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A kinetic model of iron trafficking in growing Saccharomyces cerevisiae cells; applying mathematical methods to minimize the problem of sparse data and generate viable autoregulatory mechanisms.
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- PLoS Computational Biology, 2023, v. 19, n. 12, p. 1, doi. 10.1371/journal.pcbi.1011701
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- Article
Low-temperature Mössbauer spectroscopy of organs from <sup>57</sup>Fe-enriched HFE<sup>(−/−)</sup> hemochromatosis mice: an iron-dependent threshold for generating hemosiderin.
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- Journal of Biological Inorganic Chemistry (JBIC), 2023, v. 28, n. 2, p. 173, doi. 10.1007/s00775-022-01975-y
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Mössbauer-based molecular-level decomposition of the Saccharomyces cerevisiae ironome, and preliminary characterization of isolated nuclei.
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- Metallomics, 2022, v. 14, n. 11, p. 1, doi. 10.1093/mtomcs/mfac080
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Low-molecular-mass labile metal pools in Escherichia coli: advances using chromatography and mass spectrometry.
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- Journal of Biological Inorganic Chemistry (JBIC), 2021, v. 26, n. 4, p. 479, doi. 10.1007/s00775-021-01864-w
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Chromatographic detection of low-molecular-mass metal complexes in the cytosol of Saccharomyces cerevisiae.
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- Metallomics, 2020, v. 12, n. 7, p. 1094, doi. 10.1039/c9mt00312f
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- Article
A comprehensive mechanistic model of iron metabolism in Saccharomyces cerevisiae.
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- Metallomics, 2019, v. 11, n. 11, p. 1779, doi. 10.1039/c9mt00199a
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Low-molecular-mass iron complexes in blood plasma of iron-deficient pigs do not originate directly from nutrient iron.
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- Metallomics, 2019, v. 11, n. 11, p. 1900, doi. 10.1039/c9mt00152b
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- Article
Isolated Saccharomyces cerevisiae vacuoles contain low-molecular-mass transition-metal polyphosphate complexes.
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- Metallomics, 2019, v. 11, n. 7, p. 1298, doi. 10.1039/c9mt00104b
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- Article
A mathematical model of iron import and trafficking in wild-type and Mrs3/4ΔΔ yeast cells.
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- BMC Systems Biology, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s12918-019-0702-2
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Low-molecular-mass iron in healthy blood plasma is not predominately ferric citrate.
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- Metallomics, 2018, v. 10, n. 6, p. 802, doi. 10.1039/c8mt00055g
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Ferric ions accumulate in the walls of metabolically inactivating Saccharomyces cerevisiae cells and are reductively mobilized during reactivation.
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- Metallomics, 2016, v. 8, n. 7, p. 692, doi. 10.1039/c6mt00070c
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Risk Management For Legionellosis.
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- ASHRAE Journal, 2015, v. 57, n. 10, p. 14
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Speciation of iron in mouse liver during development, iron deficiency, IRP2 deletion and inflammatory hepatitis.
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- Metallomics, 2015, v. 7, n. 1, p. 88, doi. 10.1039/c4mt00215f
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- Article
Cold Weather Operation Of Cooling Towers.
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- ASHRAE Journal, 2014, v. 56, n. 3, p. 26
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Mathematical model for positioning the FtsZ contractile ring in Escherichia coli.
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- Journal of Mathematical Biology, 2014, v. 68, n. 4, p. 911, doi. 10.1007/s00285-013-0652-z
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The catalase activity of diiron adenine deaminase.
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- Protein Science: A Publication of the Protein Society, 2011, v. 20, n. 12, p. 2080, doi. 10.1002/pro.748
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Mathematical Model of a Cell Size Checkpoint.
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- PLoS Computational Biology, 2010, v. 6, n. 12, p. 1, doi. 10.1371/journal.pcbi.1001036
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Kinetic Modeling of the Assembly, Dynamic Steady State, and Contraction of the FtsZ Ring in Prokaryotic Cytokinesis.
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- PLoS Computational Biology, 2008, v. 4, n. 7, p. 1, doi. 10.1371/journal.pcbi.1000102
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Implications of a Carboxylate-Bound C-Cluster Structure of Carbon Monoxide Dehydrogenase.
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- Angewandte Chemie International Edition, 2008, v. 47, n. 22, p. 4054, doi. 10.1002/anie.200800223
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Tunnel mutagenesis and Ni-dependent reduction and methylation of the α subunit of acetyl coenzyme A synthase/carbon monoxide dehydrogenase.
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- Journal of Biological Inorganic Chemistry (JBIC), 2008, v. 13, n. 5, p. 771, doi. 10.1007/s00775-008-0363-x
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Function of the tunnel in acetylcoenzyme A synthase/carbon monoxide dehydrogenase.
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- Journal of Biological Inorganic Chemistry (JBIC), 2006, v. 11, n. 3, p. 371, doi. 10.1007/s00775-006-0086-9
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LdpA: a component of the circadian clock senses redox state of the cell.
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- EMBO Journal, 2005, v. 24, n. 6, p. 1202, doi. 10.1038/sj.emboj.7600606
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Stepwise Evolution of Nonliving to Living Chemical Systems.
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- Origins of Life & Evolution of the Biosphere, 2004, v. 34, n. 4, p. 371, doi. 10.1023/B:ORIG.0000029880.76881.f5
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Acetyl-coenzyme A synthase: the case for a Ni<sub>p</sub><sup>0</sup>-based mechanism of catalysis.
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- Journal of Biological Inorganic Chemistry (JBIC), 2004, v. 9, n. 5, p. 516, doi. 10.1007/s00775-004-0564-x
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Autocatalytic activation of acetyl-CoA synthase.
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- Journal of Biological Inorganic Chemistry (JBIC), 2004, v. 9, n. 3, p. 316, doi. 10.1007/s00775-004-0528-1
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Ni-Zn-[Fe<sub>4</sub>-S<sub>4</sub>] and Ni-Ni-[Fe<sub>4</sub>-S<sub>4</sub>] clusters in closed and open a subunits of acetyl-CoA synthase/carbon monoxide dehydrogenase.
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- Nature Structural Biology, 2003, v. 10, n. 4, p. 271, doi. 10.1038/nsb912
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The Evolution of Acetyl-CoA Synthase.
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- Origins of Life & Evolution of the Biosphere, 2001, v. 31, n. 4/5, p. 403, doi. 10.1023/A:1011809430237
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- Article