statistiche ricercatore

Nome	#
A Single Intravenous Injection of AAV-PHP.B-hNDUFS4 Ameliorates the Phenotype of Ndufs4−/− Mice	181
Genome editing in mitochondria corrects a pathogenic mtDNA mutation in vivo	80
In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis	74
NAD+-dependent activation of Sirt1 corrects the phenotype in a mouse model of mitochondrial disease	70
Rapamycin rescues mitochondrial myopathy via coordinated activation of autophagy and lysosomal biogenesis	70
TTC19 Plays a Husbandry Role on UQCRFS1 Turnover in the Biogenesis of Mitochondrial Respiratory Complex III	68
Perturbed Redox Signaling Exacerbates a Mitochondrial Myopathy	66
Defective PITRM1 mitochondrial peptidase is associated with Aβ amyloidotic neurodegeneration	63
Opa1 Overexpression Protects from Early-Onset Mpv17−/−-Related Mouse Kidney Disease	51
DNA polymerase gamma mutations that impair holoenzyme stability cause catalytic subunit depletion	40
TTC19 Plays a Husbandry Role on UQCRFS1 Turnover in the Biogenesis of Mitochondrial Respiratory Complex III	12
APOPT1/COA8 assists COX assembly and is oppositely regulated by UPS and ROS	12
Defective PITRM1 mitochondrial peptidase is associated with Aβ amyloidotic neurodegeneration	10
Double administration of self-complementary AAV9(NDUFS4) prevents Leigh disease in Ndufs4(-/-) mice	8
The ferredoxin-NADP+ reductase/ferredoxin electron transfer system of Plasmodium falciparum	7
SURF1 knockout cloned pigs: Early onset of a severe lethal phenotype	3
Totale	815

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	160	0	0	0	0	0	0	20	28	41	32	29	10
2020/2021	234	25	18	30	42	1	5	3	28	30	19	11	22
2021/2022	179	14	13	25	17	3	14	13	18	3	6	22	31
2022/2023	103	19	2	3	6	7	15	12	4	8	1	16	10
2023/2024	139	15	28	9	8	4	2	10	61	1	1	0	0
Totale													815