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

Ankyrin repeat and SAM domain containing 1

Odin, ANKS1A
Top mentioned proteins: PTB, Epidermal Growth Factor, EphA2, AGE, Eph
Papers on Odin
Peptide Fragments of Odin-Sam1: Conformational Analysis and Interaction Studies with EphA2-Sam.
Leone et al., Napoli, Italy. In Chembiochem, Aug 2015
Odin is a protein belonging to the ANKS family, and has two tandem Sam domains.
In Vivo Expression of the PTB-deleted Odin Mutant Results in Hydrocephalus.
Park et al., Seoul, South Korea. In Mol Cells, May 2015
Odin has been implicated in the downstream signaling pathway of receptor tyrosine kinases, such as the epidermal growth factor and Eph receptors.
Rezolsta® (Darunavir/Cobicistat): First Boosted Protease Inhibitor Co-formulated with Cobicistat.
Molt├│ et al., Barcelona, Spain. In Aids Rev, Apr 2015
Data from the single-arm, open-label, phase III GS-US-216-130 trial showed virological efficacy rates comparable to those from ARTEMIS and ODIN.
Detecting differential peaks in ChIP-seq signals with ODIN.
Costa et al., Recife, Brazil. In Bioinformatics, 2015
RESULTS: We propose an One-stage DIffereNtial peak caller (ODIN); an Hidden Markov Model-based approach to detect and analyze differential peaks (DPs) in pairs of ChIP-seq data.
ANKS1B Interacts with the Cerebral Cavernous Malformation Protein-1 and Controls Endothelial Permeability but Not Sprouting Angiogenesis.
Fischer et al., Heidelberg, Germany. In Plos One, 2014
Silencing of ANKS1B or the related gene ANKS1A in primary human endothelial cells had no significant effects on cellular proliferation, migration and sprouting angiogenesis.
Subgroup analysis of virological response rates with once- and twice-daily darunavir/ritonavir in treatment-experienced patients without darunavir resistance-associated mutations in the ODIN trial.
Tomaka et al., Fort Lauderdale, United States. In Hiv Med, 2013
BACKGROUND: ODIN (once-daily darunavir in treatment-experienced patients) was a 48-week, phase III, randomized, open-label trial comparing once-daily (qd) darunavir/ritonavir (DRV/r) 800/100 mg with twice-daily (bid) DRV/r 600/100 mg, both with an optimized background regimen [OBR; at least two nucleoside reverse transcriptase inhibitors (NRTIs)], in treatment-experienced, HIV-1-infected adults with no DRV resistance-associated mutations (RAMs) at screening.
Prognostic implications of genetic variants in advanced non-small cell lung cancer: a genome-wide association study.
Lee et al., South Korea. In Carcinogenesis, 2013
These SNPs were located in the genomic regions of the FAM154A, ANKS1A, DLST, THSD7B, NCOA2, CDH8, SLC35D2, NALCN and EGF genes.
Heterotypic Sam-Sam association between Odin-Sam1 and Arap3-Sam: binding affinity and structural insights.
Leone et al., Napoli, Italy. In Chembiochem, 2013
Recently, we reported a novel interaction between the first Sam domain of Odin (Odin-Sam1), a protein belonging to the ANKS (ANKyrin repeat and Sam domain containing) family, and EphA2-Sam.
Odin (ANKS1A) modulates EGF receptor recycling and stability.
Moran et al., Toronto, Canada. In Plos One, 2012
The ANKS1A gene product, also known as Odin, was first identified as a tyrosine-phosphorylated component of the epidermal growth factor receptor network.
Virological analysis of once-daily and twice-daily darunavir/ritonavir in the ODIN trial of treatment-experienced patients.
Picchio et al., Beerse, Belgium. In Antivir Ther, 2012
BACKGROUND: The aim of this analysis was to characterize viral resistance in the Phase III, randomized ODIN trial, which demonstrated non-inferiority of once-daily darunavir/ritonavir (DRV/r) 800/100 mg to DRV/r 600/100 mg twice daily, each combined with an optimized background regimen in treatment-experienced patients with no DRV resistance-associated mutations (RAMs) at screening.
Solution structure of the first Sam domain of Odin and binding studies with the EphA2 receptor.
Leone et al., Napoli, Italy. In Biochemistry, 2012
Sam (sterile alpha motif) domains of Odin, a member of the ANKS (ankyrin repeat and sterile alpha motif domain-containing) family of proteins, are important for the regulation of EphA2 endocytosis.
RINL, guanine nucleotide exchange factor Rab5-subfamily, is involved in the EphA8-degradation pathway with odin.
Katada et al., Tokyo, Japan. In Plos One, 2011
RINL, as a GEF for Rab5 subfamily, is implicated in the EphA8-degradation pathway via its interaction with odin.
A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.
Montgomery et al., Saint Louis, United States. In Biol Psychiatry, 2011
Convergent findings for quantitative consumption and diagnostic and quantitative dependence measures suggest possible roles for a transmembrane protein gene (TMEM108) and for ANKS1A.
Week 48 analysis of once-daily vs. twice-daily darunavir/ritonavir in treatment-experienced HIV-1-infected patients.
Tomaka et al., Buenos Aires, Argentina. In Aids, 2011
OBJECTIVE: ODIN (Once-daily Darunavir In treatment-experieNced patients) was a phase III, 48-week, open-label study comparing once-daily vs. twice-daily darunavir/ritonavir (DRV/r) in treatment-experienced patients with no DRV resistance-associated mutations (RAMs) at screening.
The interactome of a PTB domain-containing adapter protein, Odin, revealed by SILAC.
Pandey et al., Baltimore, United States. In J Proteomics, 2011
We have previously identified Odin (also known as ankyrin repeat and sterile alpha motif domain-containing 1A; gene symbol ANKS1A) as a negative regulator of growth factor signaling; however, the mechanisms through which Odin regulates these pathways remain to be elucidated.
The SAM domains of Anks family proteins are critically involved in modulating the degradation of EphA receptors.
Park et al., Seoul, South Korea. In Mol Cell Biol, 2010
Data suggest that Odin levels play a critical role in regulating the stability of EphA2 and A8 in response to ligand stimulation and by modulating the ubiquitination process.
Trait-stratified genome-wide association study identifies novel and diverse genetic associations with serologic and cytokine phenotypes in systemic lupus erythematosus.
Niewold et al., Chicago, United States. In Arthritis Res Ther, 2009
The seven loci were: leucine-rich repeat containing 20 (LRRC20); protein phosphatase 1 H (PPM1H); lysophosphatidic acid receptor 1 (LPAR1); ankyrin repeat and sterile alpha motif domain 1A (ANKS1A); protein tyrosine phosphatase, receptor type M (PTPRM); ephrin A5 (EFNA5); and V-set and immunoglobulin domain containing 2 (VSIG2).
Mouse embryonic fibroblasts derived from Odin deficient mice display a hyperproliiferative phenotype.
Mann et al., Baltimore, United States. In Dna Res, 2004
Odin expression in mice is not essential for any major developmental pathway; it could play a significant functional role to negatively regulate growth factor receptor signaling pathways. [Odin]
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