Michael T. Zimmermann, Ph.D.
Affiliations: | 2011 | Biochemistry, Biophysics, and Molecular Biology | Iowa State University, Ames, IA, United States |
Area:
Bioinformatics Biology, General BiophysicsGoogle:
"Michael Zimmermann"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Robert L. Jernigan | grad student | 2011 | Iowa State | |
| (Mechanistic insights on important biomolecules derived using simple dynamics models from extending the reach of elastic network modeling.) | ||||
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Publications
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| Mathison A, Milech De Assuncao T, Dsouza NR, et al. (2020) Discovery, expression, cellular localization, and molecular properties of a novel, alternative spliced HP1γ isoform, lacking the chromoshadow domain. Plos One. 15: e0217452 |
| Gupta A, Zimmermann MT, Wang H, et al. (2019) Molecular characterization of known and novel ACVR1 variants in phenotypes of aberrant ossification. American Journal of Medical Genetics. Part A |
| Zimmermann MT, Williams MM, Klee EW, et al. (2019) Modeling Post-Translational Modifications and Cancer-Associated Mutations that Impact the Heterochromatin Protein 1α-Importin Α Heterodimers. Proteins |
| Klee EW, Zimmermann MT. (2019) Molecular modeling of LDLR aids interpretation of genomic variants. Journal of Molecular Medicine (Berlin, Germany) |
| Zimmermann MT, Urrutia R, Cousin MA, et al. (2018) Assessing Human Genetic Variations in Glucose Transporter SLC2A10 and Their Role in Altering Structural and Functional Properties. Frontiers in Genetics. 9: 276 |
| Zimmermann MT, Urrutia R, Oliver GR, et al. (2017) Molecular modeling and molecular dynamic simulation of the effects of variants in the TGFBR2 kinase domain as a paradigm for interpretation of variants obtained by next generation sequencing. Plos One. 12: e0170822 |
| Blackburn PR, Tischer A, Zimmermann MT, et al. (2017) A Novel Kleefstra Syndrome Associated Variant that Affects the Conserved TPLX Motif within the Ankyrin Repeat of EHMT1 Leads to Abnormal Protein Folding. The Journal of Biological Chemistry |
| Nasr SH, Dasari S, Mills JR, et al. (2017) Hereditary Lysozyme Amyloidosis Variant p.Leu102Ser Associates with Unique Phenotype. Journal of the American Society of Nephrology : Jasn |
| Long PA, Zimmermann MT, Kim M, et al. (2016) De novo RRAGC mutation activates mTORC1 signaling in syndromic fetal dilated cardiomyopathy. Human Genetics |
| Huang J, Eilbeck K, Smith B, et al. (2016) The Non-Coding RNA Ontology (NCRO): a comprehensive resource for the unification of non-coding RNA biology. Journal of Biomedical Semantics. 7: 24 |