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S Fulton

Showing results (321-330 of 387) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|August 5, 2009
Acquired copy number alterations in adult acute myeloid leukemia genomesMatthew J Walter, Jacqueline E Payton, Rhonda E Ries, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2000
Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genesR E Ellsworth, D C Jamison, J W Touchman, et al.
Nature Genetics|December 14, 2011
Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromesTimothy A Graubert, Dong Shen, Li Ding, et al.
Nature Communications|September 19, 2018
Recurrent WNT pathway alterations are frequent in relapsed small cell lung cancerAlex H Wagner, Siddhartha Devarakonda, Zachary L Skidmore, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 30, 2021
Immunosuppression and outcomes in adult patients with de novo acute myeloid leukemia with normal karyotypesFrancesca Ferraro, Christopher A Miller, Keegan A Christensen, et al.
Nature Communications|May 8, 2021
Co-evolution of tumor and immune cells during progression of multiple myelomaRuiyang Liu, Qingsong Gao, Steven M Foltz, et al.
The Journal of Clinical Investigation|March 26, 2011
Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progressionLukas D Wartman, David E Larson, Zhifu Xiang, et al.
Nature Communications|September 6, 2018
The prognostic effects of somatic mutations in ER-positive breast cancerObi L Griffith, Nicholas C Spies, Meenakshi Anurag, et al.
Plos Genetics|February 6, 2014
Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS lociSusan K Service, Tanya M Teslovich, Christian Fuchsberger, et al.
Neuron|May 1, 2012
De novo gene disruptions in children on the autistic spectrumIvan Iossifov, Michael Ronemus, Dan Levy, et al.
Pageof 39

Showing results (321-330 of 387) with videos related to

Sort By:
Pageof 39
Proceedings of the National Academy of Sciences of the United States of America|August 5, 2009
Acquired copy number alterations in adult acute myeloid leukemia genomesMatthew J Walter, Jacqueline E Payton, Rhonda E Ries, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2000
Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genesR E Ellsworth, D C Jamison, J W Touchman, et al.
Nature Genetics|December 14, 2011
Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromesTimothy A Graubert, Dong Shen, Li Ding, et al.
Nature Communications|September 19, 2018
Recurrent WNT pathway alterations are frequent in relapsed small cell lung cancerAlex H Wagner, Siddhartha Devarakonda, Zachary L Skidmore, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 30, 2021
Immunosuppression and outcomes in adult patients with de novo acute myeloid leukemia with normal karyotypesFrancesca Ferraro, Christopher A Miller, Keegan A Christensen, et al.
Nature Communications|May 8, 2021
Co-evolution of tumor and immune cells during progression of multiple myelomaRuiyang Liu, Qingsong Gao, Steven M Foltz, et al.
The Journal of Clinical Investigation|March 26, 2011
Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progressionLukas D Wartman, David E Larson, Zhifu Xiang, et al.
Nature Communications|September 6, 2018
The prognostic effects of somatic mutations in ER-positive breast cancerObi L Griffith, Nicholas C Spies, Meenakshi Anurag, et al.
Plos Genetics|February 6, 2014
Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS lociSusan K Service, Tanya M Teslovich, Christian Fuchsberger, et al.
Neuron|May 1, 2012
De novo gene disruptions in children on the autistic spectrumIvan Iossifov, Michael Ronemus, Dan Levy, et al.
Pageof 39