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Showing 1-7 of 7 results for "G1149" within Papers
Eric A Josephs et al.
DNA repair, 35, 71-84 (2015-10-16)
In Escherichia coli, errors in newly-replicated DNA, such as the incorporation of a nucleotide with a mis-paired base or an accidental insertion or deletion of nucleotides, are corrected by a methyl-directed mismatch repair (MMR) pathway. While the enzymology of MMR
The HCM-linked W792R mutation in cardiac myosin-binding protein C reduces C6 FnIII domain stability
Smelter DF, et al.
American Journal of Physiology. Heart and Circulatory Physiology, 314(6), H1179-H1191 (2018)
Robbin Schnieders et al.
Current protocols in nucleic acid chemistry, 82(1), e116-e116 (2020-09-23)
NMR spectroscopy is a potent method for the structural and biophysical characterization of RNAs. The application of NMR spectroscopy is restricted in RNA size and most often requires isotope-labeled or even selectively labeled RNAs. Additionally, new NMR pulse sequences, such
Stability and solution structure of binary and ternary Cu (II) complexes with l-glutamic acid and diamines as well as adducts in metal-free systems in aqueous solution
Bregier-JR
Journal of Solution Chemistry, 43(12), 2144-2162 (2014)
Cell Type-Specific Imaging of Calcium Signaling in Arabidopsis thaliana Seedling Roots Using GCaMP3.
William Krogman et al.
International journal of molecular sciences, 21(17) (2020-09-06)
Cytoplasmic calcium ([Ca2+]cyt) is a well-characterized second messenger in eukaryotic cells. An elevation in [Ca2+]cyt levels is one of the earliest responses in plant cells after exposure to a range of environmental stimuli. Advances in understanding the role of [Ca2+]cyt
Oksana Forostyak et al.
Stem cells and development, 22(10), 1506-1521 (2013-01-09)
Human embryonic stem cell-derived neural precursors (hESC NPs) are considered to be a promising tool for cell-based therapy in central nervous system injuries and neurodegenerative diseases. The Ca(2+) ion is an important intracellular messenger essential for the regulation of various
Oleg Dmitriev et al.
Proceedings of the National Academy of Sciences of the United States of America, 103(14), 5302-5307 (2006-03-29)
Wilson disease protein (ATP7B) is a copper-transporting P(1B)-type ATPase that regulates copper homeostasis and biosynthesis of copper-containing enzymes in human tissues. Inactivation of ATP7B or related ATP7A leads to severe neurodegenerative disorders, whereas their overexpression contributes to cancer cell resistance
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