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 no Mol Cells (2020)

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 em 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 no J Clin Neurol (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 em 2014

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

Por Yu, Seon-Mi, Cho, Hongsik, Kim, Gwang-Hoon, Chung, Ki-Wha, Seo, Sung-Yum, Kim, Song-Ja
Publicado no 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

Por Park, Saeyoung, Jung, Namhee, Myung, Seoha, Choi, Yoonyoung, Chung, Ki Wha, Choi, Byung-Ok, Jung, Sung-Chul
Publicado no Int J Mol Sci (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 no J Clin Neurol (2019)

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

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

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 no J Clin Neurol (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 no 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...

Por Won, So Yeon, Kwon, Soojin, Jeong, Hui Su, Chung, Ki Wha, Choi, Byung‐Ok, Chang, Jong Wook, Lee, Ji Eun
Publicado no Stem Cells (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 no Mol Cells (2016)

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 no J Clin Neurol (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 em 2007

A MELAS syndrome family harboring two mutations in mitochondrial genome

Por 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
Publicado em 2008

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

Por 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
Publicado em 2008

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

Por 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
Publicado em 2013

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

Por 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
Publicado em 2010

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

Por 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
Publicado em 2011

miR-27a and miR-449b polymorphisms associated with a risk of idiopathic recurrent pregnancy loss

Por Rah, HyungChul, Chung, Ki Wha, Ko, Ki Han, Kim, Eun Sun, Kim, Jung Oh, Sakong, Jung Hyun, Kim, Ji Hyang, Lee, Woo Sik, Kim, Nam Keun
Publicado no PLoS One (2017)