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Showing results for code wilson
Search for Codie Wilson instead (3 results)
A genetic study of Wilson's disease in the United Kingdom.
Coffey AJ, Durkie M, Hague S, McLay K, Emmerson J, Lo C, Klaffke S, Joyce CJ, Dhawan A, Hadzic N, Mieli-Vergani G, Kirk R, Elizabeth Allen K, Nicholl D, Wong S, Griffiths W, Smithson S, Giffin N, Taha A, Connolly S, Gillett GT, Tanner S, Bonham J, Sharrack B, Palotie A, Rattray M, Dalton A, Bandmann O. Coffey AJ, et al. Brain. 2013 May;136(Pt 5):1476-87. doi: 10.1093/brain/awt035. Epub 2013 Mar 21. Brain. 2013. PMID: 23518715 Free PMC article.
The likelihood of mutations in genes other than ATP7B causing a Wilson's disease phenotype is therefore very low. We report the first cases with Wilson's disease due to segmental uniparental isodisomy as well as three patients with three ATP7B mutation …
The likelihood of mutations in genes other than ATP7B causing a Wilson's disease phenotype is therefore very low. We report th …
Archetypes and code biology.
Major JC. Major JC. Biosystems. 2021 Oct;208:104501. doi: 10.1016/j.biosystems.2021.104501. Epub 2021 Aug 6. Biosystems. 2021. PMID: 34364930 Review.
As a clinical psychologist, I observe stereotyped formulas of behavior in action every day in the consulting room, despite differences in age, race, or culture; they present themselves as codified rules or typical modes of behavior in archetypical situations. ...From the p …
As a clinical psychologist, I observe stereotyped formulas of behavior in action every day in the consulting room, despite difference …
WIlsON: Web-based Interactive Omics VisualizatioN.
Schultheis H, Kuenne C, Preussner J, Wiegandt R, Fust A, Bentsen M, Looso M. Schultheis H, et al. Bioinformatics. 2019 Mar 15;35(6):1055-1057. doi: 10.1093/bioinformatics/bty711. Bioinformatics. 2019. PMID: 30535135 Free PMC article.
AVAILABILITY AND IMPLEMENTATION: We implemented WIlsON in R with a focus on extensibility using the modular Shiny and Plotly frameworks. A demo of the interactive workbench without limitations may be accessed at http://loosolab.mpi-bn.mpg.de. A standalone Docker container …
AVAILABILITY AND IMPLEMENTATION: We implemented WIlsON in R with a focus on extensibility using the modular Shiny and Plotly framewor …
[Wilson's disease].
Brůha R, Marecek Z, Martásek P, Nevsímalová S, Petrtýl J, Urbánek P, Kalistová H, Pospísilová L. Brůha R, et al. Cas Lek Cesk. 2009;148(11):544-8. Cas Lek Cesk. 2009. PMID: 20662462 Review. Czech.
Wilson's disease is an inherited disorder leading to accumulation of copper in tissues, mainly in the liver and brain. ...Up to now, more then 500 mutations causing Wilson's disease were described. The most frequent mutation in Central Europe is mutati
Wilson's disease is an inherited disorder leading to accumulation of copper in tissues, mainly in the liver and brain. ...Up t
ncRNAs in Type-2 Immunity.
Guidi R, Wedeles CJ, Wilson MS. Guidi R, et al. Noncoding RNA. 2020 Mar 6;6(1):10. doi: 10.3390/ncrna6010010. Noncoding RNA. 2020. PMID: 32155783 Free PMC article. Review.
As we slowly untangle and better appreciate these complex genetic and environment-influenced diseases, new therapeutically targetable pathways are emerging. Non-coding RNA species, which regulate epigenetic, transcriptional and translational responses are critical regulato …
As we slowly untangle and better appreciate these complex genetic and environment-influenced diseases, new therapeutically targetable pathwa …
Are the new genetic tools for diagnosis of Wilson disease helpful in clinical practice?
Espinós C, Ferenci P. Espinós C, et al. JHEP Rep. 2020 Apr 18;2(4):100114. doi: 10.1016/j.jhepr.2020.100114. eCollection 2020 Aug. JHEP Rep. 2020. PMID: 32613181 Free PMC article. Review.
If sequencing the entire ATP7B gene cannot identify 2 variants and the suspicion for Wilson disease is high, after reviewing the clinical data, WES (whole-exome sequencing) or WGS (whole-genome sequencing) could be applied. A workflow based on the type and number of …
If sequencing the entire ATP7B gene cannot identify 2 variants and the suspicion for Wilson disease is high, after reviewing the c
Gestational Hypoxia and Developmental Plasticity.
Ducsay CA, Goyal R, Pearce WJ, Wilson S, Hu XQ, Zhang L. Ducsay CA, et al. Physiol Rev. 2018 Jul 1;98(3):1241-1334. doi: 10.1152/physrev.00043.2017. Physiol Rev. 2018. PMID: 29717932 Free PMC article. Review.
Hypoxia during gestation impacts both the mother and fetal development through interactions with an individual's genetic traits acquired over multiple generations by natural selection and changes in gene expression patterns by altering the epigenetic code. Changes in the e …
Hypoxia during gestation impacts both the mother and fetal development through interactions with an individual's genetic traits acquired ove …
Cryo-electron microscopy of chromatin biology.
Wilson MD, Costa A. Wilson MD, et al. Acta Crystallogr D Struct Biol. 2017 Jun 1;73(Pt 6):541-548. doi: 10.1107/S2059798317004430. Epub 2017 Apr 20. Acta Crystallogr D Struct Biol. 2017. PMID: 28580916 Free PMC article. Review.
A tRNA- and Anticodon-Centric View of the Evolution of Aminoacyl-tRNA Synthetases, tRNAomes, and the Genetic Code.
Kim Y, Opron K, Burton ZF. Kim Y, et al. Life (Basel). 2019 May 4;9(2):37. doi: 10.3390/life9020037. Life (Basel). 2019. PMID: 31060233 Free PMC article. Review.
Pathways of standard genetic code evolution remain conserved and apparent, particularly upon analysis of aminoacyl-tRNA synthetase (aaRS) lineages. ...We posit that second- and third-position tRNA anticodon sequence preference (C>(U~G)>A) powerfully selected the sect …
Pathways of standard genetic code evolution remain conserved and apparent, particularly upon analysis of aminoacyl-tRNA synthetase (a …
A primacy code for odor identity.
Wilson CD, Serrano GO, Koulakov AA, Rinberg D. Wilson CD, et al. Nat Commun. 2017 Nov 14;8(1):1477. doi: 10.1038/s41467-017-01432-4. Nat Commun. 2017. PMID: 29133907 Free PMC article.
Here we propose that, in olfaction, a small and relatively stable set comprised of the earliest activated receptors forms a code for concentration-invariant odor identity. One prediction of this "primacy coding" scheme is that decisions based on odor identity can be …
Here we propose that, in olfaction, a small and relatively stable set comprised of the earliest activated receptors forms a code for …
956 results