Ah-ra Ko
Seoul, 135710, Republic of Korea
Last Updated: 09/26/2026
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Found 19 publications
A Liquid Chromatography-Quadrupole-Time-of-Flight Mass Spectrometric Assay for the Quantification of Fabry Disease Biomarker Globotriaosylceramide (GB3) in Fabry Model Mouse.
Journal: Pharmaceutics
Published: April 16, 2018
The efficacy of intracerebroventricular idursulfase-beta enzyme replacement therapy in mucopolysaccharidosis II murine model: heparan sulfate in cerebrospinal fluid as a clinical biomarker of neuropathology.
Journal: Journal of inherited metabolic disease
Published: November 03, 2017
BGN Mutations in X-Linked Spondyloepimetaphyseal Dysplasia.
Journal: American journal of human genetics
Published: December 19, 2015
AAV8-mediated expression of N-acetylglucosamine-1-phosphate transferase attenuates bone loss in a mouse model of mucolipidosis II.
Journal: Molecular genetics and metabolism
Published: November 24, 2015
Pharmacokinetics, Pharmacodynamics, and Efficacy of a Novel Long-Acting Human Growth Hormone: Fc Fusion Protein.
Journal: Molecular pharmaceutics
Published: September 16, 2015
Decreased performance in IDUA knockout mouse mimic limitations of joint function and locomotion in patients with Hurler syndrome.
Journal: Orphanet journal of rare diseases
Published: July 08, 2015
Effect of systemic high dose enzyme replacement therapy on the improvement of CNS defects in a mouse model of mucopolysaccharidosis type II.
Journal: Orphanet journal of rare diseases
Published: July 08, 2015
Morphological, Molecular, and Biochemical Characterization of Monounsaturated Fatty Acids-Rich Chlamydomonas sp. KIOST-1 Isolated from Korea.
Journal: Journal of microbiology and biotechnology
Published: March 05, 2015
Morphological, molecular, and biochemical characterization of astaxanthin-producing green microalga Haematococcus sp. KORDI03 (Haematococcaceae, Chlorophyta) isolated from Korea.
Journal: Journal of microbiology and biotechnology
Published: November 11, 2014
Heterozygous mutations in cyclic AMP phosphodiesterase-4D (PDE4D) and protein kinase A (PKA) provide new insights into the molecular pathology of acrodysostosis.
Journal: Cellular signalling
Published: June 14, 2014
Improvement of cardiac function by short-term enzyme replacement therapy in a murine model of cardiomyopathy associated with Hunter syndrome evaluated by serial echocardiography with speckle tracking 2-D strain analysis.
Journal: Molecular genetics and metabolism
Published: March 10, 2014
A biochemical and physicochemical comparison of two recombinant enzymes used for enzyme replacement therapies of hunter syndrome.
Journal: Glycoconjugate journal
Published: August 30, 2013
Last Updated: 09/26/2026