Funke H - Search Results

1

Screening for naturally occurring apolipoprotein A-I variants: apo A-I(delta K107) is associated with low HDL-cholesterol levels in men but not in women.

Nofer JR, von Eckardstein A, Wiebusch H, Weng W, Funke H, Schulte H, Köhler E, Assmann G. Nofer JR, et al. Among authors: funke h. Hum Genet. 1995 Aug;96(2):177-82. doi: 10.1007/BF00207375. Hum Genet. 1995. PMID: 7635466

2

Nonsynonymous polymorphic sites in the apolipoprotein (apo) A-IV gene are associated with changes in the concentration of apo B- and apo A-I-containing lipoproteins in a normal population.

von Eckardstein A, Funke H, Schulte M, Erren M, Schulte H, Assmann G. von Eckardstein A, et al. Among authors: funke h. Am J Hum Genet. 1992 May;50(5):1115-28. Am J Hum Genet. 1992. PMID: 1349197 Free PMC article.

3

HDL metabolism and atherosclerosis.

Assmann G, Funke H. Assmann G, et al. Among authors: funke h. J Cardiovasc Pharmacol. 1990;16 Suppl 9:S15-20. J Cardiovasc Pharmacol. 1990. PMID: 1710740 Review.

4

Apolipoprotein C-III(Lys58----Glu). Identification of an apolipoprotein C-III variant in a family with hyperalphalipoproteinemia.

von Eckardstein A, Holz H, Sandkamp M, Weng W, Funke H, Assmann G. von Eckardstein A, et al. Among authors: funke h. J Clin Invest. 1991 May;87(5):1724-31. doi: 10.1172/JCI115190. J Clin Invest. 1991. PMID: 2022742 Free PMC article.

5

Apolipoprotein A-I variants. Naturally occurring substitutions of proline residues affect plasma concentration of apolipoprotein A-I.

von Eckardstein A, Funke H, Henke A, Altland K, Benninghoven A, Assmann G. von Eckardstein A, et al. Among authors: funke h. J Clin Invest. 1989 Dec;84(6):1722-30. doi: 10.1172/JCI114355. J Clin Invest. 1989. PMID: 2512329 Free PMC article.

6

Deficiency of lecithin:cholesterol acyltransferase due to compound heterozygosity of two novel mutations (Gly33Arg and 30 bp ins) in the LCAT gene.

Wiebusch H, Cullen P, Owen JS, Collins D, Sharp PS, Funke H, Assmann G. Wiebusch H, et al. Among authors: funke h. Hum Mol Genet. 1995 Jan;4(1):143-5. doi: 10.1093/hmg/4.1.143. Hum Mol Genet. 1995. PMID: 7711728 No abstract available.

7

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 S, Wiebusch H, Funke H, Ros E, Seedorf U, Assmann G. Muntoni S, et al. Among authors: funke h. Hum Genet. 1995 May;95(5):491-4. doi: 10.1007/BF00223858. Hum Genet. 1995. PMID: 7759067

8

A nonsense mutation in the apolipoprotein A-I gene is associated with high-density lipoprotein deficiency and periorbital xanthelasmas.

Römling R, von Eckardstein A, Funke H, Motti C, Fragiacomo GC, Noseda G, Assmann G. Römling R, et al. Among authors: funke h. Arterioscler Thromb. 1994 Dec;14(12):1915-22. doi: 10.1161/01.atv.14.12.1915. Arterioscler Thromb. 1994. PMID: 7981179

9

Sex-specific effects of the glutamine/histidine polymorphism in apo A-IV on HDL metabolism.

von Eckardstein A, Funke H, Chirazi A, Chen-Haudenschild C, Schulte H, Schönfeld R, Köhler E, Schwarz S, Steinmetz A, Assmann G. von Eckardstein A, et al. Among authors: funke h. Arterioscler Thromb. 1994 Jul;14(7):1114-20. doi: 10.1161/01.atv.14.7.1114. Arterioscler Thromb. 1994. PMID: 8018667

10

Electrophoretic screening for human apolipoprotein C-II variants: repeated identification of apolipoprotein C-II(K19T).

Wiebusch H, Nofer JR, von Eckardstein A, Funke H, Wahrburg U, Martin H, Köhler E, Assmann G. Wiebusch H, et al. Among authors: funke h. J Mol Med (Berl). 1995 Jul;73(7):373-8. doi: 10.1007/BF00192889. J Mol Med (Berl). 1995. PMID: 8520970

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