Catalogo dei prodotti della ricerca

FORTINA, PAOLO MARIA
 Distribuzione geografica
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Continente #
NA - Nord America 6.708
EU - Europa 1.055
AS - Asia 919
SA - Sud America 32
AF - Africa 14
OC - Oceania 2
Totale 8.730
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Nazione #
US - Stati Uniti d'America 6.660
IT - Italia 376
IN - India 368
SG - Singapore 328
FI - Finlandia 181
CN - Cina 178
UA - Ucraina 166
SE - Svezia 134
DE - Germania 52
CA - Canada 44
IE - Irlanda 38
GB - Regno Unito 37
AR - Argentina 25
NL - Olanda 22
RO - Romania 15
IR - Iran 12
BE - Belgio 10
ZA - Sudafrica 9
KR - Corea 8
BG - Bulgaria 6
CH - Svizzera 6
CL - Cile 6
FR - Francia 6
HK - Hong Kong 6
PK - Pakistan 6
MY - Malesia 5
MX - Messico 4
ES - Italia 2
GR - Grecia 2
JP - Giappone 2
RU - Federazione Russa 2
TG - Togo 2
TR - Turchia 2
VN - Vietnam 2
AU - Australia 1
EC - Ecuador 1
ID - Indonesia 1
KG - Kirghizistan 1
MU - Mauritius 1
NG - Nigeria 1
NZ - Nuova Zelanda 1
SC - Seychelles 1
Totale 8.730
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Città #
Fairfield 1.366
Woodbridge 600
Ashburn 561
Houston 511
Seattle 494
Cambridge 426
Wilmington 371
Chandler 334
Ann Arbor 332
Princeton 208
Singapore 202
Plano 183
Rome 178
Beijing 149
San Paolo di Civitate 131
Lawrence 100
San Diego 96
Boston 84
Des Moines 71
Jacksonville 61
Andover 59
Millbury 47
Dublin 38
Norwalk 38
Toronto 33
Stockholm 26
Federal 25
Philadelphia 24
Falls Church 21
Phoenix 20
Bühl 18
Mannheim 17
Boardman 14
Dearborn 12
San Mateo 12
Santa Clara 10
Buffalo 9
New York 9
London 8
Long Beach 8
Brussels 7
Muizenberg 7
Ottawa 7
Indiana 6
Milan 6
Seongnam 6
Sofia 6
Bern 5
Falkenstein 5
Kota Bharu 5
Kunming 5
Lappeenranta 5
Provo 5
Chicago 4
Dallas 4
Helsinki 4
Irving 4
Prineville 4
Quetta 4
Southend 4
Tehran 4
Florence 3
Hong Kong 3
Hyderabad 3
Mexico City 3
Palermo 3
Portland 3
Prescot 3
Pune 3
Trumbull 3
Waanrode 3
Auburn Hills 2
Bologna 2
Chiswick 2
Córdoba 2
Duncan 2
Hanoi 2
Hefei 2
Kilburn 2
Las Vegas 2
Lomé 2
Lucca 2
Mainz 2
Montréal 2
Nanchang 2
Opera 2
Phoenixville 2
Redwood City 2
Riva 2
Saint-Fons 2
San Jose 2
Seoul 2
Shanghai 2
Sialkot 2
Silverton 2
Zhengzhou 2
Albinea 1
Anaheim 1
Antwerp 1
Athens 1
Totale 7.097
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Nome #
CARD15 genotyping in inflammatory bowel disease patients by multiplex pyrosequencing 111
Clinical exome performance for reporting secondary genetic findings. 109
Multigene Next-Generation Sequencing Panel Identifies Pathogenic Variants in Patients with Unknown Subtype of Epidermolysis Bullosa: Subclassification with Prognostic Implications 106
Analytical Ancestry: “Firsts” in Fluorescent Labeling of Nucleosides, Nucleotides, and Nucleic Acids 85
Transcriptomic profiling of 39 commonly-used neuroblastoma cell lines 85
High-resolution SNP arrays in mental retardation diagnostics: how much do we gain? 83
DOP-PCR amplification of whole genomic DNA and microchip-based capillary electrophoresis. 77
Linkage of ulcerative colitis to the pericentromeric region of chromosome 16 in Italian inflammatory bowel disease families is independent of the presence of common CARD15 mutations 76
Analysis of 13 cell types reveals evidence for the expression of numerous novel primate- And tissue-specific microRNAs 76
Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy 76
Miniaturized detection technology in molecular diagnostics 73
Stat5 promotes metastatic behavior of human prostate cancer cells in vitro and in vivo 72
Whole exome sequencing identifies a germline MET mutation in two siblings with hereditary wild-type RET medullary thyroid cancer 72
Dystrophic Epidermolysis Bullosa: COL7A1 Mutation Landscape in a Multi-Ethnic Cohort of 152 Extended Families with High Degree of Customary Consanguineous Marriages 72
Ethanol potentiates HIV-1 gp120-induced apoptosis in human neurons via both the death receptor and NMDA receptor pathways 71
The future of laboratory medicine - A 2014 perspective. 71
Whole-exome sequencing of DNA from peripheral blood mononuclear cells (PBMC) and EBV-transformed lymphocytes from the same donor 69
A de novo supernumerary genomic discontinuous ring chromosome 21 in a child with mild intellectual disability 69
Duchenne/Becker muscular dystrophy carrier detection using quantitative PCR and fluorescence-based strategies. 68
Pyrosequencing for detection of mutations in the connexin 26 (GJB2) and mitochondrial 12S RNA (MTRNR1) genes associated with hereditary hearing loss 67
Analytical ancestry: evolution of the array in analysis. 67
Detection and characterization of circulating tumor associated cells in metastatic breast cancer 66
MicroRNAs as new players in the genomic galaxy and disease puzzles 65
Use of linkage analysis, genome-wide association studies, and next-generation sequencing in the identification of disease-causing mutations. 65
Polymorphic changes in the 5' flanking region of factor VII have a combined effect on promoter strength. 65
Opportunities for near-infrared thermal ablation of colorectal metastases by guanylyl cyclase C-targeted gold nanoshells 65
Variants in genes involved in functional pathways associated with hypertension in African Americans. 64
Revealing genes associated with vitellogenesis in the liver of the zebrafish (Danio rerio) by transcriptome profiling 64
Applications of emerging technologies to the study of human genetics. 64
Analysis of short tandem repeat markers by capillary array electrophoresis. 64
Region specific detection of neuroblastoma loss of heterozygosity at multiple loci simultaneously using a SNP-based tag-array platform. 63
Next generation sequencing in cancer: opportunities and challenges for precision cancer medicine 63
Kinase-independent role of cyclin D1 in chromosomal instability and mammary tumorigenesis 62
Substrate uptake and metabolism are preserved in hypertrophic caveolin-3 knockout hearts. 61
Beyond Microtechnology - Nanotechnology in Molecular Diagnosis 60
Nanobiotechnology: the promise and reality of new approaches to molecular recognition 60
Detection of activating estrogen receptor gene (ESR1) mutations in single circulating tumor cells 60
Micropillar array chip for integrated white blood cell isolation and PCR 59
Hearts lacking caveolin-1 develop hypertrophy with normal cardiac substrate metabolism 59
Development of an Automated and Sensitive Microfluidic Device for Capturing and Characterizing Circulating Tumor Cells (CTCs) from Clinical Blood Samples 59
International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16 59
Effects of genetic variation in protease activated receptor 4 after an acute coronary syndrome: Analysis from the TRACER trial 59
Gene-Targeted Next Generation Sequencing Identifies PNPLA1 Mutations in Patients with a Phenotypic Spectrum of Autosomal Recessive Congenital Ichthyosis: The Impact of Consanguinity 59
Structure-based screen identifies a potent small molecule inhibitor of Stat5a/b with therapeutic potential for prostate cancer and chronic myeloid leukemia 59
Caveolin-1 overexpression enhances androgen-dependent growth and proliferation in the mouse prostate 58
Fabrication of plastic microchips by hot embossing. 58
Absence of the fragile X CGG trinucleotide repeat expansion in girls diagnosed with a pervasive developmental disorder. 58
The frame-shift mutation of the NOD2/CARD15 gene is significantly increased in ulcerative colitis: an *IG-IBD study. 57
Bridging genomics research between developed and developing countries: The Genomic Medicine Alliance 57
Protein microarrays: a literature survey. 56
Transcription factor Stat3 stimulates metastatic behavior of human prostate cancer cells in vivo, whereas Stat5b has a preferential role in the promotion of prostate cancer cell viability and tumor growth. 56
The retinoblastoma tumor suppressor modulates DNA repair and radioresponsiveness. 56
In vivo E2F reporting reveals efficacious schedules of MEK1/2–CDK4/6 targeting and mTOR–s6 resistance mechanisms 56
Homozygosity for the V37I Connexin 26 mutation in three unrelated children with sensorineural hearing loss. 55
The use of microelectronic-based techniques in molecular diagnostic assays. 55
Institutional Profile: Golden Helix Institute of Biomedical Research: interdisciplinary research and educational activities in pharmacogenomics and personalized medicine. 55
Genetic Analysis in Translational Medicine: The 2010 GOLDEN HELIX Symposium 54
In the presence of other inherited or acquired high-risk situations, the FV Cambridge mutation may be an additional thrombophilic risk factor, through its effect on APC sensitivity. 54
Angiotensin converting enzyme gene deletion allele is independently and strongly associated with coronary atherosclerosis and myocardial infarction. 54
RB and p53 cooperate to prevent liver tumorigenesis in response to tissue damage. 53
Analysis of 31 CFTR mutations by polymerase chain reaction/oligonucleotide ligation assay in a pilot screening of 4476 newborns for cystic fibrosis. 53
Establishment of an orthotopic patient-derived xenograft mouse model using uveal melanoma hepatic metastasis 53
Exosomal αvβ6 integrin is required for monocyte M2 polarization in prostate cancer 53
Concordance study of 3 direct-to-consumer genetic-testing services. 52
Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology 52
Circulating tumor DNA to monitor metastatic breast cancer. 52
RB loss contributes to aggressive tumor phenotypes in MYC-driven triple negative breast cancer 52
A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing. 52
Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci. 52
Microchips: An all-language literature survey including books and patents 51
Allelic association of microsatellites of 6p in Italian hemochromatosis patients. 51
Loss of stromal caveolin-1 leads to oxidative stress, mimics hypoxia and drives inflammation in the tumor microenvironment, conferring the "reverse Warburg effect": a transcriptional informatics analysis with validation. 51
A tandem duplication of chromosome 21 in a newborn showing non-down like features. 50
Molecular diagnostics: hurdles for clinical implementation 50
Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigels. 50
Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy. 50
Mutation detection using ligase chain reaction in passivated silicon-glass microchips and microchip capillary electrophoresis 49
Mechanisms of Endothelial Cell Attachment, Proliferation, and Differentiation on 4 Types of Platinum-Based Endovascular Coils 49
Applications of nanoparticles to diagnostics and therapeutics in colorectal cancer 49
Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans. 49
Submicroscopic deletion in cousins with Prader-Willi syndrome causes a grandmatrilineal inheritance pattern: effects of imprinting. 49
Increased amplification efficiency of microchip-based PCR by dynamic surface passivation. 49
Test pricing and reimbursement in genomic medicine: towards a general strategy 49
System for preparing microhybridization arrays on glass slides. 48
Surface effects on PCR reactions in multichip microfluidic platforms 48
The Otto Aufranc Award: Identification of a 4 Mb Region on Chromosome 17q21 Linked to Developmental Dysplasia of the Hip in One 18-member, Multigeneration Family 48
The reverse Warburg effect: aerobic glycolysis in cancer associated fibroblasts and the tumor stroma. 48
Integrated cell isolation and polymerase chain reaction analysis using silicon microfilter chambers. 47
Acute Myeloid Leukemia 47
Sighting acute myocardial infarction through platelet gene expression 47
Microchip module for blood sample preparation and nucleic acid amplification reactions. 47
Genotyping beta-globin gene mutations on copolymer-coated glass slides with the ligation detection reaction. 46
The Use of Microelectronic-Based Techniques in Molecular Diagnostic Assays 46
Reversine enhances generation of progenitor-like cells by dedifferentiation of annulus fibrosus cells. 46
Nucleic acid detection using non-radioactive labelling methods. 46
Performance of exome sequencing for pharmacogenomics 46
The presurgical management with erythrocytapheresis of a patient with a high-oxygen-affinity, unstable Hb variant (Hb Bryn Mawr). 46
Kinetics of heterogeneous hybridization on indium tin oxide surfaces with and without an applied potential 46
Infundibulopelvic stenosis, multicystic kidney, and calyectasis in a kindred: clinical observations and genetic analysis. 45
Vestibular and hearing loss in genetic and metabolic disorders. 45
Totale 5.930
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Categoria #
all - tutte 26.386
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 26.386
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.973 0 0 32 112 269 251 298 297 271 157 187 99
2020/2021683 85 130 27 57 33 33 20 89 77 75 48 9
2021/20221.857 8 153 233 31 271 28 57 229 130 159 219 339
2022/20231.249 388 310 23 128 104 127 17 32 79 5 29 7
2023/2024507 49 61 26 28 20 13 15 17 2 114 60 102
2024/2025207 88 34 85 0 0 0 0 0 0 0 0 0
Totale 8.954