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Page 1
Analysis of protein function in clinical C. albicans isolates.
Gerami-Nejad M, Forche A, McClellan M, Berman J. Gerami-Nejad M, et al. Yeast. 2012 Aug;29(8):303-9. doi: 10.1002/yea.2910. Epub 2012 Jul 9. Yeast. 2012. PMID: 22777821 Free PMC article.
We constructed novel plasmids containing HA-NAT1 or MYC-NAT1 cassettes to facilitate PCR-mediated construction of strains with C-terminal epitope-tagged proteins and a NAT1-pMet3-GFP plasmid to enable conditional expression of proteins with or without the green fluorescent protei …
We constructed novel plasmids containing HA-NAT1 or MYC-NAT1 cassettes to facilitate PCR-mediated construction of strains with C-terminal ep …
Neocentromeres form efficiently at multiple possible loci in Candida albicans.
Ketel C, Wang HS, McClellan M, Bouchonville K, Selmecki A, Lahav T, Gerami-Nejad M, Berman J. Ketel C, et al. Among authors: gerami nejad m. PLoS Genet. 2009 Mar;5(3):e1000400. doi: 10.1371/journal.pgen.1000400. Epub 2009 Mar 6. PLoS Genet. 2009. PMID: 19266018 Free PMC article.
Additional cassettes for epitope and fluorescent fusion proteins in Candida albicans.
Gerami-Nejad M, Dulmage K, Berman J. Gerami-Nejad M, et al. Yeast. 2009 Jul;26(7):399-406. doi: 10.1002/yea.1674. Yeast. 2009. PMID: 19504625 Free PMC article.
Finally, we describe a construct that directs PCR-mediated two-step insertion of GFP internal to a coding sequence, which facilitates tagging of secreted proteins, including GPI-anchor cell wall proteins that require endogenous N- and C-termini for function. These reagents …
Finally, we describe a construct that directs PCR-mediated two-step insertion of GFP internal to a coding sequence, which facilitates taggin …
11 results