NOLLI, Cecilia
 Distribuzione geografica
Continente #
NA - Nord America 333
EU - Europa 309
AS - Asia 141
AF - Africa 2
OC - Oceania 1
SA - Sud America 1
Totale 787
Nazione #
US - Stati Uniti d'America 327
IT - Italia 113
CN - Cina 81
IE - Irlanda 62
SE - Svezia 58
FI - Finlandia 40
SG - Singapore 39
TR - Turchia 18
DE - Germania 15
BE - Belgio 7
UA - Ucraina 6
CA - Canada 5
GB - Regno Unito 4
KR - Corea 2
PL - Polonia 2
AR - Argentina 1
CI - Costa d'Avorio 1
CZ - Repubblica Ceca 1
DM - Dominica 1
FR - Francia 1
MA - Marocco 1
NZ - Nuova Zelanda 1
PH - Filippine 1
Totale 787
Città #
Dublin 62
Chandler 45
Parma 43
Dearborn 39
Santa Clara 35
Singapore 28
Ann Arbor 26
Ashburn 20
Izmir 18
Nanjing 17
Boardman 13
Shanghai 12
Princeton 9
Wilmington 9
Beijing 8
Brussels 7
Jacksonville 6
Nanchang 5
Zhengzhou 5
Hefei 4
Shenyang 4
Helsinki 3
Jinan 3
Ottawa 3
Redmond 3
San Mateo 3
Tianjin 3
Ardea 2
Changsha 2
Falls Church 2
Fremont 2
London 2
Los Angeles 2
New York 2
Norwalk 2
Pittsburgh 2
San Remo 2
Seattle 2
Toronto 2
Vicenza 2
Abidjan 1
Alghero 1
Auckland 1
Bologna 1
Buenos Aires 1
Catanzaro 1
Chengde 1
Chongqing 1
Daejeon 1
Dongying 1
Düsseldorf 1
Great Malvern 1
Guangzhou 1
Hebei 1
Houston 1
Huzhou 1
Kraków 1
Kunming 1
Manila 1
Marseille 1
Modena 1
Munich 1
Pingdingshan 1
Reggio Nell'emilia 1
Rockville 1
Roseau 1
Rubiera 1
Scafati 1
Taizhou 1
Turin 1
Wuhan 1
Xian 1
Totale 491
Nome #
DNA polymerase [gamma] and disease: what we have learned from yeast 120
Biallelic Mutations in DNM1L are Associated with a Slowly Progressive Infantile Encephalopathy 109
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models 100
Screening of thiosemicarbazones as antimycotic drugs 96
S. cerevisiae carrying a MGM1/OPA1 chimeric gene: a model for the study of dominant optic atrophy and for drug discovery 96
Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy 95
Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy 95
Mitochondrial disorders caused by mutations impairing miotchondrial dynamics 72
A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency 52
Totale 835
Categoria #
all - tutte 2.562
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 2.562


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202076 0 0 0 0 0 28 18 3 19 4 2 2
2020/202146 2 3 5 2 7 4 3 2 10 2 4 2
2021/202243 2 0 5 4 0 1 2 5 3 2 3 16
2022/2023197 19 22 22 9 16 19 1 17 68 2 2 0
2023/202464 6 9 2 3 2 17 3 5 2 2 4 9
2024/2025107 1 10 14 21 25 36 0 0 0 0 0 0
Totale 835