The lipoprotein lipase (Asn291->Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia

Hoffer, M.J.V.
Bredie, S.J.H.
Snieder, H.
Reymer, P.W.A.
Demacker, P.N.M.
Havekes, L.M.
Boomsma, D.I.
Stalenhoef, A.F.H.
Frants, R.R.
Kastelein, J.J.P.

January 1998

Familial combined hyperlipidemia (FCHL) is a frequent cause of premature coronary artery disease. Af...

Lysosomal acid lipase deficiency: a hidden disease among cohorts of familial hypercholesterolemia?

Chora, J.R.
Alves, A.C.
Medeiros, A.M.
Mariano, C.
Lobarinhas, G.
Guerra, A.
Mansilha, H.
Cortez-Pinto, H.
Bourbon, M.

March 2017

Highlights: - Dyslipidemia phenotype of patients with familial hypercholesterolemia and lysosomal ac...

Small and dense LDL in Familial Combined Hyperlipidemia and N291S polymorphism of the lipoprotein lipase gene

López, Antonio
Jarabo, Maria M.
Martinez-Triguero, Maria L.
Morales, María
Sola, Eva
Banuls, Celia
Casado, Marta
Hernández Mijares, Antonio

March 2009

18 pagesm 2 figures. -- PMID: 19335919 [PubMed]There is a predominance of small and dense LDL choles...

The lipoprotein lipase (Asn 291 Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia

Hoffer, M.J.V.
Bredie, S.J.H.
Boomsma, D.I.
Reymer, P.W.A.
Kastelein, J.J.P.
de Knijff, P.
Demacker, P.N.M.
Stalenhoef, A.F.H.
Havekes, L.M.
Frants, R.R.

January 1996

Familial combined hyperlipidaemia (FCHL) is one of the major genetic causes of coronary heart diseas...

Metabolic and genetic aspects of familial combined hyperlipidaemia with emphasis on low-density lipoprotein heterogeneity

Bredie, S.J.H.
Demacker, P.N.M.
Stalenhoef, A.F.H.

January 1997

Contains fulltext : 24395___.PDF (publisher's version ) (Open Access

Familial combined hyperlipidemia: metabolic and genetic aspects

Bredie, S.J.H.

January 1997

Contains fulltext : mmubn000001_255044194.pdf (publisher's version ) (Open Access)...

Paraoxonase (PON1) is associated with familial combined hyperlipidemia.

Himbergen, T.M. van
Tits, L.J.H. van
Avest, E. ter
Roest, M.
Voorbij, H.A.
Graaf, J. de
Stalenhoef, A.F.H.

January 2008

Contains fulltext : 71837.pdf ( ) (Closed access)Familial combined hyperlipidemia ...

A frequent mutation in the lipoprotein lipase gene (D9N) deteriorates the biochemical and clinical phenotype of familial hypercholesterolemia

Wittekoek, ME
Moll, E
Pimstone, SN
Lansberg, PJ
Defesche, JC
van Doormaal, JJ
Hayden, MR
Kastelein, JJP

November 1999

The D9N substitution is a common mutation in the lipoprotein lipase (LPL) gene, This mutation has be...

Identification of a Gain-of-Function LIPC Variant as a Novel Cause of Familial Combined Hypocholesterolemia

Dijk, W.
Filippo, M. di
Kooijman, S.
Eenige, R. van
Rimbert, A.
Caillaud, A.
Thedrez, A.
Arnaud, L.
Pronk, A.
Garcon, D.
Sotin, T.
Lindenbaum, P.
Garcia, E.O.
Barros, J.P.P. de
Duvillard, L.
Si-Tayeb, K.
Amigo, N.
Questel, J.Y. le
Rensen, P.C.N.
May, C. le
Moulin, P.
Cariou, B.

September 2022

Background: Atherosclerotic cardiovascular disease is the main cause of mortality worldwide and is s...

Interaction between the Asn291Ser variant of the LPL gene and insulin resistance on dyslipidaemia in high risk individuals for Type 2 diabetes mellitus

Klannemark, Mia
Suurinkeroinen, L
Orho-Melander, Marju
Groop, Leif
Taskinen, M R

January 2000

AIMS: Lipoprotein lipase (LPL) is a major regulator of triglyceride clearance. A genetic variant of ...

Hoffer, M.J.V.
Bredie, S.J.H.
Snieder, H.
Reymer, P.W.A.
Demacker, P.N.M.
Havekes, L.M.
Boomsma, D.I.
Stalenhoef, A.F.H.
Frants, R.R.
Kastelein, J.J.P.

January 1998

Familial combined hyperlipidemia (FCHL) is a frequent cause of premature coronary artery disease. Af...

Lysosomal acid lipase deficiency: a hidden disease among cohorts of familial hypercholesterolemia?

Chora, J.R.
Alves, A.C.
Medeiros, A.M.
Mariano, C.
Lobarinhas, G.
Guerra, A.
Mansilha, H.
Cortez-Pinto, H.
Bourbon, M.

March 2017

Highlights: - Dyslipidemia phenotype of patients with familial hypercholesterolemia and lysosomal ac...

Small and dense LDL in Familial Combined Hyperlipidemia and N291S polymorphism of the lipoprotein lipase gene

López, Antonio
Jarabo, Maria M.
Martinez-Triguero, Maria L.
Morales, María
Sola, Eva
Banuls, Celia
Casado, Marta
Hernández Mijares, Antonio

March 2009

18 pagesm 2 figures. -- PMID: 19335919 [PubMed]There is a predominance of small and dense LDL choles...

The lipoprotein lipase (Asn 291 Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia

Hoffer, M.J.V.
Bredie, S.J.H.
Boomsma, D.I.
Reymer, P.W.A.
Kastelein, J.J.P.
de Knijff, P.
Demacker, P.N.M.
Stalenhoef, A.F.H.
Havekes, L.M.
Frants, R.R.

January 1996

Familial combined hyperlipidaemia (FCHL) is one of the major genetic causes of coronary heart diseas...

Metabolic and genetic aspects of familial combined hyperlipidaemia with emphasis on low-density lipoprotein heterogeneity

Bredie, S.J.H.
Demacker, P.N.M.
Stalenhoef, A.F.H.

January 1997

Contains fulltext : 24395___.PDF (publisher's version ) (Open Access

Familial combined hyperlipidemia: metabolic and genetic aspects

Bredie, S.J.H.

January 1997

Contains fulltext : mmubn000001_255044194.pdf (publisher's version ) (Open Access)...

Paraoxonase (PON1) is associated with familial combined hyperlipidemia.

Himbergen, T.M. van
Tits, L.J.H. van
Avest, E. ter
Roest, M.
Voorbij, H.A.
Graaf, J. de
Stalenhoef, A.F.H.

January 2008

Contains fulltext : 71837.pdf ( ) (Closed access)Familial combined hyperlipidemia ...

A frequent mutation in the lipoprotein lipase gene (D9N) deteriorates the biochemical and clinical phenotype of familial hypercholesterolemia

Wittekoek, ME
Moll, E
Pimstone, SN
Lansberg, PJ
Defesche, JC
van Doormaal, JJ
Hayden, MR
Kastelein, JJP

November 1999

The D9N substitution is a common mutation in the lipoprotein lipase (LPL) gene, This mutation has be...

Identification of a Gain-of-Function LIPC Variant as a Novel Cause of Familial Combined Hypocholesterolemia

Dijk, W.
Filippo, M. di
Kooijman, S.
Eenige, R. van
Rimbert, A.
Caillaud, A.
Thedrez, A.
Arnaud, L.
Pronk, A.
Garcon, D.
Sotin, T.
Lindenbaum, P.
Garcia, E.O.
Barros, J.P.P. de
Duvillard, L.
Si-Tayeb, K.
Amigo, N.
Questel, J.Y. le
Rensen, P.C.N.
May, C. le
Moulin, P.
Cariou, B.

September 2022

Background: Atherosclerotic cardiovascular disease is the main cause of mortality worldwide and is s...

Interaction between the Asn291Ser variant of the LPL gene and insulin resistance on dyslipidaemia in high risk individuals for Type 2 diabetes mellitus

Klannemark, Mia
Suurinkeroinen, L
Orho-Melander, Marju
Groop, Leif
Taskinen, M R

January 2000

AIMS: Lipoprotein lipase (LPL) is a major regulator of triglyceride clearance. A genetic variant of ...

Hoffer, M.J.V.
Bredie, S.J.H.
Snieder, H.
Reymer, P.W.A.
Demacker, P.N.M.
Havekes, L.M.
Boomsma, D.I.
Stalenhoef, A.F.H.
Frants, R.R.
Kastelein, J.J.P.

January 1998

Familial combined hyperlipidemia (FCHL) is a frequent cause of premature coronary artery disease. Af...

Lysosomal acid lipase deficiency: a hidden disease among cohorts of familial hypercholesterolemia?

Chora, J.R.
Alves, A.C.
Medeiros, A.M.
Mariano, C.
Lobarinhas, G.
Guerra, A.
Mansilha, H.
Cortez-Pinto, H.
Bourbon, M.

March 2017

Highlights: - Dyslipidemia phenotype of patients with familial hypercholesterolemia and lysosomal ac...

Small and dense LDL in Familial Combined Hyperlipidemia and N291S polymorphism of the lipoprotein lipase gene

López, Antonio
Jarabo, Maria M.
Martinez-Triguero, Maria L.
Morales, María
Sola, Eva
Banuls, Celia
Casado, Marta
Hernández Mijares, Antonio

March 2009

18 pagesm 2 figures. -- PMID: 19335919 [PubMed]There is a predominance of small and dense LDL choles...

The lipoprotein lipase (Asn291->Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia

Abstract

Extracted data

The lipoprotein lipase (Asn291->Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia

Abstract

Extracted data

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