Engelke UFH - Search Results

1

Identification of Δ-1-pyrroline-5-carboxylate derived biomarkers for hyperprolinemia type II.

Merx J, van Outersterp RE, Engelke UFH, Hendriks V, Wevers RA, Huigen MCDG, Waterval HWAH, Körver-Keularts IMLW, Mecinović J, Rutjes FPJT, Oomens J, Coene KLM, Martens J, Boltje TJ. Merx J, et al. Among authors: engelke ufh. Commun Biol. 2022 Sep 21;5(1):997. doi: 10.1038/s42003-022-03960-2. Commun Biol. 2022. PMID: 36131087 Free PMC article.

2

Structural and functional analysis of ypt2, an essential ras-related gene in the fission yeast Schizosaccharomyces pombe encoding a Sec4 protein homologue.

Haubruck H, Engelke U, Mertins P, Gallwitz D. Haubruck H, et al. EMBO J. 1990 Jun;9(6):1957-62. doi: 10.1002/j.1460-2075.1990.tb08323.x. EMBO J. 1990. PMID: 2112089 Free PMC article.

3

Defect in dimethylglycine dehydrogenase, a new inborn error of metabolism: NMR spectroscopy study.

Moolenaar SH, Poggi-Bach J, Engelke UF, Corstiaensen JM, Heerschap A, de Jong JG, Binzak BA, Vockley J, Wevers RA. Moolenaar SH, et al. Clin Chem. 1999 Apr;45(4):459-64. Clin Chem. 1999. PMID: 10102904

4

1H-NMR spectroscopy of body fluids: inborn errors of purine and pyrimidine metabolism.

Wevers RA, Engelke UF, Moolenaar SH, Bräutigam C, de Jong JG, Duran R, de Abreu RA, van Gennip AH. Wevers RA, et al. Clin Chem. 1999 Apr;45(4):539-48. Clin Chem. 1999. PMID: 10102915

5

Leukoencephalopathy associated with a disturbance in the metabolism of polyols.

van der Knaap MS, Wevers RA, Struys EA, Verhoeven NM, Pouwels PJ, Engelke UF, Feikema W, Valk J, Jakobs C. van der Knaap MS, et al. Ann Neurol. 1999 Dec;46(6):925-8. doi: 10.1002/1531-8249(199912)46:6<925::aid-ana18>3.0.co;2-j. Ann Neurol. 1999. PMID: 10589548

6

High-resolution proton nuclear magnetic resonance spectroscopy of ovarian cyst fluid.

Boss EA, Moolenaar SH, Massuger LF, Boonstra H, Engelke UF, de Jong JG, Wevers RA. Boss EA, et al. NMR Biomed. 2000 Aug;13(5):297-305. doi: 10.1002/1099-1492(200008)13:5<297::aid-nbm648>3.0.co;2-i. NMR Biomed. 2000. PMID: 10960920

7

Hypoxia in fetal lambs: a study with (1)H-MNR spectroscopy of cerebrospinal fluid.

van Cappellen van Walsum AM, Jongsma HW, Wevers RA, Nijhuis JG, Crevels J, Engelke UF, Moolenaar SH, Oeseburg B, Nijland R. van Cappellen van Walsum AM, et al. Pediatr Res. 2001 May;49(5):698-704. doi: 10.1203/00006450-200105000-00015. Pediatr Res. 2001. PMID: 11328955

8

In vivo and in vitro NMR spectroscopy reveal a putative novel inborn error involving polyol metabolism.

Moolenaar SH, van der Knaap MS, Engelke UF, Pouwels PJ, Janssen-Zijlstra FS, Verhoeven NM, Jakobs C, Wevers RA. Moolenaar SH, et al. NMR Biomed. 2001 May;14(3):167-76. doi: 10.1002/nbm.690. NMR Biomed. 2001. PMID: 11357181

9

beta-Ureidopropionase deficiency: a novel inborn error of metabolism discovered using NMR spectroscopy on urine.

Moolenaar SH, Göhlich-Ratmann G, Engelke UF, Spraul M, Humpfer E, Dvortsak P, Voit T, Hoffmann GF, Bräutigam C, van Kuilenburg AB, van Gennip A, Vreken P, Wevers RA. Moolenaar SH, et al. Magn Reson Med. 2001 Nov;46(5):1014-7. doi: 10.1002/mrm.1289. Magn Reson Med. 2001. PMID: 11675655 Free article.

10

Prolidase deficiency diagnosed by 1H NMR spectroscopy of urine.

Moolenaar SH, Engelke UF, Abeling NG, Mandel H, Duran M, Wevers RA. Moolenaar SH, et al. J Inherit Metab Dis. 2001 Dec;24(8):843-50. doi: 10.1023/a:1013940207973. J Inherit Metab Dis. 2001. PMID: 11916317

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

96 results

Search Page