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Showing results (531-540 of 565) with videos related to

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Scientific Reports|May 17, 2016
Fast machine-learning online optimization of ultra-cold-atom experimentsP B Wigley, P J Everitt, A van den Hengel, et al.
Genes, Brain, and Behavior|October 3, 2012
Genetic variation in DNMT3B and increased global DNA methylation is associated with suicide attempts in psychiatric patientsT M Murphy, N Mullins, M Ryan, et al.
JMIR Research Protocols|May 5, 2023
Impact of California's Senate Bill 27 on Antimicrobial-Resistant Escherichia coli Urinary Tract Infection in Humans: Protocol for a Study of Methods and Baseline DataAna Florea, Joan A Casey, Keeve Nachman, et al.
Journal of Neurology|February 22, 2019
The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutationsG J Knuiman, B Küsters, L Eshuis, et al.
Human Molecular Genetics|May 1, 2019
MRPS25 mutations impair mitochondrial translation and cause encephalomyopathyEnrico Bugiardini, Alice L Mitchell, Ilaria Dalla Rosa, et al.
Brain : a Journal of Neurology|September 20, 2007
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycanCaroline Godfrey, Emma Clement, Rachael Mein, et al.
Muscle & Nerve|October 4, 2021
Genotype-related respiratory progression in Duchenne muscular dystrophy-A multicenter international studyFederica Trucco, Deborah Ridout, Joana Domingos, et al.
American Journal of Human Genetics|June 14, 2011
A congenital muscular dystrophy with mitochondrial structural abnormalities caused by defective de novo phosphatidylcholine biosynthesisSatomi Mitsuhashi, Aya Ohkuma, Beril Talim, et al.
Nature Communications|November 7, 2022
Specialist multidisciplinary input maximises rare disease diagnoses from whole genome sequencingWilliam L Macken, Micol Falabella, Caroline McKittrick, et al.
Annals of Neurology|September 15, 2010
RYR1 mutations are a common cause of congenital myopathies with central nucleiJ M Wilmshurst, S Lillis, H Zhou, et al.
Pageof 57

Showing results (531-540 of 565) with videos related to

Sort By:
Pageof 57
Scientific Reports|May 17, 2016
Fast machine-learning online optimization of ultra-cold-atom experimentsP B Wigley, P J Everitt, A van den Hengel, et al.
Genes, Brain, and Behavior|October 3, 2012
Genetic variation in DNMT3B and increased global DNA methylation is associated with suicide attempts in psychiatric patientsT M Murphy, N Mullins, M Ryan, et al.
JMIR Research Protocols|May 5, 2023
Impact of California's Senate Bill 27 on Antimicrobial-Resistant Escherichia coli Urinary Tract Infection in Humans: Protocol for a Study of Methods and Baseline DataAna Florea, Joan A Casey, Keeve Nachman, et al.
Journal of Neurology|February 22, 2019
The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutationsG J Knuiman, B Küsters, L Eshuis, et al.
Human Molecular Genetics|May 1, 2019
MRPS25 mutations impair mitochondrial translation and cause encephalomyopathyEnrico Bugiardini, Alice L Mitchell, Ilaria Dalla Rosa, et al.
Brain : a Journal of Neurology|September 20, 2007
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycanCaroline Godfrey, Emma Clement, Rachael Mein, et al.
Muscle & Nerve|October 4, 2021
Genotype-related respiratory progression in Duchenne muscular dystrophy-A multicenter international studyFederica Trucco, Deborah Ridout, Joana Domingos, et al.
American Journal of Human Genetics|June 14, 2011
A congenital muscular dystrophy with mitochondrial structural abnormalities caused by defective de novo phosphatidylcholine biosynthesisSatomi Mitsuhashi, Aya Ohkuma, Beril Talim, et al.
Nature Communications|November 7, 2022
Specialist multidisciplinary input maximises rare disease diagnoses from whole genome sequencingWilliam L Macken, Micol Falabella, Caroline McKittrick, et al.
Annals of Neurology|September 15, 2010
RYR1 mutations are a common cause of congenital myopathies with central nucleiJ M Wilmshurst, S Lillis, H Zhou, et al.
Pageof 57