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

od Chung, Ki Wha, Kim, Ju Seong, Lee, Kyung Suk
Izdano u Mol Cells (2020)

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

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

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

od Chung, Ki Wha, Yoo, Da Hye, Lee, Soo Jung, Choi, Byung-Ok, Lee, Sang-Soo
Izdano u J Clin Neurol (2016)

Dynamic Transcriptional Events in Distal Sural Nerve Revealed by Transcriptome Analysis

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

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

od Yu, Seon-Mi, Cho, Hongsik, Kim, Gwang-Hoon, Chung, Ki-Wha, Seo, Sung-Yum, Kim, Song-Ja
Izdano u 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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

A Family Harboring CMT1A Duplication and HNPP Deletion

od 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
Izdano 2007

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

od 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
Izdano u BMC Med Genomics (2021)

A MELAS syndrome family harboring two mutations in mitochondrial genome

od 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
Izdano 2008

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

od 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
Izdano 2008

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

od 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
Izdano 2013

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

od 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
Izdano 2010

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

od 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
Izdano 2011