Song SM - Search Results

1

Activating mutation of GS alpha in McCune-Albright syndrome causes skin pigmentation by tyrosinase gene activation on affected melanocytes.

Kim IS, Kim ER, Nam HJ, Chin MO, Moon YH, Oh MR, Yeo UC, Song SM, Kim JS, Uhm MR, Beck NS, Jin DK. Kim IS, et al. Among authors: song sm. Horm Res. 1999;52(5):235-40. doi: 10.1159/000023467. Horm Res. 1999. PMID: 10844413

2

Morphologic evaluation and integrin expression profile of renal tubular cells cultured from percutaneous renal biopsy specimen.

Kim JS, Hwang HZ, Yeo SH, Ko SW, Song SM, Kim YK, Kim DJ, Oh HY, Choi HY, Kim MK, Toru S, Kohsaka T, Kim Y, Jin DK. Kim JS, et al. Among authors: song sm. Ren Fail. 2001 Jan;23(1):21-9. doi: 10.1081/jdi-100001280. Ren Fail. 2001. PMID: 11256526 Free article.

3

A simple method for the detection of neurologic disorders associated with CAG repeat expansion using PCR-microtiter plate hybridization.

Lee Y, Oh MR, Kim CH, Hwang HZ, Kim JS, Song SM, Jin DK. Lee Y, et al. Among authors: song sm. J Biotechnol. 2002 May 23;95(3):215-23. doi: 10.1016/s0168-1656(02)00024-x. J Biotechnol. 2002. PMID: 12007862 Clinical Trial.

4

Correlation between fasting plasma ghrelin levels and age, body mass index (BMI), BMI percentiles, and 24-hour plasma ghrelin profiles in Prader-Willi syndrome.

Paik KH, Jin DK, Song SY, Lee JE, Ko SH, Song SM, Kim JS, Oh YJ, Kim SW, Lee SH, Kim SH, Kwon EK, Choe YH. Paik KH, et al. Among authors: song sy, song sm. J Clin Endocrinol Metab. 2004 Aug;89(8):3885-9. doi: 10.1210/jc.2003-032137. J Clin Endocrinol Metab. 2004. PMID: 15292322

5

Frequency of spinocerebellar ataxia types 1,2,3,6,7 and dentatorubral pallidoluysian atrophy mutations in Korean patients with spinocerebellar ataxia.

Jin DK, Oh MR, Song SM, Koh SW, Lee M, Kim GM, Lee WY, Chung CS, Lee KH, Im JH, Lee MJ, Kim JW, Lee MS. Jin DK, et al. Among authors: song sm. J Neurol. 1999 Mar;246(3):207-10. doi: 10.1007/s004150050335. J Neurol. 1999. PMID: 10323319

6

Mutational spectrum of the iduronate 2 sulfatase gene in 25 unrelated Korean Hunter syndrome patients: identification of 13 novel mutations.

Kim CH, Hwang HZ, Song SM, Paik KH, Kwon EK, Moon KB, Yoon JH, Han CK, Jin DK. Kim CH, et al. Among authors: song sm. Hum Mutat. 2003 Apr;21(4):449-50. doi: 10.1002/humu.9128. Hum Mutat. 2003. PMID: 12655569

7

Identification of mutations in the GNPTA (MGC4170) gene coding for GlcNAc-phosphotransferase alpha/beta subunits in Korean patients with mucolipidosis type II or type IIIA.

Paik KH, Song SM, Ki CS, Yu HW, Kim JS, Min KH, Chang SH, Yoo EJ, Lee IJ, Kwan EK, Han SJ, Jin DK. Paik KH, et al. Among authors: song sm. Hum Mutat. 2005 Oct;26(4):308-14. doi: 10.1002/humu.20205. Hum Mutat. 2005. PMID: 16116615

8

Frequency analysis and clinical characterization of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Korean patients.

Lee WY, Jin DK, Oh MR, Lee JE, Song SM, Lee EA, Kim GM, Chung JS, Lee KH. Lee WY, et al. Among authors: song sm. Arch Neurol. 2003 Jun;60(6):858-63. doi: 10.1001/archneur.60.6.858. Arch Neurol. 2003. PMID: 12810491 Clinical Trial.

9

Mutational analysis of the alpha-L-iduronidase gene in 10 unrelated Korean type I mucopolysaccharidosis patients: Identification of four novel mutations.

Lee IJ, Hwang SH, Jeon BH, Song SM, Kim JS, Paik KH, Kwon EK, Jin DK. Lee IJ, et al. Among authors: song sm. Clin Genet. 2004 Dec;66(6):575-6. doi: 10.1111/j.1399-0004.2004.00374.x. Clin Genet. 2004. PMID: 15521993 No abstract available.

10

Stereoselective synthesis of geminal bromofluoroalkenes by kinetically controlled selective conversion of oxaphosphetane intermediates.

Jin J, Song SM, Choi JH, Chung WJ. Jin J, et al. Among authors: song sm. Sci Adv. 2024 Nov;10(44):eadq5316. doi: 10.1126/sciadv.adq5316. Epub 2024 Oct 30. Sci Adv. 2024. PMID: 39475612 Free article.

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