His primary areas of investigation include Genetics, Phenotype, Mutation, Mutant and Endocrinology. His Phenotype research is multidisciplinary, incorporating elements of Gene knockout, Ribosomopathy, Genome-wide association study and Ribosomal protein. His Mutation study combines topics from a wide range of disciplines, such as Molecular biology, Hearing loss and Melanin.
His Mutant research is multidisciplinary, relying on both T cell, Autoimmunity, Immune system and Autoantibody. His biological study spans a wide range of topics, including Sphingosine, Sphingosine-1-phosphate and Internal medicine. His Gene research incorporates elements of Evolutionary biology and Sexual dimorphism.
Mutant, Genetics, Internal medicine, Phenotype and Endocrinology are his primary areas of study. His Mutant study combines topics from a wide range of disciplines, such as Mutation and Molecular biology. His study ties his expertise on Cell biology together with the subject of Mutation.
His Molecular biology research incorporates themes from Signal transduction and Knockout mouse. His research in Genetics intersects with topics in Hair cell and Hearing loss. The study incorporates disciplines such as Gene knockout, Regulation of gene expression, Neuroscience and Pathology in addition to Phenotype.
His scientific interests lie mostly in Endocrinology, Internal medicine, Cell biology, Phenotype and Allele. His studies examine the connections between Endocrinology and genetics, as well as such issues in FGF21, with regards to Endogeny, Obesity and Brown adipose tissue. He has included themes like Diabetes mellitus, SNP and Sucrose in his Internal medicine study.
His Phenotype study combines topics in areas such as Mutation, Genetic traits, Neuroscience and Quantitative trait locus. His Retinal ganglion research focuses on subjects like Eye development, which are linked to Mutant. Gene and Genetics are inherently bound to his Methyltransferase studies.
Helmut Fuchs mostly deals with Cell biology, Methyltransferase, Phenotype, Translation and Genetics. His study on Respiratory chain and Alternative oxidase is often connected to Metabolome and BCS1L as part of broader study in Cell biology. His Methyltransferase study incorporates themes from Intellectual disability, Messenger RNA, Immune system and Mutation.
His studies in Phenotype integrate themes in fields like Synaptic plasticity, Postsynaptic potential, Cognitive skill, SRC Family Tyrosine Kinase and Candidate gene. His work focuses on many connections between Translation and other disciplines, such as RNA, that overlap with his field of interest in Stem cell, Ribosomal RNA and Enzyme. His work on Genetics deals in particular with TRNA Methyltransferases, Gene, Genetic traits, Quantitative trait locus and Phenome.
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Mutations in Dynein Link Motor Neuron Degeneration to Defects in Retrograde Transport
Majid Hafezparast;Rainer Klocke;Christiana Ruhrberg;Andreas Marquardt.
Science (2003)
High-throughput discovery of novel developmental phenotypes
Mary E. Dickinson;Ann M. Flenniken;Xiao Ji;Lydia Teboul.
Nature (2016)
Cardioprotection and lifespan extension by the natural polyamine spermidine
Tobias Eisenberg;Mahmoud Abdellatif;Sabrina Schroeder;Uwe Primessnig;Uwe Primessnig.
Nature Medicine (2016)
A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice
Wolfgang Enard;Sabine Gehre;Kurt Hammerschmidt;Sabine M. Hölter.
Cell (2009)
Aberrant methylation of tRNAs links cellular stress to neuro‐developmental disorders
Sandra Blanco;Sabine Dietmann;Joana V Flores;Shobbir Hussain.
The EMBO Journal (2014)
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains
Michelle M Simon;Simon Greenaway;Jacqueline K White;Helmut Fuchs.
Genome Biology (2013)
Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects
Kelly A McGowan;Jun Z Li;Jun Z Li;Christopher Y Park;Veronica Beaudry.
Nature Genetics (2008)
Rapamycin extends murine lifespan but has limited effects on aging
Frauke Neff;Diana Flores-Dominguez;Devon P. Ryan;Marion Horsch.
Journal of Clinical Investigation (2013)
An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice.
Morag A Lewis;Elizabeth Quint;Anne M Glazier;Helmut Fuchs.
Nature Genetics (2009)
Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.
Sarah Vreugde;Alexandra Erven;Corné J. Kros;Walter Marcotti.
Nature Genetics (2002)
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Technical University of Munich
Ludwig-Maximilians-Universität München
German Center for Neurodegenerative Diseases
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