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Acyl-CoA thioesterase 11

This gene encodes a member of the acyl-CoA thioesterase family which catalyse the conversion of activated fatty acids to the corresponding non-esterified fatty acid and coenzyme A. Expression of a mouse homolog in brown adipose tissue is induced by low temperatures and repressed by warm temperatures. Higher levels of expression of the mouse homolog has been found in obesity-resistant mice compared with obesity-prone mice, suggesting a role of acyl-CoA thioesterase 11 in obesity. Alternative splicing results in transcript variants. [provided by RefSeq, Nov 2010] (from NCBI)
Top mentioned proteins: ACID, HAD, Monarch, POLYMERASE, INa
Papers on KIAA0707
Human brown fat inducible thioesterase variant 2 cellular localization and catalytic function.
Dunaway-Mariano et al., Albuquerque, United States. In Biochemistry, 2012
The N-terminal region of human fat inducible thioesterase variant 2 constitutes a mitochondrial location signal sequence, which undergoes mitochondrion-dependent posttranslational cleavage.
Transfection property of a new cholesterol-based cationic lipid containing tri-2-hydroxyethylamine as gene delivery vehicle.
Seu et al., Taegu, South Korea. In J Microbiol Biotechnol, 2012
A novel cholesterol-based cationic lipid containing a tri-2- hydroxyethylamine head group and ether linker (Chol- THEA) was synthesized and examined as a potent gene delivery vehicle.
[Effects of high thoracic epidural anesthesia on ventricular remodeling and expression of beta(3)-adrenoceptor in rats with heart failure induced by acute myocardial infarction].
Jiang et al., Fuzhou, China. In Zhonghua Yi Xue Za Zhi, 2010
beta(3)AR and eNOS mRNA levels were significantly decreased in the group THEA compared with the group CHF.
Cowpeas as growth substrate do not support the production of aflatoxin byAspergillus sp.
Jakobsen et al., Porto-Novo, Benin. In Mycotoxin Res, 2008
Two additional strains neither fit with theA.
Three thioesterases are involved in the biosynthesis of phosphinothricin tripeptide in Streptomyces viridochromogenes Tü494.
Schinko et al., Tübingen, Germany. In Antimicrob Agents Chemother, 2008
In addition, two external thioesterase genes, theA and theB, are located within the PTT biosynthetic gene cluster.
[Expression of myeloid cell triggering receptor-1 in monocytes at early post-burn stage].
Huang et al., Changsha, China. In Zhonghua Shao Shang Za Zhi, 2007
METHODS: The monocytes of 8 healthy volunteers (A group), 29 patients with mild and moderate burn (B group), and 9 patients with severe and very serious burns (C group) were isolated from the blood, and the THEM-1 mRNA and protein expression were determined by semi-quantitative RT-PCR and flow cytometry, respectively.
Temporal and spatial expression of homeotic genes is important for segment-specific neuroblast 6-4 lineage formation in Drosophila.
Jeon et al., Seoul, South Korea. In Mol Cells, 2006
As homeotic genes determine the identities of embryonic segments along theA/P axis, we investigated if temporal and specific expression of homeotic genes affects MM-CBG patterns in thorax and abdomen.
Molecular modeling of the interleukin-19 receptor complex. Novel aspects of receptor recognition in the interleukin-10 cytokine family.
Sticht et al., Erlangen, Germany. In J Mol Model, 2004
Comparison of the ligand/receptor interfaces in theA IL-10/IL-10R1,B IL-19/IL-20R1 andC IFN-gamma/receptor complexes.
BFIT, a unique acyl-CoA thioesterase induced in thermogenic brown adipose tissue: cloning, organization of the human gene and assessment of a potential link to obesity.
Lewin et al., San Francisco, United States. In Biochem J, 2001
BFIT supports the transition of thermogenic brown adipose tissue towards increased metabolic activity, probably through alteration of intracellular fatty acyl-CoA concentration.
Regeneration andAgrobacterium-mediated transformation ofForsythia xintermedia "Spring Glory".
Duron et al., Angers, France. In Plant Cell Rep, 1996
Internode explants ofin vitro plants ofForsythia x intermedia "Spring Glory" were transformed with thegus andnpt II genes after inoculation with theA.
A new model of lateral plate morph inheritance in the threespine stickleback,Gasterosteus aculeatus.
Banbura, Montpellier, France. In Theor Appl Genet, 1994
The dominance of theA allele is modified to semidominance by a dominant alleleC at a second locus.
Crude extracts of asteraceous weeds : Growth inhibitors for variegated cutworm.
Isman et al., Victoria, Canada. In J Chem Ecol, 1989
suaveolens petrol extract to the diet resulted in significant reduction in the relative growth rate of larvae, although theA.
Plant-determined variation in the cardenolide content, thin-layer chromatography profiles, and emetic potency of monarch butterflies,Danaus plexippus L. Reared on milkweed plants in California: 2.Asclepias speciosa.
Holland et al., Gainesville, United States. In J Chem Ecol, 1984
Thin-layer Chromatographie separation of the cardenolides in two different solvent systems showed that there are 23 cardenolides in theA.
Nucleotide sequence of the T-DNA region from theA grobacterium tumefaciens octopine Ti plasmid pTi15955.
Kemp et al., Madison, United States. In Plant Mol Biol, 1983
The complete nucleotide sequence of the transferred region (T-DNA) of an octopine tumor inducing (Ti) plasmid fromAgrobacterium tumefaciens (pTi15955) has been determined.
Plant-determined variation in the cardenolide content, thin-layer chromatography profiles, and emetic potency of monarch butterflies,Danaus plexippus reared on the milkweed,Asclepias eriocarpa in California.
Tuskes et al., Gainesville, United States. In J Chem Ecol, 1982
Forced-feeding of blue jays with powdered butterfly and plant material and with one of the constituent plant cardenolides, labriformin, established that theA.
Theoretical foundations for a quantitative approach to paleogenetics : Part II: Proteins.
Holmquist, Berkeley, United States. In J Mol Evol, 1972
The formulas developed in this paper are shown to be capable of detectinga priori, and with statistical significance, the nonrandomness that is known from experiment to exist in theA fibrinopeptides of ox, reindeer, sheep, and goat; the formulas also show, with statistical significance, that the assumption of a single ancestral DNA does not suffice to explain the known number of amino acid differences which occur between pairs of these fibrinopeptides.More explicitly, the following problems are solved: 1.
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