Mi-hyun Park

Chungcheongbuk Do, Republic of Korea

Last Updated: 09/26/2026

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Found 17 publications

Simple differentiation method using FBS identifies DUSP6 as a marker for fine-tuning of FGF-ERK signaling activity in human pluripotent stem cells.

Simple differentiation method using FBS identifies DUSP6 as a marker for fine-tuning of FGF-ERK signaling activity in human pluripotent stem cells.

Journal: Biochemical and biophysical research communications
Published: September 18, 2019

Generation of a PDX1-EGFP reporter human induced pluripotent stem cell line, KSCBi005-A-3, using the CRISPR/Cas9 system.

Generation of a PDX1-EGFP reporter human induced pluripotent stem cell line, KSCBi005-A-3, using the CRISPR/Cas9 system.

Journal: Stem cell research
Published: September 06, 2019

Optimized detection of insertions/deletions (INDELs) in whole-exome sequencing data.

Optimized detection of insertions/deletions (INDELs) in whole-exome sequencing data.

Journal: PloS one
Published: February 23, 2017

Discovery of CDH23 as a Significant Contributor to Progressive Postlingual Sensorineural Hearing Loss in Koreans.

Discovery of CDH23 as a Significant Contributor to Progressive Postlingual Sensorineural Hearing Loss in Koreans.

Journal: PloS one
Published: August 14, 2016

Mimulone-induced autophagy through p53-mediated AMPK/mTOR pathway increases caspase-mediated apoptotic cell death in A549 human lung cancer cells.

Mimulone-induced autophagy through p53-mediated AMPK/mTOR pathway increases caspase-mediated apoptotic cell death in A549 human lung cancer cells.

Journal: PloS one
Published: July 02, 2014

Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.

Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.

Journal: BMC medical genetics
Published: December 23, 2013

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

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

Journal: Neurogenetics
Published: December 19, 2013

Patterns of gene expression associated with Pten deficiency in the developing inner ear.

Patterns of gene expression associated with Pten deficiency in the developing inner ear.

Journal: PloS one
Published: September 27, 2013

Comprehensive analysis to improve the validation rate for single nucleotide variants detected by next-generation sequencing.

Comprehensive analysis to improve the validation rate for single nucleotide variants detected by next-generation sequencing.

Journal: PloS one
Published: September 06, 2013

Influence of the vitrification solution on the angiogenic factors in vitrificated mouse ovarian tissue.

Influence of the vitrification solution on the angiogenic factors in vitrificated mouse ovarian tissue.

Journal: Obstetrics & gynecology science
Published: April 12, 2013

Identification of a genetic locus on chromosome 4q34-35 for type 2 diabetes with overweight.

Identification of a genetic locus on chromosome 4q34-35 for type 2 diabetes with overweight.

Journal: Experimental & molecular medicine
Published: February 09, 2013

Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families.

Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families.

Journal: BMC medical genetics
Published: January 08, 2013
Showing 1-12 of 17

Last Updated: 09/26/2026