Jin DK - 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: jin dk. Horm Res. 1999;52(5):235-40. doi: 10.1159/000023467. Horm Res. 1999. PMID: 10844413

2

Six novel mutations of the fibrillin-1 gene in Korean patients with Marfan syndrome.

Oh MR, Kim JS, Beck NS, Yoo HW, Lee HJ, Kohsaka T, Jin DK. Oh MR, et al. Among authors: jin dk. Pediatr Int. 2000 Oct;42(5):488-91. doi: 10.1046/j.1442-200x.2000.01268.x. Pediatr Int. 2000. PMID: 11059536

3

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: jin dk. Ren Fail. 2001 Jan;23(1):21-9. doi: 10.1081/jdi-100001280. Ren Fail. 2001. PMID: 11256526 Free article.

4

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: jin dk. J Biotechnol. 2002 May 23;95(3):215-23. doi: 10.1016/s0168-1656(02)00024-x. J Biotechnol. 2002. PMID: 12007862 Clinical Trial.

5

CAG repeats of CTG18.1 and KCNN3 in Korean patients with bipolar affective disorder.

Jin DK, Hwang HZ, Oh MR, Kim JS, Lee M, Kim S, Lim SW, Seo MY, Kim JH, Kim DK. Jin DK, et al. J Affect Disord. 2001 Sep;66(1):19-24. doi: 10.1016/s0165-0327(00)00291-3. J Affect Disord. 2001. PMID: 11532529

6

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. J Neurol. 1999 Mar;246(3):207-10. doi: 10.1007/s004150050335. J Neurol. 1999. PMID: 10323319

7

IgE-mediated anaphylaxis and allergic reactions to idursulfase in patients with Hunter syndrome.

Kim J, Park MR, Kim DS, Lee JO, Maeng SH, Cho SY, Han Y, Ahn K, Jin DK. Kim J, et al. Among authors: jin dk. Allergy. 2013 Jun;68(6):796-802. doi: 10.1111/all.12155. Epub 2013 Apr 29. Allergy. 2013. PMID: 23621439

8

Transcriptional regulation of PDGF-A and TGF-beta by +KTS WT1 deletion mutants and a mutant mimicking Denys-Drash syndrome.

Jin DK, Kang SJ, Kim SJ, Bang EH, Hwang HZ, Tadokoro K, Yamada M, Kohsaka T. Jin DK, et al. Ren Fail. 1999 Nov;21(6):685-94. doi: 10.3109/08860229909094162. Ren Fail. 1999. PMID: 10586431 Free article.

9

Relationships of cell proliferation and expression of integrin subunits and type I collagen in skin fibroblasts with renal lesions in patients with IDDM.

Jin DK, Kim Y, Mauer M, Fioretto P, Vats A, Fish AJ. Jin DK, et al. Am J Kidney Dis. 1998 Feb;31(2):293-300. doi: 10.1053/ajkd.1998.v31.pm9469500. Am J Kidney Dis. 1998. PMID: 9469500

10

Novel mutations of the PKD1 gene in Korean patients with autosomal dominant polycystic kidney disease.

Kim UK, Jin DK, Ahn C, Shin JH, Lee KB, Kim SH, Chae JJ, Hwang DY, Lee JG, Namkoong Y, Lee CC. Kim UK, et al. Among authors: jin dk. Mutat Res. 2000 Feb;432(1-2):39-45. doi: 10.1016/s1383-5726(99)00013-8. Mutat Res. 2000. PMID: 10729710

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