Kastelein JJ - Search Results

1

Lipid-free apolipoprotein (apo) A-I is converted into alpha-migrating high density lipoproteins by lipoprotein-depleted plasma of normolipidemic donors and apo A-I-deficient patients but not of Tangier disease patients.

von Eckardstein A, Huang Y, Kastelein JJ, Geisel J, Real JT, Kuivenhoven JA, Miccoli R, Noseda G, Assmann G. von Eckardstein A, et al. Among authors: kastelein jj. Atherosclerosis. 1998 May;138(1):25-34. doi: 10.1016/s0021-9150(97)00280-3. Atherosclerosis. 1998. PMID: 9678768

2

Plasma and fibroblasts of Tangier disease patients are disturbed in transferring phospholipids onto apolipoprotein A-I.

von Eckardstein A, Chirazi A, Schuler-Lüttmann S, Walter M, Kastelein JJ, Geisel J, Real JT, Miccoli R, Noseda G, Höbbel G, Assmann G. von Eckardstein A, et al. Among authors: kastelein jj. J Lipid Res. 1998 May;39(5):987-98. J Lipid Res. 1998. PMID: 9610765 Free article.

3

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: kastelein 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.

4

A unique genetic and biochemical presentation of fish-eye disease.

Kuivenhoven JA, van Voorst tot Voorst EJ, Wiebusch H, Marcovina SM, Funke H, Assmann G, Pritchard PH, Kastelein JJ. Kuivenhoven JA, et al. Among authors: kastelein jj. J Clin Invest. 1995 Dec;96(6):2783-91. doi: 10.1172/JCI118348. J Clin Invest. 1995. PMID: 8675648 Free PMC article.

5

Compound heterozygosity for a known (D250N) and a novel (E410K) missense mutation in the C-terminal domain of lipoprotein lipase causes familial chylomicronemia.

Wiebusch H, Funke H, Bruin T, Bucher H, von Eckardstein A, Kastelein JJ, Assmann G. Wiebusch H, et al. Among authors: kastelein jj. Hum Mutat. 1996;8(4):381-3. doi: 10.1002/(SICI)1098-1004(1996)8:4<381::AID-HUMU16>3.0.CO;2-Z. Hum Mutat. 1996. PMID: 8956048 No abstract available.

6

Heterozygosity for ABCA1 gene mutations: effects on enzymes, apolipoproteins and lipoprotein particle size.

Kuivenhoven JA, Hovingh GK, van Tol A, Jauhiainen M, Ehnholm C, Fruchart JC, Brinton EA, Otvos JD, Smelt AH, Brownlee A, Zwinderman AH, Hayden MR, Kastelein JJ. Kuivenhoven JA, et al. Among authors: kastelein jj. Atherosclerosis. 2003 Dec;171(2):311-9. doi: 10.1016/j.atherosclerosis.2003.08.014. Atherosclerosis. 2003. PMID: 14644402

7

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. J Intern Med. 1992 Apr;231(4):413-9. doi: 10.1111/j.1365-2796.1992.tb00953.x. J Intern Med. 1992. PMID: 1588268

8

Parental history of myocardial infarction: lipid traits, gene polymorphisms and lifestyle.

Boer JM, Feskens EJ, Kuivenhoven JA, Schouten EG, Havekes LM, Kastelein JJ, Seidell JC, Kromhout D. Boer JM, et al. Among authors: kastelein jj. Atherosclerosis. 2001 Mar;155(1):149-56. doi: 10.1016/s0021-9150(00)00521-9. Atherosclerosis. 2001. PMID: 11223436

9

Are high-density lipoprotein genes and their products targets for therapy?

Motazacker MM, Kastelein JJ, Kuivenhoven JA. Motazacker MM, et al. Among authors: kastelein jj. Curr Opin Lipidol. 2010 Apr;21(2):157-8. doi: 10.1097/MOL.0b013e3283376923. Curr Opin Lipidol. 2010. PMID: 20616629 No abstract available.

10

Proteinuria in early childhood due to familial LCAT deficiency caused by loss of a disulfide bond in lecithin:cholesterol acyl transferase.

Holleboom AG, Kuivenhoven JA, van Olden CC, Peter J, Schimmel AW, Levels JH, Valentijn RM, Vos P, Defesche JC, Kastelein JJ, Hovingh GK, Stroes ES, Hollak CE. Holleboom AG, et al. Among authors: kastelein jj. Atherosclerosis. 2011 May;216(1):161-5. doi: 10.1016/j.atherosclerosis.2011.01.025. Epub 2011 Jan 21. Atherosclerosis. 2011. PMID: 21315357

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