A. Ko

发表

Heterozygous mutations in cyclic AMP phosphodiesterase-4D (PDE4D) and protein kinase A (PKA) provide new insights into the molecular pathology of acrodysostosis.

N. Niikawa, Jooyoung Lee, K. Joo, 2014, Cellular signalling.

Identification of signal peptide domain SOST mutations in autosomal dominant craniodiaphyseal dysplasia

C. Ki, Y. Sohn, S. Kim, 2011, Human Genetics.

A Korean patient with Morquio B disease with a novel c.13_14insA mutation in the GLB1 gene.

C. Ki, Y. Sohn, H. Park, 2012, Annals of clinical and laboratory science.

Effect of systemic high dose enzyme replacement therapy on the improvement of CNS defects in a mouse model of mucopolysaccharidosis type II

Y. Sohn, Jeehun Lee, D. Jin, 2015, Orphanet Journal of Rare Diseases.

Differential effects of insufflated, subcutaneous, and intravenous growth hormone on bone growth, cognitive function, and NMDA receptor subunit expression.

So Young Park, Y. Sohn, S. Kim, 2010, Endocrinology.

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.

Y. Sohn, Y. Yook, E. Jeon, 2014, Molecular genetics and metabolism.

AAV8-mediated expression of N-acetylglucosamine-1-phosphate transferase attenuates bone loss in a mouse model of mucolipidosis II.

Y. Sohn, S. Kim, Seng H. Cheng, 2016, Molecular genetics and metabolism.

A Liquid Chromatography-Quadrupole-Time-of-Flight Mass Spectrometric Assay for the Quantification of Fabry Disease Biomarker Globotriaosylceramide (GB3) in Fabry Model Mouse

Jinwook Seo, Y. Shin, D. Jin, 2018, Pharmaceutics.

Gene Expression Related to Cognitive Function in Growth Hormone-treated Mice with Prader-Willi Syndrome

A. Ko, 2016 .

A polymorphism in the growth hormone receptor is associated with height in children with Prader–Willi syndrome

Jong-Won Kim, Y. Sohn, J. Kwon, 2011, American journal of medical genetics. Part A.

Auditory characteristics and therapeutic effects of enzyme replacement in mouse model of the mucopolysaccharidosis (MPS) II

Y. Sohn, Myung-Whan Suh, D. Jin, 2012, American journal of medical genetics. Part A.

BGN Mutations in X-Linked Spondyloepimetaphyseal Dysplasia.

Dongsup Kim, W. Park, K. Girisha, 2016, American journal of human genetics.

Improvement of CNS Defects Via Continuous Intrathecal Enzyme Replacement by Osmotic Pump in Mucopolysaccharidosis Type II Mice

Y. Sohn, S. Kim, Jeehun Lee, 2013, American journal of medical genetics. Part A.

Identification of 11 novel mutations in 49 Korean patients with mucopolysaccharidosis type II

C. Ki, Y. Yook, D. Jin, 2012, Clinical genetics.

The feasibility of assessing the diets of minke whale (Balaenoptera acutorostrata) in the East Sea through fatty acid composition in blubber and stable isotopic ratio of skin

Se-Jong Ju, K. Shin, A. Ko, 2016, Ocean Science Journal.

Calpain-mediated Proteolysis of Polycystin-1 C-terminus Induces JAK2 and ERK signal Alterations.

I. So, C. Ahn, H. Park, 2013, Experimental cell research.

Understanding the Nutritional Sources of Gastropods and Anomura from the Mangrove Forest of Weno Island, Micronesia

Se-Jong Ju, Min-Seob Kim, A. Ko, 2013 .

Phase I/II clinical trial of enzyme replacement therapy with idursulfase beta in patients with mucopolysaccharidosis II (Hunter Syndrome)

Y. Sohn, S. Kim, D. Jin, 2013, Orphanet Journal of Rare Diseases.

Enzyme replacement therapy improves joint motion and outcome of the 12‐min walk test in a mucopolysaccharidosis type VI patient previously treated with bone marrow transplantation

Y. Sohn, Jeehun Lee, D. Jin, 2012, American journal of medical genetics. Part A.

Decreased performance in IDUA knockout mouse mimic limitations of joint function and locomotion in patients with Hurler syndrome

J. Kwon, D. Jin, Chihwa Kim, 2015, Orphanet Journal of Rare Diseases.

Thermal effects on the growth and fatty acid composition of four harmful algal bloom species: Possible implications for ichthyotoxicity

S. Jung, Se-Jong Ju, K. Shin, 2016, Ocean Science Journal.

Morphological, molecular, and biochemical characterization of astaxanthin-producing green microalga Haematococcus sp. KORDI03 (Haematococcaceae, Chlorophyta) isolated from Korea.

D. Kang, C. Oh, S. Heo, 2015, Journal of microbiology and biotechnology.

Clinical, biochemical, and genetic analysis of two Korean patients with Trichorhinophalangeal syndrome type I and growth hormone deficiency

C. Ki, Y. Sohn, M. Kwon, 2012, International Journal of Pediatric Endocrinology.

LIN28B polymorphisms are associated with central precocious puberty and early puberty in girls

Jong-Won Kim, Y. Sohn, D. Jin, 2012, Korean journal of pediatrics.

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

Y. Sohn, T. Okuyama, M. Kosuga, 2018, Journal of Inherited Metabolic Disease.

Two novel PEX1 mutations in a patient with Zellweger syndrome: the first Korean case confirmed by biochemical, and molecular evidence.

Y. Sohn, H. Park, D. Jin, 2011, Annals of clinical and laboratory science.

Diet of Chaetognaths Sagitta crassa and S. nagae in the Yellow Sea Inferred from Gut Content and Fatty Acid Analyses

J. Choi, Se-Jong Ju, Jung-Hoon Kang, 2016 .

Comparisons of Feeding Ecology of Euphausia pacifica from Korean Waters Using Lipid Composition

Se-Jong Ju, A. Ko, H. Kim, 2010 .

Stratification of Lipid Content and Composition in Blubber of Marine Cetacean from Korean Waters

Se-Jong Ju, D. Moon, K. Shin, 2011 .

Latitudinal Variation of Nutritional Condition and Diet for Copepod Species , Euchaeta sp . and Pleuromamma spp . , from the Northwest Pacific Ocean Using Lipid Biomarkers

Se-Jong Ju, A. Ko, Chang-rae Lee, 2011 .

Pharmacokinetics, Pharmacodynamics, and Efficacy of a Novel Long-Acting Human Growth Hormone: Fc Fusion Protein.

Y. Sohn, S. Kim, Jinsup Kim, 2015, Molecular pharmaceutics.

High-dose enzyme replacement therapy attenuates cerebroventriculomegaly in a mouse model of mucopolysaccharidosis type II

Y. Sohn, Y. Chang, W. Park, 2013, Journal of Human Genetics.

A study of the relationship between clinical phenotypes and plasma iduronate-2-sulfatase enzyme activities in Hunter syndrome patients

Y. Sohn, Y. Yook, Su-jin Kim, 2012, Korean Journal of Pediatrics.

Five novel mutations of GALNS in Korean patients with mucopolysaccharidosis IVA

C. Ki, Jong-Won Kim, Y. Sohn, 2013, American journal of medical genetics. Part A.

PKD2 gene mutation analysis in Korean autosomal dominant polycystic kidney disease patients using two‐dimensional gene scanning

C. Ahn, K. Oh, Y. Hwang, 2006, Clinical genetics.

A biochemical and physicochemical comparison of two recombinant enzymes used for enzyme replacement therapies of hunter syndrome

Y. Sohn, Y. Yook, D. Jin, 2014, Glycoconjugate Journal.

First record of Sinocorophium homoceratum (Yu, 1938) (Crustacea, Amphipoda, Corophiidae) from Korea

A. Ko, K. Park, Soo-Gun Jo, 2017, Ocean Science Journal.

Mutational spectrum in eight Korean patients with 3‐methylcrotonyl‐CoA carboxylase deficiency

C. Ki, D. Jin, Ch Kim, 2012, Clinical genetics.

Mutations of ACADS gene associated with short-chain acyl-coenzyme A dehydrogenase deficiency.

Y. Sohn, S. Kim, H. Park, 2011, Annals of clinical and laboratory science.

Trophodynamics of euphausiids in the Amundsen Sea during the austral summer by fatty acid and stable isotopic signatures

Se-Jong Ju, E. Yang, Min-Seob Kim, 2016 .

Therapeutic effects of repetitive transcranial magnetic stimulation in an animal model of Parkinson's disease

Sung-Rae Cho, J. Seo, B. Cho, 2013, Brain Research.

Morphological, Molecular, and Biochemical Characterization of Monounsaturated Fatty Acids-Rich Chlamydomonas sp. KIOST-1 Isolated from Korea.

D. Kang, C. Oh, W. Shim, 2015, Journal of microbiology and biotechnology.

Heterozygous mutations in cyclic AMP phosphodiesterase-4D (PDE4D) and protein kinase A (PKA) provide new insights into the molecular pathology of acrodysostosis.

N. Niikawa, Jooyoung Lee, K. Joo, 2014, Cellular signalling.