Havelaar AC - Search Results

1

Interindividual and intraindividual variability in plasma fibrinogen, TPA antigen, PAI activity, and CRP in healthy, young volunteers and patients with angina pectoris.

de Maat MP, de Bart AC, Hennis BC, Meijer P, Havelaar AC, Mulder PG, Kluft C. de Maat MP, et al. Among authors: havelaar ac. Arterioscler Thromb Vasc Biol. 1996 Sep;16(9):1156-62. doi: 10.1161/01.atv.16.9.1156. Arterioscler Thromb Vasc Biol. 1996. PMID: 8792769

2

PCR detection of a dinucleotide repeat in the human histidine-rich glycoprotein (HRG) gene.

Hennis BC, Havelaar AC, Kluft C. Hennis BC, et al. Among authors: havelaar ac. Hum Mol Genet. 1992 Dec;1(9):781. doi: 10.1093/hmg/1.9.781-a. Hum Mol Genet. 1992. PMID: 1302626 No abstract available.

3

A role for the transient increase of cytoplasmic free calcium in cell rescue after photodynamic treatment.

Penning LC, Rasch MH, Ben-Hur E, Dubbelman TM, Havelaar AC, Van der Zee J, Van Steveninck J. Penning LC, et al. Among authors: havelaar ac. Biochim Biophys Acta. 1992 Jun 30;1107(2):255-60. doi: 10.1016/0005-2736(92)90412-f. Biochim Biophys Acta. 1992. PMID: 1504070

4

A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases.

Verheijen FW, Verbeek E, Aula N, Beerens CE, Havelaar AC, Joosse M, Peltonen L, Aula P, Galjaard H, van der Spek PJ, Mancini GM. Verheijen FW, et al. Among authors: havelaar ac. Nat Genet. 1999 Dec;23(4):462-5. doi: 10.1038/70585. Nat Genet. 1999. PMID: 10581036

5

Fibroblast silver loading for the diagnosis of Menkes disease.

Verheijen FW, Beerens CE, Havelaar AC, Kleijer WJ, Mancini GM. Verheijen FW, et al. Among authors: havelaar ac. J Med Genet. 1998 Oct;35(10):849-51. doi: 10.1136/jmg.35.10.849. J Med Genet. 1998. PMID: 9783711 Free PMC article.

6

Purification of the lysosomal sialic acid transporter. Functional characteristics of a monocarboxylate transporter.

Havelaar AC, Mancini GM, Beerens CE, Souren RM, Verheijen FW. Havelaar AC, et al. J Biol Chem. 1998 Dec 18;273(51):34568-74. doi: 10.1074/jbc.273.51.34568. J Biol Chem. 1998. PMID: 9852127 Free article.

7

Transport of organic anions by the lysosomal sialic acid transporter: a functional approach towards the gene for sialic acid storage disease.

Havelaar AC, Beerens CE, Mancini GM, Verheijen FW. Havelaar AC, et al. FEBS Lett. 1999 Mar 5;446(1):65-8. doi: 10.1016/s0014-5793(99)00187-8. FEBS Lett. 1999. PMID: 10100616 Free article.

8

Characterization of a heavy metal ion transporter in the lysosomal membrane.

Havelaar AC, de Gast IL, Snijders S, Beerens CE, Mancini GM, Verheijen FW. Havelaar AC, et al. FEBS Lett. 1998 Oct 2;436(2):223-7. doi: 10.1016/s0014-5793(98)01133-8. FEBS Lett. 1998. PMID: 9781683 Free article.

9

Lysosomal transport disorders.

Mancini GM, Havelaar AC, Verheijen FW. Mancini GM, et al. Among authors: havelaar ac. J Inherit Metab Dis. 2000 May;23(3):278-92. doi: 10.1023/a:1005640214408. J Inherit Metab Dis. 2000. PMID: 10863944 Review.

10

NPT4, a new microsomal phosphate transporter: mutation analysis in glycogen storage disease type Ic.

Melis D, Havelaar AC, Verbeek E, Smit GP, Benedetti A, Mancini GM, Verheijen F. Melis D, et al. Among authors: havelaar ac. J Inherit Metab Dis. 2004;27(6):725-33. doi: 10.1023/B:BOLI.0000045755.89308.2f. J Inherit Metab Dis. 2004. PMID: 15505377

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