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Jacob C Ulirsch

Showing results (31-40 of 60) with videos related to

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Nature Communications|March 8, 2020
Prioritizing disease and trait causal variants at the TNFAIP3 locus using functional and genomic featuresJohn P Ray, Carl G de Boer, Charles P Fulco, et al.
Medrxiv : the Preprint Server for Health Sciences|March 22, 2023
RNA Polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiationDanya J Martell, Hope E Merens, Claudia Fiorini, et al.
Elife|May 10, 2019
Gene-centric functional dissection of human genetic variation uncovers regulators of hematopoiesisSatish K Nandakumar, Sean K McFarland, Laura M Mateyka, et al.
Developmental Cell|August 16, 2023
RNA polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiationDanya J Martell, Hope E Merens, Alexis Caulier, et al.
Nature Genetics|September 5, 2018
Detecting genome-wide directional effects of transcription factor binding on polygenic disease riskYakir A Reshef, Hilary K Finucane, David R Kelley, et al.
Cell|March 5, 2019
Lineage Tracing in Humans Enabled by Mitochondrial Mutations and Single-Cell GenomicsLeif S Ludwig, Caleb A Lareau, Jacob C Ulirsch, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2023
Rare penetrant mutations confer severe risk of common diseasesPetko Fiziev, Jeremy McRae, Jacob C Ulirsch, et al.
Pain|May 28, 2013
Polymorphisms in the glucocorticoid receptor co-chaperone FKBP5 predict persistent musculoskeletal pain after traumatic stress exposureAndrey V Bortsov, Jennifer E Smith, Luda Diatchenko, et al.
Cell|March 12, 2017
Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO MutationAh Ram Kim, Jacob C Ulirsch, Stephan Wilmes, et al.
Nature Genetics|January 22, 2020
Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translationAnindita Basak, Mathias Munschauer, Caleb A Lareau, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
Nature Communications|March 8, 2020
Prioritizing disease and trait causal variants at the TNFAIP3 locus using functional and genomic featuresJohn P Ray, Carl G de Boer, Charles P Fulco, et al.
Medrxiv : the Preprint Server for Health Sciences|March 22, 2023
RNA Polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiationDanya J Martell, Hope E Merens, Claudia Fiorini, et al.
Elife|May 10, 2019
Gene-centric functional dissection of human genetic variation uncovers regulators of hematopoiesisSatish K Nandakumar, Sean K McFarland, Laura M Mateyka, et al.
Developmental Cell|August 16, 2023
RNA polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiationDanya J Martell, Hope E Merens, Alexis Caulier, et al.
Nature Genetics|September 5, 2018
Detecting genome-wide directional effects of transcription factor binding on polygenic disease riskYakir A Reshef, Hilary K Finucane, David R Kelley, et al.
Cell|March 5, 2019
Lineage Tracing in Humans Enabled by Mitochondrial Mutations and Single-Cell GenomicsLeif S Ludwig, Caleb A Lareau, Jacob C Ulirsch, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2023
Rare penetrant mutations confer severe risk of common diseasesPetko Fiziev, Jeremy McRae, Jacob C Ulirsch, et al.
Pain|May 28, 2013
Polymorphisms in the glucocorticoid receptor co-chaperone FKBP5 predict persistent musculoskeletal pain after traumatic stress exposureAndrey V Bortsov, Jennifer E Smith, Luda Diatchenko, et al.
Cell|March 12, 2017
Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO MutationAh Ram Kim, Jacob C Ulirsch, Stephan Wilmes, et al.
Nature Genetics|January 22, 2020
Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translationAnindita Basak, Mathias Munschauer, Caleb A Lareau, et al.
Pageof 6