IRIS Institutional Research Information System - OPENBS Open Archive UniBS

BORSANI, GIUSEPPE
 Distribuzione geografica
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Continente #
NA - Nord America 6.446
EU - Europa 3.691
AS - Asia 1.472
AF - Africa 11
OC - Oceania 10
SA - Sud America 8
Continente sconosciuto - Info sul continente non disponibili 5
Totale 11.643
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Nazione #
US - Stati Uniti d'America 6.420
PL - Polonia 1.246
CN - Cina 904
UA - Ucraina 778
IT - Italia 441
DE - Germania 366
FR - Francia 239
HK - Hong Kong 220
GB - Regno Unito 196
FI - Finlandia 187
SG - Singapore 144
IE - Irlanda 124
IN - India 76
VN - Vietnam 57
TR - Turchia 32
BE - Belgio 30
SE - Svezia 27
CA - Canada 21
CZ - Repubblica Ceca 18
RU - Federazione Russa 14
IR - Iran 12
NL - Olanda 12
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 11.643
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Città #
Warsaw 1.245
Fairfield 1.046
Woodbridge 705
Jacksonville 550
Houston 526
Ashburn 439
Ann Arbor 431
Seattle 390
Cambridge 387
Wilmington 366
Chandler 320
Princeton 245
Hong Kong 220
Brescia 200
Nanjing 174
Dublin 124
New York 123
Beijing 122
Helsinki 92
Dearborn 86
Nanchang 80
Des Moines 72
Singapore 72
Shenyang 60
Dong Ket 56
Hebei 56
San Diego 53
Changsha 49
Tianjin 49
Jinan 44
Milan 43
Shanghai 40
Hangzhou 33
Lancaster 32
Brussels 30
Kocaeli 28
Jiaxing 27
London 26
Ningbo 26
Zhengzhou 26
Augusta 23
San Mateo 23
Toronto 19
Kunming 18
San Francisco 18
Haikou 17
Boardman 16
Los Angeles 15
Monmouth Junction 15
Grafing 14
Guangzhou 14
Lanzhou 14
Pune 14
Leawood 13
Taizhou 13
Verona 13
Ardabil 9
Brno 9
Norwalk 9
Olomouc 9
Phoenix 9
Chiswick 8
Munich 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
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
Totale 9.154
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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 295
Mesenchymal stromal cells (MSCs) induce ex vivo proliferation and erythroid commitment of cord blood haematopoietic stem cells (CB-CD34+ cells) 260
Identification of p53-target genes in Danio rerio 241
Characterization of the AP-1 μ1A and μ1B adaptins in zebrafish (Danio rerio) 219
Gene expression profile in fibroblasts of Huntington's disease patients and controls 211
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. 195
Analysis of three μ1-AP1 subunits during zebrafish development 194
Zebrafish disease models in hematology: Highlights on biological and translational impact 171
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 141
Senataxin modulates neurite growth through fibroblast growth factor 8 signalling. 127
Use of CRISPR/Cas9 technique to understand the role of AP-1 complex in zebrafish 124
Real-world clinical applicability of pathogenicity predictors assessed on SERPINA1 mutations in alpha-1-antitrypsin deficiency 124
X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and a novel gene containing WD-40 repeats 123
Hypocretins or hyporexins? 121
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 118
Gene expression profile in fibroblasts of Huntington's disease patients and controls 116
Molecular cloning and knockdown of galactocerebrosidase in zebrafish: New insights into the pathogenesis of Krabbe's disease. 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 115
Sialidase NEU3 is a peripheral membrane protein localized on the cell surface and in endosomal structures 114
Genomic and biochemical characterization of sialic acid acetylesterase (siae) in zebrafish 112
Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomes 111
SLC7A8, a gene mapping within the lysinuric protein intolerance critical region, encodes a new member of the glycoprotein associated amino acid transporter family 110
Gallus gallus NEU3 sialidase as model to study protein evolution mechanism based on rapid evolving loops 110
Human sialic acid acetyl esterase: Towards a better understanding of a puzzling enzyme 109
A new submicroscopic deletion that refines the 9p region for sex reversal 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 105
An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3 105
Structure of the mouse growth/differentiation factor 9 gene 105
Genetic and physical mapping of a voltage-dependent chloride channel gene to human 4q32 and to mouse 8 104
Overexpression of wild type and mutant mucolipin proteins in mammalian cells: effects on the late endocytic compartment organization 104
A Fish-Specific Transposable Element Shapes the Repertoire of p53 Target Genes in Zebrafish 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
Sialidase NEU3 is a peripheral membrane protein localized on the cell surface and in endosomal structures 103
A gene from the Xp22.3 region shares homology with voltage-gated chloride channels 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
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. 101
Identification and characterisation of human xCT that co-expresses, with 4F2 heavy chain, the amino acid transport activity system xc- 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
Different chromosomal localization of the Clcn4 gene in Mus spretus and C57BL/6J mice 99
Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching 98
Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype 98
Molecular cloning of an adducin-like protein: evidence of a polymorphism in the normotensive and hypertensive rats of the Milan strain 98
Characterization of a human and murine gene (CLCN3) sharing similarities to voltage-gated chloride channels and to a yeast integral membrane protein 98
New insights on the sialidase protein family revealed by a phylogenetic analysis in metazoa 98
Molecular cloning and characterization of NEU4, the fourth member of the human sialidase gene family 96
A novel X gene with a widely transcribed Y-linked homologue escapes X-inactivation in mouse and human 95
Structure of the SLC7A7 gene and mutational analysis of patients affected by lysinuric protein intolerance 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
Cloning of the gene encoding a novel integral membrane protein, mucolipidin-and identification of the two major founder mutations causing mucolipidosis type IV 93
Molecular cloning and biochemical characterization of sialidases from zebrafish (Danio rerio) 93
Cloning and characterization of NEU2, a human gene homologous to rodent soluble sialidases. 92
MOLECULAR CLONING AND BIOCHEMICAL CHARACTERIZATION OF SIALIDASES FROM ZEBRAFISH (Danio rerio) 92
The amino acid transporter asc-1 is not involved in cystinuria 91
SNP prioritization using a bayesian probability of association 91
Importance of different types of prior knowledge in selecting genome-wide findings for follow-up 90
Atypical chemokine receptor 3 generates guidance cues for CXCL12-mediated endothelial cell migration 90
A homeobox gene, vax2, controls the patterning of the eye dorsoventral axis. 89
Caratterizzazione ed espressione di slc2a10, l’ortologo in Danio rerio del gene umano coinvolto nella sindrome delle arterie tortuose. 89
Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targeting 89
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation 88
TargetFinder: searching annotated sequence databases for target genes of transcription factors 88
Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuria 88
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 88
DRES search engine: of flies, men and ESTs 86
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 86
Slc7a7 disruption causes fetal growth retardation by downregulating Igf1 in the mouse model of lysinuric protein intolerance. 86
Biochemical characterization of Neu2, a novel human cytosolic sialidase 86
Identification and expression of NEU3, a novel human sialidase associated to the plasma membrane 85
Gene expression profiling of mucolipidosis type IV fibroblasts reveals deregulation of genes with relevant functions in lysosome physiology 84
Down-regulation of µ1-AP1 subunit impairs zebrafish development 84
Study of the genetic architecture behind mood disorders by whole exome sequencing on a large Italian pedigree 84
The expression pattern of a mouse doublesex-related gene is consistent with a role in gonadal differentiation 83
Metodo di elaborazione e visualizzazione di simboli grafici in un codice colore e relativa rappresentazione su supporti 79
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 79
Biochemical studies on recombinant Neu2, a novel human cytosolic sialidase. 78
γ2 and γ1AP-1 complexes: Different essential functions and regulatory mechanisms in clathrin-dependent protein sorting 77
Knock-down and knock-out: use of two techniques to understand the role of AP-1 complex in zebrafish 77
The molecular bases of cystinuria and lysinuric protein intolerance 75
The zebrafish knockdown of galactocerebrosidase contributes to understand the human Krabbe Disease 74
Krabbe Disease and zebrafish: key-role of galactocerebrosidase in CNS development 73
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 73
Zebrafish as a model for the study ofvthe possible role of sialidase neu4 in the development of vertebrates 71
µ1-AP1 gene knock-down induces several defects during zebrafish organogenesis 71
Cellular expression and alternative splicing of SLC25A23, a member of the mitochondrial Ca2+ dependent solute carrier protein family 70
cDNA sequence of human beta-NGF 69
Beta-nerve growth factor (beta-NGF) mRNA expression in the parkinsonian adrenal gland 68
SLC7A7, encoding a putative permease-related protein, is mutated in patients with lysinuric protein intolerance 67
Development of BCR-ABL1 Transgenic Zebrafish Model Reproducing Chronic Myeloid Leukemia (CML) Like-Disease and Providing a New Insight into CML Mechanisms 67
NF-kappaB pathway: a target for preventing beta-amyloid (Abeta)-induced neuronal damage and Abeta42 production 65
Totale 11.003
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Categoria #
all - tutte 52.061
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 52.061
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203.093 0 147 156 392 208 383 353 376 259 469 171 179
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
2023/2024954 52 33 90 62 43 168 40 47 230 22 15 152
2024/202531 28 3 0 0 0 0 0 0 0 0 0 0
Totale 12.034