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Angshumoy Roy

Showing results (31-40 of 92) with videos related to

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Human Molecular Genetics|October 19, 2006
Non-invasive genetic diagnosis of male infertility using spermatozoal RNA: KLHL10 mutations in oligozoospermic patients impair homodimerizationAlexander N Yatsenko, Angshumoy Roy, Ruihong Chen, et al.
Cancer Genetics|February 25, 2014
Cytogenetically cryptic and FISH-negative PML/RARA rearrangement in acute promyelocytic leukemia detected only by PCR: an exceedingly rare phenomenonElvia Martinez Blanco, Choladda V Curry, Xinyan Y Lu, et al.
Journal of Pediatric Hematology/Oncology|October 23, 2020
Adjuvant Maintenance Larotrectinib Therapy in 2 Children With NTRK Fusion-positive High-grade CancersMaria Carter-Febres, Netta Schneller, Douglas Fair, et al.
Molecular Human Reproduction|September 14, 2011
Association of mutations in the zona pellucida binding protein 1 (ZPBP1) gene with abnormal sperm head morphology in infertile menAlexander N Yatsenko, Derek S O'Neil, Angshumoy Roy, et al.
Genetics in Medicine Open|December 13, 2024
Combined bioinformatic and splicing analysis of likely benign intronic and synonymous variants reveals evidence for pathogenicityOwen R Hirschi, Stephanie A Felker, Surya P Rednam, et al.
Medrxiv : the Preprint Server for Health Sciences|November 14, 2023
Combined Bioinformatic and Splicing Analysis of Likely Benign Intronic and Synonymous Variants Reveals Evidence for PathogenicityOwen R Hirschi, Stephanie A Felker, Surya P Rednam, et al.
AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|June 12, 2018
Standardizing And Democratizing Access To Cancer Molecular Diagnostic Test Data From Patients To Drive Translational ResearchSubha Madhavan, Deborah Ritter, Christine Micheel, et al.
Molecular Genetics and Metabolism|April 12, 2011
Deoxyguanosine kinase deficiency presenting as neonatal hemochromatosisNeil A Hanchard, Oleg A Shchelochkov, Angshumoy Roy, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 9, 2017
ClinGen Cancer Somatic Working Group - standardizing and democratizing access to cancer molecular diagnostic data to drive translational researchSubha Madhavan, Deborah Ritter, Christine Micheel, et al.
The Journal of Molecular Diagnostics : JMD|April 25, 2025
Clinical Bioinformatician Body of Knowledge-Molecular Diagnostics Core: A Report of the Association for Molecular PathologyAnnette Leon, Eduardo Castro-Echeverry, Amber M Fussell, et al.
Pageof 10

Showing results (31-40 of 92) with videos related to

Sort By:
Pageof 10
Human Molecular Genetics|October 19, 2006
Non-invasive genetic diagnosis of male infertility using spermatozoal RNA: KLHL10 mutations in oligozoospermic patients impair homodimerizationAlexander N Yatsenko, Angshumoy Roy, Ruihong Chen, et al.
Cancer Genetics|February 25, 2014
Cytogenetically cryptic and FISH-negative PML/RARA rearrangement in acute promyelocytic leukemia detected only by PCR: an exceedingly rare phenomenonElvia Martinez Blanco, Choladda V Curry, Xinyan Y Lu, et al.
Journal of Pediatric Hematology/Oncology|October 23, 2020
Adjuvant Maintenance Larotrectinib Therapy in 2 Children With NTRK Fusion-positive High-grade CancersMaria Carter-Febres, Netta Schneller, Douglas Fair, et al.
Molecular Human Reproduction|September 14, 2011
Association of mutations in the zona pellucida binding protein 1 (ZPBP1) gene with abnormal sperm head morphology in infertile menAlexander N Yatsenko, Derek S O'Neil, Angshumoy Roy, et al.
Genetics in Medicine Open|December 13, 2024
Combined bioinformatic and splicing analysis of likely benign intronic and synonymous variants reveals evidence for pathogenicityOwen R Hirschi, Stephanie A Felker, Surya P Rednam, et al.
Medrxiv : the Preprint Server for Health Sciences|November 14, 2023
Combined Bioinformatic and Splicing Analysis of Likely Benign Intronic and Synonymous Variants Reveals Evidence for PathogenicityOwen R Hirschi, Stephanie A Felker, Surya P Rednam, et al.
AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|June 12, 2018
Standardizing And Democratizing Access To Cancer Molecular Diagnostic Test Data From Patients To Drive Translational ResearchSubha Madhavan, Deborah Ritter, Christine Micheel, et al.
Molecular Genetics and Metabolism|April 12, 2011
Deoxyguanosine kinase deficiency presenting as neonatal hemochromatosisNeil A Hanchard, Oleg A Shchelochkov, Angshumoy Roy, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 9, 2017
ClinGen Cancer Somatic Working Group - standardizing and democratizing access to cancer molecular diagnostic data to drive translational researchSubha Madhavan, Deborah Ritter, Christine Micheel, et al.
The Journal of Molecular Diagnostics : JMD|April 25, 2025
Clinical Bioinformatician Body of Knowledge-Molecular Diagnostics Core: A Report of the Association for Molecular PathologyAnnette Leon, Eduardo Castro-Echeverry, Amber M Fussell, et al.
Pageof 10