statistiche ricercatore

statistiche per DALPRA', LEDA

Distribuzione geografica
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Continente #
NA - Nord America 6241
EU - Europa 1840
AS - Asia 730
SA - Sud America 8
Continente sconosciuto - Info sul continente non disponibili 7
OC - Oceania 4
Totale 8830
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Nazione #
US - Stati Uniti d'America 6075
CN - Cina 590
UA - Ucraina 471
IT - Italia 329
SE - Svezia 313
GB - Regno Unito 218
CA - Canada 165
DE - Germania 135
AT - Austria 100
FI - Finlandia 87
FR - Francia 73
RU - Federazione Russa 54
IN - India 44
DK - Danimarca 41
TR - Turchia 41
VN - Vietnam 31
IR - Iran 12
EU - Europa 7
KR - Corea 5
NL - Olanda 5
AU - Australia 4
BE - Belgio 4
RO - Romania 3
BR - Brasile 2
CL - Cile 2
CO - Colombia 2
EC - Ecuador 2
ES - Italia 2
IQ - Iraq 2
JP - Giappone 2
BD - Bangladesh 1
BG - Bulgaria 1
CH - Svizzera 1
IL - Israele 1
LB - Libano 1
NO - Norvegia 1
PL - Polonia 1
PR - Porto Rico 1
PT - Portogallo 1
Totale 8830
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Città #
Ann Arbor 1507
Woodbridge 918
Houston 632
Fairfield 630
Jacksonville 523
Dearborn 360
Wilmington 313
Seattle 242
Ashburn 238
Cambridge 196
Milan 155
Nanjing 154
Vienna 99
Lachine 87
San Diego 61
Ottawa 59
Beijing 55
Nanchang 55
Fremont 45
Hebei 37
Shenyang 37
Guangzhou 31
Tianjin 30
Jinan 27
Jiaxing 24
Changsha 23
Falls Church 23
Norwalk 21
Mountain View 20
Zhengzhou 19
Auburn Hills 18
Ningbo 17
University Park 17
Taizhou 15
Kunming 14
Dong Ket 12
Meldola 10
Edmonton 8
Hangzhou 8
Kiev 8
Lecco 8
Mcallen 8
Phoenix 8
Pisa 8
San Mateo 8
Toronto 8
Hefei 7
Lanzhou 7
Lissone 7
Redmond 7
Rome 7
Chicago 6
Como 6
Leawood 6
Los Angeles 6
Zanjan 6
Kemerovo 5
Villeneuve-le-roi 5
Andover 4
Daejeon 4
Monmouth Junction 4
Shanghai 4
Waanrode 4
Waltham 4
Bari 3
Chengdu 3
Dallas 3
Detroit 3
Fuzhou 3
Loreto 3
Montréal 3
Napoli 3
New Delhi 3
Nürnberg 3
Omegna 3
Appiano Gentile 2
Ardabil 2
Bogotá 2
Bologna 2
Cermenate 2
Changchun 2
Chilly-mazarin 2
Cislago 2
Enterprise 2
Fasano 2
Fontenay-sous-bois 2
Haikou 2
Livorno 2
Newport Beach 2
Novosibirsk 2
Orange 2
Qingdao 2
Quito 2
Roskilde 2
Saint Petersburg 2
Segrate 2
Siena 2
Varese 2
Verona 2
Washington 2
Totale 6978
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Nome #
Refining the Phenotype of Recurrent Rearrangements of Chromosome 16 306
Familiar unbalanced complex rearrangements involving 13 p-arm: Description of two cases 232
Potential role of BCL2 in the recurrence of uterine smooth muscle tumors of uncertain malignant potential 199
The effect of culture on human bone marrow mesenchymal stem cells: Focus on DNA methylation profiles 192
Instability of short arm of acrocentric chromosomes: Lesson from non-acrocentric satellited chromosomes. report of 24 unrelated cases 166
Chromosome territories, X;Y translocation and Premature Ovarian Failure: is there a relationship? 157
A complete duplication of X chromosome resulting in a tricentric isochromosome originated by centromere repositioning 151
Resveratrol impairs glioma stem cells proliferation and motility by modulating the wnt signaling pathway 150
Interstitial 11q deletion: genomic characterization and neuropsychiatric follow up from early infancy to adolescence and literature review 145
Epigenetic targeting of glioma stem cells: Short-term and long-term treatments with valproic acid modulate DNA methylation and differentiation behavior, but not temozolomide sensitivity 144
Clinical and genetic evaluation of a family showing both autism and epilepsy 141
Maternal polymorphisms for methyltetrahydrofolate reductase and methionine synthetase reductase and risk of children with Down syndrome 136
Maternal polymorphisms for methyltetrahydrofolate reductase (MTHFR) and methioninesynthetasi-reductase (MTRR) and risk of children with down syndrome: A geographic effect? 135
Unexpected frequency of genomic alterations in histologically normal colonic tissue from colon cancer patients 133
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy 133
Cytogenetics of Premature Ovarian Failure: An Investigation on 269 Affected Women 131
Multi-transgenic pigs expressing three fluorescent proteins produced with high efficiency by sperm mediated gene transfer 127
Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B 124
In vitro anticancer drug test: A new method emerges from the model of glioma stem cells 124
UroVysion Multiprobe FISH on transitional cell carcinoma of the urinary bladder: comparative analysis on fresh isolated interphasic nuclei and paraffin-embedded tissue 116
Using copy number alterations to identify new therapeutic targets for bladder carcinoma 114
Monitoring the genomic stability of in vitro cultured rat bone-marrow-derived mesenchymal stem cells 112
Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated families 112
A de novo supernumerary genomic discontinuous ring chromosome 21 in a child with mild intellectual disability 111
Biological heterogeneity of putative bladder cancer stem-like cell populations from human bladder transitional cell carcinoma samples 110
Decreased platelet glutamate uptake and genetic risk factors in patients with Parkinson's disease 110
Mutations in MAPT gene cause chromosome instability and introduce copy number variations widely in the genome 110
14q32.3-qter trisomic segment: A case report and literature review 108
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy 106
Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone gene 106
Distinct pools of cancer stem-like cells coexist within human glioblastomas and display different tumorigenicity and independent genomic evolution 105
Molecular cytogenetic comparison between stem-like cell lines isolated from glioblastoma multiforme 105
Role of FISH on uncultured amniocytes for the diagnosis of aneuploidies in the presence of fetal anomalies 104
Mutations in MAPT give rise to aneuploidy in animal models of tauopathy 103
A new human cell line, PDSS-26, from poorly differentiated synovial sarcoma, with unique chromosomal anomalies 103
Evaluation of Danusertib effects on cell viability and cytomorphological parameters in cancer stem cell lines from glioblastoma multiforme 102
Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation 102
Tumor stem cell lines from glioblastoma multiforme: evaluation of antineoplastics drugs effects on cytologic, cytogenetic and genomic parameters 102
Systematic chromosomal analysis of cultured mouse neural stem cell lines 100
Tau protein and chromosome stability 99
A new function of microtubule-associated protein tau: involvement in chromosome stability 98
A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome 98
Maternal heterodisomy/isodisomy and paternal supernumerary ring of chromosome 7 in a child with Silver-Russel syndrome 98
Methods for determining the sensitivity or resistance of cancer cells to at least one anticancer drug and/or therapeutically active molecule 98
Gene Symbol: SCN1A 95
Delineating the Cytogenomic and Epigenomic Landscapes of Glioma Stem Cell Lines 94
Valproic Acid Inhibits Proliferation and Reduces Invasiveness in Glioma Stem Cells Through Wnt/β Catenin Signalling Activation 93
Synchrotron-based photon activation therapy effect on cisplatin pre-treated human glioma stem-like cells 93
Chromosomal aberrations in bladder cancer: fresh versus formalin fixed paraffin embedded tissue and targeted FISH versus wide microarray-based CGH analysis 91
Looking for the perfect test (if it exists) for the assessment of chromosome alterations in bladder cancer: UroVysion test and microarray-based CGH analysis 91
Characterisation of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams-Beuren syndrome region in chromosomal rearrangements 90
Investigating the role of X chromosome breakpoints in premature ovarian failure 90
Chromosomal imbalances in human bladder urothelial carcinoma: Similarities and differences between biopsy samples and cancer stem-like cells 90
Autosomal dominant nocturnal frontal lobe epilepsy - A critical overview 90
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal survey 89
X;Y translocations and POF 89
Resveratrol effects on cell viability, morphology and migration in cancer stem cell lines from glioblastoma multiforme 88
Clinical and genetic evaluation of a family showing both autism and epilepsy 87
Ophthalmic features in a dysmorphic boy with chromosome 4q deletion and duplication 84
Mutation analysis of the inhibin alpha gene in an Italian survey of women affected by ovarian failure 82
Blood Cell Mitochondrial DNA Content and Premature Ovarian Aging 82
A rescuable folding defective Nav1.1 (SCN1A) Na+channel mutant causes GEFS+: common mechanism in Nav1.1 related epilepsies? 80
Endometrioid-like yolk sac and Sertoli-Leydig cell tumors in the same subject carrier of a Y heterochromatin insertion into 1qh region: casual or causal association? 78
Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: cooperative study of 19 Italian laboratories 76
aCGH analysis of two families showing both autism and epilepsy 74
Clinical and genetic familial study of 61 children showing different epileptic phenotypes. 73
Wnt signaling pathway VPA-induced modulation in cancer stem cell lines from glioblastoma multiforme 72
DNA copy number alterations and PPARG amplification in a patient with multifocal bladder urothelial carcinoma 71
Cytologic, cytogenetic and genomic study of tumor stem cell lines from glioblastoma multiforme and evaluation of antineoplastic drug effects 71
Partial duplication of the PARK2 gene in a child with developmental delay and her normal mother: a second report 69
Synchrotron-based photon activation therapy effect on cisplatin pre-treated human glioma stem cells 69
Familial subtelomeric rearrangement of chromosomes 19 and 20: a new contribution to partial distal 19q trisomy 68
Familiar Febrile Seizures and Mutations in the Nav1.1 Sodium Channel 68
Two new susceptibility loci for ADNFLE 67
Two new putative loci for ADNFLE identified in an Italian family suggest a digenic inheritance for the disease 66
Characterization of cancer stem-like cells by detecting chromosomal aberrations in bladder cancer 65
DNA copy number alterations in bladder urothelial carcinoma: concordance between biopsy samples and cancer stem-like cells 64
Genetic study on 231 women affected by premature ovarian failure (POF) 63
Cytogenetic and genomic profiles of 5 cancer stem-like cell lines from glioblastoma multiforme 63
Resveratrol effects on migration and wnt signaling pathway in cancer stem cell lines from glioblastoma multiforme 62
Evaluation of Danusertib Effects on Cell Viability and Citomorphological Parameters in Cancer Stem Cell Lines from Glioblastoma Multiforme 62
Down-modulation of SEL1L, an unfolded protein response and endoplasmic reticulum-associated degradation protein, sensitizes glioma stem cells to the cytotoxic effect of valproic acid 62
Evaluation of Danusertib Effects on Cell Viability and Citomorphological Parameters in Cancer Stem Cell Lines from Glioblastoma Multiforme 60
Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011 60
DNA Methylation Changes during In Vitro Propagation of Human Mesenchymal Stem Cells: Implications for Their Genomic Stability? 60
Role of the SCN1A gene in the pathogenesis of familial febrile seizures and GEFS+ 60
Fetal trisomy 5 mosaicism: case report and literature review 57
Severe intrauterine growth restriction and trisomy 15 confined placental mosaicism: a case report and review of literature. 57
De novo balanced chromosome rearrangements in prenatal diagnosis 51
A balanced chromosomal translocation disrupting ARHGEF9 is associated with epilepsy, anxiety, aggression, and mental retardation 51
From cytogenomic to epigenomic profiles: monitoring the biologic behavior of in vitro cultured human bone marrow mesenchymal stem cells. 51
Mutational analysis of nicotinic acetylcholine receptor beta 2 subunit gene (CHRNB2) in a representative cohort of Italian probands affected by autosomal dominant nocturnal frontal lobe epilepsy 49
Analisi dei profili di metilazione di linee staminali tumorali da glioblastoma multiforme con acido valproico e paclitaxel 47
Comparative analysis of the methylation profile of tumor stem cell lines from glioblastoma multiforme and fetal neural stem cells 43
Totale 9265
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Categoria #
all - tutte 9265
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 9265
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2016/2017296 0000 00 00 000296
2017/20181912 34358270267 2912 2135 24303631
2018/20191228 28181312 35170 8557 98135236341
2019/20202446 325117196164 241318 366149 22511717553
2020/20211593 121106189176 129129 149102 14316087102
2021/20221117 59117213141 40121 4179 47749986
Totale 9265
 
 
 
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