Seo ME[Author] - Search Results

Year	Number of Results
2011	1
2013	1
2017	2
2018	1
2019	1
2020	2
2021	2
2022	1
2023	1
2024	0

1

Flat Pattern Peaks of Tacrolimus Absorption and Associated Pharmacogenomic Variants in Kidney Transplantation Recipients.

Kim SM, Lim Y, Min S, Min BJ, Seo ME, Lee KH, Kim JH, Ha J. Kim SM, et al. Among authors: seo me. J Korean Med Sci. 2022 Feb 7;37(5):e33. doi: 10.3346/jkms.2022.37.e33. J Korean Med Sci. 2022. PMID: 35132839 Free PMC article.

2

Comprehensive in vitro and in silico assessments of metabolic capabilities of 24 genomic variants of CYP2C19 using two different substrates.

Seo ME, Min BJ, Heo N, Lee KH, Kim JH. Seo ME, et al. Front Pharmacol. 2023 Jan 12;14:1055991. doi: 10.3389/fphar.2023.1055991. eCollection 2023. Front Pharmacol. 2023. PMID: 36713839 Free PMC article.

3

APEX1 Polymorphism and Mercaptopurine-Related Early Onset Neutropenia in Pediatric Acute Lymphoblastic Leukemia.

Kim H, Seo H, Park Y, Min BJ, Seo ME, Park KD, Shin HY, Kim JH, Kang HJ. Kim H, et al. Among authors: seo me. Cancer Res Treat. 2018 Jul;50(3):823-834. doi: 10.4143/crt.2017.351. Epub 2017 Sep 4. Cancer Res Treat. 2018. PMID: 28882023 Free PMC article.

4

Unveiling the genetic variation of severe continuous/mixed-type ossification of the posterior longitudinal ligament by whole-exome sequencing and bioinformatic analysis.

Lee CH, Kim KT, Kim CH, Lee EY, Lee SG, Seo ME, Kim JH, Chung CK. Lee CH, et al. Among authors: seo me. Spine J. 2021 Nov;21(11):1847-1856. doi: 10.1016/j.spinee.2021.07.005. Epub 2021 Jul 15. Spine J. 2021. PMID: 34273568

5

Development and Validation of Targeted Gene Sequencing Panel Based Companion Diagnostic for Korean Patients with Solid Tumors.

Min BJ, Lee WS, Seo ME, Lee KH, Jeong SY, Ku JL, Kim YH, Shin SW, Kim JH. Min BJ, et al. Among authors: seo me. Cancers (Basel). 2021 Oct 12;13(20):5112. doi: 10.3390/cancers13205112. Cancers (Basel). 2021. PMID: 34680263 Free PMC article.

6

Homozygote CRIM1 variant is associated with thiopurine-induced neutropenia in leukemic patients with both wildtype NUDT15 and TPMT.

Park Y, Kim H, Seo H, Choi JY, Ma Y, Yun S, Min BJ, Seo ME, Yoo KH, Kang HJ, Im HJ, Kim JH. Park Y, et al. Among authors: seo me. J Transl Med. 2020 Jul 1;18(1):265. doi: 10.1186/s12967-020-02416-7. J Transl Med. 2020. PMID: 32611418 Free PMC article.

7

Evaluation of exome variants using the Ion Proton Platform to sequence error-prone regions.

Seo H, Park Y, Min BJ, Seo ME, Kim JH. Seo H, et al. Among authors: seo me. PLoS One. 2017 Jul 24;12(7):e0181304. doi: 10.1371/journal.pone.0181304. eCollection 2017. PLoS One. 2017. PMID: 28742110 Free PMC article.

8

An interstitial, apparently-balanced chromosomal insertion in the etiology of Langer-Giedion syndrome in an Asian family.

Min BJ, Ko JM, Seo ME, Choi JS, Oh SK, Jeon J, Kim E, Moon JE, Choi IH, Lee C, Kim OH, Cho TJ, Park WY. Min BJ, et al. Among authors: seo me. Eur J Med Genet. 2013 Oct;56(10):561-5. doi: 10.1016/j.ejmg.2013.06.011. Epub 2013 Jul 5. Eur J Med Genet. 2013. PMID: 23832104

9

Star Allele-Based Haplotyping versus Gene-Wise Variant Burden Scoring for Predicting 6-Mercaptopurine Intolerance in Pediatric Acute Lymphoblastic Leukemia Patients.

Park Y, Kim H, Choi JY, Yun S, Min BJ, Seo ME, Im HJ, Kang HJ, Kim JH. Park Y, et al. Among authors: seo me. Front Pharmacol. 2019 Jun 11;10:654. doi: 10.3389/fphar.2019.00654. eCollection 2019. Front Pharmacol. 2019. PMID: 31244663 Free PMC article.

10

Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type.

Min BJ, Kim N, Chung T, Kim OH, Nishimura G, Chung CY, Song HR, Kim HW, Lee HR, Kim J, Kang TH, Seo ME, Yang SD, Kim DH, Lee SB, Kim JI, Seo JS, Choi JY, Kang D, Kim D, Park WY, Cho TJ. Min BJ, et al. Among authors: seo me. Am J Hum Genet. 2011 Dec 9;89(6):760-6. doi: 10.1016/j.ajhg.2011.10.015. Am J Hum Genet. 2011. PMID: 22152677 Free PMC article.

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