Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

POLLACCIA, Daniela
 Distribuzione geografica
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Continente #
NA - Nord America 996
EU - Europa 602
AS - Asia 176
OC - Oceania 1
Totale 1.775
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Nazione #
US - Stati Uniti d'America 996
FI - Finlandia 173
CN - Cina 133
UA - Ucraina 128
IT - Italia 93
IE - Irlanda 36
DE - Germania 35
SE - Svezia 26
FR - Francia 25
GB - Regno Unito 25
SG - Singapore 16
RU - Federazione Russa 15
PL - Polonia 13
BE - Belgio 11
KR - Corea 10
RO - Romania 10
IN - India 9
NL - Olanda 5
TR - Turchia 5
CH - Svizzera 3
IR - Iran 3
AT - Austria 2
AU - Australia 1
BG - Bulgaria 1
GR - Grecia 1
Totale 1.775
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Città #
Ashburn 95
Ann Arbor 88
Jacksonville 72
Fairfield 71
Chandler 65
Houston 59
Wilmington 57
Woodbridge 50
Dublin 36
Seattle 29
Medford 28
Nanjing 28
Cambridge 25
Des Moines 24
New York 23
Princeton 18
Tulsa 18
Boardman 17
Jinan 13
Kraków 12
Singapore 12
Brussels 11
Dearborn 11
Shenyang 10
Beijing 9
Changsha 9
Guangzhou 9
Venice 9
Nanchang 8
Palermo 8
Seongnam 8
Milan 6
Ningbo 6
San Diego 6
Tianjin 6
Groningen 5
Izmir 5
Kumar 5
Kunming 5
Ludwigshafen am Rhein 5
Haikou 4
Hebei 4
Helsinki 4
Washington 4
Altamura 3
Catania 3
Düsseldorf 3
Hangzhou 3
Jiaxing 3
Lanzhou 3
London 3
Pune 3
Taizhou 3
Verona 3
Castelvetrano 2
Chengdu 2
Edinburgh 2
Lawrence 2
Lerici 2
Los Angeles 2
Redwood City 2
Seoul 2
Stockholm 2
Taiyuan 2
Tehran 2
Zhengzhou 2
Adliswil 1
Auburn Hills 1
Bremen 1
Columbus 1
Durham 1
Falkenstein 1
Hefei 1
Mehlingen 1
Moscow 1
Orange 1
Paris 1
Saint Petersburg 1
San Mateo 1
San Paolo di Civitate 1
Sofia 1
Southend 1
Sydney 1
Zanjan 1
Zurich 1
Totale 1.070
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Nome #
CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE 189
A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol. 150
PREVALENCE OF APOB VARIANTS IN A SAMPLE OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 132
A NOVEL COMPOUND HETEROZYGOUS MUTATION OF THE LIPOPROTEIN LIPASE GENE IN A NEWBORN WITH CHYLOMICRONEMIA 129
CLINICAL AND MOLECULAR CHARACTERIZATION OF HYPERCHOLESTEROLEMIC SICILIAN FAMILIES AND DESCRIPTION OF 3 NOVEL MUTATIONS IN THE LDLR GENE 127
A novel putative interactor for the low density lipoprotein receptor cytoplasmic domain 111
HYPOBETALIPOPROTEINEMIA AND FATTY LIVER: WHO IS THE CULPRIT 95
ΒETA ARRESTIN-2: A NEW “ACTOR” IN THE LDL-R ENDOCYTOSIS? 94
A metallothionein family member interacts with the intracellular domain of the low density lipoprotein (LDL) receptor 92
A metallothionein family member interacts with the intracellular domain of the low density lipoprotein (ldl) receptor. 86
THE METABOLIC SYNDROME IS A PREDICTOR OF CARDIOVASCULAR EVENTS IN A SICILIAN POPULATION. RESULT OF A 15 YEARS FOLLOW UP 83
INTERACTION OF THE INTRACELLULAR DOMAIN OF THE LOW DENSITY LIPOPROTEIN (LDL) RECPTOR WITH METALLOTHIONEIN2 (MT2). 83
VARIABLE PHENOTYPIC ESPRESSION IN A LIPID ABSORPTION DISORDER DUE TO A MOLECULAR DEFECT IN THE SARA2 GENE 80
COMPOUND HETEROZYGOUS FH AND FDB: IDENTIFICATION OF A SICILIAN FAMILY HARBOURING THE FDB3531 MUTATION AND THE Y398X MUTATION OF THE LDL RECEPTOR GENE. 78
A NOVEL LOSS OF FUCTION MUTATION OF PCSK9 GENE IN CAUCASIANS WITH LOW PLASMA LDL-CHOLESTEROL 75
Metallotionein 2A: a possible candidate able to interact with LDL-R cytoplasmic tail 71
METALLOTHIONEIN 2A: A POSSIBLE CANDIDATE ABLE TO INTERACT WITH LDL-R CYTOPLASMIC TAIL 63
PREVALENCE OF PCSK9 VARIANTS IN A COHORT OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 59
Totale 1.797
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Categoria #
all - tutte 5.232
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 5.232
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020453 60 27 43 37 49 47 49 14 39 12 55 21
2020/2021215 4 29 13 21 24 5 18 6 33 14 22 26
2021/2022148 3 33 0 7 4 4 2 8 21 24 5 37
2022/2023226 37 12 3 17 34 40 17 24 31 1 9 1
2023/2024157 4 23 12 16 11 34 13 14 0 1 5 24
2024/20251 1 0 0 0 0 0 0 0 0 0 0 0
Totale 1.797