Stoffel W - Search Results

1

Human mitochondrial enoyl-CoA hydratase gene (ECHS1): structural organization and assignment to chromosome 10q26.2-q26.3.

Janssen U, Davis EM, Le Beau MM, Stoffel W. Janssen U, et al. Among authors: stoffel w. Genomics. 1997 Mar 15;40(3):470-5. doi: 10.1006/geno.1996.4597. Genomics. 1997. PMID: 9073515

2

Human mitochondrial 3,2-trans-enoyl-CoA isomerase (DCI): gene structure and localization to chromosome 16p13.3.

Janssen U, Fink T, Lichter P, Stoffel W. Janssen U, et al. Among authors: stoffel w. Genomics. 1994 Sep 1;23(1):223-8. doi: 10.1006/geno.1994.1480. Genomics. 1994. PMID: 7829074

3

Enoyl-CoA hydratase and isomerase form a superfamily with a common active-site glutamate residue.

Müller-Newen G, Janssen U, Stoffel W. Müller-Newen G, et al. Among authors: stoffel w. Eur J Biochem. 1995 Feb 15;228(1):68-73. doi: 10.1111/j.1432-1033.1995.tb20230.x. Eur J Biochem. 1995. PMID: 7883013 Free article.

Their substrates and reaction mechanisms are similar [Muller-Newen, G. & Stoffel, W. (1993) Biochemistry 32, 11,405-11,412]. Glu164 of mECH is the only amino acid with a protic side chain that is conserved in these monofunctional and polyfunctional enzymes with …

Their substrates and reaction mechanisms are similar [Muller-Newen, G. & Stoffel, W. (1993) Biochemistry 32, 11,405-11,412 …

4

The human gene CGT encoding the UDP-galactose ceramide galactosyl transferase (cerebroside synthase): cloning, characterization, and assignment to human chromosome 4, band q26.

Bosio A, Binczek E, Le Beau MM, Fernald AA, Stoffel W. Bosio A, et al. Among authors: stoffel w. Genomics. 1996 May 15;34(1):69-75. doi: 10.1006/geno.1996.0242. Genomics. 1996. PMID: 8661025

5

Disruption of mitochondrial beta -oxidation of unsaturated fatty acids in the 3,2-trans-enoyl-CoA isomerase-deficient mouse.

Janssen U, Stoffel W. Janssen U, et al. Among authors: stoffel w. J Biol Chem. 2002 May 31;277(22):19579-84. doi: 10.1074/jbc.M110993200. Epub 2002 Mar 26. J Biol Chem. 2002. PMID: 11916962 Free article.

6

Human neutral amino acid transporter ASCT1: structure of the gene (SLC1A4) and localization to chromosome 2p13-p15.

Hofmann K, Düker M, Fink T, Lichter P, Stoffel W. Hofmann K, et al. Among authors: stoffel w. Genomics. 1994 Nov 1;24(1):20-6. doi: 10.1006/geno.1994.1577. Genomics. 1994. PMID: 7896285

7

Molecular cloning and characterization of the mouse CGT gene encoding UDP-galactose ceramide-galactosyltransferase (cerebroside synthetase).

Bosio A, Binczek E, Stoffel W. Bosio A, et al. Among authors: stoffel w. Genomics. 1996 Jul 1;35(1):223-6. doi: 10.1006/geno.1996.0342. Genomics. 1996. PMID: 8661124

8

Molecular cloning and gene organization of the mouse mitochondrial 3,2-trans-enoyl-CoA isomerase.

Stoffel W, Düker M, Hofmann K. Stoffel W, et al. FEBS Lett. 1993 Oct 25;333(1-2):119-22. doi: 10.1016/0014-5793(93)80387-a. FEBS Lett. 1993. PMID: 8224148 Free article.

9

Functional redundancy of mitochondrial enoyl-CoA isomerases in the oxidation of unsaturated fatty acids.

van Weeghel M, te Brinke H, van Lenthe H, Kulik W, Minkler PE, Stoll MS, Sass JO, Janssen U, Stoffel W, Schwab KO, Wanders RJ, Hoppel CL, Houten SM. van Weeghel M, et al. Among authors: stoffel w. FASEB J. 2012 Oct;26(10):4316-26. doi: 10.1096/fj.12-206326. Epub 2012 Jul 10. FASEB J. 2012. PMID: 22782973

10

Site-directed mutagenesis of putative active-site amino acid residues of 3,2-trans-enoyl-CoA isomerase, conserved within the low-homology isomerase/hydratase enzyme family.

Müller-Newen G, Stoffel W. Müller-Newen G, et al. Among authors: stoffel w. Biochemistry. 1993 Oct 26;32(42):11405-12. doi: 10.1021/bi00093a018. Biochemistry. 1993. PMID: 8218206

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