CAPPATO, SERENA
 Distribuzione geografica
Continente #
EU - Europa 1.656
AS - Asia 124
SA - Sud America 11
NA - Nord America 7
AF - Africa 2
Totale 1.800
Nazione #
IT - Italia 1.653
SG - Singapore 49
CN - Cina 34
VN - Vietnam 32
HK - Hong Kong 6
BR - Brasile 5
US - Stati Uniti d'America 5
AR - Argentina 4
MX - Messico 2
CL - Cile 1
DE - Germania 1
DZ - Algeria 1
HR - Croazia 1
IN - India 1
IR - Iran 1
NL - Olanda 1
PY - Paraguay 1
SN - Senegal 1
TJ - Tagikistan 1
Totale 1.800
Città #
Genova 780
Genoa 631
Vado Ligure 116
Rapallo 109
Singapore 14
Beijing 13
Bordighera 13
Ho Chi Minh City 13
Hong Kong 6
Hanoi 5
Ashburn 4
Haiphong 4
Biên Hòa 2
Mexico City 2
São Paulo 2
Tianjin 2
Algiers 1
Asunción 1
Balneário Camboriú 1
Bắc Ninh 1
Can Tho 1
Coronel 1
Da Nang 1
Dakar 1
Dallas 1
General Rodríguez 1
Jaguariúna 1
Jequié 1
Khujand 1
Linfen 1
Ningbo 1
Nuremberg 1
Ramos Mejía 1
Resistencia 1
Shanghai 1
Thái Nguyên 1
Ulhasnagar 1
Victoria 1
Xiamen 1
Xianyang 1
Yên Bái 1
Zagreb 1
Totale 1.742
Nome #
High-throughput screening for modulators of ACVR1 transcription: discovery of potential therapeutics for fibrodysplasia ossificans progressiva. 263
The Horizon of a Therapy for Rare Genetic Diseases: A "Druggable" Future for Fibrodysplasia Ossificans Progressiva 194
Identification and characterization of regulatory elements in the promoter of ACVR1, the gene mutated in Fibrodysplasia Ossificans Progressiva. 171
STUDY OF THE ACVR1 GENE EXPRESSION AND REGULATION: THE PROMOTER REGION AND THE 5'-UTR 160
The Role of the 3′UTR Region in the Regulation of the ACVR1/Alk-2 Gene Expression 152
Hints on transcriptional control of essential players in heterotopic ossification of Fibrodysplasia Ossificans Progressiva 140
Identification of reference genes for quantitative PCR during C3H10T1/2 chondrogenic differentiation 139
Peripheral blood mononuclear cell immunophenotyping in fibrodysplasia ossificans progressiva patients: Evidence for monocyte DNAM1 up-regulation 130
P63 modulates the expression of the WDFY2 gene which is implicated in cancer regulation and limb development 98
A case of Fibrodysplasia Ossificans Progressiva associated with a novel variant of the ACVR1 gene 92
Identification of novel anti-fibrotic agents 83
Genetic and Acquired Heterotopic Ossification: A Translational Tale of Mice and Men 72
Functional analysis of a novel 5’UTR variant of the LMX1B gene associated with a familial case of Nail-Patella Syndrome 58
Antisense oligonucleotides as a precision therapy for developmental and epileptic encephalopathies 39
Chromosomal Deletion Involving ANKRD26 Leads to Expression of a Fusion Protein Responsible for ANKRD26-Related Thrombocytopenia 22
Functional Characterization of a Novel Intronic Variant in PIEZO2 in a Recessive Form of Distal Arthrogryposis With Impaired Proprioception and Touch (DAIPT) 20
A hypomorphic FLVCR2 variant resulting in moderate transport deficiency causes hydranencephaly syndrome with brain calcifications 18
Totale 1.851
Categoria #
all - tutte 6.150
article - articoli 5.136
book - libri 0
conference - conferenze 1.014
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 12.300


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021105 0 0 0 0 0 30 9 11 15 12 16 12
2021/2022142 5 9 1 13 8 18 7 26 12 16 5 22
2022/2023141 15 16 0 17 17 16 2 10 22 2 14 10
2023/2024134 6 6 1 14 11 31 10 14 4 10 5 22
2024/2025443 7 21 11 13 45 55 83 92 37 15 37 27
2025/2026310 70 16 43 46 131 4 0 0 0 0 0 0
Totale 1.851