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

ανά Chung, Ki Wha, Kim, Ju Seong, Lee, Kyung Suk
Τόπος έκδοσης Mol Cells (2020)

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

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

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

ανά Chung, Ki Wha, Yoo, Da Hye, Lee, Soo Jung, Choi, Byung-Ok, Lee, Sang-Soo
Τόπος έκδοσης J Clin Neurol (2016)

Dynamic Transcriptional Events in Distal Sural Nerve Revealed by Transcriptome Analysis

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

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

ανά Yu, Seon-Mi, Cho, Hongsik, Kim, Gwang-Hoon, Chung, Ki-Wha, Seo, Sung-Yum, Kim, Song-Ja
Τόπος έκδοσης 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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

A Family Harboring CMT1A Duplication and HNPP Deletion

ανά 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
Έκδοση 2007

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

ανά 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
Τόπος έκδοσης BMC Med Genomics (2021)

A MELAS syndrome family harboring two mutations in mitochondrial genome

ανά 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
Έκδοση 2008

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

ανά 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
Έκδοση 2008

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

ανά 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
Έκδοση 2013

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

ανά 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
Έκδοση 2010

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

ανά 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
Έκδοση 2011