statistiche ricercatore

Continente	#
NA - Nord America	787
EU - Europa	730
AS - Asia	713
AF - Africa	62
Continente sconosciuto - Info sul continente non disponibili	47
SA - Sud America	34
Totale	2.373

Nazione	#
US - Stati Uniti d'America	773
IT - Italia	359
SG - Singapore	209
CN - Cina	205
VN - Vietnam	167
GB - Regno Unito	76
DE - Germania	61
SE - Svezia	46
FR - Francia	32
KR - Corea	31
HK - Hong Kong	29
NL - Olanda	29
RU - Federazione Russa	26
CI - Costa d'Avorio	23
IN - India	23
IE - Irlanda	22
BR - Brasile	20
CH - Svizzera	15
FI - Finlandia	15
TG - Togo	15
SC - Seychelles	11
AT - Austria	9
BD - Bangladesh	8
BG - Bulgaria	8
JP - Giappone	8
ZA - Sudafrica	8
ES - Italia	7
EE - Estonia	6
AR - Argentina	5
CA - Canada	5
IQ - Iraq	5
PH - Filippine	5
BE - Belgio	4
ID - Indonesia	4
JO - Giordania	4
TW - Taiwan	4
CO - Colombia	3
CZ - Repubblica Ceca	3
MX - Messico	3
PK - Pakistan	3
PL - Polonia	3
CL - Cile	2
EC - Ecuador	2
JM - Giamaica	2
MA - Marocco	2
RO - Romania	2
SA - Arabia Saudita	2
TR - Turchia	2
UA - Ucraina	2
AE - Emirati Arabi Uniti	1
BB - Barbados	1
BJ - Benin	1
CR - Costa Rica	1
CY - Cipro	1
DK - Danimarca	1
DZ - Algeria	1
EU - Europa	1
GR - Grecia	1
GT - Guatemala	1
HN - Honduras	1
HR - Croazia	1
MG - Madagascar	1
MY - Malesia	1
PY - Paraguay	1
SI - Slovenia	1
SK - Slovacchia (Repubblica Slovacca)	1
UZ - Uzbekistan	1
VE - Venezuela	1
XK - ???statistics.table.value.countryCode.XK???	1
Totale	2.328

Nome	#
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy	333
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism	276
COQ7 defect causes prenatal onset of mitochondrial CoQ10 deficiency with cardiomyopathy and gastrointestinal obstruction	260
Unravelling the Effects of the Mutation m.3571insC/MT-ND1 on Respiratory Complexes Structural Organization	218
Mild phenotypes and proper supercomplex assembly in human cells carrying the homoplasmic m.15557G > A mutation in cytochrome b gene	207
Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys	200
The cytochrome B p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes	196
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance.	182
Cellular and mitochondrial determination of low molecular mass organic acids by LC-MS/MS	146
Complex II phosphorylation is triggered by unbalanced redox homeostasis in cells lacking complex III	137
null	109
null	109
Totale	2.373

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	166	0	6	17	5	14	6	2	10	16	17	46	27
2022/2023	262	18	44	9	34	15	24	5	13	41	3	30	26
2023/2024	118	4	8	3	6	9	30	5	6	14	13	15	5
2024/2025	466	42	32	63	32	52	34	29	14	13	29	43	83
2025/2026	879	86	111	72	94	108	37	81	17	151	63	42	17
2026/2027	42	22	20	0	0	0	0	0	0	0	0	0	0
Totale													2.373

CRIS Current Research Information System