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

ROGAIA, Daniela
 Distribuzione geografica
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Continente #
NA - Nord America 532
EU - Europa 382
AS - Asia 221
OC - Oceania 1
Totale 1.136
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Nazione #
US - Stati Uniti d'America 529
IE - Irlanda 105
UA - Ucraina 79
SG - Singapore 71
VN - Vietnam 59
IT - Italia 50
HK - Hong Kong 44
SE - Svezia 44
CN - Cina 31
DE - Germania 31
FI - Finlandia 24
RU - Federazione Russa 16
GB - Regno Unito 12
KR - Corea 9
BE - Belgio 5
AT - Austria 4
CA - Canada 3
CH - Svizzera 3
LB - Libano 3
FR - Francia 2
PL - Polonia 2
TR - Turchia 2
AD - Andorra 1
CZ - Repubblica Ceca 1
GR - Grecia 1
IM - Isola di Man 1
JP - Giappone 1
NL - Olanda 1
NZ - Nuova Zelanda 1
UZ - Uzbekistan 1
Totale 1.136
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Città #
Chandler 114
Dublin 105
Dong Ket 59
Singapore 57
Hong Kong 44
San Mateo 44
Jacksonville 34
Boardman 33
Ann Arbor 31
Santa Clara 30
Medford 23
Princeton 23
Altamura 19
Lawrence 19
Des Moines 18
Perugia 18
Wilmington 17
Beijing 11
Andover 10
Seoul 9
Helsinki 8
Ashburn 5
Brussels 5
Falls Church 5
New York 4
Redwood City 4
Saint Petersburg 4
Los Angeles 3
Norwalk 3
Ottawa 3
San Diego 3
Izmir 2
Mountain View 2
Munich 2
Woodbridge 2
Andorra la Vella 1
Auburn Hills 1
Benevento 1
Birmingham 1
Brno 1
Charlotte 1
Dallas 1
Douglas 1
Due West 1
Fremont 1
Grefrath 1
Groningen 1
Gulfport 1
Houston 1
Hwang Chow 1
Kiev 1
Landshut 1
Lausanne 1
Ludwigshafen 1
Milan 1
Moscow 1
Nuremberg 1
Redmond 1
Rovato 1
San Paolo di Civitate 1
Shanghai 1
Stockholm 1
Tasman 1
Tokyo 1
Totale 802
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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 91
Molecular Pathogenesis of Acute Promyelocytic Leukaemia. 67
Deletion 2p15-16.1 syndrome: Case Report and Review 66
Autosomal Dominant PTH Gene Signal Sequence Mutation in a Family With Familial Isolated Hypoparathyroidism 65
Acute promyelocytic leukemia cells resistant to retinoic acid show further perturbation of the RARa signal transduction system. 63
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. 59
Aicardi Syndrome Associated with Autosomal Genomic Imbalance: Coincidence or Evidence for Autosomal Inheritance with Sex-Limited Expression? 57
Effects on differentiation by the promyelocytic leukemia PML/RARa protein depend on the fusion of the PML protein-dimerization and RARa DNA binding domains. 56
Pathogenetic Relevance Of The Acute Promyelocytic Leukemia-Specific PML/RARa Fusion Protein 55
Terminal megakaryocytic differentiationof TF-1 cells is induced by phorbol esters and thrombopoietin and is blocked by expression of PML/RARa fusion protein. 53
Craniometaphyseal dysplasia with severe craniofacial involvement shows homozygosity at 6q21-22.1 locus. 48
Familial pericentric inversion of chromosome 18: intrafamilial variability of the recombinant dup(18q). 48
Lethal and non-lethal GLIS1 related malformation syndromes 45
The localization of the HRX proteinto specific nuclear subomains is altered by fusion with its eps15 translocation partner 43
Molecular Genetics Of The T(15;17) Of Acute Promyelocytic Leukemia 43
Nablus mask-like facial syndrome: deletion of chromosome 8q22.1 is necessary but not sufficient to cause the phenotype. 43
Trisomy 2 mosaicism with caudal dysgenesis, Hirschsprung disease, and micro-anophthalmia. 41
Recurrent ∼100 Kb microdeletion in the chromosomal region 14q11.2, involving CHD8 gene, is associated with autism and macrocephaly. 41
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 39
Identification of a dna methylation episignature in the 22q11.2 deletion syndrome 38
Schilbach-Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene 35
A patient with novel MBOAT7 variant: The cerebellar atrophy is progressive and displays a peculiar neurometabolic profile 34
A rare case of brachyolmia with amelogenesis imperfecta caused by a new pathogenic splicing variant in ltbp3 29
A New De Novo Missense Variant of the TET3 Gene in a Patient with Epilepsy and Macrocephaly 8
Totale 1.167
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Categoria #
all - tutte 5.467
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 5.467
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202060 0 0 0 0 9 1 14 1 16 14 0 5
2020/2021214 4 13 5 16 49 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
2024/2025118 11 28 32 14 33 0 0 0 0 0 0 0
Totale 1.167