Mutations in the human lipoprotein lipase gene and their relationship to hyperlipidaemia

Clinical biochemistry of lipoproteins Altered expression of LDL-R and PDGF-A genes in hyperlipidaemia

Adbeish, I.S

January 1996

SIGLEAvailable from British Library Document Supply Centre-DSC:DXN005688 / BLDSC - British Library D...

A COMMON VARIANT IN THE GENE FOR LIPOPROTEIN-LIPASE (ASP9-]ASN) - FUNCTIONAL IMPLICATIONS AND PREVALENCE IN NORMAL AND HYPERLIPIDEMIC SUBJECTS

OLIVECRONA, G
KASTELEIN, JJP
HAMSTEN, A
HUMPHRIES, SE
TALMUD, PJ
MAILLY, F
TUGRUL, Y
REYMER, PWA
BRUIN, T
SEED, M
GROENEMEYER, BF
ASPLUNDCARLSON, A
VALLANCE, D
WINDER, AF
MILLER, GJ

January 1995

Subjects with combined hyperlipidemia (CHL) were screened for mutations in the lipoprotein lipase (L...

Identification and the relationship between mutations in the lipoprotein lipase gene, dyslipidemia and coronary heart disease

Gagné, S. Eric

January 1999

Lipoprotein lipase (LPL) is a critical enzyme which primary function is to hydrolyze triglycerides ...

Identification and characterization of mutations in the low-density-lipoprotein (LDL) receptor gene in patients with familial hypercholesterolaemia

Sun, X

January 1995

SIGLEAvailable from British Library Document Supply Centre-DSC:DXN005113 / BLDSC - British Library D...

Molecular genetics of lipoprotein (a)

Gaw, A.

January 1995

SIGLEAvailable from British Library Document Supply Centre-DSC:DXN024853 / BLDSC - British Library D...

Genetic varients of the lipid transport genes, dyslipaemia, and coronary heart disease

Zhang, Q.

January 1997

SIGLEAvailable from British Library Document Supply Centre-DSC:DXN022210 / BLDSC - British Library D...

Reverse genetics of familial combined hyperlipidaemia

Worsley, A.P

January 1993

SIGLEAvailable from British Library Document Supply Centre- DSC:DXN003289 / BLDSC - British Library ...

Pathogenic mutations of the lipoprotein lipase gene in Chinese patients with hypertriglyceridemic type 2 diabetes.

Poon, PM
Yang, T
Pang, CP
Tsang, MW
Lam, CW
Chan, LY
Wu, XQ
Tomlinson, B
Baum, L

January 2003

Elevated plasma triglyceride and nonesterified fatty acid concentrations may cause insulin resistanc...

The molecular genetics of familial hypercholesterolaemia in Northern Ireland

Ward, A.J

January 1995

Available from British Library Document Supply Centre-DSC:DXN004132 / BLDSC - British Library Docume...

Lipoprotein metabolism Inherited disorders of apolipoprotein B metabolism

Hamed, A.M

January 1995

SIGLEAvailable from British Library Document Supply Centre-DSC:DX189360 / BLDSC - British Library Do...

Molecular basis of lipoprotein lipase deficiency in two Austrian families with type I hyperlipoproteinemia.

Paulweber, B
Wiebusch, H
Miesenboeck, G
Funke, H
Assmann, G
Hoelzl, B
Sippl, MJ
Friedl, W
Patsch, JR
Sandhofer, F

February 1991

To determine the molecular basis for type I hyperlipoproteinemia in two Austrian families, the lipop...

Identification and characterization of two novel mutations in the LPL gene causing type I hyperlipoproteinemia

Pingitore P.
Lepore S. M.
Pirazzi C.
Mancina R. M.
Motta B. M.
Valenti L.
Berge K. E.
Retterstol K.
Leren T. P.
Wiklund O.
Romeo S.

January 2016

Background Type 1 hyperlipoproteinemia is a rare autosomal recessive disorder most often caused by m...

Identification and characterization of two novel mutations in the LPL gene causing type I hyperlipoproteinemia

Pingitore P.
Lepore S. M.
Pirazzi C.
Mancina R. M.
Motta B. M.
Valenti L.
Berge K. E.
Retterstol K.
Leren T. P.
Wiklund O.
Romeo S.

January 2016

Background Type 1 hyperlipoproteinemia is a rare autosomal recessive disorder most often caused by m...

Identification and characterization of two novel mutations in the LPL gene causing type I hyperlipoproteinemia

Pingitore P.
Lepore S. M.
Pirazzi C.
Mancina R. M.
Motta B. M.
Valenti L.
Berge K. E.
Retterstol K.
Leren T. P.
Wiklund O.
Romeo S.

January 2016

Background Type 1 hyperlipoproteinemia is a rare autosomal recessive disorder most often caused by m...

Identification and characterization of two novel mutations in the LPL gene causing type I hyperlipoproteinemia

Pingitore P.
Lepore S. M.
Pirazzi C.
Mancina R. M.
Motta B. M.
Valenti L.
Berge K. E.
Retterstol K.
Leren T. P.
Wiklund O.
Romeo S.

January 2016

Background Type 1 hyperlipoproteinemia is a rare autosomal recessive disorder most often caused by m...

Clinical biochemistry of lipoproteins Altered expression of LDL-R and PDGF-A genes in hyperlipidaemia

Adbeish, I.S

January 1996

SIGLEAvailable from British Library Document Supply Centre-DSC:DXN005688 / BLDSC - British Library D...

A COMMON VARIANT IN THE GENE FOR LIPOPROTEIN-LIPASE (ASP9-]ASN) - FUNCTIONAL IMPLICATIONS AND PREVALENCE IN NORMAL AND HYPERLIPIDEMIC SUBJECTS

OLIVECRONA, G
KASTELEIN, JJP
HAMSTEN, A
HUMPHRIES, SE
TALMUD, PJ
MAILLY, F
TUGRUL, Y
REYMER, PWA
BRUIN, T
SEED, M
GROENEMEYER, BF
ASPLUNDCARLSON, A
VALLANCE, D
WINDER, AF
MILLER, GJ

January 1995

Subjects with combined hyperlipidemia (CHL) were screened for mutations in the lipoprotein lipase (L...

Identification and the relationship between mutations in the lipoprotein lipase gene, dyslipidemia and coronary heart disease

Gagné, S. Eric

January 1999

Lipoprotein lipase (LPL) is a critical enzyme which primary function is to hydrolyze triglycerides ...

Identification and characterization of mutations in the low-density-lipoprotein (LDL) receptor gene in patients with familial hypercholesterolaemia

Sun, X

January 1995

SIGLEAvailable from British Library Document Supply Centre-DSC:DXN005113 / BLDSC - British Library D...

Molecular genetics of lipoprotein (a)

Gaw, A.

January 1995

SIGLEAvailable from British Library Document Supply Centre-DSC:DXN024853 / BLDSC - British Library D...

Genetic varients of the lipid transport genes, dyslipaemia, and coronary heart disease

Zhang, Q.

January 1997

SIGLEAvailable from British Library Document Supply Centre-DSC:DXN022210 / BLDSC - British Library D...

Reverse genetics of familial combined hyperlipidaemia

Worsley, A.P

January 1993

SIGLEAvailable from British Library Document Supply Centre- DSC:DXN003289 / BLDSC - British Library ...

Pathogenic mutations of the lipoprotein lipase gene in Chinese patients with hypertriglyceridemic type 2 diabetes.

Poon, PM
Yang, T
Pang, CP
Tsang, MW
Lam, CW
Chan, LY
Wu, XQ
Tomlinson, B
Baum, L

January 2003

Elevated plasma triglyceride and nonesterified fatty acid concentrations may cause insulin resistanc...

The molecular genetics of familial hypercholesterolaemia in Northern Ireland

Ward, A.J

January 1995

Available from British Library Document Supply Centre-DSC:DXN004132 / BLDSC - British Library Docume...

Lipoprotein metabolism Inherited disorders of apolipoprotein B metabolism

Hamed, A.M

January 1995

SIGLEAvailable from British Library Document Supply Centre-DSC:DX189360 / BLDSC - British Library Do...

Molecular basis of lipoprotein lipase deficiency in two Austrian families with type I hyperlipoproteinemia.

Paulweber, B
Wiebusch, H
Miesenboeck, G
Funke, H
Assmann, G
Hoelzl, B
Sippl, MJ
Friedl, W
Patsch, JR
Sandhofer, F

February 1991

To determine the molecular basis for type I hyperlipoproteinemia in two Austrian families, the lipop...

Identification and characterization of two novel mutations in the LPL gene causing type I hyperlipoproteinemia

Pingitore P.
Lepore S. M.
Pirazzi C.
Mancina R. M.
Motta B. M.
Valenti L.
Berge K. E.
Retterstol K.
Leren T. P.
Wiklund O.
Romeo S.

January 2016

Background Type 1 hyperlipoproteinemia is a rare autosomal recessive disorder most often caused by m...

Identification and characterization of two novel mutations in the LPL gene causing type I hyperlipoproteinemia

Pingitore P.
Lepore S. M.
Pirazzi C.
Mancina R. M.
Motta B. M.
Valenti L.
Berge K. E.
Retterstol K.
Leren T. P.
Wiklund O.
Romeo S.

January 2016

Background Type 1 hyperlipoproteinemia is a rare autosomal recessive disorder most often caused by m...

Identification and characterization of two novel mutations in the LPL gene causing type I hyperlipoproteinemia

Pingitore P.
Lepore S. M.
Pirazzi C.
Mancina R. M.
Motta B. M.
Valenti L.
Berge K. E.
Retterstol K.
Leren T. P.
Wiklund O.
Romeo S.

January 2016

Background Type 1 hyperlipoproteinemia is a rare autosomal recessive disorder most often caused by m...

Identification and characterization of two novel mutations in the LPL gene causing type I hyperlipoproteinemia

Pingitore P.
Lepore S. M.
Pirazzi C.
Mancina R. M.
Motta B. M.
Valenti L.
Berge K. E.
Retterstol K.
Leren T. P.
Wiklund O.
Romeo S.

January 2016

Background Type 1 hyperlipoproteinemia is a rare autosomal recessive disorder most often caused by m...

Clinical biochemistry of lipoproteins Altered expression of LDL-R and PDGF-A genes in hyperlipidaemia

Adbeish, I.S

January 1996

SIGLEAvailable from British Library Document Supply Centre-DSC:DXN005688 / BLDSC - British Library D...

A COMMON VARIANT IN THE GENE FOR LIPOPROTEIN-LIPASE (ASP9-]ASN) - FUNCTIONAL IMPLICATIONS AND PREVALENCE IN NORMAL AND HYPERLIPIDEMIC SUBJECTS

OLIVECRONA, G
KASTELEIN, JJP
HAMSTEN, A
HUMPHRIES, SE
TALMUD, PJ
MAILLY, F
TUGRUL, Y
REYMER, PWA
BRUIN, T
SEED, M
GROENEMEYER, BF
ASPLUNDCARLSON, A
VALLANCE, D
WINDER, AF
MILLER, GJ

January 1995

Subjects with combined hyperlipidemia (CHL) were screened for mutations in the lipoprotein lipase (L...

Identification and the relationship between mutations in the lipoprotein lipase gene, dyslipidemia and coronary heart disease

Gagné, S. Eric

January 1999

Lipoprotein lipase (LPL) is a critical enzyme which primary function is to hydrolyze triglycerides ...

Mutations in the human lipoprotein lipase gene and their relationship to hyperlipidaemia

Abstract

Extracted data

Mutations in the human lipoprotein lipase gene and their relationship to hyperlipidaemia

Abstract

Extracted data

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