Jang JH - Search Results

1

Identification of two novel COL3A1 variants in patients with vascular Ehlers-Danlos syndrome.

Heo WY, Jang SY, Park TK, Ki CS, Kim JW, Kim DK, Jang JH. Heo WY, et al. Among authors: jang jh, jang sy. Mol Genet Genomic Med. 2023 Sep;11(9):e2240. doi: 10.1002/mgg3.2240. Epub 2023 Jul 17. Mol Genet Genomic Med. 2023. PMID: 37461200 Free PMC article.

2

Peripheral contributions to the mechanical hyperalgesia following a lumbar 5 spinal nerve lesion in rats.

Jang JH, Lee BH, Nam TS, Kim JW, Kim DW, Leem JW. Jang JH, et al. Neuroscience. 2010 Jan 13;165(1):221-32. doi: 10.1016/j.neuroscience.2009.09.082. Epub 2009 Oct 3. Neuroscience. 2010. PMID: 19804816

3

JAK2 V617F and MPL W515L/K mutations in Korean patients with essential thrombocythemia.

Kim HJ, Jang JH, Yoo EH, Kim HJ, Ki CS, Kim JW, Kim SH. Kim HJ, et al. Among authors: jang jh. Korean J Lab Med. 2010 Oct;30(5):474-6. doi: 10.3343/kjlm.2010.30.5.474. Korean J Lab Med. 2010. PMID: 20890078

4

Multiplex ligation-dependent probe amplification assay for diagnosis of congenital adrenal hyperplasia.

Jang JH, Jin DK, Kim JH, Tan HK, Kim JW, Lee SY, Ki CS, Park HD. Jang JH, et al. Ann Clin Lab Sci. 2011 Fall;41(1):44-7. Ann Clin Lab Sci. 2011. PMID: 21325254

5

Streptococcus suis meningitis with bilateral sensorineural hearing loss.

Huh HJ, Park KJ, Jang JH, Lee M, Lee JH, Ahn YH, Kang CI, Ki CS, Lee NY. Huh HJ, et al. Among authors: jang jh. Korean J Lab Med. 2011 Jul;31(3):205-11. doi: 10.3343/kjlm.2011.31.3.205. Epub 2011 Jun 28. Korean J Lab Med. 2011. PMID: 21779197 Free PMC article.

6

Spectra of BRCA1 and BRCA2 mutations in Korean patients with breast cancer: the importance of whole-gene sequencing.

Jang JH, Lee JE, Kwon MJ, Ki CS, Kim JW, Nam SJ, Yang JH. Jang JH, et al. J Hum Genet. 2012 Mar;57(3):212-5. doi: 10.1038/jhg.2011.139. Epub 2012 Jan 5. J Hum Genet. 2012. PMID: 22217648

7

Respiratory viral infections during the first 28 days after transplantation in pediatric hematopoietic stem cell transplant recipients.

Lee JH, Jang JH, Lee SH, Kim YJ, Yoo KH, Sung KW, Lee NY, Ki CS, Koo HH. Lee JH, et al. Among authors: jang jh. Clin Transplant. 2012 Sep-Oct;26(5):736-40. doi: 10.1111/j.1399-0012.2012.01607.x. Epub 2012 Mar 4. Clin Transplant. 2012. PMID: 22385011

8

Identification of clinical mold isolates by sequence analysis of the internal transcribed spacer region, ribosomal large-subunit D1/D2, and β-tubulin.

Jang JH, Lee JH, Ki CS, Lee NY. Jang JH, et al. Ann Lab Med. 2012 Mar;32(2):126-32. doi: 10.3343/alm.2012.32.2.126. Epub 2012 Feb 23. Ann Lab Med. 2012. PMID: 22389879 Free PMC article.

9

Clinical implication of highly sensitive detection of the BRAF V600E mutation in fine-needle aspirations of thyroid nodules: a comparative analysis of three molecular assays in 4585 consecutive cases in a BRAF V600E mutation-prevalent area.

Lee ST, Kim SW, Ki CS, Jang JH, Shin JH, Oh YL, Kim JW, Chung JH. Lee ST, et al. Among authors: jang jh. J Clin Endocrinol Metab. 2012 Jul;97(7):2299-306. doi: 10.1210/jc.2011-3135. Epub 2012 Apr 12. J Clin Endocrinol Metab. 2012. PMID: 22500044

10

Familial Xp22.33-Xp22.12 deletion delineated by chromosomal microarray analysis causes proportionate short stature.

Cho SY, Ki CS, Jang JH, Sohn YB, Park SW, Kim SH, Kim SJ, Jin DK. Cho SY, et al. Among authors: jang jh. Am J Med Genet A. 2012 Jun;158A(6):1462-6. doi: 10.1002/ajmg.a.35357. Epub 2012 May 11. Am J Med Genet A. 2012. PMID: 22581654

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