CNR Institutional Research Information System

VEZZONI, PAOLO MARIA
 Distribuzione geografica
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Continente #
AS - Asia 1.741
NA - Nord America 1.195
EU - Europa 419
SA - Sud America 304
Continente sconosciuto - Info sul continente non disponibili 44
AF - Africa 37
Totale 3.740
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Nazione #
US - Stati Uniti d'America 1.129
SG - Singapore 680
CN - Cina 438
BR - Brasile 232
HK - Hong Kong 171
VN - Vietnam 160
IT - Italia 133
KR - Corea 101
FR - Francia 83
BD - Bangladesh 46
GB - Regno Unito 38
CA - Canada 36
DE - Germania 33
NL - Olanda 33
JP - Giappone 29
IN - India 25
FI - Finlandia 22
EC - Ecuador 21
CO - Colombia 19
AR - Argentina 17
IQ - Iraq 15
MX - Messico 14
IL - Israele 11
ID - Indonesia 10
RU - Federazione Russa 10
PL - Polonia 9
SE - Svezia 8
UA - Ucraina 8
ZA - Sudafrica 8
PH - Filippine 7
VE - Venezuela 7
CI - Costa d'Avorio 6
CR - Costa Rica 6
ES - Italia 6
PK - Pakistan 6
UZ - Uzbekistan 6
CZ - Repubblica Ceca 5
MA - Marocco 5
SA - Arabia Saudita 5
TR - Turchia 5
AE - Emirati Arabi Uniti 4
EG - Egitto 4
GT - Guatemala 4
IE - Irlanda 4
LT - Lituania 4
MY - Malesia 4
AL - Albania 3
AT - Austria 3
KE - Kenya 3
PY - Paraguay 3
SK - Slovacchia (Repubblica Slovacca) 3
TN - Tunisia 3
AZ - Azerbaigian 2
CY - Cipro 2
DZ - Algeria 2
EE - Estonia 2
GY - Guiana 2
KZ - Kazakistan 2
NI - Nicaragua 2
PS - Palestinian Territory 2
SN - Senegal 2
TT - Trinidad e Tobago 2
BB - Barbados 1
BE - Belgio 1
BG - Bulgaria 1
BM - Bermuda 1
BO - Bolivia 1
BY - Bielorussia 1
CH - Svizzera 1
GE - Georgia 1
HR - Croazia 1
HU - Ungheria 1
IR - Iran 1
KG - Kirghizistan 1
LB - Libano 1
LU - Lussemburgo 1
LV - Lettonia 1
MG - Madagascar 1
MK - Macedonia 1
ML - Mali 1
MM - Myanmar 1
MN - Mongolia 1
NP - Nepal 1
OM - Oman 1
PE - Perù 1
PT - Portogallo 1
RO - Romania 1
SC - Seychelles 1
SI - Slovenia 1
SR - Suriname 1
SY - Repubblica araba siriana 1
TG - Togo 1
TJ - Tagikistan 1
Totale 3.696
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Città #
Singapore 396
Santa Clara 270
Hefei 208
Hong Kong 167
San Jose 158
Ashburn 118
Seoul 100
Beijing 94
Los Angeles 71
Lauterbourg 70
Ho Chi Minh City 63
Hanoi 36
Milan 24
New York 24
Cagliari 19
São Paulo 18
Helsinki 15
Tokyo 15
Dallas 14
Buffalo 12
Brasília 11
Düsseldorf 11
Montreal 11
Frankfurt am Main 10
Guayaquil 10
Minamishinagawa 10
Orem 9
Rome 9
Belo Horizonte 8
Chicago 8
Mexico City 8
Phoenix 8
Warsaw 8
Bengaluru 7
Council Bluffs 7
Da Nang 7
Houston 7
Poplar 7
Rio de Janeiro 7
Stockholm 7
Abidjan 6
London 6
Miami 6
Munich 6
Quito 6
Shanghai 6
Tashkent 6
Florence 5
Hortolândia 5
Johannesburg 5
Las Vegas 5
Turku 5
Amsterdam 4
Assemini 4
Brooklyn 4
Cairo 4
Caracas 4
Charlotte 4
Curitiba 4
Denver 4
Dhaka 4
Dublin 4
Haiphong 4
Hải Dương 4
Naples 4
Padova 4
Philadelphia 4
Porcari 4
Porto Alegre 4
Portsmouth 4
Queens 4
Quận Mười 4
San José 4
Thái Nguyên 4
Toronto 4
Austin 3
Baghdad 3
Basra 3
Biên Hòa 3
Boardman 3
Bogotá 3
Bologna 3
Boston 3
Campinas 3
Cape Town 3
Chennai 3
Cleveland 3
Detroit 3
Goiânia 3
Guangzhou 3
Hyderabad 3
Krasnodar 3
Manaus 3
Medina 3
Nairobi 3
Newark 3
Orlando 3
Palermo 3
Poggiomarino 3
Recife 3
Totale 2.296
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Nome #
B lymphocytes limit senescence-driven fibrosis resolution and favor hepatocarcinogenesis in mouse liver injury. 113
Intestinal microbiota sustains inflammation and autoimmunity induced by hypomorphic RAG defects 107
Chromosome Transplantation: Opportunities and Limitations 107
Homeostatic expansion of autoreactive immunoglobulin-secreting cells in the Rag2 mouse model of Omenn syndrome. 102
Hypomorphic mutation in the RAG2 gene affects dendritic cell distribution and migration. 99
Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis 85
X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations 79
Recapitulation of the Roberts syndrome cellular phenotype by inhibition of INCENP, ZWINT-1 and ZW10 genes 78
The complete sequence of the Host Cell Factor 1 (HCFC1) gene and its promoter: A role for YY1 transcription factor in the regulation of its expression 76
A pre-screening FISH-based method to detect CRISPR/Cas9 off-targets in mouse embryonic stem cells 74
Generation of an immunodeficient mouse model of tcirg1-deficient autosomal recessive osteopetrosis 74
The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy 72
Chromosome Transplantation: Correction of the Chronic Granulomatous Disease Defect in Mouse Induced Pluripotent Stem Cells 70
Computer gene mapping by EagI-based STSs 69
Anti-CD3ε mAb improves thymic architecture and prevents autoimmune manifestations in a mouse model of Omenn syndrome: therapeutic implications 67
Generation of 3 clones of induced pluripotent stem cells (iPSCs) from a patient affected by Autosomal Recessive Osteopetrosis due to mutations in TCIRG1 gene. 65
As little as needed: The extraordinary case of a mild recessive osteopetrosis owing to a novel splicing hypomorphic mutation in the TCIRG1 gene 60
Motor neuron degeneration, severe myopathy and TDP-43 increase in a transgenic pig model of SOD1-linked familiar ALS. 60
Anti-VEGF agents confer survival advantages to tumor-bearing mice by improving cancer-associated systemic syndrome 59
IL-10 Critically Modulates B Cell Responsiveness in Rankl(-/-) Mice 58
Cell fusion in the liver, revisited 57
PBX1-directed stem cell transcriptional program drives tumor progression in myeloproliferative neoplasm 54
RANK-dependent autosomal recessive osteopetrosis: characterisation of 5 new cases with novel mutations. 51
Mutations in the Neuroblastoma Amplified Sequence gene in a family affected by Acrofrontofacionasal Dysostosis type 1 50
TCIRG1-dependent recessive osteopetrosis: Mutation analysis, functional identification of the splicing defects, and in vitro rescue by U1 snRNA. 49
Fusion between cancer cells and macrophages occurs in a murine model of spontaneous neu+ breast cancer without increasing its metastatic potential 49
SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity. 48
In utero transplantation of adult bone marrow decreases perinatal lethality and rescues the bone phenotype in the knockin murine model for classical, dominant osteogenesis imperfecta. 47
Autosomal recessive osteopetrosis: report of 41 novel mutations in the TCIRG1 gene and diagnostic implications 47
Synonymous Mutations Add a Layer of Complexity in the Diagnosis of Human Osteopetrosis. 47
Motor neuron degeneration, severe myopathy and TDP-43 increase in a transgenic pig model of SOD1-linked familiar ALS 47
Cell fusion is a physiological process in Mouse liver. 46
Autofluorescence and metabolic signatures in a pig model of differentiation based on induced pluripotent cells and embryonic bodies 45
SMC1 involvement in fragile site expression 44
Dendritic cells cause bone lesions in a new mouse model of histiocytosis 44
Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement. 44
Effects of IL-12 gene therapy on spontaneous transgenic and transplanted breast tumors. 43
Dome formation in cell cultures as expression of an early stage of lactogenic differentiation of the mammary gland. 43
Establishment and characterization of new mammary adenocarcinoma cell lines derived from double transgenic mice expressing GFP and neu oncogene 42
Defect of regulatory T cells in patients with Omenn syndrome. 41
Autofluorescence properties of murine embryonic stem cells during spontaneous differentiation phases. 41
Defects in the TCIRG1-encoded 116kD subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis. 40
Methylation and sequence analysis around EagI sites: identification of 28 new CpG islands in XQ24-XQ28. 40
Autofluorescence properties of murine stem cells during early differentiation phases. 40
Generation of 3 clones of induced pluripotent stem cells (iPSCs) from a patient affected by Autosomal Recessive Osteopetrosis due to mutations in TCIRG1 gene. 40
SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity 39
Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations. 38
RANKL Cytokine: From Pioneer of the Osteoimmunology Era to Cure for a Rare Disease. 37
Damaging-agent sensitivity of Artemis-deficient cell lines. 36
Physiologic oxygen enhances human embryonic stem cell clonal recovery and reduces chromosomal abnormalities. 36
Exome sequencing identifies CTSK mutations in patients originally diagnosed as intermediate osteopetrosis 35
In vitro and in vivo antisense-mediated growth inhibition of a mammary adenocarcinoma from MMTV-neu transgenic mice 35
Chromosomes, genes, and cancer breakpoints. 35
Nephrogenic diabetes insipidus: Functional analysis of new AVPR2 mutations identified in Italian families 35
Autofluorescence properties of murine embryonic stem cells during spontaneous differentiation phases 32
Molecular cloning of ILP-2, a novel member of the inhibitor of apoptosis protein family 32
Type 2 Vasopressin Receptor Gene, the Gene Responsible for Nephrogenic Diabetes Insipidus, Maps to XQ28 Close to the L1CAM Gene 31
A transgenic mouse model for the detection of cellular stress induced by toxic inorganic compounds. 30
CHARACTERIZATION OF 9 NOVEL MUTATIONS IN THE CD40 LIGAND GENE IN PATIENTS WITH X-LINKED HYPER IGM SYNDROME OF VARIOUS ANCESTRY 30
Mapping of two genes encoding isoforms of the actin binding protein ABP-280, a dystrophin like protein, to Xq28 and to chromosome 7 30
Impaired Osteoblastogenesis in a Murine Model of Dominant Osteogenesis Imperfecta (OI), A New Target for OI Pharmacological Therapy. Stem Cells 30:1465-1476, 2012 29
THE HUMAN GENES ENCODING RENIN-BINDING PROTEIN AND HOST-CELL FACTOR ARE CLOSELY LINKED IN XQ28 AND TRANSCRIBED IN THE SAME DIRECTION 29
Genotype-Phenotype Relationship in Human ATP6i-Dependent Autosomal Recessive Osteopetrosis. 29
Artemis C-terminal region facilitates V(D)J recombination through its interactions with DNA Ligase IV and DNA-PKcs. 29
Inhibition of BUB1 results in genomic instability and anchorage-independent growth of normal human fibroblasts. 28
Reduced mammary tumor progression in a transgenic mouse model fed an isoflavone-poor soy protein concentrate. 28
Analysis of mutations from SCID and Omenn syndrome patients reveals the central role of the Rag2 PHD domain in regulating V(D)J recombination 28
A new mutation (TTR ala-47) in the transthyretin gene associated with hereditary amyloidosis 27
The Dissection of Human Autosomal Recessive Osteopetrosis Identifies an Osteoclast-Poor Form due to RANKL Deficiency. 27
SMC1 inhibition results in FRA3B expression but has no effect on its delayed replication 27
Polymorphisms of the CLCN7 Gene Are Associated With BMD in Women. 26
Mutation of the WASP gene in X-linked Thrombocytopenia 26
Iron, neuromelanin and ferritin content in the substantia nigra of normal subjects at different ages: consequences for iron storage and neurodegenerative processes. 25
Osteoclast morphology in autosomal recessive malignant osteopetrosis due to a TCIRG1 gene mutation. 24
Identification and genomic organization of a gene coding for a new member of the cell adhesion molecule family mapping to Xq25 24
Response to Gribaldo and Hartung: New hepatocytes for toxicolgoy? 24
Inhibition of BUB1 results in genomic instability and anchorage-independent growth of normal human fibroblasts. 24
The chromosome localization and the HCF repeats of the human host cell factor gene (HCFC1) are conserved in the mouse homologue 24
Combined antiestrogen, antiangiogenic and anti-invasion therapy inhibits primary and metastatic tumor growth in the MMTVneu model of breast cancer. 22
Chromosomal Instability in Mouse-Induced Pluripotent Stem Cells: Insights into X and Y Aneuploidies 13
null 3
Totale 3.740
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Categoria #
all - tutte 13.116
article - articoli 13.009
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 26.125
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202428 0 0 0 0 0 0 0 0 1 1 21 5
2024/20251.228 1 4 106 43 259 51 36 75 49 60 285 259
2025/20262.129 135 240 173 378 378 79 340 78 109 97 58 64
2026/2027355 68 90 197 0 0 0 0 0 0 0 0 0
Totale 3.740