Targeted recombination of homologous chromosomes using CRISPR‐Cas9

por Son, Wonseok, Chung, Ki Wha
Publicado 2023

A Database of Caenorhabditis elegans Locomotion and Body Posture Phenotypes for the Peripheral Neuropathy Model

por Chung, Ki Wha, Kim, Ju Seong, Lee, Kyung Suk
Publicado 2020

Wide Phenotypic Spectrum of PNMHH Patients With p.R941L Mutation in MYH14

por Kwon, Hye Mi, Park, Jin Hee, Chung, Ki Wha, Choi, Byung-Ok
Publicado 2022

Enhancement of the CRISPR/Cas9-Based Genome Editing System in Lettuce (Lactuca sativa L.) Using the Endogenous U6 Promoter

por Riu, Young-Sun, Kim, Gwang Hoon, Chung, Ki Wha, Kong, Sam-Geun
Publicado 2023

Charcot-Marie-Tooth 1A Concurrent with Schwannomas of the Spinal Cord and Median Nerve

por Kwon, Joo Young, Chung, Ki Wha, Park, Eun Kyung, Park, Sun Wha, Choi, Byung-Ok
Publicado 2009

A Large Dominant Myotonia Congenita Family with a V1293I Mutation in SCN4A

por Chung, Ki Wha, Yoo, Da Hye, Lee, Soo Jung, Choi, Byung-Ok, Lee, Sang-Soo
Publicado 2016

Dynamic Transcriptional Events in Distal Sural Nerve Revealed by Transcriptome Analysis

por Hong, Young Bin, Jung, Sung-Chul, Lee, Jinho, Moon, Heui-Soo, Chung, Ki Wha, Choi, Byung-Ok
Publicado 2014

Differentiation of Human Tonsil-Derived Mesenchymal Stem Cells into Schwann-Like Cells Improves Neuromuscular Function in a Mouse Model of Charcot-Marie-Tooth Disease Type 1A

por Park, Saeyoung, Jung, Namhee, Myung, Seoha, Choi, Yoonyoung, Chung, Ki Wha, Choi, Byung-Ok, Jung, Sung-Chul
Publicado 2018

A POLG2 Homozygous Mutation in an Autosomal Recessive Epilepsy Family Without Ophthalmoplegia

por Lee, Su Jeong, Kanwal, Sumaira, Yoo, Da Hye, Park, Hye Ri, Choi, Byung-Ok, Chung, Ki Wha
Publicado 2019

Therapeutic Potential of CKD-504, a Novel Selective Histone Deacetylase 6 Inhibitor, in a Zebrafish Model of Neuromuscular Junction Disorders

por Jeong, Hui Su, Kim, Hye Jin, Kim, Deok-Ho, Chung, Ki Wha, Choi, Byung-Ok, Lee, Ji Eun
Publicado 2022

Microsatellite Dataset for Cultivar Discrimination in Spring Orchid (Cymbidium goeringii)

por Nam, Da Eun, Cha, Min Ju, Kim, Yae Dam, Awasthi, Manisha, Do, Yuno, Kong, Sam-Geun, Chung, Ki Wha
Publicado 2023

A Novel Nonsense Mutation in Leucine-Rich, Glioma-Inactivated-1 Gene as the Underlying Cause of Familial Temporal Lobe Epilepsy

por Kanwal, Sumaira, Yoo, Da Hye, Tahir, Shahzad, Lee, Su Jung, Lee, Min Hee, Choi, Byung-Ok, Chung, Ki Wha
Publicado 2018

Novel Compound Heterozygous Nonsense PRX Mutations in a Korean Dejerine-Sottas Neuropathy Family

por Choi, Ye Ji, Hyun, Young Se, Nam, Soo Hyun, Koo, Heasoo, Hong, Young Bin, Chung, Ki Wha, Choi, Byung-Ok
Publicado 2015

Fibulin 5, a human Wharton's jelly‐derived mesenchymal stem cells‐secreted paracrine factor, attenuates peripheral nervous system myelination defects through the Integrin‐RAC1 sign...

por Won, So Yeon, Kwon, Soojin, Jeong, Hui Su, Chung, Ki Wha, Choi, Byung‐Ok, Chang, Jong Wook, Lee, Ji Eun
Publicado 2020

Identification of Genetic Causes of Inherited Peripheral Neuropathies by Targeted Gene Panel Sequencing

por Nam, Soo Hyun, Hong, Young Bin, Hyun, Young Se, Nam, Da Eun, Kwak, Geon, Hwang, Sun Hee, Choi, Byung-Ok, Chung, Ki Wha
Publicado 2016

Peripheral Myelin Protein 22 Gene Mutations in Charcot-Marie-Tooth Disease Type 1E Patients

por Jung, Na Young, Kwon, Hye Mi, Nam, Da Eun, Tamanna, Nasrin, Lee, Ah Jin, Kim, Sang Beom, Choi, Byung-Ok, Chung, Ki Wha
Publicado 2022

Molecular Genetic Diagnosis of a Bethlem Myopathy Family with an Autosomal-Dominant COL6A1 Mutation, as Evidenced by Exome Sequencing

por Park, Hyung Jun, Choi, Young-Chul, Kim, Seung Min, Kim, Se Hoon, Hong, Young Bin, Yoon, Bo Ram, Chung, Ki Wha, Choi, Byung-Ok
Publicado 2015

A Family Harboring CMT1A Duplication and HNPP Deletion

por Lee, Jung Hwa, Kang, Hee Jin, Song, Hyunseok, Hwang, Su Jin, Cho, Sun-Young, Kim, Sang-Beom, Kim, Joonki, Chung, Ki Wha, Choi, Byung-Ok
Publicado 2007

Novel homozygous mutations in Pakistani families with Charcot–Marie–Tooth disease

por Kanwal, Sumaira, Choi, Yu JIn, Lim, Si On, Choi, Hee Ji, Park, Jin Hee, Nuzhat, Rana, khan, Aneela, Perveen, Shazia, Choi, Byung-Ok, Chung, Ki Wha
Publicado 2021

Genetic and Clinical Studies of Peripheral Neuropathies with Three Small Heat Shock Protein Gene Variants in Korea

por Lim, Si On, Jung, Na Young, Lee, Ah Jin, Choi, Hee Ji, Kwon, Hye Mi, Son, Wonseok, Nam, Soo Hyun, Choi, Byung-Ok, Chung, Ki Wha
Publicado 2022