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Grace Yoon

Showing results (101-110 of 177) with videos related to

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The British Journal of Dermatology|November 23, 2024
Genome sequencing reveals novel IKBKG structural variants associated with incontinentia pigmentiNeta Pipko, Rachel Youjin Oh, Aiyana Kaplan, et al.
Bioinformatics (Oxford, England)|July 1, 2016
Estimating and testing high-dimensional mediation effects in epigenetic studiesHaixiang Zhang, Yinan Zheng, Zhou Zhang, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|May 11, 2021
Subchondral Bone Length in Knee Osteoarthritis: A Deep Learning-Derived Imaging Measure and Its Association With Radiographic and Clinical OutcomesGary H Chang, Lisa K Park, Nina A Le, et al.
Movement Disorders Clinical Practice|May 12, 2026
Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case-Series and Literature ReviewSangeetha Yoganathan, Laura Tochen, Jacky Ganguly, et al.
American Journal of Medical Genetics. Part A|August 14, 2012
A novel nonsense CDK5RAP2 mutation in a Somali child with primary microcephaly and sensorineural hearing lossAlistair T Pagnamenta, Jennie E Murray, Grace Yoon, et al.
Nature Communications|May 20, 2024
Homozygous EPRS1 missense variant causing hypomyelinating leukodystrophy-15 alters variant-distal mRNA m<sup>6</sup>A site accessibilityDebjit Khan, Iyappan Ramachandiran, Kommireddy Vasu, et al.
Brain : a Journal of Neurology|December 12, 2017
POLR3A variants in hereditary spastic paraplegia and ataxiaLaurence Gauquelin, Martine Tétreault, Isabelle Thiffault, et al.
International Journal of Innovative Research in Medical Science|October 16, 2023
Evidence For Cannabidiol Modulation of Serotonergic Transmission in a Model of Osteoarthritis via <i>in vivo</i> PET Imaging and Behavioral AssessmentYu-Shin Ding, Jiacheng Wang, Vinay Kumar, et al.
Human Molecular Genetics|December 23, 2020
De Novo variants in EEF2 cause a neurodevelopmental disorder with benign external hydrocephalusMaria J Nabais Sá, Alexandra N Olson, Grace Yoon, et al.
Neurology|July 11, 2022
Natural History of Friedreich Ataxia: Heterogeneity of Neurologic Progression and Consequences for Clinical Trial DesignChristian Rummey, Louise A Corben, Martin Delatycki, et al.
Pageof 18

Showing results (101-110 of 177) with videos related to

Sort By:
Pageof 18
The British Journal of Dermatology|November 23, 2024
Genome sequencing reveals novel IKBKG structural variants associated with incontinentia pigmentiNeta Pipko, Rachel Youjin Oh, Aiyana Kaplan, et al.
Bioinformatics (Oxford, England)|July 1, 2016
Estimating and testing high-dimensional mediation effects in epigenetic studiesHaixiang Zhang, Yinan Zheng, Zhou Zhang, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|May 11, 2021
Subchondral Bone Length in Knee Osteoarthritis: A Deep Learning-Derived Imaging Measure and Its Association With Radiographic and Clinical OutcomesGary H Chang, Lisa K Park, Nina A Le, et al.
Movement Disorders Clinical Practice|May 12, 2026
Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case-Series and Literature ReviewSangeetha Yoganathan, Laura Tochen, Jacky Ganguly, et al.
American Journal of Medical Genetics. Part A|August 14, 2012
A novel nonsense CDK5RAP2 mutation in a Somali child with primary microcephaly and sensorineural hearing lossAlistair T Pagnamenta, Jennie E Murray, Grace Yoon, et al.
Nature Communications|May 20, 2024
Homozygous EPRS1 missense variant causing hypomyelinating leukodystrophy-15 alters variant-distal mRNA m<sup>6</sup>A site accessibilityDebjit Khan, Iyappan Ramachandiran, Kommireddy Vasu, et al.
Brain : a Journal of Neurology|December 12, 2017
POLR3A variants in hereditary spastic paraplegia and ataxiaLaurence Gauquelin, Martine Tétreault, Isabelle Thiffault, et al.
International Journal of Innovative Research in Medical Science|October 16, 2023
Evidence For Cannabidiol Modulation of Serotonergic Transmission in a Model of Osteoarthritis via <i>in vivo</i> PET Imaging and Behavioral AssessmentYu-Shin Ding, Jiacheng Wang, Vinay Kumar, et al.
Human Molecular Genetics|December 23, 2020
De Novo variants in EEF2 cause a neurodevelopmental disorder with benign external hydrocephalusMaria J Nabais Sá, Alexandra N Olson, Grace Yoon, et al.
Neurology|July 11, 2022
Natural History of Friedreich Ataxia: Heterogeneity of Neurologic Progression and Consequences for Clinical Trial DesignChristian Rummey, Louise A Corben, Martin Delatycki, et al.
Pageof 18