statistiche ricercatore

Nome	#
Molecular characterisation of six patients with prolidase deficiency: identification of the first small duplication in the prolidase gene and of a mutation generating symptomatic and asymptomatic outcomes within the same family.	93
Mutation analysis of five new patients affected by prolidase deficiency: the lack of enzyme activity causes necrosis-like cell death in cultured fibroblasts	82
Human recombinant prolidase from eukaryotic and prokaryotic sources. Expression, purification, characterization and long-term stability studies.	80
Differential expression of both extracellular and intracellular proteins is involved in the lethal or nonlethal phenotypic variation of BrtlIV, a murine model for osteogenesis imperfecta	79
Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure-function relationship.	73
Totale	407

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	36	0	0	0	0	0	5	0	7	1	6	17	0
2020/2021	45	7	7	0	5	2	4	1	7	0	4	8	0
2021/2022	33	1	3	0	1	2	0	1	2	3	1	6	13
2022/2023	107	7	15	0	14	14	10	0	2	43	0	2	0
2023/2024	38	5	9	1	2	2	7	0	1	3	7	0	1
2024/2025	20	3	8	3	3	3	0	0	0	0	0	0	0
Totale													407