Basal ganglia echogenicity in tauopathies

por Sadowski, Krzysztof, Serafin-Król, Małgorzata, Szlachta, Karol, Friedman, Andrzej
Publicado 2014

CNCC: an analysis tool to determine genome-wide DNA break end structure at single-nucleotide resolution

por Szlachta, Karol, Raimer, Heather M., Comeau, Laurey D., Wang, Yuh-Hwa
Publicado 2020

Brain tissue echogenicity—implications for substantia nigra studies in parkinsonian patients

por Sadowski, Krzysztof, Szlachta, Karol, Serafin-Król, Małgorzata, Gałązka-Friedman, Jolanta, Friedman, Andrzej
Publicado 2011

Genomic analysis of DNA repair genes and androgen signaling in prostate cancer

por Jividen, Kasey, Kedzierska, Katarzyna Z, Yang, Chun-Song, Szlachta, Karol, Ratan, Aakrosh, Paschal, Bryce M
Publicado 2018

Alternative DNA secondary structure formation affects RNA polymerase II promoter-proximal pausing in human

por Szlachta, Karol, Thys, Ryan G., Atkin, Naomi D., Pierce, Levi C. T., Bekiranov, Stefan, Wang, Yuh-Hwa
Publicado 2018

Topoisomerase II contributes to DNA secondary structure-mediated double-stranded breaks

por Szlachta, Karol, Manukyan, Arkadi, Raimer, Heather M, Singh, Sandeep, Salamon, Anita, Guo, Wenying, Lobachev, Kirill S, Wang, Yuh-Hwa
Publicado 2020

Complex DNA structures trigger copy number variation across the Plasmodium falciparum genome

por Huckaby, Adam C, Granum, Claire S, Carey, Maureen A, Szlachta, Karol, Al-Barghouthi, Basel, Wang, Yuh-Hwa, Guler, Jennifer L
Publicado 2019

Live cell imaging of low- and non-repetitive chromosome loci using CRISPR-Cas9

por Qin, Peiwu, Parlak, Mahmut, Kuscu, Cem, Bandaria, Jigar, Mir, Mustafa, Szlachta, Karol, Singh, Ritambhara, Darzacq, Xavier, Yildiz, Ahmet, Adli, Mazhar
Publicado 2017

Convergent evolution and multi-wave clonal invasion in H3 K27-altered diffuse midline gliomas treated with a PDGFR inhibitor

por Arunachalam, Sasi, Szlachta, Karol, Brady, Samuel W., Ma, Xiaotu, Ju, Bensheng, Shaner, Bridget, Mulder, Heather L., Easton, John, Raphael, Benjamin J., Myers, Matthew, Tinkle, Christopher, Allen, Sariah J., Orr, Brent A., Wetmore, Cynthia J., Baker, Suzanne J., Zhang, Jinghui
Publicado 2022

CRISPR knockout screening identifies combinatorial drug targets in pancreatic cancer and models cellular drug response

por Szlachta, Karol, Kuscu, Cem, Tufan, Turan, Adair, Sara J., Shang, Stephen, Michaels, Alex D., Mullen, Matthew G., Fischer, Natasha Lopes, Yang, Jiekun, Liu, Limin, Trivedi, Prasad, Stelow, Edward B., Stukenberg, P. Todd, Parsons, J. Thomas, Bauer, Todd W., Adli, Mazhar
Publicado 2018

SequencErr: measuring and suppressing sequencer errors in next-generation sequencing data

por Davis, Eric M., Sun, Yu, Liu, Yanling, Kolekar, Pandurang, Shao, Ying, Szlachta, Karol, Mulder, Heather L., Ren, Dongren, Rice, Stephen V., Wang, Zhaoming, Nakitandwe, Joy, Gout, Alexander M., Shaner, Bridget, Hall, Salina, Robison, Leslie L., Pounds, Stanley, Klco, Jeffery M., Easton, John, Ma, Xiaotu
Publicado 2021

CICERO: a versatile method for detecting complex and diverse driver fusions using cancer RNA sequencing data

por Tian, Liqing, Li, Yongjin, Edmonson, Michael N., Zhou, Xin, Newman, Scott, McLeod, Clay, Thrasher, Andrew, Liu, Yu, Tang, Bo, Rusch, Michael C., Easton, John, Ma, Jing, Davis, Eric, Trull, Austyn, Michael, J. Robert, Szlachta, Karol, Mullighan, Charles, Baker, Suzanne J., Downing, James R., Ellison, David W., Zhang, Jinghui
Publicado 2020

Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X

por Liu, Yu, Li, Chunliang, Shen, Shuhong, Chen, Xiaolong, Szlachta, Karol, Edmonson, Michael N., Shao, Ying, Ma, Xiaotu, Hyle, Judith, Wright, Shaela, Ju, Bensheng, Rusch, Michael C., Liu, Yanling, Li, Benshang, Macias, Michael, Tian, Liqing, Easton, John, Qian, Maoxiang, Yang, Jun J., Hu, Shaoyan, Look, A. Thomas, Zhang, Jinghui
Publicado 2020