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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1999 | 2 |
2001 | 1 |
2004 | 1 |
2012 | 1 |
2014 | 1 |
2018 | 1 |
2024 | 0 |
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A radiochemical assay for beta-ureidopropionase using radiolabeled N-carbamyl-beta-alanine obtained via hydrolysis of [2-(14)C]5, 6-dihydrouracil.
Anal Biochem. 1999 Aug 1;272(2):250-3. doi: 10.1006/abio.1999.4181.
Anal Biochem. 1999.
PMID: 10415095
cDNA cloning, genomic structure and chromosomal localization of the human BUP-1 gene encoding beta-ureidopropionase.
Vreken P, van Kuilenburg AB, Hamajima N, Meinsma R, van Lenthe H, Göhlich-Ratmann G, Assmann BE, Wevers RA, van Gennip AH.
Vreken P, et al.
Biochim Biophys Acta. 1999 Oct 28;1447(2-3):251-7. doi: 10.1016/s0167-4781(99)00182-7.
Biochim Biophys Acta. 1999.
PMID: 10542323
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Expression and properties of human liver beta-ureidopropionase.
Sakamoto T, Sakata SF, Matsuda K, Horikawa Y, Tamaki N.
Sakamoto T, et al.
J Nutr Sci Vitaminol (Tokyo). 2001 Apr;47(2):132-8. doi: 10.3177/jnsv.47.132.
J Nutr Sci Vitaminol (Tokyo). 2001.
PMID: 11508704
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beta-Ureidopropionase deficiency: an inborn error of pyrimidine degradation associated with neurological abnormalities.
van Kuilenburg AB, Meinsma R, Beke E, Assmann B, Ribes A, Lorente I, Busch R, Mayatepek E, Abeling NG, van Cruchten A, Stroomer AE, van Lenthe H, Zoetekouw L, Kulik W, Hoffmann GF, Voit T, Wevers RA, Rutsch F, van Gennip AH.
van Kuilenburg AB, et al.
Hum Mol Genet. 2004 Nov 15;13(22):2793-801. doi: 10.1093/hmg/ddh303. Epub 2004 Sep 22.
Hum Mol Genet. 2004.
PMID: 15385443
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ß-ureidopropionase deficiency: phenotype, genotype and protein structural consequences in 16 patients.
van Kuilenburg AB, Dobritzsch D, Meijer J, Krumpel M, Selim LA, Rashed MS, Assmann B, Meinsma R, Lohkamp B, Ito T, Abeling NG, Saito K, Eto K, Smitka M, Engvall M, Zhang C, Xu W, Zoetekouw L, Hennekam RC.
van Kuilenburg AB, et al.
Biochim Biophys Acta. 2012 Jul;1822(7):1096-108. doi: 10.1016/j.bbadis.2012.04.001. Epub 2012 Apr 14.
Biochim Biophys Acta. 2012.
PMID: 22525402
Free article.
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Clinical, biochemical and molecular analysis of 13 Japanese patients with β-ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation [corrected].
Nakajima Y, Meijer J, Dobritzsch D, Ito T, Meinsma R, Abeling NG, Roelofsen J, Zoetekouw L, Watanabe Y, Tashiro K, Lee T, Takeshima Y, Mitsubuchi H, Yoneyama A, Ohta K, Eto K, Saito K, Kuhara T, van Kuilenburg AB.
Nakajima Y, et al.
J Inherit Metab Dis. 2014 Sep;37(5):801-12. doi: 10.1007/s10545-014-9682-y. Epub 2014 Feb 14.
J Inherit Metab Dis. 2014.
PMID: 24526388
Free PMC article.
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Crystal structure and pH-dependent allosteric regulation of human β-ureidopropionase, an enzyme involved in anticancer drug metabolism.
Maurer D, Lohkamp B, Krumpel M, Widersten M, Dobritzsch D.
Maurer D, et al.
Biochem J. 2018 Jul 31;475(14):2395-2416. doi: 10.1042/BCJ20180222.
Biochem J. 2018.
PMID: 29976570
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