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David R Bentley

Showing results (11-20 of 46) with videos related to

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Genome Research|May 9, 2002
Transcriptional regulation of the stem cell leukemia gene (SCL)--comparative analysis of five vertebrate SCL lociBerthold Göttgens, Linda M Barton, Michael A Chapman, et al.
Genome Biology|December 21, 2019
Paragraph: a graph-based structural variant genotyper for short-read sequence dataSai Chen, Peter Krusche, Egor Dolzhenko, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 24, 2012
The gene involved in X-linked agammaglobulinaemia is a member of the Src family of protein-tyrosine kinases. 1993David Vetrie, Igor Vořechovský, Paschalis Sideras, et al.
Epilepsy Research|June 11, 2011
Q8IYL2 is a candidate gene for the familial epilepsy syndrome of Partial Epilepsy with Pericentral Spikes (PEPS)Guy D Leschziner, Alison J Coffey, Toby Andrew, et al.
Cell Genomics|February 23, 2023
Reactive gene curation to support interpretation and reporting of a clinical genome test for rare disease: Experience from over 1,000 casesAmanda R Clause, Julie P Taylor, Revathi Rajkumar, et al.
Pharmacogenomics|December 19, 2007
The association between polymorphisms in RLIP76 and drug response in epilepsyGuy D Leschziner, Andrea L Jorgensen, Toby Andrew, et al.
American Journal of Human Genetics|March 5, 2005
A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphismsMarcos M Miretti, Emily C Walsh, Xiayi Ke, et al.
The Lancet. Neurology|July 22, 2006
Clinical factors and ABCB1 polymorphisms in prediction of antiepileptic drug response: a prospective cohort studyGuy Leschziner, Andrea L Jorgensen, Toby Andrew, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 19, 2020
Spinal muscular atrophy diagnosis and carrier screening from genome sequencing dataXiao Chen, Alba Sanchis-Juan, Courtney E French, et al.
Genome Research|December 2, 2016
A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigreeMichael A Eberle, Epameinondas Fritzilas, Peter Krusche, et al.
Pageof 5

Showing results (11-20 of 46) with videos related to

Sort By:
Pageof 5
Genome Research|May 9, 2002
Transcriptional regulation of the stem cell leukemia gene (SCL)--comparative analysis of five vertebrate SCL lociBerthold Göttgens, Linda M Barton, Michael A Chapman, et al.
Genome Biology|December 21, 2019
Paragraph: a graph-based structural variant genotyper for short-read sequence dataSai Chen, Peter Krusche, Egor Dolzhenko, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 24, 2012
The gene involved in X-linked agammaglobulinaemia is a member of the Src family of protein-tyrosine kinases. 1993David Vetrie, Igor Vořechovský, Paschalis Sideras, et al.
Epilepsy Research|June 11, 2011
Q8IYL2 is a candidate gene for the familial epilepsy syndrome of Partial Epilepsy with Pericentral Spikes (PEPS)Guy D Leschziner, Alison J Coffey, Toby Andrew, et al.
Cell Genomics|February 23, 2023
Reactive gene curation to support interpretation and reporting of a clinical genome test for rare disease: Experience from over 1,000 casesAmanda R Clause, Julie P Taylor, Revathi Rajkumar, et al.
Pharmacogenomics|December 19, 2007
The association between polymorphisms in RLIP76 and drug response in epilepsyGuy D Leschziner, Andrea L Jorgensen, Toby Andrew, et al.
American Journal of Human Genetics|March 5, 2005
A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphismsMarcos M Miretti, Emily C Walsh, Xiayi Ke, et al.
The Lancet. Neurology|July 22, 2006
Clinical factors and ABCB1 polymorphisms in prediction of antiepileptic drug response: a prospective cohort studyGuy Leschziner, Andrea L Jorgensen, Toby Andrew, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 19, 2020
Spinal muscular atrophy diagnosis and carrier screening from genome sequencing dataXiao Chen, Alba Sanchis-Juan, Courtney E French, et al.
Genome Research|December 2, 2016
A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigreeMichael A Eberle, Epameinondas Fritzilas, Peter Krusche, et al.
Pageof 5