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K D Kim

Showing results (101-110 of 121) with videos related to

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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.
Experimental & Molecular Medicine|August 6, 2016
Targeted exome sequencing resolves allelic and the genetic heterogeneity in the genetic diagnosis of nephronophthisis-related ciliopathyHee Gyung Kang, Hyun Kyung Lee, Yo Han Ahn, et al.
Journal for Immunotherapy of Cancer|October 20, 2020
Clinical advantage of targeted sequencing for unbiased tumor mutational burden estimation in samples with low tumor purityTae Hee Hong, Hongui Cha, Joon Ho Shim, et al.
American Journal of Human Genetics|May 31, 2016
BGN Mutations in X-Linked Spondyloepimetaphyseal DysplasiaSung Yoon Cho, Jun-Seok Bae, Nayoung K D Kim, et al.
Pageof 13

Showing results (101-110 of 121) with videos related to

Sort By:
Pageof 13
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.
Experimental & Molecular Medicine|August 6, 2016
Targeted exome sequencing resolves allelic and the genetic heterogeneity in the genetic diagnosis of nephronophthisis-related ciliopathyHee Gyung Kang, Hyun Kyung Lee, Yo Han Ahn, et al.
Journal for Immunotherapy of Cancer|October 20, 2020
Clinical advantage of targeted sequencing for unbiased tumor mutational burden estimation in samples with low tumor purityTae Hee Hong, Hongui Cha, Joon Ho Shim, et al.
American Journal of Human Genetics|May 31, 2016
BGN Mutations in X-Linked Spondyloepimetaphyseal DysplasiaSung Yoon Cho, Jun-Seok Bae, Nayoung K D Kim, et al.
Pageof 13