Froese DS - Search Results

1

Structure of MMACHC reveals an arginine-rich pocket and a domain-swapped dimer for its B12 processing function.

Froese DS, Krojer T, Wu X, Shrestha R, Kiyani W, von Delft F, Gravel RA, Oppermann U, Yue WW. Froese DS, et al. Biochemistry. 2012 Jun 26;51(25):5083-90. doi: 10.1021/bi300150y. Epub 2012 Jun 14. Biochemistry. 2012. PMID: 22642810

2

Integrated multi-omics reveals anaplerotic rewiring in methylmalonyl-CoA mutase deficiency.

Forny P, Bonilla X, Lamparter D, Shao W, Plessl T, Frei C, Bingisser A, Goetze S, van Drogen A, Harshman K, Pedrioli PGA, Howald C, Poms M, Traversi F, Bürer C, Cherkaoui S, Morscher RJ, Simmons L, Forny M, Xenarios I, Aebersold R, Zamboni N, Rätsch G, Dermitzakis ET, Wollscheid B, Baumgartner MR, Froese DS. Forny P, et al. Among authors: froese ds. Nat Metab. 2023 Jan;5(1):80-95. doi: 10.1038/s42255-022-00720-8. Epub 2023 Jan 26. Nat Metab. 2023. PMID: 36717752 Free PMC article.

3

Cellular and computational models reveal environmental and metabolic interactions in MMUT-type methylmalonic aciduria.

Ramon C, Traversi F, Bürer C, Froese DS, Stelling J. Ramon C, et al. Among authors: froese ds. J Inherit Metab Dis. 2023 May;46(3):421-435. doi: 10.1002/jimd.12575. Epub 2022 Nov 23. J Inherit Metab Dis. 2023. PMID: 36371683

4

Insights into energy balance dysregulation from a mouse model of methylmalonic aciduria.

Lucienne M, Gerlini R, Rathkolb B, Calzada-Wack J, Forny P, Wueest S, Kaech A, Traversi F, Forny M, Bürer C, Aguilar-Pimentel A, Irmler M, Beckers J, Sauer S, Kölker S, Dewulf JP, Bommer GT, Hoces D, Gailus-Durner V, Fuchs H, Rozman J, Froese DS, Baumgartner MR, de Angelis MH. Lucienne M, et al. Among authors: froese ds. Hum Mol Genet. 2023 Aug 26;32(17):2717-2734. doi: 10.1093/hmg/ddad100. Hum Mol Genet. 2023. PMID: 37369025 Free PMC article.

5

Restricted role for methionine synthase reductase defined by subcellular localization.

Froese DS, Wu X, Zhang J, Dumas R, Schoel WM, Amrein M, Gravel RA. Froese DS, et al. Mol Genet Metab. 2008 May;94(1):68-77. doi: 10.1016/j.ymgme.2007.11.019. Epub 2008 Jan 24. Mol Genet Metab. 2008. PMID: 18221906 Free PMC article.

6

Mechanism of vitamin B12-responsiveness in cblC methylmalonic aciduria with homocystinuria.

Froese DS, Zhang J, Healy S, Gravel RA. Froese DS, et al. Mol Genet Metab. 2009 Dec;98(4):338-43. doi: 10.1016/j.ymgme.2009.07.014. Epub 2009 Aug 3. Mol Genet Metab. 2009. PMID: 19700356

7

Thermolability of mutant MMACHC protein in the vitamin B12-responsive cblC disorder.

Froese DS, Healy S, McDonald M, Kochan G, Oppermann U, Niesen FH, Gravel RA. Froese DS, et al. Mol Genet Metab. 2010 May;100(1):29-36. doi: 10.1016/j.ymgme.2010.02.005. Epub 2010 Feb 15. Mol Genet Metab. 2010. PMID: 20219402 Free PMC article.

8

Structures of the human GTPase MMAA and vitamin B12-dependent methylmalonyl-CoA mutase and insight into their complex formation.

Froese DS, Kochan G, Muniz JR, Wu X, Gileadi C, Ugochukwu E, Krysztofinska E, Gravel RA, Oppermann U, Yue WW. Froese DS, et al. J Biol Chem. 2010 Dec 3;285(49):38204-13. doi: 10.1074/jbc.M110.177717. Epub 2010 Sep 28. J Biol Chem. 2010. PMID: 20876572 Free PMC article.

9

Genetic disorders of vitamin B₁₂ metabolism: eight complementation groups--eight genes.

Froese DS, Gravel RA. Froese DS, et al. Expert Rev Mol Med. 2010 Nov 29;12:e37. doi: 10.1017/S1462399410001651. Expert Rev Mol Med. 2010. PMID: 21114891 Free PMC article. Review.

10

Conformational plasticity of glycogenin and its maltosaccharide substrate during glycogen biogenesis.

Chaikuad A, Froese DS, Berridge G, von Delft F, Oppermann U, Yue WW. Chaikuad A, et al. Among authors: froese ds. Proc Natl Acad Sci U S A. 2011 Dec 27;108(52):21028-33. doi: 10.1073/pnas.1113921108. Epub 2011 Dec 12. Proc Natl Acad Sci U S A. 2011. PMID: 22160680 Free PMC article.

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