Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Brittany E. Sandoval"'
Autor:
Aaron A. Burkey, Neda Ghousifam, Alexander V. Hillsley, Zachary W. Brotherton, Mahboobeh Rezaeeyazdi, Taylor A. Hatridge, Dale T. Harris, William W. Sprague, Brittany E. Sandoval, Adrianne M. Rosales, Marissa Nichole Rylander, Nathaniel A. Lynd
Publikováno v:
Biomacromolecules. 24:1475-1482
Autor:
Stephen S. Rich, Donna Neuberg, Michael H. Cho, Bing Yu, Matthew Leventhal, George T. O'Connor, Ani Manichaikul, Weiwei Shi, Lynette M. Sholl, Michael C. Honigberg, Abhishek Niroula, Benjamin L. Ebert, Joselyn Rojas-Quintero, R. Graham Barr, Matthew Moll, Stephanie J. London, L. Adrienne Cupples, Siddhartha Jaiswal, Elizabeth C. Oelsner, Brittany E Sandoval, Pradeep Natarajan, Brian E. Cade, Peter van Galen, Susan Redline, Yohannes Tesfaigzi, Christopher J. Gibson, Stephanie M. Gogarten, COPDGene Study Investigators, Deepti Jain, Adolfo Correa, Bruce D. Levy, Sina A. Gharib, Peter Miller, Kaushik Viswanathan, Caroline A. Owen, Edwin K. Silverman, Lillian Werner, Jerome I. Rotter, Dandi Qiao, Brian C. Miller, Adam S. Sperling, Leslie A. Lange, Alexander G. Bick, Marie McConkey, Vasan S. Ramachandran
Publikováno v:
Blood. 139:357-368
Chronic obstructive pulmonary disease (COPD) is associated with age and smoking, but other determinants of the disease are incompletely understood. Clonal hematopoiesis of indeterminate potential (CHIP) is a common, age-related state in which somatic
UBR5 Is a Hect E3 Ubiquitin Ligase That Regulates Chromatin Bound Nuclear Hormone Receptor Stability
Autor:
Jonathan M Tsai, Jacob D Aguirre, Jared Brown, Vivian Focht, Yen-Der Li, Georg Kempf, Lukas Kater, Pius Galli, Simone Cavadini, Brittany E Sandoval, Charles Zou, Justine Rutter, Katherine Donovan, Quinlan Sievers, Paul Park, Jevon A. Cutler, Charlie Hatton, Elizabeth Ener, Micah T Sperling, Mikolaj Slabicki, Peter G. Miller, Roger Belizaire, Adam S. Sperling, Scott A. Armstrong, Eric S. Fischer, Nicolas Thomä, Benjamin L. Ebert
Publikováno v:
Blood. 140:2968-2969
Autor:
Rebecca Georgakopoulou, Maria Gavriatopoulou, Nikolaos Kanellias, Brittany E Sandoval, Mehmet Kemal Samur, Christine Liacos, Nikhil C. Munshi, Efstathios Kastritis, Evangelos Terpos, Flora Zagouri, Meletios A. Dimopoulos, Evangelos Eleutherakis-Papaiakovou, Adam S. Sperling, Ioannis Ntanasis-Stathopoulos, Magdalini Migkou, Despina Fotiou
Publikováno v:
Blood. 136:8-8
Introduction: An increased inherited risk for the development of plasma cell dyscrasias (PCDs) has long been suspected, however to date, only a limited number of potential genomic risk loci have been described. To characterize the inherited risk and