statistiche ricercatore

Continente	#
NA - Nord America	866
EU - Europa	604
AS - Asia	515
SA - Sud America	67
Continente sconosciuto - Info sul continente non disponibili	14
AF - Africa	9
OC - Oceania	1
Totale	2.076

Nazione	#
US - Stati Uniti d'America	844
RU - Federazione Russa	221
CN - Cina	209
SG - Singapore	168
GB - Regno Unito	161
IT - Italia	73
BR - Brasile	57
VN - Vietnam	52
HK - Hong Kong	35
FR - Francia	32
SE - Svezia	27
DE - Germania	21
FI - Finlandia	20
KR - Corea	17
IE - Irlanda	15
CA - Canada	13
BE - Belgio	12
IN - India	9
ZA - Sudafrica	7
BD - Bangladesh	4
ES - Italia	4
CR - Costa Rica	3
JP - Giappone	3
NL - Olanda	3
PK - Pakistan	3
PL - Polonia	3
TR - Turchia	3
UY - Uruguay	3
AR - Argentina	2
EC - Ecuador	2
GT - Guatemala	2
ID - Indonesia	2
IL - Israele	2
LV - Lettonia	2
MX - Messico	2
UA - Ucraina	2
AE - Emirati Arabi Uniti	1
AM - Armenia	1
AU - Australia	1
BG - Bulgaria	1
BO - Bolivia	1
CL - Cile	1
CW - ???statistics.table.value.countryCode.CW???	1
CZ - Repubblica Ceca	1
GL - Groenlandia	1
IQ - Iraq	1
LT - Lituania	1
MD - Moldavia	1
MY - Malesia	1
NG - Nigeria	1
NP - Nepal	1
PT - Portogallo	1
RO - Romania	1
RS - Serbia	1
SA - Arabia Saudita	1
SK - Slovacchia (Repubblica Slovacca)	1
SV - El Salvador	1
TN - Tunisia	1
TW - Taiwan	1
UZ - Uzbekistan	1
VE - Venezuela	1
XK - ???statistics.table.value.countryCode.XK???	1
Totale	2.064

Nome	#
THE DEFICIT OF ALANINE:GLYOXYLATE AMINOTRANSFERASE LEADS TO PRIMARY HYPEROXALURIA TYPE I: A BIOCHEMICAL STUDY TO UNDERSTAND THE ROLE OF INTERALLELIC COMPLEMENTATION IN COMPOUND HETEROZYGOUS PATIENTS AND TO PROJECT THE DEVELOPMENT OF AN ENZYME ADMINISTRATION THERAPY.	322
Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferase	321
Allele-specific Characterization of Alanine: Glyoxylate Aminotransferase Variants Associated with Primary Hyperoxaluria	311
S250F variant associated with aromatic amino acid decarboxylase deficiency: molecular defects and intracellular rescue by pyridoxine	233
Misfolding caused by the pathogenic mutation G47R on the minor allele of alanine:glyoxylate aminotransferase and chaperoning activity of pyridoxine	215
S81 L and G170R mutations causing Primary Hyperoxaluria Type I in homozygosis and heterozygosis: an example of positive interallelic complementation.	178
Tat-mediated delivery of human alanine:glyoxylate aminotransferase in a cellular model of Primary Hyperoxaluria Type I	177
Use of polymer conjugates for the intraperoxisomal delivery of engineered human alanine:glyoxylate aminotransferase as a protein therapy for primary hyperoxaluria type I	161
Rapid profiling of disease alleles using a tunable reporter of protein misfolding	158
Totale	2.076

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	59	0	0	0	2	6	5	5	6	5	3	7	20
2022/2023	188	13	28	17	31	18	32	3	12	22	0	7	5
2023/2024	80	6	5	4	4	11	13	2	14	0	6	13	2
2024/2025	234	13	21	4	40	9	12	16	10	40	21	21	27
2025/2026	764	54	33	91	105	190	69	71	44	29	45	12	21
2026/2027	190	7	8	34	141	0	0	0	0	0	0	0	0
Totale													2.076

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