NETSeq reveals heterogeneous nucleotide incorporation by RNA polymerase I

por Clarke, Andrew M., Engel, Krysta L., Giles, Keith E., Petit, Chad M., Schneider, David A.
Publicado 2018

Direct Characterization of Transcription Elongation by RNA Polymerase I

por Ucuncuoglu, Suleyman, Engel, Krysta L., Purohit, Prashant K., Dunlap, David D., Schneider, David A., Finzi, Laura
Publicado 2016

LABRAT reveals association of alternative polyadenylation with transcript localization, RNA binding protein expression, transcription speed, and cancer survival

por Goering, Raeann, Engel, Krysta L., Gillen, Austin E., Fong, Nova, Bentley, David L., Taliaferro, J. Matthew
Publicado 2021

Analysis of subcellular transcriptomes by RNA proximity labeling with Halo-seq

por Engel, Krysta L, Lo, Hei-Yong G, Goering, Raeann, Li, Ying, Spitale, Robert C, Taliaferro, J Matthew
Publicado 2021

Rate of transcription elongation and sequence-specific pausing by RNA polymerase I directly influence rRNA processing

por Huffines, Abigail K., Engel, Krysta L., French, Sarah L., Zhang, Yinfeng, Viktorovskaya, Olga V., Schneider, David A.
Publicado 2022

PB1761: PRECLINICAL EVALUATION OF THE MENIN INHIBITOR ZIFTOMENIB IN PRIMARY AML SPECIMENS

por Stevens, Brett, Engel, Krysta, Gillen, Austin, Pei, Shanshan, Krug, Anna, Ransom, Monica, Staggs, Sarah, Burrows, Francis, Tomkinson, Blake, Kessler, Linda, Jordan, Craig, Smith, Clayton
Publicado 2023

Systematic mutagenesis of TFIIH subunit p52/Tfb2 identifies residues required for XPB/Ssl2 subunit function and genetic interactions with TFB6

por Bassett, Jacob, Rimel, Jenna K., Basu, Shrabani, Basnet, Pratik, Luo, Jie, Engel, Krysta L., Nagel, Michael, Woyciehowsky, Alexander, Ebmeier, Christopher C., Kaplan, Craig D., Taatjes, Dylan J., Ranish, Jeffrey A.
Publicado 2022

Targeting Acute Myeloid Leukemia Stem Cells Through Perturbation of Mitochondrial Calcium

por Sheth, Anagha Inguva, Engel, Krysta, Tolison, Hunter, Althoff, Mark J, Amaya, Maria L., Krug, Anna, Young, Tracy, Pei, Shanshan, Patel, Sweta B., Minhajuddin, Mohammad, Winters, Amanda, Miller, Regan, Shelton, Ian, St-Germain, Jonathan, Ling, Tianyi, Jones, Courtney, Raught, Brian, Gillen, Austin, Ransom, Monica, Staggs, Sarah, Smith, Clayton A., Pollyea, Daniel A., Stevens, Brett M., Jordan, Craig T.
Publicado 2023

Genomic diagnosis for children with intellectual disability and/or developmental delay

por Bowling, Kevin M., Thompson, Michelle L., Amaral, Michelle D., Finnila, Candice R., Hiatt, Susan M., Engel, Krysta L., Cochran, J. Nicholas, Brothers, Kyle B., East, Kelly M., Gray, David E., Kelley, Whitley V., Lamb, Neil E., Lose, Edward J., Rich, Carla A., Simmons, Shirley, Whittle, Jana S., Weaver, Benjamin T., Nesmith, Amy S., Myers, Richard M., Barsh, Gregory S., Bebin, E. Martina, Cooper, Gregory M.
Publicado 2017

De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder

por Snijders Blok, Lot, Hiatt, Susan M., Bowling, Kevin M., Prokop, Jeremy W., Engel, Krysta L., Cochran, J. Nicholas, Bebin, E. Martina, Bijlsma, Emilia K., Ruivenkamp, Claudia A. L., Terhal, Paulien, Simon, Marleen E. H., Smith, Rosemarie, Hurst, Jane A., McLaughlin, Heather, Person, Richard, Crunk, Amy, Wangler, Michael F., Streff, Haley, Symonds, Joseph D., Zuberi, Sameer M., Elliott, Katherine S., Sanders, Victoria R., Masunga, Abigail, Hopkin, Robert J., Dubbs, Holly A., Ortiz-Gonzalez, Xilma R., Pfundt, Rolph, Brunner, Han G., Fisher, Simon E., Kleefstra, Tjitske, Cooper, Gregory M.
Publicado 2018