| Title : ANGPTL3 (Angiopoietin-Like 3) Preferentially Resides on High-Density Lipoprotein in the Human Circulation, Affecting Its Activity - Kraaijenhof_2023_J.Am.Heart.Assoc__e030476 |
| Author(s) : Kraaijenhof JM , Tromp TR , Nurmohamed NS , Reeskamp LF , Langenkamp M , Levels JHM , Boekholdt SM , Wareham NJ , Hoekstra M , Stroes ESG , Hovingh GK , Grefhorst A |
| Ref : J Am Heart Assoc , :e030476 , 2023 |
| Abstract : |
| PubMedSearch : Kraaijenhof_2023_J.Am.Heart.Assoc__e030476 |
| PubMedID: 37889183 |
| Title : ANGPTL3 (Angiopoietin-Like 3) Preferentially Resides on High-Density Lipoprotein in the Human Circulation, Affecting Its Activity - Kraaijenhof_2023_J.Am.Heart.Assoc__e030476 |
| Author(s) : Kraaijenhof JM , Tromp TR , Nurmohamed NS , Reeskamp LF , Langenkamp M , Levels JHM , Boekholdt SM , Wareham NJ , Hoekstra M , Stroes ESG , Hovingh GK , Grefhorst A |
| Ref : J Am Heart Assoc , :e030476 , 2023 |
| Abstract : |
| PubMedSearch : Kraaijenhof_2023_J.Am.Heart.Assoc__e030476 |
| PubMedID: 37889183 |
| Title : ANGPTL3 (Angiopoietin-Like 3) Preferentially Resides on High-Density Lipoprotein in the Human Circulation, Affecting Its Activity - Kraaijenhof_2023_J.Am.Heart.Assoc__e030476 |
| Author(s) : Kraaijenhof JM , Tromp TR , Nurmohamed NS , Reeskamp LF , Langenkamp M , Levels JHM , Boekholdt SM , Wareham NJ , Hoekstra M , Stroes ESG , Hovingh GK , Grefhorst A |
| Ref : J Am Heart Assoc , :e030476 , 2023 |
| Abstract : |
| PubMedSearch : Kraaijenhof_2023_J.Am.Heart.Assoc__e030476 |
| PubMedID: 37889183 |
| Title : GPIHBP1 autoantibodies in a patient with unexplained chylomicronemia - Hu_2017_J.Clin.Lipidol_11_964 |
| Author(s) : Hu X , Dallinga-Thie GM , Hovingh GK , Chang SY , Sandoval NP , Dang TLP , Fukamachi I , Miyashita K , Nakajima K , Murakami M , Fong LG , Ploug M , Young SG , Beigneux AP |
| Ref : J Clin Lipidol , 11 :964 , 2017 |
| Abstract : |
| PubMedSearch : Hu_2017_J.Clin.Lipidol_11_964 |
| PubMedID: 28666713 |
| Title : GPIHBP1 autoantibodies in a patient with unexplained chylomicronemia - Hu_2017_J.Clin.Lipidol_11_964 |
| Author(s) : Hu X , Dallinga-Thie GM , Hovingh GK , Chang SY , Sandoval NP , Dang TLP , Fukamachi I , Miyashita K , Nakajima K , Murakami M , Fong LG , Ploug M , Young SG , Beigneux AP |
| Ref : J Clin Lipidol , 11 :964 , 2017 |
| Abstract : |
| PubMedSearch : Hu_2017_J.Clin.Lipidol_11_964 |
| PubMedID: 28666713 |
| Title : GPIHBP1 autoantibodies in a patient with unexplained chylomicronemia - Hu_2017_J.Clin.Lipidol_11_964 |
| Author(s) : Hu X , Dallinga-Thie GM , Hovingh GK , Chang SY , Sandoval NP , Dang TLP , Fukamachi I , Miyashita K , Nakajima K , Murakami M , Fong LG , Ploug M , Young SG , Beigneux AP |
| Ref : J Clin Lipidol , 11 :964 , 2017 |
| Abstract : |
| PubMedSearch : Hu_2017_J.Clin.Lipidol_11_964 |
| PubMedID: 28666713 |
| Title : Clinical Features of Lysosomal Acid Lipase Deficiency - Burton_2015_J.Pediatr.Gastroenterol.Nutr_61_619 |
| Author(s) : Burton BK , Deegan PB , Enns GM , Guardamagna O , Horslen S , Hovingh GK , Lobritto SJ , Malinova V , McLin VA , Raiman J , Di Rocco M , Santra S , Sharma R , Sykut-Cegielska J , Whitley CB , Eckert S , Valayannopoulos V , Quinn AG |
| Ref : J Pediatr Gastroenterol Nutr , 61 :619 , 2015 |
| Abstract : |
| PubMedSearch : Burton_2015_J.Pediatr.Gastroenterol.Nutr_61_619 |
| PubMedID: 26252914 |
| Title : Clinical Features of Lysosomal Acid Lipase Deficiency - Burton_2015_J.Pediatr.Gastroenterol.Nutr_61_619 |
| Author(s) : Burton BK , Deegan PB , Enns GM , Guardamagna O , Horslen S , Hovingh GK , Lobritto SJ , Malinova V , McLin VA , Raiman J , Di Rocco M , Santra S , Sharma R , Sykut-Cegielska J , Whitley CB , Eckert S , Valayannopoulos V , Quinn AG |
| Ref : J Pediatr Gastroenterol Nutr , 61 :619 , 2015 |
| Abstract : |
| PubMedSearch : Burton_2015_J.Pediatr.Gastroenterol.Nutr_61_619 |
| PubMedID: 26252914 |
| Title : Clinical Features of Lysosomal Acid Lipase Deficiency - Burton_2015_J.Pediatr.Gastroenterol.Nutr_61_619 |
| Author(s) : Burton BK , Deegan PB , Enns GM , Guardamagna O , Horslen S , Hovingh GK , Lobritto SJ , Malinova V , McLin VA , Raiman J , Di Rocco M , Santra S , Sharma R , Sykut-Cegielska J , Whitley CB , Eckert S , Valayannopoulos V , Quinn AG |
| Ref : J Pediatr Gastroenterol Nutr , 61 :619 , 2015 |
| Abstract : |
| PubMedSearch : Burton_2015_J.Pediatr.Gastroenterol.Nutr_61_619 |
| PubMedID: 26252914 |
| Title : Familial LCAT deficiency: from renal replacement to enzyme replacement - Stoekenbroek_2013_Neth.J.Med_71_29 |
| Author(s) : Stoekenbroek RM , van den Bergh Weerman MA , Hovingh GK , Potter van Loon BJ , Siegert CE , Holleboom AG |
| Ref : Neth J Med , 71 :29 , 2013 |
| Abstract : |
| PubMedSearch : Stoekenbroek_2013_Neth.J.Med_71_29 |
| PubMedID: 23412821 |
| Gene_locus related to this paper: human-LCAT |
| 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 : |
| PubMedSearch : Stitziel_2013_Arterioscler.Thromb.Vasc.Biol_33_2909 |
| PubMedID: 24072694 |
| 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 : |
| PubMedSearch : Stitziel_2013_Arterioscler.Thromb.Vasc.Biol_33_2909 |
| PubMedID: 24072694 |
| Title : Familial LCAT deficiency: from renal replacement to enzyme replacement - Stoekenbroek_2013_Neth.J.Med_71_29 |
| Author(s) : Stoekenbroek RM , van den Bergh Weerman MA , Hovingh GK , Potter van Loon BJ , Siegert CE , Holleboom AG |
| Ref : Neth J Med , 71 :29 , 2013 |
| Abstract : |
| PubMedSearch : Stoekenbroek_2013_Neth.J.Med_71_29 |
| PubMedID: 23412821 |
| Gene_locus related to this paper: human-LCAT |
| Title : Familial LCAT deficiency: from renal replacement to enzyme replacement - Stoekenbroek_2013_Neth.J.Med_71_29 |
| Author(s) : Stoekenbroek RM , van den Bergh Weerman MA , Hovingh GK , Potter van Loon BJ , Siegert CE , Holleboom AG |
| Ref : Neth J Med , 71 :29 , 2013 |
| Abstract : |
| PubMedSearch : Stoekenbroek_2013_Neth.J.Med_71_29 |
| PubMedID: 23412821 |
| Gene_locus related to this paper: human-LCAT |
| 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 : |
| PubMedSearch : Stitziel_2013_Arterioscler.Thromb.Vasc.Biol_33_2909 |
| PubMedID: 24072694 |
| Title : Segregation of LIPG, CETP, and GALNT2 mutations in Caucasian families with extremely high HDL cholesterol - Tietjen_2012_PLoS.One_7_e37437 |
| Author(s) : Tietjen I , Hovingh GK , Singaraja RR , Radomski C , Barhdadi A , McEwen J , Chan E , Mattice M , Legendre A , Franchini PL , Dube MP , Kastelein JJ , Hayden MR |
| Ref : PLoS ONE , 7 :e37437 , 2012 |
| Abstract : |
| PubMedSearch : Tietjen_2012_PLoS.One_7_e37437 |
| PubMedID: 22952570 |
| Title : Segregation of LIPG, CETP, and GALNT2 mutations in Caucasian families with extremely high HDL cholesterol - Tietjen_2012_PLoS.One_7_e37437 |
| Author(s) : Tietjen I , Hovingh GK , Singaraja RR , Radomski C , Barhdadi A , McEwen J , Chan E , Mattice M , Legendre A , Franchini PL , Dube MP , Kastelein JJ , Hayden MR |
| Ref : PLoS ONE , 7 :e37437 , 2012 |
| Abstract : |
| PubMedSearch : Tietjen_2012_PLoS.One_7_e37437 |
| PubMedID: 22952570 |
| Title : Segregation of LIPG, CETP, and GALNT2 mutations in Caucasian families with extremely high HDL cholesterol - Tietjen_2012_PLoS.One_7_e37437 |
| Author(s) : Tietjen I , Hovingh GK , Singaraja RR , Radomski C , Barhdadi A , McEwen J , Chan E , Mattice M , Legendre A , Franchini PL , Dube MP , Kastelein JJ , Hayden MR |
| Ref : PLoS ONE , 7 :e37437 , 2012 |
| Abstract : |
| PubMedSearch : Tietjen_2012_PLoS.One_7_e37437 |
| PubMedID: 22952570 |
| Title : Proteinuria in early childhood due to familial LCAT deficiency caused by loss of a disulfide bond in lecithin:cholesterol acyl transferase - Holleboom_2011_Atherosclerosis_216_161 |
| Author(s) : Holleboom AG , Kuivenhoven JA , van Olden CC , Peter J , Schimmel AW , Levels JH , Valentijn RM , Vos P , Defesche JC , Kastelein JJ , Hovingh GK , Stroes ES , Hollak CE |
| Ref : Atherosclerosis , 216 :161 , 2011 |
| Abstract : |
| PubMedSearch : Holleboom_2011_Atherosclerosis_216_161 |
| PubMedID: 21315357 |
| Gene_locus related to this paper: human-LCAT |
| Title : Proteinuria in early childhood due to familial LCAT deficiency caused by loss of a disulfide bond in lecithin:cholesterol acyl transferase - Holleboom_2011_Atherosclerosis_216_161 |
| Author(s) : Holleboom AG , Kuivenhoven JA , van Olden CC , Peter J , Schimmel AW , Levels JH , Valentijn RM , Vos P , Defesche JC , Kastelein JJ , Hovingh GK , Stroes ES , Hollak CE |
| Ref : Atherosclerosis , 216 :161 , 2011 |
| Abstract : |
| PubMedSearch : Holleboom_2011_Atherosclerosis_216_161 |
| PubMedID: 21315357 |
| Gene_locus related to this paper: human-LCAT |
| Title : Proteinuria in early childhood due to familial LCAT deficiency caused by loss of a disulfide bond in lecithin:cholesterol acyl transferase - Holleboom_2011_Atherosclerosis_216_161 |
| Author(s) : Holleboom AG , Kuivenhoven JA , van Olden CC , Peter J , Schimmel AW , Levels JH , Valentijn RM , Vos P , Defesche JC , Kastelein JJ , Hovingh GK , Stroes ES , Hollak CE |
| Ref : Atherosclerosis , 216 :161 , 2011 |
| Abstract : |
| PubMedSearch : Holleboom_2011_Atherosclerosis_216_161 |
| PubMedID: 21315357 |
| Gene_locus related to this paper: human-LCAT |
| Title : Common variants of multiple genes that control reverse cholesterol transport together explain only a minor part of the variation of HDL cholesterol levels - Boekholdt_2006_Clin.Genet_69_263 |
| Author(s) : Boekholdt SM , Souverein OW , Tanck MW , Hovingh GK , Kuivenhoven JA , Peters RI , Jansen H , Schiffers PM , van der Wall EE , Doevendans PA , Reitsma PH , Zwinderman AH , Kastelein JJ , Jukema JW |
| Ref : Clin Genet , 69 :263 , 2006 |
| Abstract : |
| PubMedSearch : Boekholdt_2006_Clin.Genet_69_263 |
| PubMedID: 16542392 |
| Title : Common variants of multiple genes that control reverse cholesterol transport together explain only a minor part of the variation of HDL cholesterol levels - Boekholdt_2006_Clin.Genet_69_263 |
| Author(s) : Boekholdt SM , Souverein OW , Tanck MW , Hovingh GK , Kuivenhoven JA , Peters RI , Jansen H , Schiffers PM , van der Wall EE , Doevendans PA , Reitsma PH , Zwinderman AH , Kastelein JJ , Jukema JW |
| Ref : Clin Genet , 69 :263 , 2006 |
| Abstract : |
| PubMedSearch : Boekholdt_2006_Clin.Genet_69_263 |
| PubMedID: 16542392 |
| Title : Common variants of multiple genes that control reverse cholesterol transport together explain only a minor part of the variation of HDL cholesterol levels - Boekholdt_2006_Clin.Genet_69_263 |
| Author(s) : Boekholdt SM , Souverein OW , Tanck MW , Hovingh GK , Kuivenhoven JA , Peters RI , Jansen H , Schiffers PM , van der Wall EE , Doevendans PA , Reitsma PH , Zwinderman AH , Kastelein JJ , Jukema JW |
| Ref : Clin Genet , 69 :263 , 2006 |
| Abstract : |
| PubMedSearch : Boekholdt_2006_Clin.Genet_69_263 |
| PubMedID: 16542392 |