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Jessica Van Ziffle

Showing results (51-60 of 58) with videos related to

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Nature Communications|February 25, 2018
A recurrent kinase domain mutation in PRKCA defines chordoid glioma of the third ventricleBenjamin Goode, Gourish Mondal, Michael Hyun, et al.
NPJ Genomic Medicine|May 26, 2023
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse populationAnne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, et al.
Brain Pathology (Zurich, Switzerland)|October 15, 2019
Myxoid glioneuronal tumor, PDGFRA p.K385-mutant: clinical, radiologic, and histopathologic featuresCalixto-Hope G Lucas, Javier E Villanueva-Meyer, Nicholas Whipple, et al.
Brain Pathology (Zurich, Switzerland)|December 15, 2019
Clinicopathologic and molecular features of intracranial desmoplastic small round cell tumorsJulieann C Lee, Javier E Villanueva-Meyer, Sean P Ferris, et al.
Genetics in Medicine Open|August 23, 2024
The challenges and opportunities of offering and integrating training in clinical molecular genetics and clinical cytogenetics: A survey of LGG Fellowship Program DirectorsJoshua L Deignan, Vimla Aggarwal, Allen E Bale, et al.
Acta Neuropathologica|April 19, 2020
Pediatric bithalamic gliomas have a distinct epigenetic signature and frequent EGFR exon 20 insertions resulting in potential sensitivity to targeted kinase inhibitionGourish Mondal, Julieann C Lee, Ajay Ravindranathan, et al.
Neuro-Oncology|July 12, 2023
Novel SOX10 indel mutations drive schwannomas through impaired transactivation of myelination gene programsErik A Williams, Ajay Ravindranathan, Rohit Gupta, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 10, 2020
De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathyChiara Klöckner, Heinrich Sticht, Pia Zacher, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
Nature Communications|February 25, 2018
A recurrent kinase domain mutation in PRKCA defines chordoid glioma of the third ventricleBenjamin Goode, Gourish Mondal, Michael Hyun, et al.
NPJ Genomic Medicine|May 26, 2023
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse populationAnne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, et al.
Brain Pathology (Zurich, Switzerland)|October 15, 2019
Myxoid glioneuronal tumor, PDGFRA p.K385-mutant: clinical, radiologic, and histopathologic featuresCalixto-Hope G Lucas, Javier E Villanueva-Meyer, Nicholas Whipple, et al.
Brain Pathology (Zurich, Switzerland)|December 15, 2019
Clinicopathologic and molecular features of intracranial desmoplastic small round cell tumorsJulieann C Lee, Javier E Villanueva-Meyer, Sean P Ferris, et al.
Genetics in Medicine Open|August 23, 2024
The challenges and opportunities of offering and integrating training in clinical molecular genetics and clinical cytogenetics: A survey of LGG Fellowship Program DirectorsJoshua L Deignan, Vimla Aggarwal, Allen E Bale, et al.
Acta Neuropathologica|April 19, 2020
Pediatric bithalamic gliomas have a distinct epigenetic signature and frequent EGFR exon 20 insertions resulting in potential sensitivity to targeted kinase inhibitionGourish Mondal, Julieann C Lee, Ajay Ravindranathan, et al.
Neuro-Oncology|July 12, 2023
Novel SOX10 indel mutations drive schwannomas through impaired transactivation of myelination gene programsErik A Williams, Ajay Ravindranathan, Rohit Gupta, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 10, 2020
De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathyChiara Klöckner, Heinrich Sticht, Pia Zacher, et al.
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