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Sarah H Johnson

Showing results (31-40 of 62) with videos related to

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Cancer Genetics|April 10, 2020
Characterizing false-positive fluorescence in situ hybridization results by mate-pair sequencing in a patient with chronic myeloid leukemia and progression to myeloid blast crisisJaime L Lopes, Matthew Webley, Beth A Pitel, et al.
Leukemia & Lymphoma|December 7, 2019
Characterization of a cryptic <i>PML-RARA</i> fusion by mate-pair sequencing in a case of acute promyelocytic leukemia with a normal karyotype and negative <i>RARA</i> FISH studiesMatthew J Schultz, Patrick R Blackburn, Christopher H Cogbill, et al.
Genomics|November 4, 2020
Optimizing clinical cytology touch preparations for next generation sequencingStephen J Murphy, Faye R Harris, James B Smadbeck, et al.
Journal for Immunotherapy of Cancer|June 6, 2023
Dynamics and survival associations of T cell receptor clusters in patients with pleural mesothelioma treated with immunotherapyAakash P Desai, Farhad Kosari, Maria Disselhorst, et al.
Genes, Chromosomes & Cancer|May 5, 2018
Copy number variant analysis using genome-wide mate-pair sequencingJames B Smadbeck, Sarah H Johnson, Stephanie A Smoley, et al.
Mayo Clinic Proceedings|November 6, 2019
Integration of Comprehensive Genomic Analysis and Functional Screening of Affected Molecular Pathways to Inform Cancer TherapyGeorge Vasmatzis, Minetta C Liu, Sowjanya Reganti, et al.
Clinical Lung Cancer|December 25, 2018
Identification and Development of a Lung Adenocarcinoma PDX Model With STRN-ALK FusionHongzheng Ren, Xiaonan Hou, Patrick W Eiken, et al.
Cold Spring Harbor Molecular Case Studies|April 3, 2019
Detection of a cryptic <i>NUP214/ABL1</i> gene fusion by mate-pair sequencing (MPseq) in a newly diagnosed case of pediatric T-lymphoblastic leukemiaJess F Peterson, Beth A Pitel, Stephanie A Smoley, et al.
American Journal of Medical Genetics. Part A|January 18, 2024
Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld-Rieger SyndromeJoseph Farris, Cheryl Khanna, James B Smadbeck, et al.
Blood Cancer Journal|December 19, 2023
Unraveling the genomic underpinnings of unbalanced MYC break-apart FISH results using whole genome sequencing analysisMarie-France Gagnon, Alan R Penheiter, Faye Harris, et al.
Pageof 7

Showing results (31-40 of 62) with videos related to

Sort By:
Pageof 7
Cancer Genetics|April 10, 2020
Characterizing false-positive fluorescence in situ hybridization results by mate-pair sequencing in a patient with chronic myeloid leukemia and progression to myeloid blast crisisJaime L Lopes, Matthew Webley, Beth A Pitel, et al.
Leukemia & Lymphoma|December 7, 2019
Characterization of a cryptic <i>PML-RARA</i> fusion by mate-pair sequencing in a case of acute promyelocytic leukemia with a normal karyotype and negative <i>RARA</i> FISH studiesMatthew J Schultz, Patrick R Blackburn, Christopher H Cogbill, et al.
Genomics|November 4, 2020
Optimizing clinical cytology touch preparations for next generation sequencingStephen J Murphy, Faye R Harris, James B Smadbeck, et al.
Journal for Immunotherapy of Cancer|June 6, 2023
Dynamics and survival associations of T cell receptor clusters in patients with pleural mesothelioma treated with immunotherapyAakash P Desai, Farhad Kosari, Maria Disselhorst, et al.
Genes, Chromosomes & Cancer|May 5, 2018
Copy number variant analysis using genome-wide mate-pair sequencingJames B Smadbeck, Sarah H Johnson, Stephanie A Smoley, et al.
Mayo Clinic Proceedings|November 6, 2019
Integration of Comprehensive Genomic Analysis and Functional Screening of Affected Molecular Pathways to Inform Cancer TherapyGeorge Vasmatzis, Minetta C Liu, Sowjanya Reganti, et al.
Clinical Lung Cancer|December 25, 2018
Identification and Development of a Lung Adenocarcinoma PDX Model With STRN-ALK FusionHongzheng Ren, Xiaonan Hou, Patrick W Eiken, et al.
Cold Spring Harbor Molecular Case Studies|April 3, 2019
Detection of a cryptic <i>NUP214/ABL1</i> gene fusion by mate-pair sequencing (MPseq) in a newly diagnosed case of pediatric T-lymphoblastic leukemiaJess F Peterson, Beth A Pitel, Stephanie A Smoley, et al.
American Journal of Medical Genetics. Part A|January 18, 2024
Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld-Rieger SyndromeJoseph Farris, Cheryl Khanna, James B Smadbeck, et al.
Blood Cancer Journal|December 19, 2023
Unraveling the genomic underpinnings of unbalanced MYC break-apart FISH results using whole genome sequencing analysisMarie-France Gagnon, Alan R Penheiter, Faye Harris, et al.
Pageof 7