CNR Institutional Research Information System

ORIOLI, DONATA
 Distribuzione geografica
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Continente #
AS - Asia 2.087
NA - Nord America 1.563
SA - Sud America 502
EU - Europa 453
AF - Africa 51
Continente sconosciuto - Info sul continente non disponibili 46
OC - Oceania 6
Totale 4.708
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Nazione #
US - Stati Uniti d'America 1.498
SG - Singapore 859
CN - Cina 482
BR - Brasile 401
VN - Vietnam 268
HK - Hong Kong 174
IT - Italia 132
FR - Francia 126
KR - Corea 100
IN - India 47
GB - Regno Unito 39
AR - Argentina 36
JP - Giappone 35
DE - Germania 33
BD - Bangladesh 31
CA - Canada 31
NL - Olanda 31
ZA - Sudafrica 18
FI - Finlandia 16
IL - Israele 16
MX - Messico 15
EC - Ecuador 14
MA - Marocco 14
CO - Colombia 13
ID - Indonesia 13
IE - Irlanda 10
PY - Paraguay 10
IQ - Iraq 9
VE - Venezuela 9
ES - Italia 8
RU - Federazione Russa 8
PK - Pakistan 7
UA - Ucraina 7
UY - Uruguay 7
CL - Cile 6
EG - Egitto 6
JM - Giamaica 6
LT - Lituania 6
TH - Thailandia 6
TR - Turchia 6
AT - Austria 5
AU - Australia 5
PL - Polonia 5
SE - Svezia 5
BE - Belgio 4
PE - Perù 4
SA - Arabia Saudita 4
UZ - Uzbekistan 4
CH - Svizzera 3
CR - Costa Rica 3
MY - Malesia 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
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
BF - Burkina Faso 1
BG - Bulgaria 1
BH - Bahrain 1
CI - Costa d'Avorio 1
CU - Cuba 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
NI - Nicaragua 1
NZ - Nuova Zelanda 1
PA - Panama 1
QA - Qatar 1
SC - Seychelles 1
SV - El Salvador 1
Totale 4.662
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Città #
Santa Clara 718
Singapore 491
Hefei 238
Hong Kong 172
San Jose 124
Lauterbourg 104
Seoul 100
Ho Chi Minh City 96
Ashburn 76
Hanoi 69
Dallas 68
Beijing 62
Los Angeles 55
Pavia 35
Milan 32
São Paulo 28
New York 27
Rio de Janeiro 19
Tokyo 18
Frankfurt am Main 16
Minamishinagawa 15
Buffalo 13
Haiphong 13
Helsinki 12
London 12
Bengaluru 11
Houston 11
Toronto 11
Biên Hòa 9
Chennai 9
Dublin 9
Phoenix 9
Portsmouth 8
Brasília 7
Cremona 7
Da Nang 7
Düsseldorf 7
Quito 7
Rome 7
Asunción 6
Campina Grande 6
Council Bluffs 6
Johannesburg 6
Montevideo 6
San Francisco 6
The Dalles 6
Cape Town 5
Figino 5
Florence 5
Guarulhos 5
Hải Dương 5
Newark 5
Osasco 5
Porto Alegre 5
Stockholm 5
São José do Rio Preto 5
Uberlândia 5
Vienna 5
Washington 5
Atlanta 4
Bangkok 4
Boston 4
Brussels 4
Casablanca 4
Charlotte 4
Chicago 4
Curitiba 4
Denver 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
Sorocaba 4
Tashkent 4
Wilmington 4
Yên Bái 4
Amsterdam 3
Baltimore 3
Belo Horizonte 3
Boardman 3
Bogotá 3
Brooklyn 3
Buenos Aires 3
Cabo Frio 3
Cairo 3
Campinas 3
City of London 3
Colombo 3
Dhaka 3
Durban 3
Guayaquil 3
Isidro Casanova 3
Totale 2.987
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Nome #
Cockayne Syndrome Type a (CSA) Protein Protects Primary Human Keratinocytes from Senescence. 116
Extracellular matrix defects in trichothiodystrophy 116
From laboratory tests to functional characterisation of Cockayne syndrome 115
Protein instability associated with AARS1 and MARS1 mutations causes Trichothiodystrophy 103
Human cells mutated in the repair/transcription factor TFIIH: a model system to elucidate the UV-regulated transcriptional network 100
Dalla conferma della diagnosi clinica dei pazienti alla dissezione dei pathways coinvolti nella risposta a stress ossidativo e radiazione UV 95
TFIIH stabilization recovers the DNA repair and transcription dysfunctions in thermo-sensitive trichothiodystrophy 95
XPD mutations in trichothiodystrophy hamper collagen VI expression and reveal a role of TFIIH in transcription derepression. 91
Does CSA play a role in mitochondrial quality control? 90
Reference genes for gene expression analysis in proliferating and differentiating human keratinocytes 89
Overexpression of Matrix Metalloproteinase-I (MMP-1) in primary skin fibroblasts from patients with trichothiodystrophy. 70
Cockayne syndrome group A and ferrochelatase finely tune ribosomal gene transcription and its response to UV irradiation 70
Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype 70
Retinoic acid-induced growth arrest and differentiation of neuroblastoma cells are counteracted by N-myc and enhanced by max overexpressions 68
Reduced levels of prostaglandin I 2 synthase: a distinctive feature of the cancer-free trichothiodystrophy 68
Heterogeneity and overlaps in nucleotide excision repair disorders 68
Temperature-sensitive mutations in XPD affecting DNA repair and transcription in patients with trichothiodystrophy 67
Genotype-phenotype Relationships in Patients with Trichothiodystrophy and Xeroderma Pigmentosum. 67
TFIIH-dependent transcriptional impairments contribute to the phenotypic differences associated with distinct XPD mutations 67
Digital PCR identifies changes in CDH1 (E-cadherin) transcription pattern in intestinal-type gastric cancer 67
Expansion of the clinical and molecular spectrum of an XPD-related disorder linked to biallelic mutations in ERCC2 gene 66
Functional and clinical relevance of novel mutations in a large cohort of patients with Cockayne syndrome. 62
GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient Trichothiodystrophy 61
The role of mitochondrial dysfunction in Cockayne Syndrome 60
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
Cockayne Syndrome Type a (CSA) Protein Protects Primary Human Keratinocytes from Senescence. 59
Overexpression of parkin rescues the defective mitochondrial phenotype and the increased apoptosis of Cockayne Syndrome A cells. 58
TFIIH-dependent MMP-1 overexpression in trichothiodystrophy leads to extracellular matrix alterations in patient skin 58
TFIIH-dependent transcriptional impairments contribute to the phenotypic differences associated with distinct XPD mutations 58
Functional consequences of mutated TFIIH complexes in primary keratinocytes from patients with trichothiodystrophy 56
Phenotypic variability in xeroderma pigmentosum group G: An uncommon case with severe prenatal-onset Cockayne syndrome features 55
Riparazione del DNA e Malattie ereditarie 55
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 53
TFIIH-dependent transcription deregulation hampers the extracellular matrix in trichothiodystrophy 53
Genotype-phenotype relationships in trichothiodystrophy patients with novel splicing mutations in the XPD Gene. 53
TFIIH mutations can impact on translational fidelity of the ribosome 53
From Structure to Phenotype: Impact of Collagen Alterations on Human Health 49
Reduced amounts of collagen type VI reveal extracellular matrix defects in trichothiodystrophy and a new role of TFIIH in transcription derepression 46
Epigenetic Regulation of Skin Cells in Natural Aging and Premature Aging Diseases 46
Ribosomal Dysfunction Is a Common Pathomechanism in Different Forms of Trichothiodystrophy 45
The role of CSA in the response to oxidative DNA damage in human cells. 44
Does CSA play a role in mitochondrial quality control? 44
Rac3-induced neuritogenesis requires binding to Neurabin I. 43
Functional alterations in trichothiodystrophy: Overexpression of Matrix Metalloproteinase-I (MMP-1) in primary skin fibroblasts 41
TTD transcriptional defects are responsible for extracellular matrix alterations 40
Trichothiodystrophy: From basic mechanisms to clinical implications. 40
The Eph receptor family: Axonal guidance by contact repulsion 39
Functional characterization of temperature-sensitive XPD mutations in trichothiodystrophy patients with fever-dependent worsening of clinical features 39
Identificazione e caratterizzazione di pazienti difettivi nella riparazione del DNA 38
La tricotiodistrofia, una malattia modello per studiare i meccanismi d azione del complesso trascrizionale TFIIH 37
Malattie ereditarie difettive nella riparazione dei danni indotti sul DNA dai raggi ultravioletti. Corso di Aggiornamento: Difetti di riparo del DNA: meccanismi e patologie. 37
Malattie ereditarie difettive nella risposta al danno indotto da radiazioni UV 37
TFIIH-mutated cells as a model system to dissect the multiple roles of TFIIH in chromatin dynamics 36
A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage 35
Insights gained through clinical and molecular analysis of patients affected by trichothiodystrophy and Cockayne syndrome. 35
Reduced amounts of collagen type VI reveal extracellular matrix defects in trichothiodystrophy and a new role of TFIIH in transcription derepression 34
Functional characterization of temperature-sensitive XPD mutations in TTD patients showing fever-dependent worsening of clinical features 34
Transcriptional alterations in trichotiodystrophy affect different components of the extracellular matrix 34
A third complementation group of UV-sensitive syndrome with a mutation in the CSA gene 33
A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage 32
Malattie ereditarie difettive nella riparazione del DNA: dal quadro clinico agli ultimi aspetti della ricerca di base e applicata 31
Xeroderma pigmentosum, sindrome di Cockayne, tricotiodistrofia: caratterizzazione del difetto presente nei pazienti a livello cellulare, genetico e molecolare. 30
Defining the molecular basis of gene expression deregulation in human disorders, the example of UV-damage repair syndromes 30
A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage. 30
Aspetti clinici e molecolari della tricotiodistrofia 29
Functional alterations in trichothiodystrophy. 29
Funzioni difettive nella tricotiodistrofia. 29
Insights into the general transcription factor TFIIE 29
Transcriptional defects in keratinocytes of patients affected by trichothiodystrophy. 29
Transfer of a human chromosomal vector from a hamster cell line to a mouse embryonic stem cell line. 29
Transcriptional defects in keratinocytes of patients affected by trichothiodystrophy. 29
New patient material. 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
Expression of TTDN1 in different cell types from patients affected by trichothiodystrophy. 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
Sek4 and Nuk receptors cooperate in guidance of commissural axons and in palate formation 27
Two novel mutations in XPD associated with trichothiodystrophy result in temperature-dependent dysfunction of the transcription/repair complex TFIIH 27
New patient material. 26
Alterazioni trascrizionali associate a mutazioni in XPD 26
Altered collagen VI transcription in primary fibroblasts from patients with trichothiodystrophy reveals a new role of TFIIH in transcription derepression 25
Insights into genotype-phenotype relationships in the repair/transcription syndrome trichothiodystrophy 25
The Basal Transcription Factor TFIIE. 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
A third complementation group of UV-sensitive syndrome with a mutation in the CSA gene 24
Retinoic acid-induced growth arrest and differentiation of neuroblastoma cells are counteracted by N-myc and enhanced by max overexpressions 24
CS-B patients with unusual clinical features. 24
Difetti trascrizionali nella tricotiodistrofia 23
Complexity of the clinical outcomes of inborn defects in nucleotide-excision repair 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
Functional alterations in trichothiodystrophy. 23
Insights into the general transcription factor TFIIE. 23
Relevance of the extracellular matrix in the puzzling genotype-phenotype relationships of XPD mutations 22
Genetic, molecular and functional characterization of Cockayne syndrome, a rare transcription/repair defective hereditary disease 22
Deficiencies in DNA repair and transcription in patients affected by trichothiodystrophy 22
Rab17 regulates membrane trafficking through apical recycling endosomes in polarized epithelial cells 21
Tricotiodistrofia e difetti nel differenziamento epidermico 20
Totale 4.591
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Categoria #
all - tutte 15.743
article - articoli 6.711
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 22.454
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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
2025/20262.490 117 489 218 394 454 78 289 100 115 114 79 43
2026/2027246 165 81 0 0 0 0 0 0 0 0 0 0
Totale 4.708