MINERVINI, GIOVANNI
 Distribuzione geografica
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Continente #
NA - Nord America 4.299
EU - Europa 526
AS - Asia 485
AF - Africa 1
OC - Oceania 1
Totale 5.312
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Nazione #
US - Stati Uniti d'America 4.292
CN - Cina 267
IT - Italia 186
SG - Singapore 162
SE - Svezia 93
FI - Finlandia 88
FR - Francia 41
DE - Germania 37
GB - Regno Unito 33
VN - Vietnam 32
IE - Irlanda 10
NL - Olanda 10
IN - India 9
GR - Grecia 7
HK - Hong Kong 6
UA - Ucraina 5
CA - Canada 4
ES - Italia 4
SA - Arabia Saudita 4
MX - Messico 3
BE - Belgio 2
CZ - Repubblica Ceca 2
PT - Portogallo 2
RO - Romania 2
RU - Federazione Russa 2
TR - Turchia 2
TW - Taiwan 2
CY - Cipro 1
EE - Estonia 1
NZ - Nuova Zelanda 1
PL - Polonia 1
SC - Seychelles 1
Totale 5.312
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Città #
Fairfield 759
Chandler 445
Woodbridge 427
Ashburn 365
Ann Arbor 325
Seattle 316
Houston 305
Cambridge 272
Wilmington 241
Singapore 118
Beijing 81
Padova 76
San Diego 66
Medford 60
Princeton 60
Helsinki 46
Des Moines 45
Boardman 35
Dong Ket 32
Santa Clara 26
Roxbury 25
Nanjing 23
New York 21
Lappeenranta 19
Guangzhou 18
Milan 12
Falls Church 11
Rome 11
London 10
Dublin 8
Redwood City 8
Belluno 7
Washington 7
Dallas 6
Hebei 6
Jinan 6
Los Angeles 6
Mira 6
Nanchang 6
Shenyang 6
Changsha 5
Chicago 5
Hounslow 5
Norwalk 5
Paris 5
Taiyuan 5
Fontanelle 4
Hong Kong 4
Jiaxing 4
Ogden 4
Pune 4
Riyadh 4
Acton 3
Balestrino 3
Borås 3
Fuzhou 3
Hefei 3
Kharkiv 3
Kilburn 3
Lebanon 3
Legnago 3
Querétaro City 3
Shanghai 3
Tappahannock 3
Treviso 3
Zhengzhou 3
Arzignano 2
Barletta 2
Casalfiumanese 2
Chiswick 2
Dearborn 2
Falkenstein 2
Frankfurt am Main 2
Gallio 2
Jacksonville 2
Kraainem 2
Kunming 2
Las Vegas 2
Lavagna 2
León 2
Newport 2
Ningbo 2
Nuremberg 2
Ovada 2
Taoyuan District 2
Turin 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
Dongguan 1
Edinburgh 1
Totale 4.473
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Nome #
A targeted next-generation gene panel reveals a novel heterozygous nonsense variant in the TP63 gene in patients with arrhythmogenic cardiomyopathy 183
Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy 152
Ca2+ binding to F-ATP synthase beta subunit triggers the mitochondrial permeability transition 147
Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy 141
Isoform-specific interactions of the von Hippel-Lindau tumor suppressor protein 139
Calmodulin Enhances Cryptochrome Binding to INAD in Drosophila Photoreceptors 134
Computational analysis of prolyl hydroxylase domain-containing protein 2 (PHD2) mutations promoting polycythemia insurgence in humans 133
BOOGIE: Predicting Blood Groups from High Throughput Sequencing Data 131
Genotype-phenotype relations of the von Hippel-Lindau tumor suppressor inferred from a large-scale analysis of disease mutations and interactors 130
DisProt 7.0: A major update of the database of disordered proteins 130
The lipoprotein HP1454 of Helicobacter pylori regulates T-cell response by shaping T-cell receptor signalling 129
DisProt: intrinsic protein disorder annotation in 2020 126
CDKN2A Unclassified Variants in Familial Malignant Melanoma: Combining Functional and Computational Approaches for Their Assessment. 120
Mapping pathogenic mutations suggests an innovative structural model for the pendrin (SLC26A4) transmembrane domain 119
Design and Analysis of a Petri Net Model of the Von Hippel-Lindau (VHL) Tumor Suppressor Interaction Network. 115
Arginine 107 of yeast ATP synthase subunit g mediates sensitivity of the mitochondrial permeability transition to phenylglyoxal 109
The RING 2.0 web server for high quality residue interaction networks 108
Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI 108
RepeatsDB: a database of tandem repeat protein structures. 107
Bluues Server: electrostatic properties of wild-type and mutated protein structures. 104
RAPHAEL: Recognition, periodicity and insertion assignment of solenoid protein structures. 104
High-conductance channel formation in yeast mitochondria is mediated by F-ATP synthase e and g subunits 99
Novel interactions of the von Hippel-Lindau (pVHL) tumor suppressor with the CDKN1 family of cell cycle inhibitors 97
In silico investigation of PHD-3 specific HIF1-α proline 567 hydroxylation: a new player in the VHL/HIF-1α interaction pathway? 89
The clinical spectrum of CASQ1-related myopathy 88
Structural in silico dissection of the collagen v interactome to identify genotype-phenotype correlations in classic Ehlers-Danlos Syndrome (EDS) 87
Structural protein reorganization and fold emergence investigated through amino acid sequence permutations 87
Evaluation of the steric impact of flavin adenine dinucleotide in Drosophila melanogaster cryptochrome function 86
VHLdb: A database of von Hippel-Lindau protein interactors and mutations 82
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 81
The role of mitochondrial ATP synthase in cancer 81
FELLS: fast estimator of latent local structure 80
PED in 2021: a major update of the protein ensemble database for intrinsically disordered proteins 79
Design and dynamic simulation of minimal metallo-proteins 76
Massive non-natural proteins structure prediction using grid technologies 73
In silico structural study of random amino acid sequence proteins not present in nature 73
Insights into the proline hydroxylase (PHD) family, molecular evolution and its impact on human health 72
Novel Missense Variant in MYL2 Gene Associated with Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology 70
Assessing predictors for new post translational modification sites: A case study on hydroxylation 70
Never born proteins as a test case for ab initio protein structures prediction 69
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
The E3 ubiquitin-protein ligase MDM2 is a novel interactor of the von Hippel-Lindau tumor suppressor 62
Neurocognitive assessment and DNA sequencing expand the phenotype and genotype spectrum of Alström syndrome 61
Critical assessment of protein intrinsic disorder prediction 59
DisProt in 2022: improved quality and accessibility of protein intrinsic disorder annotation 58
Lys300 plays a major role in the catalytic mechanism of maize polyamine oxidase 55
Human haptoglobin structure and function - A molecular modelling study 54
Insights into the molecular features of the von Hippel–Lindau-like protein 54
HIF1α-dependent induction of the mitochondrial chaperone TRAP1 regulates bioenergetic adaptations to hypoxia 51
Characterization of the pVHL Interactome in Human Testis Using High-Throughput Library Screening 50
In silico blood genotyping from exome sequencing data 49
Selection dynamic of Escherichia coli host in M13 combinatorial peptide phage display libraries 49
Assessment of phenolic herbicide toxicity and mode of action by different assays 49
The pVHL neglected functions, a tale of hypoxia-dependent and -independent regulations in cancer 44
The f subunit of human ATP synthase is essential for normal mitochondrial morphology and permeability transition 43
Characterisation and functional role of a novel C1qDC protein from a colonial ascidian 41
RING 3.0: fast generation of probabilistic residue interaction networks from structural ensembles 35
Antagonistic effect of cyclin-dependent kinases and a calcium-dependent phosphatase on polyglutamine-expanded androgen receptor toxic gain of function 34
SARS-CoV-2 variants preferentially emerge at intrinsically disordered protein sites helping immune evasion 32
Mutational screening of androgen receptor gene in 8224 men of infertile couples 25
Investigating the Retained Inhibitory Effect of Cobimetinib against p.P124L Mutated MEK1: A Combined Liquid Biopsy and in Silico Approach 21
New data on c1qdc from the colonial ascidian botryllus schlosseri 21
CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods 20
RING-PyMOL: residue interaction networks of structural ensembles and molecular dynamics 19
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 19
Identification of Rare LRP5 Variants in a Cohort of Males with Impaired Bone Mass 18
A PDZ scaffolding/CaM-mediated pathway in Cryptochrome signaling 17
Catechol‐induced covalent modifications modulate the aggregation tendency of α‐synuclein: An in‐solution and in‐silico study 14
Investigating the Retained Inhibitory Effect of Cobimetinib against p.P124L Mutated MEK1: A Combined Liquid Biopsy and in Silico Approach 14
Structural Characterization of Hypoxia Inducible Factor α-Prolyl Hydroxylase Domain 2 Interaction through MD Simulations 13
RING 4.0: faster residue interaction networks with novel interaction types across over 35,000 different chemical structures 9
Molecular Effects of Mutations in Human Genetic Diseases 9
Mocafe: a comprehensive Python library for simulating cancer development with Phase Field Models 8
In Silico Exploration of AHR-HIF Pathway Interplay: Implications for Therapeutic Targeting in ccRCC 1
Totale 5.443
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Categoria #
all - tutte 23.217
article - articoli 23.021
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 46.238
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020824 0 0 0 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
2023/2024525 44 67 56 36 48 65 40 24 15 44 41 45
2024/2025305 13 142 83 67 0 0 0 0 0 0 0 0
Totale 5.443