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

by Chung, Ki Wha, Kim, Ju Seong, Lee, Kyung Suk
Published in Mol Cells (2020)

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

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

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

by Chung, Ki Wha, Yoo, Da Hye, Lee, Soo Jung, Choi, Byung-Ok, Lee, Sang-Soo
Published in J Clin Neurol (2016)

Dynamic Transcriptional Events in Distal Sural Nerve Revealed by Transcriptome Analysis

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

Berberine induces dedifferentiation by actin cytoskeleton reorganization via phosphoinositide 3-kinase/Akt and p38 kinase pathways in rabbit articular chondrocytes

by Yu, Seon-Mi, Cho, Hongsik, Kim, Gwang-Hoon, Chung, Ki-Wha, Seo, Sung-Yum, Kim, Song-Ja
Published in Exp Biol Med (Maywood) (2016)

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

by Park, Saeyoung, Jung, Namhee, Myung, Seoha, Choi, Yoonyoung, Chung, Ki Wha, Choi, Byung-Ok, Jung, Sung-Chul
Published in Int J Mol Sci (2018)

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

by Lee, Su Jeong, Kanwal, Sumaira, Yoo, Da Hye, Park, Hye Ri, Choi, Byung-Ok, Chung, Ki Wha
Published in J Clin Neurol (2019)

African American Hypertensive Nephropathy Maps to a New Locus on Chromosome 9q31-q32

by Chung, Ki Wha, Ferrell, Robert E., Ellis, Demetrius, Barmada, Michael, Moritz, Michael, Finegold, David N., Jaffe, Ronald, Vats, Abhay
Published 2003

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

by Kanwal, Sumaira, Yoo, Da Hye, Tahir, Shahzad, Lee, Su Jung, Lee, Min Hee, Choi, Byung-Ok, Chung, Ki Wha
Published in J Clin Neurol (2018)

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

by Choi, Ye Ji, Hyun, Young Se, Nam, Soo Hyun, Koo, Heasoo, Hong, Young Bin, Chung, Ki Wha, Choi, Byung-Ok
Published in J Clin Neurol (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...

by Won, So Yeon, Kwon, Soojin, Jeong, Hui Su, Chung, Ki Wha, Choi, Byung‐Ok, Chang, Jong Wook, Lee, Ji Eun
Published in Stem Cells (2020)

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

by Nam, Soo Hyun, Hong, Young Bin, Hyun, Young Se, Nam, Da Eun, Kwak, Geon, Hwang, Sun Hee, Choi, Byung-Ok, Chung, Ki Wha
Published in Mol Cells (2016)

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

by Park, Hyung Jun, Choi, Young-Chul, Kim, Seung Min, Kim, Se Hoon, Hong, Young Bin, Yoon, Bo Ram, Chung, Ki Wha, Choi, Byung-Ok
Published in J Clin Neurol (2015)

A Family Harboring CMT1A Duplication and HNPP Deletion

by 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
Published 2007

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

by 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
Published in BMC Med Genomics (2021)

A MELAS syndrome family harboring two mutations in mitochondrial genome

by Choi, Byung-Ok, Hwang, Jung Hee, Kim, Joonki, Cho, Eun Min, Cho, Sun Young, Hwang, Su Jin, Lee, Hyang Woon, Kim, Song Ja, Chung, Ki Wha
Published 2008

Distal hereditary motor neuropathy in Korean patients with a small heat shock protein 27 mutation

by Chung, Ki Wha, Kim, Sang-Beom, Cho, Sun Young, Hwang, Su Jin, Park, Sun Wha, Kang, Sung Hee, Kim, Joonki, Yoo, Jeong Hyun, Choi, Byung-Ok
Published 2008

Exome Sequencing Reveals a Novel PRPS1 Mutation in a Family with CMTX5 without Optic Atrophy

by Park, Jin, Hyun, Young Se, Kim, Ye Jin, Nam, Soo Hyun, Kim, Sung-hee, Hong, Young Bin, Park, Jin-Mo, Chung, Ki Wha, Choi, Byung-Ok
Published 2013

Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases

by Choi, Byung-Ok, Hwang, Jung Hee, Cho, Eun Min, Jeong, Eun Hye, Hyun, Young Se, Jeon, Hyeon Jeong, Seong, Ki Min, Cho, Nam Soo, Chung, Ki Wha
Published 2010

A Large Population Genetic Study of 15 Autosomal Short Tandem Repeat Loci for Establishment of Korean DNA Profile Database

by Yoo, Seong Yeon, Cho, Nam Soo, Park, Myung Jin, Seong, Ki Min, Hwang, Jung Ho, Song, Seok Bean, Han, Myun Soo, Lee, Won Tae, Chung, Ki Wha
Published 2011