statistiche ricercatore

Continente	#
NA - Nord America	720
EU - Europa	703
AS - Asia	702
AF - Africa	62
SA - Sud America	31
Continente sconosciuto - Info sul continente non disponibili	2
Totale	2.220

Nazione	#
US - Stati Uniti d'America	714
IT - Italia	336
SG - Singapore	208
CN - Cina	200
VN - Vietnam	167
GB - Regno Unito	76
DE - Germania	61
SE - Svezia	45
FR - Francia	32
KR - Corea	31
HK - Hong Kong	29
NL - Olanda	28
RU - Federazione Russa	26
CI - Costa d'Avorio	23
IE - Irlanda	22
IN - India	22
BR - Brasile	19
FI - Finlandia	15
TG - Togo	15
CH - Svizzera	13
SC - Seychelles	11
AT - Austria	9
BG - Bulgaria	8
JP - Giappone	8
ZA - Sudafrica	8
ES - Italia	7
EE - Estonia	6
BD - Bangladesh	5
IQ - Iraq	5
PH - Filippine	5
AR - Argentina	4
BE - Belgio	4
ID - Indonesia	4
JO - Giordania	4
TW - Taiwan	4
CA - Canada	3
CO - Colombia	3
CZ - Repubblica Ceca	3
MX - Messico	3
PK - Pakistan	3
PL - Polonia	3
CL - Cile	2
EC - Ecuador	2
MA - Marocco	2
RO - Romania	2
SA - Arabia Saudita	2
TR - Turchia	2
UA - Ucraina	2
AE - Emirati Arabi Uniti	1
BJ - Benin	1
CY - Cipro	1
DK - Danimarca	1
DZ - Algeria	1
EU - Europa	1
GR - Grecia	1
HR - Croazia	1
MG - Madagascar	1
SI - Slovenia	1
SK - Slovacchia (Repubblica Slovacca)	1
UZ - Uzbekistan	1
VE - Venezuela	1
XK - ???statistics.table.value.countryCode.XK???	1
Totale	2.220

Nome	#
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy	304
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism	262
COQ7 defect causes prenatal onset of mitochondrial CoQ10 deficiency with cardiomyopathy and gastrointestinal obstruction	239
Unravelling the Effects of the Mutation m.3571insC/MT-ND1 on Respiratory Complexes Structural Organization	216
Mild phenotypes and proper supercomplex assembly in human cells carrying the homoplasmic m.15557G > A mutation in cytochrome b gene	199
Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys	192
The cytochrome B p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes	192
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance.	177
Cellular and mitochondrial determination of low molecular mass organic acids by LC-MS/MS	139
Complex II phosphorylation is triggered by unbalanced redox homeostasis in cells lacking complex III	127
null	109
null	109
Totale	2.265

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	55	0	0	0	0	0	0	0	0	0	6	2	47
2021/2022	174	8	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	813	86	111	72	94	108	37	81	17	151	56	0	0
Totale													2.265

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