familiare 72
IL SUBCOMPLESSO DEI SARCOGLICANI NEL MUSCOLO LISCIO UMANO 70
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations 70
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study 67
GENETICS OF CAVERNOMAS: A CASE REPORT 66
A MOLECULAR- GENETIC ANALYSIS OF FLAVIN-CONTAINING MONOOXYGENASE3 GENE (FMO3) IN AN ITALIAN CHILD WITH A TMAURIA LIKE-PHENOTYPE 64
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa 64
Molecular analysis of CCM genes promoter regions 59
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations 58
An intronic variant in PTEN gene is probably involved in splicing alteration events 58
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations 56
LITHIUM TRANSPORT PATHWAYS IN HUMAN, CHICKEN AND EEL ERYTHROCYTES 55
Sarcoglycans in muscolar diseases of ureters: an immunohistochemical study. 54
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies 54
POLIMORFISMI DELLA GLIOSSALASI I E DELLA PARAOXONASI I IN INDIVIDUI SANI ED INDIVIDUI AFFETTI DA SCLEROSI MULTIPLA.FATTORI DI SUSCETTIBILITA'? 53
Distribuzione dell'allele mutato Δ32 del gene CCR5 nella popolazione sana del bacino del mediterraneo. 53
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation 52
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study 52
Glyoxalase I A111E, paraoxonase 1 q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? 51
Age dependent switching role of ciclyn D1 in breast cancer 51
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report 51
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation 51
Is α- sarcoglycan a member of sarcoglycan complex in human smooth muscle? 50
The interaction of haemoglobin, magnesium, organic phosphates and band 3 protein in nucleated and anucleated erythrocytes 49
Effetti contrastanti di alcuni ossidanti sul trasporto di litio in globuli rossi umani 49
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes 47
CCR5Δ32 POLYMORPHISM ASSOCIATED WITH A SLOWER RATE DISEASE PROGRESSION IN A COHORT OF RR-MS SICILIAN PATIENTS 46
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa 45
Distribution of Δ32-CCR5 polymorphism in a mediterranean basin population. 44
Sarcoglycans and integrins in muscular inactivity 43
IS α SARCOGLYCAN A MEMBER OF SARCOGLYCAN COMPLEX IN HUMAN SMOOTH MUSCLE ? 43
OSMOREGULATION IN NORMAL AND ABNORMAL HUMAN ERYTHROCYTES 43
Distribuzione dell'allele mutato delta 32 del gene CCR5 nella popolazione siciliana 41
INFLUSSO DELLO IONE SOLFATO NEI GLOBULI ROSSI IN SOGGETTI SANI,IPERTESI E DIABETICI 40
FMO3 allelic variants in Sicilian and Sardinian populations: Trimethylaminuria and absence of fish-like body odor 40
NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUSMALFORMATIONS 39
Oxidative Stress and the Neurovascular Unit 39
null 38
IMMUNOISTOCHEMICAL AND NUCLEOTIDE SEQUENCING ANALYSIS OF SARCOGLYCANS IN EPITHELIUM 38
Costameric proteins in human skeletal muscle during muscular inactivity. 38
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function? 36
A rare case of TMAU associated with suspected Currarino triad 35
Quantification of trimethylamine (TMA) and trimethylamine oxide (TMAO) for diagnostic and targeted diet purposes. 34
interazioni farmaco-cinetiche sul trasporto di litio nei globuli rossi umani 33
The biological pathways of Alzheimer disease: a review 33
Genetic and functional study of CCR5 gene in HIV-1 infection 32
LITHIUM TRANSPORT PATHWAYS IN HUMAN CHICKEN AND EEL ERYTHROCYTES 32
IMMUNOHISTOCHEMICAL AND NUCLEOTIDE SEQUENCING ANALYSIS OF SARCOGLYCANS IN EPITHELIUM 32
Distribution of the mutated delta32 allele of the CCR5 gene in a Sicilian population 32
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling 32
null 31
EXPRESSION OF SARCOGLYCANS IN THE HUMAN CEREBRAL CORTEX: AN IMMUNOHISTOCHEMICAL AND MOLECULAR STUDY 31
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null 29
PON I and GLO I Gene Polymorphisms and Their Association with Breast Cancer: A Case-Control Study in a Population from Southern Italy 28
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 27
Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration 23
null 23
Further data on a 9.1-kb insertion-deletion polymorphism: Survey of Mediterranean populations 23
Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells 19
Sarcoglycan complex in human normal and pathological prostatic tissue: An immunohistochemical and RT-PCR study 19
The impact of modifier genes on cone-rod dystrophy heterogeneity: An explorative familial pilot study and a hypothesis on neurotransmission impairment 10
Investigating G-quadruplex structures in RPGR gene: Implications for understanding X-linked retinal degeneration 8
Human retinal secretome: A cross-link between mesenchymal and retinal cells 8
Sarcoglycan subcomplex expression in normal human smooth muscle 7
Totale 3.501
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Categoria #
all - tutte 13.377
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 13.377
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020471 64 28 2 32 2 47 50 37 9 87 94 19
2020/2021477 78 23 64 23 62 45 26 38 24 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
2024/202523 23 0 0 0 0 0 0 0 0 0 0 0
Totale 3.501