CRIS Current Research Information System

MARESCA, ALESSANDRA
 Distribuzione geografica
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Continente #
NA - Nord America 2.839
EU - Europa 2.078
AS - Asia 507
AF - Africa 138
SA - Sud America 16
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 2
Totale 5.587
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Nazione #
US - Stati Uniti d'America 2.825
IT - Italia 681
GB - Regno Unito 430
SE - Svezia 268
DE - Germania 243
CN - Cina 208
IN - India 113
VN - Vietnam 108
IE - Irlanda 88
FR - Francia 67
RU - Federazione Russa 66
TG - Togo 53
UA - Ucraina 49
CI - Costa d'Avorio 43
CH - Svizzera 33
ZA - Sudafrica 33
EE - Estonia 30
BG - Bulgaria 29
JO - Giordania 26
FI - Finlandia 24
HK - Hong Kong 18
BE - Belgio 16
CA - Canada 14
CL - Cile 10
HR - Croazia 8
PL - Polonia 8
SC - Seychelles 8
AU - Australia 7
ES - Italia 7
JP - Giappone 7
NL - Olanda 7
BR - Brasile 5
GR - Grecia 5
RO - Romania 5
DK - Danimarca 4
SG - Singapore 4
TR - Turchia 4
IR - Iran 3
KR - Corea 3
TW - Taiwan 3
A2 - ???statistics.table.value.countryCode.A2??? 2
MT - Malta 2
MY - Malesia 2
SK - Slovacchia (Repubblica Slovacca) 2
AE - Emirati Arabi Uniti 1
AT - Austria 1
BD - Bangladesh 1
HU - Ungheria 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
LU - Lussemburgo 1
LV - Lettonia 1
MD - Moldavia 1
NG - Nigeria 1
PE - Perù 1
PH - Filippine 1
PK - Pakistan 1
PT - Portogallo 1
TH - Thailandia 1
UZ - Uzbekistan 1
Totale 5.587
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Città #
Southend 400
Fairfield 362
Chandler 332
Ashburn 225
Bologna 218
Woodbridge 154
Wilmington 136
Houston 133
Seattle 130
Ann Arbor 124
Cambridge 116
Princeton 114
Redmond 107
Dublin 87
Turin 61
Lomé 53
New York 45
Abidjan 43
Berlin 40
Westminster 39
Padova 36
Milan 35
Nanjing 33
Sofia 29
Bern 28
Dong Ket 28
Amman 26
Redwood City 26
Boydton 25
San Diego 22
Helsinki 21
Warrington 21
Jinan 19
Florence 18
Brussels 16
Hong Kong 16
Nanchang 16
Jacksonville 15
Saint Petersburg 15
Shenyang 15
Los Angeles 13
Beijing 12
Changsha 12
Falls Church 12
Hebei 12
Olalla 11
Ancona 10
Des Moines 10
Doylestown 10
Kuban 10
Medford 10
Dearborn 9
Phoenix 9
Pune 9
Zhengzhou 9
Modena 8
Paris 8
Sant Angelo 8
Taizhou 8
Tianjin 8
Bari 7
Hangzhou 7
London 7
Mülheim 7
Ferrara 6
Jiaxing 6
Ningbo 6
Rome 6
Taiyuan 6
Catania 5
Guangzhou 5
Livorno 5
Lynchburg 5
Ponte San Pietro 5
Toronto 5
Botticino 4
Cesena 4
Frankfurt Am Main 4
Frankfurt am Main 4
Fremont 4
Mahé 4
Marina Di Carrara 4
Mountain View 4
São Paulo 4
Verona 4
Washington 4
Amsterdam 3
Boston 3
Budrio 3
Bühl 3
Frederick 3
Madrid 3
Montreal 3
Moscow 3
Munich 3
Noicattaro 3
Parma 3
Provo 3
San Francisco 3
Tokyo 3
Totale 3.751
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Nome #
An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder. 224
Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy 191
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome 183
Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways 166
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy 153
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism 148
Mitochondrial Mass Assessment in a Selected Cell Line under Different Metabolic Conditions 146
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models 145
Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations 142
Mitochondrial abnormalities in fibroblasts carrying DNMT1 mutations 140
Haplogroup J mitogenomes are the most sensitive to the pesticide rotenone: Relevance for human diseases 139
Genetic Basis of Mitochondrial Optic Neuropathies. 137
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions. 129
Mitochondrial optic neuropathies: how two genomes may kill the same cell type? 125
Oncocytic glioblastoma: a glioblastoma showing oncocytic changes and increased mitochondrial DNA copy number 123
A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy. 121
OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions 121
Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α. 116
Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy 116
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy 113
Incomplete penetrance in mitochondrial optic neuropathies 108
Syndromic parkinsonism and dementia associated with OPA1 missense mutations 107
ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy 107
Mitochondrial DNA influences the susceptibility to Autism Spectrum Disorders and the severity of the clinical phenotype 106
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder 105
Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease Models 103
DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions 103
Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations 99
Idebenone treatment in patients with OPA1-mutant dominant optic atrophy. 98
Mitochondria: Biogenesis and mitophagy balance in segregation and clonal expansion of mitochondrial DNA mutations 97
Molecular biomarkers correlate with brain grey and white matter changes in patients with mitochondrial m.3243A > G mutation 95
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance. 93
OPA3, a new regulator of mitochondrial fission? 91
Exploring metabolic adaptations to the acidic microenvironment of osteosarcoma cells unveils sphingosine 1-phosphate as a valuable therapeutic target 85
null 83
DNA methyltransferase 1 mutations and mitochondrial pathology: Is mtDNA methylated? 83
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder 81
Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS-associated mtDNA mutations 81
null 78
Searching for genetic modifiers of Leber's hereditary optic neuropathy penetrance 77
Parsing the differences in affected with LHON: genetic versus environmental triggers of disease conversion 76
Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies 76
The optic nerve: a "mito-window" on mitochondrial neurodegeneration. 74
Screening of candidate nuclear genes for modifying role in Leber's hereditary optic neuropathy penetrance: A signal from manganese superoxide dismutase 73
The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs 64
Retinal nerve fiber layer thickness in dominant optic atrophy: measurements by optical coherence tomography and correlation with age. 62
Functional investigation of the mitochondrial protein OPA3 62
OPA3 IS AN INNER MITOCHONDRIAL MEMBRANE PROTEIN INVOLVED IN MITOCHONDRIAL DYNAMICS REGULATION 61
Expanding and validating the biomarkers for mitochondrial diseases 60
Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON) 55
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder 55
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy. 47
Exploring metabolic reprogramming in melanoma via acquired resistance to the oxidative phosphorylation inhibitor phenformin 42
Author Correction: Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome (Scientific Reports, (2020), 10, 1, (4785), 10.1038/s41598-020-61735-3) 39
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy 39
Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys 36
Mitochondrial diseases in adults 34
Impaired complex I repair causes recessive Leber's hereditary optic neuropathy 28
Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives 25
Molecular mechanisms behind inherited neurodegeneration of the optic nerve 19
Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy 11
Methyl carbamates of phosphatidylethanolamines and phosphatidylserines reveal bacterial contamination in mitochondrial lipid extracts of mouse embryonic fibroblasts 4
Totale 5.800
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Categoria #
all - tutte 14.604
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 14.604
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201953 0 0 0 0 0 0 0 0 0 0 9 44
2019/20201.230 161 27 7 55 122 114 141 178 222 65 75 63
2020/2021855 152 47 24 39 21 40 14 90 137 51 56 184
2021/20221.283 51 37 69 75 111 46 48 168 77 108 267 226
2022/20231.528 157 189 76 155 119 179 70 92 231 40 131 89
2023/2024480 27 71 28 40 38 110 49 44 18 46 9 0
Totale 5.800