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Martin Dugas

Showing results (191-200 of 336) with videos related to

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Genes, Chromosomes & Cancer|March 12, 2022
Design of a targeted next-generation DNA sequencing panel for pediatric T-cell lymphoblastic lymphoma to unravel biology and optimize treatmentCharlotte Ruether, Christian Wuensch, Gerrit Randau, et al.
JMIR Mental Health|December 1, 2020
Repeated Digitized Assessment of Risk and Symptom Profiles During Inpatient Treatment of Affective Disorder: Observational StudyMaike Frederike Richter, Michael Storck, Rogério Blitz, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 10, 2002
Acute myeloid leukemias with reciprocal rearrangements can be distinguished by specific gene expression profilesClaudia Schoch, Alexander Kohlmann, Susanne Schnittger, et al.
Andrology|December 16, 2021
Machine learning based prediction models in male reproductive health: Development of a proof-of-concept model for Klinefelter Syndrome in azoospermic patientsHenrike Krenz, Andrea Sansone, Michael Fujarski, et al.
Studies in Health Technology and Informatics|April 22, 2018
Compatibility Between Metadata Standards: Import Pipeline of CDISC ODM to the Samply.MDRAnn-Kristin Kock-Schoppenhauer, Hannes Ulrich, Stefanie Wagen-Zink, et al.
International Journal of Cancer|December 5, 2022
The CHK2 kinase is recurrently mutated and functionally impaired in the germline of pediatric cancer patientsRabea Wagener, Carolin Walter, Franziska Auer, et al.
Frontiers in Pediatrics|February 24, 2023
Resolving inherited and <i>de novo</i> germline predisposing sequence variants by means of whole exome trio analyses in childhood hematological malignanciesTriantafyllia Brozou, Layal Yasin, Danielle Brandes, et al.
Scientific Reports|June 18, 2021
Persistent symptoms and lab abnormalities in patients who recovered from COVID-19Julian Varghese, Sarah Sandmann, Kevin Ochs, et al.
Cancer Medicine|February 2, 2021
Mutation patterns in recurrent and/or metastatic oropharyngeal squamous cell carcinomas in relation to human papillomavirus statusHenrike Reder, Steffen Wagner, Nora Wuerdemann, et al.
The Journal of Molecular Diagnostics : JMD|March 1, 2011
Strategy for robust detection of insertions, deletions, and point mutations in CEBPA, a GC-rich content gene, using 454 next-generation deep-sequencing technologyVera Grossmann, Susanne Schnittger, Sonja Schindela, et al.
Pageof 34

Showing results (191-200 of 336) with videos related to

Sort By:
Pageof 34
Genes, Chromosomes & Cancer|March 12, 2022
Design of a targeted next-generation DNA sequencing panel for pediatric T-cell lymphoblastic lymphoma to unravel biology and optimize treatmentCharlotte Ruether, Christian Wuensch, Gerrit Randau, et al.
JMIR Mental Health|December 1, 2020
Repeated Digitized Assessment of Risk and Symptom Profiles During Inpatient Treatment of Affective Disorder: Observational StudyMaike Frederike Richter, Michael Storck, Rogério Blitz, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 10, 2002
Acute myeloid leukemias with reciprocal rearrangements can be distinguished by specific gene expression profilesClaudia Schoch, Alexander Kohlmann, Susanne Schnittger, et al.
Andrology|December 16, 2021
Machine learning based prediction models in male reproductive health: Development of a proof-of-concept model for Klinefelter Syndrome in azoospermic patientsHenrike Krenz, Andrea Sansone, Michael Fujarski, et al.
Studies in Health Technology and Informatics|April 22, 2018
Compatibility Between Metadata Standards: Import Pipeline of CDISC ODM to the Samply.MDRAnn-Kristin Kock-Schoppenhauer, Hannes Ulrich, Stefanie Wagen-Zink, et al.
International Journal of Cancer|December 5, 2022
The CHK2 kinase is recurrently mutated and functionally impaired in the germline of pediatric cancer patientsRabea Wagener, Carolin Walter, Franziska Auer, et al.
Frontiers in Pediatrics|February 24, 2023
Resolving inherited and <i>de novo</i> germline predisposing sequence variants by means of whole exome trio analyses in childhood hematological malignanciesTriantafyllia Brozou, Layal Yasin, Danielle Brandes, et al.
Scientific Reports|June 18, 2021
Persistent symptoms and lab abnormalities in patients who recovered from COVID-19Julian Varghese, Sarah Sandmann, Kevin Ochs, et al.
Cancer Medicine|February 2, 2021
Mutation patterns in recurrent and/or metastatic oropharyngeal squamous cell carcinomas in relation to human papillomavirus statusHenrike Reder, Steffen Wagner, Nora Wuerdemann, et al.
The Journal of Molecular Diagnostics : JMD|March 1, 2011
Strategy for robust detection of insertions, deletions, and point mutations in CEBPA, a GC-rich content gene, using 454 next-generation deep-sequencing technologyVera Grossmann, Susanne Schnittger, Sonja Schindela, et al.
Pageof 34