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Acyl-CoA:dihydroxyacetonephosphate acyltransferase: cloning of the human cDNA and resolution of the molecular basis in rhizomelic chondrodysplasia punctata type 2.
Ofman R, Hettema EH, Hogenhout EM, Caruso U, Muijsers AO, Wanders RJ. Ofman R, et al. Hum Mol Genet. 1998 May;7(5):847-53. doi: 10.1093/hmg/7.5.847. Hum Mol Genet. 1998. PMID: 9536089
Differential protein import deficiencies in human peroxisome assembly disorders.
Motley A, Hettema E, Distel B, Tabak H. Motley A, et al. J Cell Biol. 1994 May;125(4):755-67. doi: 10.1083/jcb.125.4.755. J Cell Biol. 1994. PMID: 7910611 Free PMC article.
The ABC transporter proteins Pat1 and Pat2 are required for import of long-chain fatty acids into peroxisomes of Saccharomyces cerevisiae.
Hettema EH, van Roermund CW, Distel B, van den Berg M, Vilela C, Rodrigues-Pousada C, Wanders RJ, Tabak HF. Hettema EH, et al. EMBO J. 1996 Aug 1;15(15):3813-22. EMBO J. 1996. PMID: 8670886 Free PMC article.
Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor.
Motley AM, Hettema EH, Hogenhout EM, Brites P, ten Asbroek AL, Wijburg FA, Baas F, Heijmans HS, Tabak HF, Wanders RJ, Distel B. Motley AM, et al. Nat Genet. 1997 Apr;15(4):377-80. doi: 10.1038/ng0497-377. Nat Genet. 1997. PMID: 9090382
Peroxisomal beta-oxidation of polyunsaturated fatty acids in Saccharomyces cerevisiae: isocitrate dehydrogenase provides NADPH for reduction of double bonds at even positions.
van Roermund CW, Hettema EH, Kal AJ, van den Berg M, Tabak HF, Wanders RJ. van Roermund CW, et al. EMBO J. 1998 Feb 2;17(3):677-87. doi: 10.1093/emboj/17.3.677. EMBO J. 1998. PMID: 9450993 Free PMC article.
The cytosolic DnaJ-like protein djp1p is involved specifically in peroxisomal protein import.
Hettema EH, Ruigrok CC, Koerkamp MG, van den Berg M, Tabak HF, Distel B, Braakman I. Hettema EH, et al. J Cell Biol. 1998 Jul 27;142(2):421-34. doi: 10.1083/jcb.142.2.421. J Cell Biol. 1998. PMID: 9679141 Free PMC article.
Molecular basis of rhizomelic chondrodysplasia punctata type I: high frequency of the Leu-292 stop mutation in 38 patients.
Brites P, Motley A, Hogenhout E, Hettema E, Wijburg F, Heijmans HS, Tabak HF, Distel B, Wanders RJ. Brites P, et al. J Inherit Metab Dis. 1998 Jun;21(3):306-8. doi: 10.1023/a:1005301112923. J Inherit Metab Dis. 1998. PMID: 9686382 No abstract available.
Enlargement of the endoplasmic reticulum membrane in Saccharomyces cerevisiae is not necessarily linked to the unfolded protein response via Ire1p.
Stroobants AK, Hettema EH, van den Berg M, Tabak HF. Stroobants AK, et al. FEBS Lett. 1999 Jun 18;453(1-2):210-4. doi: 10.1016/s0014-5793(99)00721-8. FEBS Lett. 1999. PMID: 10403405
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