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LCAT

Deficit di LCAT/LCAT Deficiency. La lecitina:colesterolo aciltransferasi (LCAT) è una glicoproteina di 416 aminoacidi, sintetizzata nel fegato e secreta nel plasma, dove circola per la maggior parte associata alle lipoproteine ad alta densità (High Density Lipoproteins, HDL) (1). La concentrazione plasmatica di LCAT nell’uomo (circa 5 mg/L) è scarsamente influenzata da sesso, età, abitudini alimentari, fumo.

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LCAT | lcat.it Reviews
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Deficit di LCAT/LCAT Deficiency. La lecitina:colesterolo aciltransferasi (LCAT) è una glicoproteina di 416 aminoacidi, sintetizzata nel fegato e secreta nel plasma, dove circola per la maggior parte associata alle lipoproteine ad alta densità (High Density Lipoproteins, HDL) (1). La concentrazione plasmatica di LCAT nell’uomo (circa 5 mg/L) è scarsamente influenzata da sesso, età, abitudini alimentari, fumo.
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1 lcat
2 mutazioni/mutations
3 studio mild/mild study
4 bibliografia/bibliography
5 contacts
6 credits
7 lecitina colesterolo
8 aciltransferasi lcat
9 coupons
10 reviews
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LCAT | lcat.it Reviews

https://lcat.it

Deficit di LCAT/LCAT Deficiency. La lecitina:colesterolo aciltransferasi (LCAT) è una glicoproteina di 416 aminoacidi, sintetizzata nel fegato e secreta nel plasma, dove circola per la maggior parte associata alle lipoproteine ad alta densità (High Density Lipoproteins, HDL) (1). La concentrazione plasmatica di LCAT nell’uomo (circa 5 mg/L) è scarsamente influenzata da sesso, età, abitudini alimentari, fumo.

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lcat.it lcat.it
1

LCAT

http://www.lcat.it/index_en.html

Deficit di LCAT/LCAT Deficiency. Lecithin:cholesterol acyltransferase (LCAT) is a glycoprotein of 416 residues, synthesized almost exclusively in the liver and secreted into plasma, where it circulates bound to High Density Lipoproteins (HDL) (1). The plasma concentration of LCAT in humans (about 5 mg/L) varies little with gender, age, alimentary habits, and smoking.

2

Studio MILD

http://www.lcat.it/deficit.html

Deficit di LCAT/LCAT Deficiency. Nell’uomo, il gene che codifica per l’LCAT è localizzato sul cromosoma 16 (regione 16q22) (1). Mutazioni nel gene. Sono causa di due malattie rare del metabolismo,. FLD, OMIM# 245900) e. Vedi database delle mutazioni. Progressiva, anemia e glomerulosclerosi focale. Laboratorio del Centro Grossi Paoletti all'Ospedale Niguarda Ca' Granda, Milano: per informazioni.

3

Studio MILD

http://www.lcat.it/mild.html

Deficit di LCAT/LCAT Deficiency. Lo studio MILD (Multicenter Italian Lcat Deficiency). Centro E. Grossi Paoletti, Dipartimento di Scienze Farmacologiche, Università degli Studi di Milano (Prof.ssa Laura Calabresi). L’obiettivo primario dello studio MILD è l’identificazione di probandi/famiglie portatrici di mutazioni nel gene. La relazione genotipo-fenotipo in soggetti portatori di mutazioni specifiche nel gene LCAT. Il fenotipo biochimico e clinico in soggetti portatori di 1 o 2 alleli mutati;. Se avete...

4

Credits

http://www.lcat.it/credits.html

Deficit di LCAT/LCAT Deficiency. Template personalizzato da skokoki. Basato su modello di Dieter Schneider.

5

LCAT

http://www.lcat.it/index.html

Deficit di LCAT/LCAT Deficiency. La lecitina:colesterolo aciltransferasi (LCAT) è una glicoproteina di 416 aminoacidi, sintetizzata nel fegato e secreta nel plasma, dove circola per la maggior parte associata alle lipoproteine ad alta densità (High Density Lipoproteins, HDL) (1). La concentrazione plasmatica di LCAT nell’uomo (circa 5 mg/L) è scarsamente influenzata da sesso, età, abitudini alimentari, fumo.

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Deficit di LCAT/LCAT Deficiency. La lecitina:colesterolo aciltransferasi (LCAT) è una glicoproteina di 416 aminoacidi, sintetizzata nel fegato e secreta nel plasma, dove circola per la maggior parte associata alle lipoproteine ad alta densità (High Density Lipoproteins, HDL) (1). La concentrazione plasmatica di LCAT nell’uomo (circa 5 mg/L) è scarsamente influenzata da sesso, età, abitudini alimentari, fumo.

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