statistiche ricercatore

Continente	#
NA - Nord America	736
EU - Europa	109
AS - Asia	63
SA - Sud America	5
AF - Africa	4
OC - Oceania	2
Continente sconosciuto - Info sul continente non disponibili	1
Totale	920

Nazione	#
US - Stati Uniti d'America	732
CN - Cina	35
IT - Italia	34
DE - Germania	18
SE - Svezia	14
FR - Francia	11
JP - Giappone	9
GB - Regno Unito	8
IN - India	6
VN - Vietnam	6
BR - Brasile	5
UA - Ucraina	5
CA - Canada	4
ZA - Sudafrica	4
FI - Finlandia	3
IE - Irlanda	3
NL - Olanda	3
AE - Emirati Arabi Uniti	2
AT - Austria	2
AU - Australia	2
SG - Singapore	2
SI - Slovenia	2
A2 - ???statistics.table.value.countryCode.A2???	1
BE - Belgio	1
ES - Italia	1
GR - Grecia	1
KR - Corea	1
MO - Macao, regione amministrativa speciale della Cina	1
PT - Portogallo	1
RO - Romania	1
RU - Federazione Russa	1
SA - Arabia Saudita	1
Totale	920

Nome	#
The dynamics of the β-propeller domain in Kelch protein KLHL40 changes upon nemaline myopathy-associated mutation, file e31e124c-0452-987f-e053-3705fe0a095a	213
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions, file e31e124d-a5f9-987f-e053-3705fe0a095a	207
Pre-amyloid oligomers budding:a metastatic mechanism of proteotoxicity, file e31e124b-cf44-987f-e053-3705fe0a095a	202
Electrochemical data on redox properties of human Cofilin-2 and its Mutant S3D, file e31e124e-4293-987f-e053-3705fe0a095a	132
Phosphorylated cofilin-2 is more prone to oxidative modifications on Cys39 and favors amyloid fibril formation, file e31e124e-9cb6-987f-e053-3705fe0a095a	119
Pseudoperoxidase activity, conformational stability and aggregation propensity of the His98Tyr myoglobin variant. Implications for the onset of myoglobinopathy., file d3187d60-e5eb-46f0-af33-3aebad5d2d59	44
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions, file e31e124d-a8e3-987f-e053-3705fe0a095a	25
Human Cofilin2: Towards the Comprehension of the Molecular Mechanism, file e31e124b-a35e-987f-e053-3705fe0a095a	7
Bi-allelic mutations in MYL1 cause a severe congenital myopathy, file c8ea5e3b-979f-4771-ad77-3198f97974dc	5
Totale	954

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	59	0	0	0	0	0	0	0	0	0	19	21	19
2019/2020	150	16	9	8	11	9	18	21	14	19	11	7	7
2020/2021	268	8	6	14	39	9	9	27	29	12	60	30	25
2021/2022	237	16	7	41	50	27	4	14	7	7	3	47	14
2022/2023	139	3	5	27	18	11	34	7	4	9	2	15	4
2023/2024	70	2	12	10	4	6	5	13	12	2	4	0	0
Totale													954