IRIS
ANGELIN, ALESSIA
 Distribuzione geografica
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Continente #
NA - Nord America 196
AS - Asia 152
EU - Europa 77
Totale 425
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Nazione #
US - Stati Uniti d'America 195
SG - Singapore 144
RU - Federazione Russa 44
CN - Cina 6
DE - Germania 6
FI - Finlandia 6
FR - Francia 6
IT - Italia 5
NL - Olanda 5
BG - Bulgaria 3
CA - Canada 1
JP - Giappone 1
PK - Pakistan 1
PL - Polonia 1
UA - Ucraina 1
Totale 425
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Città #
Singapore 130
Santa Clara 41
Del Norte 19
Moscow 9
Salt Lake City 9
Council Bluffs 7
North Bergen 7
Helsinki 6
Los Angeles 5
Amsterdam 3
Boston 2
Dongguan 2
Guiyang 2
Jacksonville 2
Nuremberg 2
Ashburn 1
Billings 1
Falkenstein 1
Grünwald 1
Lahore 1
Munich 1
Paris 1
Tokyo 1
Utrecht 1
Warsaw 1
Yong'an 1
Totale 257
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Nome #
Correction to: Advances and prospects for the Human BioMolecular Atlas Program (HuBMAP) (Nature Cell Biology, (2023), 25, 8, (1089-1100), 10.1038/s41556-023-01194-w) 34
Core mitochondrial genes are down-regulated during SARS-CoV-2 infection of rodent and human hosts 27
Mitochondrial DNA variant associated with Leber hereditary optic neuropathy and high-altitude Tibetans 24
Erratum: Landscape of the mitochondrial Hsp90 metabolome in tumours (Nature Communications (2013) 4 (2139) DOI:10.1038/ncomms3139) 23
SARS-CoV-2 mitochondrial metabolic and epigenomic reprogramming in COVID-19 22
Genetic analysis of dTSPO, an outer mitochondrial membrane protein, reveals its functions in apoptosis, longevity, and Aβ42-induced neurodegeneration 21
Cyclosporine a in Ullrich congenital muscular dystrophy: Long-term results 21
HDAC10 deletion promotes Foxp3+ T-regulatory cell function 21
Arachidonic acid released by phospholipase A2 activation triggers Ca2+-dependent apoptosis through the mitochondrial pathway 20
Cyclin-dependent kinases regulate the adult nervous system via the one-carbon-metabolism 20
Landscape of the mitochondrial Hsp90 metabolome in tumours 19
Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins 19
Lentiviral-mediated RNAi in vivo silencing of Col6a1, a gene with complex tissue specific expression pattern 18
SARS-COV-2 viroporins activate the NLRP3-inflammasome by the mitochondrial permeability transition pore 17
Deficiency in the mouse mitochondrial adenine nucleotide translocator isoform 2 gene is associated with cardiac noncompaction 16
H+ transport is an integral function of the mitochondrial ADP/ATP carrier 16
Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration 16
Critical evaluation of the use of cell cultures for inclusion in clinical trials of patients affected by collagen VI myopathies 15
The cyclophilin inhibitor Debio 025 normalizes mitochondrial function, muscle apoptosis and ultrastructural defects in Col6a1-/-myopathic mice 14
Premature Lambs Exhibit Normal Mitochondrial Respiration after Long-Term Extrauterine Support 14
Yessotoxin, a shellfish biotoxin, is a potent inducer of the permeability transition in isolated mitochondria and intact cells 13
Foxp3 Reprograms T Cell Metabolism to Function in Low-Glucose, High-Lactate Environments 13
Collagen VI Deficiency Results in Structural Abnormalities in the Mouse Lung 13
Mitochondrial respiration is sensitive to cytoarchitectural breakdown 12
Advances and prospects for the Human BioMolecular Atlas Program (HuBMAP) 11
Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathies 11
Lactate Limits T Cell Proliferation via the NAD(H) Redox State 10
Genetic ablation of cyclophilin D rescues mitochondrial defects and prevents muscle apoptosis in collagen VI myopathic mice 9
Essential role of mitochondrial energy metabolism in Foxp3+ T-regulatory cell function and allograft survival 9
Mitochondrial DNA Variation Dictates Expressivity and Progression of Nuclear DNA Mutations Causing Cardiomyopathy 9
Survivin promotes oxidative phosphorylation, subcellular mitochondrial repositioning, and tumor cell invasion 7
Altered threshold of the mitochondrial permeability transition pore in Ullrich congenital muscular dystrophy 7
Respiratory complex I dysfunction due to mitochondrial DNA mutations shifts the voltage threshold for opening of the permeability transition pore toward resting levels 6
Totale 527
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Categoria #
all - tutte 2.341
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 2.341
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/2024197 0 0 0 0 0 0 0 0 0 0 107 90
2024/2025330 25 183 73 39 10 0 0 0 0 0 0 0
Totale 527