statistiche ricercatore

Nome	#
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy	161
Ankrd2/ARPP is a novel Akt2 specific substrate and regulates myogenic differentiation upon cellular exposure to H(2)O(2	160
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism	156
Collagen VI–NG2 axis in human tendon fibroblasts under conditions mimicking injury response	153
DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions	113
Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease Models	109
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder	100
PI-PLCβ1b affects Akt activation, cyclin E expression, and caspase cleavage, promoting cell survival in pro-B-lymphoblastic cells exposed to oxidative stress	91
First TMEM126A missense mutation in an Italian proband with optic atrophy and deafness	84
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)	52
Dominant ACO2 mutations are a frequent cause of isolated optic atrophy	37
Totale	1.216

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	225	0	0	0	13	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	84	22	31	17	14	0	0	0	0	0	0	0	0
Totale													1.216

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