Ki CS - Search Results

1

Structural Characteristics and Properties of Cocoon and Regenerated Silk Fibroin from Different Silkworm Strains.

Kim YJ, Kim SW, Kim KY, Ki CS, Um IC. Kim YJ, et al. Among authors: ki cs. Int J Mol Sci. 2023 Mar 4;24(5):4965. doi: 10.3390/ijms24054965. Int J Mol Sci. 2023. PMID: 36902396 Free PMC article.

2

Role of NCKAP1 in the Defective Phagocytic Function of Microglia-Like Cells Derived from Rapidly Progressing Sporadic ALS.

Noh MY, Kwon MS, Oh KW, Nahm M, Park J, Kim YE, Ki CS, Jin HK, Bae JS, Kim SH. Noh MY, et al. Among authors: ki cs. Mol Neurobiol. 2023 Aug;60(8):4761-4777. doi: 10.1007/s12035-023-03339-2. Epub 2023 May 8. Mol Neurobiol. 2023. PMID: 37154887 Free PMC article.

3

Proteolytically degradable PEG hydrogel matrix mimicking tumor immune microenvironment for 3D co-culture of lung adenocarcinoma cells and macrophages.

Lee S, Ki CS. Lee S, et al. Among authors: ki cs. J Biomater Sci Polym Ed. 2023 Oct;34(14):1981-1999. doi: 10.1080/09205063.2023.2204778. Epub 2023 Apr 25. J Biomater Sci Polym Ed. 2023. PMID: 37071065

4

Carrier Frequency and Incidence of MUTYH-Associated Polyposis Based on Database Analysis in East Asians and Koreans.

Park JE, Lee T, Cho EH, Jang MA, Won D, Park B, Ki CS, Kong SY. Park JE, et al. Among authors: ki cs. Ann Lab Med. 2025 Jan 1;45(1):77-84. doi: 10.3343/alm.2024.0242. Epub 2024 Nov 5. Ann Lab Med. 2025. PMID: 39497414 Free PMC article.

5

Prevalence Estimation of the PALB2 Germline Variant in East Asians and Koreans through Population Database Analysis.

Park JE, Kang MC, Lee T, Cho EH, Jang MA, Won D, Park B, Ki CS, Kong SY. Park JE, et al. Among authors: ki cs. Cancers (Basel). 2024 Sep 28;16(19):3318. doi: 10.3390/cancers16193318. Cancers (Basel). 2024. PMID: 39409938 Free PMC article.

6

Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene.

Kim KY, Heo YJ, Ko JM, Lee YA, Shin CH, Ki CS, Lee YJ. Kim KY, et al. Among authors: ki cs. BMC Endocr Disord. 2024 Apr 15;24(1):47. doi: 10.1186/s12902-024-01574-9. BMC Endocr Disord. 2024. PMID: 38622573 Free PMC article.

7

KCNJ3 is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia identified using whole genome sequencing.

Lee WW, Lee CG, Ki CS. Lee WW, et al. Among authors: ki cs. Am J Med Genet B Neuropsychiatr Genet. 2024 Oct;195(7):e32984. doi: 10.1002/ajmg.b.32984. Epub 2024 Apr 10. Am J Med Genet B Neuropsychiatr Genet. 2024. PMID: 38597354

8

Progranulin haploinsufficiency mediates cytoplasmic TDP-43 aggregation with lysosomal abnormalities in human microglia.

Sung W, Noh MY, Nahm M, Kim YS, Ki CS, Kim YE, Kim HJ, Kim SH. Sung W, et al. Among authors: ki cs. J Neuroinflammation. 2024 Feb 13;21(1):47. doi: 10.1186/s12974-024-03039-1. J Neuroinflammation. 2024. PMID: 38347588 Free PMC article.

9

Differentiation, maturation, and collection of THP-1-derived dendritic cells based on a PEG hydrogel culture platform.

Choi J, Ki CS. Choi J, et al. Among authors: ki cs. Biotechnol Lett. 2024 Apr;46(2):235-247. doi: 10.1007/s10529-023-03457-w. Epub 2024 Jan 17. Biotechnol Lett. 2024. PMID: 38231384 Free PMC article.

10

Novel In-Frame Deletion CNOT3 Variant in a Family With Intellectual Developmental Disorder With Speech Delay and Dysmorphic Facies.

Lee CG, Kim HJ, Seol CA, Ki CS. Lee CG, et al. Among authors: ki cs. Neurol Genet. 2024 Jan 3;10(1):e200116. doi: 10.1212/NXG.0000000000200116. eCollection 2024 Feb. Neurol Genet. 2024. PMID: 38179413 Free PMC article.

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