CNR Institutional Research Information System

ORIOLI, DONATA
 Distribuzione geografica
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Continente #
AS - Asia 2.063
NA - Nord America 1.386
SA - Sud America 493
EU - Europa 404
AF - Africa 49
OC - Oceania 6
Totale 4.401
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Nazione #
US - Stati Uniti d'America 1.339
SG - Singapore 858
CN - Cina 480
BR - Brasile 397
VN - Vietnam 261
HK - Hong Kong 174
FR - Francia 123
KR - Corea 100
IT - Italia 91
IN - India 46
GB - Regno Unito 38
AR - Argentina 35
JP - Giappone 35
DE - Germania 33
NL - Olanda 31
BD - Bangladesh 22
CA - Canada 22
ZA - Sudafrica 18
FI - Finlandia 16
IL - Israele 16
EC - Ecuador 14
MA - Marocco 14
MX - Messico 14
ID - Indonesia 13
CO - Colombia 10
IE - Irlanda 10
PY - Paraguay 10
IQ - Iraq 9
VE - Venezuela 9
RU - Federazione Russa 8
PK - Pakistan 7
UY - Uruguay 7
EG - Egitto 6
LT - Lituania 6
TR - Turchia 6
UA - Ucraina 6
AT - Austria 5
AU - Australia 5
CL - Cile 5
ES - Italia 5
PL - Polonia 5
SE - Svezia 5
BE - Belgio 4
PE - Perù 4
SA - Arabia Saudita 4
TH - Thailandia 4
UZ - Uzbekistan 4
CH - Svizzera 3
OM - Oman 3
PH - Filippine 3
TN - Tunisia 3
AE - Emirati Arabi Uniti 2
AL - Albania 2
BA - Bosnia-Erzegovina 2
BB - Barbados 2
BO - Bolivia 2
DO - Repubblica Dominicana 2
GR - Grecia 2
HN - Honduras 2
JM - Giamaica 2
JO - Giordania 2
KE - Kenya 2
KZ - Kazakistan 2
LK - Sri Lanka 2
LV - Lettonia 2
NG - Nigeria 2
NP - Nepal 2
PT - Portogallo 2
AM - Armenia 1
AO - Angola 1
AZ - Azerbaigian 1
BG - Bulgaria 1
BH - Bahrain 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
CZ - Repubblica Ceca 1
DZ - Algeria 1
EE - Estonia 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LY - Libia 1
MD - Moldavia 1
MN - Mongolia 1
MT - Malta 1
MY - Malesia 1
NZ - Nuova Zelanda 1
PA - Panama 1
QA - Qatar 1
SV - El Salvador 1
Totale 4.401
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Città #
Santa Clara 715
Singapore 490
Hefei 238
Hong Kong 172
San Jose 123
Lauterbourg 104
Seoul 100
Ho Chi Minh City 91
Hanoi 68
Dallas 67
Ashburn 62
Beijing 61
Los Angeles 52
Pavia 35
São Paulo 28
New York 24
Rio de Janeiro 19
Tokyo 18
Frankfurt am Main 16
Minamishinagawa 15
Haiphong 13
Helsinki 12
London 12
Bengaluru 11
Buffalo 11
Milan 10
Biên Hòa 9
Chennai 9
Dublin 9
Toronto 9
Portsmouth 8
Brasília 7
Cremona 7
Da Nang 7
Düsseldorf 7
Quito 7
Asunción 6
Campina Grande 6
Council Bluffs 6
Houston 6
Johannesburg 6
Montevideo 6
Phoenix 6
Cape Town 5
Guarulhos 5
Hải Dương 5
Osasco 5
Porto Alegre 5
Rome 5
Stockholm 5
São José do Rio Preto 5
Uberlândia 5
Vienna 5
Atlanta 4
Boston 4
Brussels 4
Casablanca 4
Curitiba 4
Duque de Caxias 4
Elk Grove Village 4
Fortaleza 4
Franca 4
Goiânia 4
Hyderabad 4
Jakarta 4
Lappeenranta 4
Mumbai 4
New Delhi 4
Ninh Bình 4
Ottawa 4
San Francisco 4
Tashkent 4
Yên Bái 4
Amsterdam 3
Bangkok 3
Belo Horizonte 3
Boardman 3
Buenos Aires 3
Cabo Frio 3
Cairo 3
Campinas 3
Chicago 3
City of London 3
Colombo 3
Durban 3
Florence 3
Guayaquil 3
Isidro Casanova 3
Itaquaquecetuba 3
Londrina 3
Maceió 3
Medellín 3
Mexico City 3
Newark 3
Orem 3
Paranaguá 3
Parauapebas 3
Paris 3
Quận Bình Thạnh 3
Rabat 3
Totale 2.899
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Nome #
Extracellular matrix defects in trichothiodystrophy 114
From laboratory tests to functional characterisation of Cockayne syndrome 112
Protein instability associated with AARS1 and MARS1 mutations causes Trichothiodystrophy 100
Human cells mutated in the repair/transcription factor TFIIH: a model system to elucidate the UV-regulated transcriptional network 98
Dalla conferma della diagnosi clinica dei pazienti alla dissezione dei pathways coinvolti nella risposta a stress ossidativo e radiazione UV 94
TFIIH stabilization recovers the DNA repair and transcription dysfunctions in thermo-sensitive trichothiodystrophy 90
XPD mutations in trichothiodystrophy hamper collagen VI expression and reveal a role of TFIIH in transcription derepression. 89
Does CSA play a role in mitochondrial quality control? 89
Reference genes for gene expression analysis in proliferating and differentiating human keratinocytes 84
Overexpression of Matrix Metalloproteinase-I (MMP-1) in primary skin fibroblasts from patients with trichothiodystrophy. 70
Reduced levels of prostaglandin I 2 synthase: a distinctive feature of the cancer-free trichothiodystrophy 68
Retinoic acid-induced growth arrest and differentiation of neuroblastoma cells are counteracted by N-myc and enhanced by max overexpressions 67
Genotype-phenotype Relationships in Patients with Trichothiodystrophy and Xeroderma Pigmentosum. 67
Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype 67
Temperature-sensitive mutations in XPD affecting DNA repair and transcription in patients with trichothiodystrophy 66
Heterogeneity and overlaps in nucleotide excision repair disorders 66
TFIIH-dependent transcriptional impairments contribute to the phenotypic differences associated with distinct XPD mutations 65
Cockayne syndrome group A and ferrochelatase finely tune ribosomal gene transcription and its response to UV irradiation 65
Digital PCR identifies changes in CDH1 (E-cadherin) transcription pattern in intestinal-type gastric cancer 64
Expansion of the clinical and molecular spectrum of an XPD-related disorder linked to biallelic mutations in ERCC2 gene 61
Malattie ereditarie difettive nella riparazione dei danni indotti sul DNA dai raggi ultravioletti. Corso di Aggiornamento: Difetti di riparo del DNA: meccanismi e patologie. 59
TFIIH-dependent MMP-1 overexpression in trichothiodystrophy leads to extracellular matrix alterations in patient skin 58
Riparazione del DNA e Malattie ereditarie 55
Cockayne Syndrome Type a (CSA) Protein Protects Primary Human Keratinocytes from Senescence. 55
GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient Trichothiodystrophy 55
Cockayne Syndrome Type a (CSA) Protein Protects Primary Human Keratinocytes from Senescence. 55
TFIIH-dependent transcriptional impairments contribute to the phenotypic differences associated with distinct XPD mutations 54
Functional consequences of mutated TFIIH complexes in primary keratinocytes from patients with trichothiodystrophy 53
Overexpression of parkin rescues the defective mitochondrial phenotype and the increased apoptosis of Cockayne Syndrome A cells. 53
Phenotypic variability in xeroderma pigmentosum group G: An uncommon case with severe prenatal-onset Cockayne syndrome features 52
Functional and clinical relevance of novel mutations in a large cohort of patients with Cockayne syndrome. 52
Studies on the ATP Binding Site of Fyn Kinase for the Identification of New Inhibitors and Their Evaluation as Potential Agents against Tauopathies and Tumors 51
The role of mitochondrial dysfunction in Cockayne Syndrome 49
TFIIH-dependent transcription deregulation hampers the extracellular matrix in trichothiodystrophy 49
TFIIH mutations can impact on translational fidelity of the ribosome 49
Genotype-phenotype relationships in trichothiodystrophy patients with novel splicing mutations in the XPD Gene. 46
From Structure to Phenotype: Impact of Collagen Alterations on Human Health 45
Ribosomal Dysfunction Is a Common Pathomechanism in Different Forms of Trichothiodystrophy 44
Does CSA play a role in mitochondrial quality control? 43
Epigenetic Regulation of Skin Cells in Natural Aging and Premature Aging Diseases 43
Reduced amounts of collagen type VI reveal extracellular matrix defects in trichothiodystrophy and a new role of TFIIH in transcription derepression 42
The role of CSA in the response to oxidative DNA damage in human cells. 41
Functional alterations in trichothiodystrophy: Overexpression of Matrix Metalloproteinase-I (MMP-1) in primary skin fibroblasts 40
TTD transcriptional defects are responsible for extracellular matrix alterations 40
Rac3-induced neuritogenesis requires binding to Neurabin I. 40
Functional characterization of temperature-sensitive XPD mutations in trichothiodystrophy patients with fever-dependent worsening of clinical features 38
The Eph receptor family: Axonal guidance by contact repulsion 36
Identificazione e caratterizzazione di pazienti difettivi nella riparazione del DNA 36
Malattie ereditarie difettive nella risposta al danno indotto da radiazioni UV 36
Insights gained through clinical and molecular analysis of patients affected by trichothiodystrophy and Cockayne syndrome. 35
Trichothiodystrophy: From basic mechanisms to clinical implications. 35
Malattie ereditarie difettive nella riparazione dei danni indotti sul DNA dai raggi ultravioletti. Corso di Aggiornamento: Difetti di riparo del DNA: meccanismi e patologie. 35
Transcriptional alterations in trichotiodystrophy affect different components of the extracellular matrix 34
TFIIH-mutated cells as a model system to dissect the multiple roles of TFIIH in chromatin dynamics 34
La tricotiodistrofia, una malattia modello per studiare i meccanismi d azione del complesso trascrizionale TFIIH 34
A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage 32
Reduced amounts of collagen type VI reveal extracellular matrix defects in trichothiodystrophy and a new role of TFIIH in transcription derepression 32
Functional characterization of temperature-sensitive XPD mutations in TTD patients showing fever-dependent worsening of clinical features 32
A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage 30
A third complementation group of UV-sensitive syndrome with a mutation in the CSA gene 30
Xeroderma pigmentosum, sindrome di Cockayne, tricotiodistrofia: caratterizzazione del difetto presente nei pazienti a livello cellulare, genetico e molecolare. 30
Aspetti clinici e molecolari della tricotiodistrofia 29
Insights into the general transcription factor TFIIE 29
Transcriptional defects in keratinocytes of patients affected by trichothiodystrophy. 29
Malattie ereditarie difettive nella riparazione del DNA: dal quadro clinico agli ultimi aspetti della ricerca di base e applicata 29
Transfer of a human chromosomal vector from a hamster cell line to a mouse embryonic stem cell line. 29
A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage 29
Defining the molecular basis of gene expression deregulation in human disorders, the example of UV-damage repair syndromes 28
Basis of the puzzling variety of the clinical features of NER defective disorders 28
Relationships between the general transcription factor TFIIE and the transcription/repair complex TFIIH 28
Gene expression analysis by microarrays in patients affected by trichothiodystrophy. 28
Functional alterations in trichothiodystrophy. 27
Expression of TTDN1 in different cell types from patients affected by trichothiodystrophy. 27
Funzioni difettive nella tricotiodistrofia. 27
Sek4 and Nuk receptors cooperate in guidance of commissural axons and in palate formation 27
A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage. 27
Alterazioni trascrizionali associate a mutazioni in XPD 26
New patient material. 26
New patient material. 25
Altered collagen VI transcription in primary fibroblasts from patients with trichothiodystrophy reveals a new role of TFIIH in transcription derepression 25
Transcriptional defects in keratinocytes of patients affected by trichothiodystrophy. 25
Two novel mutations in XPD associated with trichothiodystrophy result in temperature-dependent dysfunction of the transcription/repair complex TFIIH 25
Genetic, molecular and functional characterization of Cockayne syndrome, a rare transcription/repair defective hereditary disease 25
Similarities and differences in the way transmembrane-type ligands interact with the Elk subclass of Eph receptors 24
Insights into genotype-phenotype relationships in the repair/transcription syndrome trichothiodystrophy 24
Insights into genotype-phenotype relationships in the repair/transcription syndrome trichothiodystrophy 24
The Basal Transcription Factor TFIIE. 24
CS-B patients with unusual clinical features. 24
A third complementation group of UV-sensitive syndrome with a mutation in the CSA gene 23
A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage 23
Retinoic acid-induced growth arrest and differentiation of neuroblastoma cells are counteracted by N-myc and enhanced by max overexpressions 23
Functional alterations in trichothiodystrophy. 23
Insights into the general transcription factor TFIIE. 23
Difetti trascrizionali nella tricotiodistrofia 22
Complexity of the clinical outcomes of inborn defects in nucleotide-excision repair 22
Rab17 regulates membrane trafficking through apical recycling endosomes in polarized epithelial cells 21
Deficiencies in DNA repair and transcription in patients affected by trichothiodystrophy 21
Tricotiodistrofia e difetti nel differenziamento epidermico 20
Relevance of the extracellular matrix in the puzzling genotype-phenotype relationships of XPD mutations 20
Difetti trascrizionali nella tricotiodistrofia a carico della matrice extracellulare 20
Totale 4.337
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Categoria #
all - tutte 14.207
article - articoli 6.011
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 20.218
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202410 0 0 0 0 0 0 0 0 1 1 6 2
2024/20251.962 3 6 128 61 634 160 4 128 82 58 386 312
2025/20262.475 117 489 218 394 454 78 289 100 115 114 79 28
Totale 4.447