CNR Institutional Research Information System

VEZZONI, PAOLO MARIA
 Distribuzione geografica
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Continente #
NA - Nord America 414
AS - Asia 264
EU - Europa 92
AF - Africa 2
SA - Sud America 2
Totale 774
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Nazione #
US - Stati Uniti d'America 412
SG - Singapore 229
IT - Italia 42
FI - Finlandia 19
KR - Corea 18
CN - Cina 6
NL - Olanda 5
DE - Germania 4
FR - Francia 4
HK - Hong Kong 3
SK - Slovacchia (Repubblica Slovacca) 3
CA - Canada 2
CH - Svizzera 2
ES - Italia 2
GB - Regno Unito 2
UZ - Uzbekistan 2
VN - Vietnam 2
AE - Emirati Arabi Uniti 1
AT - Austria 1
AZ - Azerbaigian 1
BG - Bulgaria 1
BO - Bolivia 1
BR - Brasile 1
BY - Bielorussia 1
CZ - Repubblica Ceca 1
EG - Egitto 1
KG - Kirghizistan 1
LT - Lituania 1
LU - Lussemburgo 1
LV - Lettonia 1
MA - Marocco 1
RO - Romania 1
RU - Federazione Russa 1
SA - Arabia Saudita 1
Totale 774
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Città #
Santa Clara 318
Singapore 120
Helsinki 19
Cagliari 18
Seoul 18
Ashburn 8
Los Angeles 7
Assemini 6
Milan 5
Guangzhou 4
Bratislava 3
Falkenstein 3
Hong Kong 3
Miami 3
Amsterdam 2
Benevento 2
Chennevières-sur-Marne 2
Forest City 2
Newark 2
Palermo 2
Tashkent 2
Varese 2
Zurich 2
'Asir Region 1
Aulnay-sous-Bois 1
Baku 1
Bartlesville 1
Bishkek 1
Cabiate 1
Cairo 1
Dubai 1
Edison 1
Hanoi 1
La Paz 1
London 1
Luxembourg 1
Madrid 1
Minsk 1
Padova 1
Pasadena 1
Pisa 1
Prague 1
Riga 1
Rome 1
San Jose 1
Sofia 1
São José dos Pinhais 1
Toronto 1
Vienna 1
Totale 579
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Nome #
TCIRG1-dependent recessive osteopetrosis: Mutation analysis, functional identification of the splicing defects, and in vitro rescue by U1 snRNA. 19
Generation of an immunodeficient mouse model of tcirg1-deficient autosomal recessive osteopetrosis 18
Chromosome Transplantation: A Possible Approach to Treat Human X-linked Disorders 18
Effects of IL-12 gene therapy on spontaneous transgenic and transplanted breast tumors. 17
Establishment and characterization of new mammary adenocarcinoma cell lines derived from double transgenic mice expressing GFP and neu oncogene 17
As little as needed: The extraordinary case of a mild recessive osteopetrosis owing to a novel splicing hypomorphic mutation in the TCIRG1 gene 15
Anti-CD3ε mAb improves thymic architecture and prevents autoimmune manifestations in a mouse model of Omenn syndrome: therapeutic implications 15
A recessive contiguous gene deletion in chromosome16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient. 14
Autofluorescence and metabolic signatures in a pig model of differentiation based on induced pluripotent cells and embryonic bodies 14
Molecular and clinical heterogeneity in CLCN7-dependent osteopetrosis: report of 20 novel mutations 14
Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis 14
Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL. 14
X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations 13
B lymphocytes limit senescence-driven fibrosis resolution and favor hepatocarcinogenesis in mouse liver injury. 13
SMC1 involvement in fragile site expression 12
The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy 12
Chromosomes, genes, and cancer breakpoints. 12
Autofluorescence properties of murine embryonic stem cells during spontaneous differentiation phases. 12
Cell fusion is a physiological process in Mouse liver. 12
Heterogeneous gene distribution reflects human genome complexity as detected at the cytogenetic level. 12
Dome formation in cell cultures as expression of an early stage of lactogenic differentiation of the mammary gland. 12
Prognostic potential of precise molecular diagnosis of Autosomal Recessive Osteopetrosis with respect to the outcome of bone marrow transplantation. 11
SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity 11
Recapitulation of the Roberts syndrome cellular phenotype by inhibition of INCENP, ZWINT-1 and ZW10 genes 11
Chromosome transplantation as a novel approach for correcting complex genomic disorders 11
Homozygous Contiguous Gene Deletion in Chromosome 16p13.3 Leads to Autosomal Recessive Osteopetrosis in a Jordanian Patient. 11
Intestinal microbiota sustains inflammation and autoimmunity induced by hypomorphic RAG defects 10
Cell fusion in the liver, revisited 10
Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA. 10
SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity. 10
Motor neuron degeneration, severe myopathy and TDP-43 increase in a transgenic pig model of SOD1-linked familiar ALS. 10
Nephrogenic diabetes insipidus: Functional analysis of new AVPR2 mutations identified in Italian families 10
Homeostatic expansion of autoreactive immunoglobulin-secreting cells in the Rag2 mouse model of Omenn syndrome. 9
TCIRG1-dependent recessive osteopetrosis: Mutation analysis, functional identification of the splicing defects, and in vitro rescue by U1 snRNA 9
IL-10 Critically Modulates B Cell Responsiveness in Rankl(-/-) Mice 9
Association of rat8 with Fyn protein kinase via lipid rafts is required for rat mammary cell differentiation in vitro 9
Fidelity of a YAC clone in the region of human MCF-2 gene 9
Chromosome Transplantation: Correction of the Chronic Granulomatous Disease Defect in Mouse Induced Pluripotent Stem Cells 9
Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis 9
Methylation and sequence analysis around EagI sites: identification of 28 new CpG islands in XQ24-XQ28. 9
Autofluorescence properties of murine stem cells during early differentiation phases. 9
The ZNF75 zinc finger gene subfamily: Isolation and mapping of the four members in humans and great apes 9
Targeted gene correction in osteopetrotic-induced pluripotent stem cells for the generation of functional osteoclasts 9
Hypomorphic mutation in the RAG2 gene affects dendritic cell distribution and migration. 8
Generation of 3 clones of induced pluripotent stem cells (iPSCs) from a patient affected by Autosomal Recessive Osteopetrosis due to mutations in TCIRG1 gene. 8
A pre-screening FISH-based method to detect CRISPR/Cas9 off-targets in mouse embryonic stem cells 8
PBX1-directed stem cell transcriptional program drives tumor progression in myeloproliferative neoplasm 8
Autosomal recessive osteopetrosis: report of 41 novel mutations in the TCIRG1 gene and diagnostic implications 8
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient 8
Autofluorescence properties of murine embryonic stem cells during spontaneous differentiation phases 8
Synonymous Mutations Add a Layer of Complexity in the Diagnosis of Human Osteopetrosis. 8
RANKL Cytokine: From Pioneer of the Osteoimmunology Era to Cure for a Rare Disease. 8
Fusion between cancer cells and macrophages occurs in a murine model of spontaneous neu+ breast cancer without increasing its metastatic potential 8
Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations. 8
Checkpoint adaptation leads to genome instability in human cells 8
Motor neuron degeneration, severe myopathy and TDP-43 increase in a transgenic pig model of SOD1-linked familiar ALS 8
Computer gene mapping by EagI-based STSs 7
Chromosome Transplantation: Opportunities and Limitations 7
Iron, neuromelanin and ferritin content in the substantia nigra of normal subjects at different ages: consequences for iron storage and neurodegenerative processes. 7
Exome sequencing identifies CTSK mutations in patients originally diagnosed as intermediate osteopetrosis 7
The Dissection of Human Autosomal Recessive Osteopetrosis Identifies an Osteoclast-Poor Form due to RANKL Deficiency. 7
Dendritic cells cause bone lesions in a new mouse model of histiocytosis 7
Mapping of two genes encoding isoforms of the actin binding protein ABP-280, a dystrophin like protein, to Xq28 and to chromosome 7 7
Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement. 7
Mutations in the Neuroblastoma Amplified Sequence gene in a family affected by Acrofrontofacionasal Dysostosis type 1 7
Generation of 3 clones of induced pluripotent stem cells (iPSCs) from a patient affected by Autosomal Recessive Osteopetrosis due to mutations in TCIRG1 gene. 7
Gene expression profiles of epithelial cells microscopically isolated from a breast-invasive ductal carcinoma and a nodal metastasis 7
RANK-dependent autosomal recessive osteopetrosis: characterisation of 5 new cases with novel mutations. 6
Inhibition of BUB1 results in genomic instability and anchorage-independent growth of normal human fibroblasts. 6
Damaging-agent sensitivity of Artemis-deficient cell lines. 6
A new mutation (TTR ala-47) in the transthyretin gene associated with hereditary amyloidosis 6
The genetics of dominant osteopetrosis 6
Defect of regulatory T cells in patients with Omenn syndrome. 6
Mutation of the WASP gene in X-linked Thrombocytopenia 6
CHARACTERIZATION OF 9 NOVEL MUTATIONS IN THE CD40 LIGAND GENE IN PATIENTS WITH X-LINKED HYPER IGM SYNDROME OF VARIOUS ANCESTRY 6
Genotype-Phenotype Relationship in Human ATP6i-Dependent Autosomal Recessive Osteopetrosis. 6
Osteopetroses and immunodeficiencies in humans. 6
Artemis C-terminal region facilitates V(D)J recombination through its interactions with DNA Ligase IV and DNA-PKcs. 6
Inhibition of BUB1 results in genomic instability and anchorage-independent growth of normal human fibroblasts. 6
Combined antiestrogen, antiangiogenic and anti-invasion therapy inhibits primary and metastatic tumor growth in the MMTVneu model of breast cancer. 6
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 5
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. 5
Defects in the TCIRG1-encoded 116kD subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis. 5
Molecular cloning of ILP-2, a novel member of the inhibitor of apoptosis protein family 5
Partial V(D)J recombination activity leads to Omenn syndrome. 5
Association between a Polymorphism Affecting an AP1 Binding Site in the Promoter of the TCIRG1 Gene and Bone Mass in Women 5
In vitro and in vivo antisense-mediated growth inhibition of a mammary adenocarcinoma from MMTV-neu transgenic mice 5
Mutations of JAK3 gene in patients with autosomal severe combined immunodeficiency (SCID). 5
Physiologic oxygen enhances human embryonic stem cell clonal recovery and reduces chromosomal abnormalities. 5
SMC1 inhibition results in FRA3B expression but has no effect on its delayed replication 5
The chromosome localization and the HCF repeats of the human host cell factor gene (HCFC1) are conserved in the mouse homologue 5
Analysis of mutations from SCID and Omenn syndrome patients reveals the central role of the Rag2 PHD domain in regulating V(D)J recombination 5
Anti-VEGF agents confer survival advantages to tumor-bearing mice by improving cancer-associated systemic syndrome 4
A transgenic mouse model for the detection of cellular stress induced by toxic inorganic compounds. 4
The mutational spectrum of human malignant autosomal recessive osteopetrosis 4
Polymorphisms of the CLCN7 Gene Are Associated With BMD in Women. 4
Identification and genomic organization of a gene coding for a new member of the cell adhesion molecule family mapping to Xq25 4
THE HUMAN GENES ENCODING RENIN-BINDING PROTEIN AND HOST-CELL FACTOR ARE CLOSELY LINKED IN XQ28 AND TRANSCRIBED IN THE SAME DIRECTION 4
Reduced mammary tumor progression in a transgenic mouse model fed an isoflavone-poor soy protein concentrate. 4
Osteoclast morphology in autosomal recessive malignant osteopetrosis due to a TCIRG1 gene mutation. 3
Totale 863
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Categoria #
all - tutte 3.661
article - articoli 3.600
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 7.261
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202437 0 0 0 0 0 0 0 0 4 3 25 5
2024/2025830 2 6 131 52 348 70 55 116 50 0 0 0
Totale 867