statistiche ricercatore

Continente	#
NA - Nord America	907
AS - Asia	659
EU - Europa	540
AF - Africa	51
Continente sconosciuto - Info sul continente non disponibili	45
SA - Sud America	37
OC - Oceania	2
Totale	2.241

Nazione	#
US - Stati Uniti d'America	889
VN - Vietnam	227
IT - Italia	178
SG - Singapore	158
CN - Cina	143
GB - Regno Unito	81
SE - Svezia	59
DE - Germania	53
FR - Francia	34
HK - Hong Kong	33
RU - Federazione Russa	27
IE - Irlanda	23
IN - India	23
BR - Brasile	22
CI - Costa d'Avorio	22
FI - Finlandia	20
NL - Olanda	17
BD - Bangladesh	15
KR - Corea	13
ZA - Sudafrica	9
CA - Canada	8
TG - Togo	8
AR - Argentina	7
BE - Belgio	7
CH - Svizzera	7
SC - Seychelles	7
TH - Thailandia	7
EE - Estonia	6
ID - Indonesia	6
PH - Filippine	6
JO - Giordania	5
JP - Giappone	5
BG - Bulgaria	4
ES - Italia	4
IR - Iran	4
UA - Ucraina	4
AT - Austria	3
CR - Costa Rica	3
EC - Ecuador	3
PL - Polonia	3
TR - Turchia	3
VE - Venezuela	3
AL - Albania	2
AU - Australia	2
CZ - Repubblica Ceca	2
HR - Croazia	2
JM - Giamaica	2
KE - Kenya	2
LT - Lituania	2
SA - Arabia Saudita	2
TW - Taiwan	2
AZ - Azerbaigian	1
BB - Barbados	1
CO - Colombia	1
CY - Cipro	1
IQ - Iraq	1
KZ - Kazakistan	1
LK - Sri Lanka	1
MA - Marocco	1
MX - Messico	1
MY - Malesia	1
NG - Nigeria	1
NI - Nicaragua	1
OM - Oman	1
PA - Panama	1
PE - Perù	1
PT - Portogallo	1
SK - Slovacchia (Repubblica Slovacca)	1
SV - El Salvador	1
TN - Tunisia	1
Totale	2.196

Nome	#
Ankrd2/ARPP is a novel Akt2 specific substrate and regulates myogenic differentiation upon cellular exposure to H(2)O(2	295
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism	281
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy	261
Author Correction: Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome (Scientific Reports, (2020), 10, 1, (4785), 10.1038/s41598-020-61735-3)	225
Collagen VI–NG2 axis in human tendon fibroblasts under conditions mimicking injury response	215
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder	205
Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease Models	195
PI-PLCβ1b affects Akt activation, cyclin E expression, and caspase cleavage, promoting cell survival in pro-B-lymphoblastic cells exposed to oxidative stress	167
DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions	155
First TMEM126A missense mutation in an Italian proband with optic atrophy and deafness	138
Dominant ACO2 mutations are a frequent cause of isolated optic atrophy	104
Totale	2.241

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	217	0	0	0	14	24	13	15	21	18	22	55	35
2022/2023	309	28	42	21	34	22	26	6	19	54	7	26	24
2023/2024	95	5	13	7	6	5	24	7	3	5	8	4	8
2024/2025	249	22	31	17	19	31	8	20	16	6	29	12	38
2025/2026	749	66	53	51	63	86	34	139	23	145	53	19	17
2026/2027	111	20	23	38	30	0	0	0	0	0	0	0	0
Totale													2.241

CRIS Current Research Information System