Showing results (2041-2050 of 2,491) with videos related to
Sort By:
Pageof 250
Data in Brief|June 23, 2020
Data highlighting phenotypic diversity of urine-associated Escherichia coli isolatesAllison R Eberly, Connor J Beebout, Ching Man Carmen Tong, et al.Biorxiv : the Preprint Server for Biology|September 10, 2024
H3K27M diffuse midline glioma is homologous recombination defective and sensitized to radiotherapy and NK cell-mediated antitumor immunity by PARP inhibitionYupei Guo, Zian Li, Leslie A Parsels, et al.Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|January 3, 2025
Rates of PSMA PET Staging and Positivity in Newly Diagnosed Prostate Cancer in a National Health Care SystemSean R Miller, Rachel Tucker Gonzalez, William C Jackson, et al.Journal of Molecular Biology|December 4, 2019
Defining a Molecular Signature for Uropathogenic versus Urocolonizing Escherichia coli: The Status of the Field and New Clinical OpportunitiesAllison R Eberly, Connor J Beebout, Ching Man Carmen Tong, et al.Proceedings of the National Academy of Sciences of the United States of America|June 6, 2009
Dynamic histone H3 epigenome marking during the intraerythrocytic cycle of Plasmodium falciparumAdriana M Salcedo-Amaya, Marc A van Driel, Blaise T Alako, et al.Pharmacogenetics|October 23, 2001
The human pregnane X receptor: genomic structure and identification and functional characterization of natural allelic variantsJ Zhang, P Kuehl, E D Green, et al.Proceedings of the National Academy of Sciences of the United States of America|June 6, 2012
Specific inactivation of two immunomodulatory SIGLEC genes during human evolutionXiaoxia Wang, Nivedita Mitra, Ismael Secundino, et al.The Journal of Clinical Investigation|February 16, 2021
Lysophospholipid acylation modulates plasma membrane lipid organization and insulin sensitivity in skeletal musclePatrick J Ferrara, Xin Rong, J Alan Maschek, et al.American Journal of Medical Genetics|December 20, 2000
Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: identification of a BAC contig spanning the translocation breakpoint at 7q21W L Yan, X Y Guan, E D Green, et al.Human Molecular Genetics|June 9, 1998
Two frequent missense mutations in Pendred syndromeP Van Hauwe, L A Everett, P Coucke, et al.Pageof 250