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Ankyrin repeat and sterile alpha motif domain containing 1B

This gene encodes a multi-domain protein that is predominantly expressed in brain and testis. This protein interacts with amyloid beta protein precursor (AbetaPP) and may have a role in normal brain development, and in the pathogenesis of Alzheimer's disease. Expression of this gene has been shown to be elevated in patients with pre-B cell acute lymphocytic leukemia associated with t(1;19) translocation. Alternatively spliced transcript variants encoding different isoforms (some with different subcellular localization, PMID:15004329) have been described for this gene. [provided by RefSeq, Aug 2011] (from NCBI)
Top mentioned proteins: ACID, CAN, mGluR, HAD, mGluR1
Papers using AIDA antibodies
Neuroprotective activity of selective mGlu1 and mGlu5 antagonists in vitro and in vivo.
Dryer Stuart E., In PLoS ONE, 2006
... Hyclone (USA); U0126 (MAPK-ERK kinase (MEK) inhibitor), DHPG (a group I mGlus agonist); and (RS)-1-aminoindan-1,5-dicarboxylic acid (AIDA, a group I mGlus antagonist) were from Tocris Biosciences (UK); Z-DEVD-FMK (an ...
Evaluation of an improved method for mass-rearing of thrips and a thrips parasitoid
Arimura Gen-ichiro et al., In Scientific Reports, 2000
Torenia fournieri (torenia) as a model plant for transgenic studies ...
Papers on AIDA
Pathological and bacteriological characterization of neonatal porcine diarrhoea of uncertain aetiology.
Jacobson et al., Uppsala, Sweden. In J Med Microbiol, 31 Aug 2015
Escherichia coli isolates (n = 276) were examined by PCR for virulence genes encoding LT, STa, STb, EAST1, VT2e, F4, F5, F6, F18, F41, AIDA-I, intimin, and for the genes aaiC and aggR.
AIDA: ab initio domain assembly for automated multi-domain protein structure prediction and domain-domain interaction prediction.
Godzik et al., San Diego, United States. In Bioinformatics, 01 Aug 2015
RESULTS: We have developed a fast docking algorithm ab initio domain assembly (AIDA) for assembling multi-domain protein structures, guided by the ab initio folding potential.
mGluR5 protect astrocytes from ischemic damage in postnatal CNS white matter.
Butt et al., Portsmouth, United Kingdom. In Cell Calcium, 30 Jul 2015
In addition, using Fluo-4 calcium imaging in isolated intact optic nerves, we show that the group I/II mGluR agonist ACPD and the specific group I mGluR agonist DHPG evoke glial Ca(2+) signals that were significantly inhibited by the group I mGluR antagonist AIDA.
ANKS1B Gene Product AIDA-1 Controls Hippocampal Synaptic Transmission by Regulating GluN2B Subunit Localization.
Jordan et al., New York City, United States. In J Neurosci, 17 Jul 2015
Here we report that the amyloid precursor protein intracellular domain associated-1 protein (AIDA-1), which associates with NMDARs and is encoded by ANKS1B, a gene recently linked to schizophrenia, regulates synaptic NMDAR subunit composition.
Quantitative mass spectrometry measurements reveal stoichiometry of principal postsynaptic density proteins.
Dosemeci et al., Gaithersburg, United States. In J Proteome Res, 05 Jul 2015
Average copy numbers for several proteins at the PSD were estimated for the first time, including those for AIDA-1, BRAGs, and densin.
High-throughput microfluidic method to study biofilm formation and host-pathogen interactions in pathogenic Escherichia coli.
Harel et al., Saint-Hyacinthe, Canada. In Appl Environ Microbiol, Apr 2015
As a proof of principle, the biofilm-forming ability of a diffusely adherent E. coli mutant strain lacking AIDA-I, a known mediator of attachment, was assessed in our models.
Improved cell surface display of Salmonella enterica serovar Enteritidis antigens in Escherichia coli.
Larsson et al., Stockholm, Sweden. In Microb Cell Fact, Dec 2014
We have previously reported the use of the β-autotransporter AIDA-I to express the Salmonella flagellar protein H:gm and the SE serotype-specific fimbrial protein SefA at the surface of E. coli as live bacterial vaccine vehicles.
Analysis of antibody aggregate content at extremely high concentrations using sedimentation velocity with a novel interference optics.
Krause et al., Potsdam, Germany. In Plos One, Dec 2014
With the development of our Advanced Interference Detection Array (AIDA), it has become possible to register interferograms of solutions as highly concentrated as 150 g/L.
STb and AIDA-I: the missing link?
Dubreuil, Saint-Hyacinthe, Canada. In Crit Rev Microbiol, 2010
With the recent recognition of a new adhesin, originally found in human E. coli isolates, named AIDA (adhesin involved in diffuse adherence) and its association with new E. coli pathotypes to which STb is linked, new light was shed on STb toxic potency.
The genetic background difference between diabetic patients with and without nephropathy in a Taiwanese population by linkage disequilibrium mapping using 382 autosomal STR markers.
Wu et al., Taipei, Taiwan. In Genet Test Mol Biomarkers, 2010
It is clear that some single-nucleotide polymorphisms and haplotypes of the EB-1 gene are associated with genetic difference between diabetic patients with and without nephropathy.
[Survey of recent clinical trials of the prevention and immunointervention of type 1 diabetes mellitus].
Ziegler et al., München, Germany. In Dtsch Med Wochenschr, 2010
(4) The AIDA study will test the beta-cell protective effect of interleukin-1-receptor antagonist Anakinra in 80 patients with T1DM, which has recently been shown to improve beta-cell function in patients with type 2 diabetes.
A nuclear localization signal at the SAM-SAM domain interface of AIDA-1 suggests a requirement for domain uncoupling prior to nuclear import.
Donaldson et al., Toronto, Canada. In J Mol Biol, 2009
The basic nuclear import signal for AIDA-1 is buried at the interface between the two sterile alpha motif domains.
EB1 recognizes the nucleotide state of tubulin in the microtubule lattice.
Howard et al., Dresden, Germany. In Plos One, 2008
EB1 recognizes the nucleotide state of tubulin in the microtubule lattice
The autodisplay story, from discovery to biotechnical and biomedical applications.
Meyer et al., Berlin, Germany. In Microbiol Mol Biol Rev, 2007
Various other autotransporter proteins have since been described, and the autodisplay system was developed on the basis of the natural Escherichia coli autotransporter protein AIDA-I (adhesin involved in diffuse adherence).
A beta-catenin-independent dorsalization pathway activated by Axin/JNK signaling and antagonized by aida.
Lin et al., Xiamen, China. In Dev Cell, 2007
A dorsalization pathway that is exerted by Axin/JNK signaling and its inhibitor Aida during vertebrate embryogenesis, is defined.
An influence of ligands of metabotropic glutamate receptor subtypes on parkinsonian-like symptoms and the striatopallidal pathway in rats.
Pilc et al., Kraków, Poland. In Amino Acids, 2007
Systemic or intrastriatal administration of group I mGluR antagonists (mGluR5 - MPEP, MTEP; mGluR1 - AIDA) was found to inhibit parkinsonian-like symptoms (catalepsy, muscle rigidity) in rats.
Self-associating autotransporters, SAATs: functional and structural similarities.
Sherlock et al., Denmark. In Int J Med Microbiol, 2006
In Escherichia coli, a subgroup of autotransporter proteins consists of the TibA adhesin/invasin associated with some enterotoxigenic E. coli, the AIDA adhesin from diarrhea-causing E. coli and finally, the Ag43 autoaggregation factor found in the majority of E. coli strains.
The effects of siRNA-mediated inhibition of E2A-PBX1 on EB-1 and Wnt16b expression in the 697 pre-B leukemia cell line.
Basso et al., Padova, Italy. In Haematologica, 2006
Targeted-E2A-PBX1 inhibition leads to reduced expression of the EB-1 and Wnt16b genes; aberrant expression of these genes may be a key step in leukemogenesis in t(1;19)-positive pre-B leukemia.
Extramedullary involvement at relapse in acute promyelocytic leukemia patients treated or not with all-trans retinoic acid: a report by the Gruppo Italiano Malattie Ematologiche dell'Adulto.
Mandelli et al., Bari, Italy. In J Clin Oncol, 2001
The studies investigated chemotherapy alone (LAP0389) versus RA plus chemotherapy (AIDA).
CD56 expression is an indicator of poor clinical outcome in patients with acute promyelocytic leukemia treated with simultaneous all-trans-retinoic acid and chemotherapy.
Lo Coco et al., Napoli, Italy. In J Clin Oncol, 2000
PATIENTS AND METHODS: Clinicobiologic presenting features and therapeutic results were analyzed in a series of 100 patients with genetically proven APL who were treated, according to the example of the Gruppo Italiano Malattie Ematologiche Maligne dell'Adulto multicenter trial, with ATRA plus idarubicin (AIDA) and for whom data on CD56 expression were available at diagnosis.
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