statistiche ricercatore

Nome	#
Ankrd2/ARPP is a novel Akt2 specific substrate and regulates myogenic differentiation upon cellular exposure to H(2)O(2	165
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy	163
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism	162
Collagen VI–NG2 axis in human tendon fibroblasts under conditions mimicking injury response	157
DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions	114
Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease Models	111
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder	103
PI-PLCβ1b affects Akt activation, cyclin E expression, and caspase cleavage, promoting cell survival in pro-B-lymphoblastic cells exposed to oxidative stress	94
First TMEM126A missense mutation in an Italian proband with optic atrophy and deafness	86
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)	57
Dominant ACO2 mutations are a frequent cause of isolated optic atrophy	40
Totale	1.252

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	212	0	0	0	0	18	19	32	40	41	22	23	17
2020/2021	153	29	13	6	6	10	4	5	4	15	5	6	50
2021/2022	246	10	8	11	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	120	22	31	17	19	31	0	0	0	0	0	0	0
Totale													1.252

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