Choi BO - Search Results

1

Tonsil-Derived Mesenchymal Stem Cells Differentiate into a Schwann Cell Phenotype and Promote Peripheral Nerve Regeneration.

Jung N, Park S, Choi Y, Park JW, Hong YB, Park HH, Yu Y, Kwak G, Kim HS, Ryu KH, Kim JK, Jo I, Choi BO, Jung SC. Jung N, et al. Among authors: choi bo, choi y. Int J Mol Sci. 2016 Nov 9;17(11):1867. doi: 10.3390/ijms17111867. Int J Mol Sci. 2016. PMID: 27834852 Free PMC article.

2

Common CYP7A1 promoter polymorphism associated with risk of neuromyelitis optica.

Kim HJ, Park HY, Kim E, Lee KS, Kim KK, Choi BO, Kim SM, Bae JS, Lee SO, Chun JY, Park TJ, Cheong HS, Jo I, Shin HD. Kim HJ, et al. Among authors: choi bo. Neurobiol Dis. 2010 Feb;37(2):349-55. doi: 10.1016/j.nbd.2009.10.013. Epub 2009 Oct 20. Neurobiol Dis. 2010. PMID: 19850125

3

Exome sequencing is an efficient tool for genetic screening of Charcot-Marie-Tooth disease.

Choi BO, Koo SK, Park MH, Rhee H, Yang SJ, Choi KG, Jung SC, Kim HS, Hyun YS, Nakhro K, Lee HJ, Woo HM, Chung KW. Choi BO, et al. Among authors: choi kg. Hum Mutat. 2012 Nov;33(11):1610-5. doi: 10.1002/humu.22143. Epub 2012 Jul 5. Hum Mutat. 2012. PMID: 22730194

4

Tonsil-derived mesenchymal stromal cells: evaluation of biologic, immunologic and genetic factors for successful banking.

Ryu KH, Cho KA, Park HS, Kim JY, Woo SY, Jo I, Choi YH, Park YM, Jung SC, Chung SM, Choi BO, Kim HS. Ryu KH, et al. Among authors: choi bo, choi yh. Cytotherapy. 2012 Nov;14(10):1193-202. doi: 10.3109/14653249.2012.706708. Epub 2012 Aug 17. Cytotherapy. 2012. PMID: 22900958

5

Proximal dominant hereditary motor and sensory neuropathy with proximal dominance association with mutation in the TRK-fused gene.

Lee SS, Lee HJ, Park JM, Hong YB, Park KD, Yoo JH, Koo H, Jung SC, Park HS, Lee JH, Lee MG, Hyun YS, Nakhro K, Chung KW, Choi BO. Lee SS, et al. Among authors: choi bo. JAMA Neurol. 2013 May;70(5):607-15. doi: 10.1001/jamaneurol.2013.1250. JAMA Neurol. 2013. PMID: 23553329

6

A novel MYH7 mutation with prominent paraspinal and proximal muscle involvement.

Park JM, Kim YJ, Yoo JH, Hong YB, Park JH, Koo H, Chung KW, Choi BO. Park JM, et al. Among authors: choi bo. Neuromuscul Disord. 2013 Jul;23(7):580-6. doi: 10.1016/j.nmd.2013.04.003. Epub 2013 May 24. Neuromuscul Disord. 2013. PMID: 23707328

7

SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3.

Nakhro K, Park JM, Hong YB, Park JH, Nam SH, Yoon BR, Yoo JH, Koo H, Jung SC, Kim HL, Kim JY, Choi KG, Choi BO, Chung KW. Nakhro K, et al. Among authors: choi kg, choi bo. Neurology. 2013 Jul 9;81(2):165-73. doi: 10.1212/WNL.0b013e31829a3421. Epub 2013 Jun 7. Neurology. 2013. PMID: 23749797

8

Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease.

Kim HJ, Hong YB, Park JM, Choi YR, Kim YJ, Yoon BR, Koo H, Yoo JH, Kim SB, Park M, Chung KW, Choi BO. Kim HJ, et al. Among authors: choi bo, choi yr. Orphanet J Rare Dis. 2013 Jul 12;8:104. doi: 10.1186/1750-1172-8-104. Orphanet J Rare Dis. 2013. PMID: 23844677 Free PMC article.

9

Early-onset severe hereditary sensory and autonomic neuropathy type 1 with S331F SPTLC1 mutation.

Suh BC, Hong YB, Nakhro K, Nam SH, Chung KW, Choi BO. Suh BC, et al. Among authors: choi bo. Mol Med Rep. 2014 Feb;9(2):481-6. doi: 10.3892/mmr.2013.1808. Epub 2013 Nov 18. Mol Med Rep. 2014. PMID: 24247255

10

Exome Sequencing Reveals a Novel PRPS1 Mutation in a Family with CMTX5 without Optic Atrophy.

Park J, Hyun YS, Kim YJ, Nam SH, Kim SH, Hong YB, Park JM, Chung KW, Choi BO. Park J, et al. Among authors: choi bo. J Clin Neurol. 2013 Oct;9(4):283-8. doi: 10.3988/jcn.2013.9.4.283. Epub 2013 Oct 31. J Clin Neurol. 2013. PMID: 24285972 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

753 results

Search Page