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Yan Ding

Showing results (1451-1460 of 1,465) with videos related to

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Molecular Therapy. Methods & Clinical Development|July 7, 2025
Interlaboratory assessment of candidate reference materials for lentiviral vector copy number and integration site measurementsHua-Jun He, Zhiyong He, Steven P Lund, et al.
BMJ Open|April 2, 2021
Study protocol for the Sino-Canadian Healthy Life Trajectories Initiative (SCHeLTI): a multicentre, cluster-randomised, parallel-group, superiority trial of a multifaceted community-family-mother-child intervention to prevent childhood overweight and obesityYanting Wu, Isabelle Marc, Luigi Bouchard, et al.
American Journal of Human Genetics|August 25, 2022
A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseasesStephen F Kingsmore, Laurie D Smith, Chris M Kunard, et al.
American Journal of Human Genetics|January 26, 2016
Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 MutationsSeema R Lalani, Pengfei Liu, Jill A Rosenfeld, et al.
Maturitas|December 25, 2025
Practice guideline for the treatment and management of iatrogenic premature ovarian insufficiencyXiangyan Ruan, Che Xu, Hefeng Huang, et al.
Science Translational Medicine|April 26, 2019
Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretationMichelle M Clark, Amber Hildreth, Sergey Batalov, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 15, 2024
Human-multimodal deep learning collaboration in 'precise' diagnosis of lupus erythematosus subtypes and similar skin diseasesQianwen Li, Zhi Yang, Kaili Chen, et al.
Nature|November 19, 2015
Hemichordate genomes and deuterostome originsOleg Simakov, Takeshi Kawashima, Ferdinand Marlétaz, et al.
Nature Communications|July 26, 2022
An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseasesMallory J Owen, Sebastien Lefebvre, Christian Hansen, et al.
Science (New York, N.Y.)|May 22, 2010
A catalog of reference genomes from the human microbiome, Karen E Nelson, George M Weinstock, et al.
Pageof 147

Showing results (1451-1460 of 1,465) with videos related to

Sort By:
Pageof 147
Molecular Therapy. Methods & Clinical Development|July 7, 2025
Interlaboratory assessment of candidate reference materials for lentiviral vector copy number and integration site measurementsHua-Jun He, Zhiyong He, Steven P Lund, et al.
BMJ Open|April 2, 2021
Study protocol for the Sino-Canadian Healthy Life Trajectories Initiative (SCHeLTI): a multicentre, cluster-randomised, parallel-group, superiority trial of a multifaceted community-family-mother-child intervention to prevent childhood overweight and obesityYanting Wu, Isabelle Marc, Luigi Bouchard, et al.
American Journal of Human Genetics|August 25, 2022
A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseasesStephen F Kingsmore, Laurie D Smith, Chris M Kunard, et al.
American Journal of Human Genetics|January 26, 2016
Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 MutationsSeema R Lalani, Pengfei Liu, Jill A Rosenfeld, et al.
Maturitas|December 25, 2025
Practice guideline for the treatment and management of iatrogenic premature ovarian insufficiencyXiangyan Ruan, Che Xu, Hefeng Huang, et al.
Science Translational Medicine|April 26, 2019
Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretationMichelle M Clark, Amber Hildreth, Sergey Batalov, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 15, 2024
Human-multimodal deep learning collaboration in 'precise' diagnosis of lupus erythematosus subtypes and similar skin diseasesQianwen Li, Zhi Yang, Kaili Chen, et al.
Nature|November 19, 2015
Hemichordate genomes and deuterostome originsOleg Simakov, Takeshi Kawashima, Ferdinand Marlétaz, et al.
Nature Communications|July 26, 2022
An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseasesMallory J Owen, Sebastien Lefebvre, Christian Hansen, et al.
Science (New York, N.Y.)|May 22, 2010
A catalog of reference genomes from the human microbiome, Karen E Nelson, George M Weinstock, et al.
Pageof 147