statistiche ricercatore

Continente	#
NA - Nord America	670
AS - Asia	373
EU - Europa	270
SA - Sud America	107
Continente sconosciuto - Info sul continente non disponibili	46
AF - Africa	11
OC - Oceania	1
Totale	1.478

Nazione	#
US - Stati Uniti d'America	634
IT - Italia	168
SG - Singapore	117
BR - Brasile	82
CN - Cina	82
VN - Vietnam	49
HK - Hong Kong	28
BD - Bangladesh	26
RU - Federazione Russa	25
CA - Canada	18
IN - India	15
KR - Corea	14
DE - Germania	13
GB - Regno Unito	10
AT - Austria	8
FR - Francia	8
ID - Indonesia	8
IQ - Iraq	8
FI - Finlandia	7
ZA - Sudafrica	7
EC - Ecuador	6
JP - Giappone	6
MX - Messico	6
NL - Olanda	6
AR - Argentina	5
PK - Pakistan	5
ES - Italia	4
PR - Porto Rico	4
TR - Turchia	4
VE - Venezuela	4
CL - Cile	3
CO - Colombia	3
DK - Danimarca	3
EG - Egitto	3
NI - Nicaragua	3
PE - Perù	3
PL - Polonia	3
UA - Ucraina	3
BE - Belgio	2
CH - Svizzera	2
CR - Costa Rica	2
IL - Israele	2
SE - Svezia	2
UZ - Uzbekistan	2
AL - Albania	1
AU - Australia	1
AZ - Azerbaigian	1
BY - Bielorussia	1
CW - ???statistics.table.value.countryCode.CW???	1
DO - Repubblica Dominicana	1
GT - Guatemala	1
KE - Kenya	1
LT - Lituania	1
LU - Lussemburgo	1
LV - Lettonia	1
MY - Malesia	1
NP - Nepal	1
PA - Panama	1
PH - Filippine	1
PY - Paraguay	1
RO - Romania	1
SA - Arabia Saudita	1
TH - Thailandia	1
TJ - Tagikistan	1
Totale	1.433

Nome	#
Testing lipid nanoparticles as delivery tool for genome editing of murine haematopoietic stem and progenitor cells	222
Correction of osteopetrosis in the neonate oc/oc murine model after lentiviral vector gene therapy and non-genotoxic conditioning	208
Non-genotoxic conditoning and in vivo gene transfer as new therapeutical approaches for autosomal recessive osteopetrosis	192
Pneumocystis murina lesions in lungs of experimentally infected Cd40l-/- mice	188
Partial correction of immunodeficiency by lentiviral vector gene therapy in mouse models carrying Rag1 hypomorphic mutations	178
Ionic Regulation of T-Cell Function and Anti-Tumour Immunity	154
In vivo haemopoietic stem cell gene therapy enabled by postnatal trafficking	61
A standardized protocol for assessing immunodeficiency in mouse models	53
Preclinical modeling of WHIM Syndrome to develop an adenine base editing therapeutic approach	49
Non-Genotoxic conditioning to implement therapy strategy in Autosomal Recessive Osteopetrosis	37
In vivo gene transfer as a new therapeutical approach for autosomal recessive osteopetrosis	35
Cxcr4-R334X mouse: a model to investigate the pathogenesis of WHIM Syndrome and assess novel gene correction therapy	35
Cxcr4-R334X mouse: a model to study WHIM syndrome pathogenesis and evaluate innovative gene correction treatment	34
Preclinical modeling of WHIM Syndrome to develop a base editing therapeutic approach	32
Totale	1.478

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2024/2025	206	0	0	0	16	56	5	20	8	15	31	20	35
2025/2026	758	84	97	54	76	96	30	72	34	43	40	31	101
2026/2027	514	152	68	136	158	0	0	0	0	0	0	0	0
Totale													1.478

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