NOLLI, Cecilia
 Distribuzione geografica
Continente #
EU - Europa 304
NA - Nord America 270
AS - Asia 92
SA - Sud America 1
Totale 667
Nazione #
US - Stati Uniti d'America 267
IT - Italia 113
CN - Cina 68
IE - Irlanda 62
SE - Svezia 58
FI - Finlandia 40
TR - Turchia 18
DE - Germania 14
BE - Belgio 7
UA - Ucraina 6
SG - Singapore 4
CA - Canada 2
KR - Corea 2
PL - Polonia 2
AR - Argentina 1
CZ - Repubblica Ceca 1
DM - Dominica 1
GB - Regno Unito 1
Totale 667
Città #
Dublin 62
Chandler 45
Parma 43
Dearborn 39
Ann Arbor 26
Ashburn 18
Izmir 18
Nanjing 17
Princeton 9
Wilmington 9
Shanghai 8
Beijing 7
Brussels 7
Jacksonville 6
Nanchang 5
Zhengzhou 5
Hefei 4
Shenyang 4
Boardman 3
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
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
Singapore 1
Taizhou 1
Toronto 1
Turin 1
Wuhan 1
Xian 1
Totale 398
Nome #
DNA polymerase [gamma] and disease: what we have learned from yeast 105
Biallelic Mutations in DNM1L are Associated with a Slowly Progressive Infantile Encephalopathy 94
S. cerevisiae carrying a MGM1/OPA1 chimeric gene: a model for the study of dominant optic atrophy and for drug discovery 85
Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy 84
Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy 84
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models 83
Screening of thiosemicarbazones as antimycotic drugs 82
Mitochondrial disorders caused by mutations impairing miotchondrial dynamics 58
A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency 40
Totale 715
Categoria #
all - tutte 1.859
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 1.859


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201924 0 0 0 0 0 0 0 0 0 0 21 3
2019/2020116 23 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
2023/202451 6 9 2 3 2 17 3 5 2 2 0 0
Totale 715