Albers JJ - Search Results

1

A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity.

Funke H, von Eckardstein A, Pritchard PH, Albers JJ, Kastelein JJ, Droste C, Assmann G. Funke H, et al. Among authors: albers jj. Proc Natl Acad Sci U S A. 1991 Jun 1;88(11):4855-9. doi: 10.1073/pnas.88.11.4855. Proc Natl Acad Sci U S A. 1991. PMID: 2052566 Free PMC article.

2

A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin: cholesterol-acyltransferase deficiency, and corneal opacities.

Funke H, von Eckardstein A, Pritchard PH, Karas M, Albers JJ, Assmann G. Funke H, et al. Among authors: albers jj. J Clin Invest. 1991 Jan;87(1):371-6. doi: 10.1172/JCI114997. J Clin Invest. 1991. PMID: 1898657 Free PMC article.

3

Familial high-density-lipoprotein deficiency causing corneal opacities (fish eye disease) in a family of Dutch descent.

Kastelein JJ, Pritchard PH, Erkelens DW, Kuivenhoven JA, Albers JJ, Frohlich JJ. Kastelein JJ, et al. Among authors: albers jj. J Intern Med. 1992 Apr;231(4):413-9. doi: 10.1111/j.1365-2796.1992.tb00953.x. J Intern Med. 1992. PMID: 1588268

4

Transmission of two novel mutations in a pedigree with familial lecithin:cholesterol acyltransferase deficiency: structure-function relationships and studies in a compound heterozygous proband.

Argyropoulos G, Jenkins A, Klein RL, Lyons T, Wagenhorst B, St Armand J, Marcovina SM, Albers JJ, Pritchard PH, Garvey WT. Argyropoulos G, et al. Among authors: albers jj. J Lipid Res. 1998 Sep;39(9):1870-6. J Lipid Res. 1998. PMID: 9741700 Free article.

5

Activation of lecithin:cholesterol acyltransferase by a synthetic model lipid-associating peptide.

Pownall HJ, Hu A, Gotto AM Jr, Albers JJ, Sparrow JT. Pownall HJ, et al. Among authors: albers jj. Proc Natl Acad Sci U S A. 1980 Jun;77(6):3154-8. doi: 10.1073/pnas.77.6.3154. Proc Natl Acad Sci U S A. 1980. PMID: 6774331 Free PMC article.

6

Fish eye syndrome: a molecular defect in the lecithin-cholesterol acyltransferase (LCAT) gene associated with normal alpha-LCAT-specific activity. Implications for classification and prognosis.

Klein HG, Santamarina-Fojo S, Duverger N, Clerc M, Dumon MF, Albers JJ, Marcovina S, Brewer HB Jr. Klein HG, et al. Among authors: albers jj. J Clin Invest. 1993 Jul;92(1):479-85. doi: 10.1172/JCI116591. J Clin Invest. 1993. PMID: 8326012 Free PMC article.

7

Lecithin: cholesterol acyltransferase in liver disease.

Florén CH, Chen CH, Franzén J, Albers JJ. Florén CH, et al. Among authors: albers jj. Scand J Clin Lab Invest. 1987 Oct;47(6):613-7. doi: 10.1080/00365518709168477. Scand J Clin Lab Invest. 1987. PMID: 3672034

8

Lecithin:cholesterol acyltransferase (LCAT) mass; its relationship to LCAT activity and cholesterol esterification rate.

Albers JJ, Chen CH, Adolphson JL. Albers JJ, et al. J Lipid Res. 1981 Nov;22(8):1206-13. J Lipid Res. 1981. PMID: 7320631 Free article.

9

A novel missense mutation (Asn5-->Ile) in lecithin: cholesterol acyltransferase (LCAT) gene in a Japanese patient with LCAT deficiency.

Okubo M, Aoyama Y, Shio H, Albers JJ, Murase T. Okubo M, et al. Among authors: albers jj. Int J Clin Lab Res. 1996;26(4):250-4. doi: 10.1007/BF02602958. Int J Clin Lab Res. 1996. PMID: 9007616

10

Stimulation of lecithin:cholesterol acyltransferase activity by apolipoprotein A-II in the presence of apolipoprotein A-I.

Chen CH, Albers JJ. Chen CH, et al. Among authors: albers jj. Eur J Biochem. 1986 Mar 17;155(3):589-94. doi: 10.1111/j.1432-1033.1986.tb09529.x. Eur J Biochem. 1986. PMID: 3082628 Free article.

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