statistiche ricercatore

Nazione	#
US - Stati Uniti d'America	628
RU - Federazione Russa	231
IT - Italia	149
SG - Singapore	143
CN - Cina	139
GB - Regno Unito	124
BR - Brasile	49
DE - Germania	44
VN - Vietnam	40
IN - India	39
FR - Francia	33
IE - Irlanda	33
SE - Svezia	31
HK - Hong Kong	29
FI - Finlandia	26
KR - Corea	20
TR - Turchia	10
MX - Messico	9
UA - Ucraina	9
ID - Indonesia	8
AR - Argentina	6
JP - Giappone	6
EC - Ecuador	4
ES - Italia	4
NL - Olanda	4
PE - Perù	4
CA - Canada	3
IQ - Iraq	3
PL - Polonia	3
VE - Venezuela	3
BD - Bangladesh	2
CL - Cile	2
LT - Lituania	2
NZ - Nuova Zelanda	2
UY - Uruguay	2
ZA - Sudafrica	2
AE - Emirati Arabi Uniti	1
AL - Albania	1
AT - Austria	1
AZ - Azerbaigian	1
BG - Bulgaria	1
CH - Svizzera	1
CI - Costa d'Avorio	1
CR - Costa Rica	1
DO - Repubblica Dominicana	1
EE - Estonia	1
EG - Egitto	1
HN - Honduras	1
HR - Croazia	1
IR - Iran	1
KE - Kenya	1
KG - Kirghizistan	1
LA - Repubblica Popolare Democratica del Laos	1
LU - Lussemburgo	1
LV - Lettonia	1
MA - Marocco	1
NG - Nigeria	1
PH - Filippine	1
PK - Pakistan	1
PS - Palestinian Territory	1
PY - Paraguay	1
QA - Qatar	1
RO - Romania	1
SA - Arabia Saudita	1
SN - Senegal	1
TH - Thailandia	1
TW - Taiwan	1
Totale	1.877

Nome	#
THE PATHOGENIC K650M MUTATION IN THE TYROSINE KINASE DOMAIN OF FGFR3 AFFECTS CYTOSKELETON ORGANIZATION	226
Abnormal signaling by FGFR3-K650M mutant associated with SADDAN disease targets paxillin causing cytoskeleton disorganization.	222
K650M-FGFR3 mutant causes cytoskeleton alteration and paxillin hyperphosphorylation through c-Src and FAK activation.	221
Mutant FGFR3 associated with SADDAN disease causes cytoskeleton disorganization through PLCγ1/Src-mediated paxillin hyperphosphorylation	204
SADDAN-FGFR3 signalling involves paxillin phosphorylation and causes cytoskeleton disorganization.	199
SADDAN-FGFR3 causes cytoskeleton disorganization and paxillin hyperphosphorylation by Src	183
Role of SADDAN-FGFR3 mutant in cytoskeletal disorganization from the endoplasmic reticulum	180
Correlation between the molecular effects of mutations at the dimer interface of alanine-glyoxylate aminotransferase leading to primary hyperoxaluria type I and the cellular response to vitamin B6	176
Membrane anchored polyQ-expanded androgen receptors: a role for S-palmitoylation in spinal and bulbar muscular atrophy (SBMA)?	162
The ILE56 mutation on different genetic backgrounds of alanine: Glyoxylate aminotransferase: Clinical features and biochemical characterization	142
Totale	1.915

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	8	0	0	0	0	0	0	0	0	0	1	7	0
2021/2022	81	3	33	0	4	6	0	1	4	5	3	6	16
2022/2023	202	13	27	15	27	20	51	6	11	27	2	3	0
2023/2024	142	2	11	11	12	18	5	30	12	0	12	20	9
2024/2025	266	10	7	18	40	8	11	20	16	60	14	29	33
2025/2026	736	52	24	51	154	215	47	59	34	53	47	0	0
Totale													1.915

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