Bicocca Open Archive

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DALPRA', LEDA
 Distribuzione geografica
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Continente #
NA - Nord America 8.889
EU - Europa 4.073
AS - Asia 1.950
SA - Sud America 65
AF - Africa 13
Continente sconosciuto - Info sul continente non disponibili 7
OC - Oceania 7
Totale 15.004
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Nazione #
US - Stati Uniti d'America 8.689
CN - Cina 762
SG - Singapore 750
DE - Germania 730
SE - Svezia 711
IE - Irlanda 516
UA - Ucraina 488
RU - Federazione Russa 467
IT - Italia 455
GB - Regno Unito 253
HK - Hong Kong 208
CA - Canada 192
FI - Finlandia 113
AT - Austria 111
FR - Francia 92
IN - India 57
BR - Brasile 49
DK - Danimarca 43
TR - Turchia 43
BE - Belgio 41
VN - Vietnam 35
ID - Indonesia 31
NL - Olanda 26
IR - Iran 13
UZ - Uzbekistan 11
EU - Europa 7
AU - Australia 5
BD - Bangladesh 5
CZ - Repubblica Ceca 5
EC - Ecuador 5
KR - Corea 5
MA - Marocco 5
AR - Argentina 4
IL - Israele 4
IQ - Iraq 4
JP - Giappone 4
AZ - Azerbaigian 3
CL - Cile 3
CO - Colombia 3
EE - Estonia 3
ES - Italia 3
KG - Kirghizistan 3
LK - Sri Lanka 3
MX - Messico 3
RO - Romania 3
ZA - Sudafrica 3
AM - Armenia 2
CH - Svizzera 2
EG - Egitto 2
KE - Kenya 2
NZ - Nuova Zelanda 2
PA - Panama 2
PL - Polonia 2
PT - Portogallo 2
AE - Emirati Arabi Uniti 1
AL - Albania 1
BG - Bulgaria 1
BS - Bahamas 1
BY - Bielorussia 1
DO - Repubblica Dominicana 1
GR - Grecia 1
HU - Ungheria 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LV - Lettonia 1
NO - Norvegia 1
NP - Nepal 1
PH - Filippine 1
PR - Porto Rico 1
TH - Thailandia 1
TN - Tunisia 1
UY - Uruguay 1
Totale 15.004
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Città #
Ann Arbor 1.511
Woodbridge 919
Chandler 788
Fairfield 632
Houston 632
Singapore 547
Jacksonville 523
Frankfurt am Main 518
Dublin 506
Ashburn 411
Dearborn 360
Wilmington 313
Seattle 246
New York 243
Hong Kong 208
Cambridge 196
Princeton 189
Milan 171
Santa Clara 165
Nanjing 154
Shanghai 120
Vienna 105
Lachine 87
Lawrence 76
Altamura 70
Ottawa 63
San Diego 61
Beijing 58
Nanchang 55
Fremont 45
Council Bluffs 43
Boardman 40
Andover 37
Brussels 37
Hebei 37
Shenyang 37
Guangzhou 36
Jakarta 31
Toronto 31
Tianjin 30
Jinan 28
Changsha 25
Jiaxing 25
Helsinki 24
Falls Church 23
Los Angeles 22
Norwalk 21
Moscow 20
Mountain View 20
Zhengzhou 20
Auburn Hills 18
Ningbo 17
University Park 17
Nuremberg 16
Kunming 15
Taizhou 15
Dallas 14
Huizen 13
Dong Ket 12
London 12
San Mateo 12
Hangzhou 11
Lissone 10
Meldola 10
Strasbourg 10
Chicago 9
Munich 9
Phoenix 9
Pune 9
Rome 9
Tashkent 9
Washington 9
Edmonton 8
Hefei 8
Kiev 8
Lanzhou 8
Leawood 8
Lecco 8
Mcallen 8
Pisa 8
Redmond 7
Como 6
The Dalles 6
Zanjan 6
Basiano 5
Bologna 5
Düsseldorf 5
Kemerovo 5
St Petersburg 5
Villeneuve-le-roi 5
Daejeon 4
Dhaka 4
Kilburn 4
Monmouth Junction 4
Mumbai 4
Philadelphia 4
Prescot 4
Quito 4
São Paulo 4
Waanrode 4
Totale 10.983
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Nome #
Refining the Phenotype of Recurrent Rearrangements of Chromosome 16 413
Familiar unbalanced complex rearrangements involving 13 p-arm: Description of two cases 312
The effect of culture on human bone marrow mesenchymal stem cells: Focus on DNA methylation profiles 282
Instability of short arm of acrocentric chromosomes: Lesson from non-acrocentric satellited chromosomes. report of 24 unrelated cases 264
Potential role of BCL2 in the recurrence of uterine smooth muscle tumors of uncertain malignant potential 262
Resveratrol impairs glioma stem cells proliferation and motility by modulating the wnt signaling pathway 246
A complete duplication of X chromosome resulting in a tricentric isochromosome originated by centromere repositioning 242
Interstitial 11q deletion: genomic characterization and neuropsychiatric follow up from early infancy to adolescence and literature review 236
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 233
Chromosome territories, X;Y translocation and Premature Ovarian Failure: is there a relationship? 231
Maternal polymorphisms for methyltetrahydrofolate reductase (MTHFR) and methioninesynthetasi-reductase (MTRR) and risk of children with down syndrome: A geographic effect? 216
Unexpected frequency of genomic alterations in histologically normal colonic tissue from colon cancer patients 212
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy 207
Clinical and genetic evaluation of a family showing both autism and epilepsy 203
Maternal polymorphisms for methyltetrahydrofolate reductase and methionine synthetase reductase and risk of children with Down syndrome 199
Multi-transgenic pigs expressing three fluorescent proteins produced with high efficiency by sperm mediated gene transfer 198
Using copy number alterations to identify new therapeutic targets for bladder carcinoma 195
Cytogenetics of Premature Ovarian Failure: An Investigation on 269 Affected Women 193
Mutations in MAPT give rise to aneuploidy in animal models of tauopathy 193
A de novo supernumerary genomic discontinuous ring chromosome 21 in a child with mild intellectual disability 190
Mutations in MAPT gene cause chromosome instability and introduce copy number variations widely in the genome 187
UroVysion Multiprobe FISH on transitional cell carcinoma of the urinary bladder: comparative analysis on fresh isolated interphasic nuclei and paraffin-embedded tissue 183
Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B 182
Monitoring the genomic stability of in vitro cultured rat bone-marrow-derived mesenchymal stem cells 181
In vitro anticancer drug test: A new method emerges from the model of glioma stem cells 181
Biological heterogeneity of putative bladder cancer stem-like cell populations from human bladder transitional cell carcinoma samples 179
Tumor stem cell lines from glioblastoma multiforme: evaluation of antineoplastics drugs effects on cytologic, cytogenetic and genomic parameters 178
Synchrotron-based photon activation therapy effect on cisplatin pre-treated human glioma stem-like cells 176
Molecular cytogenetic comparison between stem-like cell lines isolated from glioblastoma multiforme 176
Evaluation of Danusertib effects on cell viability and cytomorphological parameters in cancer stem cell lines from glioblastoma multiforme 175
Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation 174
Delineating the Cytogenomic and Epigenomic Landscapes of Glioma Stem Cell Lines 174
14q32.3-qter trisomic segment: A case report and literature review 173
Decreased platelet glutamate uptake and genetic risk factors in patients with Parkinson's disease 172
Tau protein and chromosome stability 171
A new function of microtubule-associated protein tau: involvement in chromosome stability 170
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 167
Role of FISH on uncultured amniocytes for the diagnosis of aneuploidies in the presence of fetal anomalies 166
Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone gene 165
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy 165
Distinct pools of cancer stem-like cells coexist within human glioblastomas and display different tumorigenicity and independent genomic evolution 165
Looking for the perfect test (if it exists) for the assessment of chromosome alterations in bladder cancer: UroVysion test and microarray-based CGH analysis 165
Valproic Acid Inhibits Proliferation and Reduces Invasiveness in Glioma Stem Cells Through Wnt/β Catenin Signalling Activation 165
Chromosomal imbalances in human bladder urothelial carcinoma: Similarities and differences between biopsy samples and cancer stem-like cells 163
Methods for determining the sensitivity or resistance of cancer cells to at least one anticancer drug and/or therapeutically active molecule 163
A new human cell line, PDSS-26, from poorly differentiated synovial sarcoma, with unique chromosomal anomalies 162
Chromosomal aberrations in bladder cancer: fresh versus formalin fixed paraffin embedded tissue and targeted FISH versus wide microarray-based CGH analysis 158
X;Y translocations and POF 157
Resveratrol effects on cell viability, morphology and migration in cancer stem cell lines from glioblastoma multiforme 156
A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome 154
Investigating the role of X chromosome breakpoints in premature ovarian failure 154
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 153
Maternal heterodisomy/isodisomy and paternal supernumerary ring of chromosome 7 in a child with Silver-Russel syndrome 153
Gene Symbol: SCN1A 152
Clinical and genetic evaluation of a family showing both autism and epilepsy 152
Autosomal dominant nocturnal frontal lobe epilepsy - A critical overview 151
DNA copy number alterations and PPARG amplification in a patient with multifocal bladder urothelial carcinoma 149
Systematic chromosomal analysis of cultured mouse neural stem cell lines 148
Wnt signaling pathway VPA-induced modulation in cancer stem cell lines from glioblastoma multiforme 147
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal survey 143
DNA copy number alterations in bladder urothelial carcinoma: concordance between biopsy samples and cancer stem-like cells 143
Mutation analysis of the inhibin alpha gene in an Italian survey of women affected by ovarian failure 142
aCGH analysis of two families showing both autism and epilepsy 139
Ophthalmic features in a dysmorphic boy with chromosome 4q deletion and duplication 138
Clinical and genetic familial study of 61 children showing different epileptic phenotypes. 137
Evaluation of Danusertib Effects on Cell Viability and Citomorphological Parameters in Cancer Stem Cell Lines from Glioblastoma Multiforme 136
Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: cooperative study of 19 Italian laboratories 134
Cytologic, cytogenetic and genomic study of tumor stem cell lines from glioblastoma multiforme and evaluation of antineoplastic drug effects 134
Characterization of cancer stem-like cells by detecting chromosomal aberrations in bladder cancer 133
A rescuable folding defective Nav1.1 (SCN1A) Na+channel mutant causes GEFS+: common mechanism in Nav1.1 related epilepsies? 132
Two new susceptibility loci for ADNFLE 131
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? 130
Genetic study on 231 women affected by premature ovarian failure (POF) 127
Cytogenetic and genomic profiles of 5 cancer stem-like cell lines from glioblastoma multiforme 127
Evaluation of Danusertib Effects on Cell Viability and Citomorphological Parameters in Cancer Stem Cell Lines from Glioblastoma Multiforme 127
Two new putative loci for ADNFLE identified in an Italian family suggest a digenic inheritance for the disease 126
DNA Methylation Changes during In Vitro Propagation of Human Mesenchymal Stem Cells: Implications for Their Genomic Stability? 126
Synchrotron-based photon activation therapy effect on cisplatin pre-treated human glioma stem cells 126
Resveratrol effects on migration and wnt signaling pathway in cancer stem cell lines from glioblastoma multiforme 126
Familiar Febrile Seizures and Mutations in the Nav1.1 Sodium Channel 126
Familial subtelomeric rearrangement of chromosomes 19 and 20: a new contribution to partial distal 19q trisomy 123
Severe intrauterine growth restriction and trisomy 15 confined placental mosaicism: a case report and review of literature. 122
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 122
Fetal trisomy 5 mosaicism: case report and literature review 118
From cytogenomic to epigenomic profiles: monitoring the biologic behavior of in vitro cultured human bone marrow mesenchymal stem cells. 114
Role of the SCN1A gene in the pathogenesis of familial febrile seizures and GEFS+ 114
Mutational analysis of nicotinic acetylcholine receptor β2 subunit gene (CHRNB2) in a representative cohort of Italian probands affected by autosomal dominant nocturnal frontal lobe epilepsy 110
Blood Cell Mitochondrial DNA Content and Premature Ovarian Aging 109
Analisi dei profili di metilazione di linee staminali tumorali da glioblastoma multiforme con acido valproico e paclitaxel 101
Comparative analysis of the methylation profile of tumor stem cell lines from glioblastoma multiforme and fetal neural stem cells 99
Partial duplication of the PARK2 gene in a child with developmental delay and her normal mother: a second report 92
Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011 86
A balanced chromosomal translocation disrupting ARHGEF9 is associated with epilepsy, anxiety, aggression, and mental retardation 80
De novo balanced chromosome rearrangements in prenatal diagnosis 78
Totale 15.440
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Categoria #
all - tutte 52.948
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 52.948
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020345 0 0 0 0 0 0 0 0 0 117 175 53
2020/20211.593 121 106 189 176 129 129 149 102 143 160 87 102
2021/20221.220 59 117 213 141 40 121 41 79 47 74 99 189
2022/20232.545 239 867 239 290 142 355 11 144 183 8 38 29
2023/20241.462 49 39 50 78 194 398 342 41 77 16 8 170
2024/20252.065 170 356 228 143 303 150 105 110 238 262 0 0
Totale 15.440