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Sleep and diurnal alternative polyadenylation sites associated with human APA-linked brain disorders.
Flores CC, Pasetto NA, Wang H, Dimitrov AG, Davis JF, Jiang Z, Davis CJ, Gerstner JR. Flores CC, et al. Among authors: davis cj. Res Sq [Preprint]. 2024 Aug 8:rs.3.rs-4707772. doi: 10.21203/rs.3.rs-4707772/v1. Res Sq. 2024. Update in: NPJ Biol Timing Sleep. 2024;1(1):11. doi: 10.1038/s44323-024-00012-2 PMID: 39149473 Free PMC article. Updated. Preprint.
Identification of sleep and circadian alternative polyadenylation sites associated with APA-linked human brain disorders.
Flores CC, Pasetto NA, Wang H, Dimitrov A, Davis JF, Jiang Z, Davis CJ, Gerstner JR. Flores CC, et al. Among authors: davis cj. Res Sq [Preprint]. 2024 Jan 18:rs.3.rs-3867797. doi: 10.21203/rs.3.rs-3867797/v1. Res Sq. 2024. Update in: NPJ Biol Timing Sleep. 2024;1(1):11. doi: 10.1038/s44323-024-00012-2 PMID: 38313253 Free PMC article. Updated. Preprint.
Humanization of the mouse Tert gene reset telomeres to human length.
Cheng D, Zhang F, Porter KI, Wang S, Zhang H, Davis CJ, Robertson GP, Zhu J. Cheng D, et al. Among authors: davis cj. Res Sq [Preprint]. 2024 Jan 5:rs.3.rs-3617723. doi: 10.21203/rs.3.rs-3617723/v1. Res Sq. 2024. PMID: 38260456 Free PMC article. Preprint.
Erratum: Measurement of the 2νββ Decay Half-Life of ^{130}Te with CUORE [Phys. Rev. Lett. 126, 171801 (2021)].
Adams DQ, Alduino C, Alfonso K, Avignone FT, Azzolini O, Bari G, Bellini F, Benato G, Biassoni M, Branca A, Brofferio C, Bucci C, Camilleri J, Caminata A, Campani A, Canonica L, Cao XG, Capelli S, Cappelli L, Cardani L, Carniti P, Casali N, Chiesa D, Clemenza M, Copello S, Cosmelli C, Cremonesi O, Creswick RJ, D'Addabbo A, Dafinei I, Davis CJ, Dell'Oro S, Di Domizio S, Dompè V, Fang DQ, Fantini G, Faverzani M, Ferri E, Ferroni F, Fiorini E, Franceschi MA, Freedman SJ, Fu SH, Fujikawa BK, Giachero A, Gironi L, Giuliani A, Gorla P, Gotti C, Gutierrez TD, Han K, Heeger KM, Huang RG, Huang HZ, Johnston J, Keppel G, Kolomensky YG, Ligi C, Ma L, Ma YG, Marini L, Maruyama RH, Mayer D, Mei Y, Moggi N, Morganti S, Napolitano T, Nastasi M, Nikkel J, Nones C, Norman EB, Nucciotti A, Nutini I, O'Donnell T, Ouellet JL, Pagan S, Pagliarone CE, Pagnanini L, Pallavicini M, Pattavina L, Pavan M, Pessina G, Pettinacci V, Pira C, Pirro S, Pozzi S, Previtali E, Puiu A, Rosenfeld C, Rusconi C, Sakai M, Sangiorgio S, Schmidt B, Scielzo ND, Sharma V, Singh V, Sisti M, Speller D, Surukuchi PT, Taffarello L, Terranova F, Tomei C, Vetter KJ, Vignati M, Wagaarachchi SL, Wang BS, Welliver B, Wilson J,… See abstract for full author list ➔ Adams DQ, et al. Among authors: davis cj. Phys Rev Lett. 2023 Dec 15;131(24):249902. doi: 10.1103/PhysRevLett.131.249902. Phys Rev Lett. 2023. PMID: 38181163 Free article.
Dominant-negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome.
Pujol-Giménez J, Mirzaa G, Blue EE, Albano G, Miller DE, Allworth A, Bennett JT, Byers PH, Chanprasert S, Chen J, Doherty D, Folta AB, Gillentine MA, Glass I, Hing A, Horike-Pyne M, Leppig KA, Parhin A, Ranchalis J, Raskind WH, Rosenthal EA, Schwarze U, Sheppeard S, Strohbehn S, Sybert VP, Timms A, Wener M; University of Washington Center for Mendelian Genomics (UW-CMG)a, Undiagnosed Diseases Network (UDN); Bamshad MJ, Hisama FM, Jarvik GP, Dipple KM, Hediger MA, Stergachis AB. Pujol-Giménez J, et al. Ann Clin Transl Neurol. 2023 Jun;10(6):1046-1053. doi: 10.1002/acn3.51786. Epub 2023 May 16. Ann Clin Transl Neurol. 2023. PMID: 37194416 Free PMC article.
267 results