Lentiviral and targeted cellular barcoding reveals ongoing clonal dynamics of cell lines in vitro and in vivo

por Porter, Shaina N, Baker, Lee C, Mittelman, David, Porteus, Matthew H
Publicado 2014

Therapeutic gene editing strategies using CRISPR-Cas9 for the β-hemoglobinopathies

por Papizan, James B., Porter, Shaina N., Sharma, Akshay, Pruett-Miller, Shondra M.
Publicado 2021

Attenuation of Zinc Finger Nuclease Toxicity by Small-Molecule Regulation of Protein Levels

por Pruett-Miller, Shondra M., Reading, David W., Porter, Shaina N., Porteus, Matthew H.
Publicado 2009

Fetal and neonatal hematopoietic progenitors are functionally and transcriptionally resistant to Flt3-ITD mutations

por Porter, Shaina N, Cluster, Andrew S, Yang, Wei, Busken, Kelsey A, Patel, Riddhi M, Ryoo, Jiyeon, Magee, Jeffrey A
Publicado 2016

Pten Cell Autonomously Modulates the Hematopoietic Stem Cell Response to Inflammatory Cytokines

por Porter, Shaina N., Cluster, Andrew S., Signer, Robert A.J., Voigtmann, Jenna, Monlish, Darlene A., Schuettpelz, Laura G., Magee, Jeffrey A.
Publicado 2016

DNA Barcoding in Nonhuman Primates Reveals Important Limitations in Retrovirus Integration Site Analysis

por Adair, Jennifer E., Enstrom, Mark R., Haworth, Kevin G., Schefter, Lauren E., Shahbazi, Reza, Humphrys, Daniel R., Porter, Shaina, Tam, Kenric, Porteus, Matthew H., Kiem, Hans-Peter
Publicado 2020

Activation of γ-globin gene expression by GATA1 and NF-Y in hereditary persistence of fetal hemoglobin

por Doerfler, Phillip A., Feng, Ruopeng, Li, Yichao, Palmer, Lance E., Porter, Shaina N., Bell, Henry W., Crossley, Merlin, Pruett-Miller, Shondra M., Cheng, Yong, Weiss, Mitchell J.
Publicado 2021

PAX3-FOXO1 dictates myogenic reprogramming and rhabdomyosarcoma identity in endothelial progenitors

por Searcy, Madeline B., Larsen, Randolph K., Stevens, Bradley T., Zhang, Yang, Jin, Hongjian, Drummond, Catherine J., Langdon, Casey G., Gadek, Katherine E., Vuong, Kyna, Reed, Kristin B., Garcia, Matthew R., Xu, Beisi, Kimbrough, Darden W., Adkins, Grace E., Djekidel, Nadhir, Porter, Shaina N., Schreiner, Patrick A., Pruett-Miller, Shondra M., Abraham, Brian J., Rehg, Jerold E., Hatley, Mark E.
Publicado 2023

Integrative network analysis reveals USP7 haploinsufficiency inhibits E-protein activity in pediatric T-lineage acute lymphoblastic leukemia (T-ALL)

por Shaw, Timothy I., Dong, Li, Tian, Liqing, Qian, Chenxi, Liu, Yu, Ju, Bensheng, High, Anthony, Kavdia, Kanisha, Pagala, Vishwajeeth R., Shaner, Bridget, Pei, Deqing, Easton, John, Janke, Laura J., Porter, Shaina N., Ma, Xiaotu, Cheng, Cheng, Pruett-Miller, Shondra M., Choi, John, Yu, Jiyang, Peng, Junmin, Gu, Wei, Look, A. Thomas, Downing, James R., Zhang, Jinghui
Publicado 2021

CCL22 mutations drive natural killer cell lymphoproliferative disease by deregulating microenvironmental crosstalk

por Baer, Constance, Kimura, Shunsuke, Rana, Mitra S., Kleist, Andrew B., Flerlage, Tim, Feith, David J., Chockley, Peter, Walter, Wencke, Meggendorfer, Manja, Olson, Thomas L., Cheon, HeeJin, Olson, Kristine C., Ratan, Aakrosh, Mueller, Martha-Lena, Foran, James M., Janke, Laura J., Qu, Chunxu, Porter, Shaina N., Pruett-Miller, Shondra M., Kalathur, Ravi C., Haferlach, Claudia, Kern, Wolfgang, Paietta, Elisabeth, Thomas, Paul G., Babu, M. Madan, Loughran, Thomas P., Iacobucci, Ilaria, Haferlach, Torsten, Mullighan, Charles G
Publicado 2022