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Modeling the Leigh syndrome nt8993 T-->C mutation in Escherichia coli F1F0 ATP synthase.
Int J Biochem Cell Biol. 1999 Jul;31(7):769-76. doi: 10.1016/s1357-2725(99)00029-1.
Int J Biochem Cell Biol. 1999.
PMID: 10467733
Second-site suppressor mutations at glycine 218 and histidine 245 in the alpha subunit of F1F0 ATP synthase in Escherichia coli.
Hartzog PE, Cain BD.
Hartzog PE, et al.
J Biol Chem. 1994 Dec 23;269(51):32313-7.
J Biol Chem. 1994.
PMID: 7798232
Free article.
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Mutagenic analysis of the a subunit of the F1F0 ATP synthase in Escherichia coli: Gln-252 through Tyr-263.
Hartzog PE, Cain BD.
Hartzog PE, et al.
J Bacteriol. 1993 Mar;175(5):1337-43. doi: 10.1128/jb.175.5.1337-1343.1993.
J Bacteriol. 1993.
PMID: 8383111
Free PMC article.
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The aleu207-->arg mutation in F1F0-ATP synthase from Escherichia coli. A model for human mitochondrial disease.
Hartzog PE, Cain BD.
Hartzog PE, et al.
J Biol Chem. 1993 Jun 15;268(17):12250-2.
J Biol Chem. 1993.
PMID: 8509361
Free article.
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Cytosine deaminase MX cassettes as positive/negative selectable markers in Saccharomyces cerevisiae.
Hartzog PE, Nicholson BP, McCusker JH.
Hartzog PE, et al.
Yeast. 2005 Jul 30;22(10):789-98. doi: 10.1002/yea.1245.
Yeast. 2005.
PMID: 16088873
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The tRNA-Tyr gene family of Saccharomyces cerevisiae: agents of phenotypic variation and position effects on mutation frequency.
Ito-Harashima S, Hartzog PE, Sinha H, McCusker JH.
Ito-Harashima S, et al. Among authors: hartzog pe.
Genetics. 2002 Aug;161(4):1395-410. doi: 10.1093/genetics/161.4.1395.
Genetics. 2002.
PMID: 12196388
Free PMC article.
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