Wiebusch H

References (18)

Title : Heterozygosity for lysosomal acid lipase E8SJM mutation and serum lipid concentrations - Muntoni_2013_Nutr.Metab.Cardiovasc.Dis_23_732
Author(s) : Muntoni S , Wiebusch H , Jansen-Rust M , Rust S , Schulte H , Berger K , Pisciotta L , Bertolini S , Funke H , Seedorf U , Assmann G
Ref : Nutr Metab Cardiovasc Dis , 23 :732 , 2013
Abstract :
PubMedSearch : Muntoni_2013_Nutr.Metab.Cardiovasc.Dis_23_732
PubMedID: 22795295
Gene_locus related to this paper: human-LIPA

Title : Detection of missense mutations in the genes for lipoprotein lipase and hepatic triglyceride lipase in patients with dyslipidemia undergoing coronary angiography - Moennig_2000_Atherosclerosis_149_395
Author(s) : Moennig G , Wiebusch H , Enbergs A , Dorszewski A , Kerber S , Schulte H , Vielhauer C , Haverkamp W , Assmann G , Breithardt G , Funke H
Ref : Atherosclerosis , 149 :395 , 2000
Abstract :
PubMedSearch : Moennig_2000_Atherosclerosis_149_395
PubMedID: 10729390

Title : Two novel mutations in the lipoprotein lipase gene in a family with marked hypertriglyceridemia in heterozygous carriers. Potential interaction with the polymorphic marker D1S104 on chromosome 1q21-q23 - Holzl_2000_J.Lipid.Res_41_734
Author(s) : Holzl B , Kraft HG , Wiebusch H , Sandhofer A , Patsch J , Sandhofer F , Paulweber B
Ref : J Lipid Res , 41 :734 , 2000
Abstract :
PubMedSearch : Holzl_2000_J.Lipid.Res_41_734
PubMedID: 10787434

Title : Further evidence for a synergistic association between APOE epsilon4 and BCHE-K in confirmed Alzheimer's disease - Wiebusch_1999_Hum.Genet_104_158
Author(s) : Wiebusch H , Poirier J , Sevigny P , Schappert K
Ref : Hum Genet , 104 :158 , 1999
Abstract :
PubMedSearch : Wiebusch_1999_Hum.Genet_104_158
PubMedID: 10190327

Title : Fatal genetic defect causing Wolman disease. -
Author(s) : Mayatepek E , Seedorf U , Wiebusch H , Lenhartz H , Assmann G
Ref : J Inherit Metab Dis , 22 :93 , 1999
PubMedID: 10070628
Gene_locus related to this paper: human-LIPA

Title : Heterozygous hepatic lipase deficiency, due to two missense mutations R186H and L334F, in the HL gene - Knudsen_1997_Atherosclerosis_128_165
Author(s) : Knudsen P , Antikainen M , Uusi-Oukari M , Ehnholm S , Lahdenpera S , Bensadoun A , Funke H , Wiebusch H , Assmann G , Taskinen MR , Ehnholm C
Ref : Atherosclerosis , 128 :165 , 1997
Abstract :
PubMedSearch : Knudsen_1997_Atherosclerosis_128_165
PubMedID: 9050773
Gene_locus related to this paper: human-LIPC

Title : A novel missense (E163G) mutation in the catalytic subunit of lipoprotein lipase causes familial chylomicronemia -
Author(s) : Wiebusch H , Funke H , Santer R , Richter W , Assmann G
Ref : Hum Mutat , 8 :392 , 1996
PubMedID: 8956052

Title : A novel missense mutation (Gly2Arg) in the human lysosomal acid lipase gene is found in individuals with and without cholesterol ester storage disease (CESD) -
Author(s) : Wiebusch H , Muntoni S , Funke H , Lu F , Seedorf U , Oberle S , Schwarzer U , Assmann G
Ref : Clin Genet , 50 :106 , 1996
PubMedID: 8937772

Title : Complete deficiency of plasma lecithin-cholesterol acyltransferase (LCAT) activity due to a novel homozygous mutation (Gly-30-Ser) in the LCAT gene -
Author(s) : Owen JS , Wiebusch H , Cullen P , Watts GF , Lima VL , Funke H , Assmann G
Ref : Hum Mutat , 8 :79 , 1996
PubMedID: 8807342

Title : A missense mutation (Thr-6Pro) in the lysosomal acid lipase (LAL) gene is present with a high frequency in three different ethnic populations: impact on serum lipoprotein concentrations - Muntoni_1996_Hum.Genet_97_265
Author(s) : Muntoni S , Wiebusch H , Funke H , Seedorf U , Roskos M , Schulte H , Saku K , Arakawa K , Balestrieri A , Assmann G
Ref : Hum Genet , 97 :265 , 1996
Abstract :
PubMedSearch : Muntoni_1996_Hum.Genet_97_265
PubMedID: 8566968

Title : Compound heterozygosity for a known and a novel defect in the lipoprotein lipase gene (Asp250-->\;Asn\; Ser251-->\;Cys) resulting in lipoprotein lipase (LPL) deficiency - Bijvoet_1996_Neth.J.Med_49_189
Author(s) : Bijvoet SM , Wiebusch H , Ma Y , Reymer PW , Bruin T , Bakker HD , Funke H , Assmann G , Hayden MR , Kastelein JJ
Ref : Neth J Med , 49 :189 , 1996
Abstract :
PubMedSearch : Bijvoet_1996_Neth.J.Med_49_189
PubMedID: 8973094

Title : Compound heterozygosity for a known (D250N) and a novel (E410K) missense mutation in the C-terminal domain of lipoprotein lipase causes familial chylomicronemia -
Author(s) : Wiebusch H , Funke H , Bruin T , Bucher H , von Eckardstein A , Kastelein JJ , Assmann G
Ref : Hum Mutat , 8 :381 , 1996
PubMedID: 8956048
Gene_locus related to this paper: human-LPL

Title : A novel variant of lysosomal acid lipase (Leu336-->\;Pro) associated with acid lipase deficiency and cholesterol ester storage disease - Seedorf_1995_Arterioscler.Thromb.Vasc.Biol_15_773
Author(s) : Seedorf U , Wiebusch H , Muntoni S , Christensen NC , Skovby F , Nickel V , Roskos M , Funke H , Ose L , Assmann G
Ref : Arterioscler Thromb Vasc Biol , 15 :773 , 1995
Abstract :
PubMedSearch : Seedorf_1995_Arterioscler.Thromb.Vasc.Biol_15_773
PubMedID: 7773732
Gene_locus related to this paper: human-LIPA

Title : A unique genetic and biochemical presentation of fish-eye disease - Kuivenhoven_1995_J.Clin.Invest_96_2783
Author(s) : Kuivenhoven JA , van Voorst tot Voorst EJ , Wiebusch H , Marcovina SM , Funke H , Assmann G , Pritchard PH , Kastelein JJ
Ref : J Clinical Investigation , 96 :2783 , 1995
Abstract :
PubMedSearch : Kuivenhoven_1995_J.Clin.Invest_96_2783
PubMedID: 8675648

Title : Homozygosity for a splice junction mutation in exon 8 of the gene encoding lysosomal acid lipase in a Spanish kindred with cholesterol ester storage disease (CESD) - Muntoni_1995_Hum.Genet_95_491
Author(s) : Muntoni S , Wiebusch H , Funke H , Ros E , Seedorf U , Assmann G
Ref : Hum Genet , 95 :491 , 1995
Abstract :
PubMedSearch : Muntoni_1995_Hum.Genet_95_491
PubMedID: 7759067

Title : Deficiency of lecithin:cholesterol acyltransferase due to compound heterozygosity of two novel mutations (Gly33Arg and 30 bp ins) in the LCAT gene -
Author(s) : Wiebusch H , Cullen P , Owen JS , Collins D , Sharp PS , Funke H , Assmann G
Ref : Hum Mol Genet , 4 :143 , 1995
PubMedID: 7711728
Gene_locus related to this paper: human-LCAT

Title : Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this disease - Funke_1993_J.Clin.Invest_91_677
Author(s) : Funke H , von Eckardstein A , Pritchard PH , Hornby AE , Wiebusch H , Motti C , Hayden MR , Dachet C , Jacotot B , Gerdes U , Faergeman O , Albers JJ , Colleoni N , Catapano A , Frohlich J , Assmann G
Ref : J Clinical Investigation , 91 :677 , 1993
Abstract :
PubMedSearch : Funke_1993_J.Clin.Invest_91_677
PubMedID: 8432868
Gene_locus related to this paper: human-LCAT

Title : Molecular basis of lipoprotein lipase deficiency in two Austrian families with type I hyperlipoproteinemia - Paulweber_1991_Atherosclerosis_86_239
Author(s) : Paulweber B , Wiebusch H , Miesenboeck G , Funke H , Assmann G , Hoelzl B , Sippl MJ , Friedl W , Patsch JR , Sandhofer F
Ref : Atherosclerosis , 86 :239 , 1991
Abstract :
PubMedSearch : Paulweber_1991_Atherosclerosis_86_239
PubMedID: 1872917