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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Aug 2016.

Chromosome 9 open reading frame 4

CG6
Top mentioned proteins: ACID, TRPC1, CAN, PKI, alpha-amylase
Papers on CG6
Evaluation of the nutritional quality of the grain protein of new amaranths varieties.
New
Escudero et al., San Luis, Argentina. In Plant Foods Hum Nutr, Mar 2015
Dorado (HD), as well as from advanced lines of Amaranthus hypochondriacus x Amaranthus cruentus H17a (H17) and Amaranthus cruentus G6/17a (CG6), was carried out in order to elucidate their nutritional contribution to human diet.
[Genotyping of Vaginal Candida glabrata Isolates Using Microsatellite Marker Analysis and DNA Sequencing to Identify Mutations Associated with Antifungal Resistance].
Ilkit et al., Mercin, Turkey. In Mikrobiyol Bul, 2013
These isolates were genotyped using multiple-locus variable number tandem repeat analysis of three microsatellite markers (RPM2, MTI, and Cg6).
Molecular analysis of Candida glabrata clinical isolates.
Subik et al., Bratislava, Slovakia. In Mycopathologia, 2010
The 14 different genotypes were found by using microsatellite marker analysis (RPM2, MTI and Cg6) and DNA sequencing for analysis of the entire ERG11 gene.
NMR spectroscopic elucidation of the B-Z transition of a DNA double helix induced by the Z alpha domain of human ADAR1.
Lee et al., Chinju, South Korea. In J Am Chem Soc, 2009
In order to characterize the molecular recognition of Z-DNA by Z alpha(ADAR1), we performed circular dichroism (CD) and NMR experiments with complexes of Zalpha(ADAR1) bound to d(CGCGCG)(2) (referred to as CG6) produced at a variety of protein-to-DNA molar ratios.
Copper-responsive magnetic resonance imaging contrast agents.
Chang et al., Berkeley, United States. In J Am Chem Soc, 2009
Addition of Cu(+) to CG2, CG3, CG4, and CG5 and either Cu(+) or Cu(2+) to CG6 triggers marked enhancements in relaxivity (r(1) = 2.3-6.9 mM(-1) s(-1)).
Switching DNA-binding specificity by unnatural amino acid substitution.
Roy et al., Calcutta, India. In Nucleic Acids Res, 2004
In the lambda-repressor-DNA complex, the epsilon-NH(2) group (hydrogen bond donor) of lysine-4 of lambda-repressor forms hydrogen bonds with the amide carbonyl atom of asparagine-55 (acceptor) and the O6 (acceptor) of CG6 of operator site O(L)1.
Multilocus sequence typing of Candida glabrata reveals geographically enriched clades.
Fox et al., Manchester, United Kingdom. In J Clin Microbiol, 2003
The technique was validated by comparison with random amplified polymorphic DNA and the complex DNA fingerprinting probes Cg6 and Cg12.
The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6.
Fujiki et al., Fukuoka, Japan. In J Hum Genet, 2000
Eleven peroxin genes, termed PEXs, responsible for PBDs have been identified, whereas pathogenic genes for PBDs of 2CGs, CG-A (the same CG as CG8 in the United States and Europe) and CG6, remained unidentified.
Phenotypic switching in Candida glabrata involves phase-specific regulation of the metallothionein gene MT-II and the newly discovered hemolysin gene HLP.
Soll et al., Iowa City, United States. In Infect Immun, 2000
Switching of C. glabrata is not associated with microevolutionary changes identified by the DNA fingerprinting probe Cg6 and does not involve tandem amplification of the MT-IIa gene, which has been shown to occur in response to elevated levels of copper.
Development and verification of fingerprinting probes for Candida glabrata.
Soll et al., Iowa City, United States. In Microbiology, 1997
The capacity of two of the probes, Cg6 and Cg12, to measure genetic distance between independent isolates is verified by comparing clustering in dendrograms based on similarity coefficients computed between all pairs of 39 independent isolates fingerprinted with Cg6, Cg12 and randomly amplified polymorphic DNA.
Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders.
Gould et al., Baltimore, United States. In J Cell Sci, 1995
This hypothesis is further supported by correlations between certain complementation groups and particular type-3 subphenotypes: all patient cell lines belonging to CG3 and CG10 showed a complete absence of peroxisomal matrix protein import while those from CG6, CG7, and CG8 imported some peroxisomal matrix proteins.
Complementation group assignments of moderately UV-sensitive CHO mutants isolated by large-scale screening (FAECB).
Thompson et al., Washington, D.C., United States. In Mutagenesis, 1994
One CG of UV mutants (CG6), which now has five identified representatives in the collection, has only been found among moderately UV-sensitive CHO cells.
Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F.
Hoeijmakers et al., Rotterdam, Netherlands. In Embo J, 1993
In cell-free extracts prepared from rodent CGs 1-5 and 11, but not in a mutant from CG6, we find an impaired repair of damage induced in plasmids by UV light and N-acetoxy-acetylaminofluorene.
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