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Sebastian Lunke

Showing results (41-50 of 117) with videos related to

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Internal Medicine Journal|November 2, 2016
Examining the impact of regular aspirin use and PIK3CA mutations on survival in stage 2 colon cancerCaitlin Murphy, Natalie Turner, Hui-Li Wong, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 26, 2024
Gene selection for genomic newborn screening: Moving toward consensus?Lilian Downie, Sophie E Bouffler, David J Amor, et al.
The Journal of Molecular Diagnostics : JMD|December 20, 2025
Piloting an Interpretive External Quality Assurance Model for Genomic Testing for Childhood Syndromes and Intellectual DisabilityBen Lundie, Sze Yee Chai, Alicia B Byrne, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology|November 1, 2018
Pitfalls of immunotherapy: lessons from a patient with CTLA-4 haploinsufficiencyLeisa Rebecca Watson, Charlotte A Slade, Samar Ojaimi, et al.
The Journal of Biological Chemistry|February 22, 2012
Contraction-induced interleukin-6 gene transcription in skeletal muscle is regulated by c-Jun terminal kinase/activator protein-1Martin Whitham, M H Stanley Chan, Martin Pal, et al.
European Journal of Human Genetics : EJHG|June 1, 2019
Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive careZornitza Stark, Amy Nisselle, Belinda McClaren, et al.
Epilepsy Research|February 16, 2017
Real-world utility of whole exome sequencing with targeted gene analysis for focal epilepsyPiero Perucca, Ingrid E Scheffer, A Simon Harvey, et al.
European Journal of Human Genetics : EJHG|July 31, 2019
Early diagnosis of Pearson syndrome in neonatal intensive care following rapid mitochondrial genome sequencing in tandem with exome sequencingLauren S Akesson, Stefanie Eggers, Clare J Love, et al.
BMJ Paediatrics Open|April 12, 2018
A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohortLilian Downie, Jane L Halliday, Rachel A Burt, et al.
Cold Spring Harbor Molecular Case Studies|February 15, 2022
Ethylmalonic encephalopathy masquerading as meningococcemiaAri Horton, Kai Mun Hong, Dinusha Pandithan, et al.
Pageof 12

Showing results (41-50 of 117) with videos related to

Sort By:
Pageof 12
Internal Medicine Journal|November 2, 2016
Examining the impact of regular aspirin use and PIK3CA mutations on survival in stage 2 colon cancerCaitlin Murphy, Natalie Turner, Hui-Li Wong, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 26, 2024
Gene selection for genomic newborn screening: Moving toward consensus?Lilian Downie, Sophie E Bouffler, David J Amor, et al.
The Journal of Molecular Diagnostics : JMD|December 20, 2025
Piloting an Interpretive External Quality Assurance Model for Genomic Testing for Childhood Syndromes and Intellectual DisabilityBen Lundie, Sze Yee Chai, Alicia B Byrne, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology|November 1, 2018
Pitfalls of immunotherapy: lessons from a patient with CTLA-4 haploinsufficiencyLeisa Rebecca Watson, Charlotte A Slade, Samar Ojaimi, et al.
The Journal of Biological Chemistry|February 22, 2012
Contraction-induced interleukin-6 gene transcription in skeletal muscle is regulated by c-Jun terminal kinase/activator protein-1Martin Whitham, M H Stanley Chan, Martin Pal, et al.
European Journal of Human Genetics : EJHG|June 1, 2019
Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive careZornitza Stark, Amy Nisselle, Belinda McClaren, et al.
Epilepsy Research|February 16, 2017
Real-world utility of whole exome sequencing with targeted gene analysis for focal epilepsyPiero Perucca, Ingrid E Scheffer, A Simon Harvey, et al.
European Journal of Human Genetics : EJHG|July 31, 2019
Early diagnosis of Pearson syndrome in neonatal intensive care following rapid mitochondrial genome sequencing in tandem with exome sequencingLauren S Akesson, Stefanie Eggers, Clare J Love, et al.
BMJ Paediatrics Open|April 12, 2018
A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohortLilian Downie, Jane L Halliday, Rachel A Burt, et al.
Cold Spring Harbor Molecular Case Studies|February 15, 2022
Ethylmalonic encephalopathy masquerading as meningococcemiaAri Horton, Kai Mun Hong, Dinusha Pandithan, et al.
Pageof 12