Catalogo dei prodotti della ricerca

FRANCISCI, Silvia
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 2.304
EU - Europa 693
AS - Asia 213
SA - Sud America 43
AF - Africa 33
Continente sconosciuto - Info sul continente non disponibili 2
Totale 3.288
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 2.288
UA - Ucraina 234
IN - India 153
SE - Svezia 152
IT - Italia 131
FI - Finlandia 85
CN - Cina 47
AR - Argentina 41
BE - Belgio 29
TG - Togo 29
GB - Regno Unito 26
CA - Canada 16
IE - Irlanda 10
BG - Bulgaria 9
DE - Germania 6
KR - Corea 6
TR - Turchia 4
RO - Romania 3
ZA - Sudafrica 3
CH - Svizzera 2
CL - Cile 2
EU - Europa 2
FR - Francia 2
MD - Moldavia 2
IL - Israele 1
NL - Olanda 1
NO - Norvegia 1
SA - Arabia Saudita 1
SC - Seychelles 1
SG - Singapore 1
Totale 3.288
Salva come PNG Salva come JPEG
Città #
Fairfield 313
Chandler 297
Woodbridge 160
Ann Arbor 158
Ashburn 121
Houston 113
Seattle 107
Cambridge 99
Wilmington 95
Princeton 87
Plano 86
Jacksonville 85
Boston 72
Rome 66
Federal 41
Beijing 37
Boardman 31
Lomé 29
Brussels 28
Lawrence 27
San Diego 26
Millbury 25
Andover 23
San Paolo di Civitate 22
Des Moines 18
Dearborn 14
Toronto 13
Norwalk 11
Dublin 10
Sofia 9
Washington 8
Falls Church 5
Istanbul 4
Bremen 3
Finsbury Park 3
Las Vegas 3
London 3
Milan 3
Nanjing 3
Buccinasco 2
Chisinau 2
Jinan 2
Maple Grove 2
Mentana 2
Muizenberg 2
New York 2
Ottawa 2
Phoenix 2
Rio Saliceto 2
Rozzano 2
San Mateo 2
Seongnam 2
Southend 2
Affile 1
Anguillara Sabazia 1
Bari 1
Bern 1
Delhi 1
Desio 1
Florence 1
Fremont 1
Fuzhou 1
Gent 1
Grafing 1
Grammichele 1
Hefei 1
Indianapolis 1
Jönköping 1
Lappeenranta 1
Latina 1
Laurel 1
Los Angeles 1
Mahé 1
Modderfontein 1
Montréal 1
Napoli 1
Noicattaro 1
Oslo 1
Paris 1
Pozza 1
Provo 1
Redmond 1
Sacramento 1
Salerno 1
San Jose 1
Santiago 1
Seoul 1
Simi Valley 1
Spadafora 1
Stockholm 1
Tappahannock 1
Tel Aviv 1
Torino 1
Trumbull 1
Yellow Springs 1
Zhengzhou 1
Totale 2.329
Salva come PNG Salva come JPEG
Nome #
Ubiquitin protease Ubp8 is necessary for S. cerevisiae respiration 88
The yeast model suggests the use of short peptides derived from mt LeuRS for the therapy of diseases due to mutations in several mt tRNAs 84
Biolistic Transformation for Delivering DNA into the Mitochondria 84
Can yeast be used to study mitochondrial diseases? Biolistic tRNA mutants for the analysis of mechanisms and suppressors 82
Evaluation of the efficacy of carbon nanotubes for delivering peptides into mitochondria 80
Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T > C mitochondrial tRNA(Ile) mutation causing hypertrophic cardiomyopathy 74
Il fattore di elongazione della sintesi proteica mitocondriale (EF-Tu) come soppressore di diverse mutazioni nei geni dei geni per tRNA mitocondriali in S.cerevisiae 65
Analyzing the suppression of respiratory defects in the yeast model of human mitochondrial tRNA diseases 65
SAGA complex and Gcn5 are necessary for respiration in budding yeast 64
Novel mutation in mitochondrial Elongation Factor EF-Tu associated to dysplastic leukoencephalopathy and defective mitochondrial DNA translation 63
The isolated carboxy-terminal domain of human mitochondrial leucyl-tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells 62
Gcn5 histone acetyltransferase is present in the mitoplasts 62
Mitochondrial diseases: Yeast as a model for the study of suppressors 58
Suppression of a nuclear frameshift mutation by a mitochondrial tRNA in the yeast Kluyveromyces lactis. 56
Structural and functional role of bases 32 and 33 in the anticodon loop of yeast mitochondrial tRNAIle 56
Characterization of two tRNAleu mutants harbouring the equivalent pathogenic human substitutions T3250C and A3260G 55
Nucleo-cytoplasmic interactions in the expression of mitochondrial tRNA genes in yeast 54
Suppression of a mitochondrial point mutation in a tRNA gene can cast light on the mechanisms of 3’end processing 53
Aminoacylation and conformational properties of yeast mitochondrial tRNA mutants with respiratory deficiency 52
Ts mutations in mitochondrial tRNA genes: characterization and effects of two point mutations in the mitochondrial gene for tRNAphe in Saccharomyces cerevisiae 51
Human mitochondrial leucyl tRNA synthetase can suppress non cognate pathogenic mt-tRNA mutations 51
Yeast as a model of human mitochondrial tRNA base substitutions: Investigation of the molecular basis of respiratory defects 51
Aminoacyl-tRNA synthetases are multivalent suppressors of defects due to human equivalent mutations in yeast mt tRNA genes 50
Analysis of transcripts of the major cluster of tRNA genes in the mitoc hondrial genome of S.cerevisiae 49
Mitochondrial genes in S.cerevisiae: release from glucose repression and transcription in the tRNA genes 47
Characterization of mitochondrial tRNA mutants of Saccharomyces cerevisiae 47
A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemia 47
Mitochondrial protein synthesizing machinery in S.cerevisiae 46
Mutations in yeast mt tRNAs: specific and general suppression by nuclear encoded tRNA interactors 46
Screening of effective pharmacological treatments for MELAS syndrome using yeasts, fibroblasts and cybrid models of the disease 46
Reintroduction of a characterized mit tRNAgly mutation into yeast mitochondria provides a new tool for the study of human neurodegenerative diseases 45
Initiation of tran-scription of Mitochondrial tRNA gene cluster in S.cerevisiae 44
Nuclearly encoded mitochondrial protein synthesis factors can “cure” the respiratory defects due to pathogenetic human equivalent base substitutions in yeast mt tRNA genes 44
Yeast respiratory defects caused by pathogenetic human equivalent base substitutions in mt tRNA genes can be rescued by overexpression of aminoacyl-tRNA synthetases 42
Peptides from aminoacyl-tRNA synthetases can cure the defects due to mutations in mt tRNA genes 40
Disruption of six novel genes from chromosome VII of Saccharomyces cerevisiae reveals one essentia gene and one gene which affects the growth rate 40
Yeast as a model for human mitochondrial mutation studies: the exemple of the tRNAleuUUR 'MELAS' mutation C3256T 39
Yeast as a model to study the molecular basis of mt tRNA pathogenic mutations and to identify suppressor molecules 38
Development of host-vector systems in dairy yeasts 36
Il lievito come modello per lo studio di mutazioni mitocondriali: l’esempio della mutazione ‘MELAS’ C3256T nel gene per il tRNAleuUUR. 36
L'equivalente di una mutazione 'MELAS' umana in lievito, provoca una grave alterazione mitocondriale che può essere soppressa dal fattore di elongazione mtEF-Tu 36
The effects of some human pathogenic mutations in mitochondrial tRNA genes can be studied and suppressed in yeast 36
Mutations releasing mitochondrial biogenesis from glucose repression in S. cerevisiae 36
Molecole peptidiche per il trattamento di patologie mitocondriali 35
Yeast biolistic tRNA mutants equivalent to pathogenic human mitochondrial mutations: a model for the study of mechanisms and suppressors 34
New complex mitochondrial functions in cell biology. 33
The contribution of yeast to understand mitochondrial diseases 32
tRNA interactors as suppressors of mitochondrial defects due to pathogenetic human equivalent base substitutions in yeast mt tRNA genes 31
Yeast as a paradigm for mitochondrial disease: defective phenotype of a "MELAS" mutation and rescue by mtEF-Tu 31
Mitochondrial DNA disorders: analysis of tRNA mutations in S. cerevisiae 31
Analisi di mutazioni nei geni per i tRNA mitocondriali di S.cerevisiae 31
Suppression of a nuclear frame-shift mutation by a mitochondrial tRNA 31
Mutated mitochondrial tRNA structures: effects on aminoacylation 31
Mitochondria in yeast cells: new approaches in the study of nucleo-cytoplasmic interactions 30
EXPRESSION OF THE CLUSTERED MITOCHONDRIAL TRNAGENES IN S.. CEREVISIAE: TRANSCRIPTION AND PRO-CESSING OF TRANSCRIPTS 30
Yeast as a model for analysis of human mitochondrial mutations related to neurodegenerative diseases 29
Mitochondrial genomes and nucleo-mitochondrial interactions in different yeast 29
A point mutation in a mitochondrial tRNA, abolishes its 3' end processing. 29
Variability of Mitochondrial alanyl-tRNA isoaccepting species in S. cerevisiae 29
Mutations in yeast mt tRNAs: specific and general supression by nuclear encoded tRNA interactors 28
Ts mutations in mitochondrial tRNA genes: characterization and effects of two point mutations in the mitochondrial gene for tRNAphe in S. cerevisiae 27
Transcripts of yeast Mitochondrial DNA: processing of a split gene transcript and expression ofRNA species during adaptation and differentiation processes 27
Development of host-vector systems in dairy yeasts 27
Transcripts of Mitochondrial tRNA genes in S.cerevisiae 26
Transcription of the large tRNA gene cluster in the mitochondrial genome of S.cerevisiae. 26
Mitochondrial tRNA base substitutions: investigation of the molecular basis of respiratory defects 26
Peptide molecules for treating mitochondrial pathologies 26
Genome organization and nucleocytoplasmic interactions in the expression of mitochondrial tRNA genes in yeast 26
Yeast as a tool for in vivo study of human mitochondrial tRNA mutations 25
Analisi di mutazioni nel gene mitocondriale per il tRNAleu di S.cerevisiae correlate alle patologie umane 24
The yeast counterpart of human 'MELAS' mutations cause mitochondrial dysfunction that can be rescued by overexpression of the mitochondrial translation factor EF-Tu 24
Mitochondrial tRNA pathogenetic human substitutions: analysis of the yeast equivalent mutants and study of suppressive effect of interactor molecules. 23
I mitocondri e l’eredità citoplasmatica 23
Symmetrical transcription in the tRNA region of the mitochondrial genome of S.cerevisie 23
Nucleo-mitochondrial interactions in Saccharomyces cerevisiae: characterisation of a nuclear gene suppressing a defect in mitochondrial tRNAAsp processing. 22
Un modello cellulare per le malattie mitocondriali 20
Strain-specific nuclear genetic background differentially affects mitochondria-related phenotypes in Saccharomyces cerevisiae 20
Yeast as a tool for in vivo study of human mitochondrial tRNA mutations: a study of nuclear suppressors in yeast 19
YEAST AS MODELS FOR MITOCHONDRIAL DISEASES 19
Mutazioni ts nei geni per i tRNA mitocondriali in S.cerevisiae quali strumenti per lo studio di interazioni nucleo citoplasmatiche 19
Transcription initiation and processing sites in the tRNA region of the yeast mitochondrial genome. 18
Bioinformatics and experimental characterization of yeast mitochondrial tRNA mutantsresponsible for defective phenotypes mirroring human pathologies 18
Mutations in yeast mitochondrial tRNA genes: respiratory defect and structure alteration. 16
Mutazioni nei geni per i tRNA mitocondriali di S.cerevisiae: uno strumento per lo studio di interazioni strutturali e funzionali 14
Yeast as a paradigm for mitochondrial disease: defective phenotype of “MELAS” mutation and rescue by mtEF-Tu 12
Soppressione frame-shift di una mutazione in un gene nucleare operata da un tRNA mitocondriale 11
Totale 3.385
Salva come PNG Salva come JPEG
Categoria #
all - tutte 6.645
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 109
selected - selezionate 0
volume - volumi 0
Totale 6.754
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019334 0 0 0 1 11 9 9 14 19 55 122 94
2019/2020644 129 30 10 42 57 64 63 71 61 64 42 11
2020/2021316 54 43 6 25 11 28 1 32 19 56 37 4
2021/2022789 2 56 65 26 101 14 14 74 79 62 101 195
2022/2023836 162 142 35 113 124 84 11 48 65 14 27 11
2023/2024101 16 64 18 3 0 0 0 0 0 0 0 0
Totale 3.385