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Emily C Oates

Showing results (1-10 of 26) with videos related to

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Communications Biology|May 27, 2026
Deep learning of 777 K bulk transcriptomes reveals human-mouse gene conservation beyond DNA sequence similarityZheng Su, Mingyan Fang, Andrei Smolnikov, et al.
Genome Biology|September 22, 2025
GeneRAIN: multifaceted representation of genes via deep learning of gene expression networksZheng Su, Mingyan Fang, Andrei Smolnikov, et al.
Briefings in Bioinformatics|February 6, 2025
Post-transcriptional regulation supports the homeostatic expression of mature RNAZheng Su, Mingyan Fang, Andrei Smolnikov, et al.
American Journal of Medical Genetics. Part A|February 22, 2013
Young Australian adults with NF1 have poor access to health care, high complication rates, and limited disease knowledgeEmily C Oates, Jonathan M Payne, Sheryl L Foster, et al.
American Journal of Medical Genetics. Part A|December 21, 2013
Longitudinal assessment of cognition and T2-hyperintensities in NF1: an 18-year studyJonathan M Payne, Tania Pickering, Melanie Porter, et al.
Journal of Molecular Medicine (Berlin, Germany)|January 23, 2013
Neuromuscular junction abnormalities in DNM2-related centronuclear myopathyElizabeth M Gibbs, Nigel F Clarke, Kristy Rose, et al.
Brain : a Journal of Neurology|May 26, 2012
Autosomal dominant congenital spinal muscular atrophy: a true form of spinal muscular atrophy caused by early loss of anterior horn cellsEmily C Oates, Stephen Reddel, Michael L Rodriguez, et al.
European Journal of Human Genetics : EJHG|September 4, 2014
Recessive ACTA1 variant causes congenital muscular dystrophy with rigid spineGina L O'Grady, Heather A Best, Emily C Oates, et al.
European Journal of Human Genetics : EJHG|August 31, 2020
Pathogenic deep intronic MTM1 variant activates a pseudo-exon encoding a nonsense codon resulting in severe X-linked myotubular myopathySamantha J Bryen, Emily C Oates, Frances J Evesson, et al.
Annals of Neurology|May 10, 2016
Diagnosis and etiology of congenital muscular dystrophy: We are halfway thereGina L O'Grady, Monkol Lek, Shireen R Lamande, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Communications Biology|May 27, 2026
Deep learning of 777 K bulk transcriptomes reveals human-mouse gene conservation beyond DNA sequence similarityZheng Su, Mingyan Fang, Andrei Smolnikov, et al.
Genome Biology|September 22, 2025
GeneRAIN: multifaceted representation of genes via deep learning of gene expression networksZheng Su, Mingyan Fang, Andrei Smolnikov, et al.
Briefings in Bioinformatics|February 6, 2025
Post-transcriptional regulation supports the homeostatic expression of mature RNAZheng Su, Mingyan Fang, Andrei Smolnikov, et al.
American Journal of Medical Genetics. Part A|February 22, 2013
Young Australian adults with NF1 have poor access to health care, high complication rates, and limited disease knowledgeEmily C Oates, Jonathan M Payne, Sheryl L Foster, et al.
American Journal of Medical Genetics. Part A|December 21, 2013
Longitudinal assessment of cognition and T2-hyperintensities in NF1: an 18-year studyJonathan M Payne, Tania Pickering, Melanie Porter, et al.
Journal of Molecular Medicine (Berlin, Germany)|January 23, 2013
Neuromuscular junction abnormalities in DNM2-related centronuclear myopathyElizabeth M Gibbs, Nigel F Clarke, Kristy Rose, et al.
Brain : a Journal of Neurology|May 26, 2012
Autosomal dominant congenital spinal muscular atrophy: a true form of spinal muscular atrophy caused by early loss of anterior horn cellsEmily C Oates, Stephen Reddel, Michael L Rodriguez, et al.
European Journal of Human Genetics : EJHG|September 4, 2014
Recessive ACTA1 variant causes congenital muscular dystrophy with rigid spineGina L O'Grady, Heather A Best, Emily C Oates, et al.
European Journal of Human Genetics : EJHG|August 31, 2020
Pathogenic deep intronic MTM1 variant activates a pseudo-exon encoding a nonsense codon resulting in severe X-linked myotubular myopathySamantha J Bryen, Emily C Oates, Frances J Evesson, et al.
Annals of Neurology|May 10, 2016
Diagnosis and etiology of congenital muscular dystrophy: We are halfway thereGina L O'Grady, Monkol Lek, Shireen R Lamande, et al.
Pageof 3