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JMIR Research Protocols
|
September 6, 2022
Proactive, Recovery-Oriented Treatment Navigation to Engage Racially Diverse Veterans in Mental Healthcare (PARTNER-MH), a Peer-Led Patient Navigation Intervention for Racially and Ethnically Minoritized Veterans in Veterans Health Administration Mental Health Services: Protocol for a Mixed Methods Randomized Controlled Feasibility Study
Johanne Eliacin, Diana J Burgess, Angela L Rollins, et al.
Gut
|
September 10, 2016
Subclonal diversity arises early even in small colorectal tumours and contributes to differential growth fates
Chelsie K Sievers, Luli S Zou, Perry J Pickhardt, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 15, 2024
GABAergic/Glycinergic and Glutamatergic Neurons Mediate Distinct Neurodevelopmental Phenotypes of <i>STXBP1</i> Encephalopathy
Joo Hyun Kim, Wu Chen, Eugene S Chao, et al.
NPJ Precision Oncology
|
July 9, 2025
RAS pathway targeted therapy in patients with DICER1-associated sarcomas
Lindy Zhang, Paige H R Mallinger, Serena Zhou, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
March 9, 2026
Comprehensive Cytogenomic Profiling of T-Lymphoblastic Leukemia by Optical Genome Mapping, Karyotyping and Next Generation Sequencing
Guilin Tang, Alexandra Reynolds, Farhad Ravandi-Kashani, et al.
The Journal of Molecular Diagnostics : JMD
|
February 12, 2021
Clinical Utility of Targeted Next-Generation Sequencing Assay to Detect Copy Number Variants Associated with Myelodysplastic Syndrome in Myeloid Malignancies
Liqun Jiang, Aparna Pallavajjala, Jialing Huang, et al.
Genes
|
June 28, 2023
Complex/cryptic <i>EWSR1::FLI1/ERG</i> Gene Fusions and 1q Jumping Translocation in Pediatric Ewing Sarcomas
Ying S Zou, Laura Morsberger, Melanie Hardy, et al.
Blood Cancer Journal
|
May 3, 2024
A comprehensive approach to evaluate genetic abnormalities in multiple myeloma using optical genome mapping
Ying S Zou, Melanie Klausner, Jen Ghabrial, et al.
The Journal of Clinical Investigation
|
May 15, 2026
Simultaneous CRISPR/Cas9-induced double-strand breaks are lethal in models of pancreatic cancer
Selina Shiqing K Teh, Akhil Kotwal, Alexis Bennett, et al.
Plos One
|
June 21, 2013
Progenitor cell line (hPheo1) derived from a human pheochromocytoma tumor
Hans K Ghayee, Vikash J Bhagwandin, Victor Stastny, et al.
Page
of 42
Search research articles
Search
Showing results (291-300 of 412) with videos related to
Sort By:
Page
of 42
JMIR Research Protocols
|
September 6, 2022
Proactive, Recovery-Oriented Treatment Navigation to Engage Racially Diverse Veterans in Mental Healthcare (PARTNER-MH), a Peer-Led Patient Navigation Intervention for Racially and Ethnically Minoritized Veterans in Veterans Health Administration Mental Health Services: Protocol for a Mixed Methods Randomized Controlled Feasibility Study
Johanne Eliacin, Diana J Burgess, Angela L Rollins, et al.
Gut
|
September 10, 2016
Subclonal diversity arises early even in small colorectal tumours and contributes to differential growth fates
Chelsie K Sievers, Luli S Zou, Perry J Pickhardt, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 15, 2024
GABAergic/Glycinergic and Glutamatergic Neurons Mediate Distinct Neurodevelopmental Phenotypes of <i>STXBP1</i> Encephalopathy
Joo Hyun Kim, Wu Chen, Eugene S Chao, et al.
NPJ Precision Oncology
|
July 9, 2025
RAS pathway targeted therapy in patients with DICER1-associated sarcomas
Lindy Zhang, Paige H R Mallinger, Serena Zhou, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
March 9, 2026
Comprehensive Cytogenomic Profiling of T-Lymphoblastic Leukemia by Optical Genome Mapping, Karyotyping and Next Generation Sequencing
Guilin Tang, Alexandra Reynolds, Farhad Ravandi-Kashani, et al.
The Journal of Molecular Diagnostics : JMD
|
February 12, 2021
Clinical Utility of Targeted Next-Generation Sequencing Assay to Detect Copy Number Variants Associated with Myelodysplastic Syndrome in Myeloid Malignancies
Liqun Jiang, Aparna Pallavajjala, Jialing Huang, et al.
Genes
|
June 28, 2023
Complex/cryptic <i>EWSR1::FLI1/ERG</i> Gene Fusions and 1q Jumping Translocation in Pediatric Ewing Sarcomas
Ying S Zou, Laura Morsberger, Melanie Hardy, et al.
Blood Cancer Journal
|
May 3, 2024
A comprehensive approach to evaluate genetic abnormalities in multiple myeloma using optical genome mapping
Ying S Zou, Melanie Klausner, Jen Ghabrial, et al.
The Journal of Clinical Investigation
|
May 15, 2026
Simultaneous CRISPR/Cas9-induced double-strand breaks are lethal in models of pancreatic cancer
Selina Shiqing K Teh, Akhil Kotwal, Alexis Bennett, et al.
Plos One
|
June 21, 2013
Progenitor cell line (hPheo1) derived from a human pheochromocytoma tumor
Hans K Ghayee, Vikash J Bhagwandin, Victor Stastny, et al.
Page
of 42