Papers authored by Ehrnhoefer DE

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IFRD1 modulates disease severity in cystic fibrosis through the regulation of neutrophil effector function.
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Ehrnhoefer DE
Clinical genetics 76(2):148-9, 2009 Aug - Who cited this? | PubMed ID: 19673948 | Fulltext
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MCAD mutations identified in newborn screening cause different levels of enzymatic dysfunction.
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Ehrnhoefer DE
Clinical genetics 76(2):146-8, 2009 Aug - Who cited this? | PubMed ID: 19673949 | Fulltext
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Mouse models of Huntington disease: variations on a theme.
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Ehrnhoefer DE, Butland SL, Pouladi MA, and Hayden MR
Disease models & mechanisms 2(3-4):123-9, 2009 Mar - Who cited this? | PubMed ID: 19259385 | Fulltext
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EGCG redirects amyloidogenic polypeptides into unstructured, off-pathway oligomers.
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Ehrnhoefer DE, Bieschke J, Boeddrich A, Herbst M, Masino L, Lurz R, Engemann S, Pastore A, and Wanker EE
Nature structural & molecular biology 15(6):558-66, 2008 Jun - Who cited this? | PubMed ID: 18511942 | Fulltext
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Green tea (-)-epigallocatechin-gallate modulates early events in huntingtin misfolding and reduces toxicity in Huntington's disease models.
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Ehrnhoefer DE, Duennwald M, Markovic P, Wacker JL, Engemann S, Roark M, Legleiter J, Marsh JL, Thompson LM, Lindquist S, Muchowski PJ, and Wanker EE
Human molecular genetics 15(18):2743, 2006 Sep 15 - Who cited this? | PubMed ID: 16893904 | Fulltext
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