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NPJ Genomic Medicine|November 8, 2024
Coding and non-coding variants in the ciliopathy gene CFAP410 cause early-onset non-syndromic retinal degenerationRiccardo Sangermano, Priya Gupta, Cherrell Price, et al.Cell|February 27, 2016
EGLN1 Inhibition and Rerouting of α-Ketoglutarate Suffice for Remote Ischemic ProtectionBenjamin A Olenchock, Javid Moslehi, Alan H Baik, et al.Circulation|February 21, 2018
Metabolic Predictors of Incident Coronary Heart Disease in WomenNina P Paynter, Raji Balasubramanian, Franco Giulianini, et al.American Journal of Hematology|July 29, 2023
Performance of IPSS-M in patients with myelodysplastic syndrome after hypomethylating agent failureSamuel Urrutia, Kelly S Chien, Ziyi Li, et al.The International Journal on Drug Policy|December 15, 2022
Barriers and facilitators to implementing a Pharmacist, Physician, and Patient Navigator-Collaborative Care Model (PPP-CCM) to treat hepatitis C among people who inject drugsElizabeth J Austin, Alexander J Gojic, Elenore P Bhatraju, et al.Science Translational Medicine|September 22, 2020
Immune responses to SARS-CoV-2 infection in hospitalized pediatric and adult patientsCarl A Pierce, Paula Preston-Hurlburt, Yile Dai, et al.Nature Communications|July 26, 2016
An exome array study of the plasma metabolomeEugene P Rhee, Qiong Yang, Bing Yu, et al.Cancer|June 25, 2021
A phase 1b/2 study of azacitidine with PD-L1 antibody avelumab in relapsed/refractory acute myeloid leukemiaKapil Saxena, Shelley M Herbrich, Naveen Pemmaraju, et al.Leukemia|January 12, 2017
A CpG island methylator phenotype in acute myeloid leukemia independent of IDH mutations and associated with a favorable outcomeA D Kelly, H Kroeger, J Yamazaki, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2025
Identification of IDH3G, encoding the gamma subunit of mitochondrial isocitrate dehydrogenase, as a novel candidate gene for X-linked retinitis pigmentosaLorenzo Bianco, Julien Navarro, Christelle Michiels, et al.Pageof 99