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Rosemary Burgess

Showing results (1-10 of 27) with videos related to

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Genetics|January 18, 2005
The WD40 repeat protein fritz links cytoskeletal planar polarity to frizzled subcellular localization in the Drosophila epidermisSimon Collier, Haeryun Lee, Rosemary Burgess, et al.
Genome Medicine|June 10, 2017
brain-coX: investigating and visualising gene co-expression in seven human brain transcriptomic datasetsSaskia Freytag, Rosemary Burgess, Karen L Oliver, et al.
The Journal of Biological Chemistry|February 22, 2005
EphB receptor-binding peptides identified by phage display enable design of an antagonist with ephrin-like affinityMitchell Koolpe, Rosemary Burgess, Monique Dail, et al.
Epilepsia|January 14, 2017
De novo SCN1A pathogenic variants in the GEFS+ spectrum: Not always a familial syndromeKenneth A Myers, Rosemary Burgess, Zaid Afawi, et al.
Epilepsia|January 19, 2017
Frequency of CNKSR2 mutation in the X-linked epilepsy-aphasia spectrumJohn A Damiano, Rosemary Burgess, Sara Kivity, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|December 21, 2017
Sensitive quantitative detection of somatic mosaic mutation in "double cortex" syndromeJohn A Damiano, Hongdo Do, Ezgi Ozturk, et al.
Radiology|June 30, 2016
Periventricular Nodular Heterotopia: Detection of Abnormal Microanatomic Fiber Structures with Whole-Brain Diffusion MR Imaging TractographyShawna Farquharson, J-Donald Tournier, Fernando Calamante, et al.
Investigative Ophthalmology & Visual Science|February 19, 2011
Functional characterization of bestrophin-1 missense mutations associated with autosomal recessive bestrophinopathyAlice E Davidson, Ian D Millar, Rosemary Burgess-Mullan, et al.
Journal of Paediatrics and Child Health|July 20, 2024
Scurvy and vitamin C deficiency in an Australian tertiary children's hospitalCarolyn van Heerden, Daryl R Cheng, Sarah McNab, et al.
Molecular Vision|January 5, 2011
A synonymous codon variant in two patients with autosomal recessive bestrophinopathy alters in vitro splicing of BEST1Alice E Davidson, Panagiotis I Sergouniotis, Rosemary Burgess-Mullan, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Genetics|January 18, 2005
The WD40 repeat protein fritz links cytoskeletal planar polarity to frizzled subcellular localization in the Drosophila epidermisSimon Collier, Haeryun Lee, Rosemary Burgess, et al.
Genome Medicine|June 10, 2017
brain-coX: investigating and visualising gene co-expression in seven human brain transcriptomic datasetsSaskia Freytag, Rosemary Burgess, Karen L Oliver, et al.
The Journal of Biological Chemistry|February 22, 2005
EphB receptor-binding peptides identified by phage display enable design of an antagonist with ephrin-like affinityMitchell Koolpe, Rosemary Burgess, Monique Dail, et al.
Epilepsia|January 14, 2017
De novo SCN1A pathogenic variants in the GEFS+ spectrum: Not always a familial syndromeKenneth A Myers, Rosemary Burgess, Zaid Afawi, et al.
Epilepsia|January 19, 2017
Frequency of CNKSR2 mutation in the X-linked epilepsy-aphasia spectrumJohn A Damiano, Rosemary Burgess, Sara Kivity, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|December 21, 2017
Sensitive quantitative detection of somatic mosaic mutation in "double cortex" syndromeJohn A Damiano, Hongdo Do, Ezgi Ozturk, et al.
Radiology|June 30, 2016
Periventricular Nodular Heterotopia: Detection of Abnormal Microanatomic Fiber Structures with Whole-Brain Diffusion MR Imaging TractographyShawna Farquharson, J-Donald Tournier, Fernando Calamante, et al.
Investigative Ophthalmology & Visual Science|February 19, 2011
Functional characterization of bestrophin-1 missense mutations associated with autosomal recessive bestrophinopathyAlice E Davidson, Ian D Millar, Rosemary Burgess-Mullan, et al.
Journal of Paediatrics and Child Health|July 20, 2024
Scurvy and vitamin C deficiency in an Australian tertiary children's hospitalCarolyn van Heerden, Daryl R Cheng, Sarah McNab, et al.
Molecular Vision|January 5, 2011
A synonymous codon variant in two patients with autosomal recessive bestrophinopathy alters in vitro splicing of BEST1Alice E Davidson, Panagiotis I Sergouniotis, Rosemary Burgess-Mullan, et al.
Pageof 3