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Arthritis & Rheumatology (Hoboken, N.J.)|August 21, 2014
Identification of a pathogenic variant in TREX1 in early-onset cerebral systemic lupus erythematosus by Whole-exome sequencingJulia I Ellyard, Rebekka Jerjen, Jaime L Martin, et al.Human Molecular Genetics|October 24, 2015
Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosisAdam P DeLuca, S Scott Whitmore, Jenna Barnes, et al.Nucleic Acids Research|January 31, 2019
ARGLU1 is a transcriptional coactivator and splicing regulator important for stress hormone signaling and developmentLilia Magomedova, Jens Tiefenbach, Emma Zilberman, et al.Journal of Medicinal Chemistry|April 26, 2021
Fragment-Based Design of a Potent MAT2a Inhibitor and in Vivo Evaluation in an MTAP Null Xenograft ModelClaudia De Fusco, Marianne Schimpl, Ulf Börjesson, et al.BMJ Open|March 11, 2026
NewbornsInSA multi-omic newborn screening: protocol for a prospective cohort studyLucy Anastasi, Ayesha Chowdhury, Alex Ashenden, et al.Bioorganic & Medicinal Chemistry|April 19, 2022
Identification and optimisation of a pyrimidopyridone series of IRAK4 inhibitorsIain A Cumming, Sébastien L Degorce, Anna Aagaard, et al.Annals of Oncology : Official Journal of the European Society for Medical Oncology|May 23, 2020
Collateral damage: the impact on outcomes from cancer surgery of the COVID-19 pandemicA Sud, M E Jones, J Broggio, et al.Blood|July 9, 2008
Interferon autoantibodies associated with AIRE deficiency decrease the expression of IFN-stimulated genesKai Kisand, Maire Link, Anette S B Wolff, et al.Journal of Medicinal Chemistry|May 2, 2012
Use of small-molecule crystal structures to address solubility in a novel series of G protein coupled receptor 119 agonists: optimization of a lead and in vivo evaluationJames S Scott, Alan M Birch, Katy J Brocklehurst, et al.NPJ Genomic Medicine|February 10, 2026
Semi-automated genomic newborn screening highlights complexities in reportingAyesha Chowdhury, Shashikanth Marri, Lucy Anastasi, et al.Pageof 203