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K-D Kim

Showing results (91-100 of 114) with videos related to

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The Journal of Molecular Diagnostics : JMD|December 28, 2019
Junction Location Identifier (JuLI): Accurate Detection of DNA Fusions in Clinical Sequencing for Precision OncologyHyun-Tae Shin, Nayoung K D Kim, Jae Won Yun, et al.
Cancers|July 2, 2021
Accurate Prognosis Prediction of Pancreatic Ductal Adenocarcinoma Using Integrated Clinico-Genomic Data of Endoscopic Ultrasound-Guided Fine Needle BiopsyJoo Kyung Park, Hyemin Kim, Dae-Soon Son, et al.
Journal of Clinical Medicine|July 2, 2020
Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental GlomerulosclerosisEujin Park, Chung Lee, Nayoung K D Kim, et al.
Journal of Clinical Medicine|June 10, 2022
Correction: Park et al. Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis. <i>J. Clin. Med.</i> 2020, <i>9</i>, 2013Eujin Park, Chung Lee, Nayoung K D Kim, et al.
Human Mutation|January 17, 2020
POLD1 variants leading to reduced polymerase activity can cause hearing loss without syndromic featuresDoo-Yi Oh, Yoshihiro Matsumoto, Shin-Ichiro Kitajiri, et al.
Translational Oncology|June 9, 2016
Genomic Alterations in Biliary Tract Cancer Using Targeted SequencingKwai Han Yoo, Nayoung K D Kim, Woo Il Kwon, et al.
Journal of Medical Genetics|September 2, 2019
Differential disruption of autoinhibition and defect in assembly of cytoskeleton during cell division decide the fate of human <i>DIAPH1</i>-related cytoskeletopathyBong Jik Kim, Takehiko Ueyama, Takushi Miyoshi, et al.
The Journal of Molecular Diagnostics : JMD|July 26, 2017
A Method to Evaluate the Quality of Clinical Gene-Panel Sequencing Data for Single-Nucleotide Variant DetectionChung Lee, Joon S Bae, Gyu H Ryu, et al.
Oncotarget|December 2, 2016
The implication of FLT3 amplification for FLT targeted therapeutics in solid tumorsSung Hee Lim, Sun-Young Kim, Kyung Kim, et al.
Scientific Reports|November 30, 2017
ATP1A3 mutations can cause progressive auditory neuropathy: a new gene of auditory synaptopathyKyu-Hee Han, Doo-Yi Oh, Seungmin Lee, et al.
Pageof 12

Showing results (91-100 of 114) with videos related to

Sort By:
Pageof 12
The Journal of Molecular Diagnostics : JMD|December 28, 2019
Junction Location Identifier (JuLI): Accurate Detection of DNA Fusions in Clinical Sequencing for Precision OncologyHyun-Tae Shin, Nayoung K D Kim, Jae Won Yun, et al.
Cancers|July 2, 2021
Accurate Prognosis Prediction of Pancreatic Ductal Adenocarcinoma Using Integrated Clinico-Genomic Data of Endoscopic Ultrasound-Guided Fine Needle BiopsyJoo Kyung Park, Hyemin Kim, Dae-Soon Son, et al.
Journal of Clinical Medicine|July 2, 2020
Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental GlomerulosclerosisEujin Park, Chung Lee, Nayoung K D Kim, et al.
Journal of Clinical Medicine|June 10, 2022
Correction: Park et al. Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis. <i>J. Clin. Med.</i> 2020, <i>9</i>, 2013Eujin Park, Chung Lee, Nayoung K D Kim, et al.
Human Mutation|January 17, 2020
POLD1 variants leading to reduced polymerase activity can cause hearing loss without syndromic featuresDoo-Yi Oh, Yoshihiro Matsumoto, Shin-Ichiro Kitajiri, et al.
Translational Oncology|June 9, 2016
Genomic Alterations in Biliary Tract Cancer Using Targeted SequencingKwai Han Yoo, Nayoung K D Kim, Woo Il Kwon, et al.
Journal of Medical Genetics|September 2, 2019
Differential disruption of autoinhibition and defect in assembly of cytoskeleton during cell division decide the fate of human <i>DIAPH1</i>-related cytoskeletopathyBong Jik Kim, Takehiko Ueyama, Takushi Miyoshi, et al.
The Journal of Molecular Diagnostics : JMD|July 26, 2017
A Method to Evaluate the Quality of Clinical Gene-Panel Sequencing Data for Single-Nucleotide Variant DetectionChung Lee, Joon S Bae, Gyu H Ryu, et al.
Oncotarget|December 2, 2016
The implication of FLT3 amplification for FLT targeted therapeutics in solid tumorsSung Hee Lim, Sun-Young Kim, Kyung Kim, et al.
Scientific Reports|November 30, 2017
ATP1A3 mutations can cause progressive auditory neuropathy: a new gene of auditory synaptopathyKyu-Hee Han, Doo-Yi Oh, Seungmin Lee, et al.
Pageof 12