MINERVINI, GIOVANNI
 Distribuzione geografica
Continente #
NA - Nord America 4.204
EU - Europa 470
AS - Asia 321
AF - Africa 1
OC - Oceania 1
Totale 4.997
Nazione #
US - Stati Uniti d'America 4.198
CN - Cina 211
IT - Italia 169
SE - Svezia 93
FI - Finlandia 88
SG - Singapore 56
DE - Germania 36
GB - Regno Unito 32
VN - Vietnam 32
IE - Irlanda 10
NL - Olanda 10
IN - India 9
FR - Francia 7
GR - Grecia 7
HK - Hong Kong 6
UA - Ucraina 5
SA - Arabia Saudita 4
CA - Canada 3
MX - Messico 3
BE - Belgio 2
CZ - Repubblica Ceca 2
PT - Portogallo 2
RO - Romania 2
RU - Federazione Russa 2
TR - Turchia 2
CY - Cipro 1
EE - Estonia 1
ES - Italia 1
NZ - Nuova Zelanda 1
PL - Polonia 1
SC - Seychelles 1
Totale 4.997
Città #
Fairfield 759
Chandler 445
Woodbridge 427
Ashburn 365
Ann Arbor 325
Seattle 316
Houston 305
Cambridge 272
Wilmington 241
Beijing 81
Padova 75
San Diego 66
Medford 60
Princeton 60
Helsinki 46
Des Moines 45
Boardman 35
Dong Ket 32
Singapore 32
Roxbury 25
Nanjing 23
New York 21
Lappeenranta 19
Guangzhou 17
Milan 12
Falls Church 11
London 10
Dublin 8
Redwood City 8
Belluno 7
Washington 7
Hebei 6
Jinan 6
Mira 6
Nanchang 6
Shenyang 6
Changsha 5
Chicago 5
Hounslow 5
Los Angeles 5
Norwalk 5
Paris 5
Fontanelle 4
Hong Kong 4
Jiaxing 4
Ogden 4
Pune 4
Riyadh 4
Acton 3
Balestrino 3
Borås 3
Hefei 3
Kharkiv 3
Kilburn 3
Lebanon 3
Legnago 3
Querétaro City 3
Rome 3
Shanghai 3
Taiyuan 3
Tappahannock 3
Treviso 3
Zhengzhou 3
Arzignano 2
Barletta 2
Casalfiumanese 2
Chiswick 2
Dearborn 2
Falkenstein 2
Fuzhou 2
Gallio 2
Jacksonville 2
Kraainem 2
Kunming 2
Las Vegas 2
Lavagna 2
Newport 2
Ningbo 2
Nuremberg 2
Ovada 2
Verona 2
Albignasego 1
Altopascio 1
Bagnatica 1
Buffalo 1
Böblingen 1
Camisano Vicentino 1
Cardiff 1
Central District 1
Chengdu 1
Chennai 1
Chongqing 1
Edinburgh 1
Eskişehir 1
Frankfurt am Main 1
Groningen 1
Hangzhou 1
Harbin 1
Imola 1
Julian 1
Totale 4.339
Nome #
A targeted next-generation gene panel reveals a novel heterozygous nonsense variant in the TP63 gene in patients with arrhythmogenic cardiomyopathy 176
Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy 141
Isoform-specific interactions of the von Hippel-Lindau tumor suppressor protein 138
Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy 137
Ca2+ binding to F-ATP synthase beta subunit triggers the mitochondrial permeability transition 136
Computational analysis of prolyl hydroxylase domain-containing protein 2 (PHD2) mutations promoting polycythemia insurgence in humans 132
BOOGIE: Predicting Blood Groups from High Throughput Sequencing Data 129
Genotype-phenotype relations of the von Hippel-Lindau tumor suppressor inferred from a large-scale analysis of disease mutations and interactors 129
The lipoprotein HP1454 of Helicobacter pylori regulates T-cell response by shaping T-cell receptor signalling 128
Calmodulin Enhances Cryptochrome Binding to INAD in Drosophila Photoreceptors 125
DisProt 7.0: A major update of the database of disordered proteins 123
DisProt: intrinsic protein disorder annotation in 2020 116
Design and Analysis of a Petri Net Model of the Von Hippel-Lindau (VHL) Tumor Suppressor Interaction Network. 114
Mapping pathogenic mutations suggests an innovative structural model for the pendrin (SLC26A4) transmembrane domain 112
CDKN2A Unclassified Variants in Familial Malignant Melanoma: Combining Functional and Computational Approaches for Their Assessment. 111
Arginine 107 of yeast ATP synthase subunit g mediates sensitivity of the mitochondrial permeability transition to phenylglyoxal 108
The RING 2.0 web server for high quality residue interaction networks 107
RepeatsDB: a database of tandem repeat protein structures. 105
Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI 105
Bluues Server: electrostatic properties of wild-type and mutated protein structures. 101
RAPHAEL: Recognition, periodicity and insertion assignment of solenoid protein structures. 99
High-conductance channel formation in yeast mitochondria is mediated by F-ATP synthase e and g subunits 97
Novel interactions of the von Hippel-Lindau (pVHL) tumor suppressor with the CDKN1 family of cell cycle inhibitors 92
In silico investigation of PHD-3 specific HIF1-α proline 567 hydroxylation: a new player in the VHL/HIF-1α interaction pathway? 88
Structural protein reorganization and fold emergence investigated through amino acid sequence permutations 86
Evaluation of the steric impact of flavin adenine dinucleotide in Drosophila melanogaster cryptochrome function 85
Structural in silico dissection of the collagen v interactome to identify genotype-phenotype correlations in classic Ehlers-Danlos Syndrome (EDS) 83
The clinical spectrum of CASQ1-related myopathy 82
VHLdb: A database of von Hippel-Lindau protein interactors and mutations 81
FELLS: fast estimator of latent local structure 80
Arg-8 of yeast subunit e contributes to the stability of F-ATP synthase dimers and to the generation of the full-conductance mitochondrial megachannel 79
The role of mitochondrial ATP synthase in cancer 77
Design and dynamic simulation of minimal metallo-proteins 74
PED in 2021: a major update of the protein ensemble database for intrinsically disordered proteins 71
Insights into the proline hydroxylase (PHD) family, molecular evolution and its impact on human health 69
In silico structural study of random amino acid sequence proteins not present in nature 69
Massive non-natural proteins structure prediction using grid technologies 68
Novel Missense Variant in MYL2 Gene Associated with Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology 66
Never born proteins as a test case for ab initio protein structures prediction 65
Probing mammalian spermine oxidase enzyme-substrate complex through molecular modeling, site-directed mutagenesis and biochemical characterization 64
Do natural proteins differ from random sequences polypeptides? natural vs. random proteins classification using an evolutionary neural network 63
Assessing predictors for new post translational modification sites: A case study on hydroxylation 59
The E3 ubiquitin-protein ligase MDM2 is a novel interactor of the von Hippel-Lindau tumor suppressor 58
DisProt in 2022: improved quality and accessibility of protein intrinsic disorder annotation 56
Lys300 plays a major role in the catalytic mechanism of maize polyamine oxidase 55
Critical assessment of protein intrinsic disorder prediction 54
Human haptoglobin structure and function - A molecular modelling study 53
Insights into the molecular features of the von Hippel–Lindau-like protein 53
Neurocognitive assessment and DNA sequencing expand the phenotype and genotype spectrum of Alström syndrome 53
In silico blood genotyping from exome sequencing data 48
Selection dynamic of Escherichia coli host in M13 combinatorial peptide phage display libraries 47
HIF1α-dependent induction of the mitochondrial chaperone TRAP1 regulates bioenergetic adaptations to hypoxia 46
The pVHL neglected functions, a tale of hypoxia-dependent and -independent regulations in cancer 44
Characterization of the pVHL Interactome in Human Testis Using High-Throughput Library Screening 44
Assessment of phenolic herbicide toxicity and mode of action by different assays 42
The f subunit of human ATP synthase is essential for normal mitochondrial morphology and permeability transition 40
Characterisation and functional role of a novel C1qDC protein from a colonial ascidian 37
RING 3.0: fast generation of probabilistic residue interaction networks from structural ensembles 30
SARS-CoV-2 variants preferentially emerge at intrinsically disordered protein sites helping immune evasion 30
Antagonistic effect of cyclin-dependent kinases and a calcium-dependent phosphatase on polyglutamine-expanded androgen receptor toxic gain of function 30
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 18
New data on c1qdc from the colonial ascidian botryllus schlosseri 17
Mutational screening of androgen receptor gene in 8224 men of infertile couples 16
Investigating the Retained Inhibitory Effect of Cobimetinib against p.P124L Mutated MEK1: A Combined Liquid Biopsy and in Silico Approach 15
RING-PyMOL: residue interaction networks of structural ensembles and molecular dynamics 13
CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods 13
Identification of Rare LRP5 Variants in a Cohort of Males with Impaired Bone Mass 11
Structural Characterization of Hypoxia Inducible Factor α-Prolyl Hydroxylase Domain 2 Interaction through MD Simulations 7
Investigating the Retained Inhibitory Effect of Cobimetinib against p.P124L Mutated MEK1: A Combined Liquid Biopsy and in Silico Approach 7
Mocafe: a comprehensive Python library for simulating cancer development with Phase Field Models 7
Molecular Effects of Mutations in Human Genetic Diseases 6
A PDZ scaffolding/CaM-mediated pathway in Cryptochrome signaling 5
Totale 5.125
Categoria #
all - tutte 20.549
article - articoli 20.379
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 40.928


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201999 0 0 0 0 0 0 0 0 0 0 0 99
2019/2020950 85 25 16 73 106 58 99 105 119 138 65 61
2020/20211.155 38 89 88 190 25 36 45 68 142 167 174 93
2021/2022922 33 62 86 83 83 69 49 105 59 29 64 200
2022/2023828 135 101 27 141 111 90 14 55 91 13 36 14
2023/2024512 44 67 56 36 48 65 40 24 15 44 41 32
Totale 5.125