CNR Institutional Research Information System

FRATTINI, ANNALISA
 Distribuzione geografica
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Continente #
AS - Asia 1.044
NA - Nord America 619
EU - Europa 264
SA - Sud America 161
AF - Africa 14
OC - Oceania 2
Totale 2.104
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Nazione #
US - Stati Uniti d'America 582
SG - Singapore 482
CN - Cina 206
BR - Brasile 124
VN - Vietnam 122
HK - Hong Kong 107
IT - Italia 90
FR - Francia 58
KR - Corea 27
NL - Olanda 27
JP - Giappone 23
BD - Bangladesh 21
CA - Canada 21
GB - Regno Unito 20
AR - Argentina 16
FI - Finlandia 16
IN - India 15
DE - Germania 12
EC - Ecuador 8
ES - Italia 8
CO - Colombia 7
ID - Indonesia 7
PL - Polonia 7
MX - Messico 5
CR - Costa Rica 4
IQ - Iraq 4
KE - Kenya 4
SA - Arabia Saudita 4
ZA - Sudafrica 4
IE - Irlanda 3
IL - Israele 3
MY - Malesia 3
PS - Palestinian Territory 3
RU - Federazione Russa 3
AT - Austria 2
AU - Australia 2
CH - Svizzera 2
KZ - Kazakistan 2
LT - Lituania 2
NP - Nepal 2
PK - Pakistan 2
PT - Portogallo 2
PY - Paraguay 2
RO - Romania 2
UA - Ucraina 2
UZ - Uzbekistan 2
VE - Venezuela 2
AE - Emirati Arabi Uniti 1
AZ - Azerbaigian 1
BE - Belgio 1
BY - Bielorussia 1
BZ - Belize 1
CI - Costa d'Avorio 1
GT - Guatemala 1
GY - Guiana 1
HU - Ungheria 1
IM - Isola di Man 1
JM - Giamaica 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LU - Lussemburgo 1
MA - Marocco 1
ML - Mali 1
MN - Mongolia 1
NI - Nicaragua 1
OM - Oman 1
PA - Panama 1
PE - Perù 1
PH - Filippine 1
PR - Porto Rico 1
RS - Serbia 1
SE - Svezia 1
SI - Slovenia 1
SO - Somalia 1
TN - Tunisia 1
TR - Turchia 1
TT - Trinidad e Tobago 1
UG - Uganda 1
Totale 2.104
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Città #
Singapore 269
Santa Clara 180
Hong Kong 103
San Jose 97
Beijing 67
Ashburn 59
Hefei 59
Ho Chi Minh City 51
Lauterbourg 50
Los Angeles 33
Hanoi 27
Seoul 26
New York 18
Tokyo 18
Assemini 15
Milan 12
Buffalo 10
Helsinki 9
Brooklyn 7
Dallas 7
Lappeenranta 7
Orem 7
Warsaw 7
Belo Horizonte 6
Montreal 6
Rome 6
Toronto 6
Brasília 5
City of London 5
Hải Dương 5
Thái Nguyên 5
Da Nang 4
Elk Grove Village 4
Frankfurt am Main 4
Marseille 4
Pavia 4
Porto Alegre 4
Rio de Janeiro 4
Sala Baganza 4
São Paulo 4
Bengaluru 3
Can Tho 3
Chennai 3
Dublin 3
Gaza 3
Haiphong 3
London 3
Minamishinagawa 3
Nha Trang 3
Phoenix 3
Piscataway 3
Poggiomarino 3
San José 3
Varese 3
Amsterdam 2
Atlanta 2
Baoding 2
Boston 2
Brighton 2
Bắc Giang 2
Campinas 2
Charlotte 2
Chicago 2
Colatina 2
Council Bluffs 2
Córdoba 2
Duque de Caxias 2
Greensburg 2
Guarulhos 2
Guayaquil 2
Houston 2
Jakarta 2
Kathmandu 2
Kuala Lumpur 2
Lucca 2
Madrid 2
Malnate 2
Modena 2
Mérida 2
Nairobi 2
Naples 2
Norwalk 2
Nuremberg 2
Osasco 2
Passo Fundo 2
Portsmouth 2
Praia Grande 2
Quận Bốn 2
Quận Mười 2
Riyadh 2
Roseburg 2
Shanghai 2
Spring 2
St Louis 2
St. Catharines 2
Staten Island 2
Surabaya 2
Tashkent 2
The Dalles 2
Trenton 2
Totale 1.352
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Nome #
Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis 76
The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations. 73
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 71
Computer gene mapping by EagI-based STSs 67
The synergism of SMC1A cohesin gene silencing and bevacizumab against colorectal cancer 66
A Distinctive Type of Mosaic Variegated Aneuploidy: Case Report and Review of the Literature 62
Ataluren improves myelopoiesis and neutrophil chemotaxis by restoring ribosome biogenesis and reducing p53 levels in Shwachman-Diamond syndrome cells 60
Chromosome Missegregation in Single Human Oocytes Is Related to the Age and Gene Expression Profile 58
Paracrine effect of human adipose-derived stem cells on lymphatic endothelial cells 57
Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene 54
A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease 53
Occurrence of L1M Elements in Chromosomal Rearrangements Associated to Chronic Myeloid Leukemia (CML): Insights from Patient-Specific Breakpoints Characterization 53
A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease. 48
Enhanced p53 levels are involved in the reduced mineralization capacity of osteoblasts derived from Shwachman-Diamond syndrome subjects 48
Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype 48
Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome 46
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. 44
TCIRG1-dependent recessive osteopetrosis: Mutation analysis, functional identification of the splicing defects, and in vitro rescue by U1 snRNA. 44
Shwachman-Diamond syndrome: diagnosis, pathogenesis and prognosis 44
A nonsynonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease 44
SDS with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability 43
OTX1 expression in breast cancer is regulated by p53 42
The human RNASET2 protein affects the polarization pattern of human macrophages in vitro 40
Case report: heterozygous germline variant in EIF6 additional to biallelic SBDS pathogenic variants in a patient with ribosomopathy Shwachman-Diamond syndrome 39
Expansion cranioplasty with jackscrew distracters for craniosynostosis and intracranial hypertension in transplanted osteopetrosis. 38
High variability of genomic instability and gene expression profiling in different HeLa clones 38
Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement. 38
Toxicogenomics applied to in vitro Cell Transformation Assay reveals mechanisms of early response to cadmium 38
Molecular study of six families originating from the Middle-East and presenting with autosomal recessive osteopetrosis. 36
Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations. 36
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature 33
In vitro and in vivo antisense-mediated growth inhibition of a mammary adenocarcinoma from MMTV-neu transgenic mice 32
Nephrogenic diabetes insipidus: Functional analysis of new AVPR2 mutations identified in Italian families 31
Isolation of a zinc finger motif (ZNF75) mapping on chromosome Xq26 30
Diagnosi molecolare di malattie genetiche 30
A low-copy repeat in Xq26 represents a novel putatively prenylated protein gene (CXX1) and its pseudogenes (DXS9914, DXS9915, and DXS9916) 30
Molecular cloning of ILP-2, a novel member of the inhibitor of apoptosis protein family 30
Type 2 Vasopressin Receptor Gene, the Gene Responsible for Nephrogenic Diabetes Insipidus, Maps to XQ28 Close to the L1CAM Gene 30
Electron microscopic findings in skin biopsies from patients with infantile osteopetrosis and neuronal storage disease. 30
ZNF75 - ISOLATION OF A CDNA CLONE OF THE KRAB ZINC-FINGER GENE SUBFAMILY MAPPED IN YACS 1 MB TELOMERIC OF HPRT 29
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
Brain lipid composition in grey-lethal mutant mouse characterized by severe malignant osteopetrosis. 26
Liposome-delivered angiostatin strongly inhibits tumor growth and metastatization in a transgenic model of spontaneous breast cancer 26
THE HUMAN GENES ENCODING RENIN-BINDING PROTEIN AND HOST-CELL FACTOR ARE CLOSELY LINKED IN XQ28 AND TRANSCRIBED IN THE SAME DIRECTION 25
Vacuolar H+-ATPase d2 Subunit: Molecular Characterization, Developmental Regulation, and Localization to Specialized Proton Pumps in Kidney and Bone. 25
Genomic organization of the human VP16 accessory protein (HCF), a housekeeping gene mapping to Xq28. 24
The Dissection of Human Autosomal Recessive Osteopetrosis Identifies an Osteoclast-Poor Form due to RANKL Deficiency. 23
Polymorphisms of the CLCN7 Gene Are Associated With BMD in Women. 22
Identification and genomic organization of a gene coding for a new member of the cell adhesion molecule family mapping to Xq25 22
Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human. 22
Identification of a new member (ZNF183) of the Ring finger gene family in Xq24-25 22
Chloride channel CICN7 mutations in a Korean patient with infantile malignant osteopetrosis initially presenting with neonatal thrombocytopenia. 21
Donor Cell Acute Myeloid Leukemia after Hematopoietic Stem Cell Transplantation for Chronic Granulomatous Disease: A Case Report and Literature Review 21
GENOMIC ORGANIZATION OF THE HUMAN VP16 ACCESSORY PROTEIN, A HOUSEKEEPING GENE (HCFC1) MAPPING TO XQ28 21
THE EXON-INTRON ORGANIZATION OF THE HUMAN X-LINKED GENE (FLN1) ENCODING ACTIN-BINDING PROTEIN-280 20
The chromosome localization and the HCF repeats of the human host cell factor gene (HCFC1) are conserved in the mouse homologue 20
SMC1B is present in mammalian somatic cells and interacts with mitotic cohesin proteins 20
Characterization and fine localization of two new genes in Xq28 using the genomic sequence EST database screening approach 19
Development of translational read-through-inducing drugs as novel therapeutic options for patients with Fanconi anemia 17
The mammary gland and the homeobox gene Otx1 12
Totale 2.269
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Categoria #
all - tutte 8.087
article - articoli 7.999
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 16.086
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202464 0 0 0 0 0 0 0 0 22 18 4 20
2024/2025819 9 2 63 31 218 52 28 57 12 30 172 145
2025/20261.354 61 92 111 169 233 69 265 58 89 99 62 46
2026/202732 32 0 0 0 0 0 0 0 0 0 0 0
Totale 2.269