NOLLI, Cecilia
 Distribuzione geografica
Continente #
EU - Europa 304
NA - Nord America 271
AS - Asia 104
AF - Africa 1
SA - Sud America 1
Totale 681
Nazione #
US - Stati Uniti d'America 268
IT - Italia 113
CN - Cina 72
IE - Irlanda 62
SE - Svezia 58
FI - Finlandia 40
TR - Turchia 18
DE - Germania 14
SG - Singapore 12
BE - Belgio 7
UA - Ucraina 6
CA - Canada 2
KR - Corea 2
PL - Polonia 2
AR - Argentina 1
CI - Costa d'Avorio 1
CZ - Repubblica Ceca 1
DM - Dominica 1
GB - Regno Unito 1
Totale 681
Città #
Dublin 62
Chandler 45
Parma 43
Dearborn 39
Ann Arbor 26
Ashburn 18
Izmir 18
Nanjing 17
Shanghai 12
Princeton 9
Wilmington 9
Beijing 7
Brussels 7
Jacksonville 6
Nanchang 5
Singapore 5
Zhengzhou 5
Boardman 4
Hefei 4
Shenyang 4
Helsinki 3
Jinan 3
Redmond 3
San Mateo 3
Tianjin 3
Ardea 2
Changsha 2
Falls Church 2
Fremont 2
New York 2
Norwalk 2
Pittsburgh 2
San Remo 2
Seattle 2
Vicenza 2
Abidjan 1
Alghero 1
Bologna 1
Buenos Aires 1
Catanzaro 1
Chongqing 1
Daejeon 1
Düsseldorf 1
Great Malvern 1
Guangzhou 1
Hebei 1
Houston 1
Huzhou 1
Kraków 1
Kunming 1
Los Angeles 1
Modena 1
Ottawa 1
Reggio Nell'emilia 1
Rockville 1
Roseau 1
Rubiera 1
Scafati 1
Taizhou 1
Toronto 1
Turin 1
Wuhan 1
Xian 1
Totale 408
Nome #
DNA polymerase [gamma] and disease: what we have learned from yeast 108
Biallelic Mutations in DNM1L are Associated with a Slowly Progressive Infantile Encephalopathy 95
S. cerevisiae carrying a MGM1/OPA1 chimeric gene: a model for the study of dominant optic atrophy and for drug discovery 87
Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy 85
Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy 85
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models 85
Screening of thiosemicarbazones as antimycotic drugs 83
Mitochondrial disorders caused by mutations impairing miotchondrial dynamics 59
A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency 42
Totale 729
Categoria #
all - tutte 2.103
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 2.103


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202093 0 6 0 1 10 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
2024/20251 1 0 0 0 0 0 0 0 0 0 0 0
Totale 729