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J Cowley

Showing results (451-460 of 489) with videos related to

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American Journal of Human Genetics|November 7, 2020
RLIM Is a Candidate Dosage-Sensitive Gene for Individuals with Varying Duplications of Xq13, Intellectual Disability, and Distinct Facial FeaturesElizabeth E Palmer, Renee Carroll, Marie Shaw, et al.
Molecular Systems Biology|October 1, 2025
High-throughput 3D engineered paediatric tumour models for precision medicineMoonSun Jung, Valentina Poltavets, Joanna N Skhinas, et al.
Genome Medicine|September 6, 2013
Clinical and molecular characterization of HER2 amplified-pancreatic cancerAngela Chou, Nicola Waddell, Mark J Cowley, et al.
Nature Medicine|March 18, 2023
Diagnostic classification of childhood cancer using multiscale transcriptomicsFederico Comitani, Joshua O Nash, Sarah Cohen-Gogo, et al.
Oncogene|October 24, 2018
Deep multi-region whole-genome sequencing reveals heterogeneity and gene-by-environment interactions in treatment-naive, metastatic lung cancerTracy L Leong, Velimir Gayevskiy, Daniel P Steinfort, et al.
Nature Communications|February 25, 2016
Mutation allele burden remains unchanged in chronic myelomonocytic leukaemia responding to hypomethylating agentsJane Merlevede, Nathalie Droin, Tingting Qin, et al.
Plos Biology|January 10, 2013
ELF5 suppresses estrogen sensitivity and underpins the acquisition of antiestrogen resistance in luminal breast cancerMaria Kalyuga, David Gallego-Ortega, Heather J Lee, et al.
Parkinsonism & Related Disorders|May 21, 2024
Genome sequencing reanalysis increases the diagnostic yield in dystoniaAvi Fellner, Gurusidheshwar M Wali, Neil Mahant, et al.
European Journal of Human Genetics : EJHG|August 15, 2022
Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysisLisa J Ewans, Andre E Minoche, Deborah Schofield, et al.
Plos One|November 20, 2013
Somatic point mutation calling in low cellularity tumorsKarin S Kassahn, Oliver Holmes, Katia Nones, et al.
Pageof 49

Showing results (451-460 of 489) with videos related to

Sort By:
Pageof 49
American Journal of Human Genetics|November 7, 2020
RLIM Is a Candidate Dosage-Sensitive Gene for Individuals with Varying Duplications of Xq13, Intellectual Disability, and Distinct Facial FeaturesElizabeth E Palmer, Renee Carroll, Marie Shaw, et al.
Molecular Systems Biology|October 1, 2025
High-throughput 3D engineered paediatric tumour models for precision medicineMoonSun Jung, Valentina Poltavets, Joanna N Skhinas, et al.
Genome Medicine|September 6, 2013
Clinical and molecular characterization of HER2 amplified-pancreatic cancerAngela Chou, Nicola Waddell, Mark J Cowley, et al.
Nature Medicine|March 18, 2023
Diagnostic classification of childhood cancer using multiscale transcriptomicsFederico Comitani, Joshua O Nash, Sarah Cohen-Gogo, et al.
Oncogene|October 24, 2018
Deep multi-region whole-genome sequencing reveals heterogeneity and gene-by-environment interactions in treatment-naive, metastatic lung cancerTracy L Leong, Velimir Gayevskiy, Daniel P Steinfort, et al.
Nature Communications|February 25, 2016
Mutation allele burden remains unchanged in chronic myelomonocytic leukaemia responding to hypomethylating agentsJane Merlevede, Nathalie Droin, Tingting Qin, et al.
Plos Biology|January 10, 2013
ELF5 suppresses estrogen sensitivity and underpins the acquisition of antiestrogen resistance in luminal breast cancerMaria Kalyuga, David Gallego-Ortega, Heather J Lee, et al.
Parkinsonism & Related Disorders|May 21, 2024
Genome sequencing reanalysis increases the diagnostic yield in dystoniaAvi Fellner, Gurusidheshwar M Wali, Neil Mahant, et al.
European Journal of Human Genetics : EJHG|August 15, 2022
Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysisLisa J Ewans, Andre E Minoche, Deborah Schofield, et al.
Plos One|November 20, 2013
Somatic point mutation calling in low cellularity tumorsKarin S Kassahn, Oliver Holmes, Katia Nones, et al.
Pageof 49