Ko AR - Search Results

1

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

Park SW, Shin S, Kim CH, Ko AR, Kwak MJ, Nam MH, Park SY, Kim SJ, Sohn YB, Galinsky RE, Kim H, Yeo Y, Jin DK. Park SW, et al. Among authors: ko ar. Endocrinology. 2010 Sep;151(9):4418-27. doi: 10.1210/en.2010-0152. Epub 2010 Jul 7. Endocrinology. 2010. PMID: 20610568

2

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

Kim SJ, Kwak HH, Cho SY, Sohn YB, Park SW, Huh R, Kim J, Ko AR, Jin DK. Kim SJ, et al. Among authors: ko ar. Mol Pharm. 2015 Oct 5;12(10):3759-65. doi: 10.1021/acs.molpharmaceut.5b00550. Epub 2015 Sep 21. Mol Pharm. 2015. PMID: 26370910

3

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

Park SW, Lee ST, Sohn YB, Kim SH, Cho SY, Ko AR, Ji ST, Kwon JY, Yeau S, Paik KH, Kim JW, Jin DK. Park SW, et al. Among authors: ko ar. Am J Med Genet A. 2011 Dec;155A(12):2970-3. doi: 10.1002/ajmg.a.34309. Epub 2011 Nov 3. Am J Med Genet A. 2011. PMID: 22052808

4

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

Ko AR, Jin DK, Cho SY, Park SW, Przybylska M, Yew NS, Cheng SH, Kim JS, Kwak MJ, Kim SJ, Sohn YB. Ko AR, et al. Mol Genet Metab. 2016 Apr;117(4):447-55. doi: 10.1016/j.ymgme.2016.02.001. Epub 2016 Feb 3. Mol Genet Metab. 2016. PMID: 26857995

5

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

Kim SH, Park HD, Sohn YB, Park SW, Cho SY, Ji S, Kim SJ, Choi EW, Kim CH, Ko AR, Yeau S, Paik KH, Jin DK. Kim SH, et al. Among authors: ko ar. Ann Clin Lab Sci. 2011 Fall;41(1):84-8. Ann Clin Lab Sci. 2011. PMID: 21325261

6

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

Cho SY, Chang YP, Park JY, Park HD, Sohn YB, Park SW, Kim SH, Ji S, Kim SJ, Choi EW, Kim CH, Ko AR, Paik KH, Jin DK. Cho SY, et al. Among authors: ko ar. Ann Clin Lab Sci. 2011 Spring;41(2):182-7. Ann Clin Lab Sci. 2011. PMID: 21844578

7

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

Sohn YB, Park HD, Park SW, Kim SH, Cho SY, Ko AR, Ki CS, Yeau S, Jin DK. Sohn YB, et al. Among authors: ko ar. Ann Clin Lab Sci. 2012 Winter;42(1):89-93. Ann Clin Lab Sci. 2012. PMID: 22371915

8

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

Park SW, Lee ST, Sohn YB, Cho SY, Kim SH, Kim SJ, Kim CH, Ko AR, Paik KH, Kim JW, Jin DK. Park SW, et al. Among authors: ko ar. Korean J Pediatr. 2012 Oct;55(10):388-92. doi: 10.3345/kjp.2012.55.10.388. Epub 2012 Oct 29. Korean J Pediatr. 2012. PMID: 23133486 Free PMC article.

9

Five novel mutations of GALNS in Korean patients with mucopolysaccharidosis IVA.

Park HD, Ko AR, Ki CS, Lee SY, Kim JW, Cho SY, Kim SH, Park SW, Sohn YB, Jin DK. Park HD, et al. Among authors: ko ar. Am J Med Genet A. 2013 Mar;161A(3):509-17. doi: 10.1002/ajmg.a.35298. Epub 2013 Feb 8. Am J Med Genet A. 2013. PMID: 23401410

10

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

Cho SY, Lee J, Ko AR, Kwak MJ, Kim S, Sohn YB, Park SW, Jin DK. Cho SY, et al. Among authors: ko ar. Orphanet J Rare Dis. 2015 Oct 31;10:141. doi: 10.1186/s13023-015-0356-0. Orphanet J Rare Dis. 2015. PMID: 26520066 Free PMC article.

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