BORSANI, GIUSEPPE
 Distribuzione geografica
Continente #
NA - Nord America 6.438
EU - Europa 3.668
AS - Asia 1.402
AF - Africa 11
OC - Oceania 10
SA - Sud America 8
Continente sconosciuto - Info sul continente non disponibili 5
Totale 11.542
Nazione #
US - Stati Uniti d'America 6.412
PL - Polonia 1.246
CN - Cina 901
UA - Ucraina 778
IT - Italia 432
DE - Germania 361
FR - Francia 239
HK - Hong Kong 220
GB - Regno Unito 196
FI - Finlandia 186
IE - Irlanda 124
SG - Singapore 77
IN - India 76
VN - Vietnam 57
TR - Turchia 32
BE - Belgio 30
SE - Svezia 27
CA - Canada 21
RU - Federazione Russa 14
IR - Iran 12
NL - Olanda 12
CZ - Repubblica Ceca 10
AU - Australia 9
MU - Mauritius 8
EU - Europa 5
KR - Corea 5
RO - Romania 4
BR - Brasile 3
CU - Cuba 3
KZ - Kazakistan 3
CL - Cile 2
DZ - Algeria 2
ES - Italia 2
HU - Ungheria 2
JP - Giappone 2
KW - Kuwait 2
UZ - Uzbekistan 2
AE - Emirati Arabi Uniti 1
AM - Armenia 1
AR - Argentina 1
AT - Austria 1
BD - Bangladesh 1
BH - Bahrain 1
CY - Cipro 1
DO - Repubblica Dominicana 1
EC - Ecuador 1
GE - Georgia 1
ID - Indonesia 1
IL - Israele 1
IM - Isola di Man 1
JO - Giordania 1
LK - Sri Lanka 1
MX - Messico 1
NZ - Nuova Zelanda 1
PH - Filippine 1
PT - Portogallo 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
TW - Taiwan 1
VE - Venezuela 1
ZA - Sudafrica 1
Totale 11.542
Città #
Warsaw 1.245
Fairfield 1.046
Woodbridge 705
Jacksonville 550
Houston 526
Ashburn 438
Ann Arbor 431
Seattle 390
Cambridge 387
Wilmington 366
Chandler 320
Princeton 245
Hong Kong 220
Brescia 197
Nanjing 174
Dublin 124
New York 123
Beijing 122
Helsinki 91
Dearborn 86
Nanchang 80
Des Moines 72
Shenyang 60
Dong Ket 56
Hebei 56
San Diego 53
Changsha 49
Tianjin 49
Jinan 44
Milan 40
Shanghai 37
Hangzhou 33
Lancaster 32
Singapore 31
Brussels 30
Kocaeli 28
Jiaxing 27
London 26
Ningbo 26
Zhengzhou 26
Augusta 23
San Mateo 23
Toronto 19
Kunming 18
Haikou 17
Boardman 16
San Francisco 16
Monmouth Junction 15
Grafing 14
Guangzhou 14
Lanzhou 14
Pune 14
Leawood 13
Taizhou 13
Verona 13
Los Angeles 12
Ardabil 9
Norwalk 9
Olomouc 9
Phoenix 9
Chiswick 8
Fuzhou 7
Mantova 7
Orange 7
Washington 7
Gottolengo 6
Hefei 6
Kilburn 6
Piemonte 6
Bologna 5
Pavia 5
Rome 5
Amsterdam 4
New Bedfont 4
Prescot 4
Sydney 4
Auburn Hills 3
Canberra 3
Changchun 3
Chiari 3
Como 3
Cremona 3
Gunzenhausen 3
Hounslow 3
Indiana 3
Islington 3
La Habana 3
Munich 3
Nürnberg 3
Taiyuan 3
Torre Del Greco 3
Bergamo 2
Berlin 2
Chicago 2
Falkenstein 2
Gavardo 2
Hanover 2
Ivry-sur-seine 2
Kostanay 2
Kuwait City 2
Totale 9.085
Nome #
Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis 313
Knock-down of pantothenate kinase 2 severely affects the development of the nervous and vascular system in zebrafish, providing new insights into PKAN disease 294
Mesenchymal stromal cells (MSCs) induce ex vivo proliferation and erythroid commitment of cord blood haematopoietic stem cells (CB-CD34+ cells) 258
Identification of p53-target genes in Danio rerio 241
Characterization of the AP-1 μ1A and μ1B adaptins in zebrafish (Danio rerio) 218
Gene expression profile in fibroblasts of Huntington's disease patients and controls 210
In silico identification of new putative pathogenic variants in the NEU1 sialidase gene affecting enzyme function and subcellular localization 200
Characterization and expression of slc2a10, the zebrafish ortholog of the human gene involved in arterial tortuosity syndrome. 194
Analysis of three μ1-AP1 subunits during zebrafish development 192
Zebrafish disease models in hematology: Highlights on biological and translational impact 170
Properties of recombinant human cytosolic sialidase HsNEU2. The enzyme hydrolyzes monomerically dispersed GM1 ganglioside molecules 151
Gene expression profile in fibroblasts of Huntington's disease patients and controls. 144
Overexpression of Human Mutant PANK2 Proteins Affects Development and Motor Behavior of Zebrafish Embryos 140
Senataxin modulates neurite growth through fibroblast growth factor 8 signalling. 127
X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and a novel gene containing WD-40 repeats 123
Use of CRISPR/Cas9 technique to understand the role of AP-1 complex in zebrafish 123
Real-world clinical applicability of pathogenicity predictors assessed on SERPINA1 mutations in alpha-1-antitrypsin deficiency 121
Hypocretins or hyporexins? 120
Cytogenetic and molecular characterization of a de-novo t(2p;7p) translocation involving TNS3 and EXOC6B genes in a boy with a complex syndromic phenotype 118
Characterization and expression analysis of mcoln1.1 and mcoln1.2, the putative zebrafish co-orthologs of the gene responsible for human mucolipidosis type IV. 118
Amplicon-based semiconductor sequencing of human exomes: performance evaluation and optimization strategies 117
Gene expression profile in fibroblasts of Huntington's disease patients and controls 116
slc7a6os Gene Plays a Critical Role in Defined Areas of the Developing CNS in Zebrafish 116
The gene encoding a cationic amino acid transporter (SLC7A4) maps to the region deleted in the velocardiofacial syndrome 114
Molecular cloning and knockdown of galactocerebrosidase in zebrafish: New insights into the pathogenesis of Krabbe's disease. 114
Sialidase NEU3 is a peripheral membrane protein localized on the cell surface and in endosomal structures 113
Genomic and biochemical characterization of sialic acid acetylesterase (siae) in zebrafish 111
Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomes 110
Gallus gallus NEU3 sialidase as model to study protein evolution mechanism based on rapid evolving loops 109
SLC7A8, a gene mapping within the lysinuric protein intolerance critical region, encodes a new member of the glycoprotein associated amino acid transporter family 108
A new submicroscopic deletion that refines the 9p region for sex reversal 108
Human sialic acid acetyl esterase: Towards a better understanding of a puzzling enzyme 108
Molecular cloning and biochemical characterization of sialidases from zebrafish (Danio rerio) 106
A practical guide to orient yourself in the labyrinth of genome databases 104
Genetic and physical mapping of a voltage-dependent chloride channel gene to human 4q32 and to mouse 8 104
An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3 104
Structure of the mouse growth/differentiation factor 9 gene 104
Down-regulation of coasy, the gene associated with NBIA-VI, reduces Bmp signaling, perturbs dorso-ventral patterning and alters neuronal development in zebrafish 104
Overexpression of wild type and mutant mucolipin proteins in mammalian cells: effects on the late endocytic compartment organization 103
Sialidase NEU3 is a peripheral membrane protein localized on the cell surface and in endosomal structures 103
A Fish-Specific Transposable Element Shapes the Repertoire of p53 Target Genes in Zebrafish 103
Functional study of a novel homozygous mutation in the GAD1 gene, detected in a patient with schizophrenia. 103
Characterization and expression pattern analysis of the facilitative glucose transporter 10 gene (slc2a10) in Danio rerio 102
A gene from the Xp22.3 region shares homology with voltage-gated chloride channels 102
Characterization of a murine gene expressed from the inactive X chromosome 101
Functional characterisation of human cells harbouring a novel t(2p;7p) translocation involving TNS3 and EXOC6B genes. 100
The embryonic expression pattern of 40 murine cDNAs homologous to Drosophila mutant genes (Dres): a comparative and topographic approach to predict gene function 99
Identification and characterisation of human xCT that co-expresses, with 4F2 heavy chain, the amino acid transport activity system xc- 99
Different chromosomal localization of the Clcn4 gene in Mus spretus and C57BL/6J mice 98
New insights on the sialidase protein family revealed by a phylogenetic analysis in metazoa 98
Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching 97
Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype 97
Molecular cloning of an adducin-like protein: evidence of a polymorphism in the normotensive and hypertensive rats of the Milan strain 97
Characterization of a human and murine gene (CLCN3) sharing similarities to voltage-gated chloride channels and to a yeast integral membrane protein 97
Molecular cloning and characterization of NEU4, the fourth member of the human sialidase gene family 95
Structure of the SLC7A7 gene and mutational analysis of patients affected by lysinuric protein intolerance 94
A novel X gene with a widely transcribed Y-linked homologue escapes X-inactivation in mouse and human 94
Expression of a novel human sialidase encoded by the NEU2 gene 94
Sequencing analysis of forty-eight human image cDNA clones similar to Drosophila mutant protein. 93
Molecular cloning and biochemical characterization of sialidases from zebrafish (Danio rerio) 93
Cloning of the gene encoding a novel integral membrane protein, mucolipidin-and identification of the two major founder mutations causing mucolipidosis type IV 92
MOLECULAR CLONING AND BIOCHEMICAL CHARACTERIZATION OF SIALIDASES FROM ZEBRAFISH (Danio rerio) 92
Cloning and characterization of NEU2, a human gene homologous to rodent soluble sialidases. 91
The amino acid transporter asc-1 is not involved in cystinuria 91
Importance of different types of prior knowledge in selecting genome-wide findings for follow-up 90
SNP prioritization using a bayesian probability of association 90
Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targeting 89
A homeobox gene, vax2, controls the patterning of the eye dorsoventral axis. 88
Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuria 88
Caratterizzazione ed espressione di slc2a10, l’ortologo in Danio rerio del gene umano coinvolto nella sindrome delle arterie tortuose. 88
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 88
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation 87
TargetFinder: searching annotated sequence databases for target genes of transcription factors 87
Rox, a novel bHLHZip protein expressed in quiescent cells that heterodimerizes with Max, binds a non-canonical E box and acts as a transcriptional repressor 85
Slc7a7 disruption causes fetal growth retardation by downregulating Igf1 in the mouse model of lysinuric protein intolerance. 85
DRES search engine: of flies, men and ESTs 84
Biochemical characterization of Neu2, a novel human cytosolic sialidase 84
Study of the genetic architecture behind mood disorders by whole exome sequencing on a large Italian pedigree 84
Atypical chemokine receptor 3 generates guidance cues for CXCL12-mediated endothelial cell migration 84
Gene expression profiling of mucolipidosis type IV fibroblasts reveals deregulation of genes with relevant functions in lysosome physiology 83
Identification and expression of NEU3, a novel human sialidase associated to the plasma membrane 83
Down-regulation of µ1-AP1 subunit impairs zebrafish development 83
The expression pattern of a mouse doublesex-related gene is consistent with a role in gonadal differentiation 82
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 79
Biochemical studies on recombinant Neu2, a novel human cytosolic sialidase. 77
Knock-down and knock-out: use of two techniques to understand the role of AP-1 complex in zebrafish 77
γ2 and γ1AP-1 complexes: Different essential functions and regulatory mechanisms in clathrin-dependent protein sorting 76
Metodo di elaborazione e visualizzazione di simboli grafici in un codice colore e relativa rappresentazione su supporti 75
The molecular bases of cystinuria and lysinuric protein intolerance 75
Krabbe Disease and zebrafish: key-role of galactocerebrosidase in CNS development 73
The zebrafish knockdown of galactocerebrosidase contributes to understand the human Krabbe Disease 73
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 73
µ1-AP1 gene knock-down induces several defects during zebrafish organogenesis 70
Cellular expression and alternative splicing of SLC25A23, a member of the mitochondrial Ca2+ dependent solute carrier protein family 69
Zebrafish as a model for the study ofvthe possible role of sialidase neu4 in the development of vertebrates 69
cDNA sequence of human beta-NGF 69
SLC7A7, encoding a putative permease-related protein, is mutated in patients with lysinuric protein intolerance 67
Beta-nerve growth factor (beta-NGF) mRNA expression in the parkinsonian adrenal gland 67
Development of BCR-ABL1 Transgenic Zebrafish Model Reproducing Chronic Myeloid Leukemia (CML) Like-Disease and Providing a New Insight into CML Mechanisms 66
Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT. 65
Totale 10.925
Categoria #
all - tutte 49.179
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 49.179


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019292 0 0 0 0 0 0 0 0 0 0 0 292
2019/20203.525 432 147 156 392 208 383 353 376 259 469 171 179
2020/20212.115 70 211 58 231 78 227 87 229 297 261 261 105
2021/20221.223 125 261 30 37 10 46 105 50 48 173 90 248
2022/2023966 144 15 22 63 90 246 3 102 155 7 53 66
2023/2024883 52 33 90 62 43 168 40 47 230 22 15 81
Totale 11.932