CNR Institutional Research Information System

VEZZONI, PAOLO MARIA
 Distribuzione geografica
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Continente #
AS - Asia 1.694
NA - Nord America 890
EU - Europa 370
SA - Sud America 282
AF - Africa 35
Totale 3.271
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Nazione #
US - Stati Uniti d'America 854
SG - Singapore 680
CN - Cina 438
BR - Brasile 231
HK - Hong Kong 170
VN - Vietnam 155
KR - Corea 100
IT - Italia 92
FR - Francia 82
GB - Regno Unito 34
DE - Germania 33
NL - Olanda 32
JP - Giappone 29
IN - India 25
CA - Canada 22
FI - Finlandia 22
BD - Bangladesh 21
AR - Argentina 16
IQ - Iraq 15
EC - Ecuador 13
MX - Messico 12
IL - Israele 11
RU - Federazione Russa 10
CO - Colombia 9
PL - Polonia 9
ID - Indonesia 8
SE - Svezia 8
ZA - Sudafrica 8
CI - Costa d'Avorio 6
ES - Italia 6
PK - Pakistan 6
UA - Ucraina 6
CZ - Repubblica Ceca 5
UZ - Uzbekistan 5
VE - Venezuela 5
AE - Emirati Arabi Uniti 4
EG - Egitto 4
IE - Irlanda 4
LT - Lituania 4
MA - Marocco 4
PH - Filippine 4
SA - Arabia Saudita 4
TR - Turchia 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
SN - Senegal 2
BE - Belgio 1
BG - Bulgaria 1
BO - Bolivia 1
BY - Bielorussia 1
CH - Svizzera 1
GT - Guatemala 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
MN - Mongolia 1
MY - Malesia 1
OM - Oman 1
PE - Perù 1
PS - Palestinian Territory 1
PT - Portogallo 1
RO - Romania 1
SI - Slovenia 1
SR - Suriname 1
SY - Repubblica araba siriana 1
TG - Togo 1
TJ - Tagikistan 1
TT - Trinidad e Tobago 1
Totale 3.271
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Città #
Singapore 396
Santa Clara 257
Hefei 208
Hong Kong 166
San Jose 129
Seoul 99
Ashburn 96
Beijing 94
Lauterbourg 70
Los Angeles 64
Ho Chi Minh City 62
Hanoi 35
New York 21
Cagliari 18
Milan 18
São Paulo 18
Helsinki 15
Tokyo 15
Brasília 11
Dallas 11
Düsseldorf 11
Buffalo 10
Frankfurt am Main 10
Minamishinagawa 10
Belo Horizonte 8
Mexico City 8
Montreal 8
Orem 8
Warsaw 8
Bengaluru 7
Da Nang 7
Poplar 7
Stockholm 7
Abidjan 6
Guayaquil 6
Houston 6
London 6
Munich 6
Rio de Janeiro 6
Shanghai 6
Florence 5
Hortolândia 5
Johannesburg 5
Phoenix 5
Rome 5
Tashkent 5
Turku 5
Amsterdam 4
Assemini 4
Chicago 4
Council Bluffs 4
Curitiba 4
Denver 4
Dublin 4
Hải Dương 4
Miami 4
Padova 4
Porcari 4
Porto Alegre 4
Portsmouth 4
Quận Mười 4
Thái Nguyên 4
Baghdad 3
Basra 3
Biên Hòa 3
Boston 3
Brooklyn 3
Cairo 3
Campinas 3
Cape Town 3
Caracas 3
Chennai 3
Dhaka 3
Goiânia 3
Guangzhou 3
Haiphong 3
Hyderabad 3
Krasnodar 3
Manaus 3
Nairobi 3
Orlando 3
Poggiomarino 3
Quito 3
Recife 3
Salvador 3
Thái Bình 3
Tirana 3
Almaty 2
Ankara 2
Arujá 2
Baku 2
Barra Mansa 2
Betim 2
Bologna 2
Bratislava 2
Bắc Giang 2
Cardiff 2
Chennevières-sur-Marne 2
City of London 2
Contagem 2
Totale 2.150
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Nome #
B lymphocytes limit senescence-driven fibrosis resolution and favor hepatocarcinogenesis in mouse liver injury. 106
Intestinal microbiota sustains inflammation and autoimmunity induced by hypomorphic RAG defects 99
Chromosome Transplantation: Opportunities and Limitations 95
Homeostatic expansion of autoreactive immunoglobulin-secreting cells in the Rag2 mouse model of Omenn syndrome. 93
Hypomorphic mutation in the RAG2 gene affects dendritic cell distribution and migration. 93
Recapitulation of the Roberts syndrome cellular phenotype by inhibition of INCENP, ZWINT-1 and ZW10 genes 75
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 70
A pre-screening FISH-based method to detect CRISPR/Cas9 off-targets in mouse embryonic stem cells 68
X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations 66
Computer gene mapping by EagI-based STSs 64
Chromosome Transplantation: Correction of the Chronic Granulomatous Disease Defect in Mouse Induced Pluripotent Stem Cells 64
Anti-CD3ε mAb improves thymic architecture and prevents autoimmune manifestations in a mouse model of Omenn syndrome: therapeutic implications 62
Generation of 3 clones of induced pluripotent stem cells (iPSCs) from a patient affected by Autosomal Recessive Osteopetrosis due to mutations in TCIRG1 gene. 61
Generation of an immunodeficient mouse model of tcirg1-deficient autosomal recessive osteopetrosis 60
Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis 58
As little as needed: The extraordinary case of a mild recessive osteopetrosis owing to a novel splicing hypomorphic mutation in the TCIRG1 gene 56
The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy 56
Cell fusion in the liver, revisited 55
IL-10 Critically Modulates B Cell Responsiveness in Rankl(-/-) Mice 55
Anti-VEGF agents confer survival advantages to tumor-bearing mice by improving cancer-associated systemic syndrome 53
PBX1-directed stem cell transcriptional program drives tumor progression in myeloproliferative neoplasm 52
Motor neuron degeneration, severe myopathy and TDP-43 increase in a transgenic pig model of SOD1-linked familiar ALS. 50
RANK-dependent autosomal recessive osteopetrosis: characterisation of 5 new cases with novel mutations. 46
SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity. 45
TCIRG1-dependent recessive osteopetrosis: Mutation analysis, functional identification of the splicing defects, and in vitro rescue by U1 snRNA. 44
Fusion between cancer cells and macrophages occurs in a murine model of spontaneous neu+ breast cancer without increasing its metastatic potential 44
Mutations in the Neuroblastoma Amplified Sequence gene in a family affected by Acrofrontofacionasal Dysostosis type 1 44
Autofluorescence and metabolic signatures in a pig model of differentiation based on induced pluripotent cells and embryonic bodies 43
SMC1 involvement in fragile site expression 43
Synonymous Mutations Add a Layer of Complexity in the Diagnosis of Human Osteopetrosis. 43
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. 42
Dendritic cells cause bone lesions in a new mouse model of histiocytosis 42
Cell fusion is a physiological process in Mouse liver. 42
Motor neuron degeneration, severe myopathy and TDP-43 increase in a transgenic pig model of SOD1-linked familiar ALS 42
Dome formation in cell cultures as expression of an early stage of lactogenic differentiation of the mammary gland. 41
Establishment and characterization of new mammary adenocarcinoma cell lines derived from double transgenic mice expressing GFP and neu oncogene 39
Autosomal recessive osteopetrosis: report of 41 novel mutations in the TCIRG1 gene and diagnostic implications 37
Methylation and sequence analysis around EagI sites: identification of 28 new CpG islands in XQ24-XQ28. 37
Effects of IL-12 gene therapy on spontaneous transgenic and transplanted breast tumors. 36
Autofluorescence properties of murine stem cells during early differentiation phases. 36
Defect of regulatory T cells in patients with Omenn syndrome. 36
Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement. 36
Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations. 36
Generation of 3 clones of induced pluripotent stem cells (iPSCs) from a patient affected by Autosomal Recessive Osteopetrosis due to mutations in TCIRG1 gene. 36
SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity 35
Autofluorescence properties of murine embryonic stem cells during spontaneous differentiation phases. 35
Damaging-agent sensitivity of Artemis-deficient cell lines. 34
Defects in the TCIRG1-encoded 116kD subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis. 33
Chromosomes, genes, and cancer breakpoints. 33
RANKL Cytokine: From Pioneer of the Osteoimmunology Era to Cure for a Rare Disease. 32
In vitro and in vivo antisense-mediated growth inhibition of a mammary adenocarcinoma from MMTV-neu transgenic mice 31
Autofluorescence properties of murine embryonic stem cells during spontaneous differentiation phases 30
Exome sequencing identifies CTSK mutations in patients originally diagnosed as intermediate osteopetrosis 30
Physiologic oxygen enhances human embryonic stem cell clonal recovery and reduces chromosomal abnormalities. 30
Nephrogenic diabetes insipidus: Functional analysis of new AVPR2 mutations identified in Italian families 29
Molecular cloning of ILP-2, a novel member of the inhibitor of apoptosis protein family 28
Type 2 Vasopressin Receptor Gene, the Gene Responsible for Nephrogenic Diabetes Insipidus, Maps to XQ28 Close to the L1CAM Gene 27
CHARACTERIZATION OF 9 NOVEL MUTATIONS IN THE CD40 LIGAND GENE IN PATIENTS WITH X-LINKED HYPER IGM SYNDROME OF VARIOUS ANCESTRY 27
A new mutation (TTR ala-47) in the transthyretin gene associated with hereditary amyloidosis 26
Mapping of two genes encoding isoforms of the actin binding protein ABP-280, a dystrophin like protein, to Xq28 and to chromosome 7 26
SMC1 inhibition results in FRA3B expression but has no effect on its delayed replication 26
THE HUMAN GENES ENCODING RENIN-BINDING PROTEIN AND HOST-CELL FACTOR ARE CLOSELY LINKED IN XQ28 AND TRANSCRIBED IN THE SAME DIRECTION 25
Analysis of mutations from SCID and Omenn syndrome patients reveals the central role of the Rag2 PHD domain in regulating V(D)J recombination 25
Inhibition of BUB1 results in genomic instability and anchorage-independent growth of normal human fibroblasts. 24
The Dissection of Human Autosomal Recessive Osteopetrosis Identifies an Osteoclast-Poor Form due to RANKL Deficiency. 23
Genotype-Phenotype Relationship in Human ATP6i-Dependent Autosomal Recessive Osteopetrosis. 23
Inhibition of BUB1 results in genomic instability and anchorage-independent growth of normal human fibroblasts. 23
Polymorphisms of the CLCN7 Gene Are Associated With BMD in Women. 22
Impaired Osteoblastogenesis in a Murine Model of Dominant Osteogenesis Imperfecta (OI), A New Target for OI Pharmacological Therapy. Stem Cells 30:1465-1476, 2012 22
Identification and genomic organization of a gene coding for a new member of the cell adhesion molecule family mapping to Xq25 22
Artemis C-terminal region facilitates V(D)J recombination through its interactions with DNA Ligase IV and DNA-PKcs. 22
A transgenic mouse model for the detection of cellular stress induced by toxic inorganic compounds. 21
Iron, neuromelanin and ferritin content in the substantia nigra of normal subjects at different ages: consequences for iron storage and neurodegenerative processes. 21
Osteoclast morphology in autosomal recessive malignant osteopetrosis due to a TCIRG1 gene mutation. 20
Response to Gribaldo and Hartung: New hepatocytes for toxicolgoy? 20
Mutation of the WASP gene in X-linked Thrombocytopenia 20
Reduced mammary tumor progression in a transgenic mouse model fed an isoflavone-poor soy protein concentrate. 20
The chromosome localization and the HCF repeats of the human host cell factor gene (HCFC1) are conserved in the mouse homologue 20
Combined antiestrogen, antiangiogenic and anti-invasion therapy inhibits primary and metastatic tumor growth in the MMTVneu model of breast cancer. 19
Chromosomal Instability in Mouse-Induced Pluripotent Stem Cells: Insights into X and Y Aneuploidies 7
null 3
Totale 3.315
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Categoria #
all - tutte 10.507
article - articoli 10.427
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 20.934
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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
2025/20262.059 135 240 173 378 378 79 340 78 109 97 52 0
Totale 3.315