CNR Institutional Research Information System

ORIOLI, DONATA
 Distribuzione geografica
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Continente #
AS - Asia 2.098
NA - Nord America 2.085
SA - Sud America 522
EU - Europa 477
AF - Africa 51
Continente sconosciuto - Info sul continente non disponibili 46
OC - Oceania 6
Totale 5.285
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Nazione #
US - Stati Uniti d'America 2.008
SG - Singapore 859
CN - Cina 482
BR - Brasile 410
VN - Vietnam 268
HK - Hong Kong 174
IT - Italia 152
FR - Francia 126
KR - Corea 100
IN - India 47
GB - Regno Unito 41
CA - Canada 38
AR - Argentina 36
BD - Bangladesh 35
JP - Giappone 35
DE - Germania 33
NL - Olanda 31
ZA - Sudafrica 18
CO - Colombia 17
EC - Ecuador 17
MX - Messico 17
FI - Finlandia 16
ID - Indonesia 16
IL - Israele 16
MA - Marocco 14
VE - Venezuela 12
IE - Irlanda 10
PY - Paraguay 10
ES - Italia 9
IQ - Iraq 9
RU - Federazione Russa 8
TR - Turchia 8
JM - Giamaica 7
PK - Pakistan 7
TH - Thailandia 7
UA - Ucraina 7
UY - Uruguay 7
CL - Cile 6
EG - Egitto 6
LT - Lituania 6
AT - Austria 5
AU - Australia 5
PL - Polonia 5
SE - Svezia 5
BE - Belgio 4
CH - Svizzera 4
PE - Perù 4
PH - Filippine 4
SA - Arabia Saudita 4
UZ - Uzbekistan 4
CR - Costa Rica 3
MY - Malesia 3
OM - Oman 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
SV - El Salvador 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
GF - Guiana Francese 1
KW - Kuwait 1
KY - Cayman, isole 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
Totale 5.239
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Città #
Santa Clara 721
Singapore 491
Hefei 238
Hong Kong 172
San Jose 160
Council Bluffs 110
Lauterbourg 104
Seoul 100
Ho Chi Minh City 96
Ashburn 91
Dallas 72
Hanoi 69
Beijing 62
Los Angeles 59
Pavia 35
Milan 34
Princeton 34
New York 33
São Paulo 28
Phoenix 26
Abbeville 23
Rio de Janeiro 19
Tokyo 18
Frankfurt am Main 16
Houston 15
Minamishinagawa 15
Buffalo 13
Chicago 13
Haiphong 13
Helsinki 12
London 12
Toronto 12
Bengaluru 11
Biên Hòa 9
Chennai 9
Dublin 9
Portsmouth 8
Quito 8
Atlanta 7
Brasília 7
Charlotte 7
Cremona 7
Da Nang 7
Düsseldorf 7
Florence 7
Rome 7
Washington 7
Asunción 6
Campina Grande 6
Figino 6
Johannesburg 6
Montevideo 6
Newark 6
Philadelphia 6
San Francisco 6
The Dalles 6
Cape Town 5
Denver 5
Guarulhos 5
Hải Dương 5
Naples 5
Osasco 5
Porto Alegre 5
Stockholm 5
São José do Rio Preto 5
Uberlândia 5
Vienna 5
Wilmington 5
Baltimore 4
Bangkok 4
Bogotá 4
Boston 4
Brooklyn 4
Brussels 4
Casablanca 4
Curitiba 4
Dhaka 4
Duque de Caxias 4
Elk Grove Village 4
Fort Lauderdale 4
Fortaleza 4
Franca 4
Goiânia 4
Guayaquil 4
Hyderabad 4
Jakarta 4
Lappeenranta 4
Las Vegas 4
Miami 4
Mumbai 4
New Delhi 4
Ninh Bình 4
Ottawa 4
Sorocaba 4
Tashkent 4
Yên Bái 4
Amsterdam 3
Belo Horizonte 3
Birmingham 3
Boardman 3
Totale 3.271
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Nome #
Extracellular matrix defects in trichothiodystrophy 122
From laboratory tests to functional characterisation of Cockayne syndrome 121
Cockayne Syndrome Type a (CSA) Protein Protects Primary Human Keratinocytes from Senescence. 120
Protein instability associated with AARS1 and MARS1 mutations causes Trichothiodystrophy 107
Human cells mutated in the repair/transcription factor TFIIH: a model system to elucidate the UV-regulated transcriptional network 105
XPD mutations in trichothiodystrophy hamper collagen VI expression and reveal a role of TFIIH in transcription derepression. 103
TFIIH stabilization recovers the DNA repair and transcription dysfunctions in thermo-sensitive trichothiodystrophy 101
Dalla conferma della diagnosi clinica dei pazienti alla dissezione dei pathways coinvolti nella risposta a stress ossidativo e radiazione UV 99
Does CSA play a role in mitochondrial quality control? 99
Reference genes for gene expression analysis in proliferating and differentiating human keratinocytes 97
Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype 79
Overexpression of Matrix Metalloproteinase-I (MMP-1) in primary skin fibroblasts from patients with trichothiodystrophy. 75
Functional and clinical relevance of novel mutations in a large cohort of patients with Cockayne syndrome. 75
Cockayne syndrome group A and ferrochelatase finely tune ribosomal gene transcription and its response to UV irradiation 75
Retinoic acid-induced growth arrest and differentiation of neuroblastoma cells are counteracted by N-myc and enhanced by max overexpressions 74
Reduced levels of prostaglandin I 2 synthase: a distinctive feature of the cancer-free trichothiodystrophy 74
TFIIH-dependent transcriptional impairments contribute to the phenotypic differences associated with distinct XPD mutations 73
Heterogeneity and overlaps in nucleotide excision repair disorders 73
Expansion of the clinical and molecular spectrum of an XPD-related disorder linked to biallelic mutations in ERCC2 gene 73
Digital PCR identifies changes in CDH1 (E-cadherin) transcription pattern in intestinal-type gastric cancer 72
Temperature-sensitive mutations in XPD affecting DNA repair and transcription in patients with trichothiodystrophy 71
Genotype-phenotype Relationships in Patients with Trichothiodystrophy and Xeroderma Pigmentosum. 71
The role of mitochondrial dysfunction in Cockayne Syndrome 68
TFIIH-dependent MMP-1 overexpression in trichothiodystrophy leads to extracellular matrix alterations in patient skin 67
GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient Trichothiodystrophy 67
Overexpression of parkin rescues the defective mitochondrial phenotype and the increased apoptosis of Cockayne Syndrome A cells. 66
Phenotypic variability in xeroderma pigmentosum group G: An uncommon case with severe prenatal-onset Cockayne syndrome features 65
Malattie ereditarie difettive nella riparazione dei danni indotti sul DNA dai raggi ultravioletti. Corso di Aggiornamento: Difetti di riparo del DNA: meccanismi e patologie. 63
Functional consequences of mutated TFIIH complexes in primary keratinocytes from patients with trichothiodystrophy 63
TFIIH mutations can impact on translational fidelity of the ribosome 63
TFIIH-dependent transcriptional impairments contribute to the phenotypic differences associated with distinct XPD mutations 63
Cockayne Syndrome Type a (CSA) Protein Protects Primary Human Keratinocytes from Senescence. 63
Riparazione del DNA e Malattie ereditarie 59
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 59
Genotype-phenotype relationships in trichothiodystrophy patients with novel splicing mutations in the XPD Gene. 59
TFIIH-dependent transcription deregulation hampers the extracellular matrix in trichothiodystrophy 58
Ribosomal Dysfunction Is a Common Pathomechanism in Different Forms of Trichothiodystrophy 55
From Structure to Phenotype: Impact of Collagen Alterations on Human Health 52
Does CSA play a role in mitochondrial quality control? 51
Epigenetic Regulation of Skin Cells in Natural Aging and Premature Aging Diseases 51
Rac3-induced neuritogenesis requires binding to Neurabin I. 51
Reduced amounts of collagen type VI reveal extracellular matrix defects in trichothiodystrophy and a new role of TFIIH in transcription derepression 50
The role of CSA in the response to oxidative DNA damage in human cells. 49
Trichothiodystrophy: From basic mechanisms to clinical implications. 47
TTD transcriptional defects are responsible for extracellular matrix alterations 46
Functional alterations in trichothiodystrophy: Overexpression of Matrix Metalloproteinase-I (MMP-1) in primary skin fibroblasts 45
A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage. 45
Malattie ereditarie difettive nella risposta al danno indotto da radiazioni UV 44
The Eph receptor family: Axonal guidance by contact repulsion 42
La tricotiodistrofia, una malattia modello per studiare i meccanismi d azione del complesso trascrizionale TFIIH 42
Functional characterization of temperature-sensitive XPD mutations in trichothiodystrophy patients with fever-dependent worsening of clinical features 41
A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage 41
Identificazione e caratterizzazione di pazienti difettivi nella riparazione del DNA 41
Malattie ereditarie difettive nella riparazione dei danni indotti sul DNA dai raggi ultravioletti. Corso di Aggiornamento: Difetti di riparo del DNA: meccanismi e patologie. 41
Reduced amounts of collagen type VI reveal extracellular matrix defects in trichothiodystrophy and a new role of TFIIH in transcription derepression 40
TFIIH-mutated cells as a model system to dissect the multiple roles of TFIIH in chromatin dynamics 39
Insights gained through clinical and molecular analysis of patients affected by trichothiodystrophy and Cockayne syndrome. 39
Functional characterization of temperature-sensitive XPD mutations in TTD patients showing fever-dependent worsening of clinical features 38
A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage 37
A third complementation group of UV-sensitive syndrome with a mutation in the CSA gene 37
Transcriptional alterations in trichotiodystrophy affect different components of the extracellular matrix 37
A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage 36
Xeroderma pigmentosum, sindrome di Cockayne, tricotiodistrofia: caratterizzazione del difetto presente nei pazienti a livello cellulare, genetico e molecolare. 35
Funzioni difettive nella tricotiodistrofia. 35
Malattie ereditarie difettive nella riparazione del DNA: dal quadro clinico agli ultimi aspetti della ricerca di base e applicata 35
Two novel mutations in XPD associated with trichothiodystrophy result in temperature-dependent dysfunction of the transcription/repair complex TFIIH 35
Gene expression analysis by microarrays in patients affected by trichothiodystrophy. 35
Aspetti clinici e molecolari della tricotiodistrofia 34
Insights into the general transcription factor TFIIE 34
Transcriptional defects in keratinocytes of patients affected by trichothiodystrophy. 34
Functional alterations in trichothiodystrophy. 33
Transfer of a human chromosomal vector from a hamster cell line to a mouse embryonic stem cell line. 33
New patient material. 33
Expression of TTDN1 in different cell types from patients affected by trichothiodystrophy. 32
Defining the molecular basis of gene expression deregulation in human disorders, the example of UV-damage repair syndromes 32
Basis of the puzzling variety of the clinical features of NER defective disorders 32
Transcriptional defects in keratinocytes of patients affected by trichothiodystrophy. 32
Genetic, molecular and functional characterization of Cockayne syndrome, a rare transcription/repair defective hereditary disease 32
Alterazioni trascrizionali associate a mutazioni in XPD 31
Sek4 and Nuk receptors cooperate in guidance of commissural axons and in palate formation 31
The Basal Transcription Factor TFIIE. 31
Relationships between the general transcription factor TFIIE and the transcription/repair complex TFIIH 31
Insights into genotype-phenotype relationships in the repair/transcription syndrome trichothiodystrophy 30
New patient material. 29
Altered collagen VI transcription in primary fibroblasts from patients with trichothiodystrophy reveals a new role of TFIIH in transcription derepression 29
Complexity of the clinical outcomes of inborn defects in nucleotide-excision repair 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
Difetti trascrizionali nella tricotiodistrofia a carico della matrice extracellulare 29
Functional alterations in trichothiodystrophy. 29
Similarities and differences in the way transmembrane-type ligands interact with the Elk subclass of Eph receptors 28
Insights into genotype-phenotype relationships in the repair/transcription syndrome trichothiodystrophy 28
Retinoic acid-induced growth arrest and differentiation of neuroblastoma cells are counteracted by N-myc and enhanced by max overexpressions 28
CS-B patients with unusual clinical features. 28
Insights into the general transcription factor TFIIE. 28
Tricotiodistrofia e difetti nel differenziamento epidermico 27
A third complementation group of UV-sensitive syndrome with a mutation in the CSA gene 27
Difetti trascrizionali nella tricotiodistrofia 26
Genetic, molecular and functional characterization of Cockayne syndrome, a rare transcription/repair defective hereditary disease 26
Relevance of the extracellular matrix in the puzzling genotype-phenotype relationships of XPD mutations 25
Rab17 regulates membrane trafficking through apical recycling endosomes in polarized epithelial cells 25
Totale 5.139
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Categoria #
all - tutte 17.284
article - articoli 7.426
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 24.710
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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
2026/2027823 165 169 248 241 0 0 0 0 0 0 0 0
Totale 5.285