Stephen C. Ekker, Ph.D.

Mayo Clinic, Rochester, MN, United States 
"Stephen Ekker"
Mean distance: 17.74 (cluster 11)


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Saulius Sumanas grad student 2000 UMN
Aidas Nasevicius grad student 2001 UMN
Eleanor Y. Chen grad student 2004 UMN
Ann E. Davidson grad student 2005 UMN
Hyon J. Kim grad student 2005 UMN
Kirk J. Wangensteen grad student 2007 UMN
Brent R. Bill grad student 2008 UMN
Andrew M. Petzold grad student 2010 UMN
Karl J. Clark post-doc 2007-2011 Mayo Clinic (Cell Biology Tree)
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Kar B, Castillo SR, Sabharwal A, et al. (2023) Mitochondrial Base Editing: Recent Advances towards Therapeutic Opportunities. International Journal of Molecular Sciences. 24
Sabharwal A, Wishman MD, Cervera RL, et al. (2022) Genetic therapy in a mitochondrial disease model suggests a critical role for liver dysfunction in mortality. Elife. 11
Ding Y, Lang D, Yan J, et al. (2022) A phenotype-based forward genetic screen identifies as a sick sinus syndrome gene. Elife. 11
Sabharwal A, Campbell JM, Schwab TL, et al. (2022) A Primer Genetic Toolkit for Exploring Mitochondrial Biology and Disease Using Zebrafish. Genes. 13
Liu F, Kambakam S, Almeida MP, et al. (2022) Cre/ regulated conditional rescue and inactivation with zebrafish UFlip alleles generated by CRISPR-Cas9 targeted integration. Elife. 11
Kar B, Sabharwal A, Restrepo-Castillo S, et al. (2022) An optimized FusX assembly-based technique to introduce mitochondrial TC-to-TT variations in human cell lines. Star Protocols. 3: 101288
Simone BW, Lee HB, Daby CL, et al. (2021) Chimeric RNA:DNA TracrRNA Improves Homology-Directed Repair and . The Crispr Journal
Sabharwal A, Kar B, Restrepo-Castillo S, et al. (2021) The FusX TALE Base Editor (FusXTBE) for Rapid Mitochondrial DNA Programming of Human Cells and Zebrafish Disease Models . The Crispr Journal. 4: 799-821
Welker JM, Wierson WA, Almeida MP, et al. (2021) GeneWeld: Efficient Targeted Integration Directed by Short Homology in Zebrafish. Bio-Protocol. 11: e4100
Saha K, Sontheimer EJ, Brooks PJ, et al. (2021) The NIH Somatic Cell Genome Editing program. Nature. 592: 195-204
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