Michael Nehls

Washington University in St. Louis — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

32h-index6.4kcitations74works0.02yr avg
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Research Topics

Genomics and Chromatin Dynamics(11), CRISPR and Genetic Engineering(7), Pluripotent Stem Cells Research(5), RNA and protein synthesis mechanisms(5), Animal Genetics and Reproduction(5)

Publications73 total

Mycobacterium tuberculosis exploits FIP200 regulated cell-death pathways to promote replication
The Journal of Immunology·2023Open Access
Determining the mechanistic basis for Irgm1 mediated control of <i>Mycobacterium tuberculosis</i> infection
The Journal of Immunology·2023Open Access
Investigating the role of BHLHE40 in host responses to <i>Mycobacterium tuberculosis</i> infection and myeloid cell development
The Journal of Immunology·2023· 1 citedOpen Access
Lebensweise und Alzheimer
Erfahrungsheilkunde·2017
Unified theory of Alzheimer’s disease (UTAD): implications for prevention and curative therapy
Journal of Molecular Psychiatry·2016· 41 citedOpen Access
Evolutionsbiologische Erklärung der Alzheimerentstehung − Mikronährstoffe in Prävention und Therapie
Zeitschrift für Orthomolekulare Medizin·2015
Pillars Article: New Member of the Winged-Helix Protein Family Disrupted In Mouse And Rat Nude Mutations. <i>Nature</i>. 1994. 372: 103-107
The Journal of Immunology·2015
Pillars article: new member of the winged-helix protein family disrupted in mouse and rat nude mutations. Nature. 1994. 372: 103-107.
PubMed·2015
18 Establishment and characterization of a Merkel Cell carcinoma PDX panel: Screening for potentially useful therapies
European Journal of Cancer·2014
97 Utilization of low passage adenoid cystic carcinoma PDX models to identify novel combination therapies
European Journal of Cancer·2014
An EF hand mutation in Stim1 causes premature platelet activation and bleeding in mice
Journal of Clinical Investigation·2007· 165 citedOpen Access
Contribution of Mucosal Maltase-Glucoamylase Activities to Mouse Small Intestinal Starch α-Glucogenesis3
Journal of Nutrition·2007· 72 cited
<i>N</i>-ethyl-<i>N</i>-nitrosourea-based generation of mouse models for mutant G protein-coupled receptors
Physiological Genomics·2006· 16 cited
Mutation of mouse Mayp/Pstpip2 causes a macrophage autoinflammatory disease
Blood·2006· 143 citedOpen Access
Mutation of Mouse MAYP/PSTPIP2 Causes a Macrophage Autoinflammatory Disease.
Blood·2005· 3 cited
Efficient and fast targeted production of murine models based on ENU mutagenesis
Mammalian Genome·2005· 67 cited
Autoimmunity and Inflammation Due to a Gain-of-Function Mutation in Phospholipase Cγ2 that Specifically Increases External Ca2+ Entry
Immunity·2005· 179 citedOpen Access
Mäuse als Modelle für menschliche Erkrankungen
mediaTUM (Technical University of Munich)·2005Open Access
Failure to degrade poly(ADP-ribose) causes increased sensitivity to cytotoxicity and early embryonic lethality
Proceedings of the National Academy of Sciences·2004· 323 citedOpen Access
The dominant alopecia phenotypes Bareskin, Rex-denuded, and Reduced Coat 2 are caused by mutations in gasdermin 3
Genomics·2004· 93 cited
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Frequent Co-authors

Sigrid Wattler(16), Thomas Boehm(14), Johannes Grosse(6), Michael Schorpp(5), Andreas Russ(5), David A. Brenner(5), Dietmar Pfeifer(4), Frank Wattler(4), P Hanke(4), Wolfgang Jagla(4), Richard A. Rippe(4), Dirk Korthaus(4), Martin Augustin(4), Philipp Yu(3), Ulrike Huffstadt(3), Helmut Fuchs(3), Martin Hrabě de Angelis(3), Andreas Marquardt(3), Jürgen Laufs(3), Carolin Schmittwolf(3)