Y. Hong

发表

Cytokines secreted by mesenchymal stem cells reduce demyelination in an animal model of Charcot-Marie-Tooth disease.

Myoung-Woo Lee, H. Jeon, H. Kim, 2022, Biochemical and biophysical research communications.

Application of differentiated human tonsil–derived stem cells to trembler‐J mice

G. Kwak, Byung-Ok Choi, Y. Hong, 2018, Muscle & nerve.

Clinical characterization and genetic analysis of Korean patients with X‐linked Charcot‐Marie‐Tooth disease type 1

Byung-Ok Choi, Y. Hong, K. Chung, 2017, Journal of the peripheral nervous system : JPNS.

Charcot‐Marie‐Tooth Disease Type 4H Resulting from Compound Heterozygous Mutations in FGD4 from Nonconsanguineous Korean Families

Deok‐Ho Kim, H. Koo, H. Kim, 2015, Annals of human genetics.

Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease

H. Koo, Byung-Ok Choi, Y. Hong, 2013, Orphanet Journal of Rare Diseases.

HDAC6 Inhibitors Rescued the Defective Axonal Mitochondrial Movement in Motor Neurons Derived from the Induced Pluripotent Stem Cells of Peripheral Neuropathy Patients with HSPB1 Mutation

Hyunjung Choi, I. Mook‐Jung, Byung-Ok Choi, 2016, Stem cells international.

HDAC 6 Inhibitors Rescued the Defective Axonal Mitochondrial Movement in Motor Neurons Derived from the Induced Pluripotent Stem Cells of Peripheral Neuropathy Patients with HSPB 1 Mutation

Hyunjung Choi, I. Mook‐Jung, Byung-Ok Choi, 2016 .

Overexpression of mutant HSP27 causes axonal neuropathy in mice

G. Kwak, Byung-Ok Choi, Y. Hong, 2015, Journal of Biomedical Science.

Farnesol Ameliorates Demyelinating Phenotype in a Cellular and Animal Model of Charcot-Marie-Tooth Disease Type 1A

H. Kim, H. Doo, G. Kwak, 2021, Current issues in molecular biology.

Human HSPB1 mutation recapitulates features of distal hereditary motor neuropathy (dHMN) in Drosophila.

H. Koh, Byung-Ok Choi, Y. Hong, 2019, Biochemical and biophysical research communications.

Distal hereditary motor neuropathy type 7B with Dynactin 1 mutation.

Byung-Ok Choi, Y. Hong, K. Chung, 2016, Molecular medicine reports.

ADSSL1 mutation relevant to autosomal recessive adolescent onset distal myopathy

Ji Eun Lee, H. Kim, Won Min Mo, 2016, Annals of neurology.

Phenotypic heterogeneity in patients with NEFL‐related Charcot–Marie–Tooth disease

H. Kim, Y. Hong, Hyun Su Kim, 2022, Molecular genetics & genomic medicine.

A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy

H. Koo, G. Kwak, Won Min Mo, 2016, PLoS genetics.

p75 and neural cell adhesion molecule 1 can identify pathologic Schwann cells in peripheral neuropathies

Se Hoon Kim, Byung-Ok Choi, Y. Hong, 2019, Annals of clinical and translational neurology.

Pmp22 mutant allele-specific siRNA alleviates demyelinating neuropathic phenotype in vivo

E. Chang, G. Kwak, Won Min Mo, 2017, Neurobiology of Disease.

Clinico-genetics in Korean Charcot-Marie-Tooth disease type 2Z with MORC2 mutations.

Byung-Ok Choi, Y. Hong, Y. S. Hyun, 2016, Brain : a journal of neurology.

Genotype–phenotype correlation of Charcot-Marie-Tooth type 1E patients with PMP22 mutations

Byung-Ok Choi, Y. Hong, K. Chung, 2016, Genes & Genomics.

A compound heterozygous mutation in HADHB gene causes an axonal Charcot-Marie-tooth disease

H. Koo, Byung-Ok Choi, Y. Hong, 2013, BMC Medical Genetics.

DGAT2 Mutation in a Family with Autosomal‐Dominant Early‐Onset Axonal Charcot‐Marie‐Tooth Disease

J. Kim, Ji Eun Lee, H. Koo, 2016, Human mutation.

Aminosalicylic acid reduces ER stress and Schwann cell death induced by MPZ mutations

H. Doo, E. Chang, Won Min Mo, 2019, International journal of molecular medicine.

Development of cell models for high-throughput screening system of Charcot-Marie-Tooth disease type 1

Byung-Ok Choi, Y. Hong, S. Yoo, 2015 .

Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1

H. Koo, Byung-Ok Choi, Y. Hong, 2016, Molecular medicine reports.

Null variants in DYSF result in earlier symptom onset

Y. Hong, J. Hong, S. M. Kim, 2020, Clinical genetics.

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

G. Kwak, Byung-Ok Choi, Y. Hong, 2016, Molecules and cells.

Tonsil-Derived Mesenchymal Stem Cells Differentiate into a Schwann Cell Phenotype and Promote Peripheral Nerve Regeneration

G. Kwak, Byung-Ok Choi, Y. Hong, 2016, International journal of molecular sciences.

Overexpression of mutant HSP27 causes axonal neuropathy in mice

G. Kwak, Byung-Ok Choi, Y. Hong, 2015, Journal of Biomedical Science.

Gene Therapy Options as New Treatment for Inherited Peripheral Neuropathy

Byung-Ok Choi, Y. Hong, N. Park, 2020, Experimental neurobiology.

Genotype–phenotype correlation of Charcot-Marie-Tooth type 1E patients with PMP22 mutations

Byung-Ok Choi, Y. Hong, K. Chung, 2016, Genes & Genomics.

A novel MYH7 mutation with prominent paraspinal and proximal muscle involvement

H. Koo, Byung-Ok Choi, Y. Hong, 2013, Neuromuscular Disorders.

Erratum to: Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease

H. Koo, Byung-Ok Choi, Y. Hong, 2013, Orphanet Journal of Rare Diseases.

X‐linked Charcot‐Marie‐Tooth disease type 6 (CMTX6) patients with a p.R158H mutation in the pyruvate dehydrogenase kinase isoenzyme 3 gene

Byung-Ok Choi, Y. Hong, Anna H. Siddell, 2016, Journal of the peripheral nervous system : JPNS.

Proximal dominant hereditary motor and sensory neuropathy with proximal dominance association with mutation in the TRK-fused gene.

Min Goo Lee, J. Lee, H. Koo, 2013, JAMA neurology.

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

H. Koo, Byung-Ok Choi, Y. Hong, 2014, Journal of clinical neurology.

Distal Myopathy with Rimmed Vacuoles Confirmed by Whole Exome Sequencing

Hyun Seok Song, H. Kim, Byung-Ok Choi, 2014 .

Small heat shock protein B3 (HSPB3) mutation in an axonal Charcot‐Marie‐Tooth disease family

Byung-Ok Choi, Y. Hong, K. Chung, 2018, Journal of the peripheral nervous system : JPNS.

Ser135Phe mutation in HSPB1 (HSP27) from Charcot–Marie–Tooth disease type 2F families

H. Kim, Byung-Ok Choi, Y. Hong, 2015, Genes & Genomics.

A novel INF2 mutation in a Korean family with autosomal dominant intermediate Charcot‐Marie‐Tooth disease and focal segmental glomerulosclerosis

H. Kim, Byung-Ok Choi, Y. Hong, 2014, Journal of the peripheral nervous system : JPNS.

A family with axonal sensorimotor polyneuropathy with TUBB3 mutation.

Ji Hoon Park, H. Koo, Byung-Ok Choi, 2015, Molecular medicine reports.

A novel homozygous MPV17 mutation in two families with axonal sensorimotor polyneuropathy

H. Koo, Byung-Ok Choi, Y. Hong, 2015, BMC Neurology.

Gait parameters as tools for analyzing phenotypic alterations of a mouse model of Charcot-Marie-Tooth disease

H. Jeon, E. Chang, G. Kwak, 2021, Animal cells and systems.

Targeted PMP22 TATA-box editing by CRISPR/Cas9 reduces demyelinating neuropathy of Charcot-Marie-Tooth disease type 1A in mice

Seokjoong Kim, H. Doo, G. Kwak, 2019, Nucleic acids research.

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

Byung-Ok Choi, Y. Hong, K. Chung, 2014, Journal of clinical neurology.

Early-onset severe hereditary sensory and autonomic neuropathy type 1 with S331F SPTLC1 mutation.

Byung-Ok Choi, Y. Hong, B. Suh, 2014, Molecular medicine reports.

SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3

H. Koo, Byung-Ok Choi, Y. Hong, 2013, Neurology.

PINK1 and Parkin Ameliorate the Loss of Motor Activity and Mitochondrial Dysfunction Induced by Peripheral Neuropathy-Associated HSPB8 Mutants in Drosophila Models

H. Koh, J. Yun, Byung-Ok Choi, 2023, Biomedicines.

Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy

H. Koo, Byung-Ok Choi, Y. Hong, 2014, neurogenetics.

Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy

H. Koo, Y. Hong, K. Chung, 2014, neurogenetics.

Cerebral white matter abnormalities in patients with charcot‐marie‐tooth disease

Chang-hyun Park, Byung-Ok Choi, Y. Hong, 2017, Annals of neurology.

miR-381 Attenuates Peripheral Neuropathic Phenotype Caused by Overexpression of PMP22

H. Kim, G. Kwak, Byung-Ok Choi, 2019, Experimental neurobiology.

Dynamic Transcriptional Events in Distal Sural Nerve Revealed by Transcriptome Analysis

Byung-Ok Choi, Y. Hong, H. Moon, 2014, Experimental neurobiology.

Ultrasonography-guided transplantation facilitates perineural delivery of stem cells

Byung-Ok Choi, Y. Hong, Sang-beom Kim, 2015 .

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

Byung-Ok Choi, Y. Hong, Sung-Hee Kim, 2013, Journal of clinical neurology.

Transcriptional control of motor pool formation and motor circuit connectivity by the LIM-HD protein Isl2

Y. Kosodo, Y. Hong, Byung-ok Choi, 2022, bioRxiv.

PINK1 and Parkin rescue motor defects and mitochondria dysfunction induced by a patient-derived HSPB3 mutant in Drosophila models

H. Koh, Y. Hong, Ji Eun Han, 2023, Biochemical and Biophysical Research Communications.