IRIS - Res&Arch Institutional Research Information System - Research & Archive

ROGAIA, Daniela
 Distribuzione geografica
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Continente #
NA - Nord America 666
EU - Europa 525
AS - Asia 517
SA - Sud America 66
AF - Africa 7
OC - Oceania 1
Totale 1.782
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Nazione #
US - Stati Uniti d'America 646
SG - Singapore 241
IE - Irlanda 105
CN - Cina 82
UA - Ucraina 80
HK - Hong Kong 76
DE - Germania 74
VN - Vietnam 71
BR - Brasile 57
IT - Italia 52
RU - Federazione Russa 51
FI - Finlandia 45
SE - Svezia 44
GB - Regno Unito 21
KR - Corea 19
FR - Francia 17
CA - Canada 13
AT - Austria 11
BE - Belgio 6
PL - Polonia 5
IN - India 4
IQ - Iraq 4
JP - Giappone 4
LT - Lituania 4
MX - Messico 4
AR - Argentina 3
CH - Svizzera 3
CL - Cile 3
DZ - Algeria 3
LB - Libano 3
TR - Turchia 3
BD - Bangladesh 2
ES - Italia 2
MA - Marocco 2
PK - Pakistan 2
AD - Andorra 1
BB - Barbados 1
CZ - Repubblica Ceca 1
DO - Repubblica Dominicana 1
EC - Ecuador 1
GR - Grecia 1
ID - Indonesia 1
IM - Isola di Man 1
JM - Giamaica 1
JO - Giordania 1
KG - Kirghizistan 1
LK - Sri Lanka 1
NL - Olanda 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PY - Paraguay 1
SN - Senegal 1
UZ - Uzbekistan 1
VE - Venezuela 1
ZA - Sudafrica 1
Totale 1.782
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Città #
Singapore 156
Chandler 114
Dublin 105
Hong Kong 76
Dong Ket 59
San Mateo 44
Jacksonville 34
Boardman 33
Ann Arbor 31
Munich 31
Santa Clara 30
Beijing 24
Medford 23
Princeton 23
Ashburn 21
Altamura 19
Lawrence 19
Seoul 19
Des Moines 18
Perugia 18
Wilmington 17
Turku 16
Helsinki 13
Andover 10
Moscow 10
New York 9
Ho Chi Minh City 7
Los Angeles 7
Nuremberg 7
Brussels 6
Denver 5
Falls Church 5
Ottawa 5
Piscataway 5
Columbus 4
Falkenstein 4
Frankfurt am Main 4
Montreal 4
Redwood City 4
Roubaix 4
Saint Petersburg 4
Tokyo 4
Belo Horizonte 3
London 3
Norwalk 3
Orem 3
Phoenix 3
Poplar 3
San Diego 3
San Francisco 3
Toronto 3
Vienna 3
Boston 2
Brooklyn 2
Campinas 2
Caraguatatuba 2
Changsha 2
Charlotte 2
Chennai 2
Da Nang 2
Houston 2
Izmir 2
Mexico City 2
Mountain View 2
Santiago 2
Seattle 2
Secaucus 2
Shanghai 2
Shijiazhuang 2
Sobral 2
St Petersburg 2
Suzano 2
São Paulo 2
The Dalles 2
Warsaw 2
Woodbridge 2
Wuhan 2
Adrogué 1
Agadir 1
Agrolândia 1
Amarah 1
Ambāla 1
Amman 1
Andorra la Vella 1
Ankara 1
Arroio Grande 1
As Samawah 1
Atlanta 1
Auburn Hills 1
Baghdad 1
Benevento 1
Bexley 1
Birmingham 1
Bishkek 1
Bloomington 1
Brno 1
Campinas do Sul 1
Campos dos Goytacazes 1
Candelária 1
Canoas 1
Totale 1.154
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Nome #
Formation of PML/RAR alpha high molecular weight nuclear complexes through the PML coiled-coil region is essential for the PML/RAR alpha-mediated retinoic acid response 120
Autosomal Dominant PTH Gene Signal Sequence Mutation in a Family With Familial Isolated Hypoparathyroidism 106
Acute promyelocytic leukemia cells resistant to retinoic acid show further perturbation of the RARa signal transduction system. 98
Deletion 2p15-16.1 syndrome: Case Report and Review 94
Molecular Pathogenesis of Acute Promyelocytic Leukaemia. 89
Effects on differentiation by the promyelocytic leukemia PML/RARa protein depend on the fusion of the PML protein-dimerization and RARa DNA binding domains. 86
Pathogenetic Relevance Of The Acute Promyelocytic Leukemia-Specific PML/RARa Fusion Protein 83
Recurrent ∼100 Kb microdeletion in the chromosomal region 14q11.2, involving CHD8 gene, is associated with autism and macrocephaly. 81
Lethal and non-lethal GLIS1 related malformation syndromes 80
Terminal megakaryocytic differentiationof TF-1 cells is induced by phorbol esters and thrombopoietin and is blocked by expression of PML/RARa fusion protein. 79
Aicardi Syndrome Associated with Autosomal Genomic Imbalance: Coincidence or Evidence for Autosomal Inheritance with Sex-Limited Expression? 78
The acute promyelocytic leukemia-specific PML/RAR alpha fusion protein reduces the frequency of commitment to apoptosis upon growth factor deprivation of GM-CSF-dependent myeloid cells. 73
Identification of a dna methylation episignature in the 22q11.2 deletion syndrome 73
Nablus mask-like facial syndrome: deletion of chromosome 8q22.1 is necessary but not sufficient to cause the phenotype. 70
Expanding the Clinical Spectrum of Sotos Syndrome in a Patient with the New "c.[5867T > A]+[=]"; "p.[Leu1956Gln]+[=]" NSD1 Missense Mutation and Complex Skin Hamartoma 70
Craniometaphyseal dysplasia with severe craniofacial involvement shows homozygosity at 6q21-22.1 locus. 69
Familial pericentric inversion of chromosome 18: intrafamilial variability of the recombinant dup(18q). 68
Molecular Genetics Of The T(15;17) Of Acute Promyelocytic Leukemia 66
Schilbach-Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene 62
Trisomy 2 mosaicism with caudal dysgenesis, Hirschsprung disease, and micro-anophthalmia. 61
A patient with novel MBOAT7 variant: The cerebellar atrophy is progressive and displays a peculiar neurometabolic profile 60
A rare case of brachyolmia with amelogenesis imperfecta caused by a new pathogenic splicing variant in ltbp3 60
The localization of the HRX proteinto specific nuclear subomains is altered by fusion with its eps15 translocation partner 51
A New De Novo Missense Variant of the TET3 Gene in a Patient with Epilepsy and Macrocephaly 37
Totale 1.814
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Categoria #
all - tutte 8.820
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 8.820
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021127 0 0 0 0 0 14 12 1 18 7 14 61
2021/2022173 3 30 12 10 8 1 2 54 4 3 20 26
2022/2023348 25 71 12 23 25 51 0 5 121 0 14 1
2023/2024173 11 17 15 3 5 4 40 0 11 3 24 40
2024/2025398 11 28 32 14 34 24 22 29 50 27 81 46
2025/2026367 63 43 37 82 124 18 0 0 0 0 0 0
Totale 1.814