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| Title : ANGPTL3 deficiency impairs lipoprotein production and produces adaptive changes in hepatic lipid metabolism - Burks_2024_J.Lipid.Res__100500 |
| Author(s) : Burks KH , Xie Y , Gildea M , Jung IH , Mukherjee S , Lee P , Pudupakkam U , Wagoner R , Patel V , Santana K , Alisio A , Goldberg IJ , Finck BN , Fisher EA , Davidson NO , Stitziel NO |
| Ref : J Lipid Res , :100500 , 2024 |
| Abstract : Burks_2024_J.Lipid.Res__100500 |
| ESTHER : Burks_2024_J.Lipid.Res__100500 |
| PubMedSearch : Burks_2024_J.Lipid.Res__100500 |
| PubMedID: 38219820 |
| Title : Functional Characterization of LIPA (Lysosomal Acid Lipase) Variants Associated With Coronary Artery Disease - Evans_2019_Arterioscler.Thromb.Vasc.Biol_39_2480 |
| Author(s) : Evans TD , Zhang X , Clark RE , Alisio A , Song E , Zhang H , Reilly MP , Stitziel NO , Razani B |
| Ref : Arterioscler Thromb Vasc Biol , 39 :2480 , 2019 |
| Abstract : Evans_2019_Arterioscler.Thromb.Vasc.Biol_39_2480 |
| ESTHER : Evans_2019_Arterioscler.Thromb.Vasc.Biol_39_2480 |
| PubMedSearch : Evans_2019_Arterioscler.Thromb.Vasc.Biol_39_2480 |
| PubMedID: 31645127 |
| Gene_locus related to this paper: human-LIPA |
| Title : Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease - Khera_2017_JAMA_317_937 |
| Author(s) : Khera AV , Won HH , Peloso GM , O'Dushlaine C , Liu D , Stitziel NO , Natarajan P , Nomura A , Emdin CA , Gupta N , Borecki IB , Asselta R , Duga S , Merlini PA , Correa A , Kessler T , Wilson JG , Bown MJ , Hall AS , Braund PS , Carey DJ , Murray MF , Kirchner HL , Leader JB , Lavage DR , Manus JN , Hartzel DN , Samani NJ , Schunkert H , Marrugat J , Elosua R , McPherson R , Farrall M , Watkins H , Lander ES , Rader DJ , Danesh J , Ardissino D , Gabriel S , Willer C , Abecasis GR , Saleheen D , Dewey FE , Kathiresan S |
| Ref : Jama , 317 :937 , 2017 |
| Abstract : Khera_2017_JAMA_317_937 |
| ESTHER : Khera_2017_JAMA_317_937 |
| PubMedSearch : Khera_2017_JAMA_317_937 |
| PubMedID: 28267856 |
| Gene_locus related to this paper: human-LPL |
| Title : Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia - Stitziel_2013_Arterioscler.Thromb.Vasc.Biol_33_2909 |
| Author(s) : Stitziel NO , Fouchier SW , Sjouke B , Peloso GM , Moscoso AM , Auer PL , Goel A , Gigante B , Barnes TA , Melander O , Orho-Melander M , Duga S , Sivapalaratnam S , Nikpay M , Martinelli N , Girelli D , Jackson RD , Kooperberg C , Lange LA , Ardissino D , McPherson R , Farrall M , Watkins H , Reilly MP , Rader DJ , de Faire U , Schunkert H , Erdmann J , Samani NJ , Charnas L , Altshuler D , Gabriel S , Kastelein JJ , Defesche JC , Nederveen AJ , Kathiresan S , Hovingh GK |
| Ref : Arterioscler Thromb Vasc Biol , 33 :2909 , 2013 |
| Abstract : Stitziel_2013_Arterioscler.Thromb.Vasc.Biol_33_2909 |
| ESTHER : Stitziel_2013_Arterioscler.Thromb.Vasc.Biol_33_2909 |
| PubMedSearch : Stitziel_2013_Arterioscler.Thromb.Vasc.Biol_33_2909 |
| PubMedID: 24072694 |