GIOIA, ROBERTA
 Distribuzione geografica
Continente #
NA - Nord America 507
EU - Europa 332
AS - Asia 218
Totale 1.057
Nazione #
US - Stati Uniti d'America 505
CN - Cina 215
IE - Irlanda 126
FI - Finlandia 44
IT - Italia 39
UA - Ucraina 36
DE - Germania 33
SE - Svezia 27
GB - Regno Unito 14
BE - Belgio 12
CA - Canada 2
JP - Giappone 2
FR - Francia 1
IN - India 1
Totale 1.057
Città #
Chandler 148
Dublin 126
Ann Arbor 58
Jacksonville 52
Nanjing 46
Beijing 37
Ashburn 25
Nanchang 23
Shanghai 19
Helsinki 18
Princeton 18
Changsha 17
Hebei 17
Lawrence 17
Shenyang 17
Wilmington 17
Medford 15
Pavia 15
Woodbridge 13
Brussels 12
Dearborn 10
Jiaxing 10
Hangzhou 9
Boardman 8
Houston 8
New York 8
Tianjin 7
Fairfield 4
Los Angeles 4
Milan 4
Des Moines 3
Ningbo 3
Norwalk 2
Seattle 2
Tokyo 2
Washington 2
Baqiao 1
Chongqing 1
Ercolano 1
Falkenstein 1
Forest City 1
Genova 1
Kunming 1
Lanzhou 1
Munich 1
Nagold 1
Piscataway 1
Pune 1
Toronto 1
Verona 1
Xingtai 1
Totale 811
Nome #
Kinetic and structural evidences on human prolidase pathological mutants suggest strategies for enzyme functional rescue 102
Improved prolidase activity assay allowed enzyme kinetic characterization and faster prolidase deficiency diagnosis 95
Allele-specific Col1a1 silencing reduces mutant collagen in fibroblasts from Brtl mouse, a model for classical osteogenesis imperfecta. 88
Differential response to intracellular stress in the skin from osteogenesis imperfecta Brtl mice with lethal and non lethal phenotype: a proteomic approach 78
Impaired osteoblastogenesis in a murine model of dominant osteogenesis imperfecta: a new target for osteogenesis imperfecta pharmacological therapy 72
TREX1 C-terminal frameshift mutations in the systemic variant of retinal vasculopathy with cerebral leukodystrophy. 71
A Mn(II)-Mn(II) center in human prolidase 67
Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and Skin 66
Lack of prolidase causes a bone phenotype both in human and in mouse 63
Regulation of NAD(P) synthesis in Bacillus subtilis 58
The chaperone activity of 4PBA ameliorates the skeletal phenotype of Chihuahua, a zebrafish model for dominant osteogenesis imperfecta 58
Altered cytoskeletal organization characterized lethal but not surviving Brtl+/- mice: insight on phenotypic variability in osteogenesis imperfecta 56
Severely impaired bone material quality in chihuahua zebrafish resembles classical dominant human Osteogenesis Imperfecta 54
In utero transplantation of adult bone marrow decreases perinatal lethality and rescues the bone phenotype in the knock-in murine model for classical, dominant osteogenesis imperfecta 51
Crtap and p3h1 knock out zebrafish support defective collagen chaperoning as the cause of their osteogenesis imperfecta phenotype 49
Characterization of stress response in human retinal epithelial cells. 43
Knocking out TMEM38B in human foetal osteoblasts hFOB 1.19 by CRISPR/Cas9: A model for recessive OI type XIV 24
Zebrafish Tric-b is required for skeletal development and bone cells differentiation 10
Structure, evolution and expression of zebrafish cartilage oligomeric matrix protein (COMP, TSP5). CRISPR-Cas mutants show a dominant phenotype in myosepta 4
Totale 1.109
Categoria #
all - tutte 3.658
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 3.658


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020278 67 93 6 9 2 9 2 20 2 28 29 11
2020/2021109 10 11 6 10 2 12 2 17 7 14 13 5
2021/202288 2 2 2 4 2 1 2 6 4 3 17 43
2022/2023363 26 40 4 38 34 32 1 18 142 6 9 13
2023/2024128 18 32 4 5 9 23 6 12 1 4 8 6
Totale 1.109