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

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

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

door Kwon, Joo Young, Chung, Ki Wha, Park, Eun Kyung, Park, Sun Wha, Choi, Byung-Ok
Gepubliceerd in 2009

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

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

Dynamic Transcriptional Events in Distal Sural Nerve Revealed by Transcriptome Analysis

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

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

door Yu, Seon-Mi, Cho, Hongsik, Kim, Gwang-Hoon, Chung, Ki-Wha, Seo, Sung-Yum, Kim, Song-Ja
Gepubliceerd 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

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

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

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

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

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

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

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

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

door Choi, Ye Ji, Hyun, Young Se, Nam, Soo Hyun, Koo, Heasoo, Hong, Young Bin, Chung, Ki Wha, Choi, Byung-Ok
Gepubliceerd 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...

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

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

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

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

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

A Family Harboring CMT1A Duplication and HNPP Deletion

door 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
Gepubliceerd in 2007

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

door 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
Gepubliceerd in BMC Med Genomics (2021)

A MELAS syndrome family harboring two mutations in mitochondrial genome

door 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
Gepubliceerd in 2008

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

door 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
Gepubliceerd in 2008

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

door 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
Gepubliceerd in 2013

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

door 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
Gepubliceerd in 2010

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

door 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
Gepubliceerd in 2011